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Subject Areas on Research
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2-Methylbutyryl-coenzyme A dehydrogenase deficiency: a new inborn error of L-isoleucine metabolism.
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440-kD ankyrinB: structure of the major developmentally regulated domain and selective localization in unmyelinated axons.
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A 6-Mb high-resolution physical and transcription map encompassing the hereditary prostate cancer 1 (HPC1) region.
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A B-cell-homing chemokine made in lymphoid follicles activates Burkitt's lymphoma receptor-1.
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A CaMK cascade activates CRE-mediated transcription in neurons of Caenorhabditis elegans.
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A blood group-related polymorphism of CD44 abolishes a hyaluronan-binding consensus sequence without preventing hyaluronan binding.
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A comparative analysis of the information content in long and short SAGE libraries.
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A comparison of methods for RNA extraction from lymphocytes for RT-PCR.
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A critical role of STAYGREEN/Mendel's I locus in controlling disease symptom development during Pseudomonas syringae pv tomato infection of Arabidopsis.
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A critical role of two positively charged amino acids in the Jas motif of Arabidopsis JAZ proteins in mediating coronatine- and jasmonoyl isoleucine-dependent interactions with the COI1 F-box protein.
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A feedback loop in the polo-like kinase activation pathway.
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A homozygous 5 base-pair deletion in exon 10 of the adenosine deaminase (ADA) gene in a child with severe combined immunodeficiency and very low levels of ADA mRNA and protein.
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A human protein related to yeast Cdc6p.
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A large-scale functional approach to uncover human genes and pathways in Drosophila.
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A major role for the EP4 receptor in regulation of renin.
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A member of a family of sulfate-activating enzymes causes murine brachymorphism.
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A membrane-associated progesterone-binding protein, 25-Dx, is regulated by progesterone in brain regions involved in female reproductive behaviors.
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A method for analysis of gene expression patterns.
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A missense mutation in exon 4 of the human adenosine deaminase gene causes severe combined immunodeficiency.
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A mutation in a mitochondrial transmembrane protein is responsible for the pleiotropic hematological and skeletal phenotype of flexed-tail (f/f) mice.
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A novel alternative splice domain in zebrafish tenascin-C.
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A novel leptin receptor isoform in rat.
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A patient with Ehlers-Danlos syndrome type VI is a compound heterozygote for mutations in the lysyl hydroxylase gene.
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A phosphorylated cytoplasmic autoantigen, GW182, associates with a unique population of human mRNAs within novel cytoplasmic speckles.
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A proteomics approach to the identification of mammalian mitochondrial small subunit ribosomal proteins.
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A role for Cdc2- and PP2A-mediated regulation of Emi2 in the maintenance of CSF arrest.
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A sea urchin genome project: sequence scan, virtual map, and additional resources.
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A single amino acid change in the para sodium channel protein is associated with knockdown-resistance (kdr) to pyrethroid insecticides in German cockroach.
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A single amino acid defines cross-species reactivity of tree shrew (Tupaia belangeri) CD1d to human invariant natural killer T (iNKT) cells.
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A spontaneous, recurrent mutation in divalent metal transporter-1 exposes a calcium entry pathway.
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A truncated isoform of c-Mpl with an essential C-terminal peptide targets the full-length receptor for degradation.
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A whole-genome analysis of premature termination codons.
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AMPK and substrate availability regulate creatine transport in cultured cardiomyocytes.
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Activation of MEF2 by muscle activity is mediated through a calcineurin-dependent pathway.
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Adenosine deaminase deficiency in adults.
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Adenovirus-mediated delivery into myocytes of muscle glycogen phosphorylase, the enzyme deficient in patients with glycogen-storage disease type V.
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Adenovirus-mediated transfer of CCAAT/enhancer-binding protein-alpha identifies a dominant antiproliferative role for this isoform in hepatocytes.
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Agonist-dependent recruitment of phosphoinositide 3-kinase to the membrane by beta-adrenergic receptor kinase 1. A role in receptor sequestration.
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Akt-directed glucose metabolism can prevent Bax conformation change and promote growth factor-independent survival.
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Alteration of the alkaloid profile in genetically modified tobacco reveals a role of methylenetetrahydrofolate reductase in nicotine N-demethylation.
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Alternative splicing of the BSC1 gene generates tissue-specific isoforms in the German cockroach.
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Amplification of cDNA ends based on template-switching effect and step-out PCR.
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An Arabidopsis thaliana lipoxygenase gene can be induced by pathogens, abscisic acid, and methyl jasmonate.
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An alternative splice form of Mdm2 induces p53-independent cell growth and tumorigenesis.
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An analysis of alternatively spliced CD45 mRNA transcripts during T cell maturation in humans.
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Analysis of erythropoietin and erythropoietin receptor genes expression in cattle during acute infection with Trypanosoma congolense.
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Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs.
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Angiogenesis-like activity of endothelial cells co-cultured with VEGF-producing smooth muscle cells.
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Angiotensin converting enzyme and genetic hypertension: cloning of rat cDNAs and characterization of the enzyme.
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Antiidiotypic antibody recognizes an amiloride binding domain within the alpha subunit of the epithelial Na+ channel.
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Antisense repression in Cryptococcus neoformans as a laboratory tool and potential antifungal strategy.
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Arabidopsis cDNA sequence encoding myrosinase.
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Arsenite transport by mammalian aquaglyceroporins AQP7 and AQP9.
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Assignment of hexokinase types 1,2,3 (Hk1,2,3) and glucokinase (Gck) to rat chromosome band 20q11, 4q34, 17q12 and 14q21 respectively, by in situ hybridization.
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Assignment of the human beta-adducin gene (ADD2) to 2p13-p14 by in situ hybridization.
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Atrial chamber-specific expression of sarcolipin is regulated during development and hypertrophic remodeling.
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BMPs induce dermal markers and ectopic feather tracts.
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BP1, a homeodomain-containing isoform of DLX4, represses the beta-globin gene.
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BP1, a new homeobox gene, is frequently expressed in acute leukemias.
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Bioinformatic design of A-kinase anchoring protein-in silico: a potent and selective peptide antagonist of type II protein kinase A anchoring.
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Bone morphogenetic protein 8A plays a role in the maintenance of spermatogenesis and the integrity of the epididymis.
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Brief report: hepatic dysfunction as a complication of adenosine deaminase deficiency.
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CD19 maps to a region of conservation between human chromosome 16 and mouse chromosome 7.
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CFTR as a cAMP-dependent regulator of sodium channels.
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CHST1 and CHST2 sulfotransferase expression by vascular endothelial cells regulates shear-resistant leukocyte rolling via L-selectin.
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CX3CR1 tyrosine sulfation enhances fractalkine-induced cell adhesion.
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Cadherin-11 expressed in association with mesenchymal morphogenesis in the head, somite, and limb bud of early mouse embryos.
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Cadherin-6 expression transiently delineates specific rhombomeres, other neural tube subdivisions, and neural crest subpopulations in mouse embryos.
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Calmodulin mediates Ca2+ sensitivity of sodium channels.
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Cardiovascular genomics: estimating the total number of genes expressed in the human cardiovascular system.
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Cell binding specificity of mouse R-cadherin and chromosomal mapping of the gene.
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Characterization of a new family of protein kinases from Arabidopsis containing phosphoinositide 3/4-kinase and ubiquitin-like domains.
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Characterization of a rat type 2 angiotensin II receptor stably expressed in 293 cells.
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Characterization of cis-regulatory regions responsible for developmental regulation of the gibberellin biosynthetic gene GA1 in Arabidopsis thaliana
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Characterization of deltamethrin metabolism by rat plasma and liver microsomes.
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Characterization of the G protein-coupled receptor kinase GRK4. Identification of four splice variants.
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Characterization of the mouse transforming growth factor alpha gene: its expression during eyelid development and in waved 1 tissues.
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Characterization of the role of cadherin in regulating cell adhesion during sea urchin development.
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Chicken perinatal troponin Ts are generated by a combination of novel and phylogenetically conserved alternative splicing pathways.
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Chromosomal distribution of the human cardiovascular transcriptome.
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Circadian clock-controlled genes isolated from Neurospora crassa are late night- to early morning-specific.
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Circulating PIG-A mutant T lymphocytes in healthy adults and patients with bone marrow failure syndromes.
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Cloning and characterization of ATRAP, a novel protein that interacts with the angiotensin II type 1 receptor.
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Cloning and characterization of SLP3: a novel member of the stomatin family expressed by olfactory receptor neurons.
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Cloning and characterization of a cAMP-specific cyclic nucleotide phosphodiesterase.
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Cloning and characterization of a mammalian lithium-sensitive bisphosphate 3'-nucleotidase inhibited by inositol 1,4-bisphosphate.
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Cloning and characterization of developmental endothelial locus-1: an embryonic endothelial cell protein that binds the alphavbeta3 integrin receptor.
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Cloning of a cDNA encoding bovine erythropoietin and analysis of its transcription in selected tissues.
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Cloning of an aquaporin homologue present in water channel containing endosomes of toad urinary bladder.
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Cloning of cDNA and analysis of the gene for mouse angiotensin II type 2 receptor.
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Cloning of human and mouse brain cDNAs coding for S1, the second member of the mammalian elongation factor-1 alpha gene family: analysis of a possible evolutionary pathway.
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Cloning of rat thymic stromal lymphopoietin receptor (TSLPR) and characterization of genomic structure of murine Tslpr gene.
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Cloning, expression, and cellular localization of a human prenylcysteine lyase.
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Clustered charged amino acids of human adenosine deaminase comprise a functional epitope for binding the adenosine deaminase complexing protein CD26/dipeptidyl peptidase IV.
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Co-amplification of a novel cyclophilin-like gene (PPIE) with L-myc in small cell lung cancer cell lines.
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Common promoter elements in odorant and vomeronasal receptor genes.
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Comparative analysis of the zeta-crystallin/quinone reductase gene in guinea pig and mouse.
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Complementary techniques: RNA amplification for gene profiling analysis.
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Components of a calmodulin-dependent protein kinase cascade. Molecular cloning, functional characterization and cellular localization of Ca2+/calmodulin-dependent protein kinase kinase beta.
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Computational and experimental analyses reveal previously undetected coding exons of the KRIT1 (CCM1) gene.
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Conformation-assisted inhibition of protein-tyrosine phosphatase-1B elicits inhibitor selectivity over T-cell protein-tyrosine phosphatase.
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Constitutive activation of the aromatic hydrocarbon receptor.
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Constitutive expression of CaSRP1, a hot pepper small rubber particle protein homolog, resulted in fast growth and improved drought tolerance in transgenic Arabidopsis plants.
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Construction and characterization of infectious cDNA clones of enterovirus 71 (EV71).
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Construction of cDNA libraries from small amounts of total RNA using the suppression PCR effect.
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Coordinated activation of corneal wound response genes in vivo as observed by in situ hybridization.
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Correction of aberrant splicing of the cystic fibrosis transmembrane conductance regulator (CFTR) gene by antisense oligonucleotides.
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Cross-clade inhibition of HIV-1 replication and cytopathology by using RNase P-associated external guide sequences.
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Cyclic AMP mediated GSTP1 gene activation in tumor cells involves the interaction of activated CREB-1 with the GSTP1 CRE: a novel mechanism of cellular GSTP1 gene regulation.
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Cysteine-rich regions of pig gastric mucin contain von willebrand factor and cystine knot domains at the carboxyl terminal(1).
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Cytokines in murine lyme carditis: Th1 cytokine expression follows expression of proinflammatory cytokines in a susceptible mouse strain.
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DNA methyltransferase levels and altered CpG methylation in the total genome and in the GSTP1 gene in human glioma cells transfected with sense and antisense DNA methyltransferase cDNA.
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DNA patents and diagnostics: not a pretty picture.
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DNA replication checkpoint control of Wee1 stability by vertebrate Hsl7.
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Decreased expression of lysyl hydroxylase 2 (LH2) in skin fibroblasts from three Ehlers-Danlos patients does not result from mutations in either the coding or proximal promoter region of the LH2 gene.
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Deep-RACE: Comprehensive Search for Novel ncRNAs Associated to a Specific Locus.
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Design of a novel small peptide targeted against a tumor-specific receptor.
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Different transcript patterns in response to specialist and generalist herbivores in the wild Arabidopsis relative Boechera divaricarpa.
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Differential effects of overexpressed glucokinase and hexokinase I in isolated islets. Evidence for functional segregation of the high and low Km enzymes.
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Differential expression of S1 and elongation factor-1 alpha during rat development.
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Differential expression of mitochondrial DNA replication factors in mammalian tissues.
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Differential expression of p63 isoforms in female reproductive organs.
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Differential gene expression patterns in HER2/neu-positive and -negative breast cancer cell lines and tissues.
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Differential screening of a human chromosome 3 library identifies hepatocyte growth factor-like/macrophage-stimulating protein and its receptor in injured lung. Possible implications for neuroendocrine cell survival.
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Differential screening of a subtracted cDNA library: a method to search for genes preferentially expressed in multiple tissues.
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Digital image analysis for rapid quantification of total RNA and cDNA for SMART-PCR.
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Dimerized Drosophila myosin VIIa: a processive motor.
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Direct interactions between autoantigen La and human immunodeficiency virus leader RNA.
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Direct reprogramming of cardiac fibroblasts to cardiomyocytes using microRNAs.
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Distinct beta-arrestin- and G protein-dependent pathways for parathyroid hormone receptor-stimulated ERK1/2 activation.
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Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene.
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Drosophila as a model for the identification of genes causing adult human heart disease.
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Drosophila p120catenin plays a supporting role in cell adhesion but is not an essential adherens junction component.
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Dual action of TGF-beta1 on nasal-polyp derived fibroblasts.
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Early elicitor induction in members of a novel multigene family coding for highly related RING-H2 proteins in Arabidopsis thaliana
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Early specialization of the superfast myosin in extraocular and laryngeal muscles.
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Effects of ligand and thyroid hormone receptor isoforms on hepatic gene expression profiles of thyroid hormone receptor knockout mice.
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Ehlers-Danlos syndrome type VI results from a nonsense mutation and a splice site-mediated exon-skipping mutation in the lysyl hydroxylase gene.
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Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1.
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Engineering DNA vaccines via co-delivery of co-stimulatory molecule genes.
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Enhanced inhibition of neointimal hyperplasia by genetically engineered endothelial progenitor cells.
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Equalizing cDNA subtraction based on selective suppression of polymerase chain reaction: cloning of Jurkat cell transcripts induced by phytohemaglutinin and phorbol 12-myristate 13-acetate.
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Erbin is a protein concentrated at postsynaptic membranes that interacts with PSD-95.
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Essential light chain of Drosophila nonmuscle myosin II.
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Evidence for a disease-resistance pathway in rice similar to the NPR1-mediated signaling pathway in Arabidopsis.
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Evidence for independent recruitment of zeta-crystallin/quinone reductase (CRYZ) as a crystallin in camelids and hystricomorph rodents.
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Evolution of regeneration and fission in annelids: insights from engrailed- and orthodenticle-class gene expression.
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Evolution of the 12 kDa FK506-binding protein gene.
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Ex vivo pediatric brain tumors express Fas (CD95) and FasL (CD95L) and are resistant to apoptosis induction.
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Exercise stimulates Pgc-1alpha transcription in skeletal muscle through activation of the p38 MAPK pathway.
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Exon 10b of the NF1 gene represents a mutational hotspot and harbors a recurrent missense mutation Y489C associated with aberrant splicing.
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Exploring the role of the beta-adrenergic receptor kinase in cardiac disease using gene-targeted mice.
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Expressed sequence tag analysis in Cycas, the most primitive living seed plant.
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Expression cloning of type 2 angiotensin II receptor reveals a unique class of seven-transmembrane receptors.
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Expression of a constitutively active Ca2+/calmodulin-dependent kinase in Aspergillus nidulans spores prevents germination and entry into the cell cycle.
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Expression of five selected human mismatch repair genes simultaneously detected in normal and cancer cell lines by a nonradioactive multiplex reverse transcription-polymerase chain reaction.
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Expression of full-length and truncated dystrophin mini-genes in transgenic mdx mice.
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Expression of glucokinase in cultured human muscle cells confers insulin-independent and glucose concentration-dependent increases in glucose disposal and storage.
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Expression of matrix metalloproteinase 1 in rodents: comment on the article by Huebner et al.
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Expression of mitofusin 2(R94Q) in a transgenic mouse leads to Charcot-Marie-Tooth neuropathy type 2A.
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Expression of recombinant human methylmalonyl-CoA mutase: in primary mut fibroblasts and Saccharomyces cerevisiae.
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Expression of stimulator of Fe transport is not enhanced in Hfe knockout mice.
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Expression of the type III TGF-beta receptor is negatively regulated by TGF-beta.
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Expression profiling and local adaptation of Boechera holboellii populations for water use efficiency across a naturally occurring water stress gradient.
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Expression profiling using microarrays fabricated by an ink-jet oligonucleotide synthesizer.
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FHIT and FRA3B 3p14.2 allele loss are common in lung cancer and preneoplastic bronchial lesions and are associated with cancer-related FHIT cDNA splicing aberrations.
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Familial erythrocytosis associated with a short deletion in the erythropoietin receptor gene.
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Finishing the euchromatic sequence of the human genome.
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Fragments of ATM which have dominant-negative or complementing activity.
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Functional analysis of the TAN-1 gene, a human homolog of Drosophila notch.
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Functional expression of an arachnid sodium channel reveals residues responsible for tetrodotoxin resistance in invertebrate sodium channels.
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Functional replacement of the mouse E2A gene with a human HEB cDNA.
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GIPC interacts with the beta1-adrenergic receptor and regulates beta1-adrenergic receptor-mediated ERK activation.
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Gene expression profiling in RAS oncogene-transformed cell lines and in solid tumors using subtractive suppression hybridization and cDNA arrays.
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Gene expression programs of human smooth muscle cells: tissue-specific differentiation and prognostic significance in breast cancers.
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Gene therapy inhibiting neointimal vascular lesion: in vivo transfer of endothelial cell nitric oxide synthase gene.
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Gene up-regulation in heart during mammalian hibernation.
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Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.
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Generation of a polyclonal fab phage display library to the human breast carcinoma cell line BT-20.
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Generation of full-length cDNA libraries enriched for differentially expressed genes for functional genomics.
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Generation of full-length cDNA libraries enriched for differentially expressed genes.
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Genetic immunization with LYVE-1 cDNA yields function-blocking antibodies against native protein.
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Genome annotation assessment in Drosophila melanogaster.
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Genome maps 7. The human transcript map. Wall chart.
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Genome nucleotide lengths that are divisible by six are not essential but enhance replication of defective interfering RNAs of the paramyxovirus simian virus 5.
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Genomic cloning of hGSTP1*C, an allelic human Pi class glutathione S-transferase gene variant and functional characterization of its retinoic acid response elements.
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Genomic organization and cloning of the human homologue of murine Sipa-1.
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Genomic organization, expression, and localization of murine Ran-binding protein 2 (RanBP2) gene.
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Genomic structure and embryonic expression of estrogen receptor beta a (ERbetaa) in zebrafish (Danio rerio).
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Germline sequences of V(H)7183 gene family members in C57BL/6 mice demonstrate natural selection of particular sequences during recent evolution.
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Globoid cell leukodystrophy (Krabbe disease): normal umbilical cord blood galactocerebrosidase activity and polymorphic mutations.
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Glycosaminoglycan binding properties of natural venezuelan equine encephalitis virus isolates.
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Gq-dependent signaling upregulates COX2 in glomerular podocytes.
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Growth arrest and DNA damage-inducible protein GADD34 assembles a novel signaling complex containing protein phosphatase 1 and inhibitor 1.
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Guinea pig and bovine zeta-crystallins have distinct functional characteristics highlighting replacements in otherwise similar structures.
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High-Frequency Illegitimate Strand Transfers of Nascent DNA Fragments During Reverse Transcription Result in Defective Retrovirus Genomes.
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Human DNA-activated protein kinase (DNA-PK) is homologous to phosphatidylinositol kinases.
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Human G(alpha q): cDNA and tissue distribution.
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Human GFRA1: cloning, mapping, genomic structure, and evaluation as a candidate gene for Hirschsprung disease susceptibility.
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Human MafG is a functional partner for p45 NF-E2 in activating globin gene expression.
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Human and rat peroxisome proliferator activated receptors (PPARs) demonstrate similar tissue distribution but different responsiveness to PPAR activators.
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Human beta-defensin 4: a novel inducible peptide with a specific salt-sensitive spectrum of antimicrobial activity.
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Human calcium-calmodulin dependent protein kinase I: cDNA cloning, domain structure and activation by phosphorylation at threonine-177 by calcium-calmodulin dependent protein kinase I kinase.
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Human lung cancer cell lines exhibit resistance to retinoic acid treatment.
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Hypermethylation of growth arrest DNA damage-inducible gene 45 beta promoter in human hepatocellular carcinoma.
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Hyperosmotic stress stimulates promoter activity and regulates cellular utilization of the serum- and glucocorticoid-inducible protein kinase (Sgk) by a p38 MAPK-dependent pathway.
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Hypertension and impaired glycine handling in mice lacking the orphan transporter XT2.
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Identification and cloning of a negative regulator of systemic acquired resistance, SNI1, through a screen for suppressors of npr1-1
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Identification and characterization of a cDNA encoding cytochrome P450 3A from the fresh water teleost medaka (Oryzias latipes).
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Identification and characterization of genes involved in the carcinogenesis of human squamous cell cervical carcinoma.
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Identification and localization of a sea urchin Notch homologue: insights into vegetal plate regionalization and Notch receptor regulation.
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Identification of a fetal exon in the human fast troponin T gene.
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Identification of a rat glomerular mesangial cell mitogenic 5-HT2A receptor.
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Identification of aberrantly regulated genes in diseased skin using the cDNA differential display technique.
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Identification of additional members of human G-protein-coupled receptor kinase multigene family.
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Identification of four proteins from the small subunit of the mammalian mitochondrial ribosome using a proteomics approach.
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Identification of molecular markers for the early detection of human squamous cell carcinoma of the uterine cervix.
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Identification of specific protein-RNA target sites using libraries of natural sequences.
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Identification of the ligand-binding domains of CD22, a member of the immunoglobulin superfamily that uniquely binds a sialic acid-dependent ligand.
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Identification, characterization, and ontogeny of a second cytochrome P450 3A gene from the fresh water teleost medaka (Oryzias latipes).
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Identification, chromosomal mapping and tissue-specific expression of hREV3 encoding a putative human DNA polymerase zeta.
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Identification, purification, and characterization of GRK5, a member of the family of G protein-coupled receptor kinases.
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Identifying mRNA subsets in messenger ribonucleoprotein complexes by using cDNA arrays.
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Identifying protein phosphatase 2A interacting proteins using the yeast two-hybrid method.
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Immobilized molecular beacons: a new strategy using UV-activated poly(methyl methacrylate) surfaces to provide large fluorescence sensitivities for reporting on molecular association events.
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In vitro selection of aptamers from RNA libraries.
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Incongruence between primary sequence data and the distribution of a mitochondrial atp1 group II intron among ferns and horsetails
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Increased E-selectin, IL-8 and IL-10 gene expression in human skin after minimal trauma.
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Increased vascular smooth muscle contractility in TRPC6-/- mice.
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Insulin-like growth factor binding protein-3 induces early apoptosis in malignant prostate cancer cells and inhibits tumor formation in vivo.
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Intracellular third loop domain of angiotensin II type-2 receptor. Role in mediating signal transduction and cellular function.
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Intron retention in mRNA encoding ancillary subunit of insect voltage-gated sodium channel modulates channel expression, gating regulation and drug sensitivity.
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Investigation of the phenylethanolamine N-methyltransferase gene as a candidate gene for hypertension.
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Isolated sulfite oxidase deficiency.
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Isolated sulfite oxidase deficiency: mutation analysis and DNA-based prenatal diagnosis.
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Isolation and biochemical characterization of LEAP-2, a novel blood peptide expressed in the liver.
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Isolation and characterization of cDNA clones encoding pig gastric mucin.
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Isolation and characterization of the CYP71D16 trichome-specific promoter from Nicotiana tabacum L.
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Isolation and functional analysis of the mouse RXRgamma1 gene promoter in anterior pituitary cells.
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Isolation and nucleotide sequence of human liver glycogen debranching enzyme mRNA: identification of multiple tissue-specific isoforms.
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Isolation of retinal proteins that interact with retinitis pigmentosa GTPase regulator by interaction trap screen in yeast.
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Isolation of song-regulated genes in the brain of songbirds.
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L-selectin binds to P-selectin glycoprotein ligand-1 on leukocytes: interactions between the lectin, epidermal growth factor, and consensus repeat domains of the selectins determine ligand binding specificity.
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L-selectin dimerization enhances tether formation to properly spaced ligand.
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LAT: the ZAP-70 tyrosine kinase substrate that links T cell receptor to cellular activation.
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LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development.
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LXRalpha functions as a cAMP-responsive transcriptional regulator of gene expression.
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Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome.
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Liver X receptors alpha and beta regulate renin expression in vivo.
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Localization of the VHR phosphatase gene and its analysis as a candidate for BRCA1.
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Localization of three genes expressed in retina on mouse chromosome 11.
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Locus-specific somatic hypermutation in germinal centre T cells.
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Long-term follow-up assessment of a phase 1 trial of angiogenic gene therapy using direct intramyocardial administration of an adenoviral vector expressing the VEGF121 cDNA for the treatment of diffuse coronary artery disease.
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Low level exposure to the flame retardant BDE-209 reduces thyroid hormone levels and disrupts thyroid signaling in fathead minnows.
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Low-abundance HIV drug-resistant viral variants in treatment-experienced persons correlate with historical antiretroviral use.
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Lutheran antigens, CD44-related antigens, and Lutheran regulatory genes.
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LvNumb works synergistically with Notch signaling to specify non-skeletal mesoderm cells in the sea urchin embryo.
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MGSA/GRO transcription is differentially regulated in normal retinal pigment epithelial and melanoma cells.
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Mammalian homologs of Drosophila ELAV localized to a neuronal subset can bind in vitro to the 3' UTR of mRNA encoding the Id transcriptional repressor.
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Mast cell regulation of inflammation and gene expression during antigen-induced bladder inflammation in mice.
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Maximization of signal derived from cDNA microarrays.
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Mechanistic studies of human molybdopterin synthase reaction and characterization of mutants identified in group B patients of molybdenum cofactor deficiency.
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MegaGate: A toxin-less gateway molecular cloning tool.
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Metabolism of methadone and levo-alpha-acetylmethadol (LAAM) by human intestinal cytochrome P450 3A4 (CYP3A4): potential contribution of intestinal metabolism to presystemic clearance and bioactivation.
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Metatranscriptomic analysis of ectomycorrhizal roots reveals genes associated with Piloderma-Pinus symbiosis: improved methodologies for assessing gene expression in situ.
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Microarray gene expression profiles in dilated and hypertrophic cardiomyopathic end-stage heart failure.
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Molecular analyses of the Arabidopsis TUBBY-like protein gene family.
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Molecular and functional characterization of voltage-gated sodium channel variants from Drosophila melanogaster.
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Molecular characterization and functional expression of the DSC1 channel.
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Molecular characterization of glycogen storage disease type III.
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Molecular cloning and characterization of a distinct human phosphodiesterase gene family: PDE11A.
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Molecular cloning and functional expression of a recombinant 72.5 kDa fragment of the 110 kDa regulatory subunit of smooth muscle protein phosphatase 1M.
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Molecular cloning and properties of a full-length putative thyroid hormone receptor coactivator.
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Molecular cloning of KS, a novel rat gene expressed exclusively in the kidney.
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Molecular cloning of TRPC3a, an N-terminally extended, store-operated variant of the human C3 transient receptor potential channel.
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Molecular cloning of acid alpha-glucosidase cDNA of Japanese quail (Coturnix coturnix japonica) and the lack of its mRNA in acid maltase deficient quails.
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Molecular cloning of human liver sulfite oxidase.
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Molecular cloning of rainbow trout (Oncorhynchus mykiss) eggshell zona radiata protein complementary DNA: mRNA expression in 17beta-estradiol- and nonylphenol-treated fish.
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Molecular cloning of rat liver sulfite oxidase. Expression of a eukaryotic Mo-pterin-containing enzyme in Escherichia coli.
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Molecular cloning of the cDNA and promoter sequences for the mouse sodium-hydrogen exchanger regulatory factor.
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Molecular cloning of the first metazoan beta-1,3 glucanase from eggs of the sea urchin Strongylocentrotus purpuratus.
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Molecular cloning, characterization, and expression in Escherichia coli of full-length cDNAs of three human glutathione S-transferase Pi gene variants. Evidence for differential catalytic activity of the encoded proteins.
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Molecular cloning, expression and functional characterization of rabbit anticoagulant vitamin-K-dependent protein S.
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Molecular composition of the node of Ranvier: identification of ankyrin-binding cell adhesion molecules neurofascin (mucin+/third FNIII domain-) and NrCAM at nodal axon segments.
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Molybdopterin synthase mutations in a mild case of molybdenum cofactor deficiency.
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Mouse Mesenchyme forkhead 2 (Mf2): expression, DNA binding and induction by sonic hedgehog during somitogenesis.
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Moving Beyond "Isolated" Gene Patents
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Mutation in collagen II alpha 1 isoforms delineates Stickler and Wagner syndrome phenotypes.
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Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease.
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Mutations of the E-cadherin gene in human gynecologic cancers.
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Myocyte nuclear factor, a novel winged-helix transcription factor under both developmental and neural regulation in striated myocytes.
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NAD(P)H:quinone oxidoreductase expression and mitomycin C resistance developed by human colon cancer HCT 116 cells.
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Negative regulation of DNA replication by the retinoblastoma protein is mediated by its association with MCM7.
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Neurabin/protein phosphatase-1 complex regulates dendritic spine morphogenesis and maturation.
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No evidence for maternal-fetal microchimerism in infantile hemangioma: a molecular genetic investigation.
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Nonspecific interstitial pneumonia, alveolar proteinosis, and abnormal proprotein trafficking resulting from a spontaneous mutation in the surfactant protein C gene.
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Novel bacterial P-type ATPases with histidine-rich heavy-metal-associated sequences.
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Novel splicing, missense, and deletion mutations in seven adenosine deaminase-deficient patients with late/delayed onset of combined immunodeficiency disease. Contribution of genotype to phenotype.
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Observation of dually decoded regions of the human genome using ribosome profiling data.
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Oligomerization and trafficking of the human dopamine transporter. Mutational analysis identifies critical domains important for the functional expression of the transporter.
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On the physiological importance of endoproteolysis of CAAX proteins: heart-specific RCE1 knockout mice develop a lethal cardiomyopathy.
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Osteopontin inhibits expression of cytochrome c oxidase in RAW 264.7 murine macrophages.
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PCGEM1, a prostate-specific gene, is overexpressed in prostate cancer.
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PP1 control of M phase entry exerted through 14-3-3-regulated Cdc25 dephosphorylation.
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Partitioning and translation of mRNAs encoding soluble proteins on membrane-bound ribosomes.
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Peritoneal and subperitoneal stroma may facilitate regional spread of ovarian cancer.
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Pharmacovirological impact of an integrase inhibitor on human immunodeficiency virus type 1 cDNA species in vivo.
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Physical and cDNA mapping in the DBH region of human chromosome 9q34.
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Physiologically regulated alternative splicing patterns of fast troponin T RNA are conserved in mammals.
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Podocan, a novel small leucine-rich repeat protein expressed in the sclerotic glomerular lesion of experimental HIV-associated nephropathy.
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Polymorphism of adhesion molecule CD31 and its role in acute graft-versus-host disease.
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Positional cloning of a temperature-sensitive mutant emmental reveals a role for sly1 during cell proliferation in zebrafish fin regeneration.
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Potential for germ line transmission after intramyocardial gene delivery by adeno-associated virus.
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Production of adrenergic receptors in yeast.
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Pronounced thrombocytosis in transgenic mice expressing reduced levels of Mpl in platelets and terminally differentiated megakaryocytes.
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Protein kinase-zeta interacts with munc18c: role in GLUT4 trafficking.
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Pseudomonas syringae infection assays in Arabidopsis.
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Pseudouridines have context-dependent mutation and stop rates in high-throughput sequencing.
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Putative human blue-light photoreceptors hCRY1 and hCRY2 are flavoproteins.
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Quantitative analysis of mRNA amplification by in vitro transcription.
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RNA-binding protein HuR enhances p53 translation in response to ultraviolet light irradiation.
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RORgamma t, a novel isoform of an orphan receptor, negatively regulates Fas ligand expression and IL-2 production in T cells.
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RTP family members induce functional expression of mammalian odorant receptors.
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Rapid, comprehensive analysis of human cytokine mRNA and its application to the study of acute renal allograft rejection.
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Reaction mechanism of (6-4) photolyase.
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Recoverin undergoes light-dependent intracellular translocation in rod photoreceptors.
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Refinement of the PARK3 locus on chromosome 2p13 and the analysis of 14 candidate genes.
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Region-specific anti-thyroid hormone receptor (TR) antibodies detect changes in TR structure due to ligand-binding and dimerization.
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Regulation of both PDK1 and the phosphorylation of PKC-zeta and -delta by a C-terminal PRK2 fragment.
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Regulation of human interleukin-8 receptor A: identification of a phosphorylation site involved in modulating receptor functions.
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Regulation of lysyl oxidase mRNA in dermal fibroblasts from normal donors and patients with inherited connective tissue disorders.
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Replication factors MCM2 and ORC1 interact with the histone acetyltransferase HBO1.
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Retina-specifically expressed novel subtypes of bovine cyclophilin.
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Reverse genetics with a full-length infectious cDNA of the Middle East respiratory syndrome coronavirus.
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Reversing established sepsis with antagonists of endogenous high-mobility group box 1.
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Reversion mutation of cDNA CA8-204 minigene construct produces a truncated functional peptide that regulates calcium release in vitro and produces profound analgesia in vivo.
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Role for ETS domain transcription factors Pea3/Erm in mouse lung development.
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Role of beta-arrestin in mediating agonist-promoted G protein-coupled receptor internalization.
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Role of decreased levels of lipid phosphate phosphatase-1 in accumulation of lysophosphatidic acid in ovarian cancer.
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Role of ubiquitin-like protein FAT10 in epithelial apoptosis in renal disease.
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S-allele diversity in a natural population of Physalis crassifolia (Solanaceae) (ground cherry) assessed by RT-PCR.
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SLLP1, a unique, intra-acrosomal, non-bacteriolytic, c lysozyme-like protein of human spermatozoa.
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SREC-I, a type F scavenger receptor, is an endocytic receptor for calreticulin.
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STAT1 is essential for antimicrobial effector function but dispensable for gamma interferon production during Toxoplasma gondii infection.
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Selection and validation of endogenous reference genes using a high throughput approach.
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Selective suppression of matrix metalloproteinase-9 in human glioblastoma cells by antisense gene transfer impairs glioblastoma cell invasion.
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Sensing of extracellular cations in CasR-deficient osteoblasts. Evidence for a novel cation-sensing mechanism.
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Sequence analysis of a cDNA for lysyl hydroxylase isolated from human skin fibroblasts from a normal donor: differences from human placental lysyl hydroxylase cDNA.
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Sequence of a Brassica campestris myrosinase gene.
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Sequences within the coding regions of clotting factor VIII and CFTR block transcriptional elongation.
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Seven transmembrane receptors: something old, something new.
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Somatic mutations in the neurofibromatosis 1 gene in gliomas and primitive neuroectodermal tumours.
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SpHnf6, a transcription factor that executes multiple functions in sea urchin embryogenesis.
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Spdeadringer, a sea urchin embryo gene required separately in skeletogenic and oral ectoderm gene regulatory networks.
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Sphingosine-phosphate lyase enhances stress-induced ceramide generation and apoptosis.
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Structure and expression of a membrane component of the inhibin receptor system.
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Structure of human Niemann-Pick C1 protein.
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Structure of the human gene (COX6A2) for the heart/muscle isoform of cytochrome c oxidase subunit VIa and its chromosomal location in humans, mice, and cattle.
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Subtractive cloning: new genes for studying inflammatory disorders.
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Successful herbivore attack due to metabolic diversion of a plant chemical defense.
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Sulfotransferases of two specificities function in the reconstitution of high endothelial cell ligands for L-selectin.
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Suppression of a P450 hydroxylase gene in plant trichome glands enhances natural-product-based aphid resistance.
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Suppression subtractive hybridization: a method for generating differentially regulated or tissue-specific cDNA probes and libraries.
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Suppression subtractive hybridization: a versatile method for identifying differentially expressed genes.
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Surgical treatment of malignant esophageal tumors in PUMC Hospital.
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Targeted inhibition of calcineurin in pressure-overload cardiac hypertrophy. Preservation of systolic function.
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TbetaRIII suppresses non-small cell lung cancer invasiveness and tumorigenicity.
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Temporal profile of replication of human chromosomes.
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Tetramerization and single-stranded DNA binding properties of native and mutated forms of murine mitochondrial single-stranded DNA-binding proteins.
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The Arabidopsis GA1 locus encodes the cyclase ent-kaurene synthetase A of gibberellin biosynthesis.
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The Arabidopsis NPR1 gene that controls systemic acquired resistance encodes a novel protein containing ankyrin repeats.
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The GA2 locus of Arabidopsis thaliana encodes ent-kaurene synthase of gibberellin biosynthesis.
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The PIG-A mutation and absence of glycosylphosphatidylinositol-linked proteins do not confer resistance to apoptosis in paroxysmal nocturnal hemoglobinuria.
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The alpha 1C-adrenoceptor in human prostate: cloning, functional expression, and localization to specific prostatic cell types.
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The ammonium transporter RhBG: requirement of a tyrosine-based signal and ankyrin-G for basolateral targeting and membrane anchorage in polarized kidney epithelial cells.
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The amphiphysin-like protein 1 (ALP1) interacts functionally with the cABL tyrosine kinase and may play a role in cytoskeletal regulation.
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The c-Jun NH2-terminal kinase 2 plays a dominant role in human epidermal neoplasia.
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The chromosomal mapping of four genes encoding winged helix proteins expressed early in mouse development.
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The effect of a single boranophosphate substitution with defined configuration on the thermal stability and conformation of a DNA duplex.
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The expression of a functional, secreted human lysyl hydroxylase in a baculovirus system.
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The fruitless gene is required for the proper formation of axonal tracts in the embryonic central nervous system of Drosophila.
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The human extraocular muscle myosin heavy chain gene (MYH13) maps to the cluster of fast and developmental myosin genes on chromosome 17.
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The inhibitor-1 C terminus facilitates hormonal regulation of cellular protein phosphatase-1: functional implications for inhibitor-1 isoforms.
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The integrity of a cholesterol-binding pocket in Niemann-Pick C2 protein is necessary to control lysosome cholesterol levels.
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The intrinsic factor-vitamin B12 receptor and target of teratogenic antibodies is a megalin-binding peripheral membrane protein with homology to developmental proteins.
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The isolation and characterization of cDNA encoding the mouse bifunctional ATP sulfurylase-adenosine 5'-phosphosulfate kinase.
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The mouse C-type transient receptor potential 2 (TRPC2) channel: alternative splicing and calmodulin binding to its N terminus.
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The near-naked hairless (Hr(N)) mutation disrupts hair formation but is not due to a mutation in the Hairless coding region.
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The nuclear hormone receptor coactivator SRC-1 is a specific target of p300.
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The physiology of jaundice: molecular and functional characterization of the Crigler-Najjar syndromes.
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The smallest membrane anchoring subunit (QPs3) of bovine heart mitochondrial succinate-ubiquinone reductase. Cloning, sequencing, topology, and Q-binding domain.
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Three new adenosine deaminase mutations that define a splicing enhancer and cause severe and partial phenotypes: implications for evolution of a CpG hotspot and expression of a transduced ADA cDNA.
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Thyroid hormone regulation of hepatic genes in vivo detected by complementary DNA microarray.
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Tissue specificity of a new splice form of the human lysyl hydroxylase 2 gene.
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Tissue-specific expression of Ran isoforms in the mouse.
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Transcriptional network of multiple capsule and melanin genes governed by the Cryptococcus neoformans cyclic AMP cascade.
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Transcriptional regulation of the mouse presenilin-1 gene.
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Transcriptome analysis of mouse stem cells and early embryos.
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Transgenic targeting of a dominant negative corepressor to liver and analyses by cDNA microarray.
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Translational inhibition of messenger RNA of the human pi class glutathione S-transferase by antisense oligodeoxyribonucleotides.
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Translocations and amplifications of chromosome 12 in liposarcoma demonstrated by the LSI CHOP breakapart rearrangement probe.
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Two mammalian longevity assurance gene (LAG1) family members, trh1 and trh4, regulate dihydroceramide synthesis using different fatty acyl-CoA donors.
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Two proteins of the Dictyostelium spore coat bind to cellulose in vitro.
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Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex.
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Ultrastructural and biochemical properties of the 120-kDa form of chick kinectin.
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Ultrastructure and function of dimeric, soluble intercellular adhesion molecule-1 (ICAM-1).
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Use of SMART-generated cDNA for gene expression studies in multiple human tumors.
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Use of immuno-LCM to identify the in situ expression profile of cellular constituents of the tumor microenvironment.
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Use of phage display to identify novel mineralocorticoid receptor-interacting proteins.
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VIAF, a conserved inhibitor of apoptosis (IAP)-interacting factor that modulates caspase activation.
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Vitamin K-dependent protein S in Leydig cells of human testis.
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Why certain antibodies cross-react with HLA-A and HLA-G: epitope mapping of two common MHC class I reagents.
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Yeast microarrays for genome wide parallel genetic and gene expression analysis.
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Zebrafish sparse corresponds to an orthologue of c-kit and is required for the morphogenesis of a subpopulation of melanocytes, but is not essential for hematopoiesis or primordial germ cell development.
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beta-Arrestin 2 expression determines the transcriptional response to lysophosphatidic acid stimulation in murine embryo fibroblasts.
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c-Myc creates an activation loop by transcriptionally repressing its own functional inhibitor, hMad4, in young fibroblasts, a loop lost in replicatively senescent fibroblasts.
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cDNA cloning and expression of rat and human protein geranylgeranyltransferase type-I.
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ePAD, an oocyte and early embryo-abundant peptidylarginine deiminase-like protein that localizes to egg cytoplasmic sheets.
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hMad4, c-Myc endogenous inhibitor, induces a replicative senescence-like state when overexpressed in human fibroblasts.
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Keywords of People
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Berchuck, Andrew,
James M. Ingram Distinguished Professor of Gynecologic Oncology,
Obstetrics and Gynecology, Gynecologic Oncology
-
Carbrey, Jennifer Mehlman,
Assistant Research Professor of Cell Biology,
Cell Biology
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Erickson, Harold Paul,
James B. Duke Distinguished Professor Emeritus,
Cell Biology
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Gunn, Michael Dee,
Professor of Medicine,
Integrative Immunobiology
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Hogan, Brigid L. M.,
Research Professor of Cell Biology,
Cell Biology
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Liu, Yutao,
Adjunct Assistant Professor in the Department of Medicine,
Medicine, Medical Genetics
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Pitt, Geoffrey Stuart,
Adjunct Professor in the Department of Medicine,
Medicine, Cardiology
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Shinohara, Mari L.,
Professor of Integrative Immunobiology,
Cell Biology
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Soderling, Scott Haydn,
George Barth Geller Distinguished Professor of Molecular Biology,
Cell Biology