Genomic Library
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Subject Areas on Research
- A functional isoform of the human granulocyte/macrophage colony-stimulating factor receptor has an unusual cytoplasmic domain.
- A highly polymorphic cDNA probe in the NF1 gene.
- An siRNA Screen Identifies the U2 snRNP Spliceosome as a Host Restriction Factor for Recombinant Adeno-associated Viruses.
- Autistic disorder and chromosome 15q11-q13: construction and analysis of a BAC/PAC contig.
- Catecholamine synthesis is mediated by tyrosinase in the absence of tyrosine hydroxylase.
- Characterization of the rat type III hexokinase gene promoter. A functional octamer 1 motif is critical for basal promoter activity.
- Cloning and characterization of the major promoter of the human protein kinase C beta gene. Regulation by phorbol esters.
- Cloning, characterization, and genetic mapping of the rat type 2 angiotensin II receptor gene.
- De novo assembly using low-coverage short read sequence data from the rice pathogen Pseudomonas syringae pv. oryzae.
- 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.
- Expansion of the alpha 2-adrenergic receptor family: cloning and characterization of a human alpha 2-adrenergic receptor subtype, the gene for which is located on chromosome 2.
- Genome-wide mapping of DNase hypersensitive sites using massively parallel signature sequencing (MPSS).
- Human type 2 angiotensin II receptor gene: cloned, mapped to the X chromosome, and its mRNA is expressed in the human lung.
- Identification and characterization of a Drosophila nuclear receptor with the ability to inhibit the ecdysone response.
- Identification of novel mediators of NF-kappaB through genome-wide survey of monocyte adherence-induced genes.
- Isolation and characterization of the genomic human CD7 gene: structural similarity with the murine Thy-1 gene.
- Molecular cloning of the structural gene for exopolygalacturonate lyase from Erwinia chrysanthemi EC16 and characterization of the enzyme product.
- Myogenic stem cell function is impaired in mice lacking the forkhead/winged helix protein MNF.
- Neuro-oncology: unmasking the multiforme in glioblastoma.
- Organization of the human zeta-crystallin/quinone reductase gene (CRYZ).
- Point mutations in retinoblastoma.
- Precise localization of the FHIT gene to the common fragile site at 3p14.2 (FRA3B) and characterization of homozygous deletions within FRA3B that affect FHIT transcription in tumor cell lines.
- Preparation and screening of an arrayed human genomic library generated with the P1 cloning system.
- Rat sulfite oxidase antibodies cross-react with two gene family-related proteins: albumin and vitamin D-binding protein.
- Refined localization of the cerebral cavernous malformation gene (CCM1) to a 4-cM interval of chromosome 7q contained in a well-defined YAC contig.
- Report of the Second International Workshop on Human Chromosome 19 mapping 1992.
- Suppression subtractive hybridization: a method for generating differentially regulated or tissue-specific cDNA probes and libraries.
- The actin gene from Cryptococcus neoformans: structure and phylogenetic analysis.
- The chromosomal mapping of four genes encoding winged helix proteins expressed early in mouse development.
- The potassium channel MBK1 (Kv1.1) is expressed in the mouse retina.
- The smallest membrane anchoring subunit (QPs3) of bovine heart mitochondrial succinate-ubiquinone reductase. Cloning, sequencing, topology, and Q-binding domain.
- Transcriptome profiling of genes involved in neural tube closure during human embryonic development using long serial analysis of gene expression (long-SAGE).
- Zebrafish as a neurotoxicological model.
- cDNA arrays and the enigma of melanoma immune responsiveness.
- cDNA sequence and genomic structure of EV12B, a gene lying within an intron of the neurofibromatosis type 1 gene.
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Keywords of People
- Hogan, Brigid L. M., Research Professor of Cell Biology, Cell Biology