In Situ Hybridization, Fluorescence
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Subject Areas on Research
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"Hairy" cells in acute promyelocytic leukemia: Excess myeloperoxidase with formation of needle-shaped crystalline projections on the cytochemical stain in a case with variant morphology.
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"Large cell/anaplastic" medulloblastomas: a Pediatric Oncology Group Study.
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A 137-kb deletion within the Potocki-Shaffer syndrome interval on chromosome 11p11.2 associated with developmental delay and hypotonia.
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A LGR5 reporter pig model closely resembles human intestine for improved study of stem cells in disease.
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A candidate gene for congenital bilateral isolated ptosis identified by molecular analysis of a de novo balanced translocation.
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A case of atypical, complete DiGeorge syndrome without 22q11 mutation.
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A case of infantile acute lymphoblastic leukemia presenting with rearrangement of MLL at 11q23 and apparent insertion or translocation at 10p12.
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A family of human Y chromosomes has dispersed throughout northern Eurasia despite a 1.8-Mb deletion in the azoospermia factor c region.
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A genetic memory initiates the epigenetic loop necessary to preserve centromere position.
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A high-resolution integrated physical, cytogenetic, and genetic map of human chromosome 11: distal p13 to proximal p15.1.
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A multimodal cell census and atlas of the mammalian primary motor cortex.
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A nCounter CNV Assay to Detect HER2 Amplification: A Correlation Study with Immunohistochemistry and In Situ Hybridization in Advanced Gastric Cancer.
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A physical map of the human genome.
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A simplified prognostic index for chronic lymphocytic leukemia treated with ibrutinib: Results from a multicenter retrospective cohort study.
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A subtle t(3;8) results in plausible juxtaposition of MYC and BCL6 in a child with Burkitt lymphoma/leukemia and ataxia-telangiectasia.
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AURKA amplification, chromosome instability, and centrosome abnormality in human pancreatic carcinoma cells.
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Acquired genomic copy number aberrations and survival in adult acute myelogenous leukemia.
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Acute graft-versus-host disease after liver transplantation diagnosed by fluorescent in situ hybridization testing of skin biopsy specimens.
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Adherent biofilms in bacterial vaginosis.
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Altered telomeres in tumors with ATRX and DAXX mutations.
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Amplification and overexpression of PPFIA1, a putative 11q13 invasion suppressor gene, in head and neck squamous cell carcinoma.
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Amplification of telomeric DNA directly correlates with metastatic potential of human and murine cancers of various histological origin.
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An integrated YAC map of the human X chromosome.
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An integrated physical map of 210 markers assigned to the short arm of human chromosome 11.
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Analysis of centromeric activity in Robertsonian translocations: implications for a functional acrocentric hierarchy.
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Analysis of primary central nervous system large B-cell lymphoma in the era of high-grade B-cell lymphoma: Detection of two cases with MYC and BCL6 rearrangements in a cohort of 12 cases.
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Anticipatory Positive Urine Tests for Bladder Cancer.
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Antiretroviral therapy effects on genetic and morphologic end points in lymphocytes and sperm of men with human immunodeficiency virus infection.
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Apocrine-eccrine carcinomas: molecular and immunohistochemical analyses.
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Application of FISH to complex chromosomal rearrangements associated with chronic myelogenous leukemia.
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Are sequence family variants useful for identifying deletions in the human Y chromosome?
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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 human protein phosphatase 2A regulatory subunit genes b56alpha, b56beta, b56gamma, b56delta, and b56epsilon (PPP2R5A-PPP2R5E), highly expressed in muscle and brain, to chromosome regions 1q41, 11q12, 3p21, 6p21.1, and 7p11.2 --> p12.
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Assignment of human transforming growth factor-beta type I and type III receptor genes (TGFBR1 and TGFBR3) to 9q33-q34 and 1p32-p33, respectively.
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Assignment of the zeta-crystallin gene (CRYZ) to human chromosome 1p22-p31 and identification of restriction fragment length polymorphisms.
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Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic origins.
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Atypical teratoid/rhabdoid tumor of the central nervous system: a highly malignant tumor of infancy and childhood frequently mistaken for medulloblastoma: a Pediatric Oncology Group study.
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Available Systemic Treatments and Emerging Therapies for Breast Cancer Brain Metastases.
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B-cell lymphoma with hyaline vascular Castleman disease-like features: a clinicopathologic study.
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BCL2 translocation defines a unique tumor subset within the germinal center B-cell-like diffuse large B-cell lymphoma.
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Bacteria localization and chorion thinning among preterm premature rupture of membranes.
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Bacterial biofilm within diseased pancreatic and biliary tracts.
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BayFish: Bayesian inference of transcription dynamics from population snapshots of single-molecule RNA FISH in single cells.
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Bilateral panocular involvement with mantle-cell lymphoma.
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CD44-SLC1A2 gene fusions in gastric cancer.
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CD5-positive follicular lymphoma: clinicopathologic correlations and outcome in 88 cases.
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Characterization of bone marrow mast cells in acute myeloid leukemia with t(8;21) (q22;q22); RUNX1-RUNX1T1.
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Characterization of chromosome 17 abnormalities in medulloblastomas.
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Characterization of de novo duplications in eight patients by using fluorescence in situ hybridization with chromosome-specific DNA libraries.
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Characterization of gains, losses, and regional amplification in testicular germ cell tumor cell lines by comparative genomic hybridization.
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Chordoid glioma: a case report and molecular characterization of five cases.
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Chromosomal aberrations of primary lung adenocarcinomas in nonsmokers.
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Chromosomal amplification of leucine-rich repeat kinase-2 (LRRK2) is required for oncogenic MET signaling in papillary renal and thyroid carcinomas.
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Chromosomal localization of gene for human glutamate receptor subunit-7.
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Chromosomal localization of the ankyrinG gene (ANK3/Ank3) to human 10q21 and mouse 10.
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Chromosome breakpoint at 17q11.2 and insertion of DNA from three different chromosomes in a glioblastoma with exceptional glial fibrillary acidic protein expression.
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Chromosomes with high gene density are preferentially repaired in human cells.
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Clinical and therapeutic relevance of PIM1 kinase in gastric cancer.
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Clinical course and origin of epithelium in cases of epithelial downgrowth after Descemet stripping automated endothelial keratoplasty.
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Clinical experience with array CGH: case presentations from nine months of practice.
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Clinical features, tumor biology, and prognosis associated with MYC rearrangement and Myc overexpression in diffuse large B-cell lymphoma patients treated with rituximab-CHOP.
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Cloning and characterization of a cAMP-specific cyclic nucleotide phosphodiesterase.
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Cloning, characterization, and genetic mapping of the rat type 2 angiotensin II receptor gene.
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Co-expression of urokinase with haptoglobin in human carcinomas.
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Colocalization of different influenza viral RNA segments in the cytoplasm before viral budding as shown by single-molecule sensitivity FISH analysis.
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Combined cDNA array comparative genomic hybridization and serial analysis of gene expression analysis of breast tumor progression.
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Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia.
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Comparative cellular analysis of motor cortex in human, marmoset and mouse.
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Comparative physical and transcript maps of approximately 1 Mb around loop-tail, a gene for severe neural tube defects on distal mouse chromosome 1 and human chromosome 1q22-q23.
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Comparison between melanoma gene expression score and fluorescence in situ hybridization for the classification of melanocytic lesions.
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Comparison of fluorescence in situ hybridization, cytogenetic analysis, and DNA index analysis to detect chromosomes 4 and 10 aneuploidy in pediatric acute lymphoblastic leukemia: a Pediatric Oncology Group study.
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Comparison of methods of measuring HER-2 in metastatic breast cancer patients treated with high-dose chemotherapy.
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Complexity of CNC transcription factors as revealed by gene targeting of the Nrf3 locus.
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Composite lymphoma of follicular B-cell and peripheral T-cell types with distinct zone distribution in a 75-year-old male patient: a case study.
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Comprehensive biomarker and genomic analysis identifies p53 status as the major determinant of response to MDM2 inhibitors in chronic lymphocytic leukemia.
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Comprehensive molecular cytogenetic investigation of chromosomal abnormalities in human medulloblastoma cell lines and xenograft.
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Concurrent acute myeloid leukemia with inv(16)(p13.1q22) and chronic lymphocytic leukemia: molecular evidence of two separate diseases.
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Connect MM Registry: The Importance of Establishing Baseline Disease Characteristics.
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Constellation of congenital abnormalities in an infant: a new syndrome or tissue-specific mosaicism for trisomy 18?
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Context-dependent effects of whole-genome duplication during mammary tumor recurrence.
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Cosmids map two incontinentia pigmenti type 1 (IP1) translocation breakpoints to a 180-kb region within a 1.2-Mb YAC contig.
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Cost savings with implementation of PNA FISH testing for identification of Candida albicans in blood cultures.
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Cytogenetic and molecular analysis of an unusual case of acute promyelocytic leukemia with a t(15;17;17)(q22;q23;q21).
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Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardation.
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Cytogenetic assignment and physical mapping of the human DGKE gene to chromosome 17q22.
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De novo MECP2 duplication derived from paternal germ line result in dysmorphism and developmental delay.
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De novo partial duplication of chromosome 7p in a male with autistic disorder.
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De novo translation initiation on membrane-bound ribosomes as a mechanism for localization of cytosolic protein mRNAs to the endoplasmic reticulum.
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Desmoplastic small round cell tumor: using FISH as an ancillary technique to support cytologic diagnosis in an unusual case.
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Detailed molecular analysis of 1p36 in neuroblastoma.
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Detection of trisomy 12 by fluorescence in situ hybridization on archival cytopathologic material in chronic lymphocytic leukemia/small lymphocytic lymphoma.
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Diagnosis and Treatment of ERBB2-Positive Metastatic Colorectal Cancer: A Review.
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Direct cloning of DNA sequences from the common fragile site region at chromosome band 3p14.2.
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Direct visualization of cardiac transcription factories reveals regulatory principles of nuclear architecture during pathological remodeling.
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Disruption of mRNA-RNP formation and sorting to dendritic synapses by antisense oligodeoxynucleotides.
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Distinct functions of two isoforms of a homeobox gene, BP1 and DLX7, in the regulation of the beta-globin gene.
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Distinctive phenotype in 9 patients with deletion of chromosome 1q24-q25.
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Does HLA-dependent chimerism underlie the pathogenesis of juvenile dermatomyositis?
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Donor cell-derived leukemias/myelodysplastic neoplasms in allogeneic hematopoietic stem cell transplant recipients: a clinicopathologic study of 10 cases and a comprehensive review of the literature.
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Ductal epithelial proliferations of the breast: a biological continuum? Comparative genomic hybridization and high-molecular-weight cytokeratin expression patterns.
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Dyspoietic changes associated with hepatosplenic T-cell lymphoma are not a manifestation of a myelodysplastic syndrome: analysis of 25 patients.
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EBV-positive diffuse large B-cell lymphoma of the elderly is an aggressive post-germinal center B-cell neoplasm characterized by prominent nuclear factor-kB activation.
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Epidermal growth factor receptor expression and gene copy number in fibrolamellar hepatocellular carcinoma.
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Epidermal growth factor receptor gene amplification and protein expression in glioblastoma multiforme: prognostic significance and relationship to other prognostic factors.
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Estrogen-independent proliferation is present in estrogen-receptor HER2-positive primary breast cancer after neoadjuvant letrozole.
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Evaluation of NF-κB subunit expression and signaling pathway activation demonstrates that p52 expression confers better outcome in germinal center B-cell-like diffuse large B-cell lymphoma in association with CD30 and BCL2 functions.
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Evaluation of the Fluorescence In Situ Hybridization Test to Predict Recurrence and/or Progression of Disease after bacillus Calmette-Guérin for Primary High Grade Nonmuscle Invasive Bladder Cancer: Results from a Prospective Multicenter Trial.
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Evidence for structural heterogeneity from molecular cytogenetic analysis of dicentric Robertsonian translocations.
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Extranodal lymphoid microstructures in inflamed muscle and disease severity of new-onset juvenile dermatomyositis.
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Extraskeletal myxoid chondrosarcoma of the jugular foramen.
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FGFR2 in gastric cancer: protein overexpression predicts gene amplification and high H-index predicts poor survival.
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Faecal microbiota transplantation from metabolically compromised human donors accelerates osteoarthritis in mice.
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Familial supernumerary marker chromosome evolution through three generations.
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Fetal exposure to the maternal microbiota in humans and mice.
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Fibroblast activation protein expression by stromal cells and tumor-associated macrophages in human breast cancer.
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Flavopiridol induces apoptosis in chronic lymphocytic leukemia cells via activation of caspase-3 without evidence of bcl-2 modulation or dependence on functional p53.
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Fluorescence in situ hybridization analysis of keratinocyte growth factor gene amplification and dispersion in evolution of great apes and humans.
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Fluorescence in situ hybridization method for measuring transfection efficiency.
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Fluorescence-based codetection with protein markers reveals distinct cellular compartments for altered MicroRNA expression in solid tumors.
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Fluorescent in situ hybridization in the diagnosis, prognosis, and treatment monitoring of chronic myeloid leukemia.
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Follicular lymphoma with hyaline-vascular Castleman-like features: analysis of 6 cases and review of the literature.
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Follicular lymphoma with prominent Dutcher body formation: a pathologic study of 3 cases in comparison with nodal or splenic lymphoplasmacytic lymphoma and marginal zone lymphoma.
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Formation of telomeric repeat-containing RNA (TERRA) foci in highly proliferating mouse cerebellar neuronal progenitors and medulloblastoma.
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Frequency of homozygous deletion at p16/CDKN2 in primary human tumours.
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Frequent TMPRSS2-ERG rearrangement in prostatic small cell carcinoma detected by fluorescence in situ hybridization: the superiority of fluorescence in situ hybridization over ERG immunohistochemistry.
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Generation of a Mouse Full-length Balancer with Versatile Cassette-shuttling Selection Strategy.
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Genetic diagnosis in Lafora disease: genotype-phenotype correlations and diagnostic pitfalls.
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Genetic heterogeneity of gingival fibromatosis on chromosome 2p.
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Genomic structure and chromosomal localization of the novel ETS factor, PE-2 (ERF).
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Genomics identifies medulloblastoma subgroups that are enriched for specific genetic alterations.
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Germline and somatic SMARCA4 mutations characterize small cell carcinoma of the ovary, hypercalcemic type.
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Global search for chromosomal abnormalities in infiltrating ductal carcinoma of the breast using array-comparative genomic hybridization.
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Gorlin syndrome and desmoplastic medulloblastoma: Report of 3 cases with unfavorable clinical course and novel mutations.
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Growth inhibition of a human lung adenocarcinoma cell line by genetic complementation with chromosome 11.
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HDMX regulates p53 activity and confers chemoresistance to 3-bis(2-chloroethyl)-1-nitrosourea.
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HER-2 gene amplification correlates with higher levels of angiogenesis and lower levels of hypoxia in primary breast tumors.
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Hand2 elevates cardiomyocyte production during zebrafish heart development and regeneration.
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High frequency of clonal immunoglobulin receptor gene rearrangements in sporadic histiocytic/dendritic cell sarcomas.
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High levels of nuclear MYC protein predict the presence of MYC rearrangement in diffuse large B-cell lymphoma.
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High mutation rates have driven extensive structural polymorphism among human Y chromosomes.
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High rate of CAD gene amplification in human cells deficient in MLH1 or MSH6.
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High resolution analysis of genomic aberrations by metaphase and array comparative genomic hybridization identifies candidate tumour genes in lung cancer cell lines.
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High-grade B cell lymphoma, unclassifiable, with blastoid features: an unusual morphological subgroup associated frequently with BCL2 and/or MYC gene rearrangements and a poor prognosis.
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High-resolution array CGH defines critical regions and candidate genes for microcephaly, abnormalities of the corpus callosum, and seizure phenotypes in patients with microdeletions of 1q43q44.
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Histiocytic sarcoma arising in indolent small B-cell lymphoma: report of two cases with molecular/genetic evidence suggestive of a 'transdifferentiation' during the clonal evolution.
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Human centromeric chromatin is a dynamic chromosomal domain that can spread over noncentromeric DNA.
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Human embryos derived from in vitro and in vivo matured oocytes: analysis for chromosomal abnormalities and nuclear morphology.
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Identification of Host Biomarkers of Epstein-Barr Virus Latency IIb and Latency III.
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Identification of a novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins.
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Identification of centromeric antigens in dicentric Robertsonian translocations: CENP-C and CENP-E are necessary components of functional centromeres.
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Identification of human and mouse p19, a novel CDK4 and CDK6 inhibitor with homology to p16ink4.
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Identification, chromosomal mapping and tissue-specific expression of hREV3 encoding a putative human DNA polymerase zeta.
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Immune checkpoint blockade as a potential therapeutic target: surveying CNS malignancies.
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Immunohistochemical double-hit score is a strong predictor of outcome in patients with diffuse large B-cell lymphoma treated with rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone.
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Immunophenotypic and gene expression analysis of monoclonal B-cell lymphocytosis shows biologic characteristics associated with good prognosis CLL.
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Incontinentia pigmenti in a boy with XXY mosaicism detected by fluorescence in situ hybridization.
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Increased chromosomal instability in peripheral lymphocytes and risk of human gliomas.
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Injection molded open microfluidic well plate inserts for user-friendly coculture and microscopy.
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Integrated genomic profiling of chronic lymphocytic leukemia identifies subtypes of deletion 13q14.
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Integrative genomics identifies RAB23 as an invasion mediator gene in diffuse-type gastric cancer.
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Interphase fluorescence in situ hybridization for trisomy 12 on archival ovarian sex cord-stromal tumors.
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Intrachromosomal triplication of 2q11.2-q21 in a severely malformed infant: case report and review of triplications and their possible mechanism.
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Intracranial Ewing sarcoma.
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Intraocular Medulloepitheliomas and Embryonal Tumors With Multilayered Rosettes of the Brain: Comparative Roles of LIN28A and C19MC.
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It May Be Time to Abandon Urine Tests for Bladder Cancer.
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Juvenile rheumatoid arthritis in velo-cardio-facial syndrome: coincidence or unusual complication?
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Lack of Targetable FGFR2 Fusions in Endemic Fluke-Associated Cholangiocarcinoma.
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Latent transcriptional variations of individual Plasmodium falciparum uncovered by single-cell RNA-seq and fluorescence imaging.
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Ligand-specific dynamics of the androgen receptor at its response element in living cells.
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Lineage-specific compaction of Tcrb requires a chromatin barrier to protect the function of a long-range tethering element.
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Lineage-specific trisomy 21 in a neonate with resolving transient myeloproliferative syndrome.
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Loss of chromosome 8p sequences in human breast carcinoma cell lines.
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Loss of chromosomes 22 and 14 in the malignant progression of meningiomas. A comparative study of fluorescence in situ hybridization (FISH) and standard cytogenetic analysis.
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MYC or BCL2 copy number aberration is a strong predictor of outcome in patients with diffuse large B-cell lymphoma.
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MYC protein expression does not correlate with MYC abnormalities detected by FISH but predicts an unfavorable prognosis in de novo acute myeloid leukemia.
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MYCC and MYCN oncogene amplification in medulloblastoma. A fluorescence in situ hybridization study on paraffin sections from the Children's Oncology Group.
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Malignant giant cell tumor of synovium (malignant pigmented villonodular synovitis).
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Malignant rhabdoid tumor of the kidney: involvement of chromosome 22.
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Mantle Cell Lymphoma With MYC Rearrangement: A Report of 17 Patients.
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Mantle cell lymphoma with plasma cell differentiation.
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Mapping and characterization of the amplicon near APOA2 in 1q23 in human sarcomas by FISH and array CGH.
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Mapping parameter spaces of biological switches.
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Melanocytic tumors with intraepidermal melanophages: a report of five cases with review of 231 archived cutaneous melanocytic tumors.
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Metachronous/concomitant B-cell neoplasms with discordant light-chain or heavy-chain isotype restrictions: evidence of distinct B-cell neoplasms rather than clonal evolutions.
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Methods of Melanoma Detection.
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Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients.
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Molecular analysis of genetic instability caused by chronic inflammation.
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Molecular analysis of recombination in a family with Duchenne muscular dystrophy and a large pericentric X chromosome inversion.
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Molecular analysis of the JAZF1-JJAZ1 gene fusion by RT-PCR and fluorescence in situ hybridization in endometrial stromal neoplasms.
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Molecular and cytogenetic characterization of a novel rearrangement involving chromosomes 9, 12, and 17 resulting in ETV6 (TEL) and ABL fusion.
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Molecular characteristics of mantle cell lymphoma presenting with clonal plasma cell component.
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Molecular characterization and localization of the human MAFG gene.
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Molecular cytogenetic analysis of the bladder carcinoma cell line BK-10 by spectral karyotyping.
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Molecular diagnosis of Burkitt's lymphoma.
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Morphologic features of 115 lymphomas of the orbit and ocular adnexa categorized according to the World Health Organization classification: are marginal zone lymphomas in the orbit mucosa-associated lymphoid tissue-type lymphomas?
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Multicenter evaluation of a Candida albicans peptide nucleic acid fluorescent in situ hybridization probe for characterization of yeast isolates from blood cultures.
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Multicenter evaluation of the Candida albicans/Candida glabrata peptide nucleic acid fluorescent in situ hybridization method for simultaneous dual-color identification of C. albicans and C. glabrata directly from blood culture bottles.
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Multicenter evaluation of the role of UroVysion FISH assay in surveillance of patients with bladder cancer: does FISH positivity anticipate recurrence?
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Multifocal mantle cell lymphoma in situ in the setting of a composite lymphoma.
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Myeloid neoplasms secondary to plasma cell myeloma: an intrinsic predisposition or therapy-related phenomenon? A clinicopathologic study of 41 cases and correlation of cytogenetic features with treatment regimens.
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NF1 inactivation in adult acute myelogenous leukemia.
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Nested Inversion Polymorphisms Predispose Chromosome 22q11.2 to Meiotic Rearrangements.
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No evidence for maternal-fetal microchimerism in infantile hemangioma: a molecular genetic investigation.
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Novel bioinformatic classification system for genetic signatures identification in diffuse large B-cell lymphoma.
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Novel integrase-defective lentiviral episomal vectors for gene transfer.
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OTX2 is critical for the maintenance and progression of Shh-independent medulloblastomas.
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Outcomes of Maintenance Therapy with Bortezomib after Autologous Stem Cell Transplantation for Patients with Multiple Myeloma.
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PRD-2 mediates clock-regulated perinuclear localization of clock gene RNAs within the circadian cycle of Neurospora.
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Paraganglioma-like dermal melanocytic tumor: a unique entity distinct from cellular blue nevus, clear cell sarcoma, and cutaneous melanoma.
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Peripheral subnuclear positioning suppresses Tcrb recombination and segregates Tcrb alleles from RAG2.
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Physical and genetic mapping of the CMT4A locus and exclusion of PMP-2 as the defect in CMT4A.
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Piroxicam treatment of IL-10-deficient mice enhances colonic epithelial apoptosis and mucosal exposure to intestinal bacteria.
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Post-Transplant Outcomes in High-Risk Compared with Non-High-Risk Multiple Myeloma: A CIBMTR Analysis.
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Posttransplant lymphoproliferative disorder after umbilical cord blood transplantation in children.
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Preleukemic phase of chronic myelogenous leukemia: morphologic and immunohistochemical characterization of 7 cases.
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Prenatal diagnosis of complete sole trisomy 1q.
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Prenatal diagnosis using fetal cells from the maternal circulation.
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Primary intracranial Ewing's sarcoma with unusual features.
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Prognosis significance of HER-2/neu overexpression/amplification in Chinese patients with curatively resected gastric cancer after the ToGA clinical trial.
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Prognostic Factors of Hepatosplenic T-cell Lymphoma: Clinicopathologic Study of 28 Cases.
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Prognostic impact of c-Rel nuclear expression and REL amplification and crosstalk between c-Rel and the p53 pathway in diffuse large B-cell lymphoma.
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Prognostic relevance of 6q deletion in Waldenström's macroglobulinemia: a multicenter study.
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Proliferation indices correlate with diagnosis and metastasis in diagnostically challenging melanocytic tumors.
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Quantitative spatial analysis of transcripts in multinucleate cells using single-molecule FISH.
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Rapid detection of submicroscopic chromosomal rearrangements in children with multiple congenital anomalies using high density oligonucleotide arrays.
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Reconstruction of gross avian genome structure, organization and evolution suggests that the chicken lineage most closely resembles the dinosaur avian ancestor.
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Recruitment of host progenitor cells in rat liver transplants.
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Recurrent glioblastoma diagnosed by fluorescence in situ hybridization for EGFR.
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Replication and preferential inheritance of hypersuppressive petite mitochondrial DNA.
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Reply by Authors.
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Rh-related antigen CD47 is the signal-transducer integrin-associated protein.
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Ring chromosome 17: phenotype variation by deletion size.
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Risk assessment for developing gliomas: a comparison of two cytogenetic approaches.
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SUN1 is required for telomere attachment to nuclear envelope and gametogenesis in mice.
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Sequential development of chronic myelogenous leukemia and primary myelofibrosis in a patient with history of large B-cell lymphoma treated with radiotherapy and chemotherapy: two myeloid neoplasms with distinct genotypic profiles suggestive of biclonality in a single individual.
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Sequential development of histiocytic sarcoma and diffuse large b-cell lymphoma in a patient with a remote history of follicular lymphoma with genotypic evidence of a clonal relationship: a divergent (bilineal) neoplastic transformation of an indolent B-cell lymphoma in a single individual.
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Single-Cell Analysis Reveals Distinct Gene Expression and Heterogeneity in Male and Female Plasmodium falciparum Gametocytes.
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Single-molecule analysis of myocyte differentiation reveals bimodal lineage commitment.
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Somatic mutations in VHL germline deletion kindred correlate with mild phenotype.
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Spatial organisation of microbiota in quiescent adenoiditis and tonsillitis.
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Spatial organization and composition of the mucosal flora in patients with inflammatory bowel disease.
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Spatial organization of bacterial flora in normal and inflamed intestine: a fluorescence in situ hybridization study in mice.
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Stable dicentric X chromosomes with two functional centromeres.
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Strict evolutionary conservation followed rapid gene loss on human and rhesus Y chromosomes.
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Study of host-microbe interactions in zebrafish.
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Subtelomeric deletions of chromosome 6p: molecular and cytogenetic characterization of three new cases with phenotypic overlap with Ritscher-Schinzel (3C) syndrome.
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Techniques for quantifying phytoplankton biodiversity.
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Telomerase reverse transcriptase is required for the localization of telomerase RNA to cajal bodies and telomeres in human cancer cells.
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Telomeres are shortened in acinar-to-ductal metaplasia lesions associated with pancreatic intraepithelial neoplasia but not in isolated acinar-to-ductal metaplasias.
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Temporal profile of replication of human chromosomes.
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The 2021 WHO Classification of Tumors of the Pleura: Advances Since the 2015 Classification.
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The combination of letrozole and trastuzumab as first or second-line biological therapy produces durable responses in a subset of HER2 positive and ER positive advanced breast cancers.
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The discovery of microdeletion syndromes in the post-genomic era: review of the methodology and characterization of a new 1q41q42 microdeletion syndrome.
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The importance of a multifaceted approach to characterizing the microbial flora of chronic wounds.
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The long noncoding RNA Chaer defines an epigenetic checkpoint in cardiac hypertrophy.
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The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes.
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The value of fluorescence in situ hybridization and polymerase chain reaction in the diagnosis of B-cell non-Hodgkin lymphoma by fine-needle aspiration.
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Three probands with autistic disorder and isodicentric chromosome 15.
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Tiling path resolution mapping of constitutional 1p36 deletions by array-CGH: contiguous gene deletion or "deletion with positional effect" syndrome?
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Transformation of follicular lymphoma to precursor B-cell lymphoblastic lymphoma with c-myc gene rearrangement as a critical event.
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Translocations and amplifications of chromosome 12 in liposarcoma demonstrated by the LSI CHOP breakapart rearrangement probe.
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Triple-hit B-cell Lymphoma With MYC, BCL2, and BCL6 Translocations/Rearrangements: Clinicopathologic Features of 11 Cases.
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Triploid mosaicism in a 45,X/69,XXY infant.
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Trisomy 8 mosaicism: selective growth advantage of normal cells vs. growth disadvantage of trisomy 8 cells.
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Unusual chromosome architecture and behaviour at an HSR.
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Use of peptide nucleic acid-fluorescence in situ hybridization for definitive, rapid identification of five common Candida species.
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Utility of EGFR and PTEN numerical aberrations in the evaluation of diffusely infiltrating astrocytomas. Laboratory investigation.
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Utility of peripheral blood dual color, double fusion fluorescent in situ hybridization for BCR/ABL fusion to assess cytogenetic remission status in chronic myeloid leukemia.
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VCL-ALK renal cell carcinoma in children with sickle-cell trait: the eighth sickle-cell nephropathy?
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m6A and YTHDF proteins contribute to the localization of select neuronal mRNAs.
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p63, a p53 homolog at 3q27-29, encodes multiple products with transactivating, death-inducing, and dominant-negative activities.
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Keywords of People
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Bennett, Vann,
George Barth Geller Distinguished Professor of Molecular Biology,
Duke Cancer Institute
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Krangel, Michael S.,
George Barth Geller Distinguished Professor of Immunology,
Integrative Immunobiology
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Lagoo, Anand Shreeram,
Professor of Pathology,
Pathology
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McLendon, Roger Edwin,
Professor of Pathology,
Pathology
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Muir, Kelly Walton,
Associate Professor of Ophthalmology,
Ophthalmology, Glaucoma
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Soderling, Scott Haydn,
George Barth Geller Distinguished Professor of Molecular Biology,
Cell Biology