Analysis of genes and chromosomes by nonisotopic in situ hybridization.
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Characterization and mapping of human genes encoding zinc finger proteinsDiagnostic gold standard for soft tissue tumours: morphology or molecular genetics?Homologous pairing is reduced but not abolished in asynaptic mutants of yeastExtra c-myc oncogene copies in high risk cutaneous malignant melanoma and melanoma metastasesLocalization of single- and low-copy sequences on tomato synaptonemal complex spreads using fluorescence in situ hybridization (FISH)Homology of lubricin and superficial zone protein (SZP): products of megakaryocyte stimulating factor (MSF) gene expression by human synovial fibroblasts and articular chondrocytes localized to chromosome 1q25.In situ visualisation of immunoglobulin genes in normal and malignant lymphoid cells.Nonrandom chromosomal numerical abnormality predicting prognosis of gastric cancer: a retrospective study of 51 cases using pathology archives.Specific metaphase and interphase detection of the breakpoint region in 8q24 of Burkitt lymphoma cells by triple-color fluorescence in situ hybridization.Simultaneous visualization of seven different DNA probes by in situ hybridization using combinatorial fluorescence and digital imaging microscopy.Mechanisms underlying losses of heterozygosity in human colorectal cancersMonitoring the course of chronic myelogenous leukemia by fluorescence in situ hybridization.American College of Medical Genetics guideline on the cytogenetic evaluation of the individual with developmental delay or mental retardation.Rapid detection of chromosome aneuploidies in uncultured amniocytes by using fluorescence in situ hybridization (FISH).Large domains of apparent delayed replication timing associated with triplet repeat expansion at FRAXA and FRAXE.Analysis of banded human chromosomes and in situ hybridization patterns by scanning force microscopy.In situ analysis of changes in telomere size during replicative aging and cell transformation.Resistance of human squamous carcinoma cells to transforming growth factor beta 1 is a recessive traitCCD microscopy and image analysis of cells and chromosomes stained by fluorescence in situ hybridization.Rapid fluorescence in situ hybridization with repetitive DNA probes: quantification by digital image analysis.Evidence for a nuclear compartment of transcription and splicing located at chromosome domain boundaries.Clarification of subtle reciprocal rearrangements using fluorescence in situ hybridization.A strategy for the characterization of minute chromosome rearrangements using multiple color fluorescence in situ hybridization with chromosome-specific DNA libraries and YAC clones.Detection of in situ hybridization to human chromosomes with the atomic force microscope.The three-dimensional study of chromosomes and upstream binding factor-immunolabeled nucleolar organizer regions demonstrates their nonrandom spatial arrangement during mitosis.A new method for identification of Trichomonas vaginalis by fluorescent DNA in situ hybridizationTumor suppression in human skin carcinoma cells by chromosome 15 transfer or thrombospondin-1 overexpression through halted tumor vascularization.Chromosomal instability correlates with poor outcome in patients with myelodysplastic syndromes irrespectively of the cytogenetic risk groupPrenatal and postnatal characterization of Y chromosome structural anomalies by molecular cytogenetic analysis.Isodicentric (X)(q13) in haematological malignancies: presentation of five new cases, application of fluorescence in situ hybridization (FISH) and review of the literature.Detection of genetic aberrations in bladder cancer using in situ hybridization.Amplification of FISH signals using intermittent microwave irradiation for analysis of chromosomal instability in gastric cancer.Inefficient processing impairs release of RNA from the site of transcription.Cytochemical detection systems for in situ hybridization, and the combination with immunocytochemistry, 'who is still afraid of red, green and blue?'.Replication timing properties of the human HPRT locus on active, inactive and reactivated X chromosomes.The mouse filensin gene: structure and evolutionary relation to other intermediate filament genes.In situ hybridization and detection using nonisotopic probes.Characterization of an inversion duplication of the short arm of chromosome 8 by fluorescent in situ hybridization.The elastin gene is disrupted in a family with a balanced translocation t(7;16)(q11.23;q13) associated with a variable expression of the Williams-Beuren syndrome.In situ hybridization to metaphase chromosomes and interphase nuclei.
P2860
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P2860
Analysis of genes and chromosomes by nonisotopic in situ hybridization.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on February 1991
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Analysis of genes and chromosomes by nonisotopic in situ hybridization.
@en
Analysis of genes and chromosomes by nonisotopic in situ hybridization.
@nl
type
label
Analysis of genes and chromosomes by nonisotopic in situ hybridization.
@en
Analysis of genes and chromosomes by nonisotopic in situ hybridization.
@nl
prefLabel
Analysis of genes and chromosomes by nonisotopic in situ hybridization.
@en
Analysis of genes and chromosomes by nonisotopic in situ hybridization.
@nl
P2093
P1476
Analysis of genes and chromosomes by nonisotopic in situ hybridization.
@en
P2093
P356
10.1016/1050-3862(91)90005-C
P577
1991-02-01T00:00:00Z