Fluorescence in situ hybridization: applications in cytogenetics and gene mapping.
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Genetic alteration and gene expression modulation during cancer progressionA draft annotation and overview of the human genomeApplications of Engineered DNA-Binding Molecules Such as TAL Proteins and the CRISPR/Cas System in Biology ResearchLocalization of single- and low-copy sequences on tomato synaptonemal complex spreads using fluorescence in situ hybridization (FISH)In situ visualisation of immunoglobulin genes in normal and malignant lymphoid cells.Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases.The gene structure and organization of mouse PG-Lb, a small chondroitin/dermatan sulphate proteoglycanCytogenetic analysis in prenatal diagnosis.Validation and implementation of array comparative genomic hybridisation as a first line test in place of postnatal karyotyping for genome imbalance.Coding exons function as tissue-specific enhancers of nearby genesMultipotential differentiation of human urine-derived stem cells: potential for therapeutic applications in urology.Direct selection of cDNAs using whole chromosomes.Detection of MYCN gene amplification in neuroblastoma by fluorescence in situ hybridization: a pediatric oncology group study.Comparison of high resolution cytogenetics, fluorescence in situ hybridisation, and DNA studies to validate the diagnosis of Prader-Willi and Angelman's syndromesHigh-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping.The large-scale organization of the centromeric region in Beta species.American College of Medical Genetics guideline on the cytogenetic evaluation of the individual with developmental delay or mental retardation.Rapid prenatal diagnosis of chromosomal aneuploidies by fluorescence in situ hybridization: clinical experience with 4,500 specimensCharacterization of supernumerary ring marker chromosomes by fluorescence in situ hybridization (FISH).Quantitative fluorescence in situ hybridization of Aureobasidium pullulans on microscope slides and leaf surfaces.Interphase cytogenetics for the detection of the t(11;22)(q24;q12) in small round cell tumors.Evidence for the organization of chromatin in megabase pair-sized loops arranged along a random walk path in the human G0/G1 interphase nucleus.A new structure for the murine Xist gene and its relationship to chromosome choice/counting during X-chromosome inactivationGenetic analysis of the mouse X inactivation center defines an 80-kb multifunction domain.Ectopic gene targeting exhibits a bimodal distribution of integration in murine cells, indicating that both intra- and interchromosomal sites are accessible to the targeting vectorOrganization of the Hox gene cluster in the grasshopper, Schistocerca gregariaPrimer-mediated in situ detection of the B-hordein gene cluster on barley chromosome 1H.Pulmonary alveolar proteinosis caused by deletion of the GM-CSFRalpha gene in the X chromosome pseudoautosomal region 1.20p12.3 microdeletion predisposes to Wolff-Parkinson-White syndrome with variable neurocognitive deficits.MCTP2 is a dosage-sensitive gene required for cardiac outflow tract development.Amplification of fluorescent in situ hybridisation signals in formalin fixed paraffin wax embedded sections of colon tumour using biotinylated tyramide.High-resolution mapping of mammalian genes by in situ hybridization to free chromatin.IFN-γ is required for cytotoxic T cell-dependent cancer genome immunoediting.Genetics of uveal melanoma and cutaneous melanoma: two of a kind?Chromosome analysis using spectral karyotyping (SKY).An Overview on Prenatal Screening for Chromosomal Aberrations.X-ray biological dosimetry performed by selective painting of human chromosomes 1 and 2.Locus-specific ChIP combined with NGS analysis reveals genomic regulatory regions that physically interact with the Pax5 promoter in a chicken B cell line.Current Role of Genetics in Hematologic Malignancies.Identification of RAPD markers linked to A and B genome sequences in Musa L.
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Fluorescence in situ hybridization: applications in cytogenetics and gene mapping.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on May 1991
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Fluorescence in situ hybridization: applications in cytogenetics and gene mapping.
@en
Fluorescence in situ hybridization: applications in cytogenetics and gene mapping.
@nl
type
label
Fluorescence in situ hybridization: applications in cytogenetics and gene mapping.
@en
Fluorescence in situ hybridization: applications in cytogenetics and gene mapping.
@nl
prefLabel
Fluorescence in situ hybridization: applications in cytogenetics and gene mapping.
@en
Fluorescence in situ hybridization: applications in cytogenetics and gene mapping.
@nl
P1433
P1476
Fluorescence in situ hybridization: applications in cytogenetics and gene mapping.
@en
P2093
P304
P356
10.1016/0168-9525(91)90378-4
P577
1991-05-01T00:00:00Z