Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization - Test2 - elhamkhani - TriplyDB

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

http://www.wikidata.org/entity/Q29616823

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Further delineation of complex chromosomal rearrangements in fertile male using multicolor banding Identification of novel candidate target genes, including EPHB3, MASP1 and SST at 3q26.2-q29 in squamous cell carcinoma of the lung A human RNA polymerase II subunit is encoded by a recently generated multigene family The interrelationship between DRIM gene expression and cytogenetic and phenotypic characteristics in human breast tumor cell lines Acinar cell apoptosis in Serpini2-deficient mice models pancreatic insufficiency The cloning and characterization of a novel human diacylglycerol kinase, DGKiota Cloning and characterization of a secreted frizzled-related protein that is expressed by the retinal pigment epithelium Rec8p, a meiotic recombination and sister chromatid cohesion phosphoprotein of the Rad21p family conserved from fission yeast to humans A nuclear factor, ASC-2, as a cancer-amplified transcriptional coactivator essential for ligand-dependent transactivation by nuclear receptors in vivo Loss-of-function mutations in a human gene related to Chlamydomonas reinhardtii dynein IC78 result in primary ciliary dyskinesia.Cancer in Radar Technicians Exposed to Radiofrequency/Microwave Radiation: Sentinel Episodes The human enamel protein gene amelogenin is expressed from both the X and the Y chromosomes Differential contributions of mammalian Rad54 paralogs to recombination, DNA damage repair, and meiosis The fragile X mental retardation syndrome protein interacts with novel homologs FXR1 and FXR2 HSF4, a new member of the human heat shock factor family which lacks properties of a transcriptional activator Human dipeptidyl-peptidase I. Gene characterization, localization, and expression Characterization of the myotubularin dual specificity phosphatase gene family from yeast to human BST-1, a surface molecule of bone marrow stromal cell lines that facilitates pre-B-cell growth The whole nucleotide sequence and chromosomal localization of the gene for human metabotropic glutamate receptor subtype 6 Duplicated KOX zinc finger gene clusters flank the centromere of human chromosome 10: evidence for a pericentric inversion during primate evolution Cloning of a putative ligand for the T1/ST2 receptor Diamond-Blackfan anaemia in a girl with a de novo balanced reciprocal X;19 translocation Centrosome amplification drives chromosomal instability in breast tumor development.A novel class of Pseudoautosomal region 1 deletions downstream of SHOX is associated with Leri-Weill dyschondrosteosis.Reciprocal mouse and human limb phenotypes caused by gain- and loss-of-function mutations affecting Lmbr1 Isolation of fetal DNA from nucleated erythrocytes in maternal blood MT-III, a brain-specific member of the metallothionein gene family Genomic organization of the murine Miller-Dieker/lissencephaly region: conservation of linkage with the human region Regional mapping of the Batten disease locus (CLN3) to human chromosome 16p12 Identification of a gene at 11q23 encoding a guanine nucleotide exchange factor: evidence for its fusion with MLL in acute myeloid leukemia Mutations of the microsomal triglyceride-transfer-protein gene in abetalipoproteinemia Alternative splicing of the human diacylglycerol kinase zeta gene in muscle Disruption of a new X linked gene highly expressed in brain in a family with two mentally retarded males Cloning of a candidate gene for ataxia-telangiectasia group D Detection of chromosomal regions showing differential gene expression in human skeletal muscle and in alveolar rhabdomyosarcoma Alteration in expression of the rat mitochondrial ATPase 6 gene during Pneumocystis carinii infection Analysis and visualization of chromosomal abnormalities in SNP data with SNPscan Novel biomarkers of genetic damage in humans: use of fluorescence in situ hybridization to detect aneuploidy and micronuclei in exfoliated cells Biomarkers of head and neck cancer, tools or a gordian knot?Mass casualties and health care following the release of toxic chemicals or radioactive material--contribution of modern biotechnology

P2860

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P2860

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

http://www.wikidata.org/entity/Q29616823

description

1986 nî lūn-bûn

@nan

1986 թուականի Մայիսին հրատարակուած գիտական յօդուած

@hyw

1986 թվականի մայիսին հրատարակված գիտական հոդված

@hy

1986年の論文

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1986年論文

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1986年論文

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1986年論文

@zh-hk

1986年論文

@zh-mo

1986年論文

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1986年论文

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name

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

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Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

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type

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Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

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Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

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prefLabel

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

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Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

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Proceedings of the National Academy of Sciences of the United States of America

P1476

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

@en

P2093

Gray JW

http://www.w3.org/2001/XMLSchema#string

Pinkel D

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Straume T

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P2860

Enzymatic synthesis of biotin-labeled polynucleotides: novel nucleic acid affinity probes.

Mapping muscle protein genes by in situ hybridization using biotin-labeled probes.

Specific staining of human chromosomes in Chinese hamster x man hybrid cell lines demonstrates interphase chromosome territories.

Unscheduled DNA synthesis after partial UV irradiation of the cell nucleus. Distribution in interphase and metaphase.

Isolation of repetitive DNA sequences from human chromosome 21

Chromosomal localization of several families of repetitive sequences by in situ hybridization.

A male-specific DNA probe detects heterochromatin sequences in a familial Yq- chromosome

Localization of the human insulin gene to the distal end of the short arm of chromosome 11.

Different central nervous system cell types display distinct and nonrandom arrangements of satellite DNA sequences.

Construction and characterization of genomic libraries from specific human chromosomes

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2934-8

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scholarly article

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1533680

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10.1073/PNAS.83.9.2934

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9

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83

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1986-05-01T00:00:00Z

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19698593

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3458254

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323421

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