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Human chromosome-specific repetitive DNA sequences: novel markers for genetic analysis.

Human chromosome-specific repetitive DNA sequences: novel markers for genetic analysis.

http://www.wikidata.org/entity/Q36473258

about

Cell cycle-dependent recruitment of telomerase RNA and Cajal bodies to human telomeres Human sat III and Drosophila hsr omega transcripts: a common paradigm for regulation of nuclear RNA processing in stressed cells Dualistic function of Daxx at centromeric and pericentromeric heterochromatin in normal and stress conditions Protein kinase A regulates molecular chaperone transcription and protein aggregation Conservation of the human telomere sequence (TTAGGG)n among vertebrates A highly conserved repetitive DNA sequence, (TTAGGG)n, present at the telomeres of human chromosomes An integrated physical map for the short arm of human chromosome 5.Saturating the region of the polycystic kidney disease gene with NotI linking clones.Highly conserved repetitive DNA sequences are present at human centromeres.Spectral imaging in preconception/preimplantation genetic diagnosis of aneuploidy: multicolor, multichromosome screening of single cells.Use of fluorescent sequence-specific polyamides to discriminate human chromosomes by microscopy and flow cytometry.JKT-1 is not a human seminoma cell line.Small marker chromosomes in man: origin from pericentric heterochromatin of chromosomes 1, 9, and 16 Genomic characterization of large heterochromatic gaps in the human genome assembly.Detection of aneuploidy involving chromosomes 13, 18, or 21, by fluorescence in situ hybridization (FISH) to interphase and metaphase amniocytes.Macromolecular organization of human centromeric regions reveals high-frequency, polymorphic macro DNA repeats Human beta satellite DNA: genomic organization and sequence definition of a class of highly repetitive tandem DNA.Tandemly repeated DNA families in the mouse genome.A view of interphase chromosomes.Cloning human telomeric DNA fragments into Saccharomyces cerevisiae using a yeast-artificial-chromosome vector.Long-range organization of tandem arrays of alpha satellite DNA at the centromeres of human chromosomes: high-frequency array-length polymorphism and meiotic stability.DNMT3B mutations and DNA methylation defect define two types of ICF syndrome.FISH in cancer diagnosis and prognostication: from cause to course of disease.Combined karyotyping, CGH and M-FISH analysis allows detailed characterization of unidentified chromosomal rearrangements in Merkel cell carcinoma.Paternal heterochromatin formation in human embryos is H3K9/HP1 directed and primed by sperm-derived histone modifications.Rubinstein-Taybi syndrome caused by submicroscopic deletions within 16p13.3.Chromosomal origin of small ring marker chromosomes in man: characterization by molecular genetics.Chromosome-specific alpha satellite DNA from the centromere of human chromosome 16 The Evolution of satellite III DNA subfamilies among primates.Correlation of DNA hypomethylation at pericentromeric heterochromatin regions of chromosomes 16 and 1 with histological features and chromosomal abnormalities of human breast carcinomas.Detection of numerical and structural alterations and fusion of chromosomes 16 and 1 in low-grade papillary breast carcinoma by fluorescence in situ hybridization.Detection of numerical chromosomal abnormalities in neoplastic hematopoietic cells by in situ hybridization with a chromosome-specific probe.The Reed-Sternberg cells of Hodgkin disease are clonal.Near-haploidy and subsequent polyploidization characterize the progression of peripheral chondrosarcoma.A homologous subfamily of satellite III DNA on human chromosomes 14 and 22.In vivo binding of active heat shock transcription factor 1 to human chromosome 9 heterochromatin during stress.Construction of a map of chromosome 16 by using radiation hybrids A transcriptomic analysis of human centromeric and pericentric sequences in normal and tumor cells.RETROTRANSPOSON MYS IS CONCENTRATED ON THE SEX CHROMOSOMES: IMPLICATIONS FOR COPY NUMBER CONTAINMENT.Demonstration of the translocation der(16)t(1;16)(q12;q11.2) in interphase nuclei of Ewing tumors.

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Human chromosome-specific repetitive DNA sequences: novel markers for genetic analysis.

http://www.wikidata.org/entity/Q36473258

description

1987 nî lūn-bûn

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1987年の論文

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1987年学术文章

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1987年学术文章

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1987年学术文章

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1987年学术文章

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1987年学术文章

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1987年學術文章

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1987年學術文章

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1987年學術文章

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name

Human chromosome-specific repetitive DNA sequences: novel markers for genetic analysis.

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Human chromosome-specific repetitive DNA sequences: novel markers for genetic analysis.

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type

label

Human chromosome-specific repetitive DNA sequences: novel markers for genetic analysis.

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Human chromosome-specific repetitive DNA sequences: novel markers for genetic analysis.

@en

prefLabel

Human chromosome-specific repetitive DNA sequences: novel markers for genetic analysis.

@ast

Human chromosome-specific repetitive DNA sequences: novel markers for genetic analysis.

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Human chromosome-specific repetitive DNA sequences: novel markers for genetic analysis.

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C E Hildebrand

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J L Longmire

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J Meyne

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K L Albright

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

L L Deaven

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

L S Cram

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M F Bartholdi

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N E Joste

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R K Moyzis

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T Schwarzacher-Robinson

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P2860

Construction of human chromosome-specific DNA libraries from flow-sorted chromosomes.

Structure, organization, and sequence of alpha satellite DNA from human chromosome 17: evidence for evolution by unequal crossing-over and an ancestral pentamer repeat shared with the human X chromosome.

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P304

375-386

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scholarly article

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10.1007/BF00333988

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6

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95

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1987-01-01T00:00:00Z

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