Cloning of human satellite III DNA: different components are on different chromosomes
about
Selective interactions between vertebrate polycomb homologs and the SUV39H1 histone lysine methyltransferase suggest that histone H3-K9 methylation contributes to chromosomal targeting of Polycomb group proteins.Genomic sequence and transcriptional profile of the boundary between pericentromeric satellites and genes on human chromosome arm 10pRepeat arrays in cellular DNA related to the Epstein-Barr virus IR3 repeatCentromere and telomere movements during early meiotic prophase of mouse and man are associated with the onset of chromosome pairingComparative genomic and in situ hybridization of germ cell tumors of the infantile testis.Genomic characterization of large heterochromatic gaps in the human genome assembly.The human Y chromosome.DNA damage, somatic aneuploidy, and malignant sarcoma susceptibility in muscular dystrophies.Cosmid clones derived from both euchromatic and heterochromatic regions of the human Y chromosomeStructural instability of human tandemly repeated DNA sequences cloned in yeast artificial chromosome vectors.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.Multicolor FISH analysis of chromosomal breaks, duplications, deletions, and numerical abnormalities in the sperm of healthy menA view of interphase chromosomes.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.A human Y-chromosome specific repeated DNA family (DYZ1) consists of a tandem array of pentanucleotides.Chromosome heteromorphism quantified by high-resolution bivariate flow karyotyping.Detection of aneuploid human sperm by fluorescence in situ hybridization: evidence for a donor difference in frequency of sperm disomic for chromosomes 1 and Y.Satellite DNA sequences in the human acrocentric chromosomes: information from translocations and heteromorphisms.Sex chromosome loss and aging: in situ hybridization studies on human interphase nucleiThe relationship between paternal age, sex ratios, and aneuploidy frequencies in human sperm, as assessed by multicolor FISH.Isolation and characterization of a major tandem repeat family from the human X chromosomeThe Evolution of satellite III DNA subfamilies among primates.Simple repeated sequences in human satellite DNAIsolation and characterization of cloned human DNA fragments carrying reiterated sequences common to both autosomes and the X chromosome.The specific organisation of satellite DNA sequences on the X-chromosome of Mus musculus: partial independence of chromosome evolution.Losses of chromosomes 1p and 3q are early genetic events in the development of sporadic pheochromocytomas.Correlation of DNA hypomethylation at pericentromeric heterochromatin regions of chromosomes 16 and 1 with histological features and chromosomal abnormalities of human breast carcinomas.Diverse involvement of isoforms and gene aberrations of Akt in human lung carcinomas.Interphase cytogenetic analysis of cervical intraepithelial neoplasia.Detection of numerical and structural alterations and fusion of chromosomes 16 and 1 in low-grade papillary breast carcinoma by fluorescence in situ hybridization.Incidence of chromosome numerical changes in multiple myeloma: fluorescence in situ hybridization analysis using 15 chromosome-specific probes.Near-haploidy and subsequent polyploidization characterize the progression of peripheral chondrosarcoma.Specific loss of chromosomes 1, 2, 6, 10, 13, 17, and 21 in chromophobe renal cell carcinomas revealed by comparative genomic hybridizationA homologous subfamily of satellite III DNA on human chromosomes 14 and 22.Aneuploidy in human sperm: the use of multicolor FISH to test various theories of nondisjunction.Histone hyperacetylation in mitosis prevents sister chromatid separation and produces chromosome segregation defectsRapid detection of prognostic genetic factors in neuroblastoma using fluorescence in situ hybridisation on tumour imprints and bone marrow smears. United Kingdom Children's Cancer Study GroupAnalysis of banded human chromosomes and in situ hybridization patterns by scanning force microscopy.
P2860
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P2860
Cloning of human satellite III DNA: different components are on different chromosomes
description
1979 nî lūn-bûn
@nan
1979年の論文
@ja
1979年論文
@yue
1979年論文
@zh-hant
1979年論文
@zh-hk
1979年論文
@zh-mo
1979年論文
@zh-tw
1979年论文
@wuu
1979年论文
@zh
1979年论文
@zh-cn
name
Cloning of human satellite III DNA: different components are on different chromosomes
@ast
Cloning of human satellite III DNA: different components are on different chromosomes
@en
type
label
Cloning of human satellite III DNA: different components are on different chromosomes
@ast
Cloning of human satellite III DNA: different components are on different chromosomes
@en
prefLabel
Cloning of human satellite III DNA: different components are on different chromosomes
@ast
Cloning of human satellite III DNA: different components are on different chromosomes
@en
P2860
P356
P1476
Cloning of human satellite III DNA: different components are on different chromosomes
@en
P2093
P2860
P304
P356
10.1093/NAR/6.10.3177
P407
P577
1979-07-01T00:00:00Z