Characterization of terminal deletions at 7q32 and 22q13.3 healed by De novo telomere addition
about
Telomere dysfunction and chromosome instabilityA novel L1 retrotransposon marker for HeLa cell line identificationIdentification of a recurrent breakpoint within the SHANK3 gene in the 22q13.3 deletion syndromeChromosome loops arising from intrachromosomal tethering of telomeres occur at high frequency in G1 (non-cycling) mitotic cells: Implications for telomere captureArray based characterization of a terminal deletion involving chromosome subband 15q26.2: an emerging syndrome associated with growth retardation, cardiac defects and developmental delayTelomere loss as a mechanism for chromosome instability in human cancerChromosome instability as a result of double-strand breaks near telomeres in mouse embryonic stem cellsRegulation of the human telomerase reverse transcriptase gene.DNA amplification by breakage/fusion/bridge cycles initiated by spontaneous telomere loss in a human cancer cell line.De novo 7p partial trisomy characterized by subtelomeric FISH and whole-genome array in a girl with mental retardation.PIF1 disruption or NBS1 hypomorphism does not affect chromosome healing or fusion resulting from double-strand breaks near telomeres in murine embryonic stem cells.Multiple pathways suppress telomere addition to DNA breaks in the Drosophila germline.Human subtelomeric copy number gains suggest a DNA replication mechanism for formation: beyond breakage-fusion-bridge for telomere stabilization.Chromosome healing by de novo telomere addition in Saccharomyces cerevisiae.Telomerase-dependent and -independent chromosome healing in mouse embryonic stem cellsMolecular mechanisms for subtelomeric rearrangements associated with the 9q34.3 microdeletion syndrome.Regulation of telomere addition at DNA double-strand breaks.Stable inheritance of telomere chromatin structure and function in the absence of telomeric repeats.Terminal 18q deletions are stabilized by neotelomeresMolecular characterization of Xp chromosome deletion in a fertile cow.Telomere healing following DNA polymerase arrest-induced breakages is likely the main mechanism generating chromosome 4p terminal deletions.Telomeres and genomic evolution.Development and validation of a CGH microarray for clinical cytogenetic diagnosis
P2860
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P2860
Characterization of terminal deletions at 7q32 and 22q13.3 healed by De novo telomere addition
description
2000 nî lūn-bûn
@nan
2000 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Characterization of terminal d ...... d by De novo telomere addition
@ast
Characterization of terminal d ...... d by De novo telomere addition
@en
Characterization of terminal d ...... d by De novo telomere addition
@nl
type
label
Characterization of terminal d ...... d by De novo telomere addition
@ast
Characterization of terminal d ...... d by De novo telomere addition
@en
Characterization of terminal d ...... d by De novo telomere addition
@nl
prefLabel
Characterization of terminal d ...... d by De novo telomere addition
@ast
Characterization of terminal d ...... d by De novo telomere addition
@en
Characterization of terminal d ...... d by De novo telomere addition
@nl
P2860
P356
P1476
Characterization of terminal d ...... d by De novo telomere addition
@en
P2860
P304
P356
10.1086/303050
P407
P577
2000-08-01T00:00:00Z