The gene for Nijmegen breakage syndrome (V2) is not located on chromosome 11
about
Nijmegen breakage syndrome. The International Nijmegen Breakage Syndrome Study GroupFine localization of the Nijmegen breakage syndrome gene to 8q21: evidence for a common founder haplotype.The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21NBS1 and multiple regulations of DNA damage response.Nijmegen breakage syndrome cells fail to induce the p53-mediated DNA damage response following exposure to ionizing radiationGenetic mapping using microcell-mediated chromosome transfer suggests a locus for Nijmegen breakage syndrome at chromosome 8q21-24.A variant of the Nijmegen breakage syndrome with unusual cytogenetic features and intermediate cellular radiosensitivity.Noncomplementation of radiation-induced chromosome aberrations in ataxia-telangiectasia/ataxia-telangiectasia-variant heterodikaryons.ATM-mediated mitochondrial damage response triggered by nuclear DNA damage in normal human lung fibroblasts.
P2860
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P2860
The gene for Nijmegen breakage syndrome (V2) is not located on chromosome 11
description
1996 nî lūn-bûn
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1996年の論文
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1996年論文
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1996年論文
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1996年論文
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1996年論文
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1996年論文
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1996年论文
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1996年论文
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1996年论文
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The gene for Nijmegen breakage syndrome (V2) is not located on chromosome 11
@en
The gene for Nijmegen breakage syndrome
@nl
type
label
The gene for Nijmegen breakage syndrome (V2) is not located on chromosome 11
@en
The gene for Nijmegen breakage syndrome
@nl
prefLabel
The gene for Nijmegen breakage syndrome (V2) is not located on chromosome 11
@en
The gene for Nijmegen breakage syndrome
@nl
P2093
P2860
P1476
The gene for Nijmegen breakage syndrome (V2) is not located on chromosome 11
@en
P2093
Matsuura S
Oshimura M
P2860
P304
P407
P577
1996-04-01T00:00:00Z