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V(D)J recombination and ataxia-telangiectasia: a review.

作者信息

Kirsch I R

机构信息

National Cancer Institute, Navy Medical Oncology Branch, Bethesda, MD 20889-5105.

出版信息

Int J Radiat Biol. 1994 Dec;66(6 Suppl):S97-108.

PMID:7836858
Abstract

I review one aspect of the A-T phenotype, the remarkable and fascinating increase of lymphocytes carrying chromosomal aberrations caused by V(D)J site-specific recombination. The review is organized to first present the facts of V(D)J recombination and the findings in this regard in A-T patients. Other populations that demonstrate similar increases in such chromosomal aberrations are then presented and a hypothesis is offered as to the basis and relevance of these increases vis-à-vis A-T. The contribution of V(D)J recombination to the clonal proliferations and frank lymphoid malignancies seen in A-T patients is briefly discussed. I conclude with some speculative comments extending the observations presented into a more global consideration of a possible function of an A-T gene.

摘要

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Occurrence of TRGV-BJ hybrid gene in SV40-transformed fibroblast cell lines.TRGV-BJ杂交基因在SV40转化的成纤维细胞系中的出现。
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Critical role for Atm in suppressing V(D)J recombination-driven thymic lymphoma.
Atm在抑制V(D)J重组驱动的胸腺淋巴瘤中起关键作用。
Genes Dev. 1999 May 15;13(10):1246-50. doi: 10.1101/gad.13.10.1246.
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Pleiotropic defects in ataxia-telangiectasia protein-deficient mice.共济失调毛细血管扩张症蛋白缺陷小鼠的多效性缺陷
Proc Natl Acad Sci U S A. 1996 Nov 12;93(23):13084-9. doi: 10.1073/pnas.93.23.13084.
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Ataxia-telangiectasia and the ATM gene: linking neurodegeneration, immunodeficiency, and cancer to cell cycle checkpoints.共济失调毛细血管扩张症与ATM基因:将神经退行性变、免疫缺陷和癌症与细胞周期检查点联系起来
J Clin Immunol. 1996 Sep;16(5):254-60. doi: 10.1007/BF01541389.
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