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Titlebook: Ataxia-Telangiectasia; Richard A. Gatti,Robert B. Painter Conference proceedings 1993 Springer-Verlag Berlin Heidelberg 1993 Ataxia-Telang

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31#
發(fā)表于 2025-3-26 23:37:07 | 只看該作者
Frankreichs Verfassung 1958–2008t approximately 5% of breast cancers may be the result of a highly penetrant autosomal dominant gene (Claus ., 1991). Such individuals tend to develop breast cancer at an early age, have a high prevalence of bilaterality and are at an elevated risk of other neoplasms (Lynch and Hirayam, 1989). Recen
32#
發(fā)表于 2025-3-27 02:29:32 | 只看該作者
33#
發(fā)表于 2025-3-27 09:15:49 | 只看該作者
Das Parteiensystem der V. Republikecificity. The mechanisms remain undefined. The physical basis for the differential accessibility in this site-specific recombination reaction has been a matter of much speculation. Possibilities have included the processes of transcription (Ferrier et al., 1989; Martin et al., 1991; Schlissel et al
34#
發(fā)表于 2025-3-27 12:01:54 | 只看該作者
35#
發(fā)表于 2025-3-27 16:01:07 | 只看該作者
36#
發(fā)表于 2025-3-27 17:46:22 | 只看該作者
Nato ASI Subseries H:http://image.papertrans.cn/b/image/163910.jpg
37#
發(fā)表于 2025-3-27 23:12:00 | 只看該作者
Isolation of Human cDNAS That Complement the Ataxia-Telangiectasia Phenotype in Cultured Fibroblastsgic degeneration as well as for cellular responses to induced and spontaneous DNA damage. However, despite extensive investigation, no A-T gene has been identified to date and the site of action of the A-T gene product(s) is unknown.
38#
發(fā)表于 2025-3-28 05:12:30 | 只看該作者
AT-like Radiosensitive Rodent Cell Mutants: An Alternative Approach to the Isolation of the A-T Geneectasia, immunodeficiency, hypersensitivity to ionizing radiation and predisposition to cancer (for review see Sedgwick and Boder, 1991). Despite extensive investigation, the molecular defect responsible for these pleiotropic abnormalities in A-T remains unknown.
39#
發(fā)表于 2025-3-28 07:24:13 | 只看該作者
Ataxia-Telangiectasia: A Brief Historical Overview1963.. By 1963 it was possible to publish a review of 101 cases world-wide illustrating the stereotyped nature of the disorder: progressive cerebellar ataxia in childhood, autosomal recessive heredity, oculocutaneous telangiectasia, frequency of sinopulmonary infection, peculiarity of eye movements,
40#
發(fā)表于 2025-3-28 11:15:06 | 只看該作者
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