G
Gary M. Jones
Researcher at National Institutes of Health
Publications - 44
Citations - 1733
Gary M. Jones is an academic researcher from National Institutes of Health. The author has contributed to research in topics: DNA repair & Chromatid. The author has an hindex of 22, co-authored 44 publications receiving 1718 citations.
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Journal ArticleDOI
Transfer of HIV-1-specific cytotoxic T lymphocytes to an AIDS patient leads to selection for mutant HIV variants and subsequent disease progression.
Scott Koenig,Anthony J. Conley,Yambasu A. Brewah,Gary M. Jones,Simon Leath,Lynn J. Boots,Victoria J. Davey,Guiseppi Pantaleo,James F. Demarest,Charles W. Carter,Christine Wannebo,John R. Yannelli,Steven A. Rosenberg,H. Clifford Lane +13 more
TL;DR: It is suggested that active CTL selection of viral variants could contribute to the pathogenesis of AIDS and that clinical progression can occur despite high levels of circulating HIV-1-specific CTLs.
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Chromatid damage after G2 phase x-irradiation of cells from cancer-prone individuals implicates deficiency in DNA repair
TL;DR: In this article, the authors compared 10 lines of skin fibroblasts from individuals with genetic disorders predisposing to a high risk of cancer with nine lines from normal adult donors with respect to chromatid damage after x-irradiation.
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Factors affecting and significance of G2 chromatin radiosensitivity in predisposition to cancer.
TL;DR: This response in skin fibroblasts from individuals with genetic conditions predisposing to cancer than in comparable cells from clinically normal controls could provide the basis of a test for detecting individuals carrying genes that predispose to a high risk of cancer.
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Enhanced Chromatid Damage in Blood Lymphocytes After G2 Phase X Irradiation, a Marker of the Ataxia-Telangiectasia Gene
Katherine K. Sanford,Ram Parshad,Floyd M. Price,Gary M. Jones,Robert E. Tarone,Lindsay Eierman,Paula Hale,Thomas A. Waldmann +7 more
TL;DR: The persistence of chromatid breaks and gaps in lymphocytes following radiation-induced DNA damage during G2 suggests a deficiency or deficiencies in DNA repair that may be the defect at the molecular level that results in the enhanced radiosensitivity and cancer proneness characterizing A-T gene carriers and patients.
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Fluorescent light-induced chromosome damage and its prevention in mouse cells in culture.
TL;DR: Most of the chromosomal abnormalities observed in long-term culture of mouse cells may result from exposure of cells or medium to fluorescent room lights in the presence of atmospheric oxygen, and can be minimized by shielding cells and medium from light, lowering the PO2 of the medium, and including reducing agents such as glutathione and ascorbic acid in the medium formulation.