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Xeroderma pigmentosum (XP) is a human autosomal recessive disease, characterised by a high incidence of sunlight-induced skin cancer. People's skin cells with this condition are hypersensitive to ultraviolet light, due to defects in the incision step of DNA excision repair. There are a minimum of seven genetic complementation groups involved in this pathway: XP-A to XP-G. XP-G is one of the most rare and phenotypically heterogeneous of XP, showing anything from slight to extreme dysfunction in DNA excision repair. XP-G can be corrected by a 133 Kd nuclear protein, XPGC . XPGC is an acidic protein that confers normal UV resistance in expressing cells . It is a magnesium-dependent, single-...
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| Globus pallidus |
100
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| Penis |
97
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| Subthalamic nucleus |
81
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| Thymus |
80
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| Adrenal gland |
76
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| Caudate nucleus |
74
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| Oxygen |
100
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| Phorbol Ester |
97
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| Dasatinib |
88
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| [14c] Alpha-amino-be… |
85
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| Transferrin |
84
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| Thymidine |
84
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Individual Studies |
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Authors: Shinsuke Ito, Isao Kuraoka, Pierre Chymkowitch, Emmanuel Compe, Arato Takedachi, Chie Ishigami, Frédéric Coin, Jean-Marc Egly, Kiyoji Tanaka
Molecular cell 2007 Apr 27Authors: Tomoyuki Furukawa, Tomohiro Imamura, Hiroko K Kitamoto, Hiroaki Shimada
Plant molecular biology 2008 MarThought leaders and organizations working on research involving XPG I.