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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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| Trachea |
100
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| Spinal cord |
90
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| Caudate nucleus |
89
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| Adrenal gland |
84
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| Thalamus |
78
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| Thyroid gland |
76
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| 5-fluorouracil Arabi… |
100
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| Pralidoxime |
99
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| Lumicolchicine |
95
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| Fusidic Acid |
92
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| Vigabatrin |
91
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| Chloropyramine |
90
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Authors: Robert A Pugh, Yuyen Lin, Chelcie Eller, Haley Leesley, Isaac K O Cann, Maria Spies
Journal of molecular biology 2008 Nov 28Authors: Richard Booton, Tim Ward, Jim Heighway, Pat Taylor, Fiona Power, Linda Ashcroft, Julie Morris, Nicholas Thatcher
Cancer 2006 Jun 1Thought leaders and organizations working on research involving Xeroderma pigmentosum group D protein.
conditions: Carcinoma, Non-Small-Cell Lung ; Chemotherapy
interventions: No
conditions: Prostate Cancer
interventions: none
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