Description:
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG
NIA AGING CELL REPOSITORY DNA PANEL - AGING SYNDROMES
Repository
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Subcollection |
Heritable Diseases |
License Required
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Class |
Repair Defective and Chromosomal Instability Syndromes |
Sample Source
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Subject Type
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Family Type
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Ethnicity
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Family Member
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Genetic Data
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IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Nucleoside Phosphorylase, Glucose-6-Phosphate Dehydrogenase, and Lactate Dehydrogenase Isoenzyme Electrophoresis |
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Panigrahi GB, Lau R, Montgomery SE, Leonard MR, Pearson CE, Slipped (CTG)*(CAG) repeats can be correctly repaired, escape repair or undergo error-prone repair Nature structural & molecular biology12:654-62 2005 |
PubMed ID: 16025129 |
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McCulloch SD, Gu L, Li GM, Nick-dependent and -independent processing of large DNA loops in human cells. J Biol Chem278(50):50803-9 2003 |
PubMed ID: 14522965 |
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Bowman KK, Smith CA, Hanawalt PC, Excision-repair patch lengths are similar for transcription-coupled repair and
global genome repair in UV-irradiated human cells. Mutat Res385(2):95-105 1997 |
PubMed ID: 9447231 |
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Moriwaki S, Stefanini M, Lehmann AR, Hoeijmakers JH, Robbins JH, Rapin I, Botta E, Tanganelli B, Vermeulen W, Broughton BC, Kraemer KH, DNA repair and ultraviolet mutagenesis in cells from a new patient with xeroderma pigmentosum group G and cockayne syndrome resemble xeroderma pigmentosum cells. J Invest Dermatol107(4):647-53 1996 |
PubMed ID: 8823375 |
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Matsunaga T, Mu D, Park CH, Reardon JT, Sancar A, Human DNA repair excision nuclease. Analysis of the roles of the subunits involved in dual incisions by using anti-XPG and anti-ERCC1 antibodies. J Biol Chem270:20862-9 1995 |
PubMed ID: 7657672 |
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