PubMed (OMIM) for id: 75657

Year	Number of Results
1979	1
1980	1
1983	1
1985	1
1987	2
1989	1
1990	1
1992	1
1993	4
1994	7
1995	1
1996	2
1997	2
1999	2
2001	3
2002	3
2004	1
2005	2
2023	0

1

Recognition of RNA polymerase II and transcription bubbles by XPG, CSB, and TFIIH: insights for transcription-coupled repair and Cockayne Syndrome.

Sarker AH, Tsutakawa SE, Kostek S, Ng C, Shin DS, Peris M, Campeau E, Tainer JA, Nogales E, Cooper PK. Sarker AH, et al. Mol Cell. 2005 Oct 28;20(2):187-98. doi: 10.1016/j.molcel.2005.09.022. Mol Cell. 2005. PMID: 16246722 Free article.

2

Retraction.

Cooper PK, Nouspikel T, Clarkson SG. Cooper PK, et al. Science. 2005 Jun 17;308(5729):1740. doi: 10.1126/science.308.5729.1740b. Science. 2005. PMID: 15961651 No abstract available.

3

Identification of the XPG region that causes the onset of Cockayne syndrome by using Xpg mutant mice generated by the cDNA-mediated knock-in method.

Shiomi N, Kito S, Oyama M, Matsunaga T, Harada YN, Ikawa M, Okabe M, Shiomi T. Shiomi N, et al. Mol Cell Biol. 2004 May;24(9):3712-9. doi: 10.1128/MCB.24.9.3712-3719.2004. Mol Cell Biol. 2004. PMID: 15082767 Free PMC article.

4

Requirement of yeast RAD2, a homolog of human XPG gene, for efficient RNA polymerase II transcription. implications for Cockayne syndrome.

Lee SK, Yu SL, Prakash L, Prakash S. Lee SK, et al. Cell. 2002 Jun 28;109(7):823-34. doi: 10.1016/s0092-8674(02)00795-x. Cell. 2002. PMID: 12110180 Free article.

5

Relationship of neurologic degeneration to genotype in three xeroderma pigmentosum group G patients.

Emmert S, Slor H, Busch DB, Batko S, Albert RB, Coleman D, Khan SG, Abu-Libdeh B, DiGiovanna JJ, Cunningham BB, Lee MM, Crollick J, Inui H, Ueda T, Hedayati M, Grossman L, Shahlavi T, Cleaver JE, Kraemer KH. Emmert S, et al. J Invest Dermatol. 2002 Jun;118(6):972-82. doi: 10.1046/j.1523-1747.2002.01782.x. J Invest Dermatol. 2002. PMID: 12060391 Free article.

6

The founding members of xeroderma pigmentosum group G produce XPG protein with severely impaired endonuclease activity.

Lalle P, Nouspikel T, Constantinou A, Thorel F, Clarkson SG. Lalle P, et al. J Invest Dermatol. 2002 Feb;118(2):344-51. doi: 10.1046/j.0022-202x.2001.01673.x. J Invest Dermatol. 2002. PMID: 11841555 Free article.

7

Sequential assembly of the nucleotide excision repair factors in vivo.

Volker M, Moné MJ, Karmakar P, van Hoffen A, Schul W, Vermeulen W, Hoeijmakers JH, van Driel R, van Zeeland AA, Mullenders LH. Volker M, et al. Mol Cell. 2001 Jul;8(1):213-24. doi: 10.1016/s1097-2765(01)00281-7. Mol Cell. 2001. PMID: 11511374 Free article.

8

Cerebro-oculo-facio-skeletal syndrome with a nucleotide excision-repair defect and a mutated XPD gene, with prenatal diagnosis in a triplet pregnancy.

Graham JM Jr, Anyane-Yeboa K, Raams A, Appeldoorn E, Kleijer WJ, Garritsen VH, Busch D, Edersheim TG, Jaspers NG. Graham JM Jr, et al. Am J Hum Genet. 2001 Aug;69(2):291-300. doi: 10.1086/321295. Epub 2001 Jul 3. Am J Hum Genet. 2001. PMID: 11443545 Free PMC article.

9

Xeroderma pigmentosum group G with severe neurological involvement and features of Cockayne syndrome in infancy.

Zafeiriou DI, Thorel F, Andreou A, Kleijer WJ, Raams A, Garritsen VH, Gombakis N, Jaspers NG, Clarkson SG. Zafeiriou DI, et al. Pediatr Res. 2001 Mar;49(3):407-12. doi: 10.1203/00006450-200103000-00016. Pediatr Res. 2001. PMID: 11228268

10

Studies on a new case of xeroderma pigmentosum (XP3BR) from complementation group G with cellular sensitivity to ionizing radiation.

Arlett CF, Harcourt SA, Lehmann AR, Stevens S, Ferguson-Smith MA, Morley WN. Arlett CF, et al. Carcinogenesis. 1980 Sep;1(9):745-51. doi: 10.1093/carcin/1.9.745. Carcinogenesis. 1980. PMID: 11219864

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