van Gool AJ - Search Results

1

Molecular analysis of mutations in the CSB (ERCC6) gene in patients with Cockayne syndrome.

Mallery DL, Tanganelli B, Colella S, Steingrimsdottir H, van Gool AJ, Troelstra C, Stefanini M, Lehmann AR. Mallery DL, et al. Among authors: van gool aj. Am J Hum Genet. 1998 Jan;62(1):77-85. doi: 10.1086/301686. Am J Hum Genet. 1998. PMID: 9443879 Free PMC article.

2

RAD26, the functional S. cerevisiae homolog of the Cockayne syndrome B gene ERCC6.

van Gool AJ, Verhage R, Swagemakers SM, van de Putte P, Brouwer J, Troelstra C, Bootsma D, Hoeijmakers JH. van Gool AJ, et al. Among authors: van de putte p. EMBO J. 1994 Nov 15;13(22):5361-9. doi: 10.1002/j.1460-2075.1994.tb06871.x. EMBO J. 1994. PMID: 7957102 Free PMC article.

3

ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes.

Troelstra C, van Gool A, de Wit J, Vermeulen W, Bootsma D, Hoeijmakers JH. Troelstra C, et al. Cell. 1992 Dec 11;71(6):939-53. doi: 10.1016/0092-8674(92)90390-x. Cell. 1992. PMID: 1339317

4

Phenotypic heterogeneity in nucleotide excision repair mutants of rodent complementation groups 1 and 4.

Busch DB, van Vuuren H, de Wit J, Collins A, Zdzienicka MZ, Mitchell DL, Brookman KW, Stefanini M, Riboni R, Thompson LH, Albert RB, van Gool AJ, Hoeijmakers J. Busch DB, et al. Among authors: van gool aj, van vuuren h. Mutat Res. 1997 Mar 12;383(2):91-106. doi: 10.1016/s0921-8777(96)00048-1. Mutat Res. 1997. PMID: 9088342

5

Defective transcription-coupled repair in Cockayne syndrome B mice is associated with skin cancer predisposition.

van der Horst GT, van Steeg H, Berg RJ, van Gool AJ, de Wit J, Weeda G, Morreau H, Beems RB, van Kreijl CF, de Gruijl FR, Bootsma D, Hoeijmakers JH. van der Horst GT, et al. Among authors: van gool aj, van steeg h, van kreijl cf. Cell. 1997 May 2;89(3):425-35. doi: 10.1016/s0092-8674(00)80223-8. Cell. 1997. PMID: 9150142 Free article.

6

Biochemical and biological characterization of wild-type and ATPase-deficient Cockayne syndrome B repair protein.

Citterio E, Rademakers S, van der Horst GT, van Gool AJ, Hoeijmakers JH, Vermeulen W. Citterio E, et al. Among authors: van gool aj, van der horst gt. J Biol Chem. 1998 May 8;273(19):11844-51. doi: 10.1074/jbc.273.19.11844. J Biol Chem. 1998. PMID: 9565609 Free article.

7

Cockayne syndrome: defective repair of transcription?

van Gool AJ, van der Horst GT, Citterio E, Hoeijmakers JH. van Gool AJ, et al. Among authors: van der horst gt. EMBO J. 1997 Jul 16;16(14):4155-62. doi: 10.1093/emboj/16.14.4155. EMBO J. 1997. PMID: 9250659 Free PMC article. Review.

8

The Cockayne syndrome B protein, involved in transcription-coupled DNA repair, resides in an RNA polymerase II-containing complex.

van Gool AJ, Citterio E, Rademakers S, van Os R, Vermeulen W, Constantinou A, Egly JM, Bootsma D, Hoeijmakers JH. van Gool AJ, et al. Among authors: van os r. EMBO J. 1997 Oct 1;16(19):5955-65. doi: 10.1093/emboj/16.19.5955. EMBO J. 1997. PMID: 9312053 Free PMC article.

9

A CHO mutant, UV40, that is sensitive to diverse mutagens and represents a new complementation group of mitomycin C sensitivity.

Busch DB, Zdzienicka MZ, Natarajan AT, Jones NJ, Overkamp WJ, Collins A, Mitchell DL, Stefanini M, Botta E, Albert RB, Liu N, White DA, van Gool AJ, Thompson LH. Busch DB, et al. Among authors: van gool aj. Mutat Res. 1996 Aug 8;363(3):209-21. doi: 10.1016/0921-8777(96)00014-6. Mutat Res. 1996. PMID: 8765162

10

UV-induced ubiquitination of RNA polymerase II: a novel modification deficient in Cockayne syndrome cells.

Bregman DB, Halaban R, van Gool AJ, Henning KA, Friedberg EC, Warren SL. Bregman DB, et al. Among authors: van gool aj. Proc Natl Acad Sci U S A. 1996 Oct 15;93(21):11586-90. doi: 10.1073/pnas.93.21.11586. Proc Natl Acad Sci U S A. 1996. PMID: 8876179 Free PMC article.

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