Vermeulen W - Search Results

1

TRiC controls transcription resumption after UV damage by regulating Cockayne syndrome protein A.

Pines A, Dijk M, Makowski M, Meulenbroek EM, Vrouwe MG, van der Weegen Y, Baltissen M, French PJ, van Royen ME, Luijsterburg MS, Mullenders LH, Vermeulen M, Vermeulen W, Pannu NS, van Attikum H. Pines A, et al. Among authors: vermeulen m, vermeulen w. Nat Commun. 2018 Mar 12;9(1):1040. doi: 10.1038/s41467-018-03484-6. Nat Commun. 2018. PMID: 29531219 Free PMC article.

2

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. Among authors: vermeulen w. Cell. 1992 Dec 11;71(6):939-53. doi: 10.1016/0092-8674(92)90390-x. Cell. 1992. PMID: 1339317

3

Xeroderma pigmentosum complementation group G associated with Cockayne syndrome.

Vermeulen W, Jaeken J, Jaspers NG, Bootsma D, Hoeijmakers JH. Vermeulen W, et al. Am J Hum Genet. 1993 Jul;53(1):185-92. Am J Hum Genet. 1993. PMID: 8317483 Free PMC article.

4

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: vermeulen w. EMBO J. 1997 Oct 1;16(19):5955-65. doi: 10.1093/emboj/16.19.5955. EMBO J. 1997. PMID: 9312053 Free PMC article.

5

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: vermeulen w. 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.

6

ATP-dependent chromatin remodeling by the Cockayne syndrome B DNA repair-transcription-coupling factor.

Citterio E, Van Den Boom V, Schnitzler G, Kanaar R, Bonte E, Kingston RE, Hoeijmakers JH, Vermeulen W. Citterio E, et al. Among authors: vermeulen w. Mol Cell Biol. 2000 Oct;20(20):7643-53. doi: 10.1128/MCB.20.20.7643-7653.2000. Mol Cell Biol. 2000. PMID: 11003660 Free PMC article.

7

Sublimiting concentration of TFIIH transcription/DNA repair factor causes TTD-A trichothiodystrophy disorder.

Vermeulen W, Bergmann E, Auriol J, Rademakers S, Frit P, Appeldoorn E, Hoeijmakers JH, Egly JM. Vermeulen W, et al. Nat Genet. 2000 Nov;26(3):307-13. doi: 10.1038/81603. Nat Genet. 2000. PMID: 11062469

8

A temperature-sensitive disorder in basal transcription and DNA repair in humans.

Vermeulen W, Rademakers S, Jaspers NG, Appeldoorn E, Raams A, Klein B, Kleijer WJ, Hansen LK, Hoeijmakers JH. Vermeulen W, et al. Nat Genet. 2001 Mar;27(3):299-303. doi: 10.1038/85864. Nat Genet. 2001. PMID: 11242112

9

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. Among authors: vermeulen w. Mol Cell. 2001 Jul;8(1):213-24. doi: 10.1016/s1097-2765(01)00281-7. Mol Cell. 2001. PMID: 11511374 Free article.

10

Rapid switching of TFIIH between RNA polymerase I and II transcription and DNA repair in vivo.

Hoogstraten D, Nigg AL, Heath H, Mullenders LH, van Driel R, Hoeijmakers JH, Vermeulen W, Houtsmuller AB. Hoogstraten D, et al. Among authors: vermeulen w. Mol Cell. 2002 Nov;10(5):1163-74. doi: 10.1016/s1097-2765(02)00709-8. Mol Cell. 2002. PMID: 12453423 Free article.

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