Vermeulen W - Search Results

1

Pollitt syndrome patients carry mutation in TTDN1.

Swagemakers SM, Jaspers NG, Raams A, Heijsman D, Vermeulen W, Troelstra C, Kremer A, Lincoln SE, Tearle R, Hoeijmakers JH, van der Spek PJ. Swagemakers SM, et al. Among authors: vermeulen w. Meta Gene. 2014 Aug 30;2:616-8. doi: 10.1016/j.mgene.2014.08.001. eCollection 2014 Dec. Meta Gene. 2014. PMID: 25606444 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 group A correcting protein from calf thymus.

Eker AP, Vermeulen W, Miura N, Tanaka K, Jaspers NG, Hoeijmakers JH, Bootsma D. Eker AP, et al. Among authors: vermeulen w. Mutat Res. 1992 Sep;274(3):211-24. doi: 10.1016/0921-8777(92)90067-d. Mutat Res. 1992. PMID: 1380654

4

Xeroderma pigmentosum complementation group H falls into complementation group D.

Vermeulen W, Stefanini M, Giliani S, Hoeijmakers JH, Bootsma D. Vermeulen W, et al. Mutat Res. 1991 Sep;255(2):201-8. doi: 10.1016/0921-8777(91)90054-s. Mutat Res. 1991. PMID: 1922152 No abstract available.

5

Effects of microinjected photoreactivating enzyme on thymine dimer removal and DNA repair synthesis in normal human and xeroderma pigmentosum fibroblasts.

Roza L, Vermeulen W, Bergen Henegouwen JB, Eker AP, Jaspers NG, Lohman PH, Hoeijmakers JH. Roza L, et al. Among authors: vermeulen w. Cancer Res. 1990 Mar 15;50(6):1905-10. Cancer Res. 1990. PMID: 2306742

6

The cloned human DNA excision repair gene ERCC-1 fails to correct xeroderma pigmentosum complementation groups A through I.

van Duin M, Vredeveldt G, Mayne LV, Odijk H, Vermeulen W, Klein B, Weeda G, Hoeijmakers JH, Bootsma D, Westerveld A. van Duin M, et al. Among authors: vermeulen w. Mutat Res. 1989 Mar;217(2):83-92. doi: 10.1016/0921-8777(89)90059-1. Mutat Res. 1989. PMID: 2918869

7

Three unusual repair deficiencies associated with transcription factor BTF2(TFIIH): evidence for the existence of a transcription syndrome.

Vermeulen W, van Vuuren AJ, Chipoulet M, Schaeffer L, Appeldoorn E, Weeda G, Jaspers NG, Priestley A, Arlett CF, Lehmann AR, et al. Vermeulen W, et al. Cold Spring Harb Symp Quant Biol. 1994;59:317-29. doi: 10.1101/sqb.1994.059.01.036. Cold Spring Harb Symp Quant Biol. 1994. PMID: 7587084 No abstract available.

8

Nucleotide excision repair syndromes: molecular basis and clinical symptoms.

Bootsma D, Weeda G, Vermeulen W, van Vuuren H, Troelstra C, van der Spek P, Hoeijmakers J. Bootsma D, et al. Among authors: vermeulen w. Philos Trans R Soc Lond B Biol Sci. 1995 Jan 30;347(1319):75-81. doi: 10.1098/rstb.1995.0012. Philos Trans R Soc Lond B Biol Sci. 1995. PMID: 7746858 Review.

9

Correction of xeroderma pigmentosum repair defect by basal transcription factor BTF2 (TFIIH).

van Vuuren AJ, Vermeulen W, Ma L, Weeda G, Appeldoorn E, Jaspers NG, van der Eb AJ, Bootsma D, Hoeijmakers JH, Humbert S, et al. van Vuuren AJ, et al. Among authors: vermeulen w. EMBO J. 1994 Apr 1;13(7):1645-53. doi: 10.1002/j.1460-2075.1994.tb06428.x. EMBO J. 1994. PMID: 8157004 Free PMC article.

10

Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3.

Vermeulen W, Scott RJ, Rodgers S, Müller HJ, Cole J, Arlett CF, Kleijer WJ, Bootsma D, Hoeijmakers JH, Weeda G. Vermeulen W, et al. Am J Hum Genet. 1994 Feb;54(2):191-200. Am J Hum Genet. 1994. PMID: 8304337 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

238 results

Search Page

Filters