Bootsma D - Search Results

1

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

2

The genetic basis of xeroderma pigmentosum.

Bootsma D, Hoeijmakers JH. Bootsma D, et al. Ann Genet. 1991;34(3-4):143-50. Ann Genet. 1991. PMID: 1809220 Review.

3

A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome.

Weeda G, van Ham RC, Vermeulen W, Bootsma D, van der Eb AJ, Hoeijmakers JH. Weeda G, et al. Among authors: bootsma d. Cell. 1990 Aug 24;62(4):777-91. doi: 10.1016/0092-8674(90)90122-u. Cell. 1990. PMID: 2167179

4

Molecular genetics of eukaryotic DNA excision repair.

Hoeijmakers JH, Bootsma D. Hoeijmakers JH, et al. Among authors: bootsma d. Cancer Cells. 1990 Oct;2(10):311-20. Cancer Cells. 1990. PMID: 2282248 Review.

5

DNA repair in human cells: from genetic complementation to isolation of genes.

Bootsma D, Westerveld A, Hoeijmakers JH. Bootsma D, et al. Cancer Surv. 1988;7(2):303-15. Cancer Surv. 1988. PMID: 3066477 Review.

6

The molecular basis of nucleotide excision repair syndromes.

Bootsma D, Hoeijmakers JH. Bootsma D, et al. Mutat Res. 1994 May 1;307(1):15-23. doi: 10.1016/0027-5107(94)90273-9. Mutat Res. 1994. PMID: 7513792 Review. No abstract available.

7

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. 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.

8

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: bootsma d. 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.

9

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. Among authors: bootsma d. Am J Hum Genet. 1994 Feb;54(2):191-200. Am J Hum Genet. 1994. PMID: 8304337 Free PMC article.

10

Xeroderma pigmentosum complementation group G associated with Cockayne syndrome.

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

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