Bootsma D - Search Results

1

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

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

3

Molecular and functional analysis of the XPBC/ERCC-3 promoter: transcription activity is dependent on the integrity of an Sp1-binding site.

Ma L, Weeda G, Jochemsen AG, Bootsma D, Hoeijmakers JH, van der Eb AJ. Ma L, et al. Among authors: bootsma d. Nucleic Acids Res. 1992 Jan 25;20(2):217-24. doi: 10.1093/nar/20.2.217. Nucleic Acids Res. 1992. PMID: 1741247 Free PMC article.

4

Characterization of the mouse homolog of the XPBC/ERCC-3 gene implicated in xeroderma pigmentosum and Cockayne's syndrome.

Weeda G, Ma L, van Ham RC, Bootsma D, van der Eb AJ, Hoeijmakers JH. Weeda G, et al. Among authors: bootsma d. Carcinogenesis. 1991 Dec;12(12):2361-8. doi: 10.1093/carcin/12.12.2361. Carcinogenesis. 1991. PMID: 1747940

5

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.

6

Molecular cloning and biological characterization of the human excision repair gene ERCC-3.

Weeda G, van Ham RC, Masurel R, Westerveld A, Odijk H, de Wit J, Bootsma D, van der Eb AJ, Hoeijmakers JH. Weeda G, et al. Among authors: bootsma d. Mol Cell Biol. 1990 Jun;10(6):2570-81. doi: 10.1128/mcb.10.6.2570-2581.1990. Mol Cell Biol. 1990. PMID: 2111438 Free PMC article.

7

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: bootsma d. Mutat Res. 1989 Mar;217(2):83-92. doi: 10.1016/0921-8777(89)90059-1. Mutat Res. 1989. PMID: 2918869

8

Correction of the DNA repair defect in xeroderma pigmentosum group E by injection of a DNA damage-binding protein.

Keeney S, Eker AP, Brody T, Vermeulen W, Bootsma D, Hoeijmakers JH, Linn S. Keeney S, et al. Among authors: bootsma d. Proc Natl Acad Sci U S A. 1994 Apr 26;91(9):4053-6. doi: 10.1073/pnas.91.9.4053. Proc Natl Acad Sci U S A. 1994. PMID: 8171034 Free PMC article.

9

Mutational analysis of ERCC3, which is involved in DNA repair and transcription initiation: identification of domains essential for the DNA repair function.

Ma L, Westbroek A, Jochemsen AG, Weeda G, Bosch A, Bootsma D, Hoeijmakers JH, van der Eb AJ. Ma L, et al. Among authors: bootsma d. Mol Cell Biol. 1994 Jun;14(6):4126-34. doi: 10.1128/mcb.14.6.4126-4134.1994. Mol Cell Biol. 1994. PMID: 8196650 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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