Hoeijmakers JH - Search Results

1

Premature aging in mice deficient in DNA repair and transcription.

de Boer J, Andressoo JO, de Wit J, Huijmans J, Beems RB, van Steeg H, Weeda G, van der Horst GT, van Leeuwen W, Themmen AP, Meradji M, Hoeijmakers JH. de Boer J, et al. Among authors: hoeijmakers jh. Science. 2002 May 17;296(5571):1276-9. doi: 10.1126/science.1070174. Epub 2002 Apr 11. Science. 2002. PMID: 11950998

2

RAD25 (SSL2), the yeast homolog of the human xeroderma pigmentosum group B DNA repair gene, is essential for viability.

Park E, Guzder SN, Koken MH, Jaspers-Dekker I, Weeda G, Hoeijmakers JH, Prakash S, Prakash L. Park E, et al. Among authors: hoeijmakers jh. Proc Natl Acad Sci U S A. 1992 Dec 1;89(23):11416-20. doi: 10.1073/pnas.89.23.11416. Proc Natl Acad Sci U S A. 1992. PMID: 1333609 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. Among authors: hoeijmakers jh. Cell. 1992 Dec 11;71(6):939-53. doi: 10.1016/0092-8674(92)90390-x. Cell. 1992. PMID: 1339317

4

Cloning and characterization of the Drosophila homolog of the xeroderma pigmentosum complementation-group B correcting gene, ERCC3.

Koken MH, Vreeken C, Bol SA, Cheng NC, Jaspers-Dekker I, Hoeijmakers JH, Eeken JC, Weeda G, Pastink A. Koken MH, et al. Among authors: hoeijmakers jh. Nucleic Acids Res. 1992 Nov 11;20(21):5541-8. doi: 10.1093/nar/20.21.5541. Nucleic Acids Res. 1992. PMID: 1454518 Free PMC article.

5

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: hoeijmakers jh. 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.

6

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: hoeijmakers jh. Carcinogenesis. 1991 Dec;12(12):2361-8. doi: 10.1093/carcin/12.12.2361. Carcinogenesis. 1991. PMID: 1747940

7

The genetic basis of xeroderma pigmentosum.

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

8

How relevant is the Escherichia coli UvrABC model for excision repair in eukaryotes?

Hoeijmakers JH. Hoeijmakers JH. J Cell Sci. 1991 Dec;100 (Pt 4):687-91. doi: 10.1242/jcs.100.4.687. J Cell Sci. 1991. PMID: 1814927 Review.

9

Localization of the xeroderma pigmentosum group B-correcting gene ERCC3 to human chromosome 2q21.

Weeda G, Wiegant J, van der Ploeg M, Geurts van Kessel AH, van der Eb AJ, Hoeijmakers JH. Weeda G, et al. Among authors: hoeijmakers jh. Genomics. 1991 Aug;10(4):1035-40. doi: 10.1016/0888-7543(91)90195-k. Genomics. 1991. PMID: 1916809

10

Structure and expression of the human XPBC/ERCC-3 gene involved in DNA repair disorders xeroderma pigmentosum and Cockayne's syndrome.

Weeda G, Ma LB, van Ham RC, van der Eb AJ, Hoeijmakers JH. Weeda G, et al. Among authors: hoeijmakers jh. Nucleic Acids Res. 1991 Nov 25;19(22):6301-8. doi: 10.1093/nar/19.22.6301. Nucleic Acids Res. 1991. PMID: 1956789 Free PMC article.

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