Weeda G - Search Results

1

Disruption of mouse ERCC1 results in a novel repair syndrome with growth failure, nuclear abnormalities and senescence.

Weeda G, Donker I, de Wit J, Morreau H, Janssens R, Vissers CJ, Nigg A, van Steeg H, Bootsma D, Hoeijmakers JH. Weeda G, et al. Curr Biol. 1997 Jun 1;7(6):427-39. doi: 10.1016/s0960-9822(06)00190-4. Curr Biol. 1997. PMID: 9197240 Free article.

2

Genetic analysis of nucleotide excision repair in mammalian cells.

Weeda G, Hoeijmakers JH. Weeda G, et al. Semin Cancer Biol. 1993 Apr;4(2):105-17. Semin Cancer Biol. 1993. PMID: 8513146 Review.

3

Defective transcription-coupled repair in Cockayne syndrome B mice is associated with skin cancer predisposition.

van der Horst GT, van Steeg H, Berg RJ, van Gool AJ, de Wit J, Weeda G, Morreau H, Beems RB, van Kreijl CF, de Gruijl FR, Bootsma D, Hoeijmakers JH. van der Horst GT, et al. Among authors: weeda g. Cell. 1997 May 2;89(3):425-35. doi: 10.1016/s0092-8674(00)80223-8. Cell. 1997. PMID: 9150142 Free article.

4

Disruption of the mouse xeroderma pigmentosum group D DNA repair/basal transcription gene results in preimplantation lethality.

de Boer J, Donker I, de Wit J, Hoeijmakers JH, Weeda G. de Boer J, et al. Among authors: weeda g. Cancer Res. 1998 Jan 1;58(1):89-94. Cancer Res. 1998. PMID: 9426063

5

A mouse model for the basal transcription/DNA repair syndrome trichothiodystrophy.

de Boer J, de Wit J, van Steeg H, Berg RJ, Morreau H, Visser P, Lehmann AR, Duran M, Hoeijmakers JH, Weeda G. de Boer J, et al. Among authors: weeda g. Mol Cell. 1998 Jun;1(7):981-90. doi: 10.1016/s1097-2765(00)80098-2. Mol Cell. 1998. PMID: 9651581 Free article.

6

The structure-specific endonuclease Ercc1-Xpf is required for targeted gene replacement in embryonic stem cells.

Niedernhofer LJ, Essers J, Weeda G, Beverloo B, de Wit J, Muijtjens M, Odijk H, Hoeijmakers JH, Kanaar R. Niedernhofer LJ, et al. Among authors: weeda g. EMBO J. 2001 Nov 15;20(22):6540-9. doi: 10.1093/emboj/20.22.6540. EMBO J. 2001. PMID: 11707424 Free PMC article.

7

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: weeda g. Science. 2002 May 17;296(5571):1276-9. doi: 10.1126/science.1070174. Epub 2002 Apr 11. Science. 2002. PMID: 11950998

8

An Xpb mouse model for combined xeroderma pigmentosum and cockayne syndrome reveals progeroid features upon further attenuation of DNA repair.

Andressoo JO, Weeda G, de Wit J, Mitchell JR, Beems RB, van Steeg H, van der Horst GT, Hoeijmakers JH. Andressoo JO, et al. Among authors: weeda g. Mol Cell Biol. 2009 Mar;29(5):1276-90. doi: 10.1128/MCB.01229-08. Epub 2008 Dec 29. Mol Cell Biol. 2009. PMID: 19114557 Free PMC article.

9

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: weeda g. 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.

10

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: weeda g. 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.

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