Hoeijmakers JH - Search Results

1

Inefficient DNA Repair Is an Aging-Related Modifier of Parkinson's Disease.

Sepe S, Milanese C, Gabriels S, Derks KW, Payan-Gomez C, van IJcken WF, Rijksen YM, Nigg AL, Moreno S, Cerri S, Blandini F, Hoeijmakers JH, Mastroberardino PG. Sepe S, et al. Among authors: hoeijmakers jh. Cell Rep. 2016 May 31;15(9):1866-75. doi: 10.1016/j.celrep.2016.04.071. Epub 2016 May 19. Cell Rep. 2016. PMID: 27210754 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: hoeijmakers jh. Cell. 1992 Dec 11;71(6):939-53. doi: 10.1016/0092-8674(92)90390-x. Cell. 1992. PMID: 1339317

3

Characterization of genes and proteins involved in excision repair of human cells.

Hoeijmakers JH. Hoeijmakers JH. J Cell Sci Suppl. 1987;6:111-25. doi: 10.1242/jcs.1984.supplement_6.7. J Cell Sci Suppl. 1987. PMID: 2821019

4

DNA repair. Nucleotide excision-repair in the test tube.

Jaspers NG, Hoeijmakers JH. Jaspers NG, et al. Among authors: hoeijmakers jh. Curr Biol. 1995 Jul 1;5(7):700-2. doi: 10.1016/s0960-9822(95)00137-0. Curr Biol. 1995. PMID: 7583107 Free article. Review.

5

Xeroderma pigmentosum group F caused by a defect in a structure-specific DNA repair endonuclease.

Sijbers AM, de Laat WL, Ariza RR, Biggerstaff M, Wei YF, Moggs JG, Carter KC, Shell BK, Evans E, de Jong MC, Rademakers S, de Rooij J, Jaspers NG, Hoeijmakers JH, Wood RD. Sijbers AM, et al. Among authors: hoeijmakers jh. Cell. 1996 Sep 6;86(5):811-22. doi: 10.1016/s0092-8674(00)80155-5. Cell. 1996. PMID: 8797827 Free article.

6

Disruption of mouse RAD54 reduces ionizing radiation resistance and homologous recombination.

Essers J, Hendriks RW, Swagemakers SM, Troelstra C, de Wit J, Bootsma D, Hoeijmakers JH, Kanaar R. Essers J, et al. Among authors: hoeijmakers jh. Cell. 1997 Apr 18;89(2):195-204. doi: 10.1016/s0092-8674(00)80199-3. Cell. 1997. PMID: 9108475 Free article.

7

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: hoeijmakers jh. Cell. 1997 May 2;89(3):425-35. doi: 10.1016/s0092-8674(00)80223-8. Cell. 1997. PMID: 9150142 Free article.

8

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. Among authors: hoeijmakers jh. Curr Biol. 1997 Jun 1;7(6):427-39. doi: 10.1016/s0960-9822(06)00190-4. Curr Biol. 1997. PMID: 9197240 Free article.

9

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: hoeijmakers jh. Mol Cell. 1998 Jun;1(7):981-90. doi: 10.1016/s1097-2765(00)80098-2. Mol Cell. 1998. PMID: 9651581 Free article.

10

Molecular mechanisms of DNA double strand break repair.

Kanaar R, Hoeijmakers JH, van Gent DC. Kanaar R, et al. Among authors: hoeijmakers jh. Trends Cell Biol. 1998 Dec;8(12):483-9. doi: 10.1016/s0962-8924(98)01383-x. Trends Cell Biol. 1998. PMID: 9861670 Review.

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