Kleijer WJ - Search Results

1

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: kleijer wj. Am J Hum Genet. 1994 Feb;54(2):191-200. Am J Hum Genet. 1994. PMID: 8304337 Free PMC article.

2

Xeroderma pigmentosum-Cockayne syndrome complex in two patients: absence of skin tumors despite severe deficiency of DNA excision repair.

Scott RJ, Itin P, Kleijer WJ, Kolb K, Arlett C, Muller H. Scott RJ, et al. Among authors: kleijer wj. J Am Acad Dermatol. 1993 Nov;29(5 Pt 2):883-9. doi: 10.1016/0190-9622(93)70263-s. J Am Acad Dermatol. 1993. PMID: 8408834

3

A temperature-sensitive disorder in basal transcription and DNA repair in humans.

Vermeulen W, Rademakers S, Jaspers NG, Appeldoorn E, Raams A, Klein B, Kleijer WJ, Hansen LK, Hoeijmakers JH. Vermeulen W, et al. Among authors: kleijer wj. Nat Genet. 2001 Mar;27(3):299-303. doi: 10.1038/85864. Nat Genet. 2001. PMID: 11242112

4

Prenatal diagnosis of xeroderma pigmentosum (group C) using assays of unscheduled DNA synthesis and postreplication repair.

Halley DJ, Keijzer W, Jaspers NG, Niermeijer MF, Kleijer WJ, Boué J, Boué A, Bootsma D. Halley DJ, et al. Among authors: kleijer wj. Clin Genet. 1979 Sep;16(3):137-46. doi: 10.1111/j.1399-0004.1979.tb00982.x. Clin Genet. 1979. PMID: 487635

5

Genetic complementation analysis of xeroderma pigmentosum.

Bootsma D, De Weerd-Kastelein EA, Kleijer WJ, Keÿzez W. Bootsma D, et al. Among authors: kleijer wj. Basic Life Sci. 1975;5B:725-8. doi: 10.1007/978-1-4684-2898-8_48. Basic Life Sci. 1975. PMID: 1191194

6

Different removal of ultraviolet photoproducts in genetically related xeroderma pigmentosum and trichothiodystrophy diseases.

Eveno E, Bourre F, Quilliet X, Chevallier-Lagente O, Roza L, Eker AP, Kleijer WJ, Nikaido O, Stefanini M, Hoeijmakers JH, et al. Eveno E, et al. Among authors: kleijer wj. Cancer Res. 1995 Oct 1;55(19):4325-32. Cancer Res. 1995. PMID: 7671243

7

Relationship between pyrimidine dimers, 6-4 photoproducts, repair synthesis and cell survival: studies using cells from patients with trichothiodystrophy.

Broughton BC, Lehmann AR, Harcourt SA, Arlett CF, Sarasin A, Kleijer WJ, Beemer FA, Nairn R, Mitchell DL. Broughton BC, et al. Among authors: kleijer wj. Mutat Res. 1990 Jan;235(1):33-40. doi: 10.1016/0921-8777(90)90020-6. Mutat Res. 1990. PMID: 2300071

8

Intermittent hair loss in a child with PIBI(D)S syndrome and trichothiodystrophy with defective DNA repair-xeroderma pigmentosum group D.

Kleijer WJ, Beemer FA, Boom BW. Kleijer WJ, et al. Am J Med Genet. 1994 Aug 15;52(2):227-30. doi: 10.1002/ajmg.1320520220. Am J Med Genet. 1994. PMID: 7802014

9

Effects of inhibitors on repair of DNA in normal human and xeroderma pigmentosum cells after exposure to x-rays and ultraviolet irradiation.

Kleijer WJ, Hoeksema JL, Sluyter ML, Bootsma D. Kleijer WJ, et al. Mutat Res. 1973 Mar;17(3):385-94. doi: 10.1016/0027-5107(73)90010-9. Mutat Res. 1973. PMID: 4631741 No abstract available.

10

Xeroderma pigmentosum--Cockayne syndrome complex: a further case.

Hamel BC, Raams A, Schuitema-Dijkstra AR, Simons P, van der Burgt I, Jaspers NG, Kleijer WJ. Hamel BC, et al. Among authors: kleijer wj. J Med Genet. 1996 Jul;33(7):607-10. doi: 10.1136/jmg.33.7.607. J Med Genet. 1996. PMID: 8818951 Free PMC article.

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