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Items: 1 to 20 of 153

1.

Phenotypic correction of the defect in xeroderma pigmentosum cells after fusion with isolated cytoplasts.

Keijzer W, Verkerk A, Bootsma D.

Exp Cell Res. 1982 Jul;140(1):119-25. No abstract available.

PMID:
7106197
2.

Different rates of restoration of the repair capacity in complementing xeroderma pigmentosum cells after fusion.

Matsukuma S, Zelle B, Keijzer W, Berends F, Bootsma D.

Exp Cell Res. 1981 Jul;134(1):103-12. No abstract available.

PMID:
7250211
3.

A third complementation group in xeroderma pigmentosum.

de Weerd-Kastelein EA, Keijzer W, Bootsma D.

Mutat Res. 1974 Jan;22(1):87-91. No abstract available.

PMID:
4842087
4.

Localization of a gene involved in complementation of the defect in xeroderma pigmentosum group A cells on human chromosome 1.

Keijzer W, Stefanini M, Bootsma D, Verkerk A, Geurts van Kessel AH, Jongkind JF, Westerveld A.

Exp Cell Res. 1987 Apr;169(2):490-501.

PMID:
3556430
5.

A sixth complementation group in xeroderma pigmentosum.

Arase S, Kozuka T, Tanaka K, Ikenaga M, Takebe H.

Mutat Res. 1979 Jan;59(1):143-6. No abstract available.

PMID:
431549
6.
7.

Genetic heterogeneity of xeroderma pigmentosum demonstrated by somatic cell hybridization.

De Weerd-Kastelein EA, Keijzer W, Bootsma D.

Nat New Biol. 1972 Jul 19;238(81):80-3. No abstract available.

PMID:
4505415
8.
9.
10.

Xeroderma pigmentosum: recent studies on the DNA repair defects.

Friedberg EC.

Arch Pathol Lab Med. 1978 Jan;102(1):3-7. Review.

PMID:
339872
11.

Clinical and photobiological characteristics of xeroderma pigmentosum complementation group F: a review of cases from Japan.

Yamamura K, Ichihashi M, Hiramoto T, Ogoshi M, Nishioka K, Fujiwara Y.

Br J Dermatol. 1989 Oct;121(4):471-80. Review.

PMID:
2696553
12.

Interspecies complementation analysis of xeroderma pigmentosum and UV-sensitive Chinese hamster cells.

Stefanini M, Keijzer W, Westerveld A, Bootsma D.

Exp Cell Res. 1985 Dec;161(2):373-80.

PMID:
4065224
13.
14.

Molecular and cellular analysis of the DNA repair defect in a patient in xeroderma pigmentosum complementation group D who has the clinical features of xeroderma pigmentosum and Cockayne syndrome.

Broughton BC, Thompson AF, Harcourt SA, Vermeulen W, Hoeijmakers JH, Botta E, Stefanini M, King MD, Weber CA, Cole J, et al.

Am J Hum Genet. 1995 Jan;56(1):167-74. Review.

15.
18.

High voltage electric pulses efficiently induce fusion of cells in monolayer culture.

Ishizaki K, Chang HR, Eguchi T, Ikenaga M.

Cell Struct Funct. 1989 Apr;14(2):173-81.

20.

A ninth complementation group in xeroderma pigmentosum, XP I.

Fischer E, Keijzer W, Thielmann HW, Popanda O, Bohnert E, Edler L, Jung EG, Bootsma D.

Mutat Res. 1985 May;145(3):217-25.

PMID:
3982437

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