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Results: 1 to 20 of 97

Similar articles for PubMed (Select 4842087)

1.

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
2.

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
3.
4.

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
5.

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
6.

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
7.

Cockayne syndrome complementation group B associated with xeroderma pigmentosum phenotype.

Itoh T, Cleaver JE, Yamaizumi M.

Hum Genet. 1996 Feb;97(2):176-9.

PMID:
8566949
8.
9.

Assignment of three Chinese xeroderma pigmentosum patients to complementation group C and one to group E.

Han ZB, Hara R, Ayaki H, Wang JH, Sun LY, You Y, Zhang YP, Qiang KX, Ikenaga M.

Br J Dermatol. 1998 Jan;138(1):131-6.

PMID:
9536236
10.
11.

Genetic complementation analysis of xeroderma pigmentosum.

Bootsma D, De Weerd-Kastelein EA, Kleijer WJ, Ke├┐zez W.

Basic Life Sci. 1975;5B:725-8.

PMID:
1191194
12.
13.

Xeroderma pigmentosum: recent studies on the DNA repair defects.

Friedberg EC.

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

PMID:
339872
15.

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.

16.

Xeroderma pigmentosum complementation group E: a case report.

Kawada A, Satoh Y, Fujiwara Y.

Photodermatol. 1986 Aug;3(4):233-8.

PMID:
3774595
17.

The genetic defect in the de Sanctis-Cacchione syndrome.

Der Kaloustian VM, de Weerd-Kastelein EA+DEWEERDAAKATELEIN EA, Kleijer WJ, Keijzer W, Bootsma D.

J Invest Dermatol. 1974 Nov;63(5):392-6. No abstract available.

PMID:
4436596
18.

DNA repair synthesis in human heterokaryons formed by normal and UV-sensitive fibroblasts.

Giannelli F, Croll PM, Lewin SA.

Exp Cell Res. 1973 Mar 30;78(1):175-85. No abstract available.

PMID:
4570579
19.

Development of a new easy complementation assay for DNA repair deficient human syndromes using cloned repair genes.

Carreau M, Eveno E, Quilliet X, Chevalier-Lagente O, Benoit A, Tanganelli B, Stefanini M, Vermeulen W, Hoeijmakers JH, Sarasin A, et al.

Carcinogenesis. 1995 May;16(5):1003-9.

PMID:
7767957
20.

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
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