Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 11

1.

Biochemical heterogeneity in xeroderma pigmentosum complementation group E.

Keeney S, Wein H, Linn S.

Mutat Res. 1992 Jan;273(1):49-56.

PMID:
1376435
2.

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.

4.

Xeroderma pigmentosum: from symptoms and genetics to gene-based skin therapy.

Magnaldo T, Sarasin A.

Cells Tissues Organs. 2004;177(3):189-98. Review.

PMID:
15388993
5.

[DNA repair defect in xeroderma pigmentosum].

Tanaka K.

Gan To Kagaku Ryoho. 1989 Mar;16(3 Pt 2):473-80. Review. Japanese.

PMID:
2650628
7.

Replication of damaged DNA: molecular defect in xeroderma pigmentosum variant cells.

Cordonnier AM, Fuchs RP.

Mutat Res. 1999 Oct 22;435(2):111-9. Review.

PMID:
10556591
8.

[Progress of research on xeroderma pigmentosum].

Tanaka K.

Gan To Kagaku Ryoho. 1990 Jun;17(6):1095-103. Review. Japanese.

PMID:
2190536
9.

Xeroderma pigmentosum: biochemical and genetic characteristics.

Cleaver JE, Bootsma D.

Annu Rev Genet. 1975;9:19-38. Review. No abstract available.

PMID:
1108765
10.

Xeroderma pigmentosum patients from Germany (the Mannheim XP collection): clinical and biochemical characteristics.

Thielmann HW.

Recent Results Cancer Res. 1993;128:275-97. Review. No abstract available.

PMID:
8356326
11.

The XPE gene of xeroderma pigmentosum, its product and biological roles.

Bennett D, Itoh T.

Adv Exp Med Biol. 2008;637:57-64. Review. No abstract available.

PMID:
19181111

Supplemental Content

Support Center