Weber CA - Search Results

1

Molecular analysis of the XP-D gene in Italian families with patients affected by trichothiodystrophy and xeroderma pigmentosum group D.

Mondello C, Nardo T, Giliani S, Arrand JE, Weber CA, Lehmann AR, Nuzzo F, Stefanini M. Mondello C, et al. Among authors: weber ca. Mutat Res. 1994 Mar;314(2):159-65. doi: 10.1016/0921-8777(94)90079-5. Mutat Res. 1994. PMID: 7510365

2

Defects in the DNA repair and transcription gene ERCC2 in the cancer-prone disorder xeroderma pigmentosum group D.

Takayama K, Salazar EP, Lehmann A, Stefanini M, Thompson LH, Weber CA. Takayama K, et al. Among authors: weber ca. Cancer Res. 1995 Dec 1;55(23):5656-63. Cancer Res. 1995. PMID: 7585650

3

Mutations in the xeroderma pigmentosum group D DNA repair/transcription gene in patients with trichothiodystrophy.

Broughton BC, Steingrimsdottir H, Weber CA, Lehmann AR. Broughton BC, et al. Among authors: weber ca. Nat Genet. 1994 Jun;7(2):189-94. doi: 10.1038/ng0694-189. Nat Genet. 1994. PMID: 7920640

4

Correction by the ERCC2 gene of UV sensitivity and repair deficiency phenotype in a subset of trichothiodystrophy cells.

Mezzina M, Eveno E, Chevallier-Lagente O, Benoit A, Carreau M, Vermeulen W, Hoeijmakers JH, Stefanini M, Lehmann AR, Weber CA, et al. Mezzina M, et al. Among authors: weber ca. Carcinogenesis. 1994 Aug;15(8):1493-8. doi: 10.1093/carcin/15.8.1493. Carcinogenesis. 1994. PMID: 8055625

5

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. Broughton BC, et al. Among authors: weber ca. Am J Hum Genet. 1995 Jan;56(1):167-74. Am J Hum Genet. 1995. PMID: 7825573 Free PMC article. Review.

6

Defects in the DNA repair and transcription gene ERCC2(XPD) in trichothiodystrophy.

Takayama K, Salazar EP, Broughton BC, Lehmann AR, Sarasin A, Thompson LH, Weber CA. Takayama K, et al. Among authors: weber ca. Am J Hum Genet. 1996 Feb;58(2):263-70. Am J Hum Genet. 1996. PMID: 8571952 Free PMC article.

7

Molecular analysis of CXPD mutations in the repair-deficient hamster mutants UV5 and UVL-13.

Weber CA, Kirchner JM, Salazar EP, Takayama K. Weber CA, et al. Mutat Res. 1994 Aug;324(4):147-52. doi: 10.1016/0165-7992(94)90012-4. Mutat Res. 1994. PMID: 8052270

8

Molecular analysis of ERCC2 mutations in the repair deficient hamster mutants UVL-1 and V-H1.

Kadkhodayan S, Salazar EP, Ramsey MJ, Takayama K, Zdzienicka MZ, Tucker JD, Weber CA. Kadkhodayan S, et al. Among authors: weber ca. Mutat Res. 1997 Oct;385(1):47-57. doi: 10.1016/s0921-8777(97)00030-x. Mutat Res. 1997. PMID: 9372848

9

DNA repair characteristics and mutations in the ERCC2 DNA repair and transcription gene in a trichothiodystrophy patient.

Takayama K, Danks DM, Salazar EP, Cleaver JE, Weber CA. Takayama K, et al. Among authors: weber ca. Hum Mutat. 1997;9(6):519-25. doi: 10.1002/(SICI)1098-1004(1997)9:6<519::AID-HUMU4>3.0.CO;2-X. Hum Mutat. 1997. PMID: 9195225

10

The human DNA repair gene, ERCC2 (XPD), corrects ultraviolet hypersensitivity and ultraviolet hypermutability of a shuttle vector replicated in xeroderma pigmentosum group D cells.

Gözükara EM, Parris CN, Weber CA, Salazar EP, Seidman MM, Watkins JF, Prakash L, Kraemer KH. Gözükara EM, et al. Among authors: weber ca. Cancer Res. 1994 Jul 15;54(14):3837-44. Cancer Res. 1994. PMID: 8033104

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