Lehmann AR - Search Results

1

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: lehmann ar. Carcinogenesis. 1994 Aug;15(8):1493-8. doi: 10.1093/carcin/15.8.1493. Carcinogenesis. 1994. PMID: 8055625

2

Prenatal diagnosis in a subset of trichothiodystrophy patients defective in DNA repair.

Sarasin A, Blanchet-Bardon C, Renault G, Lehmann A, Arlett C, Dumez Y. Sarasin A, et al. Br J Dermatol. 1992 Nov;127(5):485-91. doi: 10.1111/j.1365-2133.1992.tb14845.x. Br J Dermatol. 1992. PMID: 1281671

3

Workshop on DNA repair.

Lehmann AR, Hoeijmakers JH, van Zeeland AA, Backendorf CM, Bridges BA, Collins A, Fuchs RP, Margison GP, Montesano R, Moustacchi E, et al. Lehmann AR, et al. Mutat Res. 1992 Jan;273(1):1-28. doi: 10.1016/0921-8777(92)90046-6. Mutat Res. 1992. PMID: 1376432

4

Trichothiodystrophy, a human DNA repair disorder with heterogeneity in the cellular response to ultraviolet light.

Lehmann AR, Arlett CF, Broughton BC, Harcourt SA, Steingrimsdottir H, Stefanini M, Malcolm A, Taylor R, Natarajan AT, Green S, et al. Lehmann AR, et al. Cancer Res. 1988 Nov 1;48(21):6090-6. Cancer Res. 1988. PMID: 2458832

5

DNA repair and cancer: speculations based on studies with xeroderma pigmentosum, Cockayne's syndrome and trichothiodystrophy.

Lehmann AR, Norris PG. Lehmann AR, et al. Carcinogenesis. 1989 Aug;10(8):1353-6. doi: 10.1093/carcin/10.8.1353. Carcinogenesis. 1989. PMID: 2752510 No abstract available.

6

Molecular aspects of DNA repair.

Friedberg EC, Backendorf C, Burke J, Collins A, Grossman L, Hoeijmakers JH, Lehmann AR, Seeberg E, van der Schans GP, van Zeeland AA. Friedberg EC, et al. Among authors: lehmann ar. Mutat Res. 1987 Sep;184(2):67-86. doi: 10.1016/0167-8817(87)90063-0. Mutat Res. 1987. PMID: 3306357 Review. No abstract available.

7

A biochemical defect in the repair of alkylated DNA in cells from an immunodeficient patient (46BR).

Teo IA, Broughton BC, Day RS, James MR, Karran P, Mayne LV, Lehmann AR. Teo IA, et al. Among authors: lehmann ar. Carcinogenesis. 1983;4(5):559-64. doi: 10.1093/carcin/4.5.559. Carcinogenesis. 1983. PMID: 6850987

8

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: lehmann ar. Mutat Res. 1994 Mar;314(2):159-65. doi: 10.1016/0921-8777(94)90079-5. Mutat Res. 1994. PMID: 7510365

9

Three unusual repair deficiencies associated with transcription factor BTF2(TFIIH): evidence for the existence of a transcription syndrome.

Vermeulen W, van Vuuren AJ, Chipoulet M, Schaeffer L, Appeldoorn E, Weeda G, Jaspers NG, Priestley A, Arlett CF, Lehmann AR, et al. Vermeulen W, et al. Among authors: lehmann ar. Cold Spring Harb Symp Quant Biol. 1994;59:317-29. doi: 10.1101/sqb.1994.059.01.036. Cold Spring Harb Symp Quant Biol. 1994. PMID: 7587084 No abstract available.

10

The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIH.

Henning KA, Li L, Iyer N, McDaniel LD, Reagan MS, Legerski R, Schultz RA, Stefanini M, Lehmann AR, Mayne LV, Friedberg EC. Henning KA, et al. Among authors: lehmann ar. Cell. 1995 Aug 25;82(4):555-64. doi: 10.1016/0092-8674(95)90028-4. Cell. 1995. PMID: 7664335 Free article.

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