Lehmann AR - Search Results

1

Genetic heterogeneity of the excision repair defect associated with trichothiodystrophy.

Stefanini M, Lagomarsini P, Giliani S, Nardo T, Botta E, Peserico A, Kleijer WJ, Lehmann AR, Sarasin A. Stefanini M, et al. Among authors: lehmann ar. Carcinogenesis. 1993 Jun;14(6):1101-5. doi: 10.1093/carcin/14.6.1101. Carcinogenesis. 1993. PMID: 8508495

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

Relationship between pyrimidine dimers, 6-4 photoproducts, repair synthesis and cell survival: studies using cells from patients with trichothiodystrophy.

Broughton BC, Lehmann AR, Harcourt SA, Arlett CF, Sarasin A, Kleijer WJ, Beemer FA, Nairn R, Mitchell DL. Broughton BC, et al. Among authors: lehmann ar. Mutat Res. 1990 Jan;235(1):33-40. doi: 10.1016/0921-8777(90)90020-6. Mutat Res. 1990. PMID: 2300071

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

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

7

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

8

Cockayne's syndrome: correlation of clinical features with cellular sensitivity of RNA synthesis to UV irradiation.

Lehmann AR, Thompson AF, Harcourt SA, Stefanini M, Norris PG. Lehmann AR, et al. J Med Genet. 1993 Aug;30(8):679-82. doi: 10.1136/jmg.30.8.679. J Med Genet. 1993. PMID: 7692050 Free PMC article.

9

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

10

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: lehmann ar. Am J Hum Genet. 1996 Feb;58(2):263-70. Am J Hum Genet. 1996. PMID: 8571952 Free PMC article.

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