Taieb A - Search Results

1

Striking differences in cellular catalase activity between two DNA repair-deficient diseases: xeroderma pigmentosum and trichothiodystrophy.

Vuillaume M, Daya-Grosjean L, Vincens P, Pennetier JL, Tarroux P, Baret A, Calvayrac R, Taieb A, Sarasin A. Vuillaume M, et al. Among authors: taieb a. Carcinogenesis. 1992 Mar;13(3):321-8. doi: 10.1093/carcin/13.3.321. Carcinogenesis. 1992. PMID: 1547519

2

The relative expression of mutated XPB genes results in xeroderma pigmentosum/Cockayne's syndrome or trichothiodystrophy cellular phenotypes.

Riou L, Zeng L, Chevallier-Lagente O, Stary A, Nikaido O, Taïeb A, Weeda G, Mezzina M, Sarasin A. Riou L, et al. Among authors: taieb a. Hum Mol Genet. 1999 Jun;8(6):1125-33. doi: 10.1093/hmg/8.6.1125. Hum Mol Genet. 1999. PMID: 10332046

3

Diagnosis of Xeroderma pigmentosum variant in a young patient with two novel mutations in the POLH gene.

De Palma A, Morren MA, Ged C, Pouvelle C, Taïeb A, Aoufouchi S, Sarasin A. De Palma A, et al. Among authors: taieb a. Am J Med Genet A. 2017 Sep;173(9):2511-2516. doi: 10.1002/ajmg.a.38340. Epub 2017 Jul 8. Am J Med Genet A. 2017. PMID: 28688171

4

A mutation in the XPB/ERCC3 DNA repair transcription gene, associated with trichothiodystrophy.

Weeda G, Eveno E, Donker I, Vermeulen W, Chevallier-Lagente O, Taïeb A, Stary A, Hoeijmakers JH, Mezzina M, Sarasin A. Weeda G, et al. Among authors: taieb a. Am J Hum Genet. 1997 Feb;60(2):320-9. Am J Hum Genet. 1997. PMID: 9012405 Free PMC article.

5

Unexpected extradermatological findings in 31 patients with xeroderma pigmentosum type C.

Hadj-Rabia S, Oriot D, Soufir N, Dufresne H, Bourrat E, Mallet S, Poulhalon N, Ezzedine K, Grandchamp B, Taïeb A, Catteau B, Sarasin A, Bodemer C. Hadj-Rabia S, et al. Among authors: taieb a. Br J Dermatol. 2013 May;168(5):1109-13. doi: 10.1111/bjd.12183. Br J Dermatol. 2013. PMID: 23278166

6

New clinico-genetic classification of trichothiodystrophy.

Morice-Picard F, Cario-André M, Rezvani H, Lacombe D, Sarasin A, Taïeb A. Morice-Picard F, et al. Among authors: taieb a. Am J Med Genet A. 2009 Sep;149A(9):2020-30. doi: 10.1002/ajmg.a.32902. Am J Med Genet A. 2009. PMID: 19681155 Review.

7

A prevalent mutation with founder effect in xeroderma pigmentosum group C from north Africa.

Soufir N, Ged C, Bourillon A, Austerlitz F, Chemin C, Stary A, Armier J, Pham D, Khadir K, Roume J, Hadj-Rabia S, Bouadjar B, Taieb A, de Verneuil H, Benchiki H, Grandchamp B, Sarasin A. Soufir N, et al. Among authors: taieb a. J Invest Dermatol. 2010 Jun;130(6):1537-42. doi: 10.1038/jid.2009.409. Epub 2010 Jan 7. J Invest Dermatol. 2010. PMID: 20054342 Free article.

8

Familial predisposition to TP53/complex karyotype MDS and leukemia in DNA repair-deficient xeroderma pigmentosum.

Sarasin A, Quentin S, Droin N, Sahbatou M, Saada V, Auger N, Boursin Y, Dessen P, Raimbault A, Asnafi V, Schmutz JL, Taïeb A, Menck CFM, Rosselli F, La Rochelle LD, Robert C, Sicre de Fontbrune F, Sébert M, Leblanc T, Kannouche P, De Botton S, Solary E, Soulier J. Sarasin A, et al. Among authors: taieb a. Blood. 2019 Jun 20;133(25):2718-2724. doi: 10.1182/blood-2019-01-895698. Epub 2019 Mar 26. Blood. 2019. PMID: 30914417 Free PMC article.

9

Xeroderma pigmentosum in South Africa: Evidence for a prevalent founder effect.

Kgokolo M, Morice-Picard F, Rezvani HR, Austerlitz F, Cartault F, Sarasin A, Sathekge M, Taieb A, Ged C. Kgokolo M, et al. Among authors: taieb a. Br J Dermatol. 2019 Nov;181(5):1070-1072. doi: 10.1111/bjd.18030. Epub 2019 Jul 24. Br J Dermatol. 2019. PMID: 31017654 No abstract available.

10

Catalase overexpression reduces UVB-induced apoptosis in a human xeroderma pigmentosum reconstructed epidermis.

Rezvani HR, Ged C, Bouadjar B, de Verneuil H, Taïeb A. Rezvani HR, et al. Among authors: taieb a. Cancer Gene Ther. 2008 Apr;15(4):241-51. doi: 10.1038/sj.cgt.7701102. Epub 2008 Jan 18. Cancer Gene Ther. 2008. PMID: 18202716

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