Mezzina M - Search Results

1

The ERCC2/DNA repair protein is associated with the class II BTF2/TFIIH transcription factor.

Schaeffer L, Moncollin V, Roy R, Staub A, Mezzina M, Sarasin A, Weeda G, Hoeijmakers JH, Egly JM. Schaeffer L, et al. Among authors: mezzina m. EMBO J. 1994 May 15;13(10):2388-92. doi: 10.1002/j.1460-2075.1994.tb06522.x. EMBO J. 1994. PMID: 8194528 Free PMC article.

2

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

3

A new nucleotide-excision-repair gene associated with the disorder trichothiodystrophy.

Stefanini M, Vermeulen W, Weeda G, Giliani S, Nardo T, Mezzina M, Sarasin A, Harper JI, Arlett CF, Hoeijmakers JH, et al. Stefanini M, et al. Among authors: mezzina m. Am J Hum Genet. 1993 Oct;53(4):817-21. Am J Hum Genet. 1993. PMID: 8213812 Free PMC article.

4

Long-term complementation of DNA repair deficient human primary fibroblasts by retroviral transduction of the XPD gene.

Quilliet X, Chevallier-Lagente O, Eveno E, Stojkovic T, Destée A, Sarasin A, Mezzina M. Quilliet X, et al. Among authors: mezzina m. Mutat Res. 1996 Dec 2;364(3):161-9. doi: 10.1016/s0921-8777(96)00024-9. Mutat Res. 1996. PMID: 8960128

5

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: mezzina m. Am J Hum Genet. 1997 Feb;60(2):320-9. Am J Hum Genet. 1997. PMID: 9012405 Free PMC article.

6

Retrovirus-mediated gene transfer corrects DNA repair defect of xeroderma pigmentosum cells of complementation groups A, B and C.

Zeng L, Quilliet X, Chevallier-Lagente O, Eveno E, Sarasin A, Mezzina M. Zeng L, et al. Among authors: mezzina m. Gene Ther. 1997 Oct;4(10):1077-84. doi: 10.1038/sj.gt.3300495. Gene Ther. 1997. PMID: 9415314

7

Retroviral-mediated correction of DNA repair defect in xeroderma pigmentosum cells is associated with recovery of catalase activity.

Quilliet X, Chevallier-Lagente O, Zeng L, Calvayrac R, Mezzina M, Sarasin A, Vuillaume M. Quilliet X, et al. Among authors: mezzina m. Mutat Res. 1997 Dec;385(3):235-42. doi: 10.1016/s0921-8777(97)00049-9. Mutat Res. 1997. PMID: 9506892

8

Retrovirus-mediated DNA repair gene transfer into xeroderma pigmentosum cells: perspectives for a gene therapy.

Zeng L, Sarasin A, Mezzina M. Zeng L, et al. Among authors: mezzina m. Cell Biol Toxicol. 1998 Mar;14(2):105-10. doi: 10.1023/a:1007477820594. Cell Biol Toxicol. 1998. PMID: 9553721

9

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: mezzina m. Hum Mol Genet. 1999 Jun;8(6):1125-33. doi: 10.1093/hmg/8.6.1125. Hum Mol Genet. 1999. PMID: 10332046

10

Functional retroviral vector for gene therapy of xeroderma pigmentosum group D patients.

Carreau M, Quilliet X, Eveno E, Salvetti A, Danos O, Heard JM, Mezzina M, Sarasin A. Carreau M, et al. Among authors: mezzina m. Hum Gene Ther. 1995 Oct;6(10):1307-15. doi: 10.1089/hum.1995.6.10-1307. Hum Gene Ther. 1995. PMID: 8590735

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