Chevallier-Lagente O - Search Results

1

Different removal of ultraviolet photoproducts in genetically related xeroderma pigmentosum and trichothiodystrophy diseases.

Eveno E, Bourre F, Quilliet X, Chevallier-Lagente O, Roza L, Eker AP, Kleijer WJ, Nikaido O, Stefanini M, Hoeijmakers JH, et al. Eveno E, et al. Cancer Res. 1995 Oct 1;55(19):4325-32. Cancer Res. 1995. PMID: 7671243

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

Stable SV40-transformation and characterisation of some DNA repair properties of fibroblasts from a trichothiodystrophy patient.

Eveno E, Quilliet X, Chevallier-Lagente O, Daya-Grosjean L, Stary A, Zeng L, Benoit A, Savini E, Ciarrocchi G, Kannouche P, et al. Eveno E, et al. Biochimie. 1995;77(11):906-12. doi: 10.1016/0300-9084(95)90011-x. Biochimie. 1995. PMID: 8824772

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. Mutat Res. 1996 Dec 2;364(3):161-9. doi: 10.1016/s0921-8777(96)00024-9. Mutat Res. 1996. PMID: 8960128

5

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. Gene Ther. 1997 Oct;4(10):1077-84. doi: 10.1038/sj.gt.3300495. Gene Ther. 1997. PMID: 9415314

6

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. Mutat Res. 1997 Dec;385(3):235-42. doi: 10.1016/s0921-8777(97)00049-9. Mutat Res. 1997. PMID: 9506892

7

Genetic correction of DNA repair-deficient/cancer-prone xeroderma pigmentosum group C keratinocytes.

Arnaudeau-Bégard C, Brellier F, Chevallier-Lagente O, Hoeijmakers J, Bernerd F, Sarasin A, Magnaldo T. Arnaudeau-Bégard C, et al. Among authors: chevallier lagente o. Hum Gene Ther. 2003 Jul 1;14(10):983-96. doi: 10.1089/104303403766682241. Hum Gene Ther. 2003. PMID: 12869216

8

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

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

10

Ultraviolet irradiation represses PATCHED gene transcription in human epidermal keratinocytes through an activator protein-1-dependent process.

Brellier F, Marionnet C, Chevallier-Lagente O, Toftgard R, Mauviel A, Sarasin A, Magnaldo T. Brellier F, et al. Among authors: chevallier lagente o. Cancer Res. 2004 Apr 15;64(8):2699-704. doi: 10.1158/0008-5472.can-03-3477. Cancer Res. 2004. PMID: 15087382

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