Sarasin A - Search Results

1

The amyloid peptide induces early genotoxic damage in human preneuron NT2.

Santiard-Baron D, Lacoste A, Ellouk-Achard S, Soulié C, Nicole A, Sarasin A, Ceballos-Picot I. Santiard-Baron D, et al. Among authors: sarasin a. Mutat Res. 2001 Aug 8;479(1-2):113-20. doi: 10.1016/s0027-5107(01)00154-3. Mutat Res. 2001. PMID: 11470486

2

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

3

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

4

Induction of apoptosis in rat hepatocarcinoma cells by expression of IGF-I antisense c-DNA.

Ellouk-Achard S, Djenabi S, De Oliveira GA, Desauty G, Duc HT, Zohair M, Trojan J, Claude JR, Sarasin A, Lafarge-Frayssinet C. Ellouk-Achard S, et al. Among authors: sarasin a. J Hepatol. 1998 Nov;29(5):807-18. doi: 10.1016/s0168-8278(98)80263-8. J Hepatol. 1998. PMID: 9833920

5

Variability in nucleotide excision repair and cancer risk: a review.

Benhamou S, Sarasin A. Benhamou S, et al. Among authors: sarasin a. Mutat Res. 2000 Apr;462(2-3):149-58. doi: 10.1016/s1383-5742(00)00032-6. Mutat Res. 2000. PMID: 10767626 Review.

6

Hypothetical role of RNA damage avoidance in preventing human disease.

Brégeon D, Sarasin A. Brégeon D, et al. Among authors: sarasin a. Mutat Res. 2005 Sep 4;577(1-2):293-302. doi: 10.1016/j.mrfmmm.2005.04.002. Mutat Res. 2005. PMID: 15916782 Review.

7

Identification of new RECQL4 mutations in Caucasian Rothmund-Thomson patients and analysis of sensitivity to a wide range of genotoxic agents.

Cabral RE, Queille S, Bodemer C, de Prost Y, Neto JB, Sarasin A, Daya-Grosjean L. Cabral RE, et al. Among authors: sarasin a. Mutat Res. 2008 Aug 25;643(1-2):41-7. doi: 10.1016/j.mrfmmm.2008.06.002. Epub 2008 Jun 21. Mutat Res. 2008. PMID: 18616953

8

DNA damage and gene therapy of xeroderma pigmentosum, a human DNA repair-deficient disease.

Dupuy A, Sarasin A. Dupuy A, et al. Among authors: sarasin a. Mutat Res. 2015 Jun;776:2-8. doi: 10.1016/j.mrfmmm.2014.08.007. Epub 2014 Sep 6. Mutat Res. 2015. PMID: 26255934 Review.

9

Description of a new amplifiable shuttle vector for mutagenesis studies in human cells: application to N-methyl-N'-nitro-N-nitrosoguanidine-induced mutation spectrum.

Stary A, Menck CF, Sarasin A. Stary A, et al. Among authors: sarasin a. Mutat Res. 1992 Oct;272(2):101-10. doi: 10.1016/0165-1161(92)90038-n. Mutat Res. 1992. PMID: 1383742

10

Comparative study of Epstein-Barr virus and SV40-based shuttle-expression vectors in human repair-deficient cells.

James MR, Stary A, Daya-Grosjean L, Drougard C, Sarasin A. James MR, et al. Among authors: sarasin a. Mutat Res. 1989 Mar-May;220(2-3):169-85. doi: 10.1016/0165-1110(89)90023-7. Mutat Res. 1989. PMID: 2538738

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