Robert C - Search Results

1

Genomic mutation landscape of skin cancers from DNA repair-deficient xeroderma pigmentosum patients.

Yurchenko AA, Rajabi F, Braz-Petta T, Fassihi H, Lehmann A, Nishigori C, Wang J, Padioleau I, Gunbin K, Panunzi L, Morice-Picard F, Laplante P, Robert C, Kannouche PL, Menck CFM, Sarasin A, Nikolaev SI. Yurchenko AA, et al. Among authors: robert c. Nat Commun. 2023 May 4;14(1):2561. doi: 10.1038/s41467-023-38311-0. Nat Commun. 2023. PMID: 37142601 Free PMC article.

2

[Xeroderma pigmentosum. What may be expected from biological studies?].

Robert C, Sarasin A. Robert C, et al. Ann Dermatol Venereol. 1994;121(5):434-9. Ann Dermatol Venereol. 1994. PMID: 7702274 Review. French. No abstract available.

3

High mutation frequency in ras genes of skin tumors isolated from DNA repair deficient xeroderma pigmentosum patients.

Daya-Grosjean L, Robert C, Drougard C, Suarez H, Sarasin A. Daya-Grosjean L, et al. Among authors: robert c. Cancer Res. 1993 Apr 1;53(7):1625-9. Cancer Res. 1993. PMID: 8453633

4

[Cancers of the skin, relations to ultraviolet rays].

Robert C, Dubertret L. Robert C, et al. Presse Med. 1995 Nov 11;24(34):1610-6. Presse Med. 1995. PMID: 8545368 Review. French.

5

Cell survival and shuttle vector mutagenesis induced by ultraviolet A and ultraviolet B radiation in a human cell line.

Robert C, Muel B, Benoit A, Dubertret L, Sarasin A, Stary A. Robert C, et al. J Invest Dermatol. 1996 Apr;106(4):721-8. doi: 10.1111/1523-1747.ep12345616. J Invest Dermatol. 1996. PMID: 8618011 Free article.

6

Deleterious effects of ultraviolet A radiation in human cells.

Stary A, Robert C, Sarasin A. Stary A, et al. Among authors: robert c. Mutat Res. 1997 Jan 31;383(1):1-8. doi: 10.1016/s0921-8777(96)00041-9. Mutat Res. 1997. PMID: 9042414 Review. No abstract available.

7

[Trichothiodystrophies: anomalies of the repair and transcription of genes].

Robert C, Sarasin A. Robert C, et al. Ann Dermatol Venereol. 1999 Oct;126(10):669-71. Ann Dermatol Venereol. 1999. PMID: 10604001 French. No abstract available.

8

Gene expression signature associated with BRAF mutations in human primary cutaneous melanomas.

Kannengiesser C, Spatz A, Michiels S, Eychène A, Dessen P, Lazar V, Winnepenninckx V, Lesueur F, Druillennec S, Robert C, van den Oord JJ, Sarasin A, Bressac-de Paillerets B; EORTC Melanoma group. Kannengiesser C, et al. Among authors: robert c. Mol Oncol. 2008 Apr;1(4):425-30. doi: 10.1016/j.molonc.2008.01.002. Epub 2008 Jan 12. Mol Oncol. 2008. PMID: 19383316 Free PMC article.

9

Skin tumors induced by sorafenib; paradoxic RAS-RAF pathway activation and oncogenic mutations of HRAS, TP53, and TGFBR1.

Arnault JP, Mateus C, Escudier B, Tomasic G, Wechsler J, Hollville E, Soria JC, Malka D, Sarasin A, Larcher M, André J, Kamsu-Kom N, Boussemart L, Lacroix L, Spatz A, Eggermont AM, Druillennec S, Vagner S, Eychène A, Dumaz N, Robert C. Arnault JP, et al. Among authors: robert c. Clin Cancer Res. 2012 Jan 1;18(1):263-72. doi: 10.1158/1078-0432.CCR-11-1344. Epub 2011 Nov 17. Clin Cancer Res. 2012. PMID: 22096025

10

Correlation of phenotype/genotype in a cohort of 23 xeroderma pigmentosum-variant patients reveals 12 new disease-causing POLH mutations.

Opletalova K, Bourillon A, Yang W, Pouvelle C, Armier J, Despras E, Ludovic M, Mateus C, Robert C, Kannouche P, Soufir N, Sarasin A. Opletalova K, et al. Among authors: robert c. Hum Mutat. 2014 Jan;35(1):117-28. doi: 10.1002/humu.22462. Hum Mutat. 2014. PMID: 24130121

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