Lenoir G - Search Results

1

Germ-line exclusion of a single p53 allele by premature termination of translation in a Li-Fraumeni syndrome family.

Stolzenberg MC, Brugières L, Gardes M, Dessarps-Freichey F, Chompret A, Bressac B, Lenoir G, Bonaïti-Pellié C, Lemerle J, Feunteun J. Stolzenberg MC, et al. Among authors: lenoir g. Oncogene. 1994 Oct;9(10):2799-804. Oncogene. 1994. PMID: 8084585

2

BRCA1, a gene involved in inherited predisposition to breast and ovarian cancer.

Feunteun J, Lenoir GM. Feunteun J, et al. Among authors: lenoir gm. Biochim Biophys Acta. 1996 Mar 18;1242(3):177-80. doi: 10.1016/0304-419x(95)00016-9. Biochim Biophys Acta. 1996. PMID: 8603070 Review. No abstract available.

3

Gamma-rays-induced death of human cells carrying mutations of BRCA1 or BRCA2.

Foray N, Randrianarison V, Marot D, Perricaudet M, Lenoir G, Feunteun J. Foray N, et al. Among authors: lenoir g. Oncogene. 1999 Dec 2;18(51):7334-42. doi: 10.1038/sj.onc.1203165. Oncogene. 1999. PMID: 10602489

4

Mitotic catastrophe constitutes a special case of apoptosis whose suppression entails aneuploidy.

Castedo M, Perfettini JL, Roumier T, Valent A, Raslova H, Yakushijin K, Horne D, Feunteun J, Lenoir G, Medema R, Vainchenker W, Kroemer G. Castedo M, et al. Among authors: lenoir g. Oncogene. 2004 May 27;23(25):4362-70. doi: 10.1038/sj.onc.1207572. Oncogene. 2004. PMID: 15048075

5

PDGFRA germline mutation in a family with multiple cases of gastrointestinal stromal tumor.

Chompret A, Kannengiesser C, Barrois M, Terrier P, Dahan P, Tursz T, Lenoir GM, Bressac-De Paillerets B. Chompret A, et al. Gastroenterology. 2004 Jan;126(1):318-21. doi: 10.1053/j.gastro.2003.10.079. Gastroenterology. 2004. PMID: 14699510

6

Heterozygote BRCA1 status and skewed chromosome X inactivation.

Helbling-Leclere A, Lenoir GM, Feunteun J. Helbling-Leclere A, et al. Fam Cancer. 2007;6(1):153-7. doi: 10.1007/s10689-006-9102-z. Fam Cancer. 2007. PMID: 16944269

7

Comprehensive analysis of CDKN2A (p16INK4A/p14ARF) and CDKN2B genes in 53 melanoma index cases considered to be at heightened risk of melanoma.

Laud K, Marian C, Avril MF, Barrois M, Chompret A, Goldstein AM, Tucker MA, Clark PA, Peters G, Chaudru V, Demenais F, Spatz A, Smith MW, Lenoir GM, Bressac-de Paillerets B; French Hereditary Melanoma Study Group. Laud K, et al. Among authors: lenoir gm. J Med Genet. 2006 Jan;43(1):39-47. doi: 10.1136/jmg.2005.033498. Epub 2005 Jun 3. J Med Genet. 2006. PMID: 15937071 Free PMC article.

8

Nucleotide sequence polymorphism in a hotspot mutation region of the p53 gene.

Mazars GR, Jeanteur P, Lynch HT, Lenoir G, Theillet C. Mazars GR, et al. Among authors: lenoir g. Oncogene. 1992 Apr;7(4):781-2. Oncogene. 1992. PMID: 1565474

9

BRCA1, BRCA2, TP53, and CDKN2A germline mutations in patients with breast cancer and cutaneous melanoma.

Monnerat C, Chompret A, Kannengiesser C, Avril MF, Janin N, Spatz A, Guinebretière JM, Marian C, Barrois M, Boitier F, Lenoir GM, Bressac-de Paillerets B. Monnerat C, et al. Fam Cancer. 2007;6(4):453-61. doi: 10.1007/s10689-007-9143-y. Epub 2007 Jul 12. Fam Cancer. 2007. PMID: 17624602

10

A breast-ovarian cancer susceptibility gene maps to chromosome 17q21.

Feunteun J, Narod SA, Lynch HT, Watson P, Conway T, Lynch J, Parboosingh J, O'Connell P, White R, Lenoir GM. Feunteun J, et al. Among authors: lenoir gm. Am J Hum Genet. 1993 Apr;52(4):736-42. Am J Hum Genet. 1993. PMID: 8460639 Free PMC article.

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