Lenoir G - Search Results

1

Maternally inherited duplication of the mitochondrial genome in a syndrome of proximal tubulopathy, diabetes mellitus, and cerebellar ataxia.

Rötig A, Bessis JL, Romero N, Cormier V, Saudubray JM, Narcy P, Lenoir G, Rustin P, Munnich A. Rötig A, et al. Among authors: lenoir g. Am J Hum Genet. 1992 Feb;50(2):364-70. Am J Hum Genet. 1992. PMID: 1531167 Free PMC article.

2

Various mechanisms cause RET-mediated signaling defects in Hirschsprung's disease.

Pelet A, Geneste O, Edery P, Pasini A, Chappuis S, Atti T, Munnich A, Lenoir G, Lyonnet S, Billaud M. Pelet A, et al. Among authors: lenoir g. J Clin Invest. 1998 Mar 15;101(6):1415-23. doi: 10.1172/JCI375. J Clin Invest. 1998. PMID: 9502784 Free PMC article.

3

Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma.

Gardie B, Remenieras A, Kattygnarath D, Bombled J, Lefèvre S, Perrier-Trudova V, Rustin P, Barrois M, Slama A, Avril MF, Bessis D, Caron O, Caux F, Collignon P, Coupier I, Cremin C, Dollfus H, Dugast C, Escudier B, Faivre L, Field M, Gilbert-Dussardier B, Janin N, Leport Y, Leroux D, Lipsker D, Malthieu F, McGilliwray B, Maugard C, Méjean A, Mortemousque I, Plessis G, Poppe B, Pruvost-Balland C, Rooker S, Roume J, Soufir N, Steinraths M, Tan MH, Théodore C, Thomas L, Vabres P, Van Glabeke E, Meric JB, Verkarre V, Lenoir G, Joulin V, Deveaux S, Cusin V, Feunteun J, Teh BT, Bressac-de Paillerets B, Richard S; French National Cancer Institute "Inherited predisposition to kidney cancer" network. Gardie B, et al. Among authors: lenoir g. J Med Genet. 2011 Apr;48(4):226-34. doi: 10.1136/jmg.2010.085068. Epub 2011 Mar 12. J Med Genet. 2011. PMID: 21398687 Free article.

4

A high incidence of BRCA1 mutations in 20 breast-ovarian cancer families.

Serova O, Montagna M, Torchard D, Narod SA, Tonin P, Sylla B, Lynch HT, Feunteun J, Lenoir GM. Serova O, et al. Among authors: lenoir gm. Am J Hum Genet. 1996 Jan;58(1):42-51. Am J Hum Genet. 1996. PMID: 8554067 Free PMC article.

5

Mutations in BRCA1 and BRCA2 in breast cancer families: are there more breast cancer-susceptibility genes?

Serova OM, Mazoyer S, Puget N, Dubois V, Tonin P, Shugart YY, Goldgar D, Narod SA, Lynch HT, Lenoir GM. Serova OM, et al. Among authors: lenoir gm. Am J Hum Genet. 1997 Mar;60(3):486-95. Am J Hum Genet. 1997. PMID: 9042907 Free PMC article.

6

The gene for MEN 2A is tightly linked to the centromere of chromosome 10.

Narod SA, Sobol H, Schuffenecker I, Lavoué MF, Lenoir GM. Narod SA, et al. Among authors: lenoir gm. Hum Genet. 1991 Mar;86(5):529-30. doi: 10.1007/BF00194649. Hum Genet. 1991. PMID: 1673115

7

Distinct BRCA1 rearrangements involving the BRCA1 pseudogene suggest the existence of a recombination hot spot.

Puget N, Gad S, Perrin-Vidoz L, Sinilnikova OM, Stoppa-Lyonnet D, Lenoir GM, Mazoyer S. Puget N, et al. Am J Hum Genet. 2002 Apr;70(4):858-65. doi: 10.1086/339434. Epub 2002 Mar 5. Am J Hum Genet. 2002. PMID: 11880951 Free PMC article.

8

NF2 gene in neurofibromatosis type 2 patients.

Zucman-Rossi J, Legoix P, Der Sarkissian H, Cheret G, Sor F, Bernardi A, Cazes L, Giraud S, Ollagnon E, Lenoir G, Thomas G. Zucman-Rossi J, et al. Among authors: lenoir g. Hum Mol Genet. 1998 Dec;7(13):2095-101. doi: 10.1093/hmg/7.13.2095. Hum Mol Genet. 1998. PMID: 9817927

9

A 100-kb physical and transcriptional map around the EDH17B2 gene: identification of three novel genes and a pseudogene of a human homologue of the rat PRL-1 tyrosine phosphatase.

Montagna M, Serova O, Sylla BS, Feunteun J, Lenoir GM. Montagna M, et al. Among authors: lenoir gm. Hum Genet. 1995 Nov;96(5):532-8. doi: 10.1007/BF00197407. Hum Genet. 1995. PMID: 8529999

10

Localization of the human phosphotyrosine phosphatase-related genes (h-PRL-1) to chromosome bands 1p35-p34, 17q12-q21, 11q24-q25 and 12q24.

Montagna M, Serova O, Sylla BS, Mattei MG, Lenoir GM. Montagna M, et al. Among authors: lenoir gm. Hum Genet. 1996 Dec;98(6):738-40. doi: 10.1007/s004390050295. Hum Genet. 1996. PMID: 8931711

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