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Gilbert Lenoir

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Virginie Maillard; Kiyonori Kuriki; Benoît Lefebvre; Marie-Christine Boutron-Ruault; Gilbert M Lenoir; Virginie Joulin; Françoise Clavel-Chapelon; Véronique Chajès
Serum carotenoid, tocopherol and retinol concentrations and breast cancer risk in the E3N-EPIC study.
Caroline Kannengiesser; Sharon Brookes; Anna Gutierrez del Arroyo; Danielle Pham; Johny Bombled; Michel Barrois; Olivier Mauffret; Marie-Françoise M Avril; Agnès Chompret; Gilbert M Lenoir; Alain Sarasin; Gordon Peters; Brigitte Bressac-de Paillerets
Functional, structural, and genetic evaluation of 20 CDKN2A germ line mutations identified in melanoma-prone families or patients.
Fabienne LESUEUR; M de Lichy; Michel Barrois; G Durand; Johny Bombled; Marie-Françoise Avril; Agnès Chompret; Françoise Boitier; Gilbert M Lenoir; B Bressac-de Paillerets; Monique Baccard; Bertrand Bachollet; Pascaline Berthet; Valérie Bonadona; Jean-Marie Bonnetblanc; Olivier Caron; Jacqueline Chevrant-Breton; Jean-François Cuny; Stéphane Dalle; Michèle Delaunay; Liliane Demange; Julie De Quatrebarbes; Jean-François Doré; Marc Frénay; Jean-Pierre Fricker; Marion Gauthier-Villars; Paul Gesta; Sophie Giraud; Philippe Gorry; Florent Grange; Andrew Green; Laetitia Huiart; Nicolas Janin; Pascal Joly; Delphine Kérob; Christine Lasset; Dominique Leroux; Jean-Marc Limacher; Michel Longy; Sandrine Mansard; Karine Marrou; Tanguy Martin-Denavit; Christine Mateus; Eve Maubec; Laurence Olivier-Faivre; Vincent Orlandini; Pascal Pujol; Bruno Sassolas; Dominique Stoppa-Lyonnet; Luc Thomas; Pierre Vabres; Laurence Venat; Ewa Wierzbicka; Hélène Zattara
The contribution of large genomic deletions at the CDKN2A locus to the burden of familial melanoma.

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2010: Virginie Maillard; Kiyonori Kuriki; Benoît Lefebvre; Marie-Christine Boutron-Ruault; Gilbert M Lenoir; Virginie Joulin; Françoise Clavel-Chapelon; Véronique Chajès
Serum carotenoid, tocopherol and retinol concentrations and breast cancer risk in the E3N-EPIC study.
International journal of cancer. Journal international du cancer 2010;127(5):1188-96.
2009: Caroline Kannengiesser; Sharon Brookes; Anna Gutierrez del Arroyo; Danielle Pham; Johny Bombled; Michel Barrois; Olivier Mauffret; Marie-Françoise M Avril; Agnès Chompret; Gilbert M Lenoir; Alain Sarasin; Gordon Peters; Brigitte Bressac-de Paillerets
Functional, structural, and genetic evaluation of 20 CDKN2A germ line mutations identified in melanoma-prone families or patients.
Human mutation 2009;30(4):564-74.
2008: Fabienne LESUEUR; M de Lichy; Michel Barrois; G Durand; Johny Bombled; Marie-Françoise Avril; Agnès Chompret; Françoise Boitier; Gilbert M Lenoir; B Bressac-de Paillerets; Monique Baccard; Bertrand Bachollet; Pascaline Berthet; Valérie Bonadona; Jean-Marie Bonnetblanc; Olivier Caron; Jacqueline Chevrant-Breton; Jean-François Cuny; Stéphane Dalle; Michèle Delaunay; Liliane Demange; Julie De Quatrebarbes; Jean-François Doré; Marc Frénay; Jean-Pierre Fricker; Marion Gauthier-Villars; Paul Gesta; Sophie Giraud; Philippe Gorry; Florent Grange; Andrew Green; Laetitia Huiart; Nicolas Janin; Pascal Joly; Delphine Kérob; Christine Lasset; Dominique Leroux; Jean-Marc Limacher; Michel Longy; Sandrine Mansard; Karine Marrou; Tanguy Martin-Denavit; Christine Mateus; Eve Maubec; Laurence Olivier-Faivre; Vincent Orlandini; Pascal Pujol; Bruno Sassolas; Dominique Stoppa-Lyonnet; Luc Thomas; Pierre Vabres; Laurence Venat; Ewa Wierzbicka; Hélène Zattara
The contribution of large genomic deletions at the CDKN2A locus to the burden of familial melanoma.
British journal of cancer 2008;99(2):364-70.
2008: Véronique Chajès; Anne C M Thiébaut; Maxime Rotival; Estelle Gauthier; Virginie Maillard; Marie-Christine Boutron-Ruault; Virginie Joulin; Gilbert M Lenoir; Françoise Clavel-Chapelon
Association between serum trans-monounsaturated fatty acids and breast cancer risk in the E3N-EPIC Study.
American journal of epidemiology 2008;167(11):1312-20.
2007: Christian Monnerat; Agnès Chompret; Caroline Kannengiesser; Marie-Françoise Avril; Nicolas Janin; Alain Spatz; Jean-Marc Guinebretière; Catalin Marian; Michel Barrois; Françoise Boitier; Gilbert M Lenoir; Brigitte Bressac De-Paillerets
BRCA1, BRCA2, TP53, and CDKN2A germline mutations in patients with breast cancer and cutaneous melanoma.
Familial cancer 2007;6(4):453-61.
2007: Valérie Bonadona; Sophie Dussart-Moser; Nicolas Voirin; Olga M Sinilnikova; Hervé Mignotte; Patrice Mathevet; Alain Brémond; Isabelle Treilleux; Alain Martin; Pascale Romestaing; Daniel Raudrant; René-Charles Rudigoz; Gilbert M Lenoir; Christine Lasset
Prognosis of early-onset breast cancer based on BRCA1/2 mutation status in a French population-based cohort and review.
Breast cancer research and treatment 2007;101(2):233-45.
2007: Anne Helbling-Leclere; Gilbert M Lenoir; Jean Feunteun
Heterozygote BRCA1 status and skewed chromosome X inactivation.
Familial cancer 2007;6(1):153-7.
2006: Véronique Chajès; Marie Cambot; Karen Moreau; Gilbert M Lenoir; Virginie Joulin
Acetyl-CoA carboxylase alpha is essential to breast cancer cell survival.
Cancer research 2006;66(10):5287-94.
2006: Karen Moreau; Eva Dizin; Hind Ray; Celine Luquain; Etienne Lefai; Fabienne Foufelle; Marc Billaud; Gilbert M Lenoir; Nicole Dalla Venezia
BRCA1 affects lipid synthesis through its interaction with acetyl-CoA carboxylase.
The Journal of biological chemistry 2006;281(6):3172-81.
2006: Olga M Sinilnikova; Sylvie Mazoyer; Colette Bonnardel; Henry T Lynch; Steven A Narod; Gilbert M Lenoir
BRCA1 and BRCA2 mutations in breast and ovarian cancer syndrome: reflection on the Creighton University historical series of high risk families.
Familial cancer 2006;5(1):15-20.
2006: Karine Laud; Catalin Marian; Marie-Françoise Avril; Michel Barrois; Agnès Chompret; Alisa M Goldstein; Margaret A Tucker; P A Clark; G Peters; Valérie Chaudru; Florence Demenais; Alain Spatz; M W Smith; Gilbert M Lenoir; Brigitte Bressac De-Paillerets
Comprehensive analysis of CDKN2A (p16INK4A/p14ARF) and CDKN2B genes in 53 melanoma index cases considered to be at heightened risk of melanoma.
Journal of medical genetics 2006;43(1):39-47.
2005: David J Hughes; Sophie M Ginolhac; Isabelle Coupier; Laure Barjhoux; Valerie Gaborieau; Brigitte Bressac De-Paillerets; Agnès Chompret; Yves-Jean Bignon; Nancy Uhrhammer; Christine Lasset; Sophie Giraud; Hagay Sobol; Agnès Hardouin; Pascaline Berthet; Jean-Philippe Peyrat; Joëlle Fournier; Catherine Nogues; Rosette Lidereau; Danièle Muller; Jean-Pierre Fricker; Michel Longy; Christine Toulas; Rosine Guimbaud; Drakoulis Yannoukakos; Sylvie Mazoyer; Henry T Lynch; Gilbert M Lenoir; David E Goldgar; Dominique Stoppa-Lyonnet; Olga M Sinilnikova
Breast cancer risk in BRCA1 and BRCA2 mutation carriers and polyglutamine repeat length in the AIB1 gene.
International journal of cancer. Journal international du cancer 2005;117(2):230-3.
2005: Sandrine Giscard d'Estaing; Delphine Perrin; Gilbert M Lenoir; Jean François Guérin; Robert Dante
Upregulation of the BRCA1 gene in human germ cells and in preimplantation embryos.
Fertility and sterility 2005;84(3):785-8.
2005: Valérie Bonadona; Olga M Sinilnikova; Sandrine Chopin; Antonis C Antoniou; Hervé Mignotte; Patrice Mathevet; Alain Brémond; Alain Martin; Jean-Yves Bobin; Pascale Romestaing; Daniel Raudrant; René-Charles Rudigoz; Mélanie Léoné; Franck Chauvin; Douglas F Easton; Gilbert M Lenoir; Christine Lasset
Contribution of BRCA1 and BRCA2 germ-line mutations to the incidence of breast cancer in young women: results from a prospective population-based study in France.
Genes, chromosomes & cancer 2005;43(4):404-13.
2005: Georgia Chenevix-Trench; Olga M Sinilnikova; Graeme Suthers; N Pandeya; Sylvie Mazoyer; Joseph Sambrook; S Goldup; David E Goldgar; H T Lynch; Gilbert M Lenoir; G Cheetham
Ratio of male to female births in the offspring of BRCA1 and BRCA2 carriers.
Familial cancer 2005;4(2):73-5.
2005: Maureen T Travers; Marie Cambot; Helen T Kennedy; Gilbert M Lenoir; Michael Barber; Virginie Joulin
Asymmetric expression of transcripts derived from the shared promoter between the divergently oriented ACACA and TADA2L genes.
Genomics 2005;85(1):71-84.
2004: Olga M Sinilnikova; Sophie M Ginolhac; Clémence Magnard; Mélanie Léoné; Olga Anczukow; David Hughes; Karen Moreau; Deborah Thompson; Christine Coutanson; Janet Hall; Pascale Romestaing; Jean-Pierre Gérard; Valérie Bonadona; Christine Lasset; David E Goldgar; Virginie Joulin; Nicole Dalla Venezia; Gilbert M Lenoir
Acetyl-CoA carboxylase alpha gene and breast cancer susceptibility.
Carcinogenesis 2004;25(12):2417-24.
2004: Alexander Valent; Marine Guillaud-Bataille; Chantal Farra; François Lozach; Barbara Spengler; Marie-José Terrier-Lacombe; Dominique Valteau-Couanet; Gisèle Danglot; Gilbert M Lenoir; Olivier Brison; Jean Bénard; Alain BERNHEIM
Alternative pathways of MYCN gene copy number increase in primary neuroblastoma tumors.
Cancer genetics and cytogenetics 2004;153(1):10-5.
2004: Agnès Chompret; Caroline Kannengiesser; Michel Barrois; Philippe Terrier; Philippe Dahan; Thomas Tursz; Gilbert M Lenoir; Brigitte Bressac De-Paillerets
PDGFRA germline mutation in a family with multiple cases of gastrointestinal stromal tumor.
Gastroenterology 2004;126(1):318-21.
2003: Caroline Kannengiesser; Marie-Françoise Avril; Alain Spatz; Karine Laud; Gilbert M Lenoir; Brigitte Bressac De-Paillerets
CDKN2A as a uveal and cutaneous melanoma susceptibility gene.
Genes, chromosomes & cancer 2003;38(3):265-8.
2003: Silvia de Sanjosé; Mélanie Léoné; Victoria Bérez; Angel Izquierdo; Rebeca Font; Joan M Brunet; Thierry Louat; Loreto Vilardell; Joan Borras; Pau Viladiu; F Xavier Bosch; Gilbert M Lenoir; Olga M Sinilnikova
Prevalence of BRCA1 and BRCA2 germline mutations in young breast cancer patients: a population-based study.
International journal of cancer. Journal international du cancer 2003;106(4):588-93.
2003: Karine Laud; Caroline Kannengiesser; Marie-Françoise Avril; Agnès Chompret; Dominique Stoppa-Lyonnet; Laurence Desjardins; Alain Eychene; Florence Demenais; Gilbert M Lenoir; Brigitte Bressac De-Paillerets
BRAF as a melanoma susceptibility candidate gene?
Cancer research 2003;63(12):3061-5.
2002: Xiangcheng Zhi; Csilla I Szabo; Sandrine Chopin; Nicola Suter; Qing-Sheng Wang; Elaine A Ostrander; Olga M Sinilnikova; Gilbert M Lenoir; David E Goldgar; Yu-rong Shi
BRCA1 and BRCA2 sequence variants in Chinese breast cancer families.
Human mutation 2002;20(6):474.
2002: Laure Perrin-Vidoz; Olga M Sinilnikova; Dominique Stoppa-Lyonnet; Gilbert M Lenoir; Sylvie Mazoyer
The nonsense-mediated mRNA decay pathway triggers degradation of most BRCA1 mRNAs bearing premature termination codons.
Human molecular genetics 2002;11(23):2805-14.
2002: Valérie Bonadona; Olga M Sinilnikova; Gilbert M Lenoir; Christine Lasset
Pretest prediction of BRCA1 or BRCA2 mutation by risk counselors and the computer model BRCAPRO.
Journal of the National Cancer Institute 2002;94(20):1582-3; author reply 1583-4.
2002: Clémence Magnard; Richard Bachelier; Anne Vincent; Michel Jaquinod; Sylvie Kieffer; Gilbert M Lenoir; Nicole Dalla Venezia
BRCA1 interacts with acetyl-CoA carboxylase through its tandem of BRCT domains.
Oncogene 2002;21(44):6729-39.
2002: Pimpicha Patmasiriwat; Kris Bhothisuwan; Olga M Sinilnikova; Sandrine Chopin; Suthida Methakijvaroon; Michael D Badzioch; Puchong Padungsutt; Paiboon Vattanaviboon; Vanchai Vattanasapt; Csilla I Szabo; Grady F Saunders; David E Goldgar; Gilbert M Lenoir
Analysis of breast cancer susceptibility genes BRCA1 and BRCA2 in Thai familial and isolated early-onset breast and ovarian cancer.
Human mutation 2002;20(3):230.
2002: Virginie Wautot; Cécile Vercherat; James Lespinasse; Béatrice Chambe; Gilbert M Lenoir; Chang X Zhang; Nicole Porchet; Martine Cordier; Christophe Béroud; Alain Calender
Germline mutation profile of MEN1 in multiple endocrine neoplasia type 1: search for correlation between phenotype and the functional domains of the MEN1 protein.
Human mutation 2002;20(1):35-47.
2002: Francisco X Real; Núria Malats; Gaëtan Lesca; Miquel Porta; Sandrine Chopin; Gilbert M Lenoir; Olga M Sinilnikova
Family history of cancer and germline BRCA2 mutations in sporadic exocrine pancreatic cancer.
Gut 2002;50(5):653-7.
2002: Lise-Marie Billard; Frédérique Magdinier; Gilbert M Lenoir; Lucien Frappart; Robert Dante
MeCP2 and MBD2 expression during normal and pathological growth of the human mammary gland.
Oncogene 2002;21(17):2704-12.
2002: Nadine Puget; Sophie Gad; Laure Perrin-Vidoz; Olga M Sinilnikova; Dominique Stoppa-Lyonnet; Gilbert M Lenoir; Sylvie Mazoyer
Distinct BRCA1 rearrangements involving the BRCA1 pseudogene suggest the existence of a recombination hot spot.
American journal of human genetics 2002;70(4):858-65.
2002: Richard Bachelier; Anne Vincent; Patrice Mathevet; Frédérique Magdinier; Gilbert M Lenoir; Lucien Frappart
Retroviral transduction of splice variant Brca1-Delta11 or mutant Brca1-W1777Stop causes mouse epithelial mammary atypical duct hyperplasia.
Virchows Archiv : an international journal of pathology 2002;440(3):261-6.
2001: Gilles Freyer; Blandine Ligneau; M Schlumberger; Cécile Blandy; B Contedevolx; Véronique Trillet-Lenoir; Gilbert M Lenoir; N Chau; A Dazord
Quality of life in patients at risk of medullary thyroid carcinoma and followed by a comprehensive medical network: trends for future evaluations.
Annals of oncology : official journal of the European Society for Medical Oncology / ESMO 2001;12(10):1461-5.
2000: Richard Bachelier; N Dalla Venezia; Sylvie Mazoyer; Lucien Frappart; Gilbert M Lenoir; Anne Vincent
Differential expression and subcellular localization of murine BRCA1 and BRCA1-delta 11 isoforms in murine and human cell lines.
International journal of cancer. Journal international du cancer 2000;88(4):519-24.
2000: M A Unger; Katherine L Nathanson; Kathleen A Calzone; Danielle Antin-Ozerkis; Helen A Shih; Anne-Marie Martin; Gilbert M Lenoir; Sylvie Mazoyer; Barbara L Weber
Screening for genomic rearrangements in families with breast and ovarian cancer identifies BRCA1 mutations previously missed by conformation-sensitive gel electrophoresis or sequencing.
American journal of human genetics 2000;67(4):841-50.
2000: Frédérique Magdinier; Lise-Marie Billard; G Wittmann; Lucien Frappart; M Benchaïb; Gilbert M Lenoir; Jean François Guérin; Robert Dante
Regional methylation of the 5' end CpG island of BRCA1 is associated with reduced gene expression in human somatic cells.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2000;14(11):1585-94.
2000: Gerald L Feldman; M W Edmonds; P J Ainsworth; I Schuffenecker; Gilbert M Lenoir; A W Saxe; Gary B Talpos; J Roberson; Nancie Petrucelli; CE Jackson
Variable expressivity of familial medullary thyroid carcinoma (FMTC) due to a RET V804M (GTG-->ATG) mutation.
Surgery 2000;128(1):93-8.
2000: Elizabeth M Rohlfs; Nadine Puget; Mark Graham II; Barbara L Weber; Judy E Garber; Cecile Skrzynia; J L Halperin; Gilbert M Lenoir; Lawrence M Silverman; Sylvie Mazoyer
An Alu-mediated 7.1 kb deletion of BRCA1 exons 8 and 9 in breast and ovarian cancer families that results in alternative splicing of exon 10.
Genes, chromosomes & cancer 2000;28(3):300-7.
2000: Virginie Wautot; S Khodaei; Lucien Frappart; N Buisson; E Baro; Gilbert M Lenoir; Alain Calender; Chang X Zhang; Günther Weber
Expression analysis of endogenous menin, the product of the multiple endocrine neoplasia type 1 gene, in cell lines and human tissues.
International journal of cancer. Journal international du cancer 2000;85(6):877-81.
1999: O Geneste; C Bidaud; Gabriella De Vita; R M Hofstra; S Tartare-Deckert; C H Buys; Gilbert M Lenoir; Massimo Santoro; Marc Billaud
Two distinct mutations of the RET receptor causing Hirschsprung's disease impair the binding of signalling effectors to a multifunctional docking site.
Human molecular genetics 1999;8(11):1989-99.
1999: Olga M Sinilnikova; K M Egan; J L Quinn; L Boutrand; Gilbert M Lenoir; Dominique Stoppa-Lyonnet; L Desjardins; C Levy; David E Goldgar; E S Gragoudas
Germline brca2 sequence variants in patients with ocular melanoma.
International journal of cancer. Journal international du cancer 1999;82(3):325-8.
1999: Frédérique Magdinier; N Dalla Venezia; Gilbert M Lenoir; Lucien Frappart; Robert Dante
BRCA1 expression during prenatal development of the human mammary gland.
Oncogene 1999;18(27):4039-43.
1999: Nadine Puget; Dominique Stoppa-Lyonnet; Olga M Sinilnikova; S Pagès; Henry T Lynch; Gilbert M Lenoir; Sylvie Mazoyer
Screening for germ-line rearrangements and regulatory mutations in BRCA1 led to the identification of four new deletions.
Cancer research 1999;59(2):455-61.
1999: M Takahashi; T Iwashita; M Santoro; Stanislas LYONNET; Gilbert M Lenoir; Marc Billaud
Co-segregation of MEN2 and Hirschsprung's disease: the same mutation of RET with both gain and loss-of-function?
Human mutation 1999;13(4):331-6.
1999: Gilles Freyer; A Dazord; M Schlumberger; Bernard Conte-Devolx; Blandine Ligneau; Véronique Trillet-Lenoir; Gilbert M Lenoir
Psychosocial impact of genetic testing in familial medullary-thyroid carcinoma: a multicentric pilot-evaluation.
Annals of oncology : official journal of the European Society for Medical Oncology / ESMO 1999;10(1):87-95.
1999: Nadine Puget; Olga M Sinilnikova; Dominique Stoppa-Lyonnet; C Audoynaud; S Pagès; Henry T Lynch; David E Goldgar; Gilbert M Lenoir; Sylvie Mazoyer
An Alu-mediated 6-kb duplication in the BRCA1 gene: a new founder mutation?
American journal of human genetics 1999;64(1):300-2.
1998: Frédérique Magdinier; Stéphane Ribieras; Gilbert M Lenoir; Lucien Frappart; Robert Dante
Down-regulation of BRCA1 in human sporadic breast cancer; analysis of DNA methylation patterns of the putative promoter region.
Oncogene 1998;17(24):3169-76.
1998: S Chappuis-Flament; A Pasini; Gabriella De Vita; C Ségouffin-Cariou; Alfredo Fusco; Tania Attié; Gilbert M Lenoir; Massimo Santoro; Marc Billaud
Dual effect on the RET receptor of MEN 2 mutations affecting specific extracytoplasmic cysteines.
Oncogene 1998;17(22):2851-61.
1998: Sylvie Mazoyer; Nadine Puget; Laure Perrin-Vidoz; Henry T Lynch; OM Serova-Sinilnikova; Gilbert M Lenoir
A BRCA1 nonsense mutation causes exon skipping.
American journal of human genetics 1998;62(3):713-5.
1998: I Schuffenecker; M Virally-Monod; R Brohet; David E Goldgar; Bernard Conte-Devolx; L Leclerc; Olivier Chabre; A Boneu; J Caron; C Houdent; E Modigliani; Vincent Rohmer; Martin Schlumberger; C Eng; Pierre-Jean Guillausseau; Gilbert M Lenoir
Risk and penetrance of primary hyperparathyroidism in multiple endocrine neoplasia type 2A families with mutations at codon 634 of the RET proto-oncogene. Groupe D'etude des Tumeurs à Calcitonine.
The Journal of clinical endocrinology and metabolism 1998;83(2):487-91.
1997: A Pasini; O Geneste; P Legrand; Martin Schlumberger; Mireille Rossel; Laurence Fournier; Brian B Rudkin; I Schuffenecker; Gilbert M Lenoir; Marc Billaud
Oncogenic activation of RET by two distinct FMTC mutations affecting the tyrosine kinase domain.
Oncogene 1997;15(4):393-402.
1997: J N Marcus; Patrice Watson; D L Page; Steven A Narod; P Tonin; Gilbert M Lenoir; OM Serova; Henry T Lynch
BRCA2 hereditary breast cancer pathophenotype.
Breast cancer research and treatment 1997;44(3):275-7.
1997: OM Serova-Sinilnikova; L Boutrand; Dominique Stoppa-Lyonnet; Brigitte Bressac De-Paillerets; V Dubois; Christine Lasset; Nicolas Janin; Yves-Jean Bignon; Michel Longy; Christine Maugard; Rosette Lidereau; Dominique Leroux; Thierry Frebourg; Sylvie Mazoyer; Gilbert M Lenoir
BRCA2 mutations in hereditary breast and ovarian cancer in France.
American journal of human genetics 1997;60(5):1236-9.
1997: Francine-Marie Michiels; S Chappuis; Bernard Caillou; A Pasini; Monique Talbot; Roger Monier; Gilbert M Lenoir; Jean Feunteun; Marc Billaud
Development of medullary thyroid carcinoma in transgenic mice expressing the RET protooncogene altered by a multiple endocrine neoplasia type 2A mutation.
Proceedings of the National Academy of Sciences of the United States of America 1997;94(7):3330-5.
1997: OM Serova; Sylvie Mazoyer; Nadine Puget; V Dubois; P Tonin; Yin Yao Shugart; David E Goldgar; Steven A Narod; Henry T Lynch; Gilbert M Lenoir
Mutations in BRCA1 and BRCA2 in breast cancer families: are there more breast cancer-susceptibility genes?
American journal of human genetics 1997;60(3):486-95.
1997: Nadine Puget; D Torchard; OM Serova-Sinilnikova; Henry T Lynch; Jean Feunteun; Gilbert M Lenoir; Sylvie Mazoyer
A 1-kb Alu-mediated germ-line deletion removing BRCA1 exon 17.
Cancer research 1997;57(5):828-31.
1997: Mireille Rossel; A Pasini; S Chappuis; O Geneste; Laurence Fournier; I Schuffenecker; M Takahashi; Leo van Grunsven; J L Urdiales; Brian B Rudkin; Gilbert M Lenoir; Marc Billaud
Distinct biological properties of two RET isoforms activated by MEN 2A and MEN 2B mutations.
Oncogene 1997;14(3):265-75.
1997: J Lamartine; Marco Seri; Roberta Cinti; F Heitzmann; M Creaven; N Radomski; E Jost; Gilbert M Lenoir; Giovanni Romeo; Bakary S Sylla
Molecular cloning and mapping of a human cDNA (PA2G4) that encodes a protein highly homologous to the mouse cell cycle protein p38-2G4.
Cytogenetics and cell genetics 1997;78(1):31-5.
1997: Alain Calender; Sophie Giraud; I Schuffenecker; Gilbert M Lenoir; Patrick Gaudray; Anouk Courseaux; N Porchet; J P Aubert; Chang X Zhang
Genetic testing in presymptomatic diagnosis of multiple endocrine neoplasia.
Hormone research 1997;47(4-6):199-210.
1997: I Schuffenecker; N Ginet; David E Goldgar; Charis Eng; Béatrice Chambe; A Boneu; C Houdent; D Pallo; Martin Schlumberger; C Thivolet; Gilbert M Lenoir
Prevalence and parental origin of de novo RET mutations in multiple endocrine neoplasia type 2A and familial medullary thyroid carcinoma. Le Groupe d'Etude des Tumeurs a Calcitonine.
American journal of human genetics 1997;60(1):233-7.
1996: Marco Montagna; M Santacatterina; B Corneo; Chiara Menin; OM Serova; Gilbert M Lenoir; Luigi Chieco-Bianchi; Emma D'Andrea
Identification of seven new BRCA1 germline mutations in Italian breast and breast/ovarian cancer families.
Cancer research 1996;56(23):5466-9.
1996: Marco Montagna; OM Serova; Bakary S Sylla; M G Mattei; Gilbert M Lenoir
Localization of the human phosphotyrosine phosphatase-related genes (h-PRL-1) to chromosome bands 1p35-p34, 17q12-q21, 11q24-q25 and 12q24.
Human genetics 1996;98(6):738-40.
1996: Sylvie Mazoyer; Alison M Dunning; OM Serova; J Dearden; Nadine Puget; Catherine S Healey; Simon A Gayther; J Mangion; Michael R Stratton; Henry T Lynch; David E Goldgar; Bruce A J Ponder; Gilbert M Lenoir
A polymorphic stop codon in BRCA2.
Nature genetics 1996;14(3):253-4.
1996: Jean Feunteun; Gilbert M Lenoir
BRCA1, a gene involved in inherited predisposition to breast and ovarian cancer.
Biochimica et biophysica acta 1996;1242(3):177-80.
1996: CM Phelan; Timothy R Rebbeck; Barbara L Weber; Peter Devilee; M H Ruttledge; H T Lynch; Gilbert M Lenoir; Michael R Stratton; D F Easton; Bruce A J Ponder; Lisa A Cannon-Albright; Catharina Larsson; D E Goldgar; Steven A Narod
Ovarian cancer risk in BRCA1 carriers is modified by the HRAS1 variable number of tandem repeat (VNTR) locus.
Nature genetics 1996;12(3):309-11.
1996: J N Marcus; Patrice Watson; D L Page; Steven A Narod; Gilbert M Lenoir; Patricia N Tonin; L Linder-Stephenson; G Salerno; T A Conway; Henry T Lynch
Hereditary breast cancer: pathobiology, prognosis, and BRCA1 and BRCA2 gene linkage.
Cancer 1996;77(4):697-709.
1996: J Lamartine; K E Nichols; Luo Yin; michael krainer; F Heitzmann; A Bernard; S Gaudi; Gilbert M Lenoir; J L Sullivan; J E Ikeda; G Porta; David Schlessinger; Giovanni Romeo; Daniel A Haber; Bakary S Sylla; D Paul Harkin
Physical map and cosmid contig encompassing a new interstitial deletion of the X-linked lymphoproliferative syndrome region.
European journal of human genetics : EJHG 1996;4(6):342-51.
1996: S Guichard; Sophie Giraud; H Rousset; Gilbert M Lenoir; J Salandre; P Hamon; J A Chayvialle; Jean-Paul Riou; Alain Calender
[Clinical and genetic study of a familial case of multiple endocrine neoplasia type 1 (MEN 1). From value of multidisciplinary collaboration].
Annales d'endocrinologie 1996;57(1):64-70.
1996: OM Serova; Marco Montagna; D Torchard; Steven A Narod; Patricia N Tonin; Bakary S Sylla; Henry T Lynch; Jean Feunteun; Gilbert M Lenoir
A high incidence of BRCA1 mutations in 20 breast-ovarian cancer families.
American journal of human genetics 1996;58(1):42-51.
1995: Patricia N Tonin; Parviz Ghadirian; CM Phelan; Gilbert M Lenoir; Henry T Lynch; F Letendre; D Belanger; M Monté; Steven A Narod
A large multisite cancer family is linked to BRCA2.
Journal of medical genetics 1995;32(12):982-4.
1995: Marco Montagna; OM Serova; Bakary S Sylla; Jean Feunteun; Gilbert M Lenoir
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.
Human genetics 1995;96(5):532-8.
1995: Gilbert M Lenoir
[Genetic predisposition to cancer development].
La Revue du praticien 1995;45(15):1889-94.
1995: Alain Calender; Sophie Giraud; Gilbert M Lenoir; Patrick Cougard; P Chanson; C Proye
[Hereditary multiple endocrine neoplasia. New genetic data and clinical applications in type 1 multiple endocrine neoplasia].
Presse médicale (Paris, France : 1983) 1995;24(11):542-6.
1994: I Schuffenecker; Marc Billaud; Alain Calender; B Chambe; N Ginet; C Calmettes; E Modigliani; Gilbert M Lenoir
RET proto-oncogene mutations in French MEN 2A and FMTC families.
Human molecular genetics 1994;3(11):1939-43.
1994: D Torchard; C Blanchet-Bardon; OM Serova; L Langbein; Steven A Narod; Nicolas Janin; AF Goguel; Alain BERNHEIM; W W Franke; Gilbert M Lenoir
Epidermolytic palmoplantar keratoderma cosegregates with a keratin 9 mutation in a pedigree with breast and ovarian cancer.
Nature genetics 1994;6(1):106-10.
1993: M H Ruttledge; Steven A Narod; Jan P Dumanski; Dilys M Parry; R Eldridge; W Wertelecki; J Parboosingh; M C Faucher; Gilbert M Lenoir; V Peter Collins
Presymptomatic diagnosis for neurofibromatosis 2 with chromosome 22 markers.
Neurology 1993;43(9):1753-60.
1993: Alain Calender; I Schuffenecker; S Giraud-Pinloche; Gilbert M Lenoir
[Genetics of multiple endocrine neoplasms: basic aspects, methods and implications for diagnosis].
Revue médicale de Liège 1993;48(6):335-52.
1993: Jean Feunteun; S A Narod; H T Lynch; P Watson; T Conway; J Lynch; J Parboosingh; P O'Connell; Raymond White; Gilbert M Lenoir
A breast-ovarian cancer susceptibility gene maps to chromosome 17q21.
American journal of human genetics 1993;52(4):736-42.
1993: M Cordier-Bussat; Marc Billaud; Alain Calender; Gilbert M Lenoir
Epstein-Barr virus (EBV) nuclear-antigen-2-induced up-regulation of CD21 and CD23 molecules is dependent on a permissive cellular context.
International journal of cancer. Journal international du cancer 1993;53(1):153-60.
1993: M Cordier-Bussat; Alain Calender; M Vuillaume; Georg W Bornkamm; Gilbert M Lenoir
Expression of the Epstein-Barr virus (EBV) latent membrane protein is tightly regulated, independently of EB nuclear antigen 2 and of EBV integration or copy number.
Virus research 1993;27(1):55-69.
1993: Q Wang; Y Ishikawa-Brush; Anthony P Monaco; D L Nelson; C T Caskey; S P Pauly; Gilbert M Lenoir; Bakary S Sylla
Physical mapping of Xq24-25 around loci closely linked to the X-linked lymphoproliferative syndrome locus: an overlapping YAC map and linkage between DXS12, DXS42, and DXS37.
European journal of human genetics : EJHG 1993;1(1):64-71.
1992: Gilbert M Lenoir; H Sobol
[Predictive tests for familial medullary cancer of the thyroid].
Pathologie-biologie 1992;39(9):921-2.
1992: S Joos; M H Falk; P Lichter; F G Haluska; B Henglein; Gilbert M Lenoir; Georg W Bornkamm
Variable breakpoints in Burkitt lymphoma cells with chromosomal t(8;14) translocation separate c-myc and the IgH locus up to several hundred kb.
Human molecular genetics 1992;1(8):625-32.
1992: Steven A Narod; Dilys M Parry; J Parboosingh; Gilbert M Lenoir; M Ruttledge; G Fischer; R Eldridge; R L Martuza; M Frontali; Jonathan L Haines
Neurofibromatosis type 2 appears to be a genetically homogeneous disease.
American journal of human genetics 1992;51(3):486-96.
1992: Steven A Narod; M F Lavoué; Kenneth Morgan; C Calmettes; H Sobol; Paul J Goodfellow; Gilbert M Lenoir
Genetic analysis of 24 French families with multiple endocrine neoplasia type 2A.
American journal of human genetics 1992;51(3):469-77.
1992: M H Falk; B C Trauth; Klaus-Michael Debatin; C Klas; Christopher D Gregory; A B Rickinson; Alain Calender; Gilbert M Lenoir; J W Ellwart; Peter H Krammer
Expression of the APO-1 antigen in Burkitt lymphoma cell lines correlates with a shift towards a lymphoblastoid phenotype.
Blood 1992;79(12):3300-6.
1992: Alain Calender; I Schuffenecker; Gilbert M Lenoir
The genetics of multiple endocrine neoplasia (MEN).
Hormone research 1992;38 Suppl 2():16-23.
1991: Steven A Narod; Jean Feunteun; Henry T Lynch; P Watson; T Conway; J Lynch; Gilbert M Lenoir
Familial breast-ovarian cancer locus on chromosome 17q12-q23.
Lancet 1991;338(8759):82-3.
1991: Steven A Narod; H Sobol; I Schuffenecker; M F Lavoué; Gilbert M Lenoir
The gene for MEN 2A is tightly linked to the centromere of chromosome 10.
Human genetics 1991;86(5):529-30.
1991: Ursula Zimber-Strobl; K O Suentzenich; Gerhard Laux; Dirk Eick; M Cordier; Alain Calender; Marc Billaud; Gilbert M Lenoir; Georg W Bornkamm
Epstein-Barr virus nuclear antigen 2 activates transcription of the terminal protein gene.
Journal of virology 1991;65(1):415-23.
1991: M Maillet-Vioud; Steven A Narod; D Assouline; H Sobol; G Fischer; J M Robert; Gilbert M Lenoir
[Genetics of neurofibromatosis: recent progress and prospects].
Revue neurologique 1991;147(10):644-52.
1991: I Schuffenecker; Steven A Narod; R A Ezekowitz; H Sobol; Jean Feunteun; Gilbert M Lenoir
The gene for mannose-binding protein maps to chromosome 10 and is a marker for multiple endocrine neoplasia type 2.
Cytogenetics and cell genetics 1991;56(2):99-102.
1990: Alain Calender; M Cordier; Marc Billaud; Gilbert M Lenoir
Modulation of cellular gene expression in B lymphoma cells following in vitro infection by Epstein-Barr virus (EBV).
International journal of cancer. Journal international du cancer 1990;46(4):658-63.
1990: Dirk Eick; Axel Polack; E Kofler; Gilbert M Lenoir; A B Rickinson; Georg W Bornkamm
Expression of P0- and P3-RNA from the normal and translocated c-myc allele in Burkitt's lymphoma cells.
Oncogene 1990;5(9):1397-402.
1990: Gilbert M Lenoir; Steven A Narod; B A Ponder
Workshop on linkage studies of hereditary breast cancer.
Cancer research 1990;50(14):4448-9.
1990: D Assouline; H Sobol; M Maillet-Vioud; I Schuffenecker; Steven A Narod; Gilbert M Lenoir
[Heredity and medullary cancer of the thyroid].
La Revue du praticien 1990;40(16):1487-9.
1990: B Frech; Ursula Zimber-Strobl; K O Suentzenich; O Pavlish; Gilbert M Lenoir; Georg W Bornkamm; Nikolaus Mueller-Lantzsch
Identification of Epstein-Barr virus terminal protein 1 (TP1) in extracts of four lymphoid cell lines, expression in insect cells, and detection of antibodies in human sera.
Journal of virology 1990;64(6):2759-67.
1990: Marc Billaud; F Rousset; Alain Calender; M Cordier; J P Aubry; V Laisse; Gilbert M Lenoir
Low expression of lymphocyte function-associated antigen (LFA)-1 and LFA-3 adhesion molecules is a common trait in Burkitt's lymphoma associated with and not associated with Epstein-Barr virus.
Blood 1990;75(9):1827-33.
1990: M Cordier; Alain Calender; Marc Billaud; U Zimber; G Rousselet; O Pavlish; Jacques Banchereau; Thomas Tursz; Georg W Bornkamm; Gilbert M Lenoir
Stable transfection of Epstein-Barr virus (EBV) nuclear antigen 2 in lymphoma cells containing the EBV P3HR1 genome induces expression of B-cell activation molecules CD21 and CD23.
Journal of virology 1990;64(3):1002-13.
1990: Ursula Zimber-Strobl; K Suentzenich; M Falk; Gerhard Laux; M Cordier; Alain Calender; Marc Billaud; Gilbert M Lenoir; Georg W Bornkamm
Epstein-Barr virus terminal protein gene transcription is dependent on EBNA2 expression and provides evidence for viral integration into the host genome.
Current topics in microbiology and immunology 1990;166():359-66.
1989: Bakary S Sylla; Q Wang; D Hayoz; G M Lathrop; Gilbert M Lenoir
Multipoint linkage mapping of the Xq25-q26 region in a family affected by the X-linked lymphoproliferative syndrome.
Clinical genetics 1989;36(6):459-62.
1989: Marc Billaud; Pierre Busson; D Huang; N Mueller-Lantzch; G Rousselet; O Pavlish; H Wakasugi; J M Seigneurin; Thomas Tursz; Gilbert M Lenoir
Epstein-Barr virus (EBV)-containing nasopharyngeal carcinoma cells express the B-cell activation antigen blast2/CD23 and low levels of the EBV receptor CR2.
Journal of virology 1989;63(10):4121-8.
1989: H Sobol; Steven A Narod; I Schuffenecker; C Amos; R A Ezekowitz; Gilbert M Lenoir
Hereditary medullary thyroid carcinoma: genetic annalysis of three related syndromes. Groupe d'Etude des Tumeurs a Calcitonine.
Henry Ford Hospital medical journal 1989;37(3-4):109-11.
1989: Steven A Narod; H Sobol; I Schuffenecker; R A Ezekowitz; Gilbert M Lenoir
Early detection of hereditary medullary thyroid cancer with polymorphic DNA probes. Groupe d'Etude des Tumeurs a Calcitonine.
Henry Ford Hospital medical journal 1989;37(3-4):106-8.
1989: H Sobol; Steven A Narod; D Assouline; Gilbert M Lenoir
Genetic screening of endocrine tumour syndromes with DNA probes: the example of medullary thyroid carcinoma.
Hormone research 1989;32(1-3):34-40.
1988: V E Gurtsevitch; G T O'Conor; Gilbert M Lenoir
Burkitt's lymphoma cell lines reveal different degrees of tumorigenicity in nude mice.
International journal of cancer. Journal international du cancer 1988;41(1):87-95.
1988: B Henglein; Martin Lipp; P Hartl; S Adolph; Horst Hameister; Dirk Eick; Axel Polack; S Joos; F Baas; Gilbert M Lenoir
Burkitt's lymphoma variant translocations: distribution of chromosomal breakpoints and perturbated regulation of a mutated c-myc gene.
Current topics in microbiology and immunology 1988;141():165-71.
1987: Alain Calender; Marc Billaud; J P Aubry; Jacques Banchereau; M Vuillaume; Gilbert M Lenoir
Epstein-Barr virus (EBV) induces expression of B-cell activation markers on in vitro infection of EBV-negative B-lymphoma cells.
Proceedings of the National Academy of Sciences of the United States of America 1987;84(22):8060-4.
1985: Dirk Eick; M Piechaczyk; B Henglein; Jean-Marie Blanchard; B Traub; E Kofler; S Wiest; Gilbert M Lenoir; Georg W Bornkamm
Aberrant c-myc RNAs of Burkitt's lymphoma cells have longer half-lives.
The EMBO journal 1985;4(13B):3717-25.