Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Gilbert Lenoir"'
Autor:
Valérie Camara-Clayette, Serge Koscielny, Sébastien Roux, Thierry Lamy, Jacques Bosq, Marc Bernard, Thierry Fest, Vladimir Lazar, Gilbert Lenoir, Vincent Ribrag
Publikováno v:
PLoS ONE, Vol 8, Iss 9, p e73993 (2013)
PURPOSE: We designed a gene profiling experiment to identify genes involved in secondary drug resistance in mantle cell lymphomas (MCL). EXPERIMENTAL DESIGN: We obtained paired tissue samples collected from the same patients before treatment and afte
Externí odkaz:
https://doaj.org/article/50c29ba936a3416e802079f151bafbd5
Autor:
Philip Leder, Jim Battey, Gilbert Lenoir, Christopher Moulding, William Murphy, Huntington Potter, Timothy Stewart, Rebecca Taub
Publikováno v:
Biotechnology & Biological Frontiers ISBN: 9780429050329
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::24794f8634cf1e28a2f272a265f5b6dc
https://doi.org/10.4324/9780429050329-30
https://doi.org/10.4324/9780429050329-30
Autor:
Gilbert Lenoir, Tristan Renault
Publikováno v:
Bulletin de l'Académie Vétérinaire de France.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f055428319846783f9ea48d975981361
https://doi.org/10.4267/2042/63997
https://doi.org/10.4267/2042/63997
Autor:
Michel Fougereau, Gilbert Lenoir
Publikováno v:
Bulletin de l'Académie Vétérinaire de France.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fdf1314e1f2cb496f2718992a41b01dc
https://doi.org/10.4267/2042/61938
https://doi.org/10.4267/2042/61938
Autor:
Gilbert Lenoir
Publikováno v:
Périodiques Scientifiques en Édition Électronique.
The contribution of cancer innovation to public health’s issues. The fight against cancer as previously the fight against infectious diseases has become a model for the public health system. In both situations the discovery of the causal agents and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e21db28e774360f41e3a3199c423da7f
https://www.persee.fr/doc/bavf_0001-4192_2014_num_167_1_12991
https://www.persee.fr/doc/bavf_0001-4192_2014_num_167_1_12991
Publikováno v:
Medecine sciences : M/S. 21(11)
Studies performed during these last twenty years have had a major impact on the understanding of carcinogenesis. They have opened a new field : cancer genetic predisposition. At the present time, most of the cancer predispositions linked to the alter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::49b1503db74be48154fef1ea75e19839
https://pubmed.ncbi.nlm.nih.gov/16274648
https://pubmed.ncbi.nlm.nih.gov/16274648
Publikováno v:
Bulletin du cancer. 92(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::aefdadfd9151f882fee2e264977dfd42
https://pubmed.ncbi.nlm.nih.gov/15888384
https://pubmed.ncbi.nlm.nih.gov/15888384
Autor:
Pablo, Ruiz-Flores, Olga M, Sinilnikova, Michael, Badzioch, A L, Calderon-Garcidueñas, Sandrine, Chopin, Odefrey, Fabrice, J F, González-Guerrero, Csilla, Szabo, Gilbert, Lenoir, David E, Goldgar, Hugo A, Barrera-Saldaña
Publikováno v:
Human mutation. 20(6)
The entire coding regions of BRCA1 and BRCA2 were screened for mutations by heteroduplex analysis in 51 Mexican breast cancer patients. One BRCA1 and one BRCA2 truncating mutation each was identified in the group of 32 (6%) early-onset breast cancer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::76989670e7cb8da8e498116fc61464fd
https://pubmed.ncbi.nlm.nih.gov/12442275
https://pubmed.ncbi.nlm.nih.gov/12442275
Autor:
Alexander, Valent, Gwenaëlle, Le Roux, Michel, Barrois, Marie-José, Terrier-Lacombe, Dominique, Valteau-Couanet, Bernadette, Léon, Barbara, Spengler, Gilbert, Lenoir, Jean, Bénard, Alain, Bernheim
Publikováno v:
The Journal of pathology. 198(4)
Neuroblastoma is the most frequent solid extracranial neoplasm of childhood, with a median age of presentation of under 2 years. This tumour is highly malignant in patients older than 12 months of age with metastatic disease. Clinical studies have co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c571c9563fae2db6bab0b9fa1bd39b52
https://pubmed.ncbi.nlm.nih.gov/12434419
https://pubmed.ncbi.nlm.nih.gov/12434419
Autor:
Patricia Legoix, Marie-Fernande Legrand, Elisabeth Ollagnon, Gilbert Lenoir, Gilles Thomas, Jessica Zucman-Rossi
Publikováno v:
Human mutation. 13(4)
Neurofibromatosis type 2 (NF2) is an autosomal dominant disorder that predisposes to nervous system tumors. Point mutations are evidenced in about 50% of the NF2 patients and large genomic deletions account for approximately 33% of the NF2 gene alter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c470690100bab22c2e3d174a37ed819
https://pubmed.ncbi.nlm.nih.gov/10220142
https://pubmed.ncbi.nlm.nih.gov/10220142