Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Michel Barrois"'
Autor:
Charline Ladroue, David Hoogewijs, Sophie Gad, Romain Carcenac, Federica Storti, Michel Barrois, Anne-Paule Gimenez-Roqueplo, Michel Leporrier, Nicole Casadevall, Olivier Hermine, Jean-Jacques Kiladjian, André Baruchel, Fadi Fakhoury, Brigitte Bressac-de Paillerets, Jean Feunteun, Nathalie Mazure, Jacques Pouysségur, Roland H. Wenger, Stéphane Richard, Betty Gardie
Publikováno v:
Haematologica, Vol 97, Iss 1 (2012)
Background Congenital secondary erythrocytoses are due to deregulation of hypoxia inducible factor resulting in overproduction of erythropoietin. The most common germline mutation identified in the hypoxia signaling pathway is the Arginine 200-Trypto
Externí odkaz:
https://doaj.org/article/10d5cbd37645421ea450e12673c5f481
Autor:
Romain Carcenac, Michel Leporrier, Stéphane Richard, Michel Barrois, Jean-Jacques Kiladjian, Jacques Pouysségur, André Baruchel, Nathalie M. Mazure, David Hoogewijs, Roland H. Wenger, Anne-Paule Gimenez-Roqueplo, Charline Ladroue, Brigitte Bressac-de Paillerets, Nicole Casadevall, Jean Feunteun, Betty Gardie, Sophie Gad, Fadi Fakhoury, Olivier Hermine, Federica Storti
Publikováno v:
Haematologica
Haematologica, 2012, 97 (1), pp.9-14. ⟨10.3324/haematol.2011.044644⟩
Haematologica, Ferrata Storti Foundation, 2012, 97 (1), pp.9-14. 〈10.3324/haematol.2011.044644〉
Haematologica, Ferrata Storti Foundation, 2012, 97 (1), pp.9-14. ⟨10.3324/haematol.2011.044644⟩
Haematologica, 2012, 97 (1), pp.9-14. ⟨10.3324/haematol.2011.044644⟩
Haematologica, Ferrata Storti Foundation, 2012, 97 (1), pp.9-14. 〈10.3324/haematol.2011.044644〉
Haematologica, Ferrata Storti Foundation, 2012, 97 (1), pp.9-14. ⟨10.3324/haematol.2011.044644⟩
International audience; BACKGROUND: Congenital secondary erythrocytoses are due to deregulation of hypoxia inducible factor resulting in overproduction of erythropoietin. The most common germline mutation identified in the hypoxia signaling pathway i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afb7d409443e86cc302a66b339904464
https://doi.org/10.3324/haematol.2011.044644
https://doi.org/10.3324/haematol.2011.044644
Autor:
Bertil Kågedal, Felipe Trajtenberg, Etienne Blanc, Sabrina Cantais, Gilda Raguénez, Eduardo Osinaga, Xénia Mergui, Hugues Ripoche, Philippe Dessen, Nora Berois, Jean Bénard, Michel Barrois
Publikováno v:
Clinical Chemistry. 52:1701-1712
Background: To identify new molecular markers of bone marrow dissemination in human neuroblastoma (NB), we studied the transcriptome profiles of malignant neuroblasts established from the human MYCN-amplified IGR-N-91 model. Methods: This experimenta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4247eeb682649fd2ebaa936da61e8e2
https://doi.org/10.1373/clinchem.2006.067975
https://doi.org/10.1373/clinchem.2006.067975
Autor:
Alain Spatz, Michel Barrois, Michael W Smith, Karine Laud, Gordon Peters, Margaret A. Tucker, Gilbert M. Lenoir, Brigitte Bressac-de Paillerets, Paula A. Clark, Valérie Chaudru, Catalin Marian, Florence Demenais, Alisa M. Goldstein, Agnès Chompret, Marie-Françoise Avril
Publikováno v:
Journal of Medical Genetics. 43:39-47
Objective: Comprehensive analysis of the 9p21 locus including the CDKN2A , ARF , and CDKN2B genes in 53 individuals from melanoma index cases considered to be at heightened risk of melanoma. Methods and Results: Using a combination of DNA sequencing,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7dda21902d4cfaf16bdf1c13a58ea037
https://doi.org/10.1136/jmg.2005.033498
https://doi.org/10.1136/jmg.2005.033498
Autor:
Ivan Bièche, Marie-Hélène Champème, Rosette Lidereau, Michel Barrois, Brigitte Bressac-de Paillerets, Sylvie Mazoyer
Publikováno v:
Clinical Genetics. 65:131-136
BRCA1 and BRCA2 germline mutations, mainly point mutations and other small alterations, are responsible for most hereditary cases of breast-ovarian cancer. However, the observed frequency of BRCA1 alterations is lower than that predicted by linkage a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::904a0547c7e415c86938f261efa85043
https://doi.org/10.1111/j.0009-9163.2004.00200.x
https://doi.org/10.1111/j.0009-9163.2004.00200.x
Autor:
Hedi Haddada, Etienne Blanc, Gilda Raguénez, Agnès Legrand, Sétha Douc-Rasy, Jean Bénard, Gwenaëlle Le Roux, David Goldschneider, Michel Barrois
Publikováno v:
Journal of Cell Science. 117:293-301
p73, the first p53 gene homologue, encodes an array of p73 proteins including p73 alpha full-length (TAp73 alpha) and amino-truncated isoforms (Delta Np73 alpha), two proteins with opposite biological functions. TAp73 alpha can induce tumor suppressi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f725eeb68264d7110e614586140fea0d
https://doi.org/10.1242/jcs.00834
https://doi.org/10.1242/jcs.00834
Autor:
Bernadette Léon, Marie-José Terrier-Lacombe, Gilbert M. Lenoir, Alexander Valent, Alain Bernheim, Dominique Valteau-Couanet, Jean Bénard, Michel Barrois, Barbara A. Spengler, Gwenaëlle Le Roux
Publikováno v:
The Journal of Pathology. 198:495-501
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=doi_________::4d031b8b7535c445866f42539bbe0f3e
https://doi.org/10.1002/path.1244
https://doi.org/10.1002/path.1244
Autor:
Olivier Hartmann, Daniel Caput, Jean Bénard, Ute M. Moll, David Goldschneider, Sétha Douc-Rasy, Etienne Blanc, Mourad Kaghad, Michel Barrois, Maria Echeynne, Gilda Raguénez, Marie-José Terrier-Lacombe
Publikováno v:
The American Journal of Pathology. 160:631-639
Neuroblastic tumors (NTs), occurring in early childhood, display a wide spectrum of differentiation. Recurrent deletions involving the p73 locus are frequently observed in undifferentiated NTs. To address the question of the possible implication of p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5140fd25c1c2f620fb4a30d03ba970cb
https://doi.org/10.1016/s0002-9440(10)64883-3
https://doi.org/10.1016/s0002-9440(10)64883-3
Autor:
Dominique Bellet, Sylvie Chauvin, Frank Griscelli, Stephane Lastere, Jean-Henri Bourhis, Michel Barrois
Publikováno v:
Journal of Clinical Microbiology. 39:4362-4369
A real-time PCR assay was developed to quantify human cytomegalovirus (CMV) DNA in peripheral blood leukocytes (PBLs) of bone marrow transplantation patients. Unlike other teams, we quantified CMV and the glyceraldehyde-3-phosphate dehydrogenase (GAP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::caa381596a54287c7dba880e6f415d6d
https://doi.org/10.1128/jcm.39.12.4362-4369.2001
https://doi.org/10.1128/jcm.39.12.4362-4369.2001
Autor:
Jean Bénard, Marie-Christine Mathieu, Monique G. Lê, Guy Riou, Michel Barrois, Marie‐Luce Le Bihan, Jean-Charles Ahomadegbe
Publikováno v:
International Journal of Cancer. 95:266-270
Our aim was to compare the prognostic value of c-erbB-2 gene amplification analyzed by Southern blot with that of protein (p185) over-expression measured by immunohistochemistry in 172 patients with operable breast cancer (BC). Amplification and p185
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eedc37658ccca3727bbbd8d9c66e8537
https://doi.org/10.1002/1097-0215(20010720)95:4<266::aid-ijc1045>3.0.co
https://doi.org/10.1002/1097-0215(20010720)95:4<266::aid-ijc1045>3.0.co