Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Pierre-Yves Cousin"'
Autor:
Yann Marcy, Pierre-Yves Cousin, Maxime Rattier, Gordana Cerovic, Guilhem Escalier, Gilles Béna, Maurice Guéron, Lorcan McDonagh, Françoise le Boulaire, Henri Bénisty, Claude Weisbuch, Jean-Christophe Avarre
Publikováno v:
BioTechniques, Vol 44, Iss 7, Pp 913-920 (2008)
Despite the great popularity and potential of microarrays, their use for research and clinical applications is still hampered by lengthy and costly design and optimization processes, mainly because the technology relies on the end point measurement o
Externí odkaz:
https://doaj.org/article/0178b33828624e3c80a1f1fe19946ecd
Autor:
Magdalena Benetkiewicz, Ahmed Idbaih, Pierre-Yves Cousin, Blandine Boisselier, Yannick Marie, Emmanuelle Crinière, Khê Hoang-Xuan, Jean-Yves Delattre, Marc Sanson, Olivier Delattre
Publikováno v:
PLoS ONE, Vol 4, Iss 1, p e4107 (2009)
The combined deletion of 1p and 19q chromosomal arms is frequent in oligodendrogliomas (OD) and has recently been shown to be mediated by an unbalanced t(1;19) translocation. Recent studies of 1p/19q co-deleted OD suggest that the NOTCH2 gene is impl
Externí odkaz:
https://doaj.org/article/f0820822b9044387977b233babf296fc
Autor:
Ahmed Idbaih, Magdalena Benetkiewicz, Pierre-Yves Cousin, Marc Sanson, Khê Hoang-Xuan, Jean-Yves Delattre, Olivier Delattre, Blandine Boisselier, Yannick Marie, Emmanuelle Crinière
Publikováno v:
PLoS ONE
PLoS ONE, Vol 4, Iss 1, p e4107 (2009)
PLoS ONE, Vol 4, Iss 1, p e4107 (2009)
The combined deletion of 1p and 19q chromosomal arms is frequent in oligodendrogliomas (OD) and has recently been shown to be mediated by an unbalanced t(1;19) translocation. Recent studies of 1p/19q co-deleted OD suggest that the NOTCH2 gene is impl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76c2f69311682dfb86d75cf3fb8fbb53
https://pubmed.ncbi.nlm.nih.gov/19119320
https://pubmed.ncbi.nlm.nih.gov/19119320
Autor:
Jean-Christophe Avarre, Claude Weisbuch, Henri Benisty, Yann Marcy, Françoise Le Boulaire, M. Rattier, Guilhem Escalier, Gilles Béna, Lorcan Mcdonagh, Maurice Guéron, Gordana Cerovic, Pierre-Yves Cousin
Publikováno v:
Biotechniques
Biotechniques, 2008, 44, pp.913-920. ⟨10.2144/000112758⟩
Biotechniques, Eaton Publishing, 2008, 44, pp.913-920. ⟨10.2144/000112758⟩
Biotechniques, 2008, 44, pp.913-920. ⟨10.2144/000112758⟩
Biotechniques, Eaton Publishing, 2008, 44, pp.913-920. ⟨10.2144/000112758⟩
International audience; Despite the great popularity and potential of microarrays, their use for research and clinical applications is still hampered by lengthy and costly design and optimization processes, mainly because the technology relies on the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d347e1bf4a2b510e7003eaf95c550cd6
https://hal-iogs.archives-ouvertes.fr/hal-00814717/document
https://hal-iogs.archives-ouvertes.fr/hal-00814717/document
Autor:
Alexis Brice, Lucette Lacomblez, Periquet Magali, Ebba Lohmann, Pierre-Yves Cousin, Hélio A.G. Teive, Sabine Janin, Alexandra Durr, Suzanne Lesage
Publikováno v:
Human mutation. 28(1)
Autosomal recessive mutations in the parkin gene (PARK2) have been identified as a common cause of familial and also sporadic, early-onset parkinsonism (EOPD): point mutations, exonic deletions, and duplications or triplications have been described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4957e7ff5c88e39e708ce5a747df7cae
https://pubmed.ncbi.nlm.nih.gov/17068781
https://pubmed.ncbi.nlm.nih.gov/17068781
Autor:
David J. Hughes, Dominique Stoppa-Lyonnet, Pierre-Yves Cousin, Patricia Legoix-Né, Olga M. Sinilnikova, Alexandra Trehin, Isabelle Coupier
Publikováno v:
Familial cancer. 4(4)
BAP1 whose protein interacts with BRCA1 was analysed in a series of 47 French familial breast cancer cases negatively tested for BRCA1/2 mutations. The lack of detection of deleterious mutations suggests that BAP1 is not a high risk breast cancer pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c7f6cf522c16deaa31bb18fb2c0c063
https://pubmed.ncbi.nlm.nih.gov/16341802
https://pubmed.ncbi.nlm.nih.gov/16341802
Autor:
Isabelle Coupier, Pierre-Yves Cousin, David Hughes, Patricia Legoix-Né, Alexandra Trehin, Olga Sinilnikova, Dominique Stoppa-Lyonnet
Publikováno v:
Familial Cancer; Nov2005, Vol. 4 Issue 4, p273-277, 5p