Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Bedel Ngimbous"'
Autor:
Aude-Marie Lepagnol-Bestel, Agnes Zvara, Gilles Maussion, Frédérique Quignon, Bedel Ngimbous, Nicolas Ramoz, Sandrine Imbeaud, Yann Loe-Mie, Karim Benihoud, Nicolas Agier, Paul A Salin, Ana Cardona, Suonavy Khung-Savatovsky, Pekka Kallunki, Jean-Maurice Delabar, Laszlo G Puskas, Hervé Delacroix, Lawrence Aggerbeck, Anne-Lise Delezoide, Olivier Delattre, Philip Gorwood, Jean-Marie Moalic, Michel Simonneau
Publikováno v:
Human Molecular Genetics. 31:2106-2107
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90993248733f8dd7cd43ef63a830b23e
https://doi.org/10.1093/hmg/ddab346
https://doi.org/10.1093/hmg/ddab346
Autor:
Suonavy Khung-Savatovsky, Sandrine Imbeaud, Karim Benihoud, Jean Marie Moalic, Anne Lise Delezoide, László G. Puskás, Bedel Ngimbous, Pekka Kallunki, Nicolas Ramoz, Gilles Maussion, Ana Cardona, Paul A. Salin, Hervé Delacroix, Philip Gorwood, Michel Simonneau, Yann Loe-Mie, Lawrence Aggerbeck, Aude-Marie Lepagnol-Bestel, Nicolas Agier, Jean-Maurice Delabar, Olivier Delattre, Ágnes Zvara, Frédérique Quignon
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, 2009, 18 (8), pp.1405-1414. ⟨10.1093/hmg/ddp047⟩
Human Molecular Genetics, Oxford University Press (OUP), 2009, 18 (8), pp.1405-1414. ⟨10.1093/hmg/ddp047⟩
Human Molecular Genetics, 2009, 18 (8), pp.1405-1414. ⟨10.1093/hmg/ddp047⟩
Human Molecular Genetics, Oxford University Press (OUP), 2009, 18 (8), pp.1405-1414. ⟨10.1093/hmg/ddp047⟩
International audience; The molecular mechanisms that lead to the cognitive defects characteristic of Down syndrome (DS), the most frequent cause of mental retardation, have remained elusive. Here we use a transgenic DS mouse model (152F7 line) to sh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc71ddaafd63dd0e594e2480efdf6df3
https://doi.org/10.1093/hmg/ddp047
https://doi.org/10.1093/hmg/ddp047