Torthaí cuardaigh - Saeko Ishida
- 1 - 7 toradh as 7 á dtaispeáint
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1
Depdc5 knockdown causes <scp>mTOR</scp>‐dependent motor hyperactivity in zebrafish de réir Hortense de Calbiac, Adriana Dabacan, Elise Marsan, Hervé Tostivint, Gabrielle Devienne, Saeko Ishida, Eric LeGuern, Stéphanie Baulac, Raul C. Mureșan, Edor Kabashi, Sorana Ciura
Foilsithe / Cruthaithe 2018Artigo -
2
Mutations of DEPDC5 cause autosomal dominant focal epilepsies de réir Saeko Ishida, Fabienne Picard, Gabrielle Rudolf, Eric Noé, Guillaume Achaz, Pierre Thomas, Pierre Genton, Emeline Mundwiller, Markus Wolff, Christian Marescaux, Richard Miles, Michel Baulac, Édouard Hirsch, Eric LeGuern, Stéphanie Baulac
Foilsithe / Cruthaithe 2013Artigo -
3
Glutamatergic neuron-targeted loss of LGI1 epilepsy gene results in seizures de réir Morgane Boillot, Clément Huneau, Elise Marsan, Katia Lehongre, Vincent Navarro, Saeko Ishida, Béatrice Dufresnois, Ekim Özkaynak, J.L. Garrigue, Richard Miles, Benoı̂t Martin, Eric LeGuern, Matthew P. Anderson, Stéphanie Baulac
Foilsithe / Cruthaithe 2014Artigo -
4
Familial focal epilepsy with focal cortical dysplasia due to <scp><i>DEPDC</i></scp><i>5</i> mutations de réir Stéphanie Baulac, Saeko Ishida, Elise Marsan, Catherine Miquel, Arnaud Biraben, Dang Khoa Nguyen, Doug Nordli, Patrick Cossette, Sylvie Nguyen, Virginie Lambrecq, Mihaela Bustuchina ̆ Vlaicu, Maïlys Daniau, Franck Bielle, Eva Andermann, Frédérick Andermann, Eric Leguern, Francine Chassoux, Fabienne Picard
Foilsithe / Cruthaithe 2015Artigo -
5
Generation and Characterization of Severe Combined Immunodeficiency Rats de réir Tomoji Mashimo, Akiko Takizawa, Junya Kobayashi, Yayoi Kunihiro, Kazuto Yoshimi, Saeko Ishida, Koji Tanabe, Ami Yanagi, Asato Tachibana, Jun Hirose, Jun‐ichiro Yomoda, Shiho Morimoto, Takashi Kuramoto, Birger Voigt, Takeshi Watanabe, Hiroshi Hiai, Chise Tateno, Kenshi Komatsu, Tadao Serikawa
Foilsithe / Cruthaithe 2012Artigo -
6
Depdc5 knockout rat: A novel model of mTORopathy de réir Elise Marsan, Saeko Ishida, Adrien E. Schramm, Sarah Weckhuysen, Giuseppe Muraca, Sarah Lecas, Ning Liang, Caroline Treins, Mario Pende, Delphine Roussel, Michel Le Van Quyen, Tomoji Mashimo, Takehito Kaneko, Takashi Yamamoto, Tetsushi Sakuma, Séverine Mahon, Richard Miles, Eric LeGuern, Stéphane Charpier, Stéphanie Baulac
Foilsithe / Cruthaithe 2016Artigo -
7
<i>DEPDC5</i> mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsy de réir Fabienne Picard, Periklis Makrythanasis, Vincent Navarro, Saeko Ishida, Julitta de Bellescize, Dorothée Ville, Sarah Weckhuysen, Erwin Fosselle, Arvid Suls, Peter De Jonghe, Maryline Vasselon Raina, Gaëtan Lesca, Christel Depienne, Isabelle An-Gourfinkel, Mihaela Bustuchina ̆ Vlaicu, Michel Baulac, Emeline Mundwiller, Philippe Couarch, Romina Combi, Luigi Ferini‐Strambi, Antonio Gambardella, Stylianos E. Antonarakis, Eric LeGuern, Ortrud K. Steinlein, Stéphanie Baulac
Foilsithe / Cruthaithe 2014Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Biology
Genetics
Neuroscience
Epilepsy
Gene
Medicine
Mutation
Cancer research
Cell biology
Frameshift mutation
Gene knockdown
Internal medicine
Phenotype
Signal transduction
Cortical dysplasia
Dishevelled
Downregulation and upregulation
Embryonic stem cell
Epilepsy syndromes
Exome
Exome sequencing
Frizzled
Frontal lobe
GABAergic
Genetic enhancement
Genetic model
Glutamate receptor
Glutamatergic
Haematopoiesis
Haploinsufficiency