Хайлтын үр дүнгүүд - Huashan Peng
- 7-н 1 - 7 үр дүнгүүдийг харуулж байна
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Human iPSC-derived Down syndrome astrocytes display genome-wide perturbations in gene expression, an altered adhesion profile, and increased cellular dynamics -н Blandine Ponroy Bally, W. Todd Farmer, Emma V. Jones, Selin Jessa, J. Benjamin Kacerovsky, Alexandre Mayran, Huashan Peng, Julie L. Lefebvre, Jacques Drouin, Arnold Hayer, Carl Ernst, Keith K. Murai
Хэвлэсэн 2020Artigo -
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Disruption of GRIN2B Impairs Differentiation in Human Neurons -н Scott C. Bell, Gilles Maussion, Malvin Jefri, Huashan Peng, Jean-Francois Theroux, Heika Silveira, Vincent Soubannier, Hanrong Wu, Peng Hu, Yekaterina Galat, Susana G. Torres‐Platas, Camille Boudreau‐Pinsonneault, Liam Anuj O’Leary, Vasiliy Galat, Gustavo Turecki, Thomas M. Durcan, Edward A. Fon, Naguib Mechawar, Carl Ernst
Хэвлэсэн 2018Artigo -
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Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia -н Julie Gauthier, Tabrez J. Siddiqui, Huashan Peng, Daisaku Yokomaku, Fadi F. Hamdan, Nathalie Champagne, Mathieu Lapointe, Dan Spiegelman, Anne Noreau, Ronald G. Lafrenière, Ferid Fathalli, Ridha Joober, Marie‐Odile Krebs, Lynn E. DeLisi, Laurent Mottron, Éric Fombonne, Jacques L. Michaud, Pierre Drapeau, Salvatore Carbonetto, Ann Marie Craig, Guy A. Rouleau
Хэвлэсэн 2011Artigo -
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Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia -н Gauthier, Julie, Siddiqui, Tabrez J., Huashan, Peng, Yokomaku, Daisaku, Hamdan, Fadi F., Champagne, Nathalie, Lapointe, Mathieu, Spiegelman, Dan, Noreau, Anne, Lafrenière, Ronald G., Fathalli, Ferid, Joober, Ridha, Krebs, Marie-Odile, DeLisi, Lynn E., Mottron, Laurent, Fombonne, Éric, Michaud, Jacques L., Drapeau, Pierre, Carbonetto, Salvatore, Craig, Ann Marie, Rouleau, Guy A.
Хэвлэсэн 2011текст -
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De novo mutations in the gene encoding the synaptic scaffolding protein<i>SHANK3</i>in patients ascertained for schizophrenia -н Julie Gauthier, Nathalie Champagne, Ronald G. Lafrenière, Lan Xiong, Dan Spiegelman, Edna Brustein, Mathieu Lapointe, Huashan Peng, Mélanie Côté, Anne Noreau, Fadi F. Hamdan, Anjené Addington, Judith L. Rapoport, Lynn E. DeLisi, Marie‐Odile Krebs, Ridha Joober, Ferid Fathalli, Fayçal Mouaffak, A. Pejmun Haghighi, Christian Néri, Marie‐Pierre Dubé, Mark Samuels, Claude Marineau, Eric A. Stone, Philip Awadalla, Philip Barker, Salvatore Carbonetto, Pierre Drapeau, Guy A. Rouleau, Kathleen Daignault, Ousmane Diallo, Joannie Duguay, Marina Drits, Édouard Henrion, Philippe Jolivet, Frédéric Kuku, Karine Lachapelle, Guy Laliberté, Sandra B. Laurent, Meijiang Liao, Carlos Marino, Amélie Piton, A Raymond, Annie Reynolds, Daniel Rochefort, Judith St‐Onge, Pascale Thibodeau, Kazuya Tsurudome, Yanlian Yang, Sophie Leroy, Katia Ossian, Mélanie Chayet, David Gourion
Хэвлэсэн 2010Artigo -
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Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons -н Scott C. Bell, Justine Rousseau, Huashan Peng, Zahia Aouabed, Pierre Priam, Jean-Francois Theroux, Malvin Jefri, Arnaud Tanti, Hanrong Wu, Ilaria Kolobova, Heika Silviera, Karla Manzano-Vargas, Sophie Ehresmann, Fadi F. Hamdan, Nuwan C. Hettige, Xin Zhang, Lilit Antonyan, Christina Nassif, Lina Ghaloul‐Gonzalez, Jessica Sebastian, Jerry Vockley, Amber G. Begtrup, Ingrid M. Wentzensen, Amy Crunk, Robert D. Nicholls, Kristin Herman, Joshua L. Deignan, Walla Al‐Hertani, Stéphanie Efthymiou, Vincenzo Salpietro, Noriko Miyake, Yoshio Makita, Naomichi Matsumoto, Rune Østern, Gunnar Houge, Maria Hafström, Emily Fassi, Henry Houlden, Jolien S. Klein Wassink‐Ruiter, Dominic Nelson, Amy Goldstein, Tabib Dabir, Julien Van‐Gils, Thomas Bourgeron, Richard Delorme, Gregory M. Cooper, José E. Martínez, Candice R. Finnila, Lionel Carmant, Anne Lortie, Renske Oegema, Koen L.I. van Gassen, Sarju Mehta, Dagmar Huhle, Rami Abou Jamra, Sonja Martin, Han G. Brunner, Dick Lindhout, Margaret Au, John M. Graham, Christine Coubes, Gustavo Turecki, Simon Gravel, Naguib Mechawar, Elsa Rossignol, Jacques L. Michaud, Julie Lessard, Carl Ernst, Philippe M. Campeau
Хэвлэсэн 2019Artigo
Хайх хэрэгслүүд:
Холбогдох сэдвүүд
Biology
Gene
Genetics
Neuroscience
Mutation
Cell biology
Receptor
Autism
Gene expression
Medicine
Psychiatry
Schizophrenia (object-oriented programming)
Transcriptome
Amino acid
Autism spectrum disorder
Biochemistry
Cell
Cell adhesion
Cellular differentiation
Chromatin
Copy-number variation
DNA methylation
Developmental disorder
Embryonic stem cell
Epigenomics
Epilepsy
Excitatory postsynaptic potential
Extracellular matrix
GABAA receptor
GABAergic