The Pseudopod System for Axon-Glia Interactions: Stimulation and Isolation of Schwann Cell Protrusions that Form in Response to Axonal Membranes

Por Poitelon, Yannick, Feltri, M. Laura
Publicado no Methods Mol Biol (2018)

Influence of Mechanical Stimuli on Schwann Cell Biology

Por Belin, Sophie, Zuloaga, Kristen L., Poitelon, Yannick
Publicado no Front Cell Neurosci (2017)

Myelin Fat Facts: An Overview of Lipids and Fatty Acid Metabolism

Por Poitelon, Yannick, Kopec, Ashley M., Belin, Sophie
Publicado no Cells (2020)

Myelinating cells can feel disturbances in the force

Por Poitelon, Yannick, Della-Flora Nunes, Gustavo, Feltri, M. Laura
Publicado no Oncotarget (2016)

Functional mechanism and pathogenic potential of MYRF ICA domain mutations implicated in birth defects

Por An, Hongjoo, Fan, Chuandong, Sharif, Mohamed, Kim, Dongkyeong, Poitelon, Yannick, Park, Yungki
Publicado no Sci Rep (2020)

CAMOS, a nonprogressive, autosomal recessive, congenital cerebellar ataxia, is caused by a mutant zinc-finger protein, ZNF592

Por Nicolas, Elsa, Poitelon, Yannick, Chouery, Eliane, Salem, Nabiha, Levy, Nicolas, Mégarbané, André, Delague, Valérie
Publicado em 2010

YAP and TAZ Regulate Cc2d1b and Purβ in Schwann Cells

Por Belin, Sophie, Herron, Jacob, VerPlank, Jordan J. S., Park, Yungki, Feltri, Laura M., Poitelon, Yannick
Publicado no Front Mol Neurosci (2019)

Corrigendum: YAP and TAZ Regulate Cc2d1b and Purβ in Schwann Cells

Por Belin, Sophie, Herron, Jacob, VerPlank, Jordan J. S., Park, Yungki, Feltri, Laura M., Poitelon, Yannick
Publicado no Front Mol Neurosci (2019)

Acetyl-CoA production from pyruvate is not necessary for preservation of myelin

Por Della-Flora Nunes, Gustavo, Mueller, Lauren, Silvestri, Nicholas, Patel, Mulchand S, Wrabetz, Lawrence, Feltri, M Laura, Poitelon, Yannick
Publicado no Glia (2017)

Role of sex and high-fat diet in metabolic and hypothalamic disturbances in the 3xTg-AD mouse model of Alzheimer’s disease

Por Robison, Lisa S., Gannon, Olivia J., Thomas, Melissa A., Salinero, Abigail E., Abi-Ghanem, Charly, Poitelon, Yannick, Belin, Sophie, Zuloaga, Kristen L.
Publicado no J Neuroinflammation (2020)

YAP and TAZ regulate Schwann cell proliferation and differentiation during peripheral nerve regeneration

Por Jeanette, Haley, Marziali, Leandro N., Bhatia, Urja, Hellman, Abigail, Herron, Jacob, Kopec, Ashley M., Feltri, Maria Laura, Poitelon, Yannick, Belin, Sophie
Publicado no Glia (2020)

Tead1 regulates the expression of Peripheral Myelin Protein 22 during Schwann cell development

Por Lopez-Anido, Camila, Poitelon, Yannick, Gopinath, Chetna, Moran, John J., Ma, Ki Hwan, Law, William D., Antonellis, Anthony, Feltri, M. Laura, Svaren, John
Publicado no Hum Mol Genet (2016)

A dual role for Integrin α6β4 in modulating Hereditary Neuropathy with liability to Pressure Palsies

Por Poitelon, Yannick, Matafora, Vittoria, Silvestri, Nicholas, Zambroni, Desirée, McGarry, Claire, Serghany, Nora, Rush, Thomas, Vizzuso, Domenica, Court, Felipe A., Bachi, Angela, Wrabetz, Lawrence, Feltri, Maria Laura
Publicado no J Neurochem (2018)

Mutations in FGD4 Encoding the Rho GDP/GTP Exchange Factor FRABIN Cause Autosomal Recessive Charcot-Marie-Tooth Type 4H

Por Delague, Valérie , Jacquier, Arnaud , Hamadouche, Tarik , Poitelon, Yannick , Baudot, Cécile , Boccaccio, Irène , Chouery, Eliane , Chaouch, Malika , Kassouri, Nora , Jabbour, Rosette , Grid, Djamel , Mégarbané, André , Haase, Georg , Lévy, Nicolas 
Publicado em 2007

Deficiency of Microglial Autophagy Increases the Density of Oligodendrocytes and Susceptibility to Severe Forms of Seizures

Por Alam, Mahabub Maraj, Zhao, Xiao-Feng, Liao, Yuan, Mathur, Ramkumar, McCallum, Sarah E., Mazurkiewicz, Joseph E., Adamo, Matthew A., Feustel, Paul, Belin, Sophie, Poitelon, Yannick, Zhu, Xinjun Cindy, Huang, Yunfei
Publicado no eNeuro (2021)

Schwann cell-specific JAM-C-deficient mice reveal novel expression and functions for JAM-C in peripheral nerves

Por Colom, Bartomeu, Poitelon, Yannick, Huang, Wenlong, Woodfin, Abigail, Averill, Sharon, Del Carro, Ubaldo, Zambroni, Desirée, Brain, Susan D., Perretti, Mauro, Ahluwalia, Amrita, Priestley, John V., Chavakis, Triantafyllos, Imhof, Beat A., Feltri, M. Laura, Nourshargh, Sussan
Publicado em 2012

Laminin 211 inhibits protein kinase A in Schwann cells to modulate neuregulin 1 type III-driven myelination

Por Ghidinelli, Monica, Poitelon, Yannick, Shin, Yoon Kyoung, Ameroso, Dominique, Williamson, Courtney, Ferri, Cinzia, Pellegatta, Marta, Espino, Kevin, Mogha, Amit, Monk, Kelly, Podini, Paola, Taveggia, Carla, Nave, Klaus-Armin, Wrabetz, Lawrence, Park, Hwan Tae, Feltri, Maria Laura
Publicado no PLoS Biol (2017)

GPR56/ADGRG1 regulates development and maintenance of peripheral myelin

Por Ackerman, Sarah D., Luo, Rong, Poitelon, Yannick, Mogha, Amit, Harty, Breanne L., D’Rozario, Mitchell, Sanchez, Nicholas E., Lakkaraju, Asvin K.K., Gamble, Paul, Li, Jun, Qu, Jun, MacEwan, Matthew R., Ray, Wilson Zachary, Aguzzi, Adriano, Feltri, M. Laura, Piao, Xianhua, Monk, Kelly R.
Publicado no J Exp Med (2018)

Neuregulin 1 type III improves peripheral nerve myelination in a mouse model of congenital hypomyelinating neuropathy

Por Belin, Sophie, Ornaghi, Francesca, Shackleford, Ghjuvan’Ghjacumu, Wang, Jie, Scapin, Cristina, Lopez-Anido, Camila, Silvestri, Nicholas, Robertson, Neil, Williamson, Courtney, Ishii, Akihiro, Taveggia, Carla, Svaren, John, Bansal, Rashmi, Schwab, Markus H, Nave, Klaus, Fratta, Pietro, D’Antonio, Maurizio, Poitelon, Yannick, Feltri, M Laura, Wrabetz, Lawrence
Publicado no Hum Mol Genet (2019)

Corrigendum: Neuregulin 1 type III improves peripheral nerve myelination in a mouse model of congenital hypomyelinating neuropathy

Por Belin, Sophie, Ornaghi, Francesca, Shackleford, Ghjuvan’Ghjacumu, Wang, Jie, Scapin, Cristina, Lopez-Anido, Camila, Silvestri, Nicholas, Robertson, Neil, Williamson, Courtney, Ishii, Akihiro, Taveggia, Carla, Svaren, John, Bansal, Rashmi, Schwab, Markus H, Nave, Klaus, Fratta, Pietro, D’Antonio, Maurizio, Poitelon, Yannick, Feltri, M Laura, Wrabetz, Lawrence
Publicado no Hum Mol Genet (2019)