| Year |
Citation |
Score |
| 2024 |
Wilson ER, Nunes GD, Shen S, Moore S, Gawron J, Maxwell J, Syed U, Hurley E, Lanka M, Qu J, Desaubry L, Wrabetz L, Poitelon Y, Feltri ML. Loss of prohibitin 2 in Schwann cells dysregulates key transcription factors controlling developmental myelination. Biorxiv : the Preprint Server For Biology. PMID 38562812 DOI: 10.1101/2024.03.20.585915 |
0.837 |
|
| 2024 |
Hong J, Garfolo R, Kabre S, Humml C, Velanac V, Roué C, Beck B, Jeanette H, Haslam S, Bach M, Arora S, Acheta J, Nave KA, Schwab MH, Jourd'heuil D, ... Poitelon Y, et al. PMP2 regulates myelin thickening and ATP production during remyelination. Glia. PMID 38311982 DOI: 10.1002/glia.24508 |
0.731 |
|
| 2023 |
Hong J, Kirkland JM, Acheta J, Marziali LN, Beck B, Jeanette H, Bhatia U, Davis G, Herron J, Roué C, Abi-Ghanem C, Feltri ML, Zuloaga KL, Bechler ME, Poitelon Y, et al. YAP and TAZ regulate remyelination in the central nervous system. Glia. PMID 37724047 DOI: 10.1002/glia.24467 |
0.784 |
|
| 2023 |
Abi-Ghanem C, Salinero AE, Kordit D, Mansour FM, Kelly RD, Venkataganesh H, Kyaw NR, Gannon OJ, Riccio D, Fredman G, Poitelon Y, Belin S, Kopec AM, Robison LS, Zuloaga KL. Sex differences in the effects of high fat diet on underlying neuropathology in a mouse model of VCID. Biology of Sex Differences. 14: 31. PMID 37208759 DOI: 10.1186/s13293-023-00513-y |
0.68 |
|
| 2022 |
El-Bazzal L, Ghata A, Estève C, Gadacha J, Quintana P, Castro C, Roeckel-Trévisiol N, Lembo F, Lenfant N, Mégarbané A, Borg JP, Lévy N, Bartoli M, Poitelon Y, Roubertoux PL, et al. Imbalance of NRG1-ERBB2/3 signalling underlies altered myelination in Charcot-Marie-Tooth disease 4H. Brain : a Journal of Neurology. PMID 36314052 DOI: 10.1093/brain/awac402 |
0.804 |
|
| 2022 |
Acheta J, Bhatia U, Haley J, Hong J, Rich K, Close R, Bechler ME, Belin S, Poitelon Y. Piezo channels contribute to the regulation of myelination in Schwann cells. Glia. PMID 35903933 DOI: 10.1002/glia.24251 |
0.821 |
|
| 2022 |
Acheta J, Hong J, Jeanette H, Brar S, Yalamanchili A, Feltri ML, Manzini MC, Belin S, Poitelon Y. Contributes to the Regulation of Developmental Myelination in the Central Nervous System. Frontiers in Molecular Neuroscience. 15: 881571. PMID 35592111 DOI: 10.3389/fnmol.2022.881571 |
0.834 |
|
| 2022 |
Acheta J, Stephens SBZ, Belin S, Poitelon Y. Therapeutic Low-Intensity Ultrasound for Peripheral Nerve Regeneration - A Schwann Cell Perspective. Frontiers in Cellular Neuroscience. 15: 812588. PMID 35069118 DOI: 10.3389/fncel.2021.812588 |
0.777 |
|
| 2021 |
Della Flora Nunes G, Wilson ER, Hurley E, He B, O'Malley BW, Poitelon Y, Wrabetz L, Feltri ML. Activation of mTORC1 and c-Jun by Prohibitin1 loss in Schwann cells may link mitochondrial dysfunction to demyelination. Elife. 10. PMID 34519641 DOI: 10.7554/eLife.66278 |
0.771 |
|
| 2021 |
Della-Flora Nunes G, Wilson ER, Marziali LN, Hurley E, Silvestri N, He B, O'Malley BW, Beirowski B, Poitelon Y, Wrabetz L, Feltri ML. Prohibitin 1 is essential to preserve mitochondria and myelin integrity in Schwann cells. Nature Communications. 12: 3285. PMID 34078899 DOI: 10.1038/s41467-021-23552-8 |
0.85 |
|
| 2021 |
Hellman A, Maietta T, Clum A, Byraju K, Raviv N, Staudt MD, Jeannotte E, Nalwalk J, Belin S, Poitelon Y, Pilitsis JG. Development of a common peroneal nerve injury model in domestic swine for the study of translational neuropathic pain treatments. Journal of Neurosurgery. 1-8. PMID 33862596 DOI: 10.3171/2020.9.JNS202961 |
0.691 |
|
| 2021 |
Alam MM, Zhao XF, Liao Y, Mathur R, McCallum SE, Mazurkiewicz JE, Adamo MA, Feustel P, Belin S, Poitelon Y, Zhu XC, Huang Y. Deficiency of microglial autophagy increases the density of oligodendrocytes and susceptibility to severe forms of seizures. Eneuro. PMID 33472865 DOI: 10.1523/ENEURO.0183-20.2021 |
0.71 |
|
| 2021 |
Feltri ML, Weaver MR, Belin S, Poitelon Y. The Hippo pathway: horizons for innovative treatments of peripheral nerve diseases. Journal of the Peripheral Nervous System : Jpns. PMID 33449435 DOI: 10.1111/jns.12431 |
0.802 |
|
| 2020 |
Jeanette H, Marziali LN, Bhatia U, Hellman A, Herron J, Kopec AM, Feltri ML, Poitelon Y, Belin S. YAP and TAZ regulate Schwann cell proliferation and differentiation during peripheral nerve regeneration. Glia. PMID 33336855 DOI: 10.1002/glia.23949 |
0.796 |
|
| 2020 |
Robison LS, Gannon OJ, Thomas MA, Salinero AE, Abi-Ghanem C, Poitelon Y, Belin S, Zuloaga KL. Role of sex and high-fat diet in metabolic and hypothalamic disturbances in the 3xTg-AD mouse model of Alzheimer's disease. Journal of Neuroinflammation. 17: 285. PMID 32993686 DOI: 10.1186/s12974-020-01956-5 |
0.662 |
|
| 2020 |
Catignas KK, Frick LR, Pellegatta M, Hurley E, Kolb Z, Addabbo K, McCarty JH, Hynes RO, van der Flier A, Poitelon Y, Wrabetz L, Laura Feltri M. α integrins in Schwann cells promote attachment to axons, but are dispensable in vivo. Glia. PMID 32744761 DOI: 10.1002/Glia.23886 |
0.718 |
|
| 2020 |
Poitelon Y, Kopec AM, Belin S. Myelin Fat Facts: An Overview of Lipids and Fatty Acid Metabolism. Cells. 9. PMID 32230947 DOI: 10.3390/Cells9040812 |
0.805 |
|
| 2019 |
Belin S, Herron J, VerPlank JJS, Park Y, Feltri LM, Poitelon Y. Corrigendum: YAP and TAZ Regulate and β in Schwann Cells. Frontiers in Molecular Neuroscience. 12: 256. PMID 31680860 DOI: 10.3389/Fnmol.2019.00256 |
0.724 |
|
| 2019 |
Belin S, Ornaghi F, Shackleford G, Wang J, Scapin C, Lopez-Anido C, Silvestri N, Robertson N, Williamson C, Ishii A, Taveggia C, Svaren J, Bansal R, Schwab MH, Nave K, ... ... Poitelon Y, et al. Corrigendum: Neuregulin 1 type III improves peripheral nerve myelination in a mouse model of congenital hypomyelinating neuropathy. Human Molecular Genetics. 28: 2282. PMID 31220267 DOI: 10.1093/hmg/ddz037 |
0.843 |
|
| 2019 |
Belin S, Ornaghi F, Shackleford G, Wang J, Scapin C, Lopez-Anido C, Silvestri N, Robertson N, Williamson C, Ishii A, Taveggia C, Svaren J, Bansal R, Schwab MH, Nave K, ... ... Poitelon Y, et al. Neuregulin 1 type III improves peripheral nerve myelination in a mouse model of congenital hypomyelinating neuropathy. Human Molecular Genetics. PMID 30668730 DOI: 10.1093/hmg/ddz021 |
0.843 |
|
| 2018 |
Belin S, Ornaghi F, Shackleford G, Wang J, Scapin C, Lopez-Anido C, Silvestri N, Robertson N, Williamson C, Ishii A, Taveggia C, Svaren J, Bansal R, Markus Schwab H, Nave K, ... ... Poitelon Y, et al. Neuregulin 1 type III improves peripheral nerve myelination in a mouse model of congenital hypomyelinating neuropathy. Human Molecular Genetics. PMID 30535360 DOI: 10.1093/Hmg/Ddy420 |
0.882 |
|
| 2018 |
Poitelon Y, Feltri ML. The Pseudopod System for Axon-Glia Interactions: Stimulation and Isolation of Schwann Cell Protrusions that Form in Response to Axonal Membranes. Methods in Molecular Biology (Clifton, N.J.). 1739: 233-253. PMID 29546711 DOI: 10.1007/978-1-4939-7649-2_15 |
0.725 |
|
| 2018 |
Feltri ML, Poitelon Y. HIPPO Stampede in Nerve Sheath Tumors. Cancer Cell. 33: 160-161. PMID 29438691 DOI: 10.1016/J.Ccell.2018.01.016 |
0.644 |
|
| 2018 |
Ackerman SD, Luo R, Poitelon Y, Mogha A, Harty BL, D'Rozario M, Sanchez NE, Lakkaraju AKK, Gamble P, Li J, Qu J, MacEwan MR, Ray WZ, Aguzzi A, Feltri ML, et al. GPR56/ADGRG1 regulates development and maintenance of peripheral myelin. The Journal of Experimental Medicine. PMID 29367382 DOI: 10.1084/Jem.20161714 |
0.786 |
|
| 2018 |
Poitelon Y, Matafora V, Silvestri N, Zambroni D, McGarry C, Serghany N, Rush T, Vizzuso D, Court FA, Bachi A, Wrabetz L, Feltri ML. A dual role for Integrin α6β4 in modulating Hereditary Neuropathy with liability to Pressure Palsies. Journal of Neurochemistry. PMID 29315582 DOI: 10.1111/Jnc.14295 |
0.852 |
|
| 2017 |
Belin S, Zuloaga KL, Poitelon Y. Influence of Mechanical Stimuli on Schwann Cell Biology. Frontiers in Cellular Neuroscience. 11: 347. PMID 29209171 DOI: 10.3389/Fncel.2017.00347 |
0.856 |
|
| 2017 |
Della-Flora Nunes G, Mueller L, Silvestri N, Patel MS, Wrabetz L, Feltri ML, Poitelon Y. Acetyl-CoA production from pyruvate is not necessary for preservation of myelin. Glia. PMID 28657129 DOI: 10.1002/Glia.23184 |
0.84 |
|
| 2017 |
Ghidinelli M, Poitelon Y, Shin YK, Ameroso D, Williamson C, Ferri C, Pellegatta M, Espino K, Mogha A, Monk K, Podini P, Taveggia C, Nave KA, Wrabetz L, Park HT, et al. Laminin 211 inhibits protein kinase A in Schwann cells to modulate neuregulin 1 type III-driven myelination. Plos Biology. 15: e2001408. PMID 28636612 DOI: 10.1371/Journal.Pbio.2001408 |
0.839 |
|
| 2016 |
Poitelon Y, Nunes GD, Feltri ML. Myelinating cells can feel disturbances in the force. Oncotarget. PMID 28031544 DOI: 10.18632/Oncotarget.14240 |
0.688 |
|
| 2016 |
Lopez-Anido C, Poitelon Y, Gopinath C, Moran JJ, Ma KH, Law WD, Antonellis A, Feltri ML, Svaren J. Tead1 regulates the expression of Peripheral Myelin Protein 22 during Schwann cell development. Human Molecular Genetics. PMID 27288457 DOI: 10.1093/Hmg/Ddw158 |
0.771 |
|
| 2016 |
Poitelon Y, Lopez-Anido C, Catignas K, Berti C, Palmisano M, Williamson C, Ameroso D, Abiko K, Hwang Y, Gregorieff A, Wrana JL, Asmani M, Zhao R, Sim FJ, Wrabetz L, et al. YAP and TAZ control peripheral myelination and the expression of laminin receptors in Schwann cells. Nature Neuroscience. PMID 27273766 DOI: 10.1038/Nn.4316 |
0.851 |
|
| 2016 |
Feltri ML, Poitelon Y, Previtali SC. How Schwann Cells Sort Axons: New Concepts. The Neuroscientist : a Review Journal Bringing Neurobiology, Neurology and Psychiatry. 22: 252-65. PMID 25686621 DOI: 10.1177/1073858415572361 |
0.845 |
|
| 2015 |
Poitelon Y, Bogni S, Matafora V, Della-Flora Nunes G, Hurley E, Ghidinelli M, Katzenellenbogen BS, Taveggia C, Silvestri N, Bachi A, Sannino A, Wrabetz L, Feltri ML. Spatial mapping of juxtacrine axo-glial interactions identifies novel molecules in peripheral myelination. Nature Communications. 6: 8303. PMID 26383514 DOI: 10.1038/Ncomms9303 |
0.806 |
|
| 2012 |
Baudot C, Esteve C, Castro C, Poitelon Y, Mas C, Hamadouche T, El-Rajab M, Lévy N, Megarbané A, Delague V. Two novel missense mutations in FGD4/FRABIN cause Charcot-Marie-Tooth type 4H (CMT4H). Journal of the Peripheral Nervous System : Jpns. 17: 141-6. PMID 22734899 DOI: 10.1111/J.1529-8027.2012.00405.X |
0.601 |
|
| 2012 |
Poitelon Y, Kozlov S, Devaux J, Vallat JM, Jamon M, Roubertoux P, Rabarimeriarijaona S, Baudot C, Hamadouche T, Stewart CL, Levy N, Delague V. Behavioral and molecular exploration of the AR-CMT2A mouse model Lmna (R298C/R298C). Neuromolecular Medicine. 14: 40-52. PMID 22331516 DOI: 10.1007/S12017-012-8168-Z |
0.69 |
|
| 2012 |
Colom B, Poitelon Y, Huang W, Woodfin A, Averill S, Del Carro U, Zambroni D, Brain SD, Perretti M, Ahluwalia A, Priestley JV, Chavakis T, Imhof BA, Feltri ML, Nourshargh S. Schwann cell-specific JAM-C-deficient mice reveal novel expression and functions for JAM-C in peripheral nerves. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 26: 1064-76. PMID 22090315 DOI: 10.1096/Fj.11-196220 |
0.641 |
|
| 2010 |
Nicolas E, Poitelon Y, Chouery E, Salem N, Levy N, Mégarbané A, Delague V. CAMOS, a nonprogressive, autosomal recessive, congenital cerebellar ataxia, is caused by a mutant zinc-finger protein, ZNF592. European Journal of Human Genetics : Ejhg. 18: 1107-13. PMID 20531441 DOI: 10.1038/Ejhg.2010.82 |
0.589 |
|
| 2008 |
Hamadouche T, Poitelon Y, Genin E, Chaouch M, Tazir M, Kassouri N, Nouioua S, Chaouch A, Boccaccio I, Benhassine T, Sandre-Giovannoli AD, Grid D, Lévy N, Delague V. Founder effect and estimation of the age of the c.892C>T (p.Arg298Cys) mutation in LMNA associated to Charcot-Marie-Tooth subtype CMT2B1 in families from North Western Africa. Annals of Human Genetics. 72: 590-597. PMID 18549403 DOI: 10.1111/J.1469-1809.2008.00456.X |
0.61 |
|
| 2007 |
Delague V, Jacquier A, Hamadouche T, Poitelon Y, Baudot C, Boccaccio I, Chouery E, Chaouch M, Kassouri N, Jabbour R, Grid D, Mégarbané A, Haase G, Lévy N. Mutations in FGD4 encoding the Rho GDP/GTP exchange factor FRABIN cause autosomal recessive Charcot-Marie-Tooth type 4H. American Journal of Human Genetics. 81: 1-16. PMID 17564959 DOI: 10.1086/518428 |
0.622 |
|
| 2007 |
Delague V, Jacquier A, Hamadouche T, Poitelon Y, Baudot C, Boccaccio I, Chouery E, Chaouch M, Kassouri N, Jabbour R, Grid D, Mégarbané A, Haase G, Levy N. G.O.3 Mutations in FGD4 encoding the Rho GDP/GTP exchange factor FRABIN cause autosomal recessive Charcot-Marie-Tooth type 4H Neuromuscular Disorders. 17: 767. DOI: 10.1016/J.Nmd.2007.06.024 |
0.557 |
|
| 2006 |
Poitelon Y, Hamadouche T, Sandre-Giovannoli AD, Kozlov S, Serradj N, Tazir M, Chaouch M, Grid D, Stewart C, Jamon M, Delague V, Lévy N. G.P.4.02 Pathophysiological mechanisms of lamin A/C associated Charcot-Marie-Tooth disease (CMT2B1/ARCMT2) Neuromuscular Disorders. 16: 675. DOI: 10.1016/J.Nmd.2006.05.110 |
0.563 |
|
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