| Year |
Citation |
Score |
| 2022 |
Boueid MJ, Mikdache A, Lesport E, Delespierre B, Loisel-Duwattez J, Degerny C, Tawk M. Pals1a and aPKCλ are not essential for Schwann cell migration, division or myelination in zebrafish. Developmental Dynamics : An Official Publication of the American Association of Anatomists. PMID 36284447 DOI: 10.1002/dvdy.547 |
0.548 |
|
| 2022 |
Mikdache A, Boueid MJ, Lesport E, Delespierre B, Loisel-Duwattez J, Degerny C, Tawk M. Timely Schwann cell division drives peripheral myelination in vivo via Laminin/cAMP pathway. Development (Cambridge, England). PMID 35938454 DOI: 10.1242/dev.200640 |
0.619 |
|
| 2021 |
Mikdache A, Boueid MJ, van der Spek L, Lesport E, Delespierre B, Loisel-Duwattez J, Degerny C, Tawk M. Rgs4 is a regulator of mTOR activity required for motoneuron axon outgrowth and neuronal development in zebrafish. Scientific Reports. 11: 13338. PMID 34172795 DOI: 10.1038/s41598-021-92758-z |
0.524 |
|
| 2019 |
Mikdache A, Fontenas L, Albadri S, Revenu C, Loisel-Duwattez J, Lesport E, Degerny C, Del Bene F, Tawk M. Elmo1 function, linked to Rac1 activity, regulates peripheral neuronal numbers and myelination in zebrafish. Cellular and Molecular Life Sciences : Cmls. PMID 31161284 DOI: 10.1007/S00018-019-03167-5 |
0.616 |
|
| 2019 |
Vivanti A, Ozanne A, Grondin C, Saliou G, Quevarec L, Maurey H, Aubourg P, Benachi A, Gut M, Gut I, Martinovic J, Senat M, Tawk M, Melki J. Mutation ephb4 responsable de malformation anévrysmale de la veine de Galien Journal of Neuroradiology. 46: 72-73. DOI: 10.1016/J.Neurad.2019.01.069 |
0.337 |
|
| 2018 |
Vivanti A, Ozanne A, Grondin C, Saliou G, Quevarec L, Maurey H, Aubourg P, Benachi A, Gut M, Gut I, Martinovic J, Sénat MV, Tawk M, Melki J. Loss of function mutations in EPHB4 are responsible for vein of Galen aneurysmal malformation. Brain : a Journal of Neurology. PMID 29444212 DOI: 10.1093/Brain/Awy020 |
0.337 |
|
| 2016 |
Fontenas L, De Santis F, Di Donato V, Degerny C, Chambraud B, Del Bene F, Tawk M. Neuronal Ndrg4 Is Essential for Nodes of Ranvier Organization in Zebrafish. Plos Genetics. 12: e1006459. PMID 27902705 DOI: 10.1371/Journal.Pgen.1006459 |
0.603 |
|
| 2014 |
Laquérriere A, Maluenda J, Camus A, Fontenas L, Dieterich K, Nolent F, Zhou J, Monnier N, Latour P, Gentil D, Héron D, Desguerres I, Landrieu P, Beneteau C, Delaporte B, ... ... Tawk M, et al. Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects. Human Molecular Genetics. 23: 2279-89. PMID 24319099 DOI: 10.1093/Hmg/Ddt618 |
0.615 |
|
| 2012 |
Zhou J, Tawk M, Tiziano FD, Veillet J, Bayes M, Nolent F, Garcia V, Servidei S, Bertini E, Castro-Giner F, Renda Y, Carpentier S, Andrieu-Abadie N, Gut I, Levade T, et al. Spinal muscular atrophy associated with progressive myoclonic epilepsy is caused by mutations in ASAH1. American Journal of Human Genetics. 91: 5-14. PMID 22703880 DOI: 10.1016/J.Ajhg.2012.05.001 |
0.444 |
|
| 2011 |
Tawk M, Makoukji J, Belle M, Fonte C, Trousson A, Hawkins T, Li H, Ghandour S, Schumacher M, Massaad C. Wnt/beta-catenin signaling is an essential and direct driver of myelin gene expression and myelinogenesis. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 3729-42. PMID 21389228 DOI: 10.1523/Jneurosci.4270-10.2011 |
0.525 |
|
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