Year |
Citation |
Score |
2023 |
Fontenas L. Glial plasticity at nervous system transition zones. Biology Open. 12. PMID 37787575 DOI: 10.1242/bio.060037 |
0.567 |
|
2021 |
Ali MF, Latimer AJ, Wang Y, Hogenmiller L, Fontenas L, Isabella AJ, Moens CB, Yu G, Kucenas S. Met is required for oligodendrocyte progenitor cell migration in Danio rerio. G3 (Bethesda, Md.). 11. PMID 34568921 DOI: 10.1093/g3journal/jkab265 |
0.693 |
|
2021 |
Fontenas L, Kucenas S. Spinal cord precursors utilize neural crest cell mechanisms to generate hybrid peripheral myelinating glia. Elife. 10. PMID 33554855 DOI: 10.7554/eLife.64267 |
0.77 |
|
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 |
0.75 |
|
2019 |
Fontenas L, Welsh TG, Piller M, Coughenour P, Gandhi AV, Prober DA, Kucenas S. The Neuromodulator Adenosine Regulates Oligodendrocyte Migration at Motor Exit Point Transition Zones. Cell Reports. 27: 115-128.e5. PMID 30943395 DOI: 10.1016/J.Celrep.2019.03.013 |
0.643 |
|
2018 |
Fontenas L, Kucenas S. Motor Exit Point (MEP) Glia: Novel Myelinating Glia That Bridge CNS and PNS Myelin. Frontiers in Cellular Neuroscience. 12: 333. PMID 30356886 DOI: 10.3389/Fncel.2018.00333 |
0.768 |
|
2017 |
Fontenas L, Kucenas S. Livin' On The Edge: glia shape nervous system transition zones. Current Opinion in Neurobiology. 47: 44-51. PMID 28957729 DOI: 10.1016/J.Conb.2017.09.008 |
0.742 |
|
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 |
0.712 |
|
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, 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 |
0.729 |
|
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