Laura Fontenas - Publications

2016- University of Virginia, Charlottesville, VA 

7 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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