Jerome Devaux - Publications

Affiliations: 
2003-2006 Neurology University of Pennsylvania, Philadelphia, PA, United States 

18 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
2022 Deck M, Van Hameren G, Campbell G, Bernard-Marissal N, Devaux J, Berthelot J, Lattard A, Médard JJ, Gautier B, Guelfi S, Abbou S, Quintana P, Chao de la Barca JM, Reynier P, Lenaers G, et al. Physiology of PNS axons relies on glycolytic metabolism in myelinating Schwann cells. Plos One. 17: e0272097. PMID 36194565 DOI: 10.1371/journal.pone.0272097  0.369
2022 Vallat JM, Deschamps N, Richard L, Magy L, Devaux J, Mathis S. Widening of myelin lamellae in polyneuropathy with immunoglobulin-M monoclonal gammopathy, without activity against myelin-associated glycoprotein, responsive to treatment. Neuromuscular Disorders : Nmd. PMID 35618575 DOI: 10.1016/j.nmd.2022.05.001  0.314
2020 Eshed-Eisenbach Y, Devaux J, Vainshtein A, Golani O, Lee SJ, Feinberg K, Sukhanov N, Greenspan DS, Susuki K, Rasband MN, Peles E. Precise Spatiotemporal Control of Nodal Na Channel Clustering by Bone Morphogenetic Protein-1/Tolloid-like Proteinases. Neuron. PMID 32209430 DOI: 10.1016/J.Neuron.2020.03.001  0.557
2019 Efthymiou S, Salpietro V, Malintan N, Poncelet M, Kriouile Y, Fortuna S, De Zorzi R, Payne K, Henderson LB, Cortese A, Maddirevula S, Alhashmi N, Wiethoff S, Ryten M, Botia JA, ... ... Devaux J, et al. Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination. Brain : a Journal of Neurology. PMID 31501903 DOI: 10.1093/Brain/Awz248  0.411
2017 Bang ML, Vainshtein A, Yang HJ, Eshed-Eisenbach Y, Devaux J, Werner HB, Peles E. Glial M6B stabilizes the axonal membrane at peripheral nodes of Ranvier. Glia. PMID 29282769 DOI: 10.1002/Glia.23285  0.62
2016 Martin PM, Cifuentes-Diaz C, Devaux J, Garcia M, Bureau J, Thomasseau S, Klingler E, Girault JA, Goutebroze L. Schwannomin-interacting protein 1 isoform IQCJ-SCHIP1 is a multi-partner ankyrin and spectrin binding protein involved in the organization of nodes of Ranvier. The Journal of Biological Chemistry. PMID 27979964 DOI: 10.1074/Jbc.M116.758029  0.472
2016 Maluenda J, Manso C, Quevarec L, Vivanti A, Marguet F, Gonzales M, Guimiot F, Petit F, Toutain A, Whalen S, Grigorescu R, Coeslier AD, Gut M, Gut I, Laquerrière A, ... Devaux J, et al. Mutations in GLDN, Encoding Gliomedin, a Critical Component of the Nodes of Ranvier, Are Responsible for Lethal Arthrogryposis. American Journal of Human Genetics. PMID 27616481 DOI: 10.1016/j.ajhg.2016.07.021  0.443
2016 Devaux J, Abidi A, Roubertie A, Molinari F, Becq H, Lacoste C, Villard L, Milh M, Aniksztejn L. A Kv7.2 mutation associated with early onset epileptic encephalopathy with suppression-burst enhances Kv7/M channel activity. Epilepsia. PMID 27030113 DOI: 10.1111/Epi.13366  0.476
2016 Manso C, Querol L, Mekaouche M, Illa I, Devaux JJ. Contactin-1 IgG4 antibodies cause paranode dismantling and conduction defects. Brain : a Journal of Neurology. 139: 1700-12. PMID 27017186 DOI: 10.1093/brain/aww062  0.344
2015 Abidi A, Devaux JJ, Molinari F, Alcaraz G, Michon FX, Sutera-Sardo J, Becq H, Lacoste C, Altuzarra C, Afenjar A, Mignot C, Doummar D, Isidor B, Guyen SN, Colin E, et al. A recurrent KCNQ2 pore mutation causing early onset epileptic encephalopathy has a moderate effect on M current but alters subcellular localization of Kv7 channels. Neurobiology of Disease. 80: 80-92. PMID 26007637 DOI: 10.1016/J.Nbd.2015.04.017  0.423
2014 Liu W, Devaux JJ. Calmodulin orchestrates the heteromeric assembly and the trafficking of KCNQ2/3 (Kv7.2/3) channels in neurons. Molecular and Cellular Neurosciences. 58: 40-52. PMID 24333508 DOI: 10.1016/j.mcn.2013.12.005  0.379
2012 Bangratz M, Sarrazin N, Devaux J, Zambroni D, Echaniz-Laguna A, René F, Boërio D, Davoine CS, Fontaine B, Feltri ML, Benoit E, Nicole S. A mouse model of Schwartz-Jampel syndrome reveals myelinating Schwann cell dysfunction with persistent axonal depolarization in vitro and distal peripheral nerve hyperexcitability when perlecan is lacking. The American Journal of Pathology. 180: 2040-55. PMID 22449950 DOI: 10.1016/j.ajpath.2012.01.035  0.451
2011 Cifuentes-Diaz C, Chareyre F, Garcia M, Devaux J, Carnaud M, Levasseur G, Niwa-Kawakita M, Harroch S, Girault JA, Giovannini M, Goutebroze L. Protein 4.1B contributes to the organization of peripheral myelinated axons. Plos One. 6: e25043. PMID 21966409 DOI: 10.1371/Journal.Pone.0025043  0.472
2008 Gow A, Devaux J. A model of tight junction function in central nervous system myelinated axons. Neuron Glia Biology. 4: 307-17. PMID 20102674 DOI: 10.1017/S1740925X09990391  0.356
2008 Devaux J, Gow A. Tight junctions potentiate the insulative properties of small CNS myelinated axons. The Journal of Cell Biology. 183: 909-21. PMID 19047465 DOI: 10.1083/Jcb.200808034  0.436
2005 Devaux JJ, Scherer SS. Altered ion channels in an animal model of Charcot-Marie-Tooth disease type IA. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 25: 1470-80. PMID 15703401 DOI: 10.1523/Jneurosci.3328-04.2005  0.614
2004 Devaux JJ, Kleopa KA, Cooper EC, Scherer SS. KCNQ2 is a nodal K+ channel. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 24: 1236-44. PMID 14762142 DOI: 10.1523/Jneurosci.4512-03.2004  0.421
2003 Devaux J, Alcaraz G, Grinspan J, Bennett V, Joho R, Crest M, Scherer SS. Kv3.1b is a novel component of CNS nodes. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 23: 4509-18. PMID 12805291 DOI: 10.1523/Jneurosci.23-11-04509.2003  0.589
Show low-probability matches.