Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ankur M. Thomas"'
Autor:
Ashley N. Nelson, Michael S. Calhoun, Ankur M. Thomas, Jennifer L. Tavares, Daniel M. Ferretti, Gregory M. Dillon, Yael Mandelblat-Cerf
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 14 (2020)
Ischemic stroke is recognized as one of the leading causes of adult disability, morbidity, and death worldwide. Following stroke, acute neuronal excitotoxicity can lead to many deleterious consequences, one of which is the dysregulation of intracellu
Externí odkaz:
https://doaj.org/article/5592c98416e14b32b4800f26c4a8e30a
Autor:
Ankur M. Thomas, Chris Ehrenfels, Ru Wei, Ramiro H. Massol, Dávid Nagy, Ashley Nelson, Susan C. Su, Stefka Gyoneva, Katelin A. Ennis, Luke Jandreski, Benbo Gao, Linda C. Burkly, Rong-Fang Gu, Christopher A Hinckley, Mihály Hajós
Publikováno v:
Proc Natl Acad Sci U S A
Identifying molecular mediators of neural circuit development and/or function that contribute to circuit dysfunction when aberrantly reengaged in neurological disorders is of high importance. The role of the TWEAK/Fn14 pathway, which was recently rep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::079742a52073fbc500e03b3bb0e72f38
https://doi.org/10.1073/pnas.2001679118
https://doi.org/10.1073/pnas.2001679118
Autor:
Suzanne Szak, Robert H. Scannevin, Ralf Gold, Robert Hoepner, Katrin Strassburger-Krogias, Maximilian Pistor, Melanie S. Brennan, Andrew T. Chan, Davide Gianni, Brian T. Wipke, Ankur M. Thomas
Publikováno v:
Wipke, Brian T; Hoepner, Robert; Strassburger-Krogias, Katrin; Thomas, Ankur M; Gianni, Davide; Szak, Suzanne; Brennan, Melanie S; Pistor, Maximilian; Gold, Ralf; Chan, Andrew; Scannevin, Robert H (2021). Different Fumaric Acid Esters Elicit Distinct Pharmacologic Responses. Neurology: Neuroimmunology and Neuroinflammation, 8(2) Wolters Kluwer Health 10.1212/NXI.0000000000000950
Neurology® Neuroimmunology & Neuroinflammation
article-version (Version of Record) 3
Neurology® Neuroimmunology & Neuroinflammation
article-version (Version of Record) 3
ObjectiveTo test the hypothesis that dimethyl fumarate (DMF, Tecfidera) elicits different biological changes from DMF combined with monoethyl fumarate (MEF) (Fumaderm, a psoriasis therapy), we investigated DMF and MEF in rodents and cynomolgus monkey
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9942fb198d350807c36bb9ace37f271f
https://doi.org/10.1212/nxi.0000000000000950
https://doi.org/10.1212/nxi.0000000000000950
Autor:
Jilin Bai, Joseph J. LoTurco, Juha Kere, J. Voskuil, Nina Kaminen-Ahola, Murugan Paramasivam, Ankur M Thomas, Albert M. Galaburda, Yu Wang, Glenn D. Rosen
Publikováno v:
Neuroscience. 143:515-522
Rodent homologues of two candidate dyslexia susceptibility genes, Kiaa0319 and Dcdc2, have been shown to play roles in neuronal migration in developing cerebral neocortex. This functional role is consistent with the hypothesis that dyslexia susceptib
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8bc3213c39f14620bc7a1b7d20417511
https://doi.org/10.1016/j.neuroscience.2006.08.022
https://doi.org/10.1016/j.neuroscience.2006.08.022
Autor:
James B. Ackman, Joseph J. LoTurco, Ankur M Thomas, Jilin Bai, Richard V. Lee, Raddy L. Ramos
Publikováno v:
Nature Neuroscience. 6:1277-1283
Mutations in the doublecortin gene (DCX) in humans cause malformation of the cerebral neocortex. Paradoxically, genetic deletion of Dcx in mice does not cause neocortical malformation. We used electroporation of plasmids encoding short hairpin RNA to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60cc7e81fb20eb7b44cd94bef9dae4e6
https://doi.org/10.1038/nn1153
https://doi.org/10.1038/nn1153
Autor:
Yu Wang, Julian C. Knight, Alex J. Richardson, Sandra Castro, Douglas F. Hacking, Cecilia Lai, Thomas S. Scerri, Murugan Paramasivam, Clyde Francks, Ankur M Thomas, Joseph J. LoTurco, Anthony P. Monaco, Andrew J. Copp, Brendan J. Keating, Jennifer M. Taylor, Richard Wade-Martins, John F. Stein, Silvia Paracchini
Publikováno v:
Human Molecular Genetics
Dyslexia is one of the most prevalent childhood cognitive disorders, affecting approximately 5% of school-age children. We have recently identified a risk haplotype associated with dyslexia on chromosome 6p22.2 which spans the TTRAP gene and portions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41f71105a2461273912f4278a36ed2f6
https://pubmed.ncbi.nlm.nih.gov/16600991
https://pubmed.ncbi.nlm.nih.gov/16600991