Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Marcel Tawk"'
Autor:
Emilie Lesport, Lucie Commeau, Mélanie Genet, Etienne-Emile Baulieu, Marcel Tawk, Julien Giustiniani
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 18 (2024)
The failure of the autophagy-lysosomal pathway to clear the pathogenic forms of Tau exacerbates the pathogenesis of tauopathies. We have previously shown that the immunophilin FKBP52 interacts both physically and functionally with Tau, and that a dec
Externí odkaz:
https://doaj.org/article/51a5cd0174404aa1b1f736aa034c62c1
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
Estrogens induce several regulatory signals in the nervous system that are mainly mediated through estrogen receptors (ERs). ERs are largely expressed in the nervous system, yet the importance of ERs to neural development has only been elucidated ove
Externí odkaz:
https://doaj.org/article/7b69593715034e179bcc85a635c75eeb
Autor:
Aya Mikdache, Marie-José Boueid, Lorijn van der Spek, Emilie Lesport, Brigitte Delespierre, Julien Loisel-Duwattez, Cindy Degerny, Marcel Tawk
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-18 (2021)
Abstract The Regulator of G protein signaling 4 (Rgs4) is a member of the RGS proteins superfamily that modulates the activity of G-protein coupled receptors. It is mainly expressed in the nervous system and is linked to several neuronal signaling pa
Externí odkaz:
https://doaj.org/article/ae7d4224c42a4f8bbfeb4badcf76ef5e
Autor:
Berivan Tas, Daniele Starnoni, Stanislas Smajda, Alexandre J. Vivanti, Catherine Adamsbaum, Mélanie Eyries, Judith Melki, Marcel Tawk, Augustin Ozanne, Nicole Revencu, Florent Soubrier, Selima Siala, Miikka Vikkula, Kumaran Deiva, Guillaume Saliou
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
ObjectiveTo study the genotypes and phenotypes of cerebral arteriovenous fistulas that drain or do not drain through the vein of Galen, and true vein of Galen aneurysmal malformations, in order to determine whether genotyping could help improve class
Externí odkaz:
https://doaj.org/article/f2cfff4171da43f9be891ec0852947f9
Publikováno v:
Cells, Vol 9, Iss 12, p 2634 (2020)
Cells encounter countless external cues and the specificity of their responses is translated through a myriad of tightly regulated intracellular signals. For this, Rho GTPases play a central role and transduce signals that contribute to fundamental c
Externí odkaz:
https://doaj.org/article/111bf6c3a8a54f108bcf69ba49a9e725
Autor:
Laura Fontenas, Flavia De Santis, Vincenzo Di Donato, Cindy Degerny, Béatrice Chambraud, Filippo Del Bene, Marcel Tawk
Publikováno v:
PLoS Genetics, Vol 12, Iss 11, p e1006459 (2016)
Axon ensheathment by specialized glial cells is an important process for fast propagation of action potentials. The rapid electrical conduction along myelinated axons is mainly due to its saltatory nature characterized by the accumulation of ion chan
Externí odkaz:
https://doaj.org/article/55ec8d10f48d45d7b47b7035fd301169
Autor:
Marie‐José Boueid, Aya Mikdache, Emilie Lesport, Brigitte Delespierre, Julien Loisel‐Duwattez, Cindy Degerny, Marcel Tawk
Publikováno v:
Developmental dynamics : an official publication of the American Association of AnatomistsREFERENCES. 252(1)
Schwann cells (SCs) are specialized glial cells of the peripheral nervous system that produce myelin and promote fast action potential propagation. In order to myelinate, SCs engage in a series of events that include migration and division along axon
Autor:
Aya Mikdache, Marie-José Boueid, Emilie Lesport, Brigitte Delespierre, Julien Loisel-Duwattez, Cindy Degerny, Marcel Tawk
Publikováno v:
Development (Cambridge, England). 149(17)
Schwann cells (SCs) migrate along peripheral axons and divide intensively to generate the right number of cells prior to axonal ensheathment; however, little is known regarding the temporal and molecular control of their division and its impact on my
Autor:
Berivan, Tas, Daniele, Starnoni, Stanislas, Smajda, Alexandre J, Vivanti, Catherine, Adamsbaum, Mélanie, Eyries, Judith, Melki, Marcel, Tawk, Augustin, Ozanne, Nicole, Revencu, Florent, Soubrier, Selima, Siala, Miikka, Vikkula, Kumaran, Deiva, Guillaume, Saliou
Publikováno v:
Frontiers in pediatrics, Vol. 10, p. 871565 (2022)
Frontiers in Pediatrics, Vol. 10 (2022)
Frontiers in Pediatrics, Vol. 10 (2022)
To study the genotypes and phenotypes of cerebral arteriovenous fistulas that drain or do not drain through the vein of Galen, and true vein of Galen aneurysmal malformations, in order to determine whether genotyping could help improve classification
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::4721fd7224f0cd6851902f9caaf35036
https://hdl.handle.net/2078.1/261994
https://hdl.handle.net/2078.1/261994
Autor:
Ivo Gut, Sarah Grotto, Céline Bellesme, Arnold Munnich, Cyril Gitiaux, Jeanne Amiel, Chloé Quélin, Annie Laquerrière, Suonavy Khung, Hanitra Ranjatoelina-Randrianaivo, Luc Rigonnot, Christine Francannet, Loic Quevarec, Jérôme Bouligand, Fabienne Prieur, Alexandra Benachi, Valérie Cormier-Daire, Laurence Perrin, Judith Melki, Pierre-Simon Jouk, Flora Nolent, Tania Attié-Bitach, Delphine Héron, Marie-Line Jacquemont, Claire Beneteau, Fabien Guimiot, Laetitia Lambert, Sandra Mercier, Valérie Biancalana, Fanny Laffargue, Elise Boucher, Jean-Louis Bessereau, P. Landrieu, Annick Toutain, Alain Verloes, Alice Goldenberg, Philippe Latour, Dominique Martin-Coignard, Anne Guiochon-Mantel, Dan Mejlachowicz, Damien Sternberg, Haluk Topaloglu, Bruno Eymard, Géraldine Viot, Catherine Fallet-Bianco, Julien Saada, Isabelle Desguerre, Marie-Hélène Saint-Frison, Catherine Vincent-Delorme, Sophie Blesson, Radka Stoeva, Alexandre J. Vivanti, Martine Bucourt, Pascaline Letard, Jérome Maluenda, Laurence Loeuillet, Lionel Van Maldergem, Didier Lacombe, Marcel Tawk, Michèle Granier, Stanislas Lyonnet, Anne-Lise Delezoide, Andrée Delahaye-Duriez, André Mégarbané, Marie Gonzales, Florence Petit, Juliette Piard, Laurence Faivre, Helene Verhelst, Bettina Bessières, Sabine Sigaudy, Sandra Whalen, Valérie Layet, Yline Capri, Fanny Pelluard, Emanuela Abiusi, Klaus Dieterich, Marie Vincent, Marine Legendre, Dana Jaber, Romulus Grigorescu, Florent Marguet, Eric Bieth, Helge Amthor, Christine Barnerias, Estelle Colin, Laetitia Trestard, Mathilde Nizon, Jelena Martinovic, Daniel Amram, Nicoletta Resta
Publikováno v:
JOURNAL OF MEDICAL GENETICS
BackgroundArthrogryposis multiplex congenita (AMC) is characterised by congenital joint contractures in two or more body areas. AMC exhibits wide phenotypic and genetic heterogeneity. Our goals were to improve the genetic diagnosis rates of AMC, to e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e5ca5c2b4280785da88a26155872ce7
https://hdl.handle.net/1854/LU-8759575
https://hdl.handle.net/1854/LU-8759575