Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Nadège, Diedhiou"'
Autor:
Laura Pérez-Guàrdia, Emma Lafabrie, Nadège Diedhiou, Coralie Spiegelhalter, Jocelyn Laporte, Johann Böhm
Publikováno v:
Cells, Vol 13, Iss 22, p 1829 (2024)
Store-operated Ca2+ entry (SOCE) controls Ca2+ homeostasis and mediates multiple Ca2+-dependent signaling pathways and cellular processes. It relies on the concerted activity of the reticular Ca2+ sensor STIM1 and the plasma membrane Ca2+ channel ORA
Externí odkaz:
https://doaj.org/article/433bc148b6a54aa5a066d77dc9c3a24e
Autor:
Nicole M. Sayles, Jill S. Napierala, Josef Anrather, Nadège Diedhiou, Jixue Li, Marek Napierala, Hélène Puccio, Giovanni Manfredi
Publikováno v:
Disease Models & Mechanisms, Vol 17, Iss 1 (2024)
Externí odkaz:
https://doaj.org/article/729b9a5043944924a6bc981023634e12
Autor:
Nicole M. Sayles, Jill S. Napierala, Josef Anrather, Nadège Diedhiou, Jixue Li, Marek Napierala, Hélène Puccio, Giovanni Manfredi
Publikováno v:
Disease Models & Mechanisms, Vol 16, Iss 10 (2023)
Externí odkaz:
https://doaj.org/article/b108419737af43439a6188f425d2817c
Autor:
Valentina Maria Lionello, Christine Kretz, Evelina Edelweiss, Corinne Crucifix, Raquel Gómez-Oca, Nadia Messaddeq, Suzie Buono, Pascale Koebel, Xènia Massana Muñoz, Nadège Diedhiou, Belinda S. Cowling, Marc Bitoun, Jocelyn Laporte
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 119(9)
Significance Membrane remodeling and trafficking is essential for intracellular organization under normal conditions and can be altered in a plethora of diseases. Here we characterized the action of amphiphysin (BIN1) and dynamin (DNM2), two main reg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56a47859f93f44c1fbc97c308f4bd117
https://pubmed.ncbi.nlm.nih.gov/35217605
https://pubmed.ncbi.nlm.nih.gov/35217605
Autor:
Aleksandra Nadaj-Pakleza, Lucas Corti, Hélène Puccio, Mathieu Anheim, Jamel Chelly, Cecilia Marelli, Julien Tarabeux, Nicolas Dondaine, Nadège Diedhiou, Odile Gebus, Marilyne Almeras, Pauline Fahrer, Cécile Cauquil, Jean-Baptiste Chanson, Béatrice Lannes, Laura Robelin, Marie Claire Vincent, Mehdi Benkirane, Guillaume Taieb, Christine Tranchant, Gabrielle Rudolf, Matthieu Canuet, Andoni Echaniz-Laguna, Lise Larrieu, Solveig Montaut, Benoit Lhermitte
Publikováno v:
Journal of Neurology.
Cerebellar ataxia with neuropathy and vestibular areflexia syndrome (CANVAS) is a recessively inherited multisystem ataxia compromising cerebellar, vestibular, and sensory nerves, which has been associated to a pathogenic AAGGG(n) biallelic expansion
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f95fc877c929ba0614a59f2502a73ce
https://doi.org/10.1007/s00415-021-10499-5
https://doi.org/10.1007/s00415-021-10499-5
Autor:
Solveig, Montaut, Nadège, Diedhiou, Pauline, Fahrer, Cécilia, Marelli, Benoit, Lhermitte, Laura, Robelin, Marie Claire, Vincent, Lucas, Corti, Guillaume, Taieb, Odile, Gebus, Gabrielle, Rudolf, Julien, Tarabeux, Nicolas, Dondaine, Matthieu, Canuet, Marilyne, Almeras, Mehdi, Benkirane, Lise, Larrieu, Jean-Baptiste, Chanson, Aleksandra, Nadaj-Pakleza, Andoni, Echaniz-Laguna, Cécile, Cauquil, Béatrice, Lannes, Jamel, Chelly, Mathieu, Anheim, Hélène, Puccio, Christine, Tranchant
Publikováno v:
Journal of neurology. 268(9)
Cerebellar ataxia with neuropathy and vestibular areflexia syndrome (CANVAS) is a recessively inherited multisystem ataxia compromising cerebellar, vestibular, and sensory nerves, which has been associated to a pathogenic AAGGG(n) biallelic expansion
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a3f7002d60d223f8e6490c246c50d181
https://pubmed.ncbi.nlm.nih.gov/33666721
https://pubmed.ncbi.nlm.nih.gov/33666721
Autor:
Béatrice Lannes, Nadège Diedhiou, Solveig Montaut, Lhermitte Benoit, Mathieu Anheim, Hélène Puccio, Christine Tranchant
Publikováno v:
Revue Neurologique. 177:S48-S49
Introduction Le cerebellar ataxia with neuropathy and vestibular areflexia syndrome (CANVAS) correspond a une ataxie plurisystemique, de transmission recessive, associee a une expansion biallelique pathogene AAGGG(n) dans le gene RFC1. Objectifs Notr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ad5228f1abd25d03fcb747e7d2f6ccd
https://doi.org/10.1016/j.neurol.2021.02.187
https://doi.org/10.1016/j.neurol.2021.02.187