Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Yoan Arribat"'
Autor:
Dogan Grepper, Cassandra Tabasso, Nadège Zanou, Axel K.F. Aguettaz, Mauricio Castro-Sepulveda, Dorian V. Ziegler, Sylviane Lagarrigue, Yoan Arribat, Adrien Martinotti, Ammar Ebrahimi, Jean Daraspe, Lluis Fajas, Francesca Amati
Publikováno v:
iScience, Vol 27, Iss 8, Pp 110510- (2024)
Summary: The physical connection between mitochondria and endoplasmic reticulum (ER) is an essential signaling hub to ensure organelle and cellular functions. In skeletal muscle, ER-mitochondria calcium (Ca2+) signaling is crucial to maintain cellula
Externí odkaz:
https://doaj.org/article/5ccb21c1b3074b46860b81ba3f848cf6
Autor:
Sarah Bahraoui, Gautier Tejedor, Anne-Laure Mausset-Bonnefont, François Autelitano, Audrey Barthelaix, Claudia Terraza-Aguirre, Vincent Gisbert, Yoan Arribat, Christian Jorgensen, Mingxing Wei, Farida Djouad
Publikováno v:
Stem Cell Research & Therapy, Vol 15, Iss 1, Pp 1-14 (2024)
Abstract Background Initially discovered for its ability to regenerate ear holes, the Murphy Roth Large (MRL) mouse has been the subject of multiple research studies aimed at evaluating its ability to regenerate other body tissues and at deciphering
Externí odkaz:
https://doaj.org/article/530faf1c79e540e0bfd8dc943c480b42
Autor:
Evgeniya Trofimenko, Gianvito Grasso, Mathieu Heulot, Nadja Chevalier, Marco A Deriu, Gilles Dubuis, Yoan Arribat, Marc Serulla, Sebastien Michel, Gil Vantomme, Florine Ory, Linh Chi Dam, Julien Puyal, Francesca Amati, Anita Lüthi, Andrea Danani, Christian Widmann
Publikováno v:
eLife, Vol 10 (2021)
Cell-penetrating peptides (CPPs) allow intracellular delivery of bioactive cargo molecules. The mechanisms allowing CPPs to enter cells are ill-defined. Using a CRISPR/Cas9-based screening, we discovered that KCNQ5, KCNN4, and KCNK5 potassium channel
Externí odkaz:
https://doaj.org/article/98b234728cca409a8a4e7ab3072baed6
Publikováno v:
PLoS Genetics, Vol 16, Iss 4, p e1008665 (2020)
Lipid droplets (LD) are affected in multiple human disorders. These highly dynamic organelles are involved in many cellular roles. While their intracellular dispersion is crucial to ensure their function and other organelles-contact, underlying mecha
Externí odkaz:
https://doaj.org/article/dddd12ae689347068de717598048fe3c
Autor:
Yoan Arribat, Dogan Grepper, Sylviane Lagarrigue, Joy Richard, Mélanie Gachet, Philipp Gut, Francesca Amati
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 7 (2019)
Organogenesis is well characterized in vertebrates. However, the anatomical and functional development of intracellular compartments during this phase of development remains unknown. Taking an organellogenesis point of view, we characterize the spati
Externí odkaz:
https://doaj.org/article/33713e13d1c349b29e34dcaa7b9274ef
Autor:
Ali Seifinejad, Mergim Ramosaj, Ling Shan, Sha Li, Marie-Laure Possovre, Corinne Pfister, Rolf Fronczek, Lee A. Garrett-Sinha, David Frieser, Makoto Honda, Yoan Arribat, Dogan Grepper, Francesca Amati, Marie Picot, Andrea Agnoletto, Christian Iseli, Nicolas Chartrel, Roland Liblau, Gert J. Lammers, Anne Vassalli, Mehdi Tafti
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 120(19). National Academy of Sciences
Narcolepsy with cataplexy is a sleep disorder caused by deficiency in the hypothalamic neuropeptide hypocretin/orexin (HCRT), unanimously believed to result from autoimmune destruction of hypocretin-producing neurons. HCRT deficiency can also occur i
Autor:
Alexandre Reymond, Paolo Gasparini, Jacqueline Chrast, Hannie Kremer, Sissy Bassani, Giorgia Girotto, Jiddeke M. van de Kamp, Massimiliano Cocca, Nicolas Guex, Benjamin Delprat, Mireille Rossel, Francesca Amati, Flavio Faletra, Heiko Locher, Yoan Arribat, Sylvain Pradervand, Alban Ziegler, Jeroen Smits, Sandrine Marlin, Norine Voisin, Giuliana Giannuzzi, Tangui Maurice, Anna Morgan, Roxane Machavoine, Edward S A van Beelen, Nicolas Chatron
Publikováno v:
Bassani, S, van Beelen, E, Rossel, M, Voisin, N, Morgan, A, Arribat, Y, Chatron, N, Chrast, J, Cocca, M, Delprat, B, Faletra, F, Giannuzzi, G, Guex, N, Machavoine, R, Pradervand, S, Smits, J J, van de Kamp, J M, Ziegler, A, Amati, F, Marlin, S, Kremer, H, Locher, H, Maurice, T, Gasparini, P, Girotto, G & Reymond, A 2021, ' Variants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss ', Human Molecular Genetics, vol. 30, no. 19, pp. 1785-1796 . https://doi.org/10.1093/hmg/ddab145
Human Molecular Genetics, 30(19), 1785-1796. OXFORD UNIV PRESS
Human Molecular Genetics, 30(19), 1785-1796. Oxford University Press
Human Molecular Genetics, 30, 19, pp. 1785-1796
Human Molecular Genetics, 30, 1785-1796
Human Molecular Genetics, 30(19), 1785-1796. OXFORD UNIV PRESS
Human Molecular Genetics, 30(19), 1785-1796. Oxford University Press
Human Molecular Genetics, 30, 19, pp. 1785-1796
Human Molecular Genetics, 30, 1785-1796
Non-Syndromic Hereditary Hearing Loss (NSHHL) is a genetically heterogeneous sensory disorder with about 120 genes already associated. Through exome sequencing (ES) and data aggregation, we identified a family with six affected individuals and one un
Autor:
Yoan Arribat
Publikováno v:
Brain. 144:362-365
This scientific commentary refers to ‘Bi-allelic truncating mutations in VWA1 cause neuromyopathy’, by Deschauer et al. (doi:10.1093/brain/awaa418) and ‘An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy’
Autor:
Anja Holm, Marie-Laure Possovre, Mojtaba Bandarabadi, Kristine F. Moseholm, Jessica L. Justinussen, Ivan Bozic, René Lemcke, Yoan Arribat, Francesca Amati, Asli Silahtaroglu, Maxime Juventin, Antoine Adamantidis, Mehdi Tafti, Birgitte R. Kornum
Publikováno v:
Holm, Anja; Possovre, Marie-Laure; Bandarabadi, Mojtaba; Moseholm, Kristine F; Justinussen, Jessica L; Bozic, Ivan; Lemcke, René; Arribat, Yoan; Amati, Francesca; Silahtaroglu, Asli; Juventin, Maxime; Adamantidis, Antoine; Tafti, Mehdi; Kornum, Birgitte R (2022). The evolutionarily conserved miRNA-137 targets the neuropeptide hypocretin/orexin and modulates the wake to sleep ratio. Proceedings of the National Academy of Sciences of the United States of America-PNAS, 119(17), e2112225119. National Academy of Sciences NAS 10.1073/pnas.2112225119
Holm, A, Possovre, M-L, Bandarabadi, M, Moseholm, K F, Justinussen, J L, Bozic, I, Lemcke, R, Arribat, Y, Amati, F, Silahtaroglu, A, Juventin, M, Adamantidis, A, Tafti, M & Kornum, B R 2022, ' The evolutionarily conserved miRNA-137 targets the neuropeptide hypocretin/orexin and modulates the wake to sleep ratio ', Proceedings of the National Academy of Sciences of the United States of America, vol. 119, no. 17, e2112225119, pp. e2112225119 . https://doi.org/10.1073/pnas.2112225119
Holm, A, Possovre, M L, Bandarabadi, M, Moseholm, K F, Justinussen, J L, Bozic, I, Lemcke, R, Arribat, Y, Amati, F, Silahtaroglu, A, Juventin, M, Adamantidis, A, Tafti, M & Kornum, B R 2022, ' The evolutionarily conserved miRNA-137 targets the neuropeptide hypocretin/orexin and modulates the wake to sleep ratio ', Proceedings of the National Academy of Sciences of the United States of America, vol. 119, no. 17 . https://doi.org/10.1073/pnas.2112225119
Proceedings of the National Academy of Sciences of the United States of America, vol. 119, no. 17, pp. e2112225119
Holm, A, Possovre, M-L, Bandarabadi, M, Moseholm, K F, Justinussen, J L, Bozic, I, Lemcke, R, Arribat, Y, Amati, F, Silahtaroglu, A, Juventin, M, Adamantidis, A, Tafti, M & Kornum, B R 2022, ' The evolutionarily conserved miRNA-137 targets the neuropeptide hypocretin/orexin and modulates the wake to sleep ratio ', Proceedings of the National Academy of Sciences of the United States of America, vol. 119, no. 17, e2112225119, pp. e2112225119 . https://doi.org/10.1073/pnas.2112225119
Holm, A, Possovre, M L, Bandarabadi, M, Moseholm, K F, Justinussen, J L, Bozic, I, Lemcke, R, Arribat, Y, Amati, F, Silahtaroglu, A, Juventin, M, Adamantidis, A, Tafti, M & Kornum, B R 2022, ' The evolutionarily conserved miRNA-137 targets the neuropeptide hypocretin/orexin and modulates the wake to sleep ratio ', Proceedings of the National Academy of Sciences of the United States of America, vol. 119, no. 17 . https://doi.org/10.1073/pnas.2112225119
Proceedings of the National Academy of Sciences of the United States of America, vol. 119, no. 17, pp. e2112225119
Hypocretin (Hcrt), also known as orexin, neuropeptide signaling stabilizes sleep and wakefulness in all vertebrates. A lack of Hcrt causes the sleep disorder narcolepsy, and increased Hcrt signaling has been speculated to cause insomnia, but while th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5daa4e77ffd8aa8cbc665cd9fc957acc
https://boris.unibe.ch/169463/1/pnas.2112225119.pdf
https://boris.unibe.ch/169463/1/pnas.2112225119.pdf
Publikováno v:
International Journal of Molecular Sciences, Vol 19, Iss 3, p 744 (2018)
Structural microtubule associated protein Tau is found in high amount in axons and is involved in several neurodegenerative diseases. Although many studies have highlighted the toxicity of an excess of Tau in neurons, the in vivo understanding of the
Externí odkaz:
https://doaj.org/article/6687bc03c16e44389d888debc468e893