Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Olivier Biondi"'
Autor:
Elias Abi Akar, Laure Weill, Mirella El Khoury, Cédric Caradeuc, Gildas Bertho, Suzan Boutary, Cynthia Bezier, Zoé Clerc, Delphine Sapaly, Sabrina Bendris, Flore Cheguillaume, Nicolas Giraud, Assaad A. Eid, Frédéric Charbonnier, Olivier Biondi
Publikováno v:
Molecular Medicine, Vol 30, Iss 1, Pp 1-16 (2024)
Abstract Background Type 2 diabetes mellitus (T2DM) is a chronic metabolic disease that commonly results from a high-calorie diet and sedentary lifestyle, leading to insulin resistance and glucose homeostasis perturbation. Physical activity is recomm
Externí odkaz:
https://doaj.org/article/08581acfbdf54fc68bb47baec3268e46
Autor:
Mirella El Khoury, Olivier Biondi, Gaelle Bruneteau, Delphine Sapaly, Sabrina Bendris, Cynthia Bezier, Zoé Clerc, Elias Abi Akar, Laure Weill, Assaad A. Eid, Frédéric Charbonnier
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 17 (2023)
IntroductionSpinal muscular atrophy (SMA) is a fatal neurodegenerative disorder, characterized by motor neuron (MN) degeneration and severe muscular atrophy and caused by Survival of Motor Neuron (SMN) depletion. Therapies aimed at increasing SMN in
Externí odkaz:
https://doaj.org/article/b187f5fb340440b7ab9572622915223a
Autor:
Zherui Wu, Nicolas Stadler, Amazigh Abbaci, Jin Liu, Agnès Boullier, Nicolas Marie, Olivier Biondi, Marthe Moldes, Romain Morichon, Bruno Feve, Olle Melander, Patricia Forgez
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
BackgroundObesity is a major public health problem of our time as a risk factor for cardiometabolic disease and the available pharmacological tools needed to tackle the obesity pandemic are insufficient. Neurotensin (NTS) is a 13 amino acid peptide,
Externí odkaz:
https://doaj.org/article/17486a3e01ca49d0b67a718be10d7ebc
Autor:
Léo Houdebine, Domenico D’Amico, Jean Bastin, Farah Chali, Céline Desseille, Valentin Rumeau, Judy Soukkari, Carole Oudot, Thaïs Rouquet, Bruno Bariohay, Julien Roux, Delphine Sapaly, Laure Weill, Philippe Lopes, Fatima Djouadi, Cynthia Bezier, Frédéric Charbonnier, Olivier Biondi
Publikováno v:
Frontiers in Physiology, Vol 10 (2019)
Spinal Muscular Atrophy (SMA), an autosomal recessive neurodegenerative disease characterized by the loss of spinal-cord motor-neurons, is caused by mutations on Survival-of-Motor Neuron (SMN)-1 gene. The expression of SMN2, a SMN1 gene copy, partial
Externí odkaz:
https://doaj.org/article/0b7e68d9487c4a4d90e01f37457cf285
Autor:
Laia Just-Borràs, Víctor Cilleros-Mañé, Erica Hurtado, Olivier Biondi, Frédéric Charbonnier, Marta Tomàs, Neus Garcia, Josep Tomàs, Maria A. Lanuza
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 9, p 4577 (2021)
Physical exercise improves motor control and related cognitive abilities and reinforces neuroprotective mechanisms in the nervous system. As peripheral nerves interact with skeletal muscles at the neuromuscular junction, modifications of this bidirec
Externí odkaz:
https://doaj.org/article/0bf0c45d099d4238b4f6f836eb1b7c40
Autor:
Céline Desseille, Séverine Deforges, Olivier Biondi, Léo Houdebine, Domenico D’amico, Antonin Lamazière, Cédric Caradeuc, Gildas Bertho, Gaëlle Bruneteau, Laure Weill, Jean Bastin, Fatima Djouadi, François Salachas, Philippe Lopes, Christophe Chanoine, Charbel Massaad, Frédéric Charbonnier
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 10 (2017)
Amyotrophic Lateral Sclerosis is an adult-onset neurodegenerative disease characterized by the specific loss of motor neurons, leading to muscle paralysis and death. Although the cellular mechanisms underlying amyotrophic lateral sclerosis (ALS)-indu
Externí odkaz:
https://doaj.org/article/93e08f1473ec471cac23c066507b727c
Autor:
Anne-Sophie Armand, Iman Laziz, Dounia Djeghloul, Sylvie Lécolle, Anne T Bertrand, Olivier Biondi, Leon J De Windt, Christophe Chanoine
Publikováno v:
PLoS ONE, Vol 6, Iss 11, p e27283 (2011)
Apoptosis Inducing Factor (AIF) is a highly conserved, ubiquitous flavoprotein localized in the mitochondrial intermembrane space. In vivo, AIF provides protection against neuronal and cardiomyocyte apoptosis induced by oxidative stress. Conversely i
Externí odkaz:
https://doaj.org/article/cd65edbb7d954aa8a79f6e7af60092b8
Autor:
Domenico D'Amico, Olivier Biondi, Camille Januel, Cynthia Bezier, Delphine Sapaly, Zoé Clerc, Mirella El Khoury, Venkat Krishnan Sundaram, Léo Houdebine, Thibaut Josse, Bruno Della Gaspera, Cécile Martinat, Charbel Massaad, Laure Weill, Frédéric Charbonnier
Publikováno v:
Neuropathology and applied neurobiologyREFERENCES. 48(5)
Spinal muscular atrophy (SMA) is a neuromuscular disease caused by survival of motor neuron (SMN) deficiency that induces motor neuron (MN) degeneration and severe muscular atrophy. Gene therapies that increase SMN have proven their efficacy but not
Autor:
Domenico D’Amico, Laure Weill, Valentin Rumeau, Thaïs Rouquet, Bruno Bariohay, Farah Chali, Cynthia Bezier, Céline Desseille, Julien Roux, Philippe Lopes, Léo Houdebine, Carole Oudot, Frédéric Charbonnier, Delphine Sapaly, Jean Bastin, Olivier Biondi, Judy Soukkari, Fatima Djouadi
Publikováno v:
Frontiers in Physiology
Frontiers in Physiology, Frontiers, 2019, 10, pp.1258. ⟨10.3389/fphys.2019.01258⟩
Frontiers in Physiology, Vol 10 (2019)
Frontiers in Physiology, 2019, 10, pp.1258. ⟨10.3389/fphys.2019.01258⟩
Frontiers in Physiology, Frontiers, 2019, 10, pp.1258. ⟨10.3389/fphys.2019.01258⟩
Frontiers in Physiology, Vol 10 (2019)
Frontiers in Physiology, 2019, 10, pp.1258. ⟨10.3389/fphys.2019.01258⟩
International audience; Spinal Muscular Atrophy (SMA), an autosomal recessive neurodegenerative disease characterized by the loss of spinal-cord motor-neurons, is caused by mutations on Survival-of-Motor Neuron (SMN)-1 gene. The expression of SMN2, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f1322e110ebc3740027f4fa4c141044
https://www.hal.inserm.fr/inserm-02893893/document
https://www.hal.inserm.fr/inserm-02893893/document
Autor:
Erica Hurtado, Neus Garcia, Laia Just-Borràs, Víctor Cilleros-Mañé, Marta Tomàs, Olivier Biondi, Frédéric Charbonnier, Josep Tomàs, Maria A. Lanuza
Publikováno v:
Cellular and molecular life sciences : CMLS. 77(15)
Nerve-induced muscle contraction regulates the BDNF/TrkB neurotrophic signalling to retrogradely modulate neurotransmission and protect the neuromuscular junctions and motoneurons. In muscles with amyotrophic lateral sclerosis, this pathway is strong