Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Sabine, de la Porte"'
Autor:
Antoine de Zélicourt, Abdallah Fayssoil, Mbarka Dakouane‐Giudicelli, Isley De Jesus, Ahmed Karoui, Faouzi Zarrouki, Florence Lefebvre, Arnaud Mansart, Jean‐Marie Launay, Jerome Piquereau, Mariana G Tarragó, Marcel Bonay, Anne Forand, Sophie Moog, France Piétri‐Rouxel, Elise Brisebard, Claudia C S Chini, Sonu Kashyap, Matthew J Fogarty, Gary C Sieck, Mathias Mericskay, Eduardo N Chini, Ana Maria Gomez, José‐Manuel Cancela, Sabine de la Porte
Publikováno v:
EMBO Molecular Medicine, Vol 14, Iss 5, Pp 1-23 (2022)
Abstract Duchenne muscular dystrophy (DMD) is characterized by progressive muscle degeneration. Two important deleterious features are a Ca2+ dysregulation linked to Ca2+ influxes associated with ryanodine receptor hyperactivation, and a muscular nic
Externí odkaz:
https://doaj.org/article/ff8aa5831114408f802cc62d7a45fce4
Autor:
Lora L. Martucci, Jean-Marie Launay, Natsuko Kawakami, Cécile Sicard, Nathalie Desvignes, Mbarka Dakouane-Giudicelli, Barbara Spix, Maude Têtu, Franck-Olivier Gilmaire, Sloane Paulcan, Jacques Callebert, Cyrille Vaillend, Franz Bracher, Christian Grimm, Philippe Fossier, Sabine de la Porte, Hirotaka Sakamoto, John Morris, Antony Galione, Sylvie Granon, José-Manuel Cancela
Publikováno v:
Proceedings of the National Academy of Sciences. 120
Oxytocin (OT) is a prominent regulator of many aspects of mammalian social behavior and stored in large dense-cored vesicles (LDCVs) in hypothalamic neurons. It is released in response to activity-dependent Ca 2+ influx, but is also dependent on Ca 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9fc8b7b5712e85f0c955136ea1c08c7
https://doi.org/10.1073/pnas.2213682120
https://doi.org/10.1073/pnas.2213682120
Autor:
Sara Vianello, Sophie Bouyon, Evelyne Benoit, Catherine Sebrié, Delphine Boerio, Marc Herbin, Morgane Roulot, Yves Fromes, Sabine de la Porte
Publikováno v:
Neurobiology of Disease, Vol 71, Iss , Pp 325-333 (2014)
Duchenne muscular dystrophy (DMD) is a progressive neuromuscular disease caused by lack of dystrophin, a sub-sarcolemmal protein, which leads to dramatic muscle deterioration. We studied in mdx mice, the effects of oral administration of arginine but
Externí odkaz:
https://doaj.org/article/33657da37cff4ec583b976a8f26d6b70
Publikováno v:
Neurobiology of Disease, Vol 36, Iss 2, Pp 252-258 (2009)
Duchenne muscular dystrophy (DMD), the most common and severe X-linked myopathy, is characterized by the lack of dystrophin, a sub-sarcolemmal protein necessary for normal muscle functions. In a previous study of the lipid content of skeletal muscles
Externí odkaz:
https://doaj.org/article/61fce4d5c4bc4b2898ea90558f28da70
Publikováno v:
Journal of Lipid Research, Vol 49, Iss 2, Pp 438-454 (2008)
Human striated muscle samples, from male control and Duchenne muscular dystrophy-affected children, were subjected to cluster-time-of-flight secondary ion mass spectrometry (cluster-ToF-SIMS) imaging using a 25 keV Bi3+ liquid metal ion gun under sta
Externí odkaz:
https://doaj.org/article/4fe8ec866ef64394a99f5c483604a65d
Autor:
Vincent Voisin, Catherine Sébrié, Stéfan Matecki, Hua Yu, Brigitte Gillet, Michèle Ramonatxo, Maurice Israël, Sabine De la Porte
Publikováno v:
Neurobiology of Disease, Vol 20, Iss 1, Pp 123-130 (2005)
A possible treatment for Duchenne muscular dystrophies would be to compensate for dystrophin loss by increasing the expression of utrophin, another cytoskeletal protein of the muscle membrane. We previously found that l-arginine, the substrate for ni
Externí odkaz:
https://doaj.org/article/8f11f0c88a914c9e8f33fb4a69c65746
Publikováno v:
Journal of Lipid Research, Vol 46, Iss 7, Pp 1388-1395 (2005)
Imaging with time-of-flight secondary ion mass spectrometry (TOF-SIMS) has expanded very rapidly with the development of gold cluster ion sources (Au3+). It is now possible to acquire ion density maps (ion images) on a tissue section without any trea
Externí odkaz:
https://doaj.org/article/072f5dc00e384013923d44e921ee7ac6
Autor:
José-Manuel Cancela, Oscar Bauer, Jean-Marc Edeline, Gabriel Benet, Antoine De Zelicourt, Catherine Sebrié, Cyrille Vaillend, Muriel Amar, Sabine De La Porte, Antony Galione, Philippe Fossier, Lora L Martucci, Anne Nosjean, Jacques Callebert, Rémi Chaussenot, Sylvie Granon, Jean-Marie Launay
Publikováno v:
FASEB Journal
FASEB Journal, 2019, 54, pp.fj.201800489R. ⟨10.1096/fj.201800489R⟩
FASEB Journal, Federation of American Society of Experimental Biology, 2019, 54, pp.fj.201800489R. ⟨10.1096/fj.201800489R⟩
FASEB Journal, Federation of American Society of Experimental Biology, 2019, 33 (5), pp.5823-5835. ⟨10.1096/fj.201800489R⟩
FASEB Journal, 2019, 54, pp.fj.201800489R. ⟨10.1096/fj.201800489R⟩
FASEB Journal, Federation of American Society of Experimental Biology, 2019, 54, pp.fj.201800489R. ⟨10.1096/fj.201800489R⟩
FASEB Journal, Federation of American Society of Experimental Biology, 2019, 33 (5), pp.5823-5835. ⟨10.1096/fj.201800489R⟩
International audience; Autism spectrum disorder (ASD) is characterized by early onset of behavioral and cognitive alterations. Low plasma levels of oxytocin (OT) have also been found in ASD patients; recently, a critical role for the enzyme CD38 in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6302ec700c2754cce805314269bdb029
https://doi.org/10.1096/fj.201800489r
https://doi.org/10.1096/fj.201800489r
Autor:
Emmanuel Chaubourt, Philippe Fossier, Gérard Baux, Christine Leprince, Maurice Israël, Sabine De La Porte
Publikováno v:
Neurobiology of Disease, Vol 6, Iss 6, Pp 499-507 (1999)
Duchenne muscular dystrophy (DMD), a severe X-linked recessive disorder which results in progressive muscle degeneration, is due to a lack of dystrophin, a membrane cytoskeletal protein. An approach to treatment is to compensate for dystrophin loss w
Externí odkaz:
https://doaj.org/article/d2300b663fb94273a070a27c8d8b0df5
Autor:
Alfredo D Guerron, Rashmi Rawat, Arpana Sali, Christopher F Spurney, Emidio Pistilli, Hee-Jae Cha, Gouri S Pandey, Ramkishore Gernapudi, Dwight Francia, Viken Farajian, Diana M Escolar, Laura Bossi, Magali Becker, Patricia Zerr, Sabine de la Porte, Heather Gordish-Dressman, Terence Partridge, Eric P Hoffman, Kanneboyina Nagaraju
Publikováno v:
PLoS ONE, Vol 5, Iss 6, p e11220 (2010)
The number of promising therapeutic interventions for Duchenne Muscular Dystrophy (DMD) is increasing rapidly. One of the proposed strategies is to use drugs that are known to act by multiple different mechanisms including inducing of homologous feta
Externí odkaz:
https://doaj.org/article/172d4c8d76d54f2eb4e255e3054e1d0a