Torthaí cuardaigh - Benjamin Delprat
- 1 - 7 toradh as 7 á dtaispeáint
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1
Wolfram syndrome: MAMs’ connection? de réir Benjamin Delprat, Tangui Maurice, Cécile Delettre
Foilsithe / Cruthaithe 2018Revisão -
2
FXYD6 Is a Novel Regulator of Na,K-ATPase Expressed in the Inner Ear de réir Benjamin Delprat, Danièle Schaer, Sophie Roy, Jing Wang, Jean‐Luc Puel, Käthi Geering
Foilsithe / Cruthaithe 2007Artigo -
3
Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells de réir Avital Adato, G. Lefèvre, Benjamin Delprat, Vincent Michel, Nicolas Michalski, Sébastien Chardenoux, Dominique Weil, A. Amraoui, Christine Petit
Foilsithe / Cruthaithe 2005Artigo -
4
Tmprss3, a Transmembrane Serine Protease Deficient in Human DFNB8/10 Deafness, Is Critical for Cochlear Hair Cell Survival at the Onset of Hearing de réir Lydie Fasquelle, Hamish S. Scott, Marc Lenoir, Jing Wang, Guy Rebillard, Sophie Gaboyard-Niay, Stéphanie Ventéo, Florence François, Anne-Laure Mausset-Bonnefont, Stylianos E. Antonarakis, Elizabeth Neidhart, Christian Chabbert, Jean‐Luc Puel, Michel Guipponi, Benjamin Delprat
Foilsithe / Cruthaithe 2011Artigo -
5
Activation of the sigma-1 receptor chaperone alleviates symptoms of Wolfram syndrome in preclinical models de réir Lucie Crouzier, Alberto Danese, Yuko Yasui, Élodie M. Richard, Jean-Charles Liévens, Simone Patergnani, Simon Couly, Camille Diez, Morgane Denus, Nicolas Cubedo, Mireille Rossel, Marc Thiry, Tsung‐Ping Su, Paolo Pinton, Tangui Maurice, Benjamin Delprat
Foilsithe / Cruthaithe 2022Artigo -
6
ER-mitochondria cross-talk is regulated by the Ca <sup>2+</sup> sensor NCS1 and is impaired in Wolfram syndrome de réir Claire Angebault, Jérémy Fauconnier, Simone Patergnani, Jennifer Rieusset, Alberto Danese, Corentin Affortit, Jolanta Jagodzinska, Camille Mégy, Mélanie Quilès, Chantal Cazevieille, Julia Korchagina, Delphine Bonnet-Wersinger, Dan Miléa, Christian Hamel, Paolo Pinton, Marc Thiry, Alain Lacampagne, Benjamin Delprat, Cécile Delettre
Foilsithe / Cruthaithe 2018Artigo -
7
Impairment of SLC17A8 Encoding Vesicular Glutamate Transporter-3, VGLUT3, Underlies Nonsyndromic Deafness DFNA25 and Inner Hair Cell Dysfunction in Null Mice de réir Jérôme Ruel, Sarah B. Emery, Régis Nouvian, Tiphaine Bersot, Bénédicte Amilhon, Jana M. Van Rybroek, Guy Rebillard, Marc Lenoir, Michel Eybalin, Benjamin Delprat, Theru A. Sivakumaran, Bruno Giros, Salah El Mestikawy, Tobias Moser, Richard J. Smith, Marci M. Lesperance, Jean‐Luc Puel
Foilsithe / Cruthaithe 2008Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Biology
Cell biology
Medicine
Anatomy
Biochemistry
Chemistry
Gene
Genetics
Hair cell
Inner ear
Mitochondrion
Neuroscience
Pathology
Receptor
Apoptosis
Audiology
Cochlea
Endocrinology
Endoplasmic reticulum
Hearing loss
Immunology
Unfolded protein response
ATPase
Agonist
Amyotrophic lateral sclerosis
Atrophy
Auditory neuropathy
Auditory system
Autophagy
Bioinformatics