Výsledky vyhledávání - Christian Hamel
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Molecular cloning and expression of RPE65, a novel retinal pigment epithelium-specific microsomal protein that is post-transcriptionally regulated in vitro Autor Christian Hamel, Ekaterini Tsilou, Bruce A. Pfeffer, John J. Hooks, Barbara Detrick, T. Michael Redmond
Vydáno 1993Artigo -
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OPA1 gene therapy prevents retinal ganglion cell loss in a Dominant Optic Atrophy mouse model Autor Emmanuelle Sarzi, Marie Seveno, Camille Piro-Mégy, Lucie Elzière, Mélanie Quilès, Marie O. Péquignot, Agnès Müller, Christian Hamel, Guy Lenaers, Cécile Delettre
Vydáno 2018Artigo -
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Mutations in CNNM4 Cause Recessive Cone-Rod Dystrophy with Amelogenesis Imperfecta Autor Bozena Polok, Pascal Escher, Aude Ambresin, Éliane Chouery, Sylvain Bolay, Isabelle Meunier, Francis Nan, Christian Hamel, Francis L. Munier, Bernard Thilo, André Mégarbané, Daniel F. Schorderet
Vydáno 2009Artigo -
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The Clinical Phenotype of <i>CNGA3</i>-Related Achromatopsia: Pretreatment Characterization in Preparation of a Gene Replacement Therapy Trial Autor Ditta Zobor, Annette Werner, Franco Stanzial, Francesco Benedicenti, Günther Rudolph, Ulrich Kellner, Christian Hamel, Sten Andréasson, Gergely Zobor, Torsten Straßer, Bernd Wissinger, Susanne Kohl, Eberhart Zrenner
Vydáno 2017Artigo -
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The human dynamin‐related protein OPA1 is anchored to the mitochondrial inner membrane facing the inter‐membrane space Autor Aurélien Olichon, Laurent J. Emorine, Eric Descoins, Laetitia Pelloquin, Laetitia Brichese, Nicole Gas, Emmanuelle Guillou, Cécile Delettre, Annie Valette, Christian Hamel, Bernard Ducommun, Guy Lenaers, Pascale Belenguer
Vydáno 2002Artigo -
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Enrichment of LOVD-USHbases with 152<i>USH2A</i>Genotypes Defines an Extensive Mutational Spectrum and Highlights Missense Hotspots Autor David Baux, Catherine Blanchet, Christian Hamel, Isabelle Meunier, Lise Larrieu, Valérie Faugère, Christel Vaché, Pierangela Castorina, Bernard Puech, Dominique Bonneau, Sue Malcolm, Mireille Claustres, Anne‐Françoise Roux
Vydáno 2014Artigo -
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TRPV4 channels mediate the infrared laser-evoked response in sensory neurons Autor Emmanuelle S. Albert, Jean‐Michel Bec, Gilles Desmadryl, Karim Chekroud, C. Travo, Sophie Gaboyard-Niay, Fabrice Bardin, Isabelle Marc, M. Dumas, Guy Lenaers, Christian Hamel, Andreas Müller, Christian Chabbert
Vydáno 2012Artigo -
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Effects of OPA1 mutations on mitochondrial morphology and apoptosis: Relevance to ADOA pathogenesis Autor Aurélien Olichon, Thomas Landes, Laetitia Pelloquin, Laurent J. Emorine, Valérie Mils, Agnès Guichet, Cécile Delettre, Christian Hamel, Patrizia Amati‐Bonneau, Dominique Bonneau, Pascal Reynier, Guy Lenaers, Pascale Belenguer
Vydáno 2006Artigo -
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Mutation in NDUFA13/GRIM19 leads to early onset hypotonia, dyskinesia and sensorial deficiencies, and mitochondrial complex I instability Autor Claire Angebault, Majida Charif, Naïg Guegen, Camille Piro-Mégy, Bénédicte Mousson de Camaret, Vincent Procaccio, Pierre‐Olivier Guichet, Maxime Hebrard, Gaël Manès, Nicolas Leboucq, François Rivier, Christian Hamel, Guy Lenaers, Agathe Roubertie
Vydáno 2015Artigo -
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Comprehensive survey of mutations in RP2 and RPGR in patients affected with distinct retinal dystrophies: genotype–phenotype correlations and impact on genetic counseling Autor Valérie Pelletier, Marguerite Jambou, Nathalie Delphin, Elena Zinovieva, Morgane Stum, Nadine Gigarel, Hélène Dollfus, Christian Hamel, Annick Toutain, Jean‐Louis Dufier, Olivier Roche, Arnold Münnich, Jean‐Paul Bonnefont, Josseline Kaplan, Jean‐Michel Rozet
Vydáno 2006Artigo -
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Clinical Outcome After Rectal Replacement With Side-to-End, Colon-J-Pouch, or Straight Colorectal Anastomosis Following Total Mesorectal Excision Autor Walter R. Marti, Gaudenz Curti, H Wehrli, Felix Grieder, Michael Graf, Beat Gloor, Markus Zuber, Nicolas Demartines, Fabrizio Fasolini, B. Lerf, Christoph Kettelhack, Christiane Andrieu, Martin Bigler, Stefanie Hayoz, Karin Ribi, Christian Hamel
Vydáno 2018Artigo -
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Leber congenital amaurosis: Comprehensive survey of the genetic heterogeneity, refinement of the clinical definition, and genotype-phenotype correlations as a strategy for molecula... Autor Sylvain Hanein, Isabelle Perrault, S. Gerber, Gaëlle Tanguy, Fabienne Barbet, Dominique Ducroq, Patrick Calvas, Hélène Dollfus, Christian Hamel, Tuija Löppönen, Francis L. Munier, Louisa Santos, Stavit A. Shalev, Dimitrios Zafeiriou, Jean‐Louis Dufier, Arnold Munnich, Jean‐Michel Rozet, Josseline Kaplan
Vydáno 2004Artigo -
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ER-mitochondria cross-talk is regulated by the Ca <sup>2+</sup> sensor NCS1 and is impaired in Wolfram syndrome Autor 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
Vydáno 2018Artigo -
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OPA1 links human mitochondrial genome maintenance to mtDNA replication and distribution Autor Ghizlane Elachouri, Sara Vidoni, Claudia Zanna, Alexandre Pattyn, Hassan Boukhaddaoui, Karen Gaget, Patrick Yu‐Wai‐Man, Giuseppe Gasparre, Emmanuelle Sarzi, Cécile Delettre, Aurélien Olichon, Dominique Loiseau, Pascal Reynier, Patrick F. Chinnery, Agnès Rötig, Valério Carelli, Christian Hamel, Michela Rugolo, Guy Lenaers
Vydáno 2010Artigo
Vyhledávací nástroje:
Související témata
Biology
Genetics
Gene
Medicine
Mutation
Retinal
Mitochondrion
Missense mutation
Ophthalmology
Pathology
Phenotype
Retinitis pigmentosa
Atrophy
Biochemistry
Cell biology
Mitochondrial DNA
Neuroscience
Anatomy
Blindness
Chemistry
Internal medicine
Optic nerve
Optic neuropathy
Optometry
Bardet–Biedl syndrome
Computational biology
Disease
Exome sequencing
Genetic heterogeneity
Molecular biology