Cecile Delettre INSERM U1051, Institut of Neurosciences of Montpellier Biography Publications Institution JoVE Articles Cecile Delettre has not added a biography. If you are Cecile Delettre and would like to personalize this page please email our Author Liaison for assistance. Publications WFS1 in Optic Neuropathies: Mutation Findings in Nonsyndromic Optic Atrophy and Assessment of Clinical Severity Ophthalmology. Sep, 2016 | Pubmed ID: 27395765 Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neuropathies American Journal of Human Genetics. Nov, 2015 | Pubmed ID: 26593267 Impairment of Visual Function and Retinal ER Stress Activation in Wfs1-deficient Mice PloS One. 2014 | Pubmed ID: 24823368 A Novel Heterozygous OPA3 Mutation Located in the Mitochondrial Target Sequence Results in Altered Steady-state Levels and Fragmented Mitochondrial Network Journal of Medical Genetics. Dec, 2013 | Pubmed ID: 24136862 Relative Frequencies of Inherited Retinal Dystrophies and Optic Neuropathies in Southern France: Assessment of 21-year Data Management Ophthalmic Epidemiology. 2013 | Pubmed ID: 23350551 The Human OPA1delTTAG Mutation Induces Premature Age-related Systemic Neurodegeneration in Mouse Brain : a Journal of Neurology. Dec, 2012 | Pubmed ID: 23250881 Dominant Optic Atrophy Orphanet Journal of Rare Diseases. Jul, 2012 | Pubmed ID: 22776096 OPA1 Links Human Mitochondrial Genome Maintenance to MtDNA Replication and Distribution Genome Research. Jan, 2011 | Pubmed ID: 20974897 [From Yeast to Neurodegenerative Diseases: Ten Years of Exploration of Mitochondrial Dynamic Disorders] Medecine Sciences : M/S. Oct, 2010 | Pubmed ID: 20929674 OPA1 Functions in Mitochondria and Dysfunctions in Optic Nerve The International Journal of Biochemistry & Cell Biology. Oct, 2009 | Pubmed ID: 19389483 Reversible Optic Neuropathy with OPA1 Exon 5b Mutation Annals of Neurology. May, 2008 | Pubmed ID: 18360822 Effects of OPA1 Mutations on Mitochondrial Morphology and Apoptosis: Relevance to ADOA Pathogenesis Journal of Cellular Physiology. May, 2007 | Pubmed ID: 17167772 Homozygous Deletion Related to Alu Repeats in RLBP1 Causes Retinitis Punctata Albescens Investigative Ophthalmology & Visual Science. Nov, 2006 | Pubmed ID: 17065479 Mitochondrial Dynamics and Disease, OPA1 Biochimica Et Biophysica Acta. May-Jun, 2006 | Pubmed ID: 16737747 Identification and Characterization of AIFsh2, a Mitochondrial Apoptosis-inducing Factor (AIF) Isoform with NADH Oxidase Activity The Journal of Biological Chemistry. Jul, 2006 | Pubmed ID: 16644725 AIFsh, a Novel Apoptosis-inducing Factor (AIF) Pro-apoptotic Isoform with Potential Pathological Relevance in Human Cancer The Journal of Biological Chemistry. Mar, 2006 | Pubmed ID: 16365034 Expression of the Opa1 Mitochondrial Protein in Retinal Ganglion Cells: Its Downregulation Causes Aggregation of the Mitochondrial Network Investigative Ophthalmology & Visual Science. Nov, 2005 | Pubmed ID: 16249510 Fourteen Novel OPA1 Mutations in Autosomal Dominant Optic Atrophy Including Two De Novo Mutations in Sporadic Optic Atrophy Human Mutation. Jun, 2003 | Pubmed ID: 14961560 Mitochondrial Dysfunction in CD47-mediated Caspase-independent Cell Death: ROS Production in the Absence of Cytochrome C and AIF Release Biochimie. Aug, 2003 | Pubmed ID: 14585540 Gene Structure and Chromosomal Localization of Mouse Opa1 : Its Exclusion from the Bst Locus BMC Genetics. May, 2003 | Pubmed ID: 12735796 Identification of Preferentially Expressed MRNAs in Retina and Cochlea DNA and Cell Biology. Nov, 2002 | Pubmed ID: 12489989 What Similarity Between Human and Fission Yeast Proteins is Required for Orthology? Yeast (Chichester, England). Sep, 2002 | Pubmed ID: 12237853 The Human Dynamin-related Protein OPA1 is Anchored to the Mitochondrial Inner Membrane Facing the Inter-membrane Space FEBS Letters. Jul, 2002 | Pubmed ID: 12123827 OPA1 (Kjer Type) Dominant Optic Atrophy: a Novel Mitochondrial Disease Molecular Genetics and Metabolism. Feb, 2002 | Pubmed ID: 11855928 التصوير المقطعي التماسك البصري: التصوير الماوس العقدة الشبكية خلايا في فيفو Jolanta Jagodzinska*1, Emmanuelle Sarzi*1, Mélanie Cavalier1, Marie Seveno1, Volker Baecker2, Christian Hamel1,3,4, Marie Péquignot1, Cecile Delettre1 1INSERM U1051, Institut of Neurosciences of Montpellier, 2CNRS UMS3426, BioCampus Montepellier, 3University of Montpellier, 4CHRU Montpellier, Centre of Reference for Genetic Sensory Diseases, CHU Gui de Chauliac Hospital JoVE 55865 Neurociência
التصوير المقطعي التماسك البصري: التصوير الماوس العقدة الشبكية خلايا في فيفو Jolanta Jagodzinska*1, Emmanuelle Sarzi*1, Mélanie Cavalier1, Marie Seveno1, Volker Baecker2, Christian Hamel1,3,4, Marie Péquignot1, Cecile Delettre1 1INSERM U1051, Institut of Neurosciences of Montpellier, 2CNRS UMS3426, BioCampus Montepellier, 3University of Montpellier, 4CHRU Montpellier, Centre of Reference for Genetic Sensory Diseases, CHU Gui de Chauliac Hospital JoVE 55865 Neurociência