Emmanuelle Sarzi INSERM U1051, Institut of Neurosciences of Montpellier Biography Publications Institution JoVE Articles Emmanuelle Sarzi has not added a biography. If you are Emmanuelle Sarzi and would like to personalize this page please email our Author Liaison for assistance. Publications Targeted Metabolomics Reveals Early Dominant Optic Atrophy Signature in Optic Nerves of Opa1delTTAG/+ Mice Investigative Ophthalmology & Visual Science. Feb, 2017 | Pubmed ID: 28159969 Increase in Cardiac Ischemia-Reperfusion Injuries in Opa1+/- Mouse Model PloS One. 2016 | Pubmed ID: 27723783 Increased Steroidogenesis Promotes Early-onset and Severe Vision Loss in Females with OPA1 Dominant Optic Atrophy Human Molecular Genetics. Jun, 2016 | Pubmed ID: 27260406 OPA1-related Disorders: Diversity of Clinical Expression, Modes of Inheritance and Pathophysiology Neurobiology of Disease. Jun, 2016 | Pubmed ID: 26311407 In Vivo Time-lapse Imaging of Mitochondria in Healthy and Diseased Peripheral Myelin Sheath Mitochondrion. Jul, 2015 | Pubmed ID: 26031781 Neuroradiological Findings Expand the Phenotype of OPA1-related Mitochondrial Dysfunction Journal of the Neurological Sciences. Feb, 2015 | Pubmed ID: 25641387 Why Mitochondria Must Fuse to Maintain Their Genome Integrity Antioxidants & Redox Signaling. Aug, 2013 | Pubmed ID: 23350575 The Human OPA1delTTAG Mutation Induces Premature Age-related Systemic Neurodegeneration in Mouse Brain : a Journal of Neurology. Dec, 2012 | Pubmed ID: 23250881 OPA1 Links Human Mitochondrial Genome Maintenance to MtDNA Replication and Distribution Genome Research. Jan, 2011 | Pubmed ID: 20974897 [Mitochondrial Genome Instability and Associated Diseases] Medecine Sciences : M/S. Feb, 2010 | Pubmed ID: 20188049 Twinkle Helicase (PEO1) Gene Mutation Causes Mitochondrial DNA Depletion Annals of Neurology. Dec, 2007 | Pubmed ID: 17722119 Mutation of RRM2B, Encoding P53-controlled Ribonucleotide Reductase (p53R2), Causes Severe Mitochondrial DNA Depletion Nature Genetics. Jun, 2007 | Pubmed ID: 17486094 Mitochondrial DNA Depletion is a Prevalent Cause of Multiple Respiratory Chain Deficiency in Childhood The Journal of Pediatrics. May, 2007 | Pubmed ID: 17452231 A Novel Recurrent Mitochondrial DNA Mutation in ND3 Gene is Associated with Isolated Complex I Deficiency Causing Leigh Syndrome and Dystonia American Journal of Medical Genetics. Part A. Jan, 2007 | Pubmed ID: 17152068 MPV17 Encodes an Inner Mitochondrial Membrane Protein and is Mutated in Infantile Hepatic Mitochondrial DNA Depletion Nature Genetics. May, 2006 | Pubmed ID: 16582910 Molecular Diagnostics of Mitochondrial Disorders Biochimica Et Biophysica Acta. Dec, 2004 | Pubmed ID: 15576044 Optical Coherence Tomography: Imaging Mouse Retinal Ganglion Cells In Vivo 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 Neuroscience
Optical Coherence Tomography: Imaging Mouse Retinal Ganglion Cells In Vivo 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 Neuroscience
