Cecile Delettre

INSERM U1051, Institut of Neurosciences of Montpellier

Affiliated withINSERM U1051, Institut of Neurosciences of Montpellier

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 13	2017

Other Publications

Article	Year
OPA1 (Kjer type) dominant optic atrophy: a novel mitochondrial disease. Molecular genetics and metabolism\| PubMed ID: 11855928	2002
The human dynamin-related protein OPA1 is anchored to the mitochondrial inner membrane facing the inter-membrane space. FEBS letters\| PubMed ID: 12123827	2002
What similarity between human and fission yeast proteins is required for orthology? Yeast (Chichester, England)\| PubMed ID: 12237853	2002
Identification of preferentially expressed mRNAs in retina and cochlea. DNA and cell biology\| PubMed ID: 12489989	2002
Gene structure and chromosomal localization of mouse Opa1 : its exclusion from the Bst locus. BMC genetics\| PubMed ID: 12735796	2003
Mitochondrial dysfunction in CD47-mediated caspase-independent cell death: ROS production in the absence of cytochrome c and AIF release. Biochimie\| PubMed ID: 14585540	2003
Fourteen novel OPA1 mutations in autosomal dominant optic atrophy including two de novo mutations in sporadic optic atrophy. Human mutation\| PubMed ID: 14961560	2003
Expression of the Opa1 mitochondrial protein in retinal ganglion cells: its downregulation causes aggregation of the mitochondrial network. Investigative ophthalmology & visual science\| PubMed ID: 16249510	2005
AIFsh, a novel apoptosis-inducing factor (AIF) pro-apoptotic isoform with potential pathological relevance in human cancer. The Journal of biological chemistry\| PubMed ID: 16365034	2006
Identification and characterization of AIFsh2, a mitochondrial apoptosis-inducing factor (AIF) isoform with NADH oxidase activity. The Journal of biological chemistry\| PubMed ID: 16644725	2006
Mitochondrial dynamics and disease, OPA1. Biochimica et biophysica acta\| PubMed ID: 16737747	2006
Homozygous deletion related to Alu repeats in RLBP1 causes retinitis punctata albescens. Investigative ophthalmology & visual science\| PubMed ID: 17065479	2006
Effects of OPA1 mutations on mitochondrial morphology and apoptosis: relevance to ADOA pathogenesis. Journal of cellular physiology\| PubMed ID: 17167772	2007
Reversible optic neuropathy with OPA1 exon 5b mutation. Annals of neurology\| PubMed ID: 18360822	2008
OPA1 functions in mitochondria and dysfunctions in optic nerve. The international journal of biochemistry & cell biology\| PubMed ID: 19389483	2009
[From yeast to neurodegenerative diseases: ten years of exploration of mitochondrial dynamic disorders]. Medecine sciences : M/S\| PubMed ID: 20929674	2010
OPA1 links human mitochondrial genome maintenance to mtDNA replication and distribution. Genome research\| PubMed ID: 20974897	2011
Dominant optic atrophy. Orphanet journal of rare diseases\| PubMed ID: 22776096	2012
The human OPA1delTTAG mutation induces premature age-related systemic neurodegeneration in mouse. Brain : a journal of neurology\| PubMed ID: 23250881	2012
Relative frequencies of inherited retinal dystrophies and optic neuropathies in Southern France: assessment of 21-year data management. Ophthalmic epidemiology\| PubMed ID: 23350551	2013
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\| PubMed ID: 24136862	2013
Impairment of visual function and retinal ER stress activation in Wfs1-deficient mice. PloS one\| PubMed ID: 24823368	2014
Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neuropathies. American journal of human genetics\| PubMed ID: 26593267	2015
WFS1 in Optic Neuropathies: Mutation Findings in Nonsyndromic Optic Atrophy and Assessment of Clinical Severity. Ophthalmology\| PubMed ID: 27395765	2016