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JOURNAL OF NEUROCHEMISTRY (2017)
Dysregulated mitophagy and mitochondrial organization in optic atrophy due to OPA1 mutations
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Restoration of Opa1-long isoform inhibits retinal injury-induced neurodegeneration
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JOURNAL OF MOLECULAR MEDICINE-JMM (2016)
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ACTA NEUROPATHOLOGICA (2016)
OPA1 functionally interacts with MIC60 but is dispensable for crista junction formation
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BNIP3 Protein Suppresses PINK1 Kinase Proteolytic Cleavage to Promote Mitophagy
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JOURNAL OF BIOLOGICAL CHEMISTRY (2016)
OPA1-related disorders: Diversity of clinical expression, modes of inheritance and pathophysiology
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Mitochondrial dysfunction in an Opa1Q285STOP mouse model of dominant optic atrophy results from Opa1 haploinsufficiency
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Loss of functional OPA1 unbalances redox state: implications in dominant optic atrophy pathogenesis
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ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY (2016)
Syndromic parkinsonism and dementia associated with OPA1 missense mutations
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ANNALS OF NEUROLOGY (2015)
Mitochondrial Ca2+ uptake correlates with the severity of the symptoms in autosomal dominant optic atrophy
Laszlo Fueloep et al.
CELL CALCIUM (2015)
Validation of a MGM1/OPA1 chimeric gene for functional analysis in yeast of mutations associated with dominant optic atrophy
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Trans-mitochondrial coordination of cristae at regulated membrane junctions
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'Behr syndrome' with OPA1 compound heterozygote mutations
Valerio Carelli et al.
BRAIN (2015)
Improved Locus-Specific Database for OPA1 Mutations Allows Inclusion of Advanced Clinical Data
Marc Ferre et al.
HUMAN MUTATION (2015)
Disturbed mitochondrial dynamics and neurodegenerative disorders
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NATURE REVIEWS NEUROLOGY (2015)
Early-onset Behr syndrome due to compound heterozygous mutations in OPA1
Dominique Bonneau et al.
BRAIN (2014)
Morphological and bioenergetic demands underlying the nnitophagy in post-mitotic neurons: the pink parkin pathway
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FRONTIERS IN AGING NEUROSCIENCE (2014)
Mitochondrial morphology in mitophagy and macroautophagy
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BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2013)
OPA1 loss of function affects in vitro neuronal maturation
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Mitochondrial Cristae Shape Determines Respiratory Chain Supercomplexes Assembly and Respiratory Efficiency
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Rheb Regulates Mitophagy Induced by Mitochondrial Energetic Status
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CELL METABOLISM (2013)
The E3 Ligase Parkin Maintains Mitochondrial Integrity by Increasing Linear Ubiquitination of NEMO
Anne Kathrin Mueller-Rischart et al.
MOLECULAR CELL (2013)
Dominant optic atrophy, OPA1, and mitochondrial quality control: understanding mitochondrial network dynamics
Marcel V. Alavi et al.
MOLECULAR NEURODEGENERATION (2013)
Guidelines for the use and interpretation of assays for monitoring autophagy
Daniel J. Klionsky et al.
AUTOPHAGY (2012)
The human OPA1delTTAG mutation induces premature age-related systemic neurodegeneration in mouse
Emmanuelle Sarzi et al.
BRAIN (2012)
Down-regulation of OPA1 alters mouse mitochondrial morphology, PTP function, and cardiac adaptation to pressure overload
Jerome Piquereau et al.
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OPA1 links human mitochondrial genome maintenance to mtDNA replication and distribution
Ghizlane Elachouri et al.
GENOME RESEARCH (2011)
Multi-system neurological disease is common in patients with OPA1 mutations
P. Yu-Wai-Man et al.
BRAIN (2010)
Selective degradation of p62 by autophagy
Yoshinobu Ichimura et al.
SEMINARS IN IMMUNOPATHOLOGY (2010)
A novel link between autophagy and the ubiquitin-proteasome system
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AUTOPHAGY (2009)
MONITORING AUTOPHAGY BY ELECTRON MICROSCOPY IN MAMMALIAN CELLS
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METHODS IN ENZYMOLOGY: AUTOPHAGY IN MAMMALIAN SYSTEMS, VOL 452, PT B (2009)
OPA1 Deficiency Associated with Increased Autophagy in Retinal Ganglion Cells in a Murine Model of Dominant Optic Atrophy
Kathryn E. White et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2009)
Hereditary optic neuropathies share a common mitochondrial coupling defect
Arnaud Chevrollier et al.
ANNALS OF NEUROLOGY (2008)
Mitochondrial oxidative phosphorylation in autosomal dominant optic atrophy
Vladimir I Mayorov et al.
BMC BIOCHEMISTRY (2008)
OPA1 mutations induce mitochondrial DNA instability and optic atrophy plus phenotypes
Patrizia Amati-Bonneau et al.
BRAIN (2008)
Fission and selective fusion govern mitochondrial segregation and elimination by autophagy
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EMBO JOURNAL (2008)
Characterization of OPA1 isoforms isolated from mouse tissues
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JOURNAL OF NEUROCHEMISTRY (2008)
The C-elegans opa1 homologue EAT-3 is essential for resistance to free radicals
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Proteolytic processing of OPA1 links mitochondrial dysfunction to alterations in mitochondrial morphology
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JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
OPA1 controls apoptotic cristae remodeling independently from mitochondrial fusion
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CELL (2006)
Mitochondrial dynamics and disease, OPA1
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BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2006)
OPA1 R445H mutation in optic atrophy associated with sensorineural deafness
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ANNALS OF NEUROLOGY (2005)
Another way to die: autophagic programmed cell death
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CELL DEATH AND DIFFERENTIATION (2005)
Msp1p is an intermembrane space dynamin-related protein that mediates mitochondrial fusion in a Dnm1p-dependent manner in S-pombe
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FEBS LETTERS (2005)
Mitochondrial fission in apoptosis, neurodegeneration and aging
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CURRENT OPINION IN CELL BIOLOGY (2003)
Loss of OPA1 perturbates the mitochondrial inner membrane structure and integrity, leading to cytochrome c release and apoptosis
A Olichon et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Mutation spectrum and splicing variants in the OPA1 gene
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HUMAN GENETICS (2001)
OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritance
UEA Pesch et al.
HUMAN MOLECULAR GENETICS (2001)
Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy
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NATURE GENETICS (2000)
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