Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A

Mitofusins Mfn1 and Mfn2 coordinately regulate mitochondrial fusion and are essential for embryonic development

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Control of mitochondrial morphology by a human mitofusin

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Spatial and temporal association of Bax with mitochondrial fission sites, Drp1, and Mfn2 during apoptosis

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Mitofusin-2 Determines Mitochondrial Network Architecture and Mitochondrial Metabolism

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Charcot-Marie-Tooth Disease Type 2A Caused by Mutation in a Microtubule Motor KIF1Bβ

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Developmentally Regulated Mitochondrial Fusion Mediated by a Conserved, Novel, Predicted GTPase

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Membrane topology and mitochondrial targeting of mitofusins, ubiquitous mammalian homologs of the transmembrane GTPase Fzo

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Mitochondrial transmission during mating in Saccharomyces cerevisiae is determined by mitochondrial fusion and fission and the intramitochondrial segregation of mitochondrial DNA.

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Mitochondrial filaments and clusters as intracellular power-transmitting cables

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Human cells are protected from mitochondrial dysfunction by complementation of DNA products in fused mitochondria

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Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies

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Small molecule agonist of mitochondrial fusion repairs mitochondrial dysfunction

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Mitochondrial Fragmentation Is Involved in Methamphetamine-Induced Cell Death in Rat Hippocampal Neural Progenitor Cells

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Cell Death Pathways in Parkinson's Disease: Role of Mitochondria

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Molecular Events Underlying Parkinson’s Disease – An Interwoven Tapestry

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Mitochondrial Dynamics and Parkinson's Disease: Focus on Parkin

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Signalling endosomes in axonal transport: Travel updates on the molecular highway

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MFN2-associated lipomatosis: Clinical spectrum and impact on adipose tissue

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Implications of mitochondrial dynamics on neurodegeneration and on hypothalamic dysfunction

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Molecular Genetics of Autosomal-Dominant Axonal Charcot-Marie-Tooth Disease

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An emerging role for mitochondrial dynamics in schizophrenia

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Lethal Disorder of Mitochondrial Fission Caused by Mutations in DNM1L

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Development of pharmacological strategies for mitochondrial disorders

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Axonal Transport Defects in a Mitofusin 2 Loss of Function Model of Charcot-Marie-Tooth Disease in Zebrafish

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Rapid degradation of mutant SLC25A46 by the ubiquitin-proteasome system results in MFN1/2-mediated hyperfusion of mitochondria

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GARS axonopathy: not every neuron's cup of tRNA

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Disorders of mitochondrial function

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Sequencing of C harcot– M arie– T ooth disease genes in a toxic polyneuropathy

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Translating m-AAA protease function in mitochondria to hereditary spastic paraplegia

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Whole-exome sequencing in patients with inherited neuropathies: outcome and challenges

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Charcot–Marie–Tooth disease and intracellular traffic

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The Gdap1 knockout mouse mechanistically links redox control to Charcot–Marie–Tooth disease

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Mitochondrial Dysfunction in Neuromuscular Disorders

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Regulation and Physiologic Functions of GTPases in Mitochondrial Fusion and Fission in Mammals

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Mitochondrial Dynamics in Cancer and Neurodegenerative and Neuroinflammatory Diseases

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Different Roles of Mitochondria in Cell Death and Inflammation: Focusing on Mitochondrial Quality Control in Ischemic Stroke and Reperfusion

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Cerebral involvement in axonal Charcot-Marie-Tooth neuropathy caused by mitofusin2 mutations

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Key Targets for Multi-Target Ligands Designed to Combat Neurodegeneration

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Mitochondrial morphology and dynamics in hepatocytes from normal and ethanol-fed rats

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Molecular mechanism of mitochondrial membrane fusion

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Analysis of functional domains of rat mitochondrial Fis1, the mitochondrial fission-stimulating protein

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Synaptic Deficits at Neuromuscular Junctions in Two Mouse Models of Charcot–Marie–Tooth Type 2d

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Loss of MICOS complex integrity and mitochondrial damage, but not TDP-43 mitochondrial localisation, are likely associated with severity of CHCHD10-related diseases

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Sorting out the inherited neuropathies.

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Mitochondrial dynamics in the regulation of neuronal cell death

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Domain Interactions within Fzo1 Oligomers Are Essential for Mitochondrial Fusion

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Mitochondrial regulation of local supply of energy in neurons

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Charcot-Marie-Tooth neuropathy type 2A: novel mutations in the mitofusin 2 gene (MFN2)

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Impact of nitric oxide on metabolism in health and age‐related disease

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Sodium Channels Contribute to Degeneration of Dorsal Root Ganglion Neurites Induced by Mitochondrial Dysfunction in anIn VitroModel of Axonal Injury

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Altered expression and coregulation of dopamine signalling genes in schizophrenia and bipolar disorder

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Loss of SLC25A46 causes neurodegeneration by affecting mitochondrial dynamics and energy production in mice

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Regulation of Mitochondrial Dynamics and Cell Fate

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Potential for therapeutic targeting of AKAP signaling complexes in nervous system disorders

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Down-regulation of Mortalin Exacerbates Aβ-mediated Mitochondrial Fragmentation and Dysfunction

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Mitochondrial trafficking and morphology in neuronal injury

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A novel mechanism causing imbalance of mitochondrial fusion and fission in human myopathies

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Mitofusins as mitochondrial anchors and tethers

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TRPV4 disrupts mitochondrial transport and causes axonal degeneration via a CaMKII-dependent elevation of intracellular Ca2+

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Lipodystrophy: A paradigm for understanding the consequences of "overloading" adipose tissue

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Mitochondrial dynamics and mitochondrial autophagy: Molecular structure, orchestrating mechanism and related disorders

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Mitochondrial biogenesis and fragmentation as regulators of protein degradation in striated muscles

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Loss of Drp1 function alters OPA1 processing and changes mitochondrial membrane organization

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Cell signaling and mitochondrial dynamics: Implications for neuronal function and neurodegenerative disease

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Mitochondrial Genetics and Disease

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Genes Linking Mitochondrial Function, Cognitive Impairment and Depression are Associated with Endophenotypes Serving Precision Medicine

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Inhibition of histone deacetylase 6 (HDAC6) protects against vincristine-induced peripheral neuropathies and inhibits tumor growth

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Lipid signaling on the mitochondrial surface

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Mitochondrial protein import regulates cytosolic protein homeostasis and neuronal integrity

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Mitochondrially-targeted treatment strategies

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Gender-specific regulation of mitochondrial fusion and fission gene transcription and viability of cortical astrocytes by steroid hormones

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Mitochondria and the Brain: Bioenergetics and Beyond

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Optic atrophy 3 as a protein of the mitochondrial outer membrane induces mitochondrial fragmentation

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Zebrafish as a model system for mitochondrial biology and diseases

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Reduction of endoplasmic reticulum stress attenuates the defects caused by Drosophila mitofusin depletion

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Measuring Mitochondrial Shape with ImageJ

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Mitochondrial Dynamics

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Mitochondrial Involvement in Amyotrophic Lateral Sclerosis: Trigger or Target?

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Functional characterisation of ganglioside-induced differentiation-associated protein 1 as a glutathione transferase

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Insights on altered mitochondrial function and dynamics in the pathogenesis of neurodegeneration

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Selective mitochondrial depletion, apoptosis resistance, and increased mitophagy in human Charcot-Marie-Tooth 2A motor neurons

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Mitochondrial dynamics in exercise physiology

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Adult skeletal muscle deletion of Mitofusin 1 and 2 impedes exercise performance and training capacity

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HDAC6 inhibition promotes α-tubulin acetylation and ameliorates CMT2A peripheral neuropathy in mice

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Mfn2 localization in the ER is necessary for its bioenergetic function and neuritic development

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Less than perfect divorces: dysregulated mitochondrial fission and neurodegeneration

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Ugo1p Is a Multipass Transmembrane Protein with a Single Carrier Domain Required for Mitochondrial Fusion

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Normal role of the low‐molecular‐weight neurofilament protein in mitochondrial dynamics and disruption in Charcot‐Marie‐Tooth disease

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Relationship between OPA1 and cardiolipin in mitochondrial inner-membrane fusion

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Intersection of mitochondrial fission and fusion machinery with apoptotic pathways: Role of Mcl‐1

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Burst mitofusin activation reverses neuromuscular dysfunction in murine CMT2A

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Mitochondria, Bioenergetics and Excitotoxicity: New Therapeutic Targets in Perinatal Brain Injury

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Phenotypic spectrum of MFN2 mutations in the Spanish population

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GASZ and mitofusin‐mediated mitochondrial functions are crucial for spermatogenesis

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OPA1: 516 unique variants and 831 patients registered in an updated centralized Variome database

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Mitochondria and heart failure: new insights into an energetic problem.

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Induced pluripotent stem cell-derived motor neurons of CMT type 2 patients reveal progressive mitochondrial dysfunction

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Mitochondrial GTPase mitofusin 2 mutation in Charcot?Marie?Tooth neuropathy type 2A

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Mitochondrial fusion protein mutated in CMT2A

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Clinical and Genetic Characteristics in Patients of Charcot-Marie-Tooth type 2A with Mitofusin 2 (MFN2) Mutations

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Mitofusin 2 (MFN2) �쑀�쟾�옄 �룎�뿰蹂��씠媛� �엳�뒗 Charcot-Marie-Tooth 2A �솚�옄�뱾�쓽 �엫�긽 諛� �쑀�쟾�븰�쟻 �듅�꽦

源��꽭�썕, 源��듅誘�, & �꽑�슦�씪�궓 (2006) · YUHSpace (Yonsei University Medical Library)

Mitochondrial GTPase mitofusin 2 mutations in Korean patients with Charcot‐Marie‐Tooth neuropathy type 2

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