相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Molecular mechanisms and physiological functions of mitophagy
Mashun Onishi et al.
EMBO JOURNAL (2021)
Self-assembly of multi-component mitochondrial nucleoids via phase separation
Marina Feric et al.
EMBO JOURNAL (2021)
ATAD3B is a mitophagy receptor mediating clearance of oxidative stress-induced damaged mitochondrial DNA
Li Shu et al.
EMBO JOURNAL (2021)
Function and regulation of the divisome for mitochondrial fission
Felix Kraus et al.
NATURE (2021)
Motor proteins at the mitochondria cytoskeleton interface
Antonina J. Kruppa et al.
JOURNAL OF CELL SCIENCE (2021)
Distinct fission signatures predict mitochondrial degradation or biogenesis
Tatjana Kleele et al.
NATURE (2021)
A549 cells contain enlarged mitochondria with independently functional clustered mtDNA nucleoids
Aleksandrs Nasonovs et al.
PLOS ONE (2021)
NMR identification of a conserved Drp1 cardiolipin-binding motif essential for stress-induced mitochondrial fission
Mukesh Mahajan et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2021)
Mitochondrial Dynamics and Its Involvement in Disease
David C. Chan
ANNUAL REVIEW OF PATHOLOGY: MECHANISMS OF DISEASE, VOL 15, 2020 (2020)
Fission and fusion machineries converge at ER contact sites to regulate mitochondrial morphology
Robert G. Abrisch et al.
JOURNAL OF CELL BIOLOGY (2020)
Comprehensive molecular characterization of mitochondrial genomes in human cancers
Yuan Yuan et al.
NATURE GENETICS (2020)
The MICOS complex, a structural element of mitochondria with versatile functions
Siavash Khosravi et al.
BIOLOGICAL CHEMISTRY (2020)
DNA-editing enzymes as potential treatments for heteroplasmic mtDNA diseases
U. Zekonyte et al.
JOURNAL OF INTERNAL MEDICINE (2020)
Reciprocal Regulation of Mitochondrial Fission and Fusion
Rasha Sabouny et al.
TRENDS IN BIOCHEMICAL SCIENCES (2020)
OPA1-Exon4b Binds to mtDNA D-Loop for Transcriptional and Metabolic Modulation, Independent of Mitochondrial Fusion
Liang Yang et al.
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY (2020)
FBXL4 deficiency increases mitochondrial removal by autophagy
David Alsina et al.
EMBO MOLECULAR MEDICINE (2020)
Lysocardiolipin acyltransferase regulates NSCLC cell proliferation and migration by modulating mitochondrial dynamics
Long Shuang Huang et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2020)
A novel homozygous variant in MICOS13/QIL1causes hepato-encephalopathy with mitochondrial DNA depletion syndrome
Yoshihito Kishita et al.
MOLECULAR GENETICS & GENOMIC MEDICINE (2020)
A bacterial cytidine deaminase toxin enables CRISPR-free mitochondrial base editing
Beverly Y. Mok et al.
NATURE (2020)
Visualizing, quantifying, and manipulating mitochondrial DNA in vivo
David L. Prole et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2020)
ER-mitochondria contacts promote mtDNA nucleoids active transportation via mitochondrial dynamic tubulation
Jinshan Qin et al.
NATURE COMMUNICATIONS (2020)
The Maintenance of Mitochondrial DNA Integrity and Dynamics by Mitochondrial Membranes
James Chapman et al.
LIFE-BASEL (2020)
The Functional Impact of Mitochondrial Structure Across Subcellular Scales
Brian Glancy et al.
FRONTIERS IN PHYSIOLOGY (2020)
Autophagy induction via STING trafficking is a primordial function of the cGAS pathway
Xiang Gui et al.
NATURE (2019)
The Expanding and Unexpected Functions of Mitochondria Contact Sites
Laura L. Lackner
TRENDS IN CELL BIOLOGY (2019)
Mechanisms of Mitochondrial DNA Deletion Formation
Nadee Nissanka et al.
TRENDS IN GENETICS (2019)
FBXL4-Related Mitochondrial DNA Depletion Syndrome 13 (MTDPS13): A Case Report With a Comprehensive Mutation Review
Rami A. Ballout et al.
FRONTIERS IN GENETICS (2019)
Mitochondrial dynamics and their potential as a therapeutic target
B. N. Whitley et al.
MITOCHONDRION (2019)
PINK1 attenuates mtDNA release in alveolar epithelial cells and TLR9 mediated profibrotic responses
Marta Bueno et al.
PLOS ONE (2019)
Mitochondrial fusion is required for regulation of mitochondrial DNA replication
Eduardo Silva Ramos et al.
PLOS GENETICS (2019)
The R941L mutation in MYH14 disrupts mitochondrial fission and associates with peripheral neuropathy
Walaa Almutawa et al.
EBIOMEDICINE (2019)
MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement
S. Donkervoort et al.
ACTA NEUROPATHOLOGICA (2019)
Characterization of the C584R variant in the mtDNA depletion syndrome gene FBXL4, reveals a novel role for FBXL4 as a regulator of mitochondrial fusion
Rasha Sabouny et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2019)
The Cellular Mitochondrial Genome Landscape in Diesease
Anne Hahn et al.
TRENDS IN CELL BIOLOGY (2019)
Relationship between OPA1 and cardiolipin in mitochondrial inner-membrane fusion
Tadato Ban et al.
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS (2018)
Mitophagy and Quality Control Mechanisms in Mitochondrial Maintenance
Sarah Pickles et al.
CURRENT BIOLOGY (2018)
A novel mechanism causing imbalance of mitochondrial fusion and fission in human myopathies
Marina Bartsakoulia et al.
HUMAN MOLECULAR GENETICS (2018)
ATAD3 controls mitochondrial cristae structure in mouse muscle, influencing mtDNA replication and cholesterol levels
Susana Peralta et al.
JOURNAL OF CELL SCIENCE (2018)
Novel recessive mutations in MSTO1 cause cerebellar atrophy with pigmentary retinopathy
Kazuhiro Iwama et al.
JOURNAL OF HUMAN GENETICS (2018)
BAK/BAX macropores facilitate mitochondrial herniation and mtDNA efflux during apoptosis
Kate McArthur et al.
SCIENCE (2018)
Linear mitochondrial DNA is rapidly degraded by components of the replication machinery
Viktoriya Peeva et al.
NATURE COMMUNICATIONS (2018)
The mitochondrial DNA polymerase gamma degrades linear DNA fragments precluding the formation of deletions
Nadee Nissanka et al.
NATURE COMMUNICATIONS (2018)
Endonuclease G promotes mitochondrial genome cleavage and replication
Rahel Stefanie Wiehe et al.
Oncotarget (2018)
Sam50 Regulates PINK1-Parkin-Mediated Mitophagy by Controlling PINK1 Stability and Mitochondrial Morphology
Fenglei Jian et al.
CELL REPORTS (2018)
Mitochondrial inner membrane permeabilisation enables mtDNA release during apoptosis
Joel S. Riley et al.
EMBO JOURNAL (2018)
Parkin and PINK1 mitigate STING-induced inflammation
Danielle A. Sliter et al.
NATURE (2018)
Separating and Segregating the Human Mitochondrial Genome
Thomas J. Nicholls et al.
TRENDS IN BIOCHEMICAL SCIENCES (2018)
Mesenchymal Stem Cells Shift Mitochondrial Dynamics and Enhance Oxidative Phosphorylation in Recipient Cells
Christopher Newell et al.
FRONTIERS IN PHYSIOLOGY (2018)
Clinical and Biochemical Features in a Patient With Mitochondrial Fission Factor Gene Alteration
Alessia Nasca et al.
FRONTIERS IN GENETICS (2018)
Mitochondrial-cytoskeletal interactions: dynamic associations that facilitate network function and remodeling
Andrew S. Moore et al.
CURRENT OPINION IN PHYSIOLOGY (2018)
Identification of New Activators of Mitochondrial Fusion Reveals a Link between Mitochondrial Morphology and Pyrimidine Metabolism
Laia Miret-Casals et al.
CELL CHEMICAL BIOLOGY (2018)
Molecular and clinical spectra of FBXL4 deficiency
Ayman W. El-Hattab et al.
HUMAN MUTATION (2017)
Recessive mutations in MSTO1 cause mitochondrial dynamics impairment, leading to myopathy and ataxia
Alessia Nasca et al.
HUMAN MUTATION (2017)
MtDNA-maintenance defects: syndromes and genes
Carlo Viscomi et al.
JOURNAL OF INHERITED METABOLIC DISEASE (2017)
Single-Molecule Analysis of mtDNA Replication Uncovers the Basis of the Common Deletion
Aaron F. Phillips et al.
MOLECULAR CELL (2017)
Molecular basis of selective mitochondrial fusion by heterotypic action between OPA1 and cardiolipin
Tadato Ban et al.
NATURE CELL BIOLOGY (2017)
Extracellular Mitochondrial DNA Is Generated by Fibroblasts and Predicts Death in Idiopathic Pulmonary Fibrosis
Changwan Ryu et al.
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE (2017)
MSTO1 is a cytoplasmic pro-mitochondrial fusion protein, whose mutation induces myopathy and ataxia in humans
Aniko Gal et al.
EMBO MOLECULAR MEDICINE (2017)
ATAD3 gene cluster deletions cause cerebellar dysfunction associated with altered mitochondrial DNA and cholesterol metabolism
Radha Desai et al.
BRAIN (2017)
FBXL4 defects are common in patients with congenital lactic acidemia and encephalomyopathic mitochondrial DNA depletion syndrome
H. Dai et al.
CLINICAL GENETICS (2017)
Mic60/Mitofilin determines MICOS assembly essential for mitochondrial dynamics and mtDNA nucleoid organization
H. Li et al.
CELL DEATH AND DIFFERENTIATION (2016)
CHCHD10 mutations promote loss of mitochondrial cristae junctions with impaired mitochondrial genome maintenance and inhibition of apoptosis
Emmanuelle C. Genin et al.
EMBO MOLECULAR MEDICINE (2016)
DNM1L-related mitochondrial fission defect presenting as refractory epilepsy
Jason R. Vanstone et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2016)
Tissue-specific modulation of mitochondrial DNA segregation by a defect in mitochondrial division
Riikka Jokinen et al.
HUMAN MOLECULAR GENETICS (2016)
Fatal infantile mitochondrial encephalomyopathy, hypertrophic cardiomyopathy and optic atrophy associated with a homozygous OPA1 mutation
Ronen Spiegel et al.
JOURNAL OF MEDICAL GENETICS (2016)
A novel de novo dominant negative mutation in DNM1L impairs mitochondrial fission and presents as childhood epileptic encephalopathy
Jill A. Fahrner et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2016)
Maintenance and Expression of Mammalian Mitochondrial DNA
Claes M. Gustafsson et al.
ANNUAL REVIEW OF BIOCHEMISTRY, VOL 85 (2016)
A novel mutation in FBXL4 in a Norwegian child with encephalomyopathic mitochondrial DNA depletion syndrome 13
Tuva Baroy et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS (2016)
Biallelic Mutations in DNM1L are Associated with a Slowly Progressive Infantile Encephalopathy
Alessia Nasca et al.
HUMAN MUTATION (2016)
Disturbed mitochondrial and peroxisomal dynamics due to loss of MFF causes Leigh-like encephalopathy, optic atrophy and peripheral neuropathy
Johannes Koch et al.
JOURNAL OF MEDICAL GENETICS (2016)
ER-mitochondria contacts couple mtDNA synthesis with mitochondrial division in human cells
Samantha C. Lewis et al.
SCIENCE (2016)
Mitochondrial nucleoid clusters protect newly synthesized mtDNA during Doxorubicin- and Ethidium Bromide-induced mitochondrial stress
Lukas Alan et al.
TOXICOLOGY AND APPLIED PHARMACOLOGY (2016)
Selective removal of deletion-bearing mitochondrial DNA in heteroplasmic Drosophila
Nikolay P. Kandul et al.
NATURE COMMUNICATIONS (2016)
Mitochondrial diseases
Grainne S. Gorman et al.
NATURE REVIEWS DISEASE PRIMERS (2016)
Mitochondrial cholesterol: mechanisms of import and effects on mitochondrial function
Laura A. Martin et al.
JOURNAL OF BIOENERGETICS AND BIOMEMBRANES (2016)
Cardiolipin is a key determinant for mtDNA stability and segregation during mitochondrial stress
Luis Alberto Luevano-Martinez et al.
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS (2015)
Mitochondrial DNA mutations in neurodegeneration
Michael J. Keogh et al.
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS (2015)
Titration of mitochondrial fusion rescues Mff-deficient cardiomyopathy
Hsiuchen Chen et al.
JOURNAL OF CELL BIOLOGY (2015)
Clinical, morphological, biochemical, imaging and outcome parameters in 21 individuals with mitochondrial maintenance defect related to FBXL4 mutations
Martina Huemer et al.
JOURNAL OF INHERITED METABOLIC DISEASE (2015)
Parkin modulates heteroplasmy of truncated mtDNA in Caenorhabditis elegans
Itay Valenci et al.
MITOCHONDRION (2015)
Mitochondrial DNA stress primes the antiviral innate immune response
A. Phillip West et al.
NATURE (2015)
The dynamics of mitochondrial DNA heteroplasmy: implications for human health and disease
James B. Stewart et al.
NATURE REVIEWS GENETICS (2015)
Endogenous Parkin Preserves Dopaminergic Substantia Nigral Neurons following Mitochondrial DNA Mutagenic Stress
Alicia M. Pickrell et al.
NEURON (2015)
Recurrent Stroke-Like Episodes in FBXL4-Associated Early-Onset Mitochondrial Encephalomyopathy
Darius Ebrahimi-Fakhari et al.
PEDIATRIC NEUROLOGY (2015)
A novel quantitative assay of mitophagy: Combining high content fluorescence microscopy and mitochondrial DNA load to quantify mitophagy and identify novel pharmacological tools against pathogenic heteroplasmic mtDNA
Alan Diot et al.
PHARMACOLOGICAL RESEARCH (2015)
Human Mitochondrial DNA-Protein Complexes Attach to a Cholesterol-Rich Membrane Structure
Joachim M. Gerhold et al.
SCIENTIFIC REPORTS (2015)
MICOS coordinates with respiratory complexes and lipids to establish mitochondrial inner membrane architecture
Jonathan R. Friedman et al.
ELIFE (2015)
A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement
Sylvie Bannwarth et al.
BRAIN (2014)
Proteolytic Cleavage of Opa1 Stimulates Mitochondrial Inner Membrane Fusion and Couples Fusion to Oxidative Phosphorylation
Prashant Mishra et al.
CELL METABOLISM (2014)
A new pathway for mitochondrial quality control: mitochondrial-derived vesicles
Ayumu Sugiura et al.
EMBO JOURNAL (2014)
Rapamycin drives selection against a pathogenic heteroplasmic mitochondrial DNA mutation
Ying Dai et al.
HUMAN MOLECULAR GENETICS (2014)
MPV17L2 is required for ribosome assembly in mitochondria
Ilaria Dalla Rosa et al.
NUCLEIC ACIDS RESEARCH (2014)
Mitofusin 2 mutations affect mitochondrial function by mitochondrial DNA depletion
Stefan Vielhaber et al.
ACTA NEUROPATHOLOGICA (2013)
Mutations in FBXL4 Cause Mitochondrial Encephalopathy and a Disorder of Mitochondrial DNA Maintenance
Penelope E. Bonnen et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2013)
Mutations in FBXL4, Encoding a Mitochondrial Protein, Cause Early-Onset Mitochondrial Encephalomyopathy
Xiaowu Gai et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2013)
Why Mitochondria Must Fuse to Maintain Their Genome Integrity
Sara Vidoni et al.
ANTIOXIDANTS & REDOX SIGNALING (2013)
Dihydro-orotate dehydrogenase is physically associated with the respiratory complex and its loss leads to mitochondrial dysfunction
JingXian Fang et al.
BIOSCIENCE REPORTS (2013)
Distribution of mitochondrial nucleoids upon mitochondrial network fragmentation and network reintegration in HEPG2 cells
Jan Tauber et al.
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY (2013)
UVC-Induced Mitochondrial Degradation via Autophagy Correlates with mtDNA Damage Removal in Primary Human Fibroblasts
Amanda S. Bess et al.
JOURNAL OF BIOCHEMICAL AND MOLECULAR TOXICOLOGY (2013)
Fis1, Mff, MiD49, and MiD51 mediate Drp1 recruitment in mitochondrial fission
Oliver C. Loson et al.
MOLECULAR BIOLOGY OF THE CELL (2013)
Dynamics of nucleoid structure regulated by mitochondrial fission contributes to cristae reformation and release of cytochrome c
Reiko Ban-Ishihara et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2013)
PINK1-Phosphorylated Mitofusin 2 Is a Parkin Receptor for Culling Damaged Mitochondria
Yun Chen et al.
SCIENCE (2013)
mtDNA makes a U-turn for the mitochondrial nucleoid
Christian Kukat et al.
TRENDS IN CELL BIOLOGY (2013)
Fusion and Fission: Interlinked Processes Critical for Mitochondrial Health
David C. Chan
ANNUAL REVIEW OF GENETICS, VOL 46 (2012)
Mitophagy in cells with mtDNA mutations Being sick is not enough
Rosa L. A. de Vries et al.
AUTOPHAGY (2012)
The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype
Cecile Rouzier et al.
BRAIN (2012)
MFN2, a new gene responsible for mitochondrial DNA depletion
Florence Renaldo et al.
BRAIN (2012)
Mitochondria: In Sickness and in Health
Jodi Nunnari et al.
CELL (2012)
Mitochondrial autophagy in cells with mtDNA mutations results from synergistic loss of transmembrane potential and mTORC1 inhibition
Robert W. Gilkerson et al.
HUMAN MOLECULAR GENETICS (2012)
Lysocardiolipin acyltransferase 1 (ALCAT1) controls mitochondrial DNA fidelity and biogenesis through modulation of MFN2 expression
Jia Li et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2012)
Role of MINOS in mitochondrial membrane architecture and biogenesis
Martin van der Laan et al.
TRENDS IN CELL BIOLOGY (2012)
Human mitochondrial transcription factor A is required for the segregation of mitochondrial DNA in cultured cells
Katsumi Kasashima et al.
EXPERIMENTAL CELL RESEARCH (2011)
OPA1 links human mitochondrial genome maintenance to mtDNA replication and distribution
Ghizlane Elachouri et al.
GENOME RESEARCH (2011)
A Complex Phenotype of Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss is Linked to an Autosomal Dominant Mutation in MYH14
Byung-Ok Choi et al.
HUMAN MUTATION (2011)
During autophagy mitochondria elongate, are spared from degradation and sustain cell viability
Ligia C. Gomes et al.
NATURE CELL BIOLOGY (2011)
Actin and myosin contribute to mammalian mitochondrial DNA maintenance
A. Reyes et al.
NUCLEIC ACIDS RESEARCH (2011)
Tubular network formation protects mitochondria from autophagosomal degradation during nutrient starvation
Angelika S. Rambold et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
Super-resolution microscopy reveals that mammalian mitochondrial nucleoids have a uniform size and frequently contain a single copy of mtDNA
Christian Kukat et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
ER Tubules Mark Sites of Mitochondrial Division
Jonathan R. Friedman et al.
SCIENCE (2011)
Physiological functions of mitochondrial fusion
Hsiuchen Chen et al.
MITOCHONDRIAL RESEARCH IN TRANSLATIONAL MEDICINE (2010)
Functional complementation of mitochondrial DNAs: Mobilizing mitochondrial genetics against dysfunction
Eric A. Schon et al.
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS (2010)
Mitochondrial Fusion Is Required for mtDNA Stability in Skeletal Muscle and Tolerance of mtDNA Mutations
Hsiuchen Chen et al.
CELL (2010)
Parkin overexpression selects against a deleterious mtDNA mutation in heteroplasmic cybrid cells
Der-Fen Suen et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Inhibition of mitochondrial fission favours mutant over wild-type mitochondrial DNA
Adriana Malena et al.
HUMAN MOLECULAR GENETICS (2009)
Anticancer DNA intercalators cause p53-dependent mitochondrial DNA nucleoid re-modelling
N. Ashley et al.
ONCOGENE (2009)
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
Gilad Twig et al.
EMBO JOURNAL (2008)
Mitochondrial nucleoids maintain genetic autonomy but allow for functional complementation
Robert W. Gilkerson et al.
JOURNAL OF CELL BIOLOGY (2008)
Preventing Mitochondrial Fission Impairs Mitochondrial Function and Leads to Loss of Mitochondrial DNA
Philippe A. Parone et al.
PLOS ONE (2008)
The layered structure of human mitochondrial DNA nucleoids
Daniel F. Bogenhagen et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions:: a novel disorder of mtDNA maintenance
Gavin Hudson et al.
BRAIN (2008)
Mitochondrial fusion protects against neurodegeneration in the cerebellum
Hsiuchen Chen et al.
CELL (2007)
A lethal defect of mitochondrial and peroxisomal fission
Hans R. Waterham et al.
NEW ENGLAND JOURNAL OF MEDICINE (2007)
The AAA+ protein ATAD3 has displacement loop binding properties and is involved in mitochondrial nucleoid organization
Jiuya He et al.
JOURNAL OF CELL BIOLOGY (2007)
Cardiolipin metabolism and Barth Syndrome
KD Hauff et al.
PROGRESS IN LIPID RESEARCH (2006)
The functional organization of mitochondrial genomes in human cells
Francisco J. Iborra et al.
BMC BIOLOGY (2004)
Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A
S Züchner et al.
NATURE GENETICS (2004)
Evidence for a two membrane-spanning autonomous mitochondrial DNA replisome
S Meeusen et al.
JOURNAL OF CELL BIOLOGY (2003)
Dynamics of mitochondrial morphology in healthy cells and during apoptosis
M Karbowski et al.
CELL DEATH AND DIFFERENTIATION (2003)
Mitofusins Mfn1 and Mfn2 coordinately regulate mitochondrial fusion and are essential for embryonic development
HC Chen et al.
JOURNAL OF CELL BIOLOGY (2003)
OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28
C Alexander et al.
NATURE GENETICS (2000)
分享论文
