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Mitofusin-2 Determines Mitochondrial Network Architecture and Mitochondrial Metabolism
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Mitochondrial movement and morphology depend on an intact actin cytoskeleton in Aspergillus nidulans
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Yeast mitochondrial dynamics: Fusion, division, segregation, and shape
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The Use of the Reverse Transcription-Competitive Polymerase Chain Reaction to Investigate thein VivoRegulation of Gene Expression in Small Tissue Samples
inferredcites →https://doi.org/10.1007/bf00324678openalex-snapshot
Normal mitochondrial structure and genome maintenance in yeast requires the dynamin-like product of the MGM1 gene
inferredcites →https://doi.org/10.1007/s001250051163openalex-snapshot
Defective regulation of phosphatidylinositol-3-kinase gene expression in skeletal muscle and adipose tissue of non-insulin-dependent diabetes mellitus patients
inferredcites →https://doi.org/10.1016/0005-2728(78)90104-4openalex-snapshot
Mitochondrial framework (reticulum mitochondriale) in rat diaphragm muscle
inferredcites →https://doi.org/10.1016/s0021-9258(17)37547-6openalex-snapshot
Perinatal hypothyroidism impairs the normal transition of GLUT4 and GLUT1 glucose transporters from fetal to neonatal levels in heart and brown adipose tissue. Evidence for tissue-specific regulation of GLUT4 expression by thyroid hormone.
inferredcites →https://doi.org/10.1016/s0074-7696(08)61205-xopenalex-snapshot
Behavior of Mitochondria in the Living Cell
inferredcites →https://doi.org/10.1016/s0092-8674(00)80319-0openalex-snapshot
Developmentally Regulated Mitochondrial Fusion Mediated by a Conserved, Novel, Predicted GTPase
inferredcites →https://doi.org/10.1016/s0303-7207(98)00132-4openalex-snapshot
Longitudinal study of tissue- and subunit-specific obesity-induced regulation of the pyruvate dehydrogenase complex
inferredcites →https://doi.org/10.1016/s0962-8924(01)02246-2openalex-snapshot
Mitochondrial dynamics and division in budding yeast
inferredcites →https://doi.org/10.1016/s0968-0004(00)01735-7openalex-snapshot
Mitochondrial filaments and clusters as intracellular power-transmitting cables
inferredcites →https://doi.org/10.1038/79936openalex-snapshot
Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy
inferredcites →https://doi.org/10.1038/79944openalex-snapshot
OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28
inferredcites →https://doi.org/10.1038/ng0596-18openalex-snapshot
Leptin receptor missense mutation in the fatty Zucker rat
inferredcites →https://doi.org/10.1038/nm1195-1155openalex-snapshot
Leptin levels in human and rodent: Measurement of plasma leptin and ob RNA in obese and weight-reduced subjects
inferredcites →https://doi.org/10.1042/bj1780733openalex-snapshot
Glucose metabolism in perfused skeletal muscle. Demonstration of insulin resistance in the obese Zucker rat
inferredcites →https://doi.org/10.1042/bj1860525openalex-snapshot
Insulin resistance in soleus muscle from obese Zucker rats. Involvement of several defective sites
inferredcites →https://doi.org/10.1042/bj3240455openalex-snapshot
Heterologous expression of rab4 reduces glucose transport and GLUT4 abundance at the cell surface in oocytes
inferredcites →https://doi.org/10.1073/pnas.91.19.8802openalex-snapshot
An efficient and flexible system for construction of adenovirus vectors with insertions or deletions in early regions 1 and 3.
inferredcites →https://doi.org/10.1074/jbc.273.32.20150openalex-snapshot
Fzo1p Is a Mitochondrial Outer Membrane Protein Essential for the Biogenesis of Functional Mitochondria in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1074/jbc.274.25.17626openalex-snapshot
Factors Involved in GLUT-1 Glucose Transporter Gene Transcription in Cardiac Muscle
inferredcites →https://doi.org/10.1074/jbc.m203036200openalex-snapshot
Human Mitochondrial Thioredoxin
inferredcites →https://doi.org/10.1083/jcb.107.2.481openalex-snapshot
Coupling membranes as energy-transmitting cables. I. Filamentous mitochondria in fibroblasts and mitochondrial clusters in cardiomyocytes.
inferredcites →https://doi.org/10.1083/jcb.143.2.333openalex-snapshot
The Dynamin-related GTPase, Dnm1p, Controls Mitochondrial Morphology in Yeast
inferredcites →https://doi.org/10.1083/jcb.143.2.351openalex-snapshot
A Human Dynamin-related Protein Controls the Distribution of Mitochondria
inferredcites →https://doi.org/10.1083/jcb.144.4.711openalex-snapshot
The Yeast Dynamin-like Protein, Mgm1p, Functions on the Mitochondrial Outer Membrane to Mediate Mitochondrial Inheritance
inferredcites →https://doi.org/10.1083/jcb.151.2.333openalex-snapshot
Gag3p, an Outer Membrane Protein Required for Fission of Mitochondrial Tubules
inferredcites →https://doi.org/10.1083/jcb.151.2.341openalex-snapshot
The Dynamin-Related Gtpase, Mgm1p, Is an Intermembrane Space Protein Required for Maintenance of Fusion Competent Mitochondria
inferredcites →https://doi.org/10.1083/jcb.151.2.353openalex-snapshot
Mdv1p Is a Wd Repeat Protein That Interacts with the Dynamin-Related Gtpase, Dnm1p, to Trigger Mitochondrial Division
inferredcites →https://doi.org/10.1083/jcb.151.2.367openalex-snapshot
Dnm1p Gtpase-Mediated Mitochondrial Fission Is a Multi-Step Process Requiring the Novel Integral Membrane Component Fis1p
inferredcites →https://doi.org/10.1091/mbc.8.7.1233openalex-snapshot
Mitochondrial transmission during mating in Saccharomyces cerevisiae is determined by mitochondrial fusion and fission and the intramitochondrial segregation of mitochondrial DNA.
inferredcites →https://doi.org/10.1093/dnares/3.5.321openalex-snapshot
Prediction of the Coding Sequences of Unidentified Human Genes. VI. The Coding Sequences of 80 New Genes (KIAA0201-KIAA0280) Deduced by Analysis of cDNA Clones from Cell Line KG-1 and Brain
inferredcites →https://doi.org/10.1093/emboj/21.7.1616openalex-snapshot
Mitochondria are morphologically and functionally heterogeneous within cells
inferredcites →https://doi.org/10.1093/jn/116.9.1841openalex-snapshot
Effect of Treadmill Training on Muscle Oxidative Capacity and Accretion in Young Male Obese and Nonobese Zucker Rats
inferredcites →https://doi.org/10.1096/fasebj.12.15.1739openalex-snapshot
Overexpression of muscle uncoupling protein 2 content in human obesity associates with reduced skeletal muscle lipid utilization
inferredcites →https://doi.org/10.1111/j.1365-2818.1986.tb04282.xopenalex-snapshot
Estimation of surface area from vertical sections
inferredcites →https://doi.org/10.1111/j.1471-4159.1991.tb11435.xopenalex-snapshot
Fatty Acid Oxidation and Ketogenesis by Astrocytes in Primary Culture
inferredcites →https://doi.org/10.1113/jphysiol.1995.sp020786openalex-snapshot
Mitochondrial membrane potential in single living adult rat cardiac myocytes exposed to anoxia or metabolic inhibition.
inferredcites →https://doi.org/10.1152/ajpcell.1986.251.3.c395openalex-snapshot
Mitochondrial reticulum in limb skeletal muscle
inferredcites →https://doi.org/10.1152/jappl.1989.67.5.1807openalex-snapshot
Muscle morphological and biochemical adaptations to training in obese Zucker rats
inferredcites →https://doi.org/10.1172/jci108559openalex-snapshot
Decreased basal, noninsulin-stimulated glucose uptake and metabolism by skeletal soleus muscle isolated from obese-hyperglycemic (ob/ob) mice.
inferredcites →https://doi.org/10.1210/endo.139.12.6360openalex-snapshot
p70 S6 Kinase Activation Is Not Required for Insulin-Like Growth Factor-Induced Differentiation of Rat, Mouse, or Human Skeletal Muscle Cells**This work was supported by research grants from the Direccion General de Investigacion Cientifica y Tecnica (PB95/0971), Fondo de Investigacion Sanitaria…
inferredcites →https://doi.org/10.1242/jcs.114.5.867openalex-snapshot
Control of mitochondrial morphology by a human mitofusin
inferredcites →https://doi.org/10.1242/jcs.115.8.1663openalex-snapshot
Membrane topology and mitochondrial targeting of mitofusins, ubiquitous mammalian homologs of the transmembrane GTPase Fzo
inferredcites →https://doi.org/10.2337/diabetes.49.5.677openalex-snapshot
Fuel selection in human skeletal muscle in insulin resistance: a reexamination.
inferredcites →https://doi.org/10.2337/diabetes.50.6.1389openalex-snapshot
Increased Fatty Acid Uptake and Altered Fatty Acid Metabolism in Insulin-Resistant Muscle of Obese Zucker Rats
inferredcites →https://doi.org/10.2337/diabetes.51.10.2944openalex-snapshot
Dysfunction of Mitochondria in Human Skeletal Muscle in Type 2 Diabetes
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Dual GLP-1/GIP agonist tirzepatide modulates hepatic mitochondrial fusion–fission gene expression and oxidative stress in diabetic rats
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Molecular evolution of proteins mediating mitochondrial fission–fusion dynamics
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Functional interplay of lipid droplets and mitochondria
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Mitofusin 1 Drives Preimplantation Development by Enhancing Chromatin Incorporation of Histone H3.3
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FABP4 as a Mediator of Lipid Metabolism and Pregnant Uterine Dysfunction in Obesity
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Oxidative Phosphorylation in Uncoupled Mitochondria
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Compromised hepatic mitochondrial fatty acid oxidation and reduced markers of mitochondrial turnover in human NAFLD
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Role of Skeletal Muscle in Insulin Resistance and Glucose Uptake
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Insulin resistance is improved in high‐fat fed mice by photobiomodulation therapy at 630 nm
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Crosstalk between mitochondrial (dys)function and mitochondrial abundance
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Electron microscopic observations on the alterations of tegumental surface of Raillietina echinobothrida treated with root‐peel extract of Potentilla fulgens
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Adaptations of Skeletal Muscle Mitochondria to Obesity, Exercise, and Polyunsaturated Fatty Acids
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Do mitochondria provide a common link between diabetes and Parkinson's disease?
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Resveratrol induces apoptosis and inhibits adipogenesis in 3T3‐L1 adipocytes
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Traditional and novel tools to probe the mitochondrial metabolism in health and disease
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6.3 Mitochondria-Nucleus Energetic Communication: Role for Phosphotransfer Networks in Processing Cellular Information
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Mechanical View on the Mitochondria
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Mitochondrial Biogenesis and Dynamics in Health and Disease
inferred← citeshttps://doi.org/10.1007/978-3-031-17362-2_6openalex-snapshot
Autophagy in Muscle Stem Cells
inferred← citeshttps://doi.org/10.1007/978-3-031-26576-1_15openalex-snapshot
Ageing, Metabolic Dysfunction, and the Therapeutic Role of Antioxidants
inferred← citeshttps://doi.org/10.1007/978-3-031-39721-9_4openalex-snapshot
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Role of Antioxidant Signaling in Mitochondrial Adaptation to Muscle Contraction
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Cristae Remodeling and Mitochondrial Fragmentation: A Checkpoint for Cytochrome c Release and Apoptosis?
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Mitochondrial Dynamics and Apoptosis
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Role of the Mitochondrial Fission Protein Drp1 in Synaptic Damage and Neurodegeneration
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Role of Mitochondrial Function in Insulin Resistance
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Mitochondrial dynamics in cell death and neurodegeneration
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Mitofusins: from mitochondria to fertility
inferred← citeshttps://doi.org/10.1007/s00109-010-0675-5openalex-snapshot
Role of mitofusin 2 in cardiovascular oxidative injury
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MiR-125a regulates mitochondrial homeostasis through targeting mitofusin 1 to control hypoxic pulmonary vascular remodeling
inferred← citeshttps://doi.org/10.1007/s00125-004-1394-7openalex-snapshot
Expression of key genes of fatty acid oxidation, including adiponectin receptors, in skeletal muscle of Type 2 diabetic patients
inferred← citeshttps://doi.org/10.1007/s00125-005-1918-9openalex-snapshot
Could the low level of expression of the gene encoding skeletal muscle mitofusin-2 account for the metabolic inflexibility of obesity?
inferred← citeshttps://doi.org/10.1007/s00125-007-0782-1openalex-snapshot
Upregulation of peroxisome proliferator-activated receptor gamma coactivator gene (PGC1A) during weight loss is related to insulin sensitivity but not to energy expenditure
inferred← citeshttps://doi.org/10.1007/s00125-009-1403-yopenalex-snapshot
Genes involved in mitochondrial biogenesis/function are induced in response to bilio-pancreatic diversion in morbidly obese individuals with normal glucose tolerance but not in type 2 diabetic patients
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Mitochondrial fragmentation and superoxide anion production in coronary endothelial cells from a mouse model of type 1 diabetes
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Longitudinal metabolic profiling of cardiomyocytes derived from human-induced pluripotent stem cells
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Effects of insulin on the skin: possible healing benefits for diabetic foot ulcers
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Cerebral involvement in axonal Charcot-Marie-Tooth neuropathy caused by mitofusin2 mutations
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Substrate use and biochemical response to a 3,211-km bicycle tour in trained cyclists
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Characterization of distinct single-channel properties of Ca2+ inward currents in mitochondria
inferred← citeshttps://doi.org/10.1007/s00439-004-1199-2openalex-snapshot
Mitochondrial GTPase mitofusin 2 mutation in Charcot?Marie?Tooth neuropathy type 2A
inferred← citeshttps://doi.org/10.1007/s00441-006-0320-3openalex-snapshot
Mitofusin 2 (Mfn2): a key player in insulin-dependent myogenesis in vitro
inferred← citeshttps://doi.org/10.1007/s00709-013-0515-xopenalex-snapshot
Do we age because we have mitochondria?
inferred← citeshttps://doi.org/10.1007/s10048-009-0207-zopenalex-snapshot
Adenine nucleotide translocase is involved in a mitochondrial coupling defect in MFN2-related Charcot–Marie–Tooth type 2A disease
inferred← citeshttps://doi.org/10.1007/s10048-011-0285-6openalex-snapshot
A novel mitofusin 2 mutation causes canine fetal-onset neuroaxonal dystrophy
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Photobiomodulation therapy with light-emitting diode in stimulating adipose tissue mitochondria
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Mitochondrial dynamics in the regulation of neuronal cell death
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Mitochondrial dysfunction in metabolism and ageing: shared mechanisms and outcomes?
inferred← citeshttps://doi.org/10.1007/s10534-012-9543-9openalex-snapshot
Hepatic and adipocyte cells respond differentially to iron overload, hypoxic and inflammatory challenge
inferred← citeshttps://doi.org/10.1007/s10545-005-0307-3openalex-snapshot
Dominance in mitochondrial disorders
inferred← citeshttps://doi.org/10.1007/s10545-008-1018-3openalex-snapshot
Organelle dynamics and dysfunction: A closer link between peroxisomes and mitochondria
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Metabolic manipulators: a well founded strategy to combat mitochondrial dysfunction
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Mitochondrial transplantation as a potential and novel master key for treatment of various incurable diseases
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Mitochondria in heart failure: the emerging role of mitochondrial dynamics
inferred← citeshttps://doi.org/10.1007/s10863-005-6572-xopenalex-snapshot
Proteins That Fuse and Fragment Mitochondria in Apoptosis: Con-Fissing a Deadly Con-Fusion?
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The complex interplay between mitochondrial dynamics and cardiac metabolism
inferred← citeshttps://doi.org/10.1007/s11033-014-3584-9openalex-snapshot
Mitofusin 2 deficiency leads to oxidative stress that contributes to insulin resistance in rat skeletal muscle cells
inferred← citeshttps://doi.org/10.1007/s11154-025-09954-9openalex-snapshot
Skeletal muscle atrophy and dysfunction in obesity and type-2 diabetes mellitus: Myocellular mechanisms involved
inferred← citeshttps://doi.org/10.1007/s11332-018-0430-9openalex-snapshot
The effect of 12 weeks of aerobic exercise on mitochondrial dynamics in cardiac myocytes of type 2 diabetic rats
inferred← citeshttps://doi.org/10.1007/s11356-020-11313-xopenalex-snapshot
RETRACTED ARTICLE: Thymoquinone alleviates mitochondrial viability and apoptosis in diclofenac-induced acute kidney injury (AKI) via regulating Mfn2 and miR-34a mRNA expressions
inferred← citeshttps://doi.org/10.1007/s11428-014-1278-5openalex-snapshot
Mitochondrien als Kraftwerk der β-Zelle
inferred← citeshttps://doi.org/10.1007/s11596-009-0603-5openalex-snapshot
Liver-specific reduction of Mfn2 protein by RNAi results in impaired glycometabolism and lipid homeostasis in BALB/c mice
inferred← citeshttps://doi.org/10.1007/s11596-012-0005-yopenalex-snapshot
Valsartan inhibits angiotensin II-induced proliferation of vascular smooth muscle cells via regulating the expression of mitofusin 2
inferred← citeshttps://doi.org/10.1007/s11695-009-9987-3openalex-snapshot
Mitochondrial DNA Content in Human Omental Adipose Tissue
inferred← citeshttps://doi.org/10.1007/s12011-013-9666-zopenalex-snapshot
Effects of High Iron and Glucose Concentrations over the Relative Expression of Bcl2, Bax, and Mfn2 in MIN6 Cells
inferred← citeshttps://doi.org/10.1007/s12020-011-9555-1openalex-snapshot
Early protective effect of mitofusion 2 overexpression in STZ-induced diabetic rat kidney
inferred← citeshttps://doi.org/10.1007/s12020-024-03764-wopenalex-snapshot
Estrogen promotes fetal skeletal muscle mitochondrial distribution and ATP synthase activity important for insulin sensitivity in offspring
inferred← citeshttps://doi.org/10.1007/s12032-015-0515-0openalex-snapshot
Mitofusin-2 over-expresses and leads to dysregulation of cell cycle and cell invasion in lung adenocarcinoma
inferred← citeshttps://doi.org/10.1007/s12035-012-8311-8openalex-snapshot
Nitric Oxide in Myogenesis and Therapeutic Muscle Repair
inferred← citeshttps://doi.org/10.1007/s12035-021-02667-5openalex-snapshot
Studies on Regulation of Global Protein Profile and Cellular Bioenergetics of Differentiating SH-SY5Y Cells
inferred← citeshttps://doi.org/10.1007/s12522-015-0225-5openalex-snapshot
Sperm dysfunction and ciliopathy
inferred← citeshttps://doi.org/10.1007/s12551-021-00891-wopenalex-snapshot
Uncovering the important role of mitochondrial dynamics in oogenesis: impact on fertility and metabolic disorder transmission
inferred← citeshttps://doi.org/10.1007/s12639-023-01630-6openalex-snapshot
Anthelmintic evaluation of three ayurvedic formulations: a transmission electron microscopy study in Raillietina sp. (Cestoda)
inferred← citeshttps://doi.org/10.1007/s13679-021-00434-0openalex-snapshot
The Role of Mitochondrial Adaptation and Metabolic Flexibility in the Pathophysiology of Obesity and Insulin Resistance: an Updated Overview
inferred← citeshttps://doi.org/10.1007/s13679-022-00473-1openalex-snapshot
Hepatocyte Mitochondrial Dynamics and Bioenergetics in Obesity-Related Non-Alcoholic Fatty Liver Disease
inferred← citeshttps://doi.org/10.1007/s40618-020-01381-8openalex-snapshot
Testosterone treatment is associated with reduced adipose tissue dysfunction and nonalcoholic fatty liver disease in obese hypogonadal men
inferred← citeshttps://doi.org/10.1016/b978-0-12-404599-6.00015-9openalex-snapshot
The Emerging Role of Mitochondrial Dynamics in Cardiovascular Disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-800877-5.00025-5openalex-snapshot
Childhood-Onset Peripheral Neuropathy with Cognitive Decline
inferred← citeshttps://doi.org/10.1016/b978-0-12-801585-8.00007-5openalex-snapshot
Impact of Type 2 Diabetes on Skeletal Muscle Mass and Quality
inferred← citeshttps://doi.org/10.1016/b978-0-12-810422-4.00009-9openalex-snapshot
Skeletal Muscle Mitochondrial, Obesity, and High-Fat Feeding
inferred← citeshttps://doi.org/10.1016/b978-0-12-811752-1.00012-2openalex-snapshot
Role of Mitochondria in the Regulation of Kidney Function and Metabolism in Type 2 Diabetes
inferred← citeshttps://doi.org/10.1016/b978-0-12-811752-1.00017-1openalex-snapshot
State of Knowledge and Recent Advances in Prevention and Treatment of Mitochondrial Dysfunction in Obesity and Type 2 Diabetes
inferred← citeshttps://doi.org/10.1016/b978-0-12-813553-2.00007-5openalex-snapshot
Obesity, mitochondrial dysfunction, and obstructive lung disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-819621-2.00026-7openalex-snapshot
Modulation of the mitochondrial function with polyphenols and other natural bioactive compounds to treat obesity
inferred← citeshttps://doi.org/10.1016/bs.apcsb.2018.11.009openalex-snapshot
Relationship between mitofusin 2 and cancer
inferred← citeshttps://doi.org/10.1016/bs.ircmb.2018.05.004openalex-snapshot
Mitochondrial Dynamics: Shaping Metabolic Adaptation
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2024.107547openalex-snapshot
Insights into crucial molecules and protein channels involved in pig sperm cryopreservation
inferred← citeshttps://doi.org/10.1016/j.bbabio.2008.04.002openalex-snapshot
Mitochondrial oxidative phosphorylation and energetic status are reflected by morphology of mitochondrial network in INS-1E and HEP-G2 cells viewed by 4Pi microscopy
inferred← citeshttps://doi.org/10.1016/j.bbabio.2008.05.442openalex-snapshot
High levels of Fis1, a pro-fission mitochondrial protein, trigger autophagy
inferred← citeshttps://doi.org/10.1016/j.bbabio.2008.12.005openalex-snapshot
Calcium regulation of mitochondria motility and morphology
inferred← citeshttps://doi.org/10.1016/j.bbabio.2010.02.017openalex-snapshot
Alterations in the mitochondrial regulatory pathways constituted by the nuclear co-factors PGC-1α or PGC-1β and mitofusin 2 in skeletal muscle in type 2 diabetes
inferred← citeshttps://doi.org/10.1016/j.bbabio.2010.02.030openalex-snapshot
Multi-site control and regulation of mitochondrial energy production
inferred← citeshttps://doi.org/10.1016/j.bbabio.2010.03.018openalex-snapshot
Regulation of mitochondrial fission by intracellular Ca2+ in rat ventricular myocytes
inferred← citeshttps://doi.org/10.1016/j.bbabio.2014.01.014openalex-snapshot
Epigallocatechin gallate counteracts oxidative stress in docosahexaenoxic acid-treated myocytes
inferred← citeshttps://doi.org/10.1016/j.bbadis.2009.09.005openalex-snapshot
Mitochondrial trafficking and morphology in neuronal injury
inferred← citeshttps://doi.org/10.1016/j.bbadis.2009.09.006openalex-snapshot
Mitochondria: Joining forces to thwart cell death
inferred← citeshttps://doi.org/10.1016/j.bbadis.2019.03.013openalex-snapshot
Mitochondrial fusion and maintenance of mitochondrial homeostasis in diabetic retinopathy
inferred← citeshttps://doi.org/10.1016/j.bbagen.2009.08.007openalex-snapshot
Response of mitochondrial fusion and fission protein gene expression to exercise in rat skeletal muscle
inferred← citeshttps://doi.org/10.1016/j.bbagen.2012.11.009openalex-snapshot
Mitochondrial and sarcoplasmic reticulum abnormalities in cancer cachexia: Altered energetic efficiency?
inferred← citeshttps://doi.org/10.1016/j.bbagen.2023.130413openalex-snapshot
MFN2-mediated mitochondrial fusion facilitates acute hypobaric hypoxia-induced cardiac dysfunction by increasing glucose catabolism and ROS production
inferred← citeshttps://doi.org/10.1016/j.bbalip.2016.08.003openalex-snapshot
Regulation of autophagy by mitochondrial phospholipids in health and diseases
inferred← citeshttps://doi.org/10.1016/j.bbalip.2017.05.011openalex-snapshot
Mitochondria and endoplasmic reticulum: Targets for a better insulin sensitivity in skeletal muscle?
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2006.02.004openalex-snapshot
Get the balance right: Mitofusins roles in health and disease
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2011.01.014openalex-snapshot
Mitochondrial dysfunction in diabetic cardiomyopathy
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2012.02.012openalex-snapshot
Mitochondrial morphology in mitophagy and macroautophagy
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2012.05.002openalex-snapshot
Recent advances into the understanding of mitochondrial fission
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2012.07.016openalex-snapshot
Mechanistic perspective of mitochondrial fusion: Tubulation vs. fragmentation
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2017.03.006openalex-snapshot
Molecular regulation of mitochondrial dynamics in cardiac disease
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2019.06.006openalex-snapshot
Sphingosine kinase 1 overexpression induces MFN2 fragmentation and alters mitochondrial matrix Ca2+ handling in HeLa cells
inferred← citeshttps://doi.org/10.1016/j.bbi.2023.11.010openalex-snapshot
Gonadal Hormones Impart Male-Biased Behavioral Vulnerabilities to Immune Activation via Microglial Mitochondrial Function
inferred← citeshttps://doi.org/10.1016/j.bbrc.2003.10.008openalex-snapshot
Stage-specific enhanced expression of mitochondrial fusion and fission factors during spermatogenesis in rat testis
inferred← citeshttps://doi.org/10.1016/j.bbrc.2005.07.088openalex-snapshot
Expression of HSG is essential for mouse blastocyst formation
inferred← citeshttps://doi.org/10.1016/j.bbrc.2007.08.191openalex-snapshot
Overexpression of Mitofusin 2 inhibited oxidized low-density lipoprotein induced vascular smooth muscle cell proliferation and reduced atherosclerotic lesion formation in rabbit
inferred← citeshttps://doi.org/10.1016/j.bbrc.2010.08.108openalex-snapshot
Mitofusin-2 is a novel direct target of p53
inferred← citeshttps://doi.org/10.1016/j.bbrc.2011.10.006openalex-snapshot
Ionizing radiation accelerates Drp1-dependent mitochondrial fission, which involves delayed mitochondrial reactive oxygen species production in normal human fibroblast-like cells
inferred← citeshttps://doi.org/10.1016/j.bbrc.2019.04.037openalex-snapshot
Mitofusin 2 is involved in chemotaxis of neutrophil-like differentiated HL-60 cells
inferred← citeshttps://doi.org/10.1016/j.bbrep.2016.03.006openalex-snapshot
Subsarcolemmal mitochondria isolated with the proteolytic enzyme nagarse exhibit greater protein specific activities and functional coupling
inferred← citeshttps://doi.org/10.1016/j.beem.2012.05.003openalex-snapshot
Cellular and molecular mechanisms of mitochondrial function
inferred← citeshttps://doi.org/10.1016/j.beem.2012.05.004openalex-snapshot
Mitochondrial dynamics and morphology in beta-cells
inferred← citeshttps://doi.org/10.1016/j.biocel.2009.02.004openalex-snapshot
Role of mitochondrial dynamics proteins in the pathophysiology of obesity and type 2 diabetes
inferred← citeshttps://doi.org/10.1016/j.biocel.2009.02.014openalex-snapshot
Mitochondrial reticulum network dynamics in relation to oxidative stress, redox regulation, and hypoxia
inferred← citeshttps://doi.org/10.1016/j.biocel.2009.03.007openalex-snapshot
The cell-type specificity of mitochondrial dynamics
inferred← citeshttps://doi.org/10.1016/j.biocel.2009.04.016openalex-snapshot
Opening the doors to cytochrome c: Changes in mitochondrial shape and apoptosis
inferred← citeshttps://doi.org/10.1016/j.biocel.2012.09.024openalex-snapshot
Ex vivo measures of muscle mitochondrial capacity reveal quantitative limits of oxygen delivery by the circulation during exercise
inferred← citeshttps://doi.org/10.1016/j.biopha.2020.109849openalex-snapshot
Vitexin attenuates myocardial ischemia/reperfusion injury in rats by regulating mitochondrial dysfunction induced by mitochondrial dynamics imbalance
inferred← citeshttps://doi.org/10.1016/j.biopha.2021.111315openalex-snapshot
Adipose tissue and insulin resistance in obese
inferred← citeshttps://doi.org/10.1016/j.biopha.2022.113968openalex-snapshot
Insight into the regulation of NLRP3 inflammasome activation by mitochondria in liver injury and the protective role of natural products
inferred← citeshttps://doi.org/10.1016/j.biopsych.2020.12.003openalex-snapshot
Mitofusin-2 in the Nucleus Accumbens Regulates Anxiety and Depression-like Behaviors Through Mitochondrial and Neuronal Actions
inferred← citeshttps://doi.org/10.1016/j.bone.2024.117086openalex-snapshot
Mitofusin 2 plays a critical role in maintaining the functional integrity of the neuromuscular-skeletal axis
inferred← citeshttps://doi.org/10.1016/j.brainres.2016.09.047openalex-snapshot
MiR-195 dependent roles of mitofusin2 in the mitochondrial dysfunction of hippocampal neurons in SAMP8 mice
inferred← citeshttps://doi.org/10.1016/j.canlet.2012.03.038openalex-snapshot
Mitofusin 1 inhibits an apoptosis-associated amino-terminal conformational change in Bax, but not its mitochondrial translocation, in a GTPase-dependent manner
inferred← citeshttps://doi.org/10.1016/j.canlet.2023.216235openalex-snapshot
MSC-NPRA loop drives fatty acid oxidation to promote stemness and chemoresistance of gastric cancer
inferred← citeshttps://doi.org/10.1016/j.carbpol.2017.01.019openalex-snapshot
Effects of cultured Cordyceps mycelia polysaccharide A on tumor neurosis factor-α induced hepatocyte injury with mitochondrial abnormality
inferred← citeshttps://doi.org/10.1016/j.cbi.2017.05.003openalex-snapshot
Early energy metabolism-related molecular events in skeletal muscle of diabetic rats: The effects of l-arginine and SOD mimic
inferred← citeshttps://doi.org/10.1016/j.cbpb.2005.04.022openalex-snapshot
Nitric oxide and mitochondrial biogenesis: A key to long-term regulation of cellular metabolism
inferred← citeshttps://doi.org/10.1016/j.ceca.2016.04.006openalex-snapshot
Mitochondrial remodeling: Rearranging, recycling, and reprogramming
inferred← citeshttps://doi.org/10.1016/j.cell.2013.09.003openalex-snapshot
Mitofusin 2 in POMC Neurons Connects ER Stress with Leptin Resistance and Energy Imbalance
inferred← citeshttps://doi.org/10.1016/j.cell.2013.09.004openalex-snapshot
Mitochondrial Dynamics Controlled by Mitofusins Regulate Agrp Neuronal Activity and Diet-Induced Obesity
inferred← citeshttps://doi.org/10.1016/j.cell.2019.04.010openalex-snapshot
Deficient Endoplasmic Reticulum-Mitochondrial Phosphatidylserine Transfer Causes Liver Disease
inferred← citeshttps://doi.org/10.1016/j.cellsig.2024.111035openalex-snapshot
Mitochondrial quality control in liver fibrosis: Epigenetic hallmarks and therapeutic strategies
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.108079openalex-snapshot
Mitofusin 2 in Macrophages Links Mitochondrial ROS Production, Cytokine Release, Phagocytosis, Autophagy, and Bactericidal Activity
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.112776openalex-snapshot
Mitofusin-2 in nucleus accumbens D2-MSNs regulates social dominance and neuronal function
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.112895openalex-snapshot
PGAM5 is an MFN2 phosphatase that plays an essential role in the regulation of mitochondrial dynamics
inferred← citeshttps://doi.org/10.1016/j.chembiol.2017.12.001openalex-snapshot
Identification of New Activators of Mitochondrial Fusion Reveals a Link between Mitochondrial Morphology and Pyrimidine Metabolism
inferred← citeshttps://doi.org/10.1016/j.clnu.2025.106547openalex-snapshot
Changes in body composition, muscle function, and muscle insulin sensitivity induced by obesity and bariatric surgery: Implications for sarcopenic obesity
inferred← citeshttps://doi.org/10.1016/j.cmet.2008.03.009openalex-snapshot
When BAD Is Good for β Cells
inferred← citeshttps://doi.org/10.1016/j.cmet.2010.04.004openalex-snapshot
Regulation of Skeletal Muscle Oxidative Capacity and Insulin Signaling by the Mitochondrial Rhomboid Protease PARL
inferred← citeshttps://doi.org/10.1016/j.cmet.2012.10.005openalex-snapshot
RETRACTED: The Ubiquitin Ligase Mul1 Induces Mitophagy in Skeletal Muscle in Response to Muscle-Wasting Stimuli
inferred← citeshttps://doi.org/10.1016/j.cmet.2013.03.002openalex-snapshot
Mitochondrial Dynamics in the Regulation of Nutrient Utilization and Energy Expenditure
inferred← citeshttps://doi.org/10.1016/j.cmet.2026.01.012openalex-snapshot
Deletion of Mfn2 in endothelial cells triggers a mitohormetic response that improves systemic metabolism and healthspan in mice
inferred← citeshttps://doi.org/10.1016/j.cophys.2018.02.006openalex-snapshot
Mitochondrial dynamics and metabolic homeostasis
inferred← citeshttps://doi.org/10.1016/j.cophys.2022.100487openalex-snapshot
Energy transfer between the mitochondrial network and lipid droplets in insulin resistant skeletal muscle
inferred← citeshttps://doi.org/10.1016/j.crvi.2019.04.003openalex-snapshot
A hypercaloric diet induces hepatic oxidative stress, infiltration of lymphocytes, and mitochondrial reshuffle in Psammomys obesus, a murine model of insulin resistance
inferred← citeshttps://doi.org/10.1016/j.cub.2006.06.054openalex-snapshot
Mitochondria: More Than Just a Powerhouse
inferred← citeshttps://doi.org/10.1016/j.ejcb.2014.04.001openalex-snapshot
Epigallocatechin-3-gallate inhibits proliferation of human aortic smooth muscle cells via up-regulating expression of mitofusin 2
inferred← citeshttps://doi.org/10.1016/j.ejcb.2018.07.003openalex-snapshot
Function and regulation of mitofusin 2 in cardiovascular physiology and pathology
inferred← citeshttps://doi.org/10.1016/j.ejogrb.2013.11.024openalex-snapshot
Relationship between the expressions of mitofusin-2 and procollagen in uterosacral ligament fibroblasts of postmenopausal patients with pelvic organ prolapse
inferred← citeshttps://doi.org/10.1016/j.ejphar.2018.02.050openalex-snapshot
Pravastatin improves risk factors but not ischaemic tolerance in obese rats
inferred← citeshttps://doi.org/10.1016/j.euroneuro.2018.01.004openalex-snapshot
Second generation antipsychotic-induced mitochondrial alterations: Implications for increased risk of metabolic syndrome in patients with schizophrenia
inferred← citeshttps://doi.org/10.1016/j.exger.2023.112081openalex-snapshot
Resistance training prevents dynamics and mitochondrial respiratory dysfunction in vastus lateralis muscle of ovariectomized rats
inferred← citeshttps://doi.org/10.1016/j.expneurol.2009.05.003openalex-snapshot
Role of mitofusin 2 mutations in the physiopathology of Charcot–Marie–Tooth disease type 2A
inferred← citeshttps://doi.org/10.1016/j.expneurol.2024.115131openalex-snapshot
Astrogliosis and glial scar in ischemic stroke - focused on mechanism and treatment
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2010.08.024openalex-snapshot
H2O2-induced mitochondrial fragmentation in C2C12 myocytes
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2012.05.009openalex-snapshot
Mitochondrial respiratory chain dysfunction: Implications in neurodegeneration
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2013.09.007openalex-snapshot
Mitochondrial genetics and obesity: evolutionary adaptation and contemporary disease susceptibility
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2014.02.009openalex-snapshot
Nitrite augments glucose uptake in adipocytes through the protein kinase A-dependent stimulation of mitochondrial fusion
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2016.02.025openalex-snapshot
Exercise-induced hormesis and skeletal muscle health
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2016.04.019openalex-snapshot
Altered mitochondrial dynamics and response to insulin in cybrid cells harboring a diabetes-susceptible mitochondrial DNA haplogroup
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