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Mitochondrial fusion and fission in cell life and death
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/s004380000307openalex-snapshot
A putative mitochondrial ftsZ gene is present in the unicellular primitive red alga Cyanidioschyzon merolae
inferredcites →https://doi.org/10.1016/j.cell.2004.11.003openalex-snapshot
The Importance of Dendritic Mitochondria in the Morphogenesis and Plasticity of Spines and Synapses
inferredcites →https://doi.org/10.1016/j.cell.2005.02.001openalex-snapshot
Mitochondria, Oxidants, and Aging
inferredcites →https://doi.org/10.1016/j.cell.2006.06.021openalex-snapshot
Mitochondrial Rhomboid PARL Regulates Cytochrome c Release during Apoptosis via OPA1-Dependent Cristae Remodeling
inferredcites →https://doi.org/10.1016/j.cell.2006.09.021openalex-snapshot
Mitochondrial Inner-Membrane Fusion and Crista Maintenance Requires the Dynamin-Related GTPase Mgm1
inferredcites →https://doi.org/10.1016/j.cell.2007.06.026openalex-snapshot
Mitochondrial Fusion Protects against Neurodegeneration in the Cerebellum
inferredcites →https://doi.org/10.1016/j.cell.2010.02.026openalex-snapshot
Mitochondrial Fusion Is Required for mtDNA Stability in Skeletal Muscle and Tolerance of mtDNA Mutations
inferredcites →https://doi.org/10.1016/j.cell.2010.04.009openalex-snapshot
Mitochondria Supply Membranes for Autophagosome Biogenesis during Starvation
inferredcites →https://doi.org/10.1016/j.cub.2007.12.038openalex-snapshot
Cargo-Selected Transport from the Mitochondria to Peroxisomes Is Mediated by Vesicular Carriers
inferredcites →https://doi.org/10.1016/j.devcel.2007.01.017openalex-snapshot
Yeast Mitochondrial Division and Distribution Require the Cortical Num1 Protein
inferredcites →https://doi.org/10.1016/j.devcel.2007.02.002openalex-snapshot
Role of Mitochondrial Remodeling in Programmed Cell Death in Drosophila melanogaster
inferredcites →https://doi.org/10.1016/j.molcel.2008.07.015openalex-snapshot
Caenorhabditis elegans drp-1 and fis-2 Regulate Distinct Cell-Death Execution Pathways Downstream of ced-3 and Independent of ced-9
inferredcites →https://doi.org/10.1016/j.yexcr.2007.08.008openalex-snapshot
OPA1 cleavage depends on decreased mitochondrial ATP level and bivalent metals
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/s0968-0004(00)01735-7openalex-snapshot
Mitochondrial filaments and clusters as intracellular power-transmitting cables
inferredcites →https://doi.org/10.1016/s1097-2765(00)80391-3openalex-snapshot
C. elegans Dynamin-Related Protein DRP-1 Controls Severing of the Mitochondrial Outer Membrane
inferredcites →https://doi.org/10.1016/s1534-5807(01)00055-7openalex-snapshot
The Role of Dynamin-Related Protein 1, a Mediator of Mitochondrial Fission, in Apoptosis
inferredcites →https://doi.org/10.1038/13014openalex-snapshot
The dynamin-related GTPase Dnm1 regulates mitochondrial fission in yeast
inferredcites →https://doi.org/10.1038/35073006openalex-snapshot
Versatility of the mitochondrial protein import machinery
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/10.1038/90116openalex-snapshot
Human cells are protected from mitochondrial dysfunction by complementation of DNA products in fused mitochondria
inferredcites →https://doi.org/10.1038/90976openalex-snapshot
Inter-mitochondrial complementation: Mitochondria-specific system preventing mice from expression of disease phenotypes by mutant mtDNA
inferredcites →https://doi.org/10.1038/emboj.2009.89openalex-snapshot
SLP‐2 is required for stress‐induced mitochondrial hyperfusion
inferredcites →https://doi.org/10.1038/embor.2009.86openalex-snapshot
MAPL is a new mitochondrial SUMO E3 ligase that regulates mitochondrial fission
inferredcites →https://doi.org/10.1038/nature01633openalex-snapshot
Mitochondrial membrane remodelling regulated by a conserved rhomboid protease
inferredcites →https://doi.org/10.1038/nature03316openalex-snapshot
DRP-1-mediated mitochondrial fragmentation during EGL-1-induced cell death in C. elegans
inferredcites →https://doi.org/10.1038/nature04718openalex-snapshot
GTP-dependent twisting of dynamin implicates constriction and tension in membrane fission
inferredcites →https://doi.org/10.1038/nature05111openalex-snapshot
Role of Bax and Bak in mitochondrial morphogenesis
inferredcites →https://doi.org/10.1038/nature07534openalex-snapshot
Mitofusin 2 tethers endoplasmic reticulum to mitochondria
inferredcites →https://doi.org/10.1038/ncb1907openalex-snapshot
Mitochondrial fission factor Drp1 is essential for embryonic development and synapse formation in mice
inferredcites →https://doi.org/10.1038/ng1341openalex-snapshot
Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A
inferredcites →https://doi.org/10.1038/nrg1708openalex-snapshot
The organization and inheritance of the mitochondrial genome
inferredcites →https://doi.org/10.1038/nrm1313openalex-snapshot
The dynamin superfamily: universal membrane tubulation and fission molecules?
inferredcites →https://doi.org/10.1038/nrm2275openalex-snapshot
Functions and dysfunctions of mitochondrial dynamics
inferredcites →https://doi.org/10.1038/nrm2417openalex-snapshot
Mechanisms of membrane fusion: disparate players and common principles
inferredcites →https://doi.org/10.1038/nrn2417openalex-snapshot
Mitochondrial fragmentation in neurodegeneration
inferredcites →https://doi.org/10.1038/sj.emboj.7601184openalex-snapshot
Regulation of mitochondrial morphology through proteolytic cleavage of OPA1
inferredcites →https://doi.org/10.1038/sj.emboj.7601249openalex-snapshot
A novel mitochondrial ubiquitin ligase plays a critical role in mitochondrial dynamics
inferredcites →https://doi.org/10.1038/sj.emboj.7601963openalex-snapshot
Fission and selective fusion govern mitochondrial segregation and elimination by autophagy
inferredcites →https://doi.org/10.1038/sj.embor.7400488openalex-snapshot
Separate fusion of outer and inner mitochondrial membranes
inferredcites →https://doi.org/10.1038/sj.embor.7400790openalex-snapshot
MARCH‐V is a novel mitofusin 2‐ and Drp1‐binding protein able to change mitochondrial morphology
inferredcites →https://doi.org/10.1038/sj.embor.7401062openalex-snapshot
Reversible phosphorylation of Drp1 by cyclic AMP‐dependent protein kinase and calcineurin regulates mitochondrial fission and cell death
inferredcites →https://doi.org/10.1056/nejmoa064436openalex-snapshot
A Lethal Defect of Mitochondrial and Peroxisomal Fission
inferredcites →https://doi.org/10.1073/pnas.0401077101openalex-snapshot
Frequent fusion and fission of plant mitochondria with unequal nucleoid distribution
inferredcites →https://doi.org/10.1073/pnas.0407043101openalex-snapshot
OPA1 requires mitofusin 1 to promote mitochondrial fusion
inferredcites →https://doi.org/10.1073/pnas.0703976104openalex-snapshot
Bak regulates mitochondrial morphology and pathology during apoptosis by interacting with mitofusins
inferredcites →https://doi.org/10.1073/pnas.0706441104openalex-snapshot
Structural basis for recruitment of mitochondrial fission complexes by Fis1
inferredcites →https://doi.org/10.1073/pnas.0711845105openalex-snapshot
Pink1 regulates mitochondrial dynamics through interaction with the fission/fusion machinery
inferredcites →https://doi.org/10.1073/pnas.0803998105openalex-snapshot
The Parkinson's disease genes pink1 and parkin promote mitochondrial fission and/or inhibit fusion in Drosophila
inferredcites →https://doi.org/10.1073/pnas.0808249105openalex-snapshot
Dephosphorylation by calcineurin regulates translocation of Drp1 to mitochondria
inferredcites →https://doi.org/10.1073/pnas.082663299openalex-snapshot
A dynamin-like protein (ADL2b), rather than FtsZ, is involved in Arabidopsis mitochondrial division
inferredcites →https://doi.org/10.1073/pnas.0904875106openalex-snapshot
A hyperfused mitochondrial state achieved at G 1 –S regulates cyclin E buildup and entry into S phase
inferredcites →https://doi.org/10.1073/pnas.0913485107openalex-snapshot
Drosophila Parkin requires PINK1 for mitochondrial translocation and ubiquitinates Mitofusin
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.c200677200openalex-snapshot
Loss of OPA1 Perturbates the Mitochondrial Inner Membrane Structure and Integrity, Leading to Cytochrome c Release and Apoptosis
inferredcites →https://doi.org/10.1074/jbc.m109.035774openalex-snapshot
Loss of Parkin or PINK1 Function Increases Drp1-dependent Mitochondrial Fragmentation
inferredcites →https://doi.org/10.1074/jbc.m211311200openalex-snapshot
Processing of Mgm1 by the Rhomboid-type Protease Pcp1 Is Required for Maintenance of Mitochondrial Morphology and of Mitochondrial DNA
inferredcites →https://doi.org/10.1074/jbc.m211761200openalex-snapshot
Dynamin-like Protein 1 Is Involved in Peroxisomal Fission
inferredcites →https://doi.org/10.1074/jbc.m303758200openalex-snapshot
hFis1, a Novel Component of the Mammalian Mitochondrial Fission Machinery
inferredcites →https://doi.org/10.1074/jbc.m401363200openalex-snapshot
Ugo1p Links the Fzo1p and Mgm1p GTPases for Mitochondrial Fusion
inferredcites →https://doi.org/10.1074/jbc.m503062200openalex-snapshot
Disruption of Fusion Results in Mitochondrial Heterogeneity and Dysfunction
inferredcites →https://doi.org/10.1074/jbc.m607279200openalex-snapshot
Mitotic Phosphorylation of Dynamin-related GTPase Drp1 Participates in Mitochondrial Fission
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.143.2.359openalex-snapshot
Mitochondrial Fusion in Yeast Requires the Transmembrane GTPase Fzo1p
inferredcites →https://doi.org/10.1083/jcb.147.4.699openalex-snapshot
Division versus Fusion: Dnm1p and Fzo1p Antagonistically Regulate Mitochondrial Shape
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/10.1083/jcb.152.4.683openalex-snapshot
Connection of the Mitochondrial Outer and Inner Membranes by Fzo1 Is Critical for Organellar Fusion
inferredcites →https://doi.org/10.1083/jcb.152.6.1123openalex-snapshot
UGO1 Encodes an Outer Membrane Protein Required for Mitochondrial Fusion
inferredcites →https://doi.org/10.1083/jcb.200205031openalex-snapshot
The WD repeat protein, Mdv1p, functions as a molecular adaptor by interacting with Dnm1p and Fis1p during mitochondrial fission
inferredcites →https://doi.org/10.1083/jcb.200209124openalex-snapshot
Spatial and temporal association of Bax with mitochondrial fission sites, Drp1, and Mfn2 during apoptosis
inferredcites →https://doi.org/10.1083/jcb.200211046openalex-snapshot
Mitofusins Mfn1 and Mfn2 coordinately regulate mitochondrial fusion and are essential for embryonic development
inferredcites →https://doi.org/10.1083/jcb.200211113openalex-snapshot
The inner membrane protein Mdm33 controls mitochondrial morphology in yeast
inferredcites →https://doi.org/10.1083/jcb.200403022openalex-snapshot
Alternative topogenesis of Mgm1 and mitochondrial morphology depend on ATP and a functional import motor
inferredcites →https://doi.org/10.1083/jcb.200503148openalex-snapshot
The WD40 protein Caf4p is a component of the mitochondrial fission machinery and recruits Dnm1p to mitochondria
inferredcites →https://doi.org/10.1083/jcb.200506078openalex-snapshot
Dnm1 forms spirals that are structurally tailored to fit mitochondria
inferredcites →https://doi.org/10.1083/jcb.200610042openalex-snapshot
Bax/Bak promote sumoylation of DRP1 and its stable association with mitochondria during apoptotic cell death
inferredcites →https://doi.org/10.1083/jcb.200611064openalex-snapshot
The mitochondrial E3 ubiquitin ligase MARCH5 is required for Drp1 dependent mitochondrial division
inferredcites →https://doi.org/10.1083/jcb.200704110openalex-snapshot
OPA1 processing controls mitochondrial fusion and is regulated by mRNA splicing, membrane potential, and Yme1L
inferredcites →https://doi.org/10.1083/jcb.200704112openalex-snapshot
Regulation of the mitochondrial dynamin-like protein Opa1 by proteolytic cleavage
inferredcites →https://doi.org/10.1083/jcb.200709099openalex-snapshot
The class V myosin motor protein, Myo2, plays a major role in mitochondrial motility in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1083/jcb.200802164openalex-snapshot
CaM kinase Iα–induced phosphorylation of Drp1 regulates mitochondrial morphology
inferredcites →https://doi.org/10.1083/jcb.200809099openalex-snapshot
Mitochondrial outer and inner membrane fusion requires a modified carrier protein
inferredcites →https://doi.org/10.1083/jcb.200903065openalex-snapshot
The dynamin-related GTPase Drp1 is required for embryonic and brain development in mice
inferredcites →https://doi.org/10.1083/jcb.200906083openalex-snapshot
Inducible proteolytic inactivation of OPA1 mediated by the OMA1 protease in mammalian cells
inferredcites →https://doi.org/10.1083/jcb.200906084openalex-snapshot
Regulation of OPA1 processing and mitochondrial fusion by m -AAA protease isoenzymes and OMA1
inferredcites →https://doi.org/10.1083/jcb.200906098openalex-snapshot
Coassembly of Mgm1 isoforms requires cardiolipin and mediates mitochondrial inner membrane fusion
inferredcites →https://doi.org/10.1083/jcb.200910140openalex-snapshot
PINK1 stabilized by mitochondrial depolarization recruits Parkin to damaged mitochondria and activates latent Parkin for mitophagy
inferredcites →https://doi.org/10.1091/mbc.01-12-0588openalex-snapshot
Genetic Basis of Mitochondrial Function and Morphology in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1091/mbc.e02-10-0657openalex-snapshot
Constriction and Dnm1p Recruitment Are Distinct Processes in Mitochondrial Fission
inferredcites →https://doi.org/10.1091/mbc.e02-12-0831openalex-snapshot
Mdm30 Is an F-Box Protein Required for Maintenance of Fusion-competent Mitochondria in Yeast
inferredcites →https://doi.org/10.1091/mbc.e04-04-0294openalex-snapshot
Roles of the Mammalian Mitochondrial Fission and Fusion Mediators Fis1, Drp1, and Opa1 in Apoptosis
inferredcites →https://doi.org/10.1091/mbc.e05-02-0159openalex-snapshot
A Role for Fis1 in Both Mitochondrial and Peroxisomal Fission in Mammalian Cells
inferredcites →https://doi.org/10.1091/mbc.e05-07-0678openalex-snapshot
Role of Essential Genes in Mitochondrial Morphogenesis inSaccharomyces cerevisiae
inferredcites →https://doi.org/10.1091/mbc.e07-12-1287openalex-snapshot
The Novel Tail-anchored Membrane Protein Mff Controls Mitochondrial and Peroxisomal Fission in Mammalian Cells
inferredcites →https://doi.org/10.1091/mbc.e08-02-0227openalex-snapshot
Ubiquitin–Proteasome-dependent Degradation of a Mitofusin, a Critical Regulator of Mitochondrial Fusion
inferredcites →https://doi.org/10.1091/mbc.e09-07-0622openalex-snapshot
A Mutation Associated with CMT2A Neuropathy Causes Defects in Fzo1 GTP Hydrolysis, Ubiquitylation, and Protein Turnover
inferredcites →https://doi.org/10.1091/mbc.e10-02-0096openalex-snapshot
Mdm36 Is a Mitochondrial Fission-promoting Protein inSaccharomyces cerevisiae
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/jxb/erh073openalex-snapshot
ADL2a, like ADL2b, is involved in the control of higher plant mitochondrial morphology*
inferredcites →https://doi.org/10.1093/jxb/erj096openalex-snapshot
BIGYIN, an orthologue of human and yeast FIS1 genes functions in the control of mitochondrial size and number in Arabidopsis thaliana
inferredcites →https://doi.org/10.1101/gad.1247904openalex-snapshot
Mitochondrial fission proteins regulate programmed cell death in yeast
inferredcites →https://doi.org/10.1101/gad.1658508openalex-snapshot
Mitochondrial dynamics and apoptosis
inferredcites →https://doi.org/10.1105/tpc.108.058578openalex-snapshot
Arabidopsis ELONGATED MITOCHONDRIA1 Is Required for Localization of DYNAMIN-RELATED PROTEIN3A to Mitochondrial Fission Sites
inferredcites →https://doi.org/10.1126/science.1099793openalex-snapshot
Structural Basis of Mitochondrial Tethering by Mitofusin Complexes
inferredcites →https://doi.org/10.1126/science.1100612openalex-snapshot
Mitochondrial Fusion Intermediates Revealed in Vitro
inferredcites →https://doi.org/10.1126/science.1176921openalex-snapshot
Mechanistic Analysis of a Dynamin Effector
inferredcites →https://doi.org/10.1126/science.287.5456.1276openalex-snapshot
Mitochondrial FtsZ in a Chromophyte Alga
inferredcites →https://doi.org/10.1128/mcb.23.15.5409-5420.2003openalex-snapshot
The Mitochondrial Protein hFis1 Regulates Mitochondrial Fission in Mammalian Cells through an Interaction with the Dynamin-Like Protein DLP1
inferredcites →https://doi.org/10.1146/annurev-genet-102808-114910openalex-snapshot
Regulation Mechanisms and Signaling Pathways of Autophagy
inferredcites →https://doi.org/10.1146/annurev.biochem.76.052705.163409openalex-snapshot
Translocation of Proteins into Mitochondria
inferredcites →https://doi.org/10.1146/annurev.biochem.76.071905.090048openalex-snapshot
The Machines that Divide and Fuse Mitochondria
inferredcites →https://doi.org/10.1146/annurev.genet.38.072902.093019openalex-snapshot
Mitochondrial Morphology and Dynamics in Yeast and Multicellular Eukaryotes
inferredcites →https://doi.org/10.1177/1.4.188openalex-snapshot
AN ELECTRON MICROSCOPE STUDY OF THE MITOCHONDRIAL STRUCTURE
inferredcites →https://doi.org/10.1186/gb-2009-10-9-r95openalex-snapshot
Genome-wide deletion mutant analysis reveals genes required for respiratory growth, mitochondrial genome maintenance and mitochondrial protein synthesis in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1242/jcs.00423openalex-snapshot
Spatial and temporal dynamics of budding yeast mitochondria lacking the division component Fis1p
inferredcites →https://doi.org/10.1242/jcs.02415openalex-snapshot
The mitochondrial protein MTP18 contributes to mitochondrial fission in mammalian cells
inferredcites →https://doi.org/10.1242/jcs.03026openalex-snapshot
Fis1p and Caf4p, but not Mdv1p, determine the polar localization of Dnm1p clusters on the mitochondrial surface
inferredcites →https://doi.org/10.1242/jcs.03166openalex-snapshot
Dynamin-related proteins Vps1p and Dnm1p control peroxisome abundance inSaccharomyces cerevisiae
inferredcites →https://doi.org/10.1242/jcs.03253openalex-snapshot
Identification of a novel protein that regulates mitochondrial fusion by modulating mitofusin (Mfn) protein function
inferredcites →https://doi.org/10.1242/jcs.03418openalex-snapshot
The SUMO protease SENP5 is required to maintain mitochondrial morphology and function
inferredcites →https://doi.org/10.1242/jcs.061481openalex-snapshot
Loss of MARCH5 mitochondrial E3 ubiquitin ligase induces cellular senescence through dynamin-related protein 1 and mitofusin 1
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/10.1371/journal.pbio.1000298openalex-snapshot
PINK1 Is Selectively Stabilized on Impaired Mitochondria to Activate Parkin
inferredcites →https://doi.org/10.1371/journal.pgen.0040006openalex-snapshot
The Molecular Mechanisms of OPA1-Mediated Optic Atrophy in Drosophila Model and Prospects for Antioxidant Treatment
inferredcites →https://doi.org/10.1371/journal.pgen.1000022openalex-snapshot
The C. elegans Opa1 Homologue EAT-3 Is Essential for Resistance to Free Radicals
inferredcites →https://doi.org/10.1371/journal.pone.0003613openalex-snapshot
Mitochondrial Fusion Is Increased by the Nuclear Coactivator PGC-1β
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Micropatterning Facilitates the Long‐Term Growth and Analysis of iPSC‐Derived Individual Human Neurons and Neuronal Networks
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A Germline‐Specific Regulator of Mitochondrial Fusion is Required for Maintenance and Differentiation of Germline Stem and Progenitor Cells
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SIRT3‐Mediated Deacetylation of DRP1 K711 Prevents Mitochondrial Dysfunction in Parkinson's Disease
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Neuronal ABCA7 deficiency aggravates mitochondrial dysfunction and neurodegeneration in Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/ange.202417469openalex-snapshot
Spontaneously Blinkogenic Probe for Wash‐Free Single‐Molecule Localization‐Based Super‐Resolution Imaging in Living Cells
inferred← citeshttps://doi.org/10.1002/anie.202417469openalex-snapshot
Spontaneously Blinkogenic Probe for Wash‐Free Single‐Molecule Localization‐Based Super‐Resolution Imaging in Living Cells
inferred← citeshttps://doi.org/10.1002/asia.201900468openalex-snapshot
Design and Synthesis of 2‐(5‐Phenylindol‐3‐yl)benzimidazole Derivatives with Antiproliferative Effects towards Triple‐Negative Breast Cancer Cells by Activation of ROS‐Mediated Mitochondria Dysfunction
inferred← citeshttps://doi.org/10.1002/bies.201100179openalex-snapshot
Mitochondria: Starving to reach quorum?
inferred← citeshttps://doi.org/10.1002/bies.201200125openalex-snapshot
Quality control of mitochondria during aging: Is there a good and a bad side of mitochondrial dynamics?
inferred← citeshttps://doi.org/10.1002/bies.202400090openalex-snapshot
FAM210A: An emerging regulator of mitochondrial homeostasis
inferred← citeshttps://doi.org/10.1002/bies.70146openalex-snapshot
Mitochondrial Signaling and Stress Responses, Key Regulators of Aging and Longevity
inferred← citeshttps://doi.org/10.1002/biof.1637openalex-snapshot
The roles of melatonin on kidney injury in obese and diabetic conditions
inferred← citeshttps://doi.org/10.1002/biot.201500168openalex-snapshot
Polyphosphate as a metabolic fuel in Metazoa: A foundational breakthrough invention for biomedical applications
inferred← citeshttps://doi.org/10.1002/cbin.12206openalex-snapshot
ATAD3 is a limiting factor in mitochondrial biogenesis and adipogenesis of white adipocyte‐like 3T3‐L1 cells
inferred← citeshttps://doi.org/10.1002/cphy.c230009openalex-snapshot
Mitochondrial Function and Dysfunction in White Adipocytes and Therapeutic Implications
inferred← citeshttps://doi.org/10.1002/elps.202000125openalex-snapshot
An impedimetric assay for the identification of abnormal mitochondrial dynamics in living cells
inferred← citeshttps://doi.org/10.1002/em.70013openalex-snapshot
Mitochondria‐Nuclear Crosstalk: Orchestrating mtDNA Maintenance
inferred← citeshttps://doi.org/10.1002/embj.201386474openalex-snapshot
Stress‐induced OMA1 activation and autocatalytic turnover regulate OPA1‐dependent mitochondrial dynamics
inferred← citeshttps://doi.org/10.1002/embr.201338225openalex-snapshot
Dynamic survey of mitochondria by ubiquitin
inferred← citeshttps://doi.org/10.1002/ijc.28992openalex-snapshot
Noninvasive assessment of mitochondrial organization in three-dimensional tissues reveals changes associated with cancer development
inferred← citeshttps://doi.org/10.1002/iub.2615openalex-snapshot
Induced effect of zinc oxide nanoparticles on human acute myeloid leukemia cell apoptosis by regulating mitochondrial division
inferred← citeshttps://doi.org/10.1002/j.2040-4603.2024.tb00302.xopenalex-snapshot
Mitochondrial Function and Dysfunction in White Adipocytes and Therapeutic Implications
inferred← citeshttps://doi.org/10.1002/jat.3933openalex-snapshot
Impairment of mitochondrial dynamics involved in iron oxide nanoparticle‐induced dysfunction of dendritic cells was alleviated by autophagy inhibitor 3‐methyladenine
inferred← citeshttps://doi.org/10.1002/jbio.201960140openalex-snapshot
Insulin resistance is improved in high‐fat fed mice by photobiomodulation therapy at 630 nm
inferred← citeshttps://doi.org/10.1002/jbio.202000462openalex-snapshot
In vivo optoretinography of phototransduction activation and energy metabolism in retinal photoreceptors
inferred← citeshttps://doi.org/10.1002/jbm.a.37668openalex-snapshot
Nanoparticle‐based therapeutic strategies for mitochondrial dysfunction in cardiovascular disease
inferred← citeshttps://doi.org/10.1002/jcb.24177openalex-snapshot
Maintenance of feeder free anchorage independent cultures of ES and iPS cells by retinol/vitamin A
inferred← citeshttps://doi.org/10.1002/jcb.24671openalex-snapshot
Energy Metabolism Characterization of a Novel Cancer Stem Cell‐ L ike Line 3 AB ‐ OS
inferred← citeshttps://doi.org/10.1002/jcb.24709openalex-snapshot
Apoptosis Regulation at the Mitochondrial Outer Membrane
inferred← citeshttps://doi.org/10.1002/jcb.25016openalex-snapshot
Regulation of Mitochondrial Morphology by Positive Feedback Interaction Between PKCδ and Drp1 in Vascular Smooth Muscle Cell
inferred← citeshttps://doi.org/10.1002/jcb.25154openalex-snapshot
The Critical Role of Dynamin‐Related Protein 1 in Hypoxia‐Induced Pulmonary Vascular Angiogenesis
inferred← citeshttps://doi.org/10.1002/jcb.29311openalex-snapshot
Mitochondria could be a potential key mediator linking the intestinal microbiota to depression
inferred← citeshttps://doi.org/10.1002/jcp.23021openalex-snapshot
Crosstalk between mitochondrial (dys)function and mitochondrial abundance
inferred← citeshttps://doi.org/10.1002/jcp.25260openalex-snapshot
Autophagy as a Potential Target for Sarcopenia
inferred← citeshttps://doi.org/10.1002/jcp.25943openalex-snapshot
Polydatin impairs mitochondria fitness and ameliorates podocyte injury by suppressing Drp1 expression
inferred← citeshttps://doi.org/10.1002/jcp.26145openalex-snapshot
Tetrahydrocurcumin ameliorates homocysteine‐mediated mitochondrial remodeling in brain endothelial cells
inferred← citeshttps://doi.org/10.1002/jcp.26897openalex-snapshot
Effects of biphasic and monophasic electrical stimulation on mitochondrial dynamics, cell apoptosis, and cell proliferation
inferred← citeshttps://doi.org/10.1002/jcp.30576openalex-snapshot
N6‐methyladenosine RNA methylation: A novel regulator of the development and function of immune cells
inferred← citeshttps://doi.org/10.1002/jlb.1a0720-471ropenalex-snapshot
Mitofusin-2 regulates leukocyte adhesion and β2 integrin activation
inferred← citeshttps://doi.org/10.1002/jmor.21242openalex-snapshot
Morphogenesis of the Balbiani body in developing oocytes of an orthopteran, Metrioptera brachyptera , and multiplication of female germline mitochondria
inferred← citeshttps://doi.org/10.1002/jnr.24511openalex-snapshot
Differential mitochondrial morphology in ventral striatal projection neuron subtypes
inferred← citeshttps://doi.org/10.1002/jnr.25276openalex-snapshot
Selective vulnerability of hippocampal CA1 and CA3 pyramidal cells: What are possible pathomechanisms and should more attention be paid to the CA3 region in future studies?
inferred← citeshttps://doi.org/10.1002/jor.24828openalex-snapshot
Drp1‐mediated mitochondrial fission is involved in oxidized low‐density lipoprotein‐induced AF cella poptosis
inferred← citeshttps://doi.org/10.1002/lipd.12119openalex-snapshot
Resolvin E1 Improves Mitochondrial Function in Human Alveolar Epithelial Cells during Severe Inflammation
inferred← citeshttps://doi.org/10.1002/mnfr.201200718openalex-snapshot
Curcumin, a potential therapeutic candidate for retinal diseases
inferred← citeshttps://doi.org/10.1002/prca.201400030openalex-snapshot
Proteomics in neurodegenerative diseases: Methods for obtaining a closer look at the neuronal proteome
inferred← citeshttps://doi.org/10.1002/pro.2629openalex-snapshot
Crystal structure and functional analysis of MiD49, a receptor for the mitochondrial fission protein Drp1
inferred← citeshttps://doi.org/10.1002/slct.202403717openalex-snapshot
New Quinazolinone‐Thiouracil Derivatives: Design, Synthesis, Anticancer Evaluation, and In Silico Analysis
inferred← citeshttps://doi.org/10.1002/stem.3256openalex-snapshot
DNMT3B deficiency alters mitochondrial biogenesis and α-ketoglutarate levels in human embryonic stem cells
inferred← citeshttps://doi.org/10.1002/stem.695openalex-snapshot
The Mitochondrial Electron Transport Chain Is Dispensable for Proliferation and Differentiation of Epidermal Progenitor Cells
inferred← citeshttps://doi.org/10.1002/syn.21622openalex-snapshot
Mitochondrial plasticity of the hippocampus in a genetic rat model of depression after antidepressant treatment
inferred← citeshttps://doi.org/10.1002/yea.3062openalex-snapshot
Mdm31 protein mediates sensitivity to potassium ionophores but does not regulate mitochondrial morphology or phospholipid trafficking inSchizosaccharomyces pombe
inferred← citeshttps://doi.org/10.1007/164_2017_3openalex-snapshot
Mitochondria in Alzheimer’s Disease and Diabetes-Associated Neurodegeneration: License to Heal!
inferred← citeshttps://doi.org/10.1007/978-0-85729-701-3_3openalex-snapshot
Mutations in Nuclear Genes That Affect Mitochondrial Function in Parkinson’s Disease
inferred← citeshttps://doi.org/10.1007/978-1-4471-6702-0_10openalex-snapshot
The Nature of Living Things
inferred← citeshttps://doi.org/10.1007/978-1-4614-3381-1_7openalex-snapshot
Endoplasmic Reticulum-Targeted Bcl-2 Inhibitable Mitochondrial Fragmentation Initiates ER Stress-Induced Cell Death
inferred← citeshttps://doi.org/10.1007/978-1-4614-3573-0_2openalex-snapshot
Mitochondrial Dynamics: The Intersection of Form and Function
inferred← citeshttps://doi.org/10.1007/978-1-4614-3722-2_9openalex-snapshot
Defects in Mitochondrial Dynamics and Mitochondrial DNA Instability
inferred← citeshttps://doi.org/10.1007/978-1-4614-4599-9_17openalex-snapshot
Mitochondrial Dynamics in Health and Disease
inferred← citeshttps://doi.org/10.1007/978-1-4614-4599-9_3openalex-snapshot
Mitochondrial Structure, Composition, and Dynamics
inferred← citeshttps://doi.org/10.1007/978-1-4939-3124-8_2openalex-snapshot
Live-Cell Imaging of Mitochondria and the Actin Cytoskeleton in Budding Yeast
inferred← citeshttps://doi.org/10.1007/978-1-4939-8697-2_20openalex-snapshot
Analytical Platforms and Techniques to Study Stem Cell Metabolism
inferred← citeshttps://doi.org/10.1007/978-1-61779-606-7_10openalex-snapshot
The Role of Mitochondrial Oxidative Stress in Retinal Dysfunction
inferred← citeshttps://doi.org/10.1007/978-1-62703-487-6_17openalex-snapshot
Analyzing Membrane Dynamics with Live Cell Fluorescence Microscopy with a Focus on Yeast Mitochondria
inferred← citeshttps://doi.org/10.1007/978-3-030-40955-5_4openalex-snapshot
Mitochondrial Function in Aging
inferred← citeshttps://doi.org/10.1007/978-3-030-45607-8_14openalex-snapshot
The Nature of Living Things
inferred← citeshttps://doi.org/10.1007/978-3-030-67928-6_136-1openalex-snapshot
Synaptic and Extrasynaptic Mitochondria
inferred← citeshttps://doi.org/10.1007/978-3-030-78799-8_10openalex-snapshot
Mitochondria and Their Cell Hosts: Best of Frenemies
inferred← citeshttps://doi.org/10.1007/978-3-030-80962-1_287-1openalex-snapshot
Quantum Medicine and the Immune System
inferred← citeshttps://doi.org/10.1007/978-3-030-92392-1_136openalex-snapshot
Synaptic and Extrasynaptic Mitochondria
inferred← citeshttps://doi.org/10.1007/978-3-031-08309-9_6openalex-snapshot
Metabolic Regulation of Mitochondrial Dynamics and Cardiac Function
inferred← citeshttps://doi.org/10.1007/978-3-031-20730-3_17openalex-snapshot
Machine Learning-Based QSAR Models and Structural Alerts for Prediction of Mitochondrial Dysfunction
inferred← citeshttps://doi.org/10.1007/978-3-031-40858-8_469-1openalex-snapshot
Aurora Kinase A: Bridging Breast Cancer Therapy and Disability-Inclusive Care
inferred← citeshttps://doi.org/10.1007/978-3-031-47331-9_3openalex-snapshot
Mitochondrial Function in Health and Disease: Responses to Helicobacter pylori Metabolism and Impact in Gastric Cancer Development
inferred← citeshttps://doi.org/10.1007/978-3-032-00773-5_287openalex-snapshot
Quantum Medicine and the Immune System
inferred← citeshttps://doi.org/10.1007/978-3-032-06766-1_9openalex-snapshot
Analysis of Bush Cricket Oogenesis Provides an Insight into the Function and Anagenesis of an Enigmatic Organelle Assemblage: The Balbiani Body
inferred← citeshttps://doi.org/10.1007/978-3-319-22671-2_8openalex-snapshot
The Emerging Role of MitomiRs in the Pathophysiology of Human Disease
inferred← citeshttps://doi.org/10.1007/978-3-319-25844-7_8openalex-snapshot
8 Molecular Control of Fungal Senescence and Longevity
inferred← citeshttps://doi.org/10.1007/978-3-319-26587-2_171-1openalex-snapshot
Mitochondrial Biology in Hepatobiliary Tumors: Changes of the Cellular Energy Factory
inferred← citeshttps://doi.org/10.1007/978-3-319-26956-6_171openalex-snapshot
Mitochondrial Biology in Hepatobiliary Tumors: Changes of the Cellular Energy Factory
inferred← citeshttps://doi.org/10.1007/978-3-319-28637-2_1openalex-snapshot
An Introduction to Mitochondria, Their Structure and Functions
inferred← citeshttps://doi.org/10.1007/978-3-319-53235-6_9openalex-snapshot
Cancer Stem Cells and Tumor Microenvironment in Radiotherapy
inferred← citeshttps://doi.org/10.1007/978-3-319-58106-4_8openalex-snapshot
The Critical Role of Mitochondria in Drug-Induced Liver Injury
inferred← citeshttps://doi.org/10.1007/978-3-319-64543-8_11openalex-snapshot
Developing Circadian Therapeutics Against Age-Related Metabolic Decline
inferred← citeshttps://doi.org/10.1007/978-3-319-73344-9_11openalex-snapshot
Role of Mitochondria in Neurodegenerative Diseases: The Dark Side of the “Energy Factory”
inferred← citeshttps://doi.org/10.1007/978-3-7091-0962-5_14openalex-snapshot
The Role of Mitochondria in the Activation/Maintenance of SOCE
inferred← citeshttps://doi.org/10.1007/978-3-7091-1232-8_2openalex-snapshot
Aging in the Single-Celled Eukaryote, S. cerevisiae
inferred← citeshttps://doi.org/10.1007/978-4-431-56068-5_23openalex-snapshot
Roles of Mitochondrial Sensing and Stress Response in the Regulation of Inflammation
inferred← citeshttps://doi.org/10.1007/978-94-007-2888-2_17openalex-snapshot
Mitochondria-Associated Membranes (MAMs) as Hotspot Ca2+ Signaling Units
inferred← citeshttps://doi.org/10.1007/978-981-13-2233-4_17openalex-snapshot
Multi-localized Proteins: The Peroxisome-Mitochondria Connection
inferred← citeshttps://doi.org/10.1007/978-981-15-7586-0_6openalex-snapshot
ROS and Oxidative Stress in Cancer: Recent Advances
inferred← citeshttps://doi.org/10.1007/978-981-16-3464-2_7openalex-snapshot
Mammary Epithelial Cells: A Potential Cellular Model to Understand the Impact of Heat Stress on Mammary Gland and Milk Production in Dairy Animals
inferred← citeshttps://doi.org/10.1007/978-981-95-6099-8_4openalex-snapshot
Cellular Bioenergetics in Ubiquitin-Proteasome System Functionality
inferred← citeshttps://doi.org/10.1007/978-981-97-6695-6_5openalex-snapshot
Circadian Control of Mitochondrial Dynamics and Its Implication in Aging
inferred← citeshttps://doi.org/10.1007/978-981-99-7342-2_8openalex-snapshot
Cell Cycle, DNA Damage Repair Systems, and Impact of Redox Regulation in Cancer
inferred← citeshttps://doi.org/10.1007/s00018-012-1066-6openalex-snapshot
Regulation of mitochondrial dynamics: convergences and divergences between yeast and vertebrates
inferred← citeshttps://doi.org/10.1007/s00018-013-1428-8openalex-snapshot
Human mitochondrial Fis1 links to cell cycle regulators at G2/M transition
inferred← citeshttps://doi.org/10.1007/s00018-016-2282-2openalex-snapshot
Mitochondrial cAMP signaling
inferred← citeshttps://doi.org/10.1007/s00018-016-2364-1openalex-snapshot
Schwann cell mitochondria as key regulators in the development and maintenance of peripheral nerve axons
inferred← citeshttps://doi.org/10.1007/s00018-018-2963-0openalex-snapshot
Mitochondrial functions and melatonin: a tour of the reproductive cancers
inferred← citeshttps://doi.org/10.1007/s00018-020-03546-3openalex-snapshot
Studies of ApoD−/− and ApoD−/−ApoE−/− mice uncover the APOD significance for retinal metabolism, function, and status of chorioretinal blood vessels
inferred← citeshttps://doi.org/10.1007/s00018-023-04962-xopenalex-snapshot
Metabolic and cell cycle shift induced by the deletion of Dnm1l attenuates the dissolution of pluripotency in mouse embryonic stem cells
inferred← citeshttps://doi.org/10.1007/s00018-025-05995-0openalex-snapshot
Regulation of mitochondrial dynamics and function by melatonin type 1 receptor in parkinson’s disease
inferred← citeshttps://doi.org/10.1007/s00109-015-1258-2openalex-snapshot
Mitochondrial dynamics in cardiovascular disease: fission and fusion foretell form and function
inferred← citeshttps://doi.org/10.1007/s00109-021-02150-7openalex-snapshot
Mitochondrial dynamics and its impact on human health and diseases: inside the DRP1 blackbox
inferred← citeshttps://doi.org/10.1007/s00125-016-3891-xopenalex-snapshot
Mitochondrial network regulation and its potential interference with inflammatory signals in pancreatic beta cells
inferred← citeshttps://doi.org/10.1007/s00204-014-1401-9openalex-snapshot
Glutathione and mitochondria determine acute defense responses and adaptive processes in cadmium-induced oxidative stress and toxicity of the kidney
inferred← citeshttps://doi.org/10.1007/s00204-019-02390-0openalex-snapshot
Roles of mitochondrial fission inhibition in developmental fluoride neurotoxicity: mechanisms of action in vitro and associations with cognition in rats and children
inferred← citeshttps://doi.org/10.1007/s00204-020-02764-9openalex-snapshot
In vitro study of carbon black nanoparticles on human pulmonary artery endothelial cells: effects on calcium signaling and mitochondrial alterations
inferred← citeshttps://doi.org/10.1007/s00204-021-03160-7openalex-snapshot
Mapping the cellular response to electron transport chain inhibitors reveals selective signaling networks triggered by mitochondrial perturbation
inferred← citeshttps://doi.org/10.1007/s00204-022-03375-2openalex-snapshot
Activation of autophagy triggers mitochondrial loss and changes acetylation profile relevant for mechanotransduction in bladder cancer cells
inferred← citeshttps://doi.org/10.1007/s00204-024-03865-5openalex-snapshot
Research advances on CaMKs-mediated neurodevelopmental injury
inferred← citeshttps://doi.org/10.1007/s00204-026-04451-7openalex-snapshot
Mitochondrial dynamics in environmental neurotoxicity: beyond oxidative stress toward spatial and functional reorganization
inferred← citeshttps://doi.org/10.1007/s00210-014-1047-4openalex-snapshot
Mitochondrial NM23-H4/NDPK-D: a bifunctional nanoswitch for bioenergetics and lipid signaling
inferred← citeshttps://doi.org/10.1007/s00294-015-0542-6openalex-snapshot
Regulation of mitochondrial inner membrane fusion: divergent evolution with similar solutions?
inferred← citeshttps://doi.org/10.1007/s00395-016-0578-xopenalex-snapshot
Inhibition of mitochondrial fission as a molecular target for cardioprotection: critical importance of the timing of treatment
inferred← citeshttps://doi.org/10.1007/s00395-020-0796-0openalex-snapshot
Longitudinal metabolic profiling of cardiomyocytes derived from human-induced pluripotent stem cells
inferred← citeshttps://doi.org/10.1007/s00395-023-01009-xopenalex-snapshot
Mitophagy for cardioprotection
inferred← citeshttps://doi.org/10.1007/s00415-011-6104-zopenalex-snapshot
The role of mitochondria in neurodegenerative diseases
inferred← citeshttps://doi.org/10.1007/s00418-016-1424-9openalex-snapshot
Reactive oxygen species effect PASMCs apoptosis via regulation of dynamin-related protein 1 in hypoxic pulmonary hypertension
inferred← citeshttps://doi.org/10.1007/s00424-019-02258-3openalex-snapshot
Mitochondrial dynamics in exercise physiology
inferred← citeshttps://doi.org/10.1007/s00424-020-02357-6openalex-snapshot
Effects of aging and exercise training on mitochondrial function and apoptosis in the rat heart
inferred← citeshttps://doi.org/10.1007/s00441-016-2414-xopenalex-snapshot
Exclusion of dysfunctional mitochondria from Balbiani body during early oogenesis of Thermobia
inferred← citeshttps://doi.org/10.1007/s00592-026-02645-0openalex-snapshot
A TFAP4-UBC9-SUMO1 axis orchestrates pathological mitochondrial hyperfission in diabetic complications
inferred← citeshttps://doi.org/10.1007/s00726-021-03028-1openalex-snapshot
Bioactive peptide apelin rescues acute kidney injury by protecting the function of renal tubular mitochondria
inferred← citeshttps://doi.org/10.1007/s00775-026-02139-yopenalex-snapshot
Emerging role of mitoNEET as mitochondrial sensor of hypoxia
inferred← citeshttps://doi.org/10.1007/s10495-014-1016-xopenalex-snapshot
Beta-nodavirus B2 protein induces hydrogen peroxide production, leading to Drp1-recruited mitochondrial fragmentation and cell death via mitochondrial targeting
inferred← citeshttps://doi.org/10.1007/s10522-013-9474-zopenalex-snapshot
The systems biology of mitochondrial fission and fusion and implications for disease and aging
inferred← citeshttps://doi.org/10.1007/s10522-014-9515-2openalex-snapshot
Mitochondrial function and mitochondrial DNA maintenance with advancing age
inferred← citeshttps://doi.org/10.1007/s10522-014-9546-8openalex-snapshot
Exercise improves mitochondrial and redox-regulated stress responses in the elderly: better late than never!
inferred← citeshttps://doi.org/10.1007/s10528-017-9829-2openalex-snapshot
DNM1L Variant Alters Baseline Mitochondrial Function and Response to Stress in a Patient with Severe Neurological Dysfunction
inferred← citeshttps://doi.org/10.1007/s10545-015-9819-7openalex-snapshot
Peroxisome‐mitochondria interplay and disease
inferred← citeshttps://doi.org/10.1007/s10565-018-9447-8openalex-snapshot
Drp1-associated mitochondrial dysfunction and mitochondrial autophagy: a novel mechanism in triptolide-induced hepatotoxicity
inferred← citeshttps://doi.org/10.1007/s10565-020-09561-1openalex-snapshot
Mediators of mitophagy that regulate mitochondrial quality control play crucial role in diverse pathophysiology
inferred← citeshttps://doi.org/10.1007/s10565-021-09629-6openalex-snapshot
Vitamin D3 decreases TNF-α-induced inflammation in lung epithelial cells through a reduction in mitochondrial fission and mitophagy
inferred← citeshttps://doi.org/10.1007/s10565-021-09662-5openalex-snapshot
Mitochondrial dynamics regulators: implications for therapeutic intervention in cancer
inferred← citeshttps://doi.org/10.1007/s10565-022-09712-6openalex-snapshot
High-content high-throughput imaging reveals distinct connections between mitochondrial morphology and functionality for OXPHOS complex I, III, and V inhibitors
inferred← citeshttps://doi.org/10.1007/s10565-025-10071-1openalex-snapshot
Asperosaponin VI mitigates mitochondrial dysfunction and chondrocyte apoptosis in osteoarthritis by modulating the AMPK-SIRT3 pathway
inferred← citeshttps://doi.org/10.1007/s10571-018-0584-7openalex-snapshot
ROS as Regulators of Mitochondrial Dynamics in Neurons
inferred← citeshttps://doi.org/10.1007/s10571-023-01376-yopenalex-snapshot
Microglial Metabolic Reprogramming: Emerging Insights and Therapeutic Strategies in Neurodegenerative Diseases
inferred← citeshttps://doi.org/10.1007/s10735-020-09952-yopenalex-snapshot
Lyciumamide A, a dimer of phenolic amide, protects against NMDA-induced neurotoxicity and potential mechanisms in vitro
inferred← citeshttps://doi.org/10.1007/s10735-026-10965-2openalex-snapshot
SIRT3-mediated DRP1 acetylation changes are associated with the restoration of mitochondrial function and alleviation of anterior cruciate ligament injury-induced osteoarthritis
inferred← citeshttps://doi.org/10.1007/s10741-012-9330-2openalex-snapshot
Mitochondria in heart failure: the emerging role of mitochondrial dynamics
inferred← citeshttps://doi.org/10.1007/s10741-016-9530-2openalex-snapshot
Mitochondrial dynamics and cell death in heart failure
inferred← citeshttps://doi.org/10.1007/s10753-020-01370-2openalex-snapshot
Isoliquiritigenin Reduces LPS-Induced Inflammation by Preventing Mitochondrial Fission in BV-2 Microglial Cells
inferred← citeshttps://doi.org/10.1007/s10815-017-1006-3openalex-snapshot
Selection of mitochondria in female germline cells: is Balbiani body implicated in this process?
inferred← citeshttps://doi.org/10.1007/s10863-011-9381-4openalex-snapshot
Mammalian NADH:ubiquinone oxidoreductase (Complex I) and nicotinamide nucleotide transhydrogenase (Nnt) together regulate the mitochondrial production of H2O2—Implications for their role in disease, especially cancer
inferred← citeshttps://doi.org/10.1007/s10863-012-9494-4openalex-snapshot
Matters of the heart in bioenergetics: mitochondrial fusion into continuous reticulum is not needed for maximal respiratory activity
inferred← citeshttps://doi.org/10.1007/s10863-014-9575-7openalex-snapshot
Mitochondrial dynamics: cell-type and hippocampal region specific changes following global cerebral ischemia
inferred← citeshttps://doi.org/10.1007/s10863-014-9589-1openalex-snapshot
Evidence to support mitochondrial neuroprotection, in severe traumatic brain injury
inferred← citeshttps://doi.org/10.1007/s10863-016-9662-zopenalex-snapshot
Revisiting trends on mitochondrial mega-channels for the import of proteins and nucleic acids
inferred← citeshttps://doi.org/10.1007/s10863-019-09800-zopenalex-snapshot
Mitochondria as a possible target for nicotine action
inferred← citeshttps://doi.org/10.1007/s10863-023-09959-6openalex-snapshot
The status and trends of mitochondrial dynamics research: A global bibliometric and visualized analysis
inferred← citeshttps://doi.org/10.1007/s10895-025-04567-6openalex-snapshot
High-Photostability Perylene-Derived Probe Enables Accurate Dual-Modality Imaging of Mitochondrial Membrane Potential
inferred← citeshttps://doi.org/10.1007/s11010-014-2076-5openalex-snapshot
Mitochondrial quality control systems sustain brain mitochondrial bioenergetics in early stages of type 2 diabetes
inferred← citeshttps://doi.org/10.1007/s11033-014-3663-yopenalex-snapshot
Mitochondrial dynamic changes in health and genetic diseases
inferred← citeshttps://doi.org/10.1007/s11033-022-07959-0openalex-snapshot
Chemical inhibition of mitochondrial fission improves insulin signaling and subdues hyperglycemia induced stress in placental trophoblast cells
inferred← citeshttps://doi.org/10.1007/s11033-024-09285-zopenalex-snapshot
An integral role of mitochondrial function in the pathophysiology of preeclampsia
inferred← citeshttps://doi.org/10.1007/s11064-015-1604-3openalex-snapshot
Mitochondrial Division Inhibitor 1 Ameliorates Mitochondrial Injury, Apoptosis, and Motor Dysfunction After Acute Spinal Cord Injury in Rats
inferred← citeshttps://doi.org/10.1007/s11064-015-1631-0openalex-snapshot
Abnormal Glucose Metabolism in Alzheimer’s Disease: Relation to Autophagy/Mitophagy and Therapeutic Approaches
inferred← citeshttps://doi.org/10.1007/s11064-025-04357-3openalex-snapshot
HIV-1 gp120 Interactions with Nicotine Modulate Mitochondrial Network Properties and Amyloid Release in Microglia
inferred← citeshttps://doi.org/10.1007/s11103-022-01318-0openalex-snapshot
High temporal-resolution transcriptome landscapes of maize embryo sac and ovule during early seed development
inferred← citeshttps://doi.org/10.1007/s11154-023-09827-zopenalex-snapshot
White adipose tissue mitochondrial bioenergetics in metabolic diseases
inferred← citeshttps://doi.org/10.1007/s11357-020-00179-zopenalex-snapshot
Accelerated cerebral vascular injury in diabetes is associated with vascular smooth muscle cell dysfunction
inferred← citeshttps://doi.org/10.1007/s11357-026-02515-1openalex-snapshot
Therapeutic potential of MitoQ, a mitochondria-targeted antioxidant, in age-related physiological dysfunction
inferred← citeshttps://doi.org/10.1007/s11427-023-2552-7openalex-snapshot
LPS-related muscle loss is associated with the alteration of Bacteroidetes abundance, systemic inflammation, and mitochondrial morphology in a weaned piglet model
inferred← citeshttps://doi.org/10.1007/s11538-026-01738-9openalex-snapshot
Algebraic Representation of Mitochondrial Dynamics
inferred← citeshttps://doi.org/10.1007/s11626-020-00446-5openalex-snapshot
Heat stress induces apoptosis through disruption of dynamic mitochondrial networks in dairy cow mammary epithelial cells
inferred← citeshttps://doi.org/10.1007/s11626-021-00616-zopenalex-snapshot
Vascular endothelial growth factor ameliorated palmitate-induced cardiomyocyte injury via JNK pathway
inferred← citeshttps://doi.org/10.1007/s11684-017-0569-9openalex-snapshot
Non-genetic mechanisms of diabetic nephropathy
inferred← citeshttps://doi.org/10.1007/s11738-022-03453-zopenalex-snapshot
Codon usage bias and evolution analysis in the mitochondrial genome of Mesona chinensis Benth
inferred← citeshttps://doi.org/10.1007/s11892-019-1263-xopenalex-snapshot
Crosstalk Between Lipids and Mitochondria in Diabetic Kidney Disease
inferred← citeshttps://doi.org/10.1007/s11910-012-0260-0openalex-snapshot
Disorders of the Optic Nerve in Mitochondrial Cytopathies: New Ideas on Pathogenesis and Therapeutic Targets
inferred← citeshttps://doi.org/10.1007/s11912-022-01333-wopenalex-snapshot
Mitochondrial Dynamin-Related Protein Drp1: a New Player in Cardio-oncology
inferred← citeshttps://doi.org/10.1007/s11914-024-00874-2openalex-snapshot
Interplay Between Skeletal and Hematopoietic Cells in the Bone Marrow Microenvironment in Homeostasis and Aging
inferred← citeshttps://doi.org/10.1007/s12012-020-09626-xopenalex-snapshot
Mitochondrial Sirtuins and Doxorubicin-induced Cardiotoxicity
inferred← citeshttps://doi.org/10.1007/s12013-014-0245-5openalex-snapshot
The Interplay Between Apoptosis, Mitophagy and Mitochondrial Biogenesis Induced by Resveratrol Can Determine Activated Hepatic Stellate Cells Death or Survival
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