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Individual cristae within the same mitochondrion display different membrane potentials and are functionally independent
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1873-3468.12384openalex-snapshot
OPA1 functionally interacts with MIC60 but is dispensable for crista junction formation
inferredcites →https://doi.org/10.1002/ar.1091140304openalex-snapshot
The fine structure of mitochondria
inferredcites →https://doi.org/10.1016/j.bbamcr.2016.05.020openalex-snapshot
Role of the mitochondrial contact site and cristae organizing system in membrane architecture and dynamics
inferredcites →https://doi.org/10.1016/j.bbamcr.2017.05.004openalex-snapshot
Mitochondrial contact site and cristae organizing system: A central player in membrane shaping and crosstalk
inferredcites →https://doi.org/10.1016/j.cell.2006.06.025openalex-snapshot
OPA1 Controls Apoptotic Cristae Remodeling Independently from Mitochondrial Fusion
inferredcites →https://doi.org/10.1016/j.celrep.2016.11.049openalex-snapshot
Optic Atrophy 1 Is Epistatic to the Core MICOS Component MIC60 in Mitochondrial Cristae Shape Control
inferredcites →https://doi.org/10.1016/j.cmet.2011.04.007openalex-snapshot
Mitochondrial Phosphatase PTPMT1 Is Essential for Cardiolipin Biosynthesis
inferredcites →https://doi.org/10.1016/j.cmet.2015.04.006openalex-snapshot
Mic10 Oligomerizes to Bend Mitochondrial Inner Membranes at Cristae Junctions
inferredcites →https://doi.org/10.1016/j.devcel.2011.08.026openalex-snapshot
Dual Role of Mitofilin in Mitochondrial Membrane Organization and Protein Biogenesis
inferredcites →https://doi.org/10.1016/j.febslet.2005.09.065openalex-snapshot
Structure of dimeric ATP synthase from mitochondria: An angular association of monomers induces the strong curvature of the inner membrane
inferredcites →https://doi.org/10.1016/j.jmb.2012.05.004openalex-snapshot
Role of MINOS in Mitochondrial Membrane Architecture: Cristae Morphology and Outer Membrane Interactions Differentially Depend on Mitofilin Domains
inferredcites →https://doi.org/10.1016/j.mam.2004.03.001openalex-snapshot
Mitochondria in health and disease: perspectives on a new mitochondrial biology
inferredcites →https://doi.org/10.1016/j.tibs.2016.01.001openalex-snapshot
Mitochondrial Cristae: Where Beauty Meets Functionality
inferredcites →https://doi.org/10.1016/s0006-3495(88)83158-8openalex-snapshot
Membrane potential can be determined in individual cells from the nernstian distribution of cationic dyes
inferredcites →https://doi.org/10.1016/s0006-3495(89)82754-7openalex-snapshot
Simultaneous imaging of cell and mitochondrial membrane potentials
inferredcites →https://doi.org/10.1016/s0006-3495(93)81318-3openalex-snapshot
Imaging in five dimensions: time-dependent membrane potentials in individual mitochondria
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/s1570-0232(03)00371-4openalex-snapshot
MitoTracker Green labeling of mitochondrial proteins and their subsequent analysis by capillary electrophoresis with laser-induced fluorescence detection
inferredcites →https://doi.org/10.1021/ac403616copenalex-snapshot
Superior Fluorescent Probe for Detection of Cardiolipin
inferredcites →https://doi.org/10.1038/191144a0openalex-snapshot
Coupling of Phosphorylation to Electron and Hydrogen Transfer by a Chemi-Osmotic type of Mechanism
inferredcites →https://doi.org/10.1038/emboj.2008.35openalex-snapshot
Dimer ribbons of ATP synthase shape the inner mitochondrial membrane
inferredcites →https://doi.org/10.1038/emboj.2011.379openalex-snapshot
The mitochondrial contact site complex, a determinant of mitochondrial architecture
inferredcites →https://doi.org/10.1038/nature14614openalex-snapshot
Mitochondrial reticulum for cellular energy distribution in muscle
inferredcites →https://doi.org/10.1038/ncomms15258openalex-snapshot
Regulated membrane remodeling by Mic60 controls formation of mitochondrial crista junctions
inferredcites →https://doi.org/10.1038/ncomms4103openalex-snapshot
Lateral pH gradient between OXPHOS complex IV and F0F1 ATP-synthase in folded mitochondrial membranes
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.7601963openalex-snapshot
Fission and selective fusion govern mitochondrial segregation and elimination by autophagy
inferredcites →https://doi.org/10.1038/srep35907openalex-snapshot
Cristae remodeling causes acidification detected by integrated graphene sensor during mitochondrial outer membrane permeabilization
inferredcites →https://doi.org/10.1073/pnas.1103621108openalex-snapshot
Macromolecular organization of ATP synthase and complex I in whole mitochondria
inferredcites →https://doi.org/10.1073/pnas.1305462110openalex-snapshot
Age-dependent dissociation of ATP synthase dimers and loss of inner-membrane cristae in mitochondria
inferredcites →https://doi.org/10.1074/jbc.m606059200openalex-snapshot
Proteolytic Processing of OPA1 Links Mitochondrial Dysfunction to Alterations in Mitochondrial Morphology
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.142.4.975openalex-snapshot
Transient Mitochondrial Depolarizations Reflect Focal Sarcoplasmic Reticular Calcium Release in Single Rat Cardiomyocytes
inferredcites →https://doi.org/10.1083/jcb.200605138openalex-snapshot
Dynamic subcompartmentalization of the mitochondrial inner membrane
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.200811099openalex-snapshot
Formation of cristae and crista junctions in mitochondria depends on antagonism between Fcj1 and Su e / g
inferredcites →https://doi.org/10.1083/jcb.201107053openalex-snapshot
A mitochondrial-focused genetic interaction map reveals a scaffold-like complex required for inner membrane organization in mitochondria
inferredcites →https://doi.org/10.1091/mbc.e04-08-0697openalex-snapshot
The Mitochondrial Inner Membrane Protein Mitofilin Controls Cristae Morphology
inferredcites →https://doi.org/10.1093/brain/awm298openalex-snapshot
OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes
inferredcites →https://doi.org/10.1093/brain/awm335openalex-snapshot
OPA1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion
inferredcites →https://doi.org/10.1111/j.1432-1033.1969.tb19633.xopenalex-snapshot
Estimation of Membrane Potential and pH Difference across the Cristae Membrane of Rat Liver Mitochondria
inferredcites →https://doi.org/10.1177/1.4.188openalex-snapshot
AN ELECTRON MICROSCOPE STUDY OF THE MITOCHONDRIAL STRUCTURE
inferredcites →https://doi.org/10.1242/jcs.108852openalex-snapshot
Restricted diffusion of OXPHOS complexes in dynamic mitochondria delays their exchange between cristae and engenders a transitory mosaic distribution
inferredcites →https://doi.org/10.1371/journal.pone.0160258openalex-snapshot
Mic13 Is Essential for Formation of Crista Junctions in Mammalian Cells
inferredcites →https://doi.org/10.1515/hsz-2012-0254openalex-snapshot
Dynamics of bioenergetic microcompartments
inferredcites →https://doi.org/10.1523/jneurosci.20-19-07208.2000openalex-snapshot
Mitochondrial Membrane Potential and Glutamate Excitotoxicity in Cultured Cerebellar Granule Cells
inferredcites →https://doi.org/10.15252/embj.2018101056openalex-snapshot
Individual cristae within the same mitochondrion display different membrane potentials and are functionally independent
inferredcites →https://doi.org/10.15252/embr.201949776openalex-snapshot
Cristae undergo continuous cycles of membrane remodelling in a MICOS‐dependent manner
inferredcites →https://doi.org/10.1681/asn.2012121216openalex-snapshot
The Mitochondrial-Targeted Compound SS-31 Re-Energizes Ischemic Mitochondria by Interacting with Cardiolipin
inferredcites →https://doi.org/10.2337/db06-0757openalex-snapshot
β-Cell Mitochondria Exhibit Membrane Potential Heterogeneity That Can Be Altered by Stimulatory or Toxic Fuel Levels
inferredcites →https://doi.org/10.7554/elife.06265openalex-snapshot
QIL1 is a novel mitochondrial protein required for MICOS complex stability and cristae morphology
inferredcites →https://doi.org/10.7554/elife.07739openalex-snapshot
MICOS coordinates with respiratory complexes and lipids to establish mitochondrial inner membrane architecture
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inferred← citeshttps://doi.org/10.1021/acsami.4c09001openalex-snapshot
Dual-Modality Imaging with a Zwitterionic Fluorescent Probe for Reversible Monitoring of Mitochondrial Membrane Potential Dynamics
inferred← citeshttps://doi.org/10.1021/acscentsci.4c00616openalex-snapshot
Gentle Rhodamines for Live-Cell Fluorescence Microscopy
inferred← citeshttps://doi.org/10.1021/acsnano.3c02768openalex-snapshot
Super-Resolution Imaging of Voltages in the Interior of Individual, Vital Mitochondria
inferred← citeshttps://doi.org/10.1021/jacsau.5c00261openalex-snapshot
Rotation-Direction-Dependent Mechanism of the Inhibitor Protein IF1 for Mitochondrial ATP Synthase from Atomistic Simulations
inferred← citeshttps://doi.org/10.1038/d41586-021-01173-xopenalex-snapshot
Revolutionary view of two ways to split a mitochondrion
inferred← citeshttps://doi.org/10.1038/d41586-024-02528-wopenalex-snapshot
Inner membrane turns inside out to exit mitochondrial organelles
inferred← citeshttps://doi.org/10.1038/s41392-022-01243-0openalex-snapshot
Organelle-targeted therapies: a comprehensive review on system design for enabling precision oncology
inferred← citeshttps://doi.org/10.1038/s41419-020-03152-yopenalex-snapshot
OPA1 and MICOS Regulate mitochondrial crista dynamics and formation
inferred← citeshttps://doi.org/10.1038/s41419-023-05572-yopenalex-snapshot
The mitochondrial inhibitor IF1 binds to the ATP synthase OSCP subunit and protects cancer cells from apoptosis
inferred← citeshttps://doi.org/10.1038/s41419-023-05678-3openalex-snapshot
TIM-4 orchestrates mitochondrial homeostasis to promote lung cancer progression via ANXA2/PI3K/AKT/OPA1 axis
inferred← citeshttps://doi.org/10.1038/s41467-020-20381-zopenalex-snapshot
ATP synthase hexamer assemblies shape cristae of Toxoplasma mitochondria
inferred← citeshttps://doi.org/10.1038/s41467-022-30431-3openalex-snapshot
Mechanical instability generated by Myosin 19 contributes to mitochondria cristae architecture and OXPHOS
inferred← citeshttps://doi.org/10.1038/s41467-023-41682-zopenalex-snapshot
All-optical spatiotemporal mapping of ROS dynamics across mitochondrial microdomains in situ
inferred← citeshttps://doi.org/10.1038/s41580-020-0210-7openalex-snapshot
The cell biology of mitochondrial membrane dynamics
inferred← citeshttps://doi.org/10.1038/s41580-023-00613-yopenalex-snapshot
The multiple links between actin and mitochondria
inferred← citeshttps://doi.org/10.1038/s41580-024-00785-1openalex-snapshot
Molecular mechanisms of mitochondrial dynamics
inferred← citeshttps://doi.org/10.1038/s41580-025-00854-zopenalex-snapshot
Molecular machineries shaping the mitochondrial inner membrane
inferred← citeshttps://doi.org/10.1038/s41586-021-03510-6openalex-snapshot
Distinct fission signatures predict mitochondrial degradation or biogenesis
inferred← citeshttps://doi.org/10.1038/s41586-023-05793-3openalex-snapshot
Spatial mapping of mitochondrial networks and bioenergetics in lung cancer
inferred← citeshttps://doi.org/10.1038/s41586-023-05817-yopenalex-snapshot
Structural basis of mitochondrial membrane bending by the I–II–III2–IV2 supercomplex
inferred← citeshttps://doi.org/10.1038/s41586-024-07835-wopenalex-snapshot
Lysosomes drive the piecemeal removal of mitochondrial inner membrane
inferred← citeshttps://doi.org/10.1038/s41589-023-01450-yopenalex-snapshot
Long-term super-resolution inner mitochondrial membrane imaging with a lipid probe
inferred← citeshttps://doi.org/10.1038/s41589-026-02253-7openalex-snapshot
A ratiometric fluorescent reporter of mitochondrial sodium
inferred← citeshttps://doi.org/10.1038/s41598-020-67408-5openalex-snapshot
An ultra-high bandwidth nano-electronic interface to the interior of living cells with integrated fluorescence readout of metabolic activity
inferred← citeshttps://doi.org/10.1038/s41598-021-88400-7openalex-snapshot
Phosphopeptide interactions of the Nbs1 N-terminal FHA-BRCT1/2 domains
inferred← citeshttps://doi.org/10.1038/s41598-024-55780-5openalex-snapshot
The use of NADH anisotropy to investigate mitochondrial cristae alignment
inferred← citeshttps://doi.org/10.1038/s41598-024-65595-zopenalex-snapshot
Implications of mitochondrial membrane potential gradients on signaling and ATP production analyzed by correlative multi-parameter microscopy
inferred← citeshttps://doi.org/10.1038/s42003-021-02114-0openalex-snapshot
Aberrant activity of mitochondrial NCLX is linked to impaired synaptic transmission and is associated with mental retardation
inferred← citeshttps://doi.org/10.1038/s42003-022-03606-3openalex-snapshot
MICU1 controls spatial membrane potential gradients and guides Ca2+ fluxes within mitochondrial substructures
inferred← citeshttps://doi.org/10.1038/s42003-023-05214-1openalex-snapshot
IF1 promotes oligomeric assemblies of sluggish ATP synthase and outlines the heterogeneity of the mitochondrial membrane potential
inferred← citeshttps://doi.org/10.1038/s42003-026-10085-3openalex-snapshot
Membranes arrest the coarsening of mitochondrial condensates in human cells
inferred← citeshttps://doi.org/10.1038/s42003-026-11029-7openalex-snapshot
How mitochondrial heterogeneity fuels a dynamic organelle ecosystem
inferred← citeshttps://doi.org/10.1038/s44318-025-00632-9openalex-snapshot
Measuring mitochondrial membrane potential
inferred← citeshttps://doi.org/10.1038/s44318-026-00827-8openalex-snapshot
Mitochondrial calcium regulates lipid metabolism by modulating tethering of mitochondria to lipid droplets
inferred← citeshttps://doi.org/10.1038/s44319-024-00336-xopenalex-snapshot
Coordination of cytochrome bc1 complex assembly at MICOS
inferred← citeshttps://doi.org/10.1039/d4cc00018hopenalex-snapshot
Recent advances in FRET probes for mitochondrial imaging and sensing
inferred← citeshttps://doi.org/10.1039/d4cc02702gopenalex-snapshot
Targeting sub-cellular organelles for boosting precision photodynamic therapy
inferred← citeshttps://doi.org/10.1039/d4cc06022aopenalex-snapshot
Reaction-free mitochondrial membrane potential independent luminogens with aggregation-induced emission characteristics for live neuron imaging
inferred← citeshttps://doi.org/10.1042/bcj20260185openalex-snapshot
Re-evaluating the rationale for targeting oxidative phosphorylation in acute myeloid leukemia
inferred← citeshttps://doi.org/10.1042/bst20200742openalex-snapshot
The F1Fo-ATPase inhibitor, IF1, is a critical regulator of energy metabolism in cancer cells
inferred← citeshttps://doi.org/10.1042/bst20221364openalex-snapshot
Coordinating BNIP3/NIX-mediated mitophagy in space and time
inferred← citeshttps://doi.org/10.1042/bst20260167openalex-snapshot
The molecular mechanisms of crista formation: how mitochondria give themselves breathing room
inferred← citeshttps://doi.org/10.1063/5.0215900openalex-snapshot
Voltage mapping in subcellular nanodomains using electro-diffusion modeling
inferred← citeshttps://doi.org/10.1073/pnas.2008778118openalex-snapshot
High-resolution imaging reveals compartmentalization of mitochondrial protein synthesis in cultured human cells
inferred← citeshttps://doi.org/10.1073/pnas.2021012118openalex-snapshot
Interface mobility between monomers in dimeric bovine ATP synthase participates in the ultrastructure of inner mitochondrial membranes
inferred← citeshttps://doi.org/10.1073/pnas.2101675118openalex-snapshot
The human cytomegalovirus protein pUL13 targets mitochondrial cristae architecture to increase cellular respiration during infection
inferred← citeshttps://doi.org/10.1073/pnas.2213241120openalex-snapshot
A molecular rotor FLIM probe reveals dynamic coupling between mitochondrial inner membrane fluidity and cellular respiration
inferred← citeshttps://doi.org/10.1073/pnas.2215799119openalex-snapshot
Multi-color live-cell STED nanoscopy of mitochondria with a gentle inner membrane stain
inferred← citeshttps://doi.org/10.1073/pnas.2508911123openalex-snapshot
Multiscale mitochondrial cristae remodeling links Opa1 downregulation to reduced OXPHOS capacity in aged hearts
inferred← citeshttps://doi.org/10.1080/10409238.2020.1784084openalex-snapshot
Mitochondrial F-type ATP synthase: multiple enzyme functions revealed by the membrane-embedded FO structure
inferred← citeshttps://doi.org/10.1080/23723556.2019.1705119openalex-snapshot
Why does a mitochondrion need its individual cristae to be functionally autonomous?
inferred← citeshttps://doi.org/10.1083/jcb.202003131openalex-snapshot
Phospholipid ebb and flow makes mitochondria go
inferred← citeshttps://doi.org/10.1083/jcb.202005193openalex-snapshot
Long-lived mitochondrial cristae proteins in mouse heart and brain
inferred← citeshttps://doi.org/10.1083/jcb.202503037openalex-snapshot
Inwardly rectifying potassium channels promote directional sensing during neutrophil chemotaxis
inferred← citeshttps://doi.org/10.1088/1478-3975/adaa47openalex-snapshot
Electrical homeostasis of the inner mitochondrial membrane potential
inferred← citeshttps://doi.org/10.1089/ars.2022.0124openalex-snapshot
Molecular Determinants of Mitochondrial Shape and Function and Their Role in Glaucoma
inferred← citeshttps://doi.org/10.1089/ars.2022.0173openalex-snapshot
Mitochondrial Cristae Morphology Reflecting Metabolism, Superoxide Formation, Redox Homeostasis, and Pathology
inferred← citeshttps://doi.org/10.1089/ars.2023.0268openalex-snapshot
Mitochondrial Dynamics and Cristae Shape Changes During Metabolic Reprogramming
inferred← citeshttps://doi.org/10.1091/mbc.e21-04-0191openalex-snapshot
Discovery of bactericides as an acute mitochondrial membrane damage inducer
inferred← citeshttps://doi.org/10.1093/aob/mcad075openalex-snapshot
ATP yield of plant respiration: potential, actual and unknown
inferred← citeshttps://doi.org/10.1093/jb/mvz111openalex-snapshot
The ‘mitochondrial contact site and cristae organising system’ (MICOS) in health and human disease
inferred← citeshttps://doi.org/10.1093/molbev/msad134openalex-snapshot
A Novel Group of Dynamin-Related Proteins Shared by Eukaryotes and Giant Viruses Is Able to Remodel Mitochondria From Within the Matrix
inferred← citeshttps://doi.org/10.1093/molehr/gaaa071openalex-snapshot
Mice born to females with oocyte-specific deletion of mitofusin 2 have increased weight gain and impaired glucose homeostasis
inferred← citeshttps://doi.org/10.1093/oxfordhb/9780190932183.013.1openalex-snapshot
Mitochondrial Bioenergetics and Mitochondrial Structure with High-Resolution Imaging
inferred← citeshttps://doi.org/10.1093/plphys/kiab270openalex-snapshot
Proton motive force in plant photosynthesis dominated by ΔpH in both low and high light
inferred← citeshttps://doi.org/10.1096/fj.202001693ropenalex-snapshot
Quantitative analysis of mitochondrial membrane potential heterogeneity in unsynchronized and synchronized cancer cells
inferred← citeshttps://doi.org/10.1098/rsob.210238openalex-snapshot
Pathways shaping the mitochondrial inner membrane
inferred← citeshttps://doi.org/10.1101/2020.05.05.076109openalex-snapshot
High resolution imaging of nascent mitochondrial protein synthesis in cultured human cells
inferred← citeshttps://doi.org/10.1101/2021.04.01.438160openalex-snapshot
MICOS and F 1 F O -ATP synthase crosstalk is a fundamental property of mitochondrial cristae
inferred← citeshttps://doi.org/10.1101/2022.06.26.497646openalex-snapshot
Structural basis of mitochondrial membrane bending by I-II-III2-IV2 supercomplex
inferred← citeshttps://doi.org/10.1101/2022.10.19.512772openalex-snapshot
Long-term, super-resolution HIDE imaging of the inner mitochondrial membrane in live cells with a cell-permeant lipid probe
inferred← citeshttps://doi.org/10.1101/2023.01.07.523093openalex-snapshot
All-optical spatiotemporal mapping of ROS dynamics across mitochondrial microdomains in situ
inferred← citeshttps://doi.org/10.1101/2023.03.22.533773openalex-snapshot
Atlas of Plasmodium falciparum intraerythrocytic development using expansion microscopy
inferred← citeshttps://doi.org/10.1101/2023.04.27.538553openalex-snapshot
Live-cell super-resolution nanoscopy reveals modulation of cristae dynamics in bioenergetically compromised mitochondria
inferred← citeshttps://doi.org/10.1101/2023.06.30.547132openalex-snapshot
Mitochondria Exhibit Changes in Morphology/Function to Support Increased Glutamate Release in Tau P301L Neurons Prior to Reduction in Presynaptic Vesicle Release
inferred← citeshttps://doi.org/10.1101/2023.08.22.554375openalex-snapshot
Urolithin A induces cardioprotection and enhanced mitochondrial quality during natural aging and heart failure
inferred← citeshttps://doi.org/10.1101/2024.12.19.629456openalex-snapshot
Sprint interval exercise disrupts mitochondrial ultrastructure driving a unique mitochondrial stress response and remodelling in humans
inferred← citeshttps://doi.org/10.1101/2024.12.26.630390openalex-snapshot
FAM162A is Crucial for Mitochondrial Structure, Dynamics, and Bioenergetics, Driving Cellular Protection and Longevity
inferred← citeshttps://doi.org/10.1101/2025.01.28.634915openalex-snapshot
Mitochondrial dysfunction underlies monocyte immune deficiency in patients with severe alcohol-related hepatitis
inferred← citeshttps://doi.org/10.1101/2025.03.06.641746openalex-snapshot
Inwardly rectifying potassium channels regulate membrane potential polarization and direction sensing during neutrophil chemotaxis
inferred← citeshttps://doi.org/10.1101/2025.05.05.652276openalex-snapshot
A Platform for Mitochondrial Profiling in Enriched Kidney Segments Under Thermodynamic Control in Mice and Humans
inferred← citeshttps://doi.org/10.1101/2025.05.20.655052openalex-snapshot
MINDNet: Proximity interactome of the MICOS complex revealing a multifaceted network orchestrating mitochondrial biogenesis
inferred← citeshttps://doi.org/10.1101/2025.06.16.659894openalex-snapshot
Reversal of ATP synthase is a key attribute for cellular differentiation of the Trypanosoma brucei insect forms
inferred← citeshttps://doi.org/10.1103/physreve.102.022401openalex-snapshot
Mitochondrial cristae modeled as an out-of-equilibrium membrane driven by a proton field
inferred← citeshttps://doi.org/10.1111/acel.70508openalex-snapshot
FAM162A Is a Key Regulator of Mitochondrial Structure, Dynamics, and Bioenergetics, Driving Cellular Protection and Longevity
inferred← citeshttps://doi.org/10.1111/acel.70729openalex-snapshot
Mitochondrial Fusion and Fission in Age‐Related Cardio‐Cerebral Diseases: Mechanisms and Interventions
inferred← citeshttps://doi.org/10.1111/brv.13168openalex-snapshot
Bringing together but staying apart: decisive differences in animal and fungal mitochondrial inner membrane fusion
inferred← citeshttps://doi.org/10.1111/febs.15424openalex-snapshot
Mitochondrial light switches: optogenetic approaches to control metabolism
inferred← citeshttps://doi.org/10.1111/febs.17119openalex-snapshot
Transfer and fates of damaged mitochondria: role in health and disease
inferred← citeshttps://doi.org/10.1111/jeu.12846openalex-snapshot
Ultrastructural Changes of the Mitochondrion During the Life Cycle of Trypanosoma brucei
inferred← citeshttps://doi.org/10.1111/jmi.12891openalex-snapshot
Mitochondrial morphology and function: two for the price of one!
inferred← citeshttps://doi.org/10.1111/jmi.70050openalex-snapshot
Integrated approaches for multiscale mitochondrial structure and function analysis
inferred← citeshttps://doi.org/10.1111/joim.13031openalex-snapshot
Shaping the mitochondrial inner membrane in health and disease
inferred← citeshttps://doi.org/10.1111/ppl.70230openalex-snapshot
Lipid polymorphism of plant thylakoid membranes. The dynamic exchange model – facts and hypotheses
inferred← citeshttps://doi.org/10.1113/jp283825openalex-snapshot
Optical recordings of organellar membrane potentials and the components of membrane conductance in lysosomes
inferred← citeshttps://doi.org/10.1126/sciadv.abi8886openalex-snapshot
Cristae-dependent quality control of the mitochondrial genome
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