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Bax oligomerization is required for channel-forming activity in liposomes and to trigger cytochrome c release from mitochondria
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/prep.1997.0871openalex-snapshot
Purification and Biochemical Properties of Soluble Recombinant Human Bax
inferredcites →https://doi.org/10.1006/prep.1998.1010openalex-snapshot
Expression and Purification of Full-Length Human Bax α
inferredcites →https://doi.org/10.1016/0092-8674(94)90203-8openalex-snapshot
Cell-free apoptosis in Xenopus egg extracts: Inhibition by Bcl-2 and requirement for an organelle fraction enriched in mitochondria
inferredcites →https://doi.org/10.1016/s0092-8674(00)80434-1openalex-snapshot
Cytochrome c and dATP-Dependent Formation of Apaf-1/Caspase-9 Complex Initiates an Apoptotic Protease Cascade
inferredcites →https://doi.org/10.1016/s0960-9822(06)00136-9openalex-snapshot
Apoptosis: Bcl-2-related proteins get connected
inferredcites →https://doi.org/10.1016/s0962-8924(98)01321-xopenalex-snapshot
Bcl-2-family proteins: the role of the BH3 domain in apoptosis
inferredcites →https://doi.org/10.1021/bi00061a023openalex-snapshot
Oligomerization of the channel-forming toxin aerolysin precedes insertion into lipid bilayers
inferredcites →https://doi.org/10.1038/35160openalex-snapshot
Bcl-2 prolongs cell survival after Bax-induced release of cytochrome c
inferredcites →https://doi.org/10.1038/367292a0openalex-snapshot
Structure of the Aeromonas toxin proaerolysin in its water-soluble and membrane-channel states
inferredcites →https://doi.org/10.1038/369321a0openalex-snapshot
BH1 and BH2 domains of Bcl-2 are required for inhibition of apoptosis and heterodimerization with Bax
inferredcites →https://doi.org/10.1038/381335a0openalex-snapshot
X-ray and NMR structure of human Bcl-xL, an inhibitor of programmed cell death
inferredcites →https://doi.org/10.1038/385353a0openalex-snapshot
Bcl-xL forms an ion channel in synthetic lipid membranes
inferredcites →https://doi.org/10.1038/42867openalex-snapshot
Double identity for proteins of the Bcl-2 family
inferredcites →https://doi.org/10.1038/bjc.1972.33openalex-snapshot
Apoptosis: A Basic Biological Phenomenon with Wideranging Implications in Tissue Kinetics
inferredcites →https://doi.org/10.1038/ng0897-358openalex-snapshot
Bcl-2 and Bax function independently to regulate cell death
inferredcites →https://doi.org/10.1038/nm0697-614openalex-snapshot
The proto-oncogene Bcl-2 and its role in regulating apoptosis
inferredcites →https://doi.org/10.1073/pnas.92.17.7834openalex-snapshot
Multiple Bcl-2 family members demonstrate selective dimerizations with Bax.
inferredcites →https://doi.org/10.1073/pnas.94.10.5113openalex-snapshot
Channel formation by antiapoptotic protein Bcl-2
inferredcites →https://doi.org/10.1073/pnas.94.21.11357openalex-snapshot
Comparison of the ion channel characteristics of proapoptotic BAX and antiapoptotic BCL-2
inferredcites →https://doi.org/10.1073/pnas.94.8.3668openalex-snapshot
Cytosol-to-membrane redistribution of Bax and Bcl-X L during apoptosis
inferredcites →https://doi.org/10.1073/pnas.95.9.4997openalex-snapshot
Bax directly induces release of cytochrome c from isolated mitochondria
inferredcites →https://doi.org/10.1074/jbc.271.15.8521openalex-snapshot
A Peptide Sequence from Bax That Converts Bcl-2 into an Activator of Apoptosis
inferredcites →https://doi.org/10.1074/jbc.272.21.13829openalex-snapshot
Nonionic Detergents Induce Dimerization among Members of the Bcl-2 Family
inferredcites →https://doi.org/10.1074/jbc.272.39.24101openalex-snapshot
BH3 Domain of BAD Is Required for Heterodimerization with BCL-XL and Pro-apoptotic Activity
inferredcites →https://doi.org/10.1074/jbc.273.17.10777openalex-snapshot
Bax in Murine Thymus Is a Soluble Monomeric Protein That Displays Differential Detergent-induced Conformations
inferredcites →https://doi.org/10.1083/jcb.126.4.1059openalex-snapshot
The protein bcl-2 alpha does not require membrane attachment, but two conserved domains to suppress apoptosis.
inferredcites →https://doi.org/10.1083/jcb.139.5.1281openalex-snapshot
Movement of Bax from the Cytosol to Mitochondria during Apoptosis
inferredcites →https://doi.org/10.1083/jcb.143.1.207openalex-snapshot
Regulated Targeting of BAX to Mitochondria
inferredcites →https://doi.org/10.1083/jcb.143.1.217openalex-snapshot
Bax-induced Cytochrome C Release from Mitochondria Is Independent of the Permeability Transition Pore but Highly Dependent on Mg2+ Ions
inferredcites →https://doi.org/10.1083/jcb.144.5.891openalex-snapshot
Bid-induced Conformational Change of Bax Is Responsible for Mitochondrial Cytochrome c Release during Apoptosis
inferredcites →https://doi.org/10.1093/emboj/17.14.3878openalex-snapshot
Enforced dimerization of BAX results in its translocation, mitochondrial dysfunction and apoptosis
inferredcites →https://doi.org/10.1101/gad.10.22.2859openalex-snapshot
BID: a novel BH3 domain-only death agonist.
inferredcites →https://doi.org/10.1126/science.275.5302.983openalex-snapshot
Structure of Bcl-x L -Bak Peptide Complex: Recognition Between Regulators of Apoptosis
inferredcites →https://doi.org/10.1126/science.277.5324.370openalex-snapshot
Inhibition of Bax Channel-Forming Activity by Bcl-2
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.3921286openalex-extracted
A Kinetic Fluorescence Polarization Ligand Assay for Monitoring BAX Early-Activation
inferred← citeshttps://doi.org/10.1002/9780470429907.ch6openalex-snapshot
Unique Mitochondrial Ion Channels: Roles in Synaptic Transmission and Programmed Cell Death
inferred← citeshttps://doi.org/10.1002/9780470987575.ch10openalex-snapshot
Apoptosis in Atherosclerosis
inferred← citeshttps://doi.org/10.1002/9781119017127.ch2openalex-snapshot
The Mitochondrial Permeability Transition Pore, the c‐Subunit of the F1FoATP Synthase, Cellular Development, and Synaptic Efficiency
inferred← citeshttps://doi.org/10.1002/9783527619665.ch6openalex-snapshot
Role of Mitochondrial Proteins in Apoptosis
inferred← citeshttps://doi.org/10.1002/cph4.70012openalex-snapshot
Heat Stress‐Mediated Multi‐Organ Injury: Pathophysiology and Treatment Strategies
inferred← citeshttps://doi.org/10.1002/ddr.1155openalex-snapshot
Role of caspases in neuronal apoptosis
inferred← citeshttps://doi.org/10.1002/dneu.22042openalex-snapshot
Ethanol influences on bax associations with mitochondrial membrane proteins in neonatal rat cerebellum
inferred← citeshttps://doi.org/10.1002/ijc.29350openalex-snapshot
Resistance to UV‐induced apoptosis by β‐HPV5 E6 involves targeting of activated BAK for proteolysis by recruitment of the HERC1 ubiquitin ligase
inferred← citeshttps://doi.org/10.1002/jcb.24709openalex-snapshot
Apoptosis Regulation at the Mitochondrial Outer Membrane
inferred← citeshttps://doi.org/10.1002/jcp.10254openalex-snapshot
Cell death regulation by the Bcl‐2 protein family in the mitochondria
inferred← citeshttps://doi.org/10.1002/mnfr.201300323openalex-snapshot
Oleuropein and hydroxytyrosol activate GPER / GPR 30‐dependent pathways leading to apoptosis of ER ‐negative SKBR 3 breast cancer cells
inferred← citeshttps://doi.org/10.1002/mrc.1322openalex-snapshot
Structural studies of apoptosis and ion transport regulatory proteins in membranes
inferred← citeshttps://doi.org/10.1002/nau.20855openalex-snapshot
Unilateral ureteral obstruction evokes renal tubular apoptosis via the enhanced oxidative stress and endoplasmic reticulum stress in the rat
inferred← citeshttps://doi.org/10.1002/ptr.2028openalex-snapshot
The water extract of Omija protects H9c2 cardiomyoblast cells from hydrogen peroxide through prevention of mitochondrial dysfunction and activation of caspases pathway
inferred← citeshttps://doi.org/10.1002/yea.2918openalex-snapshot
Bax induces activation of the unfolded protein response by inducing HAC1 mRNA splicing in Saccharomyces cerevisiae
inferred← citeshttps://doi.org/10.1006/cbir.2001.0768openalex-snapshot
EXPRESSION OF BAX IN CELL NUCLEUS AFTER EXPERIMENTALLY INDUCED APOPTOSIS REVEALED BY IMMUNOGOLD AND EMBEDMENT‐FREE ELECTRON MICROSCOPY
inferred← citeshttps://doi.org/10.1006/excr.2002.5586openalex-snapshot
Subcellular Localization and Physiological Consequences of Introducing a Mitochondrial Matrix Targeting Signal Sequence in Bax and Its Mutants
inferred← citeshttps://doi.org/10.1007/0-387-23695-3_1openalex-snapshot
Apoptotic Pathways and Their Regulation
inferred← citeshttps://doi.org/10.1007/978-0-387-30411-3_26openalex-snapshot
6.5 Mitochondrial Mechanisms of Oxidative Stress and Apoptosis
inferred← citeshttps://doi.org/10.1007/978-0-387-79112-8_4openalex-snapshot
Experimental Ischemia: Summary of Metabolic Encephalopathy
inferred← citeshttps://doi.org/10.1007/978-1-4020-6191-2_18openalex-snapshot
Calcium and Cell Death: The Mitochondrial Connection
inferred← citeshttps://doi.org/10.1007/978-1-4419-6327-7_8openalex-snapshot
Permeabilization of the Outer Mitochondrial Membrane by Bcl-2 Proteins
inferred← citeshttps://doi.org/10.1007/978-1-4419-6706-0_6openalex-snapshot
The Interplay between BCL-2 Family Proteins and Mitochondrial Morphology in the Regulation of Apoptosis
inferred← citeshttps://doi.org/10.1007/978-1-4419-6706-0_7openalex-snapshot
Noncanonical Functions of BCL-2 Proteins in the Nervous System
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/10.1007/978-1-4614-9302-0_11openalex-snapshot
Structural Perspectives on BCL-2 Family of Proteins
inferred← citeshttps://doi.org/10.1007/978-1-4757-5890-0_17openalex-snapshot
The Mechanism of Apoptosis Regulation by IAP Antagonist Smac/DIABLO
inferred← citeshttps://doi.org/10.1007/978-1-4939-3612-0_4openalex-snapshot
Bcl-2 Protein Interplay on the Outer Mitochondrial Membrane
inferred← citeshttps://doi.org/10.1007/978-1-4939-6890-9_11openalex-snapshot
Examination of Mitochondrial Ion Conductance by Patch Clamp in Intact Neurons and Mitochondrial Membrane Preparations
inferred← citeshttps://doi.org/10.1007/978-1-4939-8861-7_6openalex-snapshot
Investigating BCL-2 Family Protein Interactions in Yeast
inferred← citeshttps://doi.org/10.1007/978-1-59259-361-3_6openalex-snapshot
The Mitochondrial Apoptosis Pathway
inferred← citeshttps://doi.org/10.1007/978-1-60327-381-7_23openalex-snapshot
Apoptosis in Lung Injury and Disease
inferred← citeshttps://doi.org/10.1007/978-1-60327-381-7_6openalex-snapshot
The Mitochondrial Pathway: Focus on Shape Changes
inferred← citeshttps://doi.org/10.1007/978-1-60327-579-8_7openalex-snapshot
Mitochondrial Ion Channels in Ischemic Brain
inferred← citeshttps://doi.org/10.1007/978-1-60761-314-5_9openalex-snapshot
Punching Holes in Membranes: How Oligomeric Pore-Forming Proteins and Lipids Cooperate to Form Aqueous Channels in Membranes
inferred← citeshttps://doi.org/10.1007/978-3-031-23104-9_11openalex-snapshot
Apoptosis, Autophagy, and Unfolded Protein Response and Cerebellar Development
inferred← citeshttps://doi.org/10.1007/978-3-319-20149-8_3openalex-snapshot
Electrophysiology of the Mitochondrial Apoptosis-Induced Channel, MAC
inferred← citeshttps://doi.org/10.1007/978-3-319-46248-6_1openalex-snapshot
Neurophysiological and Behavioral Dysfunctions After Electromagnetic Field Exposure: A Dose Response Relationship
inferred← citeshttps://doi.org/10.1007/978-3-319-59749-2_8openalex-snapshot
Apoptosis, Autophagy, and Unfolded Protein Response and Cerebellar Development
inferred← citeshttps://doi.org/10.1007/978-3-642-00663-0_12openalex-snapshot
Mechanisms of Acetaminophen-Induced Liver Necrosis
inferred← citeshttps://doi.org/10.1007/978-3-642-18741-4_9openalex-snapshot
Molekulare Veränderungen beim ischämischen Schlaganfall
inferred← citeshttps://doi.org/10.1007/978-3-662-04333-2_5openalex-snapshot
Events that Commit Neurons to Die After Trophic Factor Deprivation
inferred← citeshttps://doi.org/10.1007/978-90-481-9713-2_9openalex-snapshot
Nuclear Apoptosis and Sarcopenia
inferred← citeshttps://doi.org/10.1007/bf03179878openalex-snapshot
Mitochondrial control of neuron death and its role in neurodegenerative disorders
inferred← citeshttps://doi.org/10.1007/s00232-005-0799-7openalex-snapshot
Interactions of Bax and tBid with Lipid Monolayers
inferred← citeshttps://doi.org/10.1007/s00232-010-9230-0openalex-snapshot
Melatonin Reduces Apoptosis Induced by Calcium Signaling in Human Leukocytes: Evidence for the Involvement of Mitochondria and Bax Activation
inferred← citeshttps://doi.org/10.1007/s00249-007-0149-zopenalex-snapshot
Monte Carlo simulations of tBid association with the mitochondrial outer membrane
inferred← citeshttps://doi.org/10.1007/s00262-012-1258-9openalex-snapshot
Shikonin induces immunogenic cell death in tumor cells and enhances dendritic cell-based cancer vaccine
inferred← citeshttps://doi.org/10.1007/s00395-009-0004-8openalex-snapshot
The mitochondrial permeability transition pore and ischemia-reperfusion injury
inferred← citeshttps://doi.org/10.1007/s00417-011-1906-3openalex-snapshot
Staurosporine-induced differentiation of the RGC-5 cell line leads to apoptosis and cell death at the lowest differentiating concentration
inferred← citeshttps://doi.org/10.1007/s00441-001-0472-0openalex-snapshot
Bax and other pro-apoptotic Bcl-2 family "killer-proteins" and their victim the mitochondrion
inferred← citeshttps://doi.org/10.1007/s00774-008-0864-2openalex-snapshot
The flavonoid quercetin induces apoptosis and inhibits migration through a MAPK-dependent mechanism in osteoblasts
inferred← citeshttps://doi.org/10.1007/s10495-006-6315-4openalex-snapshot
Deficiency of the Bax gene attenuates denervation-induced apoptosis
inferred← citeshttps://doi.org/10.1007/s10495-006-8417-4openalex-snapshot
Water-soluble formulation of Coenzyme Q10 inhibits Bax-induced destabilization of mitochondria in mammalian cells
inferred← citeshttps://doi.org/10.1007/s10495-007-0098-0openalex-snapshot
Mitochondrial anchoring of PKCα by PICK1 confers resistance to etoposide-induced apoptosis
inferred← citeshttps://doi.org/10.1007/s10495-007-0722-zopenalex-snapshot
A tale of two mitochondrial channels, MAC and PTP, in apoptosis
inferred← citeshttps://doi.org/10.1007/s10495-007-0749-1openalex-snapshot
Bax activation and mitochondrial insertion during apoptosis
inferred← citeshttps://doi.org/10.1007/s10495-009-0389-8openalex-snapshot
Oligomerization of membrane-bound Bcl-2 is involved in its pore formation induced by tBid
inferred← citeshttps://doi.org/10.1007/s10495-009-0410-2openalex-snapshot
The Bax carboxy-terminal hydrophobic helix does not determine organelle-specific targeting but is essential for maintaining Bax in an inactive state and for stable mitochondrial membrane insertion
inferred← citeshttps://doi.org/10.1007/s10495-016-1283-9openalex-snapshot
Alpha 5/6 helix domains together with N-terminus determine the apoptotic potency of the Bcl-2 family proteins
inferred← citeshttps://doi.org/10.1007/s10620-008-0583-5openalex-snapshot
Overexpression of Mcl-1 Attenuates Liver Injury and Fibrosis in the Bile Duct–Ligated Mouse
inferred← citeshttps://doi.org/10.1007/s10741-016-9531-1openalex-snapshot
Mitochondrial involvement in myocyte death and heart failure
inferred← citeshttps://doi.org/10.1007/s10863-005-6566-8openalex-snapshot
On the Role of VDAC in Apoptosis: Fact and Fiction
inferred← citeshttps://doi.org/10.1007/s10863-005-6570-zopenalex-snapshot
The Role of the Mitochondrial Apoptosis Induced Channel MAC in Cytochrome c Release
inferred← citeshttps://doi.org/10.1007/s10863-005-6632-2openalex-snapshot
Sphingosine Forms Channels in Membranes That Differ Greatly from Those Formed by Ceramide
inferred← citeshttps://doi.org/10.1007/s10863-006-9054-xopenalex-snapshot
Alteration of mitochondrial function and cell sensitization to death
inferred← citeshttps://doi.org/10.1007/s10863-009-9202-1openalex-snapshot
Conformational changes and protein stability of the pro-apoptotic protein Bax
inferred← citeshttps://doi.org/10.1007/s10863-016-9648-xopenalex-snapshot
Complex formation and turnover of mitochondrial transporters and ion channels
inferred← citeshttps://doi.org/10.1007/s10863-016-9652-1openalex-snapshot
Physiological roles of the mitochondrial permeability transition pore
inferred← citeshttps://doi.org/10.1007/s11033-011-0760-zopenalex-snapshot
Human amniotic membrane derived-mesenchymal stem cells induce C6 glioma apoptosis in vivo through the Bcl-2/caspase pathways
inferred← citeshttps://doi.org/10.1007/s11064-007-9475-xopenalex-snapshot
Ciglitazone Induces Caspase-Independent Apoptosis through Down-Regulation of XIAP and Survivin in Human Glioma Cells
inferred← citeshttps://doi.org/10.1007/s11655-011-0846-4openalex-snapshot
Pien Tze Huang (片仔癀)-induced apoptosis in human colon cancer HT-29 cells is associated with regulation of the Bcl-2 family and activation of caspase 3
inferred← citeshttps://doi.org/10.1007/s12011-014-0221-3openalex-snapshot
Assessment of Oxidative Stress in Hippocampus, Cerebellum and Frontal Cortex in Rat Pups Exposed to Lead (Pb) During Specific Periods of Initial Brain Development
inferred← citeshttps://doi.org/10.1007/s12011-020-02215-7openalex-snapshot
Lead (Pb) Accumulation in Human THP-1 Monocytes/Macrophages In Vitro and the Influence on Cell Apoptosis
inferred← citeshttps://doi.org/10.1007/s12035-014-9043-8openalex-snapshot
Ursodeoxycholic Acid Ameliorates Apoptotic Cascade in the Rotenone Model of Parkinson’s Disease: Modulation of Mitochondrial Perturbations
inferred← citeshttps://doi.org/10.1016/b978-0-12-378638-8.00004-xopenalex-snapshot
Aging and Apoptosis in Muscle
inferred← citeshttps://doi.org/10.1016/b978-0-12-394447-4.30046-3openalex-snapshot
Mitochondria in Cell Death Regulation
inferred← citeshttps://doi.org/10.1016/b978-0-12-417158-9.00001-7openalex-snapshot
Examining the Molecular Mechanism of Bcl-2 Family Proteins at Membranes by Fluorescence Spectroscopy
inferred← citeshttps://doi.org/10.1016/b978-0-12-811304-2.00013-4openalex-snapshot
Mitochondrial Function and Neurodegenerative Diseases
inferred← citeshttps://doi.org/10.1016/bs.abl.2017.12.002openalex-snapshot
The Role of Mitochondrial Outer Membrane Permeabilization (MOMP) in Apoptosis: Studying Bax Pores by Cryo-Electron Microscopy
inferred← citeshttps://doi.org/10.1016/j.abb.2008.02.004openalex-snapshot
Insight into the apoptosis-inducing action of α-bisabolol towards malignant tumor cells: Involvement of lipid rafts and Bid
inferred← citeshttps://doi.org/10.1016/j.alcohol.2010.07.003openalex-snapshot
ER-targeted Bcl-2 and inhibition of ER-associated caspase-12 rescue cultured immortalized cells from ethanol toxicity
inferred← citeshttps://doi.org/10.1016/j.aquatox.2009.11.013openalex-snapshot
Flow cytometric analysis of BDE 47 mediated injury to rainbow trout gill epithelial cells
inferred← citeshttps://doi.org/10.1016/j.aquatox.2017.02.028openalex-snapshot
Toxic effects of 56Fe ion radiation on the zebrafish (Danio rerio) embryonic development
inferred← citeshttps://doi.org/10.1016/j.athoracsur.2004.04.031openalex-snapshot
Apoptosis-related mitochondrial dysfunction in the early postoperative neonatal lamb heart
inferred← citeshttps://doi.org/10.1016/j.athoracsur.2005.11.029openalex-snapshot
Preservation of Mitochondrial Structure and Function After Cardioplegic Arrest in the Neonate Using a Selective Mitochondrial KATP Channel Opener
inferred← citeshttps://doi.org/10.1016/j.bbabio.2006.03.016openalex-snapshot
Multiple pathways of cytochrome c release from mitochondria in apoptosis
inferred← citeshttps://doi.org/10.1016/j.bbabio.2006.07.002openalex-snapshot
Therapeutic peptides: Targeting the mitochondrion to modulate apoptosis
inferred← citeshttps://doi.org/10.1016/j.bbabio.2008.08.002openalex-snapshot
Oligomeric BAX induces mitochondrial permeability transition and complete cytochrome c release without oxidative stress
inferred← citeshttps://doi.org/10.1016/j.bbabio.2010.03.003openalex-snapshot
Apoptosis is regulated by the VDAC1 N-terminal region and by VDAC oligomerization: release of cytochrome c, AIF and Smac/Diablo
inferred← citeshttps://doi.org/10.1016/j.bbabio.2010.07.006openalex-snapshot
BAX insertion, oligomerization, and outer membrane permeabilization in brain mitochondria: Role of permeability transition and SH-redox regulation
inferred← citeshttps://doi.org/10.1016/j.bbadis.2013.11.007openalex-snapshot
Contributions of Bcl-xL to acute and long term changes in bioenergetics during neuronal plasticity
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2003.08.009openalex-snapshot
The role of Bcl-2 family members in tumorigenesis
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2003.08.011openalex-snapshot
Control of mitochondrial integrity by Bcl-2 family members and caspase-independent cell death
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2003.10.016openalex-snapshot
Control of mitochondrial permeability by Bcl-2 family members
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2003.11.001openalex-snapshot
Viral Bcl-2 homologs and their role in virus replication and associated diseases
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2010.10.017openalex-snapshot
Bcl-2 proteins and mitochondria—Specificity in membrane targeting for death
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2022.119317openalex-snapshot
Pro-apoptotic complexes of BAX and BAK on the outer mitochondrial membrane
inferred← citeshttps://doi.org/10.1016/j.bbamem.2011.10.007openalex-snapshot
Interaction of the full-length Bax protein with biomimetic mitochondrial liposomes: A small-angle neutron scattering and fluorescence study
inferred← citeshttps://doi.org/10.1016/j.bbamem.2011.10.025openalex-snapshot
The role of VDAC in cell death: Friend or foe?
inferred← citeshttps://doi.org/10.1016/j.bbamem.2014.10.040openalex-snapshot
The mitochondrial voltage-dependent anion channel 1 in tumor cells
inferred← citeshttps://doi.org/10.1016/j.bbamem.2015.07.013openalex-snapshot
Ceramide channels: destabilization by Bcl-xL and role in apoptosis
inferred← citeshttps://doi.org/10.1016/j.bbamem.2018.02.031openalex-snapshot
Mechanism of aggregation and membrane interactions of mammalian prion protein
inferred← citeshttps://doi.org/10.1016/j.bbamem.2022.184075openalex-snapshot
Cell-Free Synthesis and Reconstitution of Bax in Nanodiscs: Comparison between Wild-Type Bax and a Constitutively Active Mutant
inferred← citeshttps://doi.org/10.1016/j.bbrc.2017.06.190openalex-snapshot
BCL-2 proteins and apoptosis: Recent insights and unknowns
inferred← citeshttps://doi.org/10.1016/j.bbrc.2022.11.104openalex-snapshot
Live-cell imaging analysis on the anti-apoptotic function of the Bcl-xL transmembrane carboxyl terminal domain
inferred← citeshttps://doi.org/10.1016/j.bcp.2004.08.006openalex-snapshot
Ibuprofen-induced Walker 256 tumor cell death: cytochrome c release from functional mitochondria and enhancement by calcineurin inhibition
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.biocel.2003.09.011openalex-snapshot
Polyamine depletion switches the form of 2-deoxy-d-ribose-induced cell death from apoptosis to necrosis in HL-60 cells
inferred← citeshttps://doi.org/10.1016/j.biocel.2005.03.003openalex-snapshot
Retinoic acid determines life span of leukemic cells by inducing antagonistic apoptosis-regulatory programs
inferred← citeshttps://doi.org/10.1016/j.biocel.2009.05.001openalex-snapshot
Mitochondrial outer-membrane permeabilization and remodelling in apoptosis
inferred← citeshttps://doi.org/10.1016/j.biochi.2003.09.007openalex-snapshot
Intrinsic and extrinsic pathways signaling during HIV-1 mediated cell death
inferred← citeshttps://doi.org/10.1016/j.biombioe.2021.106176openalex-snapshot
Effective methane production from waste activated sludge in anaerobic digestion via formic acid pretreatment
inferred← citeshttps://doi.org/10.1016/j.biopha.2017.09.072openalex-snapshot
P38 MAP kinase is involved in oleuropein-induced apoptosis in A549 cells by a mitochondrial apoptotic cascade
inferred← citeshttps://doi.org/10.1016/j.bpj.2012.06.047openalex-snapshot
The Dynamics of Bax Channel Formation: Influence of Ionic Strength
inferred← citeshttps://doi.org/10.1016/j.brainres.2003.09.048openalex-snapshot
AMPA-induced dark cell degeneration of cerebellar Purkinje neurons involves activation of caspases and apparent mitochondrial dysfunction
inferred← citeshttps://doi.org/10.1016/j.brainres.2005.01.009openalex-snapshot
Isoflurane and sevoflurane affect cell survival and BCL-2/BAX ratio differently
inferred← citeshttps://doi.org/10.1016/j.brainresbull.2003.07.007openalex-snapshot
The molecular biology of retinal ganglion cell death: caveats and controversies
inferred← citeshttps://doi.org/10.1016/j.brainresbull.2017.01.024openalex-snapshot
Preventive treatment of astaxanthin provides neuroprotection through suppression of reactive oxygen species and activation of antioxidant defense pathway after stroke in rats
inferred← citeshttps://doi.org/10.1016/j.canlet.2009.04.021openalex-snapshot
MAC related mitochondrial pathway in oroxylin A induces apoptosis in human hepatocellular carcinoma HepG2 cells
inferred← citeshttps://doi.org/10.1016/j.carbpol.2012.12.048openalex-snapshot
Cardioprotective and antioxidant activities of a polysaccharide from the root bark of Aralia elata (Miq.) Seem
inferred← citeshttps://doi.org/10.1016/j.cbi.2006.04.010openalex-snapshot
Mitochondrial regulation of apoptotic cell death
inferred← citeshttps://doi.org/10.1016/j.ceb.2004.09.009openalex-snapshot
Regulation of mitochondrial membrane permeabilization by BCL-2 family proteins and caspases
inferred← citeshttps://doi.org/10.1016/j.ceb.2006.10.004openalex-snapshot
How do Bax and Bak lead to permeabilization of the outer mitochondrial membrane?
inferred← citeshttps://doi.org/10.1016/j.ceca.2014.09.006openalex-snapshot
Targeting a mitochondrial potassium channel to fight cancer
inferred← citeshttps://doi.org/10.1016/j.cell.2016.02.026openalex-snapshot
BOK Is a Non-canonical BCL-2 Family Effector of Apoptosis Regulated by ER-Associated Degradation
inferred← citeshttps://doi.org/10.1016/j.chemphyslip.2004.02.002openalex-snapshot
Membrane lipids and cell death: an overview
inferred← citeshttps://doi.org/10.1016/j.chemphyslip.2013.12.002openalex-snapshot
Involvement of cardiolipin in tBID-induced activation of BAX during apoptosis
inferred← citeshttps://doi.org/10.1016/j.crmeth.2022.100174openalex-snapshot
A kinetic fluorescence polarization ligand assay for monitoring BAX early activation
inferred← citeshttps://doi.org/10.1016/j.ejphar.2020.173299openalex-snapshot
6H2L, a novel synthetic derivative of bifendate, induces apoptosis in hepatoma cells via mitochondrial and MAPK pathway
inferred← citeshttps://doi.org/10.1016/j.exer.2010.03.004openalex-snapshot
Variations in the rheostat model of apoptosis: What studies of retinal ganglion cell death tell us about the functions of the Bcl2 family proteins
inferred← citeshttps://doi.org/10.1016/j.exer.2011.07.013openalex-snapshot
WITHDRAWN: Reprint of: Variations in the rheostat model of apoptosis: What studies of retinal ganglion cell death tell us about the functions of the Bcl2 family proteins
inferred← citeshttps://doi.org/10.1016/j.expneurol.2009.03.025openalex-snapshot
Molecular participants in mitochondrial cell death channel formation during neuronal ischemia
inferred← citeshttps://doi.org/10.1016/j.febslet.2004.10.080openalex-snapshot
Impact of pH on Bax α conformation, oligomerisation and mitochondrial integration
inferred← citeshttps://doi.org/10.1016/j.foodchem.2017.10.034openalex-snapshot
Study on the effect of reactive oxygen species-mediated oxidative stress on the activation of mitochondrial apoptosis and the tenderness of yak meat
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2005.10.064openalex-snapshot
Mechanism of cell death induction by nitroxide and hyperthermia
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2007.02.020openalex-snapshot
FLIP inhibits endothelial cell apoptosis during hyperoxia by suppressing Bax
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2009.04.007openalex-snapshot
Heme oxygenase-1, a critical arbitrator of cell death pathways in lung injury and disease
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2010.08.018openalex-snapshot
SOD1 and MitoTEMPO partially prevent mitochondrial permeability transition pore opening, necrosis, and mitochondrial apoptosis after ATP depletion recovery
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2009.11.015openalex-snapshot
Differential induction of apoptosis in human colonic carcinoma cells (Caco-2) by Atopobium, and commensal, probiotic and enteropathogenic bacteria: Mediation by the mitochondrial pathway
inferred← citeshttps://doi.org/10.1016/j.jaci.2007.11.023openalex-snapshot
Increased T-cell survival by structural bronchial cells derived from asthmatic subjects cultured in an engineered human mucosa
inferred← citeshttps://doi.org/10.1016/j.jsbmb.2008.03.007openalex-snapshot
Mechanisms involved in tissue-specific apopotosis regulated by glucocorticoids
inferred← citeshttps://doi.org/10.1016/j.jss.2013.04.079openalex-snapshot
Regulation of tumor necrosis factor-α–induced microvascular endothelial cell hyperpermeability by recombinant B-cell lymphoma-extra large
inferred← citeshttps://doi.org/10.1016/j.jtcvs.2007.05.009openalex-snapshot
Cyclosporine A prevents apoptosis-related mitochondrial dysfunction after neonatal cardioplegic arrest
inferred← citeshttps://doi.org/10.1016/j.jtcvs.2007.09.023openalex-snapshot
Inhibition of mitochondrial remodeling by cyclosporine A preserves myocardial performance in a neonatal rabbit model of cardioplegic arrest
inferred← citeshttps://doi.org/10.1016/j.jtcvs.2010.08.030openalex-snapshot
Transient mitochondrial permeability transition pore opening after neonatal cardioplegic arrest
inferred← citeshttps://doi.org/10.1016/j.jtcvs.2013.12.065openalex-snapshot
Progressive thermopreconditioning attenuates rat cardiac ischemia/reperfusion injury by mitochondria-mediated antioxidant and antiapoptotic mechanisms
inferred← citeshttps://doi.org/10.1016/j.lfs.2019.116655openalex-snapshot
MitoQ ameliorates testicular damage induced by gamma irradiation in rats: Modulation of mitochondrial apoptosis and steroidogenesis
inferred← citeshttps://doi.org/10.1016/j.mad.2016.04.007openalex-snapshot
A brewing understanding of the regulation of Bax function by Bcl-xL and Bcl-2
inferred← citeshttps://doi.org/10.1016/j.mam.2009.12.004openalex-snapshot
The Warburg effect and mitochondrial stability in cancer cells
inferred← citeshttps://doi.org/10.1016/j.mam.2010.03.002openalex-snapshot
VDAC, a multi-functional mitochondrial protein regulating cell life and death
inferred← citeshttps://doi.org/10.1016/j.mce.2012.01.017openalex-snapshot
17β-Estradiol activates GPER- and ESR1-dependent pathways inducing apoptosis in GC-2 cells, a mouse spermatocyte-derived cell line
inferred← citeshttps://doi.org/10.1016/j.meatsci.2022.109021openalex-snapshot
Exploratory study on the potential regulating role of Peroxiredoxin 6 on proteolysis and relationships with desmin early postmortem
inferred← citeshttps://doi.org/10.1016/j.mito.2004.01.001openalex-snapshot
Caspase activation precedes PTP opening in TNF-α-induced apoptosis in L929 cells
inferred← citeshttps://doi.org/10.1016/j.mito.2008.10.003openalex-snapshot
Putative partners in Bax mediated cytochrome-c release: ANT, CypD, VDAC or none of them?
inferred← citeshttps://doi.org/10.1016/j.mito.2014.07.009openalex-snapshot
VDAC phosphorylation, a lipid sensor influencing the cell fate
inferred← citeshttps://doi.org/10.1016/j.molcel.2014.09.022openalex-snapshot
Structural Model of Active Bax at the Membrane
inferred← citeshttps://doi.org/10.1016/j.molcel.2020.05.029openalex-snapshot
Homogeneous Oligomers of Pro-apoptotic BAX Reveal Structural Determinants of Mitochondrial Membrane Permeabilization
inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2016.11.001openalex-snapshot
Effects of Ru(CO)3Cl-glycinate on the developmental toxicities induced by X-ray and carbon-ion irradiation in zebrafish embryos
inferred← citeshttps://doi.org/10.1016/j.neulet.2008.03.062openalex-snapshot
Increase in bax expression and apoptosis are associated in Huntington's disease progression
inferred← citeshttps://doi.org/10.1016/j.neulet.2008.04.070openalex-snapshot
Exercise reverses chronic stress-induced Bax oligomer formation in the cerebral cortex
inferred← citeshttps://doi.org/10.1016/j.nurt.2009.11.001openalex-snapshot
Mitochondrial Damage: A Target for New Therapeutic Horizons
inferred← citeshttps://doi.org/10.1016/j.parkreldis.2003.11.005openalex-snapshot
α-Synuclein, Parkinson's disease, and Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.pep.2020.105628openalex-snapshot
A novel recombinant expression and purification approach for the full-length anti-apoptotic membrane protein Bcl-2
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2006.11.004openalex-snapshot
Therapeutic approaches for muscle wasting disorders
inferred← citeshttps://doi.org/10.1016/j.phrs.2015.04.013openalex-snapshot
Cell death disguised: The mitochondrial permeability transition pore as the c-subunit of the F1FO ATP synthase
inferred← citeshttps://doi.org/10.1016/j.phymed.2026.158624openalex-snapshot
Polysaccharides-mediated mitochondrial remodeling: role in chemotherapy resistance of gastrointestinal tumors
inferred← citeshttps://doi.org/10.1016/j.preteyeres.2017.01.002openalex-snapshot
BAX to basics: How the BCL2 gene family controls the death of retinal ganglion cells
inferred← citeshttps://doi.org/10.1016/j.reaurg.2010.06.006openalex-snapshot
Hypoxie et fonction mitochondriale
inferred← citeshttps://doi.org/10.1016/j.semcancer.2006.03.003openalex-snapshot
Dynamic 14-3-3/client protein interactions integrate survival and apoptotic pathways
inferred← citeshttps://doi.org/10.1016/j.sjbs.2015.03.005openalex-snapshot
Regulation of ceramide channel formation and disassembly: Insights on the initiation of apoptosis
inferred← citeshttps://doi.org/10.1016/j.str.2015.07.013openalex-snapshot
Solution Structure of Apoptotic BAX Oligomer: Oligomerization Likely Precedes Membrane Insertion
inferred← citeshttps://doi.org/10.1016/j.taap.2006.03.001openalex-snapshot
Activation of peroxisome proliferator-activated receptor-γ (PPARγ) induces cell death through MAPK-dependent mechanism in osteoblastic cells
inferred← citeshttps://doi.org/10.1016/j.taap.2009.07.001openalex-snapshot
Combinational chelation therapy abrogates lead-induced neurodegeneration in rats
inferred← citeshttps://doi.org/10.1016/j.tcb.2008.01.007openalex-snapshot
How do BCL-2 proteins induce mitochondrial outer membrane permeabilization?
inferred← citeshttps://doi.org/10.1016/j.tibs.2008.07.004openalex-snapshot
Disparate proteins use similar architectures to damage membranes
inferred← citeshttps://doi.org/10.1016/j.tibs.2011.08.009openalex-snapshot
BAX unleashed: the biochemical transformation of an inactive cytosolic monomer into a toxic mitochondrial pore
inferred← citeshttps://doi.org/10.1016/j.tiv.2010.06.015openalex-snapshot
The compound cis-(dichloro)tetrammineruthenium(III) chloride induces caspase-mediated apoptosis in K562 cells
inferred← citeshttps://doi.org/10.1016/j.tiv.2014.09.011openalex-snapshot
Extracellular signal-regulated kinase pathway play distinct role in acetochlor-mediated toxicity and intrinsic apoptosis in A549 cells
inferred← citeshttps://doi.org/10.1016/j.tox.2005.07.003openalex-snapshot
Role of mitogen-activated protein kinases in hydrogen peroxide-induced cell death in osteoblastic cells
inferred← citeshttps://doi.org/10.1016/j.tox.2008.03.014openalex-snapshot
15-Deoxy-Δ12,14-prostaglandin J2 induces apoptosis via JNK-mediated mitochondrial pathway in osteoblastic cells
inferred← citeshttps://doi.org/10.1016/j.toxlet.2003.12.017openalex-snapshot
Mitochondrial regulation of apoptotic cell death
inferred← citeshttps://doi.org/10.1016/j.toxlet.2017.12.022openalex-snapshot
Calpain and JNK pathways participate in isoflurane – induced nucleus translocation of apoptosis-inducing factor in the brain of neonatal rats
inferred← citeshttps://doi.org/10.1016/j.urolonc.2010.04.011openalex-snapshot
13-Methyltetradecanoic acid induces mitochondrial-mediated apoptosis in human bladder cancer cells
inferred← citeshttps://doi.org/10.1016/j.yexcr.2007.07.031openalex-snapshot
In vitro analysis of Bcl-2 proteins in mitochondria and endoplasmic reticulum: Similarities in anti-apoptotic functions and differences in regulation
inferred← citeshttps://doi.org/10.1016/j.yjmcc.2004.11.003openalex-snapshot
Apoptosis of ventricular myocytes: a means to an end
inferred← citeshttps://doi.org/10.1016/j.ymeth.2007.11.003openalex-snapshot
Apoptosis-associated mitochondrial outer membrane permeabilization assays
inferred← citeshttps://doi.org/10.1016/j.ymthe.2006.02.008openalex-snapshot
Abolishing Bax-Dependent Apoptosis Shows Beneficial Effects on Spinal Muscular Atrophy Model Mice
inferred← citeshttps://doi.org/10.1016/s0005-2728(02)00358-4openalex-snapshot
Bax and heart mitochondria: uncoupling and inhibition of respiration without permeability transition
inferred← citeshttps://doi.org/10.1016/s0006-291x(02)02544-5openalex-snapshot
Direct evidence for membrane pore formation by the apoptotic protein Bax
inferred← citeshttps://doi.org/10.1016/s0006-291x(03)00615-6openalex-snapshot
Mechanisms of cytochrome c release by proapoptotic BCL-2 family members
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