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BAX-dependent transport of cytochrome c reconstituted in pure liposomes
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-1-4684-2583-3openalex-snapshot
Modern Fluorescence Spectroscopy
inferredcites →https://doi.org/10.1016/0003-2697(81)90474-7openalex-snapshot
Fluorescence quenching studies with proteins
inferredcites →https://doi.org/10.1016/0003-2697(88)90412-5openalex-snapshot
Mechanism of fluorescence concentration quenching of carboxyfluorescein in liposomes: Energy transfer to nonfluorescent dimers
inferredcites →https://doi.org/10.1016/0005-2736(86)90315-9openalex-snapshot
Morphological changes of phosphatidylcholine bilayers induced by melittin: vesicularization, fusion, discoidal particles
inferredcites →https://doi.org/10.1016/0005-2736(92)90299-2openalex-snapshot
Kinetics of melittin induced pore formation in the membrane of lipid vesicles
inferredcites →https://doi.org/10.1016/0020-711x(94)90021-3openalex-snapshot
Enzyme kinetics; behavior and analysis of rapid equilibrium and steady state enzyme systems
inferredcites →https://doi.org/10.1016/0301-4622(92)80021-vopenalex-snapshot
Kinetics of pore-mediated release of marker molecules from liposomes or cells
inferredcites →https://doi.org/10.1016/0301-4622(95)00087-9openalex-snapshot
Pore formation induced by the peptide melittin in different lipid vesicle membranes
inferredcites →https://doi.org/10.1016/s0006-3495(90)82401-2openalex-snapshot
Pore formation kinetics in membranes, determined from the release of marker molecules out of liposomes or cells
inferredcites →https://doi.org/10.1016/s0070-2161(08)60438-4openalex-snapshot
Kinetics of Movement in Narrow Channels
inferredcites →https://doi.org/10.1038/20959openalex-snapshot
Bcl-2 family proteins regulate the release of apoptogenic cytochrome c by the mitochondrial channel VDAC
inferredcites →https://doi.org/10.1042/bj3450271openalex-snapshot
Bax oligomerization is required for channel-forming activity in liposomes and to trigger cytochrome c release from mitochondria
inferredcites →https://doi.org/10.1046/j.1432-1327.1999.00198.xopenalex-snapshot
Investigation of bax‐induced release of cytochrome c from yeast mitochondria
inferredcites →https://doi.org/10.1073/pnas.93.25.14559openalex-snapshot
BAX-induced cell death may not require interleukin 1β-converting enzyme-like proteases
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.96.10.5492openalex-snapshot
Bax, but not Bcl-x L , decreases the lifetime of planar phospholipid bilayer membranes at subnanomolar concentrations
inferredcites →https://doi.org/10.1074/jbc.273.13.7770openalex-snapshot
The Overexpression of Bax Produces Cell Death upon Induction of the Mitochondrial Permeability Transition
inferredcites →https://doi.org/10.1074/jbc.274.17.11549openalex-snapshot
An APAF-1·Cytochrome c Multimeric Complex Is a Functional Apoptosome That Activates Procaspase-9
inferredcites →https://doi.org/10.1074/jbc.274.4.2225openalex-snapshot
Bax-induced Caspase Activation and Apoptosis via Cytochromec Release from Mitochondria Is Inhibitable by Bcl-xL
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/10.1085/jgp.51.2.199openalex-snapshot
Pharmacological Modifications of the Sodium Channels of Frog Nerve
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.13.15.1899openalex-snapshot
BCL-2 family members and the mitochondria in apoptosis
inferredcites →https://doi.org/10.1126/science.277.5324.370openalex-snapshot
Inhibition of Bax Channel-Forming Activity by Bcl-2
inferredcites →https://doi.org/10.1146/annurev.ph.46.030184.003001openalex-snapshot
ION CHANNELS IN LIPOSOMES
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/1521-1878(200102)23:2<111::aid-bies1016>3.0.co;2-yopenalex-snapshot
Mitochondria-the suicide organelles
inferred← citeshttps://doi.org/10.1002/9783527639502.ch8openalex-snapshot
Synthetic Amphiphilic Peptides that Self‐Assemble to Membrane‐Active Anion Transporters
inferred← citeshttps://doi.org/10.1002/ar.22689openalex-snapshot
Growth‐Inhibitory Activity of Melatonin on Murine Foregastric Carcinoma Cells In Vitro and the Underlying Molecular Mechanism
inferred← citeshttps://doi.org/10.1002/ar.a.20229openalex-snapshot
Tumor necrosis factor‐α‐induced changes in insulin‐producing β‐cells
inferred← citeshttps://doi.org/10.1002/bab.2505openalex-snapshot
Mung bean as a potent emerging functional food having anticancer therapeutic potential: Mechanistic insight and recent updates
inferred← citeshttps://doi.org/10.1002/cbdv.200790119openalex-snapshot
Synthetic, Biologically Active Amphiphilic Peptides
inferred← citeshttps://doi.org/10.1002/cbf.4062openalex-snapshot
Synthesis, characterization, and evaluation of the anticancer properties of pH‐responsive carvacrol‐zinc oxide quantum dots on breast cancer cell line (MDA‐MB‐231)
inferred← citeshttps://doi.org/10.1002/cbin.10425openalex-snapshot
Role of c‐Jun N‐terminal kinase activation in apoptosis induced by removal of the growth factors
inferred← citeshttps://doi.org/10.1002/chem.200900898openalex-snapshot
Membrane‐Length Amphiphiles Exhibiting Structural Simplicity and Ion Channel Activity
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/dvdy.20166openalex-snapshot
Implication of bax in Xenopus laevis tail regression at metamorphosis
inferred← citeshttps://doi.org/10.1002/dvdy.20312openalex-snapshot
Apoptosis of tail muscle during amphibian metamorphosis involves a caspase 9‐dependent mechanism
inferred← citeshttps://doi.org/10.1002/eji.200324650openalex-snapshot
The mitochondrial phase of the glucocorticoid‐induced apoptotic response in thymocytes comprises sequential activation of adenine nucleotide transporter (ANT)‐independent and ANT‐dependent events
inferred← citeshttps://doi.org/10.1002/em.20552openalex-snapshot
Targeting mitochondria for cancer therapy
inferred← citeshttps://doi.org/10.1002/ijc.22977openalex-snapshot
Targeting BCL‐2 family proteins to overcome drug resistance in non‐small cell lung cancer
inferred← citeshttps://doi.org/10.1002/jcb.10203openalex-snapshot
High levels of exogenous C2‐ceramide promote morphological and biochemical evidences of necrotic features in thyroid follicular cells
inferred← citeshttps://doi.org/10.1002/jcb.20893openalex-snapshot
Molecular dynamics simulation and automated docking of the pro‐apoptotic bax protein and its complex with a peptide designed from the Bax‐binding domain of anti‐apoptotic Ku70
inferred← citeshttps://doi.org/10.1002/jcb.22785openalex-snapshot
Apoptosis of mesenchymal stem cells induced by hydrogen peroxide concerns both endoplasmic reticulum stress and mitochondrial death pathway through regulation of caspases, p38 and JNK
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/mabi.201900276openalex-snapshot
Temperature‐Sensitive Amphiphilic Non‐Ionic Triblock Copolymers for Enhanced In Vivo Skeletal Muscle Transfection
inferred← citeshttps://doi.org/10.1002/pro.536openalex-snapshot
The C. elegans B‐cell lymphoma 2 (Bcl‐2) homolog cell death abnormal 9 (CED‐9) associates with and remodels LIPID membranes
inferred← citeshttps://doi.org/10.1006/abbi.2000.2201openalex-snapshot
Mitochondrial Precursor Signal Peptide Induces a Unique Permeability Transition and Release of Cytochrome c from Liver and Brain Mitochondria
inferred← citeshttps://doi.org/10.1006/bbrc.2001.6120openalex-snapshot
Mitochondrial AAA-Type Protease Yme1p Is Involved in Bax Effects on Cytochrome c Oxidase
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/10.1007/0-306-47931-1_1openalex-snapshot
Lipid Metabolism and Release of Cytochrome c from Mitochondria
inferred← citeshttps://doi.org/10.1007/0-387-23695-3_5openalex-snapshot
The Intrinsic (Mitochondrial) Death Pathway and New Cancer Therapeutics: Bcl-2 Family in Focus
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/10.1007/978-1-4419-6327-7_8openalex-snapshot
Permeabilization of the Outer Mitochondrial Membrane by Bcl-2 Proteins
inferred← citeshttps://doi.org/10.1007/978-1-4614-5203-4_10openalex-snapshot
Functional Adaptation During the Development of Cardiac Hypertrophy and Heart Failure in Females
inferred← citeshttps://doi.org/10.1007/978-1-4615-0123-7_2openalex-snapshot
Neuronal Survival and Cell Death Signaling Pathways
inferred← citeshttps://doi.org/10.1007/978-1-4939-8861-7_18openalex-snapshot
CW EPR and DEER Methods to Determine BCL-2 Family Protein Structure and Interactions: Application of Site-Directed Spin Labeling to BAK Apoptotic Pores
inferred← citeshttps://doi.org/10.1007/978-1-59259-361-3_6openalex-snapshot
The Mitochondrial Apoptosis Pathway
inferred← citeshttps://doi.org/10.1007/978-1-60761-314-5_9openalex-snapshot
Punching Holes in Membranes: How Oligomeric Pore-Forming Proteins and Lipids Cooperate to Form Aqueous Channels in Membranes
inferred← citeshttps://doi.org/10.1007/978-3-319-19497-4_1openalex-snapshot
Apoptosis: Pathways, Molecules and Beyond
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/10.1007/978-3-662-04333-2_2openalex-snapshot
Mitochondrial Membrane Permeabilization in Physiological and Pathological Cell Death
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/10.1007/978-4-431-68430-5_7openalex-snapshot
Molecular mechanisms of neuronal survival; Roles of kinases in ischemic cell death
inferred← citeshttps://doi.org/10.1007/978-94-007-6211-4_9openalex-snapshot
BH3-Only Proteins in Cancer and Apoptosis
inferred← citeshttps://doi.org/10.1007/bf02254976openalex-snapshot
On the Release of Cytochrome c from Mitochondria during Cell Death Signaling
inferred← citeshttps://doi.org/10.1007/s00204-014-1448-7openalex-snapshot
The mystery of BCL2 family: Bcl-2 proteins and apoptosis: an update
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/s00280-002-0522-7openalex-snapshot
Current status of the molecular mechanisms of anticancer drug-induced apoptosis
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/s00441-004-0954-yopenalex-snapshot
Neuronal pathology in Parkinson?s disease
inferred← citeshttps://doi.org/10.1007/s00441-005-1081-0openalex-snapshot
Neuronal pathology in Parkinson?s disease
inferred← citeshttps://doi.org/10.1007/s10495-005-0803-9openalex-snapshot
Smac/DIABLO and cytochrome c are released from mitochondria through a similar mechanism during UV-induced apoptosis
inferred← citeshttps://doi.org/10.1007/s10495-006-0004-1openalex-snapshot
Role of HPV E6 proteins in preventing UVB-induced release of pro-apoptotic factors from the mitochondria
inferred← citeshttps://doi.org/10.1007/s10495-006-0330-3openalex-snapshot
Herpes simplex virus blocks apoptosis by precluding mitochondrial cytochrome c release independent of caspase activation in infected human epithelial cells
inferred← citeshttps://doi.org/10.1007/s10495-006-4570-zopenalex-snapshot
Heat-induced programmed cell death in Leishmania infantum is reverted by Bcl-XL expression
inferred← citeshttps://doi.org/10.1007/s10495-007-0087-3openalex-snapshot
The inhibitors of apoptosis (IAPs) as cancer targets
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/s10495-007-0723-yopenalex-snapshot
The mitochondrial permeability transition pore and its involvement in cell death and in disease pathogenesis
inferred← citeshttps://doi.org/10.1007/s10495-009-0441-8openalex-snapshot
Gender differences in apoptotic signaling in heart failure due to volume overload
inferred← citeshttps://doi.org/10.1007/s10557-006-0583-7openalex-snapshot
The Interplay between Pro-Death and Pro-Survival Signaling Pathways in Myocardial Ischemia/Reperfusion Injury: Apoptosis Meets Autophagy
inferred← citeshttps://doi.org/10.1007/s10853-013-7415-5openalex-snapshot
5-Fluorouracil-loaded poly-l-lactide fibrous membrane for the prevention of intestinal stent restenosis
inferred← citeshttps://doi.org/10.1007/s10863-005-6222-3openalex-snapshot
Mitochondrial Carrier Homolog 2: A Clue to Cracking the BCL-2 Family Riddle?
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/s11655-015-1975-yopenalex-snapshot
Matrine and CYC116 synergistically inhibit growth and induce apoptosis in multiple myeloma cells
inferred← citeshttps://doi.org/10.1007/s11655-017-2922-xopenalex-snapshot
Effects of Banxia Xiexin Decoction (半夏泻心汤) on Cisplatin-Induced Apoptosis of Human A549 Lung Cancer Cells
inferred← citeshttps://doi.org/10.1007/s12011-014-0219-xopenalex-snapshot
Inhibitive Effects of Nickel Chloride (NiCl2) on Thymocytes
inferred← citeshttps://doi.org/10.1007/s12035-021-02675-5openalex-snapshot
Bax Contributes to Retinal Ganglion Cell Dendritic Degeneration During Glaucoma
inferred← citeshttps://doi.org/10.1007/s12291-019-0817-7openalex-snapshot
Amelioration of Combination of Paclitaxel and Di Allyl Sulfide on the Alterations of Bcl2, P53 and Apoptosis Changes Against 7,12 Di Methyl Benz (A) Anthracene Induced Skin Cancer in Experimental Animals
inferred← citeshttps://doi.org/10.1007/s13273-012-0009-5openalex-snapshot
Capsaicin-induced apoptosis in the human glioblastoma U87MG cells via p-38 MAPK and Bcl-2/Bax signaling pathway
inferred← citeshttps://doi.org/10.1007/s13402-012-0086-4openalex-snapshot
Myrtenal attenuates diethylnitrosamine-induced hepatocellular carcinoma in rats by stabilizing intrinsic antioxidants and modulating apoptotic and anti-apoptotic cascades
inferred← citeshttps://doi.org/10.1016/bs.adplan.2015.01.002openalex-snapshot
Microscopy of Model Membranes
inferred← citeshttps://doi.org/10.1016/j.abb.2003.08.038openalex-snapshot
Opposing roles of δ and εPKC in cardiac ischemia and reperfusion: targeting the apoptotic machinery
inferred← citeshttps://doi.org/10.1016/j.abb.2004.08.025openalex-snapshot
Initiation of mitochondrial-mediated apoptosis during cardiac reperfusion
inferred← citeshttps://doi.org/10.1016/j.abb.2006.02.007openalex-snapshot
Preconditioning prevents loss in mitochondrial function and release of cytochrome c during prolonged cardiac ischemia/reperfusion
inferred← citeshttps://doi.org/10.1016/j.ajoms.2022.11.005openalex-snapshot
Role of hypoxia-inducible proteins in ameloblastoma: A review
inferred← citeshttps://doi.org/10.1016/j.bbabio.2006.04.011openalex-snapshot
Proapoptotic BCL-2 family members and mitochondrial dysfunction during ischemia/reperfusion injury, a study employing cardiac HL-1 cells and GFP biosensors
inferred← citeshttps://doi.org/10.1016/j.bbabio.2006.05.032openalex-snapshot
Mitochondria as the target of the pro-apoptotic protein Bax
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.2003.10.007openalex-snapshot
The intra-mitochondrial cytochrome c distribution varies correlated to the formation of a complex between VDAC and the adenine nucleotide translocase: this affects Bax-dependent cytochrome c release
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.2008.02.018openalex-snapshot
Caspase-independent apoptosis in yeast
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2010.12.019openalex-snapshot
Molecular biology of Bax and Bak activation and action
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.2012.08.006openalex-snapshot
Transmembrane pore formation by the carboxyl terminus of Bax protein
inferred← citeshttps://doi.org/10.1016/j.bbamem.2016.10.007openalex-snapshot
Pro-apoptotic cBid and Bax exhibit distinct membrane remodeling activities: An AFM study
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.bbcan.2004.09.004openalex-snapshot
Promises and challenges of targeting Bcl-2 anti-apoptotic proteins for cancer therapy
inferred← citeshttps://doi.org/10.1016/j.bbrc.2004.07.054openalex-snapshot
Bax-inhibiting peptide derived from mouse and rat Ku70
inferred← citeshttps://doi.org/10.1016/j.bbrc.2019.05.039openalex-snapshot
Time-lapse FRET analysis reveals the ability of Bax dimer to trigger mitochondrial outer membrane permeabilization
inferred← citeshttps://doi.org/10.1016/j.bcp.2004.07.006openalex-snapshot
Role of the permeability transition pore in cytochrome C release from mitochondria during ischemia-reperfusion in rat liver
inferred← citeshttps://doi.org/10.1016/j.bcp.2019.01.015openalex-snapshot
A delicate balance – The BCL-2 family and its role in apoptosis, oncogenesis, and cancer therapeutics
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.biopha.2014.10.006openalex-snapshot
Antiproliferation and induction of caspase-8-dependent mitochondria-mediated apoptosis by β-tocotrienol in human lung and brain cancer cell lines
inferred← citeshttps://doi.org/10.1016/j.bmc.2003.08.036openalex-snapshot
Functional, synthetic organic chemical models of cellular ion channels
inferred← citeshttps://doi.org/10.1016/j.bpj.2011.09.041openalex-snapshot
Bax Forms Two Types of Channels, One of Which Is Voltage-Gated
inferred← citeshttps://doi.org/10.1016/j.brainresbull.2003.08.005openalex-snapshot
BAX protein-immunoreactivity in midbrain neurons of Parkinson’s disease patients
inferred← citeshttps://doi.org/10.1016/j.brainresbull.2007.11.001openalex-snapshot
Bcl-2 or Bcl-XL gene therapy reduces apoptosis and increases plasticity protein GAP-43 in PC12 cells
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.cbi.2009.11.011openalex-snapshot
Morin fosters apoptosis in experimental hepatocellular carcinogenesis model
inferred← citeshttps://doi.org/10.1016/j.ceb.2003.10.004openalex-snapshot
Bcl-2-family proteins and the role of mitochondria in apoptosis
inferred← citeshttps://doi.org/10.1016/j.cellsig.2007.07.024openalex-snapshot
Bid is not required for Bax translocation during UV-induced apoptosis
inferred← citeshttps://doi.org/10.1016/j.cellsig.2010.05.018openalex-snapshot
RACK1 promotes Bax oligomerization and dissociates the interaction of Bax and Bcl-XL
inferred← citeshttps://doi.org/10.1016/j.cophys.2018.03.005openalex-snapshot
BH3-dependent and independent activation of BAX and BAK in mitochondrial apoptosis
inferred← citeshttps://doi.org/10.1016/j.ejmech.2018.02.057openalex-snapshot
Design, synthesis, and biological evaluation of stable β 6.3 -Helices: Discovery of non-hemolytic antibacterial peptides
inferred← citeshttps://doi.org/10.1016/j.eujim.2013.06.004openalex-snapshot
Novel anticancer activity and anticancer mechanisms of Brassica oleracea L. var. capitata f. rubra
inferred← citeshttps://doi.org/10.1016/j.febslet.2004.05.006openalex-snapshot
Some amphiphilic cations block the mitochondrial apoptosis‐induced channel, MAC
inferred← citeshttps://doi.org/10.1016/j.febslet.2007.09.063openalex-snapshot
Robustness analysis identifies the plausible model of the Bcl‐2 apoptotic switch
inferred← citeshttps://doi.org/10.1016/j.gene.2005.10.038openalex-snapshot
Bid, a BH3-only multi-functional molecule, is at the cross road of life and death
inferred← citeshttps://doi.org/10.1016/j.gene.2021.145897openalex-snapshot
PGAM1 regulates the glycolytic metabolism of SCs in tibetan sheep and its influence on the development of SCs
inferred← citeshttps://doi.org/10.1016/j.jmb.2003.10.028openalex-snapshot
Specific Interaction of the Antiapoptotic Protein Nr-13 with Phospholipid Monolayers is Prevented by the BH3 Domain of Bax
inferred← citeshttps://doi.org/10.1016/j.jmb.2005.11.032openalex-snapshot
BCL-XL Dimerization by Three-dimensional Domain Swapping
inferred← citeshttps://doi.org/10.1016/j.jmb.2007.01.016openalex-snapshot
Preprotein Transport Machineries of Yeast Mitochondrial Outer Membrane Are not Required for Bax-induced Release of Intermembrane Space Proteins
inferred← citeshttps://doi.org/10.1016/j.jmb.2008.06.037openalex-snapshot
Cholesterol Effects on BAX Pore Activation
inferred← citeshttps://doi.org/10.1016/j.jnutbio.2005.11.001openalex-snapshot
Apoptosis induction by γ-tocotrienol in human hepatoma Hep3B cells
inferred← citeshttps://doi.org/10.1016/j.jphotobiol.2019.111698openalex-snapshot
Synthesis and characterization of zinc oxide nanoparticles from Morus nigra and its anticancer activity of AGS gastric cancer cells
inferred← citeshttps://doi.org/10.1016/j.jtbi.2010.11.040openalex-snapshot
The Bcl-2-associated death promoter (BAD) lowers the threshold at which the Bcl-2-interacting domain death agonist (BID) triggers mitochondria disintegration
inferred← citeshttps://doi.org/10.1016/j.meatsci.2016.01.003openalex-snapshot
Disorder of endoplasmic reticulum calcium channel components is associated with the increased apoptotic potential in pale, soft, exudative pork
inferred← citeshttps://doi.org/10.1016/j.molcel.2009.09.030openalex-snapshot
Stepwise Activation of BAX and BAK by tBID, BIM, and PUMA Initiates Mitochondrial Apoptosis
inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2005.08.004openalex-snapshot
Survival and cell death in cells constitutively unable to synthesize glutathione
inferred← citeshttps://doi.org/10.1016/j.neulet.2008.12.021openalex-snapshot
Bax-inhibiting peptide protects glutamate-induced cerebellar granule cell death by blocking Bax translocation
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2006.07.049openalex-snapshot
Ischemic preconditioning negatively regulates plenty of SH3s–mixed lineage kinase 3–Rac1 complex and c-Jun N-terminal kinase 3 signaling via activation of Akt
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2009.03.050openalex-snapshot
Neuroprotection of preconditioning against ischemic brain injury in rat hippocampus through inhibition of the assembly of GluR6—PSD95—mixed lineage kinase 3 signaling module via nuclear and non-nuclear pathways
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.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.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.2011.07.015openalex-snapshot
Crystal Structure of a BCL-W Domain-Swapped Dimer: Implications for the Function of BCL-2 Family Proteins
inferred← citeshttps://doi.org/10.1016/j.taap.2007.08.025openalex-snapshot
Ofloxacin induces apoptosis in microencapsulated juvenile rabbit chondrocytes by caspase-8-dependent mitochondrial pathway
inferred← citeshttps://doi.org/10.1016/j.taap.2009.06.015openalex-snapshot
Neurobehavioral impairments, generation of oxidative stress and release of pro-apoptotic factors after chronic exposure to sulphur mustard in mouse brain
inferred← citeshttps://doi.org/10.1016/j.tox.2007.08.095openalex-snapshot
Interaction between caspase-8 activation and endoplasmic reticulum stress in glycochenodeoxycholic acid-induced apoptotic HepG2 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.tox.2019.04.006openalex-snapshot
Effects of TNFR1 gene silencing on early apoptosis of marbofloxacin-treated chondrocytes from juvenile dogs
inferred← citeshttps://doi.org/10.1016/j.yexcr.2006.01.026openalex-snapshot
Relative timing of redistribution of cytochrome c and Smac/DIABLO from mitochondria during apoptosis assessed by double immunocytochemistry on mammalian cells
inferred← citeshttps://doi.org/10.1016/j.yjmcc.2007.09.001openalex-snapshot
Alterations in both death and survival signals for apoptosis in heart failure due to volume overload
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
inferred← citeshttps://doi.org/10.1016/s0006-291x(03)00630-2openalex-snapshot
Mitochondrion-targeted apoptosis regulators of viral origin
inferred← citeshttps://doi.org/10.1016/s0006-3495(03)74588-3openalex-snapshot
Enlargement and Contracture of C2-Ceramide Channels
inferred← citeshttps://doi.org/10.1016/s0014-5793(01)02858-7openalex-snapshot
Oligomeric C‐terminal truncated Bax preferentially releases cytochrome c but not adenylate kinase from mitochondria, outer membrane vesicles and proteoliposomes
inferred← citeshttps://doi.org/10.1016/s0026-895x(24)12510-2openalex-snapshot
Multiple Kinetics of Mitochondrial Cytochrome cRelease in Drug-Induced Apoptosis
inferred← citeshttps://doi.org/10.1016/s0041-008x(03)00240-0openalex-snapshot
Involvement of mitochondria in acetaminophen-induced apoptosis and hepatic injury
inferred← citeshttps://doi.org/10.1016/s0083-6729(07)00010-6openalex-snapshot
Vitamin K2‐Mediated Apoptosis in Cancer Cells: Role of Mitochondrial Transmembrane Potential
inferred← citeshttps://doi.org/10.1016/s0092-8674(02)01036-xopenalex-snapshot
Bid, Bax, and Lipids Cooperate to Form Supramolecular Openings in the Outer Mitochondrial Membrane
inferred← citeshttps://doi.org/10.1016/s0161-5890(02)00252-3openalex-snapshot
The Bcl-2 protein family: sensors and checkpoints for life-or-death decisions
inferred← citeshttps://doi.org/10.1016/s0165-0173(01)00095-9openalex-snapshot
Prevention of apoptotic neuronal death by controlling procaspases? A point of view
inferred← citeshttps://doi.org/10.1016/s0278-5846(03)00016-2openalex-snapshot
Apoptotic signaling cascades
inferred← citeshttps://doi.org/10.1016/s0300-9084(02)01366-4openalex-snapshot
The adenine nucleotide translocator in apoptosis
inferred← citeshttps://doi.org/10.1016/s0300-9084(02)01370-6openalex-snapshot
The voltage-dependent anion channel: an essential player in apoptosis
inferred← citeshttps://doi.org/10.1016/s0733-8651(05)70194-6openalex-snapshot
INVOLVEMENT OF MITOCHONDRIA IN APOPTOSIS
inferred← citeshttps://doi.org/10.1016/s0960-9822(02)01433-1openalex-snapshot
Apoptosis: Mitochondrial Membrane Permeabilization – The (W)hole Story?
inferred← citeshttps://doi.org/10.1016/s0968-0004(01)01844-8openalex-snapshot
The mitochondrial apoptosome: a killer unleashed by the cytochrome seas
inferred← citeshttps://doi.org/10.1016/s1097-2765(01)00320-3openalex-snapshot
BCL-2, BCL-XL Sequester BH3 Domain-Only Molecules Preventing BAX- and BAK-Mediated Mitochondrial Apoptosis
inferred← citeshttps://doi.org/10.1016/s1097-2765(02)00751-7openalex-snapshot
Bax, along with Lipid Conspirators, Allows Cytochrome c to Escape Mitochondria
inferred← citeshttps://doi.org/10.1016/s1535-6108(03)00272-1openalex-snapshot
Pharmacologic activation of p53 elicits Bax-dependent apoptosis in the absence of transcription
inferred← citeshttps://doi.org/10.1016/s1554-4516(05)02010-7openalex-snapshot
Mechanisms of Membrane Permeabilization by Apoptosis-Regulatory Proteins of the BCL-2 Family
inferred← citeshttps://doi.org/10.1016/s1566-2772(01)00021-4openalex-snapshot
Apoptosis: its relevance to Parkinson's disease
inferred← citeshttps://doi.org/10.1017/cbo9780511544873.008openalex-snapshot
Apoptosis in neurodegenerative diseases
inferred← citeshttps://doi.org/10.1021/acs.bioconjchem.9b00366openalex-snapshot
Chemically Engineered Synthetic Lipid Vesicles for Sensing and Visualization of Protein–Bilayer Interactions
inferred← citeshttps://doi.org/10.1021/acs.jpcb.6c02290openalex-snapshot
Direct Observation of Electric Field-Driven Protein Translocation through the Single-Walled Carbon Nanotube Embedded in a Lipid Bilayer Membrane Revealed a High Dipole Moment of the Transition State
inferred← citeshttps://doi.org/10.1021/acsami.8b12393openalex-snapshot
Hyaluronan Reduces Cationic Liposome-Induced Toxicity and Enhances the Antitumor Effect of Targeted Gene Delivery in Mice
inferred← citeshttps://doi.org/10.1021/bi026979dopenalex-snapshot
Tauroursodeoxycholic Acid Prevents Bax-Induced Membrane Perturbation and CytochromecRelease in Isolated Mitochondria
inferred← citeshttps://doi.org/10.1021/bk-2012-1093.ch028openalex-snapshot
Cellular Antioxidant Defenses and Amelioration by Biopigments with Particular Focus on mRNA Oxidations
inferred← citeshttps://doi.org/10.1021/cr3002033openalex-snapshot
Mitochondrial Outer Membrane Channels
inferred← citeshttps://doi.org/10.1021/ja016784dopenalex-snapshot
SCMTR: A Chloride-Selective, Membrane-Anchored Peptide Channel that Exhibits Voltage Gating
inferred← citeshttps://doi.org/10.1021/jacs.2c06275openalex-snapshot
High-Resolution Low-Power Hyperspectral Line-Scan Imaging of Fast Cellular Dynamics Using Azo-Enhanced Raman Scattering Probes
inferred← citeshttps://doi.org/10.1021/nl073290ropenalex-snapshot
Synthesis and Characterization of Stable Fluorocarbon Nanostructures as Drug Delivery Vehicles for Cytolytic Peptides
inferred← citeshttps://doi.org/10.1023/a:1016061006256openalex-snapshot
Bcl-2 Family of Proteins: Life-or-Death Switch in Mitochondria
inferred← citeshttps://doi.org/10.1023/a:1022945107762openalex-snapshot
The mitochondrial membrane potential (Δψm) in apoptosis; an update
inferred← citeshttps://doi.org/10.1023/a:1023635510363openalex-snapshot
Caspases as Regulators of Apoptosis and Other Cell Functions
inferred← citeshttps://doi.org/10.1023/b:appt.0000045786.98031.1dopenalex-snapshot
Apoptosome dysfunction in human cancer
inferred← citeshttps://doi.org/10.1023/b:mcbi.0000009862.17396.8dopenalex-snapshot
VDAC: The channel at the interface between mitochondria and the cytosol
inferred← citeshttps://doi.org/10.1023/b:mcbi.0000009865.70898.36openalex-snapshot
Mitochondria and the Bcl-2 family proteins in apoptosis signaling pathways
inferred← citeshttps://doi.org/10.1038/35048073openalex-snapshot
The mitochondrion in apoptosis: how Pandora's box opens
inferred← citeshttps://doi.org/10.1038/cdd.2009.123openalex-snapshot
Single-cell quantification of Bax activation and mathematical modelling suggest pore formation on minimal mitochondrial Bax accumulation
inferred← citeshttps://doi.org/10.1038/cdd.2010.112openalex-snapshot
Single-point mutations of a lysine residue change function of Bax and Bcl-xL expressed in Bax- and Bak-less mouse embryonic fibroblasts: novel insights into the molecular mechanisms of Bax-induced apoptosis
inferred← citeshttps://doi.org/10.1038/cddis.2013.210openalex-snapshot
Three-dimensional structure of Bax-mediated pores in membrane bilayers
inferred← citeshttps://doi.org/10.1038/cr.2007.101openalex-snapshot
Apoptosis commitment – translating survival signals into decisions on mitochondria
inferred← citeshttps://doi.org/10.1038/cr.2015.9openalex-snapshot
Cationic nanocarriers induce cell necrosis through impairment of Na+/K+-ATPase and cause subsequent inflammatory response
inferred← citeshttps://doi.org/10.1038/ncb950openalex-snapshot
Ku70 suppresses the apoptotic translocation of Bax to mitochondria
inferred← citeshttps://doi.org/10.1038/ncomms5935openalex-snapshot
Small-molecule Bax agonists for cancer therapy
inferred← citeshttps://doi.org/10.1038/nrc2297openalex-snapshot
Diagnosing and exploiting cancer's addiction to blocks in apoptosis
inferred← citeshttps://doi.org/10.1038/nrc883openalex-snapshot
The Bcl2 family: regulators of the cellular life-or-death switch
inferred← citeshttps://doi.org/10.1038/nri931openalex-snapshot
Lymphocide: cytokines and the control of lymphoid homeostasis
inferred← citeshttps://doi.org/10.1038/nrm2952openalex-snapshot
Mitochondria and cell death: outer membrane permeabilization and beyond
inferred← citeshttps://doi.org/10.1038/onc.2009.293openalex-snapshot
A novel pro-apoptotic function of RACK1: suppression of Src activity in the intrinsic and Akt pathways
inferred← citeshttps://doi.org/10.1038/s41388-018-0123-5openalex-snapshot
Differential role of FL-BID and t-BID during verotoxin-1-induced apoptosis in Burkitt’s lymphoma cells
inferred← citeshttps://doi.org/10.1038/s41419-018-0464-6openalex-snapshot
Bax retrotranslocation potentiates Bcl-xL’s antiapoptotic activity and is essential for switch-like transitions between MOMP competency and resistance
inferred← citeshttps://doi.org/10.1038/s41419-019-2128-6openalex-snapshot
eIF2α-CHOP-BCl-2/JNK and IRE1α-XBP1/JNK signaling promote apoptosis and inflammation and support the proliferation of Newcastle disease virus
inferred← citeshttps://doi.org/10.1038/s41419-025-08258-9openalex-snapshot
Stochasticity contributes to explaining minority and majority MOMP during apoptosis
inferred← citeshttps://doi.org/10.1038/s41598-017-02825-7openalex-snapshot
Release of Cytochrome C from Bax Pores at the Mitochondrial Membrane
inferred← citeshttps://doi.org/10.1038/s41598-019-53049-wopenalex-snapshot
Completion of BAX recruitment correlates with mitochondrial fission during apoptosis
inferred← citeshttps://doi.org/10.1038/sj.cdd.4400783openalex-snapshot
Pro-apoptotic cascade activates BID, which oligomerizes BAK or BAX into pores that result in the release of cytochrome c
inferred← citeshttps://doi.org/10.1038/sj.cdd.4400910openalex-snapshot
Conformational change of Bax: a question of life or death
inferred← citeshttps://doi.org/10.1038/sj.cdd.4401566openalex-snapshot
Cardiolipin and phosphatidylglycerol are not required for the in vivo action of Bcl-2 family proteins
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