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Facilitation of Mitochondrial Outer and Inner Membrane Permeabilization and Cell Death in Oxidative Stress by a Novel Bcl-2 Homology 3 Domain Protein
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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High fluence low‐power laser irradiation induces mitochondrial permeability transition mediated by reactive oxygen species
inferredcites →https://doi.org/10.1007/s10495-006-0525-7openalex-snapshot
Role of the mitochondrial membrane permeability transition in cell death
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Inhibition of Mitochondrial Neural Cell Death Pathways by Protein Transduction of Bcl-2 Family Proteins
inferredcites →https://doi.org/10.1007/s10863-008-9147-9openalex-snapshot
Uncovering the role of VDAC in the regulation of cell life and death
inferredcites →https://doi.org/10.1016/0003-2697(90)90595-zopenalex-snapshot
Molecular cloning: A laboratory manual
inferredcites →https://doi.org/10.1016/j.bbabio.2006.03.017openalex-snapshot
Mitochondrial membrane permeability transition and cell death
inferredcites →https://doi.org/10.1016/j.bbabio.2008.08.002openalex-snapshot
Oligomeric BAX induces mitochondrial permeability transition and complete cytochrome c release without oxidative stress
inferredcites →https://doi.org/10.1016/j.bbadis.2005.10.006openalex-snapshot
Voltage-dependent anion channel (VDAC) as mitochondrial governator—Thinking outside the box
inferredcites →https://doi.org/10.1016/j.bbrc.2004.08.094openalex-snapshot
Bax increases the pore size of rat brain mitochondrial voltage-dependent anion channel in the presence of tBid
inferredcites →https://doi.org/10.1016/j.cellsig.2007.04.009openalex-snapshot
Oxyl radicals, redox-sensitive signalling cascades and antioxidants
inferredcites →https://doi.org/10.1016/j.febslet.2006.10.067openalex-snapshot
Induction of necrotic cell death and mitochondrial permeabilization by heme binding protein 2/SOUL
inferredcites →https://doi.org/10.1016/j.mito.2006.07.006openalex-snapshot
The role of the mitochondrial permeability transition in cell death
inferredcites →https://doi.org/10.1016/j.neulet.2005.06.070openalex-snapshot
Bax-regulated mitochondria-mediated apoptosis is responsible for the in vitro ischemia induced neuronal cell death of Sprague Dawley rat
inferredcites →https://doi.org/10.1016/j.peptides.2005.06.022openalex-snapshot
Pituitary adenylate cyclase activating polypeptide protects cardiomyocytes against oxidative stress-induced apoptosis
inferredcites →https://doi.org/10.1016/s0003-9861(02)00471-xopenalex-snapshot
Characterization of a human and mouse tetrapyrrole-binding protein
inferredcites →https://doi.org/10.1016/s0005-2728(98)00112-1openalex-snapshot
The mitochondrial permeability transition in cell death: a common mechanism in necrosis, apoptosis and autophagy
inferredcites →https://doi.org/10.1016/s0021-9258(18)56236-0openalex-snapshot
CYTOCHEMICAL STUDIES OF MAMMALIAN TISSUES
inferredcites →https://doi.org/10.1016/s0169-328x(99)00277-6openalex-snapshot
Discovery of a putative heme-binding protein family (SOUL/HBP) by two-tissue suppression subtractive hybridization and database searches
inferredcites →https://doi.org/10.1016/s0891-5849(01)00616-5openalex-snapshot
Direct effect of Taxol on free radical formation and mitochondrial permeability transition
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/bi00232a015openalex-snapshot
J-aggregate formation of a carbocyanine as a quantitative fluorescent indicator of membrane potential
inferredcites →https://doi.org/10.1021/bi035348wopenalex-snapshot
Transbilayer Lipid Diffusion Promoted by Bax: Implications for Apoptosis
inferredcites →https://doi.org/10.1021/bi048742iopenalex-snapshot
SOUL in Mouse Eyes Is a New Hexameric Heme-Binding Protein with Characteristic Optical Absorption, Resonance Raman Spectral, and Heme-Binding Properties
inferredcites →https://doi.org/10.1021/bi061577hopenalex-snapshot
NMR Structural Investigation of the Mitochondrial Outer Membrane Protein VDAC and Its Interaction with Antiapoptotic Bcl-xL
inferredcites →https://doi.org/10.1023/b:appt.0000038034.16230.eaopenalex-snapshot
The cardiolipin-binding domain of Bid affects mitochondrial respiration and enhances cytochrome c release
inferredcites →https://doi.org/10.1038/nature03434openalex-snapshot
Loss of cyclophilin D reveals a critical role for mitochondrial permeability transition in cell death
inferredcites →https://doi.org/10.1038/ncb1575openalex-snapshot
Voltage-dependent anion channels are dispensable for mitochondrial-dependent cell death
inferredcites →https://doi.org/10.1038/sj.cdd.4400722openalex-snapshot
Bcl-2 prevents mitochondrial permeability transition and cytochrome c release via maintenance of reduced pyridine nucleotides
inferredcites →https://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
inferredcites →https://doi.org/10.1038/sj.cdd.4400889openalex-snapshot
Bax translocation to mitochondria subsequent to a rapid loss of mitochondrial membrane potential
inferredcites →https://doi.org/10.1038/sj.cdd.4401508openalex-snapshot
Bax affects intracellular Ca2+ stores and induces Ca2+ wave propagation
inferredcites →https://doi.org/10.1038/sj.emboj.7600675openalex-snapshot
Bax forms multispanning monomers that oligomerize to permeabilize membranes during apoptosis
inferredcites →https://doi.org/10.1038/sj.onc.1201350openalex-snapshot
Bak can accelerate chemotherapy-induced cell death independently of its heterodimerization with Bcl-XL and Bcl-2
inferredcites →https://doi.org/10.1038/sj.onc.1205621openalex-snapshot
Activation of mitochondrial voltage-dependent anion channel by apro-apoptotic BH3-only protein Bim
inferredcites →https://doi.org/10.1038/sj.onc.1210638openalex-snapshot
Endoplasmic reticulum stress induces calcium-dependent permeability transition, mitochondrial outer membrane permeabilization and apoptosis
inferredcites →https://doi.org/10.1042/bj3040081openalex-snapshot
Multiple effects of haemin binding on protease susceptibility of bovine serum albumin and a novel isolation procedure for its large fragment
inferredcites →https://doi.org/10.1042/bj3060445openalex-snapshot
Control of inositol 1,4,5-trisphosphate-induced Ca2+ release by cytosolic Ca2+
inferredcites →https://doi.org/10.1046/j.1471-4159.2003.01545.xopenalex-snapshot
Two pathways for tBID‐induced cytochrome c release from rat brain mitochondria: BAK‐ versus BAX‐dependence
inferredcites →https://doi.org/10.1073/pnas.97.2.577openalex-snapshot
Proapoptotic BH3-only Bcl-2 family members induce cytochrome c release, but not mitochondrial membrane potential loss, and do not directly modulate voltage-dependent anion channel activity
inferredcites →https://doi.org/10.1074/jbc.273.47.31388openalex-snapshot
Molecular Characterization of a Newly Identified Heme-binding Protein Induced during Differentiation of urine Erythroleukemia Cells
inferredcites →https://doi.org/10.1074/jbc.m301624200openalex-snapshot
Necrotic Cell Death in Response to Oxidant Stress Involves the Activation of the Apoptogenic Caspase-8/Bid Pathway
inferredcites →https://doi.org/10.1074/jbc.m308576200openalex-snapshot
Calpain-1 Regulates Bax and Subsequent Smac-dependent Caspase-3 Activation in Neutrophil Apoptosis
inferredcites →https://doi.org/10.1074/jbc.m310593200openalex-snapshot
Bid, but Not Bax, Regulates VDAC Channels
inferredcites →https://doi.org/10.1074/jbc.m313420200openalex-snapshot
Lipidic Pore Formation by the Concerted Action of Proapoptotic BAX and tBID
inferredcites →https://doi.org/10.1074/jbc.m507075200openalex-snapshot
Pivotal Role of Akt Activation in Mitochondrial Protection and Cell Survival by Poly(ADP-ribose)polymerase-1 Inhibition in Oxidative Stress
inferredcites →https://doi.org/10.1083/jcb.200306159openalex-snapshot
PLA2 activity is required for nuclear shrinkage in caspase-independent cell death
inferredcites →https://doi.org/10.1101/gad.13.15.1899openalex-snapshot
BCL-2 family members and the mitochondria in apoptosis
inferredcites →https://doi.org/10.1111/j.1471-4159.1990.tb04189.xopenalex-snapshot
Rapid Isolation of Metabolically Active Mitochondria from Rat Brain and Subregions Using Percoll Density Gradient Centrifugation
inferredcites →https://doi.org/10.1126/science.1161302openalex-snapshot
Solution Structure of the Integral Human Membrane Protein VDAC-1 in Detergent Micelles
inferredcites →https://doi.org/10.1126/science.281.5381.1322openalex-snapshot
The Bcl-2 Protein Family: Arbiters of Cell Survival
inferredcites →https://doi.org/10.1126/science.8424176openalex-snapshot
Regulation by Heme of Mitochondrial Protein Transport Through a Conserved Amino Acid Motif
inferredcites →https://doi.org/10.1126/stke.2000.63.pe1openalex-snapshot
Protein N-myristoylation: Critical Role in Apoptosis and Salt Tolerance
inferredcites →https://doi.org/10.1152/physrev.2000.80.2.593openalex-snapshot
Tissue-Specific Bcl-2 Protein Partners in Apoptosis: An Ovarian Paradigm
inferredcites →https://doi.org/10.1161/circresaha.108.178970openalex-snapshot
Glycogen Synthase Kinase 3 Inhibition Slows Mitochondrial Adenine Nucleotide Transport and Regulates Voltage-Dependent Anion Channel Phosphorylation
inferredcites →https://doi.org/10.1242/jcs.115.8.1567openalex-snapshot
BH3-only proteins — evolutionarily conserved proapoptotic Bcl-2 family members essential for initiating programmed cell death
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Exercise and Doxorubicin Treatment Modulate Cardiac Mitochondrial Quality Control Signaling
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HEBP2 affects sensitivity to cisplatin and BCNU but not to paclitaxel in MDA-MB-231 breast cancer cells
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The SOUL family of heme-binding proteins: Structure and function 15 years later
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SARS-CoV-2 SUD2core promotes neutrophil-mediated inflammation by disabling HEBP2-mediated restraint on granule exocytosis
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Plasminogen activator inhibitor 1, fibroblast apoptosis resistance, and aging-related susceptibility to lung fibrosis
inferred← citeshttps://doi.org/10.1016/j.gep.2011.03.006openalex-snapshot
Identification and expression of soul/p22HBP genes in zebrafish
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Protein hydrolysates from tuna cooking juice inhibit cell growth and induce apoptosis of human breast cancer cell line MCF-7
inferred← citeshttps://doi.org/10.1016/j.jmgm.2010.07.008openalex-snapshot
Tetrapyrrole binding affinity of the murine and human p22HBP heme-binding proteins
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Danshou Tang alleviates mitochondrial oxidative stress and modulates apoptosis to improve recurrent spontaneous abortion outcomes
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Structural changes in the BH3 domain of SOUL protein upon interaction with the anti-apoptotic protein Bcl-xL
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