scholarly article | Q13442814 |
P2093 | author name string | Paul Schlesinger | |
Eric Christenson | |||
Sean Merlin | |||
Mitsu Saito | |||
P2860 | cites work | Apoptosis initiated when BH3 ligands engage multiple Bcl-2 homologs, not Bax or Bak | Q24296478 |
NPC1 and NPC2 Regulate Cellular Cholesterol Homeostasis through Generation of Low Density Lipoprotein Cholesterol-derived Oxysterols | Q24300768 | ||
Enforced dimerization of BAX results in its translocation, mitochondrial dysfunction and apoptosis | Q24533270 | ||
Movement of Bax from the cytosol to mitochondria during apoptosis | Q24677881 | ||
Oxysterol biosynthetic enzymes | Q28139744 | ||
Peripheral benzodiazepine receptors and mitochondrial function | Q28201926 | ||
Peripheral-type benzodiazepine receptor: structure and function of a cholesterol-binding protein in steroid and bile acid biosynthesis | Q28205153 | ||
Cell death: critical control points | Q28240722 | ||
Membrane-protein interactions in cell signaling and membrane trafficking | Q28248356 | ||
Association of Bax and Bak homo-oligomers in mitochondria. Bax requirement for Bak reorganization and cytochrome c release | Q28579372 | ||
VDAC2 inhibits BAK activation and mitochondrial apoptosis | Q28594000 | ||
The BCL-2 protein family: opposing activities that mediate cell death | Q29547380 | ||
Mitochondrial membrane permeabilization in cell death | Q29547425 | ||
The pathophysiology of mitochondrial cell death | Q29547893 | ||
BAX and BAK regulation of endoplasmic reticulum Ca2+: a control point for apoptosis | Q29620466 | ||
The voltage dependent anion channel affects mitochondrial cholesterol distribution and function | Q33292291 | ||
Cholesterol's interfacial interactions with galactosylceramides | Q33792383 | ||
Bax forms multispanning monomers that oligomerize to permeabilize membranes during apoptosis | Q33854131 | ||
BAX-dependent transport of cytochrome c reconstituted in pure liposomes | Q33912996 | ||
VDAC channels mediate and gate the flow of ATP: implications for the regulation of mitochondrial function | Q33915365 | ||
Visualizing recycling synaptic vesicles in hippocampal neurons by FM 1-43 photoconversion | Q33948072 | ||
Pro-apoptotic cascade activates BID, which oligomerizes BAK or BAX into pores that result in the release of cytochrome c. | Q34139321 | ||
Genetic ablation of calcium-independent phospholipase A2gamma leads to alterations in mitochondrial lipid metabolism and function resulting in a deficient mitochondrial bioenergetic phenotype | Q34304761 | ||
New insights into the mechanism of permeation through large channels | Q34352427 | ||
Is MAC the knife that cuts cytochrome c from mitochondria during apoptosis? | Q34522154 | ||
Liquid-liquid immiscibility in membranes | Q35062616 | ||
Peeking into a secret world of pore-forming toxins: membrane binding processes studied by surface plasmon resonance. | Q35559641 | ||
Functional, synthetic organic chemical models of cellular ion channels | Q35690277 | ||
The condensing effect of cholesterol in lipid bilayers | Q35794510 | ||
Cytochrome C-mediated apoptosis | Q35799945 | ||
Modeling of the role of a Bax-activation switch in the mitochondrial apoptosis decision | Q35812274 | ||
Procedure for preparation of liposomes with large internal aqueous space and high capture by reverse-phase evaporation | Q35989488 | ||
The enantiomer of cholesterol | Q36035615 | ||
What's so special about cholesterol? | Q36052476 | ||
Mitochondrial permeabilization relies on BH3 ligands engaging multiple prosurvival Bcl-2 relatives, not Bak. | Q36118156 | ||
Fluorescence photooxidation with eosin: a method for high resolution immunolocalization and in situ hybridization detection for light and electron microscopy | Q36234474 | ||
Regulated targeting of BAX to mitochondria. | Q36255507 | ||
On the role of VDAC in apoptosis: fact and fiction | Q36259127 | ||
Life in the balance: how BH3-only proteins induce apoptosis. | Q36294226 | ||
Cholesterol and the interaction of proteins with membrane domains. | Q36436022 | ||
Surface plasmon resonance in protein-membrane interactions | Q36439282 | ||
Proapoptotic multidomain Bcl-2/Bax-family proteins: mechanisms, physiological roles, and therapeutic opportunities | Q36490192 | ||
The Bax pore in liposomes, Biophysics | Q36501189 | ||
Ionic strength of the intermembrane space of intact mitochondria as estimated with fluorescein-BSA delivered by low pH fusion | Q36529908 | ||
Mitochondria as the target of the pro-apoptotic protein Bax. | Q36534322 | ||
Mitochondrial P450s | Q36555033 | ||
Comparison of the ion channel characteristics of proapoptotic BAX and antiapoptotic BCL-2. | Q36593741 | ||
Phase boundaries and biological membranes | Q36698591 | ||
Embedded together: the life and death consequences of interaction of the Bcl-2 family with membranes | Q36799170 | ||
Bcl-2-regulated apoptosis: mechanism and therapeutic potential | Q36880621 | ||
Transfer of cholesterol between phospholipid vesicles mediated by the steroidogenic acute regulatory protein (StAR). | Q39536902 | ||
Ion channels in liposomes | Q40141536 | ||
Mechanisms and genes of cellular suicide | Q40605270 | ||
Bcl-2 prevents Bax oligomerization in the mitochondrial outer membrane | Q40816351 | ||
Mutual amplification of apoptosis by statin-induced mitochondrial stress and doxorubicin toxicity in human rhabdomyosarcoma cells | Q41844170 | ||
Melittin and phospholipase A2 from bee (Apis mellifera) venom cause necrosis of murine skeletal muscle in vivo | Q42529079 | ||
The C- and N-Terminal Residues of Synthetic Heptapeptide Ion Channels Influence Transport Efficacy Through Phospholipid Bilayers | Q42565141 | ||
Reconstitution in planar lipid bilayers of a voltage-dependent anion-selective channel obtained from paramecium mitochondria | Q42597073 | ||
Phosphatidylcholine acyl unsaturation modulates the decrease in interfacial elasticity induced by cholesterol | Q42928959 | ||
Energetics and partition of two cecropin-melittin hybrid peptides to model membranes of different composition | Q43062959 | ||
Morphological correlates of functionally defined synaptic vesicle populations | Q43558103 | ||
Enantiospecificity of cholesterol function in vivo | Q43764671 | ||
Exploring peptide membrane interaction using surface plasmon resonance: differentiation between pore formation versus membrane disruption by lytic peptides | Q44276478 | ||
The role of cytochrome c diffusion in mitochondrial electron transport | Q44529460 | ||
Trojan horse-like behavior of a biologically representative mixture of oxysterols | Q44819905 | ||
Characterization of the cholesterol recognition amino acid consensus sequence of the peripheral-type benzodiazepine receptor | Q45140597 | ||
Distinct domains control the addressing and the insertion of Bax into mitochondria. | Q45182291 | ||
Properties of nonfused liposomes immobilized on an L1 Biacore chip and their permeabilization by a eukaryotic pore-forming toxin | Q46615466 | ||
Enantiospecific interactions between cholesterol and phospholipids | Q46826245 | ||
Bax activation and stress-induced apoptosis delayed by the accumulation of cholesterol in mitochondrial membranes | Q46847162 | ||
Changes in specific lipids regulate BAX-induced mitochondrial permeability transition | Q46889586 | ||
How might you compare mitochondria from different tissues and different species? | Q46891171 | ||
Ca2+-dependent control of the permeability properties of the mitochondrial outer membrane and voltage-dependent anion-selective channel (VDAC). | Q50113362 | ||
The effect of melittin on proliferation and death of thymocytes. | Q50527919 | ||
Characterization of the surfaces generated by liposome binding to the modified dextran matrix of a surface plasmon resonance sensor chip. | Q51604331 | ||
Colorimetric determination of phospholipids with ammonium ferrothiocyanate | Q56453315 | ||
Sterol and pH Interdependence in the Binding, Oligomerization, and Pore Formation of Listeriolysin O† | Q57365087 | ||
Organelle isolation: functional mitochondria from mouse liver, muscle and cultured filroblasts | Q60056610 | ||
The mitochondrial channel VDAC has a cation-selective open state | Q63027354 | ||
The properties of mitochondria enriched in vitro with cholesterol | Q68606951 | ||
Cholesterol and phospholipid composition of mitochondria and microsomes isolated from morris hepatoma 5123 and rat liver | Q68666774 | ||
Mitochondrial cholesterol content and membrane properties in porcine myocardial ischemia | Q70567457 | ||
Role of lipid transfer proteins in the abnormal lipid content of Morris hepatoma mitochondria and microsomes | Q71733380 | ||
Motional dynamics of functional cytochrome c delivered by low pH fusion into the intermembrane space of intact mitochondria | Q72960267 | ||
Quantitative studies on the melittin-induced leakage mechanism of lipid vesicles | Q74252243 | ||
Standardizing the free energy change of transmembrane helix-helix interactions | Q78376983 | ||
Hierarchical regulation of mitochondrion-dependent apoptosis by BCL-2 subfamilies | Q79370601 | ||
Cell biology. Cellular demolition and the rules of engagement | Q79750370 | ||
Intracellular cholesterol transport | Q80059619 | ||
Voltage gating of VDAC is regulated by nonlamellar lipids of mitochondrial membranes | Q80312005 | ||
Utilization of intramitochondrial membrane cholesterol by cytochrome P-450-dependent cholesterol side-chain cleavage reaction in bovine adrenocortical mitochondria: steroidogenic and non-steroidogenic pools of cholesterol in the mitochondrial inner | Q93573314 | ||
P433 | issue | 5 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 1168-1183 | |
P577 | publication date | 2008-06-20 | |
P1433 | published in | Journal of Molecular Biology | Q925779 |
P1476 | title | Cholesterol effects on BAX pore activation | |
P478 | volume | 381 |
Q38432040 | A Small-Molecule Inhibitor of Bax and Bak Oligomerization Prevents Genotoxic Cell Death and Promotes Neuroprotection. |
Q27002044 | BAX unleashed: the biochemical transformation of an inactive cytosolic monomer into a toxic mitochondrial pore |
Q43289014 | Bax distribution into mitochondrial detergent-resistant microdomains is related to ceramide and cholesterol content in postischemic hearts |
Q28240923 | Bioactive lipids and the control of Bax pro-apoptotic activity |
Q37705156 | Cholesterol and ion channels |
Q37433219 | Detergent-activated BAX protein is a monomer |
Q36438467 | Effect of Cholesterol on the Structure of a Five-Component Mitochondria-Like Phospholipid Membrane. |
Q35165455 | Mitochondria in apoptosis: Bcl-2 family members and mitochondrial dynamics. |
Q41579498 | Mitochondrial outer membrane permeabilization: a focus on the role of mitochondrial membrane structural organization |
Q37328406 | Molecularly targeted nanocarriers deliver the cytolytic peptide melittin specifically to tumor cells in mice, reducing tumor growth |
Q37778022 | Permeabilization of the Outer Mitochondrial Membrane by Bcl-2 Proteins |
Q41975085 | Reconstitution of proapoptotic BAK function in liposomes reveals a dual role for mitochondrial lipids in the BAK-driven membrane permeabilization process |
Q42153822 | The 2-oxoglutarate carrier promotes liver cancer by sustaining mitochondrial GSH despite cholesterol loading |
Q34198892 | The bladder tumor suppressor protein TERE1 (UBIAD1) modulates cell cholesterol: implications for tumor progression |
Q38668186 | The deadly landscape of pro-apoptotic BCL-2 proteins in the outer mitochondrial membrane |
Q36150746 | The dynamics of Bax channel formation: influence of ionic strength |
Q37138526 | The tumor suppressor TERE1 (UBIAD1) prenyltransferase regulates the elevated cholesterol phenotype in castration resistant prostate cancer by controlling a program of ligand dependent SXR target genes |
Q36985116 | Three-dimensional structure of Bax-mediated pores in membrane bilayers |
Q37356591 | ent-Steroids: novel tools for studies of signaling pathways |
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