| scholarly article | Q13442814 |
| P50 | author | Stephanie Bleicken | Q57054678 |
| Ana J García-Sáez | Q78568898 | ||
| P2093 | author name string | Gorka Basañez | |
| Olatz Landeta | |||
| Ane Landajuela | |||
| P2860 | cites work | Bcl-x(L) retrotranslocates Bax from the mitochondria into the cytosol | Q24298758 |
| Membrane remodeling induced by the dynamin-related protein Drp1 stimulates Bax oligomerization | Q24300125 | ||
| Bax crystal structures reveal how BH3 domains activate Bax and nucleate its oligomerization to induce apoptosis | Q24313049 | ||
| Membrane binding by tBid initiates an ordered series of events culminating in membrane permeabilization by Bax | Q24323186 | ||
| Endophilin B1/Bif-1 stimulates BAX activation independently from its capacity to produce large scale membrane morphological rearrangements | Q24324817 | ||
| Movement of Bax from the cytosol to mitochondria during apoptosis | Q24677881 | ||
| A new view of the lethal apoptotic pore | Q27000479 | ||
| High resolution X-ray crystallographic structure of bovine heart cytochrome c and its application to the design of an electron transfer biosensor | Q27646756 | ||
| BID-induced structural changes in BAK promote apoptosis | Q27677468 | ||
| Isolation, crystallization, crystal structure analysis and refinement of allophycocyanin from the cyanobacterium Spirulina platensis at 2.3 A resolution | Q27730274 | ||
| Proapoptotic BAX and BAK: a requisite gateway to mitochondrial dysfunction and death | Q28363890 | ||
| The combined functions of proapoptotic Bcl-2 family members bak and bax are essential for normal development of multiple tissues | Q28512628 | ||
| Bid induces the oligomerization and insertion of Bax into the outer mitochondrial membrane | Q28647586 | ||
| Bid, Bax, and lipids cooperate to form supramolecular openings in the outer mitochondrial membrane | Q29616354 | ||
| Structure of transmembrane pore induced by Bax-derived peptide: evidence for lipidic pores. | Q30157467 | ||
| Different mitochondrial intermembrane space proteins are released during apoptosis in a manner that is coordinately initiated but can vary in duration | Q30477672 | ||
| Antimicrobial peptides bind more strongly to membrane pores | Q33912494 | ||
| BAX-dependent transport of cytochrome c reconstituted in pure liposomes | Q33912996 | ||
| Dynamic interaction of cBid with detergents, liposomes and mitochondria. | Q34249427 | ||
| XIAP impairs Smac release from the mitochondria during apoptosis. | Q34545370 | ||
| A lipocentric view of peptide-induced pores. | Q34757093 | ||
| Membrane protein assembly into Nanodiscs | Q35008328 | ||
| BH3-only proteins that bind pro-survival Bcl-2 family members fail to induce apoptosis in the absence of Bax and Bak | Q35079498 | ||
| Mitochondria in apoptosis: Bcl-2 family members and mitochondrial dynamics. | Q35165455 | ||
| Translocation of a Bak C-terminus mutant from cytosol to mitochondria to mediate cytochrome C release: implications for Bak and Bax apoptotic function | Q35839831 | ||
| Mitochondrial release of apoptosis-inducing factor occurs downstream of cytochrome c release in response to several proapoptotic stimuli | Q36325547 | ||
| Bax, but not Bcl-xL, decreases the lifetime of planar phospholipid bilayer membranes at subnanomolar concentrations | Q36353924 | ||
| Where killers meet--permeabilization of the outer mitochondrial membrane during apoptosis | Q36629743 | ||
| Direct activation of full-length proapoptotic BAK | Q36692849 | ||
| Three-dimensional structure of Bax-mediated pores in membrane bilayers | Q36985116 | ||
| Mitochondrial outer membrane proteins assist Bid in Bax-mediated lipidic pore formation | Q37158414 | ||
| Assembly of the mitochondrial apoptosis-induced channel, MAC. | Q37169502 | ||
| Spatial and temporal dynamics of mitochondrial membrane permeability waves during apoptosis | Q37392644 | ||
| Conformational changes and protein stability of the pro-apoptotic protein Bax. | Q37424410 | ||
| The physicochemical properties of cardiolipin bilayers and cardiolipin-containing lipid membranes | Q37425910 | ||
| Permeabilization of the Outer Mitochondrial Membrane by Bcl-2 Proteins | Q37778022 | ||
| Homeostatic functions of BCL-2 proteins beyond apoptosis | Q37797382 | ||
| Apoptosis and oncogenesis: give and take in the BCL-2 family | Q37828794 | ||
| The secrets of the Bcl-2 family | Q38039293 | ||
| Bid-induced conformational change of Bax is responsible for mitochondrial cytochrome c release during apoptosis | Q38326924 | ||
| Sphingosine-induced apoptosis in rhabdomyosarcoma cell lines is dependent on pre-mitochondrial Bax activation and post-mitochondrial caspases | Q40181636 | ||
| Peptides derived from apoptotic Bax and Bid reproduce the poration activity of the parent full-length proteins | Q40334590 | ||
| Real-time single cell analysis of Smac/DIABLO release during apoptosis | Q40634471 | ||
| Bax exists in a dynamic equilibrium between the cytosol and mitochondria to control apoptotic priming | Q41263641 | ||
| Reconstitution of proapoptotic BAK function in liposomes reveals a dual role for mitochondrial lipids in the BAK-driven membrane permeabilization process | Q41975085 | ||
| Pore formation and translocation of melittin | Q42029147 | ||
| Pores formed by Baxα5 relax to a smaller size and keep at equilibrium | Q42183300 | ||
| Pore formation by a Bax-derived peptide: effect on the line tension of the membrane probed by AFM. | Q42183606 | ||
| Transient binding of an activator BH3 domain to the Bak BH3-binding groove initiates Bak oligomerization | Q42800693 | ||
| Molecular details of Bax activation, oligomerization, and membrane insertion. | Q42910802 | ||
| Mechanistic differences in the membrane activity of Bax and Bcl-xL correlate with their opposing roles in apoptosis. | Q42928576 | ||
| Bid induces cytochrome c-impermeable Bax channels in liposomes | Q43001510 | ||
| Transbilayer lipid diffusion promoted by Bax: implications for apoptosis. | Q44684385 | ||
| Membrane promotes tBID interaction with BCL(XL). | Q45815145 | ||
| Magainin 2-induced pore formation in the lipid membranes depends on its concentration in the membrane interface | Q46225719 | ||
| BIM and tBID are not mechanistically equivalent when assisting BAX to permeabilize bilayer membranes | Q46808299 | ||
| Lipidic pore formation by the concerted action of proapoptotic BAX and tBID. | Q47618625 | ||
| Molecular mechanism of Peptide-induced pores in membranes | Q49260601 | ||
| Peptides corresponding to helices 5 and 6 of Bax can independently form large lipid pores | Q57824114 | ||
| Mitochondrial contact sites. Lipid composition and dynamics | Q68483792 | ||
| Regulation of antiapoptotic MCL-1 function by gossypol: mechanistic insights from in vitro reconstituted systems | Q81908401 | ||
| Structure of fully hydrated fluid phase lipid bilayers with monounsaturated chains | Q83129856 | ||
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 46 | |
| P407 | language of work or name | English | Q1860 |
| P1104 | number of pages | 12 | |
| P304 | page(s) | 33241-33252 | |
| P577 | publication date | 2013-10-07 | |
| P1433 | published in | Journal of Biological Chemistry | Q867727 |
| P1476 | title | Proapoptotic Bax and Bak proteins form stable protein-permeable pores of tunable size | |
| P478 | volume | 288 |
| Q90044884 | A new perspective on membrane-embedded Bax oligomers using DEER and bioresistant orthogonal spin labels |
| Q102053969 | Anti-apoptotic BCL-2 regulation by changes in dynamics of its long unstructured loop |
| Q64286492 | Anticancer effect of nor-wogonin (5, 7, 8-trihydroxyflavone) on human triple-negative breast cancer cells via downregulation of TAK1, NF-κB, and STAT3 |
| Q39384348 | Apoptotic foci at mitochondria: in and around Bax pores |
| Q33361524 | Assembling the puzzle: Oligomerization of α-pore forming proteins in membranes |
| Q40172342 | Automated analysis of giant unilamellar vesicles using circular Hough transformation. |
| Q99418930 | BAK core dimers bind lipids and can be bridged by them |
| Q39073674 | BAX to basics: How the BCL2 gene family controls the death of retinal ganglion cells |
| Q47155532 | BCL-2 family proteins: changing partners in the dance towards death |
| Q90605928 | BFL1 modulates apoptosis at the membrane level through a bifunctional and multimodal mechanism showing key differences with BCLXL |
| Q36478810 | BH3-in-groove dimerization initiates and helix 9 dimerization expands Bax pore assembly in membranes |
| Q43156404 | Bak apoptotic pores involve a flexible C-terminal region and juxtaposition of the C-terminal transmembrane domains |
| Q39033533 | Bax and Bak Pores: Are We Closing the Circle? |
| Q38494808 | Bax assembly into rings and arcs in apoptotic mitochondria is linked to membrane pores. |
| Q36018810 | Bax monomers form dimer units in the membrane that further self-assemble into multiple oligomeric species |
| Q47305952 | Bax, Bak and beyond - mitochondrial performance in apoptosis |
| Q50195472 | Bcl-2 proteins: Unraveling the details of a complex and dynamic network. |
| Q26751456 | Control of adult neurogenesis by programmed cell death in the mammalian brain |
| Q38172752 | Control of apoptosis by the BCL-2 protein family: implications for physiology and therapy. |
| Q41141777 | Effect of Content of Sulfate Groups in Seaweed Polysaccharides on Antioxidant Activity and Repair Effect of Subcellular Organelles in Injured HK-2 Cells |
| Q47318003 | Effect of Src Kinase inhibition on Cytochrome c, Smac/DIABLO and Apoptosis Inducing Factor (AIF) Following Cerebral Hypoxia-Ischemia in Newborn Piglets |
| Q90394426 | Impacts of Dietary Protein and Prebiotic Inclusion on Liver and Spleen Gene Expression in Hy-Line Brown Caged Layers |
| Q36996518 | In Situ Characterization of Bak Clusters Responsible for Cell Death Using Single Molecule Localization Microscopy. |
| Q41570585 | Live-cell imaging to measure BAX recruitment kinetics to mitochondria during apoptosis |
| Q96023628 | Location of Peptide-Induced Submicron Discontinuities in the Membranes of Vesicles Using ImageJ |
| Q48161032 | Melilotus indicus extract induces apoptosis in hepatocellular carcinoma cells via a mechanism involving mitochondria-mediated pathways. |
| Q64922363 | Membrane Permeabilization by Bordetella Adenylate Cyclase Toxin Involves Pores of Tunable Size. |
| Q92879812 | Membrane Permeabilization by Pore-Forming RTX Toxins: What Kind of Lesions Do These Toxins Form? |
| Q47123534 | Membrane insertion of the BAX core, but not latch domain, drives apoptotic pore formation |
| Q55065193 | Micro-Economics of Apoptosis in Cancer: ncRNAs Modulation of BCL-2 Family Members. |
| Q38952396 | Milestones and recent discoveries on cell death mediated by mitochondria and their interactions with biologically active amines |
| Q28383717 | Minimalist Model Systems Reveal Similarities and Differences between Membrane Interaction Modes of MCL1 and BAK |
| Q91975627 | Mitochondria and Inflammation: Cell Death Heats Up |
| Q90859789 | Mitochondria as multifaceted regulators of cell death |
| Q90518992 | Mitochondrial inner membrane permeabilisation enables mtDNA release during apoptosis |
| Q38353200 | Molecular basis of hair cell loss |
| Q37257680 | Oncogenic Mutations Differentially Affect Bax Monomer, Dimer, and Oligomeric Pore Formation in the Membrane |
| Q39384356 | Pore formation by dimeric Bak and Bax: an unusual pore? |
| Q34853156 | Pycnogenol Induces Nuclear Translocation of Apoptosis-inducing Factor and Caspase-independent Apoptosis in MC-3 Human Mucoepidermoid Carcinoma Cell Line |
| Q41009828 | Quantitative interactome of a membrane Bcl-2 network identifies a hierarchy of complexes for apoptosis regulation. |
| Q52721187 | Regulatory role of calpain in neuronal death. |
| Q33752784 | Release of Cytochrome C from Bax Pores at the Mitochondrial Membrane |
| Q42166522 | Structural model of active Bax at the membrane. |
| Q90383179 | The Incomplete Puzzle of the BCL2 Proteins |
| Q48374835 | The membrane activity of BOK involves formation of large, stable toroidal pores and is promoted by cBID. |
| Q91304407 | Topology of active, membrane-embedded Bax in the context of a toroidal pore |
| Q41668377 | Toxicity of an α-pore-forming toxin depends on the assembly mechanism on the target membrane as revealed by single molecule imaging |
| Q34960771 | Visual and functional demonstration of growing Bax-induced pores in mitochondrial outer membranes |
| Q40757128 | cBid, Bax and Bcl-xL exhibit opposite membrane remodeling activities. |
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