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Journal Article
PLoS ONE, ISSN 1932-6203, 09/2013, Volume 8, Issue 9, p. e75812
.... It has been proposed that PHB can mediate ion transport across lipid bilayer membranes. We investigated the ability of PHB to interact with living cells and isolated mitochondria and the effects of these interactions on membrane ion transport... 
(R)-3-HYDROXYBUTANOIC ACID | INORGANIC POLYPHOSPHATE | CELLS | TRANSPORT | LIPID-BILAYERS | CHANNEL | METABOLISM | CA2 | MULTIDISCIPLINARY SCIENCES | ESCHERICHIA-COLI | IDENTIFICATION | Mitochondrial Membrane Transport Proteins - metabolism | Permeability - drug effects | Calcium - metabolism | Mitochondrial Membranes - physiology | Humans | Mitochondrial Membrane Transport Proteins - drug effects | Mitochondria - metabolism | Mitochondria - drug effects | Membrane Potential, Mitochondrial - drug effects | Mitochondrial Membranes - metabolism | Mitochondrial Membranes - drug effects | Polyesters - pharmacology | Mitochondrial Membrane Transport Proteins - physiology | Cell Line, Tumor | Membrane Potential, Mitochondrial - physiology | Ion Transport - drug effects | HeLa Cells | Hydroxybutyrates - pharmacology | Ion Transport - physiology | Mitochondria - physiology | Cyclosporine - metabolism | Proteins | Membrane lipids | Permeability | Fluorescein | Biological properties | Membranes | Calcium | Mitochondrial permeability transition pore | Free form | Membrane permeability | Lipids | Organisms | Cyclosporin A | Experiments | Accumulation | Depolarization | Polyhydroxybutyric acid | Mitochondria | Biological effects | Eukaryotes | Biological membranes | Physiology | Membrane potential | Localization | Polymers | Ion transport | Biophysics | Carbon | Studies | Polyhydroxybutyrate | Calcium transport
Journal Article
Journal of Molecular and Cellular Cardiology, ISSN 0022-2828, 2015, Volume 78, pp. 100 - 106
Abstract The mitochondrial permeability transition (PT) – an abrupt increase permeability of the inner membrane to solutes... 
Cardiovascular | Mitochondria | Ischemia–reperfusion injury | Permeability transition pore | Ischemia-reperfusion injury | DEPENDENT ANION CHANNEL | CARDIAC & CARDIOVASCULAR SYSTEMS | CA-2&-INDUCED MEMBRANE TRANSITION | CELL BIOLOGY | CYCLOPHILIN-D | CYCLOSPORINE-A | MYOCARDIAL INFARCT SIZE | ATP SYNTHASE | PERIPHERAL BENZODIAZEPINE-RECEPTOR | ADRENAL-CORTEX MITOCHONDRIA | MALIC ENZYME-ACTIVITY | Mitochondrial Membranes - drug effects | Mitochondrial Membrane Transport Proteins - metabolism | Permeability - drug effects | Animals | Mitochondria, Heart - metabolism | Cyclosporine - pharmacology | Humans | Cyclophilins - metabolism | Cardiotonic Agents - pharmacology | Mitochondria, Heart - drug effects | Mitochondrial Proton-Translocating ATPases - metabolism | Mitochondrial Membranes - metabolism | Mitochondrial DNA | Permeability | OMM, outer mitochondrial membrane | PTP, permeability transition pore | PKG, cyclic GMP-dependent protein kinase | PT, permeability transition | IMM, inner mitochondrial membrane | PKA, cyclic AMP-dependent protein kinase | Drp1, dynamin-related protein 1 | CsA, cyclosporin A | PPIase, peptidylprolyl cis-trans isomerase | ERK, extracellular signal regulated kinase | CyP, cyclophilin | ANT, adenine nucleotide translocase | R, ischemia–reperfusion | Review | TSPO, transport protein of 18 kDa | MMC, mitochondrial megachannel | Δψm, mitochondrial membrane potential | VDAC, voltage-dependent anion channel | GSK, glycogen synthase kinase | ROS, reactive oxygen species
Journal Article
American journal of physiology. Renal physiology, ISSN 1522-1466, 2014, Volume 307, Issue 3, pp. F326 - F336
.... APOL1Vs expressing podocytes displayed diffuse distribution of both Lucifer yellow dye and cathepsin L as manifestations of enhanced lysosomal membrane permeability (LMP... 
Kidney disease | Podocyte | Lysosomal membrane permeability | APOL1 risk variants | Necrosis | TRYPANOSOME LYTIC FACTOR | PHYSIOLOGY | LIPID-BINDING PROTEIN | kidney disease | AUTOPHAGIC CELL-DEATH | HUMAN SERUM | TRYPANOLYTIC FACTOR | necrosis | APOLIPOPROTEIN-L | podocyte | HIV-ASSOCIATED NEPHROPATHY | lysosomal membrane permeability | UROLOGY & NEPHROLOGY | AFRICAN-AMERICANS | CHRONIC KIDNEY-DISEASE | STAGE RENAL-DISEASE | Lipoproteins, HDL - genetics | Chloride Channels - drug effects | Glomerulosclerosis, Focal Segmental - genetics | Humans | Actins - metabolism | Lipoproteins, HDL - metabolism | Lysosomes - physiology | Chloroquine - pharmacology | Necrosis - physiopathology | Apolipoproteins - genetics | Glomerulosclerosis, Focal Segmental - ethnology | Genetic Predisposition to Disease - genetics | Chloride Channels - antagonists & inhibitors | Podocytes - metabolism | 4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid - pharmacology | Apolipoproteins - metabolism | Cells, Cultured | African Americans - genetics | Permeability | Podocytes - pathology | African Americans - ethnology | Podocytes - drug effects | Apolipoprotein L1 | Genetic Predisposition to Disease - ethnology | Genetic Variation - genetics | Lysosomes | Physiological aspects | Development and progression | Cell membranes | Apolipoproteins | Health aspects | Cells
Journal Article
Cellular and Molecular Life Sciences, ISSN 1420-682X, 08/2017, Volume 74, Issue 15, pp. 2795 - 2813
Growing number of studies provide strong evidence that the mitochondrial permeability transition pore (PTP... 
Oxidative stress | Cyclophilin D | Ischemia–reperfusion injury | Cardioprotection | Mitochondrial permeability transition pores | BIOCHEMISTRY & MOLECULAR BIOLOGY | ADP/ATP CARRIER | PHOSPHATE CARRIER | CELL-DEATH | CELL BIOLOGY | Ischemia-reperfusion injury | CYCLOSPORINE-A | MYOCARDIAL INFARCT SIZE | ATP SYNTHASE | NITRIC-OXIDE | CA2+ UPTAKE | ADENINE-NUCLEOTIDE TRANSLOCASE | Myocardial Ischemia - metabolism | Mitochondrial Membrane Transport Proteins - metabolism | Mitochondrial Membrane Transport Proteins - antagonists & inhibitors | Calcium - metabolism | Protein Interaction Maps - drug effects | Humans | Cyclophilins - metabolism | Cardiotonic Agents - pharmacology | Molecular Targeted Therapy | Drug Discovery | Myocardial Ischemia - drug therapy | Cyclophilins - antagonists & inhibitors | Myocardial Reperfusion Injury - metabolism | Animals | Protein Processing, Post-Translational - drug effects | Myocardium - metabolism | Heart - drug effects | Myocardial Reperfusion Injury - drug therapy | Oxidative Stress - drug effects | Energy Metabolism - drug effects | Medical colleges | Medical research | Ischemia | Analysis | Cardiac patients | Medicine, Experimental | Permeability | Heart | Myocardial infarction | Animal models | Mitochondrial permeability transition pore | Cyclosporins | Pathogenesis | Membrane permeability | Mitochondrial DNA | Information dissemination | Reperfusion | Bioenergetics | Attenuation | Physiology | Inhibition | Damage | Cardiology | Heart diseases | Pharmacology | Metabolism | Patients | Injury prevention | Inhibitors | Myocardium | Infarction
Journal Article
Journal of neurochemistry, ISSN 1471-4159, 2006, Volume 97, Issue 4, pp. 1071 - 1077
Journal Article
FEBS Letters, ISSN 0014-5793, 01/2014, Volume 588, Issue 1, pp. 35 - 40
•Ostreolysin A/pleurotolysin B mixture forms ion-conducting pores in cell membranes... 
Electrophysiology | Pore-forming protein | Pleurotus ostreatus | Membrane attack complex/perforin (MACPF) domain | TOXIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | EDIBLE MUSHROOM | EQUINATOXIN | CHOLESTEROL-DEPENDENT CYTOLYSIN | PNEUMOLYSIN | CELL BIOLOGY | LIPID-BILAYERS | BIOPHYSICS | PLEUROTOLYSIN | SPHINGOMYELIN | CHANNELS | ATTACK COMPLEX | Hemolysis - drug effects | Hemolysin Proteins - pharmacology | Cricetulus | Erythrocytes - ultrastructure | Porins - metabolism | Cell Membrane - physiology | Erythrocyte Membrane - physiology | Porins - pharmacology | Cattle | Erythrocytes - cytology | Cell Membrane - drug effects | CHO Cells | Membrane Potentials - drug effects | Cricetinae | Microscopy, Electron | Erythrocyte Membrane - drug effects | Erythrocytes - drug effects | Patch-Clamp Techniques | Animals | Cell Membrane Permeability - physiology | Cell Membrane Permeability - drug effects | Cell Line, Tumor | Erythrocyte Membrane - ultrastructure | Mice | Fungal Proteins - pharmacology | Pleurotus - metabolism | Hemolysin Proteins - metabolism | Fungal Proteins - metabolism | Proteins | Permeability | Index Medicus | Hemolysis | Cell Membrane | Hemolysin Proteins | Neurons and Cognition | Psychology and behavior | Erythrocytes | Neurobiology | Cell Membrane Permeability | Fungal Proteins | Erythrocyte Membrane | Porins | Life Sciences | Pleurotus | Membrane Potentials | Cognitive Sciences
Journal Article