about
Transport and metabolism of D-lactate in Jerusalem artichoke mitochondriaHaematoporphyrin derivative (Photofrin II) photosensitization of isolated mitochondria: inhibition of ADP/ATP translocatorMorphological and bioenergetic demands underlying the mitophagy in post-mitotic neurons: the pink-parkin pathwayD-Lactate transport and metabolism in rat liver mitochondriaCytochrome c is released from mitochondria in a reactive oxygen species (ROS)-dependent fashion and can operate as a ROS scavenger and as a respiratory substrate in cerebellar neurons undergoing excitotoxic deathTissue-specific mtDNA abundance from exome data and its correlation with mitochondrial transcription, mass and respiratory activity.Alzheimer's proteins, oxidative stress, and mitochondrial dysfunction interplay in a neuronal model of Alzheimer's disease.Glutamate neurotoxicity, oxidative stress and mitochondria.Functional characterization of the oxidative capacity of mitochondria and glycolytic assessment in benthic aquatic organisms.Mitochondria and L-lactate metabolism.Characterization of mitochondrial function in cells with impaired cystic fibrosis transmembrane conductance regulator (CFTR) function.AD-linked, toxic NH2 human tau affects the quality control of mitochondria in neurons.A disease with a sweet tooth: exploring the Warburg effect in Alzheimer's disease.Identification of a caspase-derived N-terminal tau fragment in cellular and animal Alzheimer's disease models.NH2-truncated human tau induces deregulated mitophagy in neurons by aberrant recruitment of Parkin and UCHL-1: implications in Alzheimer's disease.Glutamate stimulates 2-deoxyglucose uptake in rat cerebellar granule cells.L-lactate generates hydrogen peroxide in purified rat liver mitochondria due to the putative L-lactate oxidase localized in the intermembrane space.Pyruvate kinase in pig liver mitochondria.Genistein and daidzein prevent low potassium-dependent apoptosis of cerebellar granule cells.Interaction between NH(2)-tau fragment and Aβ in Alzheimer's disease mitochondria contributes to the synaptic deterioration.Carrier thiols are targets of Photofrin II photosensitization of isolated rat liver mitochondria.Proteasome inhibitors prevent cytochrome c release during apoptosis but not in excitotoxic death of cerebellar granule neurons.Extracellular ADP prevents neuronal apoptosis via activation of cell antioxidant enzymes and protection of mitochondrial ANT-1.Inhibition of phosphate transport in rat heart mitochondria by 3'-azido-3'-deoxythymidine due to stimulation of superoxide anion mitochondrial production.The apoptosis/necrosis transition in cerebellar granule cells depends on the mutual relationship of the antioxidant and the proteolytic systems which regulate ROS production and cytochrome c release en route to death.Cytochrome c, released from cerebellar granule cells undergoing apoptosis or excytotoxic death, can generate protonmotive force and drive ATP synthesis in isolated mitochondria.Glycolytic enzyme upregulation and numbness of mitochondrial activity characterize the early phase of apoptosis in cerebellar granule cells.A peptide containing residues 26-44 of tau protein impairs mitochondrial oxidative phosphorylation acting at the level of the adenine nucleotide translocator.An increase in the ATP levels occurs in cerebellar granule cells en route to apoptosis in which ATP derives from both oxidative phosphorylation and anaerobic glycolysis.Cytochrome c is released from coupled mitochondria of yeast en route to acetic acid-induced programmed cell death and can work as an electron donor and a ROS scavenger.Jerusalem artichoke mitochondria can export reducing equivalents in the form of malate as a result of D-lactate uptake and metabolism.Transport and metabolism of L-lactate occur in mitochondria from cerebellar granule cells and are modified in cells undergoing low potassium dependent apoptosis.Mitochondrial respiratory chain Complexes I and IV are impaired by β-amyloid via direct interaction and through Complex I-dependent ROS production, respectively.Early release and subsequent caspase-mediated degradation of cytochrome c in apoptotic cerebellar granule cells.Nitric oxide has dual opposite roles during early and late phases of apoptosis in cerebellar granule neurons.Glutamate neurotoxicity in rat cerebellar granule cells involves cytochrome c release from mitochondria and mitochondrial shuttle impairment.Glucose-6-phosphate tips the balance in modulating apoptosis in cerebellar granule cells.Neuronal apoptosis in rats is accompanied by rapid impairment of cellular respiration and is prevented by scavengers of reactive oxygen species.Oxaloacetate permeation in rat kidney mitochondria: pyruvate/oxaloacetate and malate/oxaloacetate translocators.Caspase-dependent alteration of the ADP/ATP translocator triggers the mitochondrial permeability transition which is not required for the low-potassium-dependent apoptosis of cerebellar granule cells.
P50
Q28255793-3356D99B-46AB-40EF-B81E-519B72E2B973Q28343044-0336F708-898F-44B5-9CEF-51DAB3B396C1Q28396161-FEEDFA0F-5EBC-4094-945A-C2255936CD9FQ28570856-7681C632-DD13-432E-81E9-20CDBC509A56Q28581047-87D0AF2B-EFCB-42A4-8F7F-9439E5BCA9E3Q30872900-A141D6BB-8B44-43B1-BC20-11050726041EQ34127614-04C3A61D-4DA3-4157-B549-E199B93CC751Q34263800-B09CF1D1-885F-4110-B446-5E37D1C55581Q35915186-7B3DA76C-3F46-4C22-807F-7CF42B133B2CQ37285242-34520B3D-0592-40CF-BFCC-B8A409FA8A1CQ38871529-2A605FF9-D2E6-406D-A45F-BEC59EB17CB7Q39035671-AFC2D784-F67C-4868-BF45-3D15902B3932Q39185516-B3FD76D1-DD2A-457E-A67B-BCEDF31B397EQ39977284-384451E4-6B8B-410B-8D1E-E0FA96621675Q41427586-174BC605-3B50-49A8-A048-2B181FF7AB13Q42447043-E6D7FD85-E378-4E23-A520-39549B0188A1Q43115738-495D499F-85CE-4C77-BCDE-5D9AF70AB385Q43212745-BDA62904-8F10-4DA4-B3B7-80DCA393E6A5Q43263175-356102C2-2CED-490F-8DA5-763CF020C867Q43509894-8CC278C5-503D-47CB-BD9F-AAD1A8EEF818Q43576993-14F3D29D-14EB-45E5-8A62-9FAA804575F4Q43953859-33C14AE9-E8DA-42C5-B496-AABF9A3CB807Q43986421-E3038DD0-485F-40ED-9EA7-1F7BE67B4621Q44068268-46017D51-D9A7-4C3D-AE21-CA039B5B9467Q44326504-3272502D-0554-4701-8A3A-0637C882964FQ44512228-F4F96CC5-5B0F-4292-933D-939CA027FB8DQ44721612-83387CCB-9115-48ED-BADF-83DAF8F987F3Q46412685-A58C211A-9F99-49CB-BFD7-BADEA2DA0784Q46540278-860B1FDF-F202-4917-9E3B-9624B659C8F9Q46658299-860A0954-EFAD-4F12-B87F-A5EEDD947019Q46675285-674EB215-C30B-4786-A270-565497B11698Q46940258-96EDB6B4-BF6B-4268-A56D-45CF366342EBQ48094013-CB1D9FA2-96B4-4A17-9190-BAA77537860EQ48112961-325E2FDA-3980-453F-AD83-6ECAD4DDDEE7Q48167788-8EE69D21-20D6-4395-8B5B-775A3D7204E1Q48175028-9EB5F234-DC4C-4AB4-8FB0-7D726F2DD215Q48346378-E1EE237F-949E-4346-B204-A316F0AB8829Q48459887-B29E3E06-A447-4084-AF24-2DA74CE02402Q48486629-9E27608F-F9BE-4222-ABFD-FFD574E48B9BQ48588017-BA9F9281-5B16-44CF-8489-E9DCC019C424
P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Anna Atlante
@ast
Anna Atlante
@en
Anna Atlante
@es
Anna Atlante
@nl
type
label
Anna Atlante
@ast
Anna Atlante
@en
Anna Atlante
@es
Anna Atlante
@nl
altLabel
anna atlante
@en
prefLabel
Anna Atlante
@ast
Anna Atlante
@en
Anna Atlante
@es
Anna Atlante
@nl
P106
P1153
7004503226
P21
P31
P496
0000-0001-6577-6414