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Wyszukujesz frazę ""Autophagy drug effects"" wg kryterium: Temat


Tytuł :
The PRKAA1/AMPKalpha1 pathway triggers autophagy during CSF1-induced human monocyte differentiation and is a potential target in CMML.
Autorzy :
Obba, Sandrine
Hizir, Zoheir
Boyer, Laurent
Selimoglu-Buet, Dorothee
Pfeifer, Anja
Michel, Gregory
Hamouda, Mohamed-Amine
Goncalves, Diogo
Cerezo, Michael
Marchetti, Sandrine
Rocchi, Stephane
Droin, Nathalie
Cluzeau, Thomas
Robert, Guillaume
Luciano, Frederic
Robaye, Bernard
Foretz, Marc
Viollet, Benoit
Legros, Laurence
Solary, Eric
Auberger, Patrick
Jacquel, Arnaud
Pokaż więcej
Temat :
AMP-Activated Protein Kinases/metabolism
Animals
Autophagy/drug effects
Calcium-Calmodulin-Dependent Protein Kinase Kinase/metabolism
Cell Differentiation/drug effects
Cell Line, Tumor
Enzyme Activation/drug effects
Humans
Leukemia, Myeloid/enzymology/pathology
Macrophage Colony-Stimulating Factor/pharmacology
Mice, Inbred C57BL
Models, Biological
Monocytes/cytology/drug effects/metabolism
Phospholipase C gamma/metabolism
Receptors, Purinergic P2/metabolism
Signal Transduction/drug effects
Uridine Diphosphate/pharmacology
ACTB actin, beta
CAMKK2, calcium/calmodulin-dependent protein kinase kinase 2, beta
CASP8, caspase 8
CFLAR CASP8 and FADD-like apoptosis regulator
CMML
CMML chronic myelomonocytic leukemia
CSF1
CSF1 colony stimulating factor 1 (macrophage)
CSF1R colony stimulating factor 1 receptor
DEFA1 defensin alpha 1
DEFA3 defensin alpha 3 neutrophil-specific
DRS
dorsomorphin
EMR1 EGF-like module-containing mucin-like hormone receptor-like 1
FADD Fas (TNFRSF6)-associated via death domain
G-protein coupled 6
ITGAM integrin alpha M
MAP1LC3B/LC3B microtubule-associated protein 1 light chain 3 beta
P2RY6
P2RY6 pyrimidinergic receptor P2Y
PLC phospholipase
PLCB3 phospholipase C
PLCG2 phospholipase C gamma 2 (phosphatidylinositol-specific)
PRKAA protein kinase AMP-activated
PRKAA1 protein kinase AMP-activated alpha 1 catalytic subunit
PRKAA1/AMPKalpha1
PRKAA2 protein kinase AMP-activated alpha 2 catalytic subunit
PRKAG1 protein kinase AMP-activated gamma 1 noncatalytic subunit
RIPK1 receptor (TNFRSF)-interacting serine-threonine kinase 1
STK11 serine/threonine kinase 11
TFRC transferrin receptor
UDP uridine diphosphate
ULK1 unc-51 like autophagy activating kinase 1
WT wild-type
apoptosis-related cysteine peptidase
autophagy
differentiation
primary monocyte
beta 3 (phosphatidylinositol-specific)
Biochemistry, biophysics & molecular biology [Life sciences]
Biochimie, biophysique & biologie moléculaire [Sciences du vivant]
Źródło :
The PRKAA1/AMPKalpha1 pathway triggers autophagy during CSF1-induced human monocyte differentiation and is a potential target in CMML. Autophagy, 11(7), 1114-29., United States. (2015).
Tytuł :
Autosis is a Na+,K+-ATPase-regulated form of cell death triggered by autophagy-inducing peptides, starvation, and hypoxia-ischemia
Autorzy :
Liu, Yang
Shoji-Kawata, Sanae
Sumpter, Rhea M.
Wei, Yongjie
Ginet, Vanessa
Zhang, Liying
Posner, Bruce
Tran, Khoa A.
Green, Douglas R.
Xavier, Ramnik J.
Shaw, Stanley Y.
Clarke, Peter G. H.
Puyal, Julien
Levine, Beth
Pokaż więcej
Temat :
Sodium-Potassium-Exchanging ATPase/metabolism
Animals
Autophagy/drug effects
Brain Ischemia/metabolism
Brain Ischemia/pathology
Cardiac Glycosides/pharmacology
Cell-Penetrating Peptides/pharmacology
HeLa Cells
Humans
Nerve Tissue Proteins/metabolism
Rats
Sodium-Potassium-Exchanging ATPase/antagonists & inhibitors
Biological Sciences
Źródło :
Proceedings of the National Academy of Sciences of the United States of America 110(51) 20364-20371
Proceedings of the National Academy of Sciences of the United States of America, vol. 110, no. 51, pp. 20364-20371
Opis pliku :
application/pdf
Tytuł :
Multiple interacting cell death mechanisms in the mediation of excitotoxicity and ischemic brain damage: A challenge for neuroprotection.
Autorzy :
Puyal, Julien
Ginet, Vanessa
Clarke, Peter G H
Pokaż więcej
Temat :
Necrosis/drug therapy
Neuroprotective Agents/pharmacology
Autophagy/physiology
Brain Injuries/drug therapy
Apoptosis/physiology
Neuronal death
Apoptosis
Necrosis
Autophagy
Stroke
Hypoxia-ischemia
Autophagy/drug effects
Brain Injuries/metabolism
Brain Ischemia/metabolism
Necrosis/metabolism
Apoptosis/drug effects
Źródło :
Progress In Neurobiology 105 24-48
Progress in Neurobiology, vol. 105, pp. 24-48
Opis pliku :
application/pdf
Tytuł :
The TP53INP2 protein is required for autophagy in mammalian cells.
Autorzy :
Nowak, Jonathan
Archange, Cendrine
Tardivel-Lacombe, Joël
Pontarotti, Pierre
Pébusque, Marie-Josèphe
Vaccaro, Maria Inés
Velasco, Guillermo
Dagorn, Jean-Charles
Iovanna, Juan Lucio
Pokaż więcej
Temat :
MESH : Membrane Proteins: metabolism
MESH : Protein Transport: drug effects
MESH: Protein Binding: drug effects
MESH : Cloning, Molecular
MESH : Apoptosis Regulatory Proteins: metabolism
MESH : Animals
MESH : Carrier Proteins: chemistry,metabolism
MESH: Cloning, Molecular
MESH: Heat-Shock Proteins: chemistry,metabolism
MESH: Phagosomes: drug effects,metabolism
MESH : Sirolimus: pharmacology
MESH : Phagosomes: drug effects,metabolism
MESH : Gene Silencing: drug effects
MESH: Mice
MESH : Cell Line
MESH: Protein Transport: drug effects
MESH : Humans
MESH : Luminescent Measurements
MESH: Phylogeny
MESH: Nuclear Proteins: chemistry,metabolism
MESH: Conserved Sequence
MESH : Molecular Sequence Data
MESH: Molecular Sequence Data
MESH: Animals
MESH : Heat-Shock Proteins: chemistry,metabolism
MESH : Phylogeny
MESH: Apoptosis Regulatory Proteins: metabolism
MESH : Amino Acid Sequence
MESH: Gene Silencing: drug effects
MESH: Amino Acid Sequence
MESH : Conserved Sequence
MESH : Nuclear Proteins: chemistry,metabolism
MESH: Autophagy: drug effects
MESH : Protein Binding: drug effects
[ SDV.OT ] Life Sciences [q-bio]/Other [q-bio.OT]
MESH : Adaptor Proteins, Signal Transducing: metabolism
MESH: Cell Line
MESH: Sirolimus: pharmacology
MESH : Microtubule-Associated Proteins: metabolism
MESH: Carrier Proteins: chemistry,metabolism
MESH: Humans
MESH: Adaptor Proteins, Signal Transducing: metabolism
MESH: Microtubule-Associated Proteins: metabolism
[SDV.OT]Life Sciences [q-bio]/Other [q-bio.OT]
MESH: Membrane Proteins: metabolism
MESH: Luminescent Measurements
MESH : Autophagy: drug effects
Articles
MESH : Mice
Źródło :
Molecular Biology of the Cell, American Society for Cell Biology, 2009, 20 (3), pp.870-81. ⟨10.1091/mbc.E08-07-0671⟩
Molecular Biology of the Cell, American Society for Cell Biology, 2009, 20 (3), pp.870-81. 〈10.1091/mbc.E08-07-0671〉
Molecular Biology of the Cell

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