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ali fraza pojavi v podobnem stavčnem kontekstu kot "astrocytes".
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Subanesthetic doses of ketamine stabilize the fusion pore in a narrow flickering state in astrocytes.
Staurosporine induces different cell death forms in cultured rat astrocytes .
Figure 11: The effect of the activation of adrenergic receptors on lipid droplet diameter and number of lipid droplets in cultured rat astrocytes.
Noradrenaline treatment increases cytosolic glucose concentration in wild-type (full circles) and GDI knockout astrocytes (empty ciricles).
Figure 9: Metabolic stress and hypoxia induce the accumulation of lipid droplets in astrocytes in organotypic brain tissue cultures.
Staurosporin sproži nekroptozo v kulturi astrocitov podgan = Staurosporine induces necroprosis in cultured rat astrocytes .
Figure 18: Distribution of cholesterol-rich domains in the plasma membrane of astrocytes after treatment with ketamine.
"primary rat astrocytes") zaradi pomanjkanja holina v gojišču z okužbo z M. fermentas.
Figure 19: Membrane current after stimulation of astrocytes with cannabinoid receptor agonists is not affected.
Figure 2: Subcellular localization of lipid droplets in cultured rat astrocytes.
Treatment of resting cultured astrocytes with 3-NPA increases [lac]i by a factor of 200 (i.e., from 0.003 mM to 0.620 mM).
Note the absence and abundance of surface MHCIIimmunofluorescence in control (f) and IFNγ-treated (h) astrocytes, respectively.
Figure 13: Changes in FRET ratio of lactate nanosensor after stimullation of astrocytes with agonists of cannabinoid receptors.
Figure 4: Starvation and ATP-stimulation lower the mobility of lipid droplets in cultured rat astrocytes.
Figure 5: Overexpressing AQP4b doesn't affect the volume change in astrocytes in hypoosmotic conditions.
Figure 10: Noradrenaline stimulation after 3-nitropropionic acid preincubation increases L-lactate concentrations in single astrocytes.
Upper pannel shows representative signal recorded from 1 cell and lower pannel shows mean response from 9 astrocytes (responsivness 9/48 = 18.8 %, *P=0.05,**P=0.01).
Figure 16: Colocalization of AQP4 with cholesterol domains in the plasma membrane lawns of astrocytes.
Figure 8: Inhibition of DGAT1 and DGAT2 enzymes in isolated astrocytes decreases cellular lipid droplet content and cell number.
Figure 20: Effect of agonists of CB1 and CB2 receptors on the height of astrocytes after hiopoosmotic shock.