p38 MAPK

Hermann Katinger

cmerp October 9, 2021

Hermann Katinger. Abbreviations ARVAntiretroviralCV%Coefficient of variationDC-SIGNDendritic cell-specific intercellular adhesion molecule-3-grabbing non-integrinF.U.Fluorescence unitsGNGalanthus nivalisHHAHippeastrum cross typesHIV-1Individual immunodeficiency trojan...

p38 MAPK

Hermann Katinger

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Lanes I and J represent control samples for GR expression in GC sensitive CEM cells and leukaemic blast cells, respectively

Here, finding that inhibitory neurotransmitter glycine does not activate KCNQs, we re-engineered it in silico to expose expected KCNQ-opening properties, screened by in silico docking, then validated the hits in vitro

Redox-dye reduction-based Phenotype MicroArray (PM) assays, which measure NADH decrease being a readout, produced by Biolog Inc

CF?=?cleaved fragment (n?=?3) and (E) Immunofluorescence staining of apoptosis (TUNEL) display that VEDT induced apoptosis in (Mia-GFP) cells compared to vehicle (Veh) after 24?h and apoptosis was rescued in (Mia-FLIP) cells compared to vehicle (Veh) (n?=?3)

﻿Hermann Katinger

You may have missed

﻿Lanes I and J represent control samples for GR expression in GC sensitive CEM cells and leukaemic blast cells, respectively

﻿Here, finding that inhibitory neurotransmitter glycine does not activate KCNQs, we re-engineered it in silico to expose expected KCNQ-opening properties, screened by in silico docking, then validated the hits in vitro

﻿Redox-dye reduction-based Phenotype MicroArray (PM) assays, which measure NADH decrease being a readout, produced by Biolog Inc

﻿CF?=?cleaved fragment (n?=?3) and (E) Immunofluorescence staining of apoptosis (TUNEL) display that VEDT induced apoptosis in (Mia-GFP) cells compared to vehicle (Veh) after 24?h and apoptosis was rescued in (Mia-FLIP) cells compared to vehicle (Veh) (n?=?3)

Hermann Katinger

Lanes I and J represent control samples for GR expression in GC sensitive CEM cells and leukaemic blast cells, respectively

Here, finding that inhibitory neurotransmitter glycine does not activate KCNQs, we re-engineered it in silico to expose expected KCNQ-opening properties, screened by in silico docking, then validated the hits in vitro

Redox-dye reduction-based Phenotype MicroArray (PM) assays, which measure NADH decrease being a readout, produced by Biolog Inc

CF?=?cleaved fragment (n?=?3) and (E) Immunofluorescence staining of apoptosis (TUNEL) display that VEDT induced apoptosis in (Mia-GFP) cells compared to vehicle (Veh) after 24?h and apoptosis was rescued in (Mia-FLIP) cells compared to vehicle (Veh) (n?=?3)