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Smart Reasoning:

C&E

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Qaagi - Book of Why

Causes

Effects

these interactionscan causeneurodegeneration in vivo

I. Cloned Th2 cells modified with DNA methylation inhibitors in vitrocauseautoimmunity in vivo

the passively acquired ABO antibodieswill causein vivo hemolysis

likelyto causein vivo hemolysis

the factcausedby in vivo hemolysis

The phenomenaleadingin vivo hemolysis

The phenomenaleadingto in vivo hemolysis

it is not clearcauseshemolysis in vivo

in vitro * melanoma cell invasioncould influencein vivo ... metastasis

because they are reactive at room temperature but not body temperature and , thereforecausehemolysis in vivo

that , in turn , release biologically active VEGF - Aresultingin angiogenesis in vivo

VEGFcausedin vivo neovascularization

Researchmay resultin vivo v

a certain potentialto influenceosseointegration in vivo

multiple physiological effects , as well as antioxidant activityresultin radioprotection in vivo

by RNAi overexpression(passive) caused byin vivo toxicities

Factorsinfluencingin vivo transduction

eventsresultsin vivo myocyte

by mutations on the surface of the peptide binding pocket , the same mutations that also influenced the in vitro activation of PP2Ai(passive) is influencedin vivo

by mutations on the surface of the peptide binding pocket , the same mutations that also influenced the in vitro activation of PP2Ai(passive) is influenced byin vivo

mutations on the surface of the peptide binding pocket , the same mutations that also influenced the in vitro activation of PP2Ai(passive) is influenced byin vivo

The combination of in vitro , ex vivo , andhas ... contributedin vivo

Studies in the mouse model using both in vitro andhave resultedin vivo

resistant cells generated in vitro ... ableto originatein vivo

Pharmacological inhibition and conditional deletion of Cpt1a in vitro andleadsin vivo

the certain effects of lipid and protein componentsmay be discoveredin vivo

the ability of cellsto causein vivo

Enhanced bone regeneration with a synthetic cell - binding peptideresultsin vivo

cells ... sufficientto causein vivo

Activation of the MAPK pathway via activating EGFR mutationscausesin vivo

The murine cells treated with TNF - in vitro andcausein vivo

Studies involving ectopic expression of SHH in vitro andresultin vivo

the precise effects of lipid and protein componentsmay be discoveredin vivo

the variations ... " using imaging methodsbeing discoveredin vivo

the ability of MAIT cellsto contributein vivo

this method of cell ablation on its owndoes ... causein vivo

these cellsto causein vivo

using ... techniquesdesignedin vivo

Our study ... sufficientto causein vivo

study ... sufficientto causein vivo

their releasecausestheir release

from acquired , hereditary , or iatrogenic conditionscan originatefrom acquired , hereditary , or iatrogenic conditions

from acquired , hereditary , or iatrogenic conditions and is not technique dependentcan originatefrom acquired , hereditary , or iatrogenic conditions and is not technique dependent

alsowill ... causealso

MSC / cartilage interactionsinfluencesMSC / cartilage interactions

MEG2 suppression(passive) caused byMEG2 suppression

to a hepatocellular carcinoma cell line with enhanced tumorigenicity and EpCAM expression , hallmark characteristics of tumor initiating cells ( TIChas ledto a hepatocellular carcinoma cell line with enhanced tumorigenicity and EpCAM expression , hallmark characteristics of tumor initiating cells ( TIC

the periprosthetic tissue gene expression profiles by diminishing the mRNA expression of TNF , IL-1 , CPK and RANKLinfluencedthe periprosthetic tissue gene expression profiles by diminishing the mRNA expression of TNF , IL-1 , CPK and RANKL

to increased melanoma primary tumor growth due to the recruitment of mesenchymal stromal cells as well as the enhanced metastasisleadsto increased melanoma primary tumor growth due to the recruitment of mesenchymal stromal cells as well as the enhanced metastasis

to the improved TIL function and subsequent tumor regression observedcontributedto the improved TIL function and subsequent tumor regression observed

to enhanced antigen - specific T - lymphocyte responsesleadingto enhanced antigen - specific T - lymphocyte responses

neuronal function indirectly as a result of its expression in non - neuronal cell types resulting in cortical dysplasia due to aberrant neuronal migrationmay influenceneuronal function indirectly as a result of its expression in non - neuronal cell types resulting in cortical dysplasia due to aberrant neuronal migration

in enhanced antitumor killing and complete tumor regressionresultedin enhanced antitumor killing and complete tumor regression

to the improved TIL function and subsequent tumor regressioncontributedto the improved TIL function and subsequent tumor regression

subsequent tumor developmentcould influencesubsequent tumor development

to a reduction in tumor growth in immune compromised miceledto a reduction in tumor growth in immune compromised mice

to an immediate and dose dependent early activation of T cellsleadsto an immediate and dose dependent early activation of T cells

to the controlled releaseleadingto the controlled release

to a change in the response of specific substrate receptorswill ... leadto a change in the response of specific substrate receptors

to a tissue - specific induction in DNA repaircan leadto a tissue - specific induction in DNA repair

to a transgene - specific T cellmight ... leadto a transgene - specific T cell

to strong inhibition of NF - B transcriptional activityledto strong inhibition of NF - B transcriptional activity

to elevated plasma homocysteineleadsto elevated plasma homocysteine

the drug response in the hostmay influencethe drug response in the host

dose - dependent inhibition of tumor growthcausesdose - dependent inhibition of tumor growth

T cells(passive) is influencedT cells

to the observed difference in neuronal lossmay contributeto the observed difference in neuronal loss

NO production , which was found to be increased in lupus T cells ( Fig . S1did ... influenceNO production , which was found to be increased in lupus T cells ( Fig . S1

in an up to 86 % reduced tumor volumeresultedin an up to 86 % reduced tumor volume

to a selective elevated expression of TNF in inflamed tissues ( skin , in the present study , or liver , as shown in Kaplan et alleadsto a selective elevated expression of TNF in inflamed tissues ( skin , in the present study , or liver , as shown in Kaplan et al

in decreased complement - dependent cytotoxicityresultingin decreased complement - dependent cytotoxicity

to tissue - specific vascular leakage after immune recognitioncould contributeto tissue - specific vascular leakage after immune recognition

to improved tumour control with adjuvant treatmentmay contributeto improved tumour control with adjuvant treatment

in greater anti - tumor activityresultedin greater anti - tumor activity

This study(passive) was designedThis study

to increased tumor cell growthleadsto increased tumor cell growth

to altered NO productionleadsto altered NO production

better suits the analysis of cytokine production and the effects of inflammation on epileptogenesissettingbetter suits the analysis of cytokine production and the effects of inflammation on epileptogenesis

from mutation or genetic recombinationcan resultfrom mutation or genetic recombination

in extended cellular apoptosisresultsin extended cellular apoptosis

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Smart Reasoning:

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