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Qaagi - Book of Why

Causes

Effects

bound to the N terminal domain of molecular chaperone Hsp90 has been usedto design5-amide analogues

The primary risk factorinfluenceglycosidated phospholipid analogues

Other mental health issues like depressioncan also causesimilar symptoms.6

kale , beans , lentils , and soy - based foodscan ... causesimilar gassiness

0.3 Billion compoundsresulted2756 structural analogues

new N - acylhydrazone derivativesdesignedas LASSBio-294 analogues

The knowledge of transition state structure has been usedto designoseltamivir analogues

using in silico modelling(passive) were designed2ME analogues

to improve the therapeutic use(passive) are designedAnalogues of Zanamivir Zanamivir analogues

to improve the therapeutic use(passive) are designedZanamivir analogues

ResearchersdesignedPGF2 analogues

subunit composition(passive) is strongly influenced byphilanthotoxin analogues

In the search for effective , selective , and nontoxic antiviral and antitumor agents , a variety of strategies have been devisedto designnucleoside analogues

two noveldesignedanalogues

which causesto inventthe analogues

by molecular simplification(passive) designed byAnalogues

structures ... the N - terminal sideto designthe analogues

decausesanalogues

to be potent and selective for p38(passive) have been designedAnalogues

who are lookingto contributethe analogues

to be incorporated into viral nucleic acids and act as chain terminators thus inhibiting efficient viral replication(passive) are designedNucleoside analogues

to time or strong points(passive) are designedThe analogues

to investigate the effects of modification of these factors on antimicrobial activities ( Table1(passive) were designedAnalogues

in order to determine new and potential antioxidant peptides(passive) were designedAnalogues of PAGY

of 2- and 4-substituted imidazoles and imidazolines attached through a methylene bridge to either the 1- or 2-naphthalene ring system(passive) were composedThe analogues

to inhibit human acetylcholinesterase for Alzheimer 's diseasedesignedto inhibit human acetylcholinesterase for Alzheimer 's disease

mitochondrial toxicityto causemitochondrial toxicity

to weight loss in patientscan leadto weight loss in patients

to weight loss in patients withcan leadto weight loss in patients with

mitochondrial toxicity to varying degreesmay causemitochondrial toxicity to varying degrees

several gastrointestinal effectscan causeseveral gastrointestinal effects

eyelash hypertrichosis ( 1can causeeyelash hypertrichosis ( 1

to weight loss incan leadto weight loss in

to weight losscan leadto weight loss

in weight lossresultedin weight loss

alsocan ... causealso

to resist DPP-4 degradationdesignedto resist DPP-4 degradation

to treat Hepatitis C Virus ( HCV ) infections and potentially other diseasesdesignedto treat Hepatitis C Virus ( HCV ) infections and potentially other diseases

significantlyhave contributedsignificantly

to supraphysiological GLP-1 levelsleadto supraphysiological GLP-1 levels

to inhibit the C - terminal portion of Hsp90 , which demonstrated the ability to decrease client protein expressiondesignedto inhibit the C - terminal portion of Hsp90 , which demonstrated the ability to decrease client protein expression

to resist inactivation by DPP-4designedto resist inactivation by DPP-4

to the acid environment for h. Pylorimay contributeto the acid environment for h. Pylori

to depletion of mitochondrial DNAledto depletion of mitochondrial DNA

to side effects like eye irritationcan leadto side effects like eye irritation

to resist inactivationdesignedto resist inactivation

excessive bleeding during tattoo treatmentsto causeexcessive bleeding during tattoo treatments

irises ( the colored part of the eyes ) to darkencan causeirises ( the colored part of the eyes ) to darken

more weight loss ( Table ) and gastrointestinal side effects than controls ( nausea , relative risk increase [ RRI ] 192 %causedmore weight loss ( Table ) and gastrointestinal side effects than controls ( nausea , relative risk increase [ RRI ] 192 %

to resist enzymatic degradationdesignedto resist enzymatic degradation

A novel triazole(passive) was discoveredA novel triazole

as substrates and inhibitors of thymidine kinase 1 ( TK1designedas substrates and inhibitors of thymidine kinase 1 ( TK1

A novel traizole(passive) was ... discoveredA novel traizole

to probe and modify enzyme interactionsdesignedto probe and modify enzyme interactions

more weight loss ( Table ) and gastrointestinal side effects than controls ( nausea , relative risk increase [ RRI ] 192 % , 95 % CI 102causedmore weight loss ( Table ) and gastrointestinal side effects than controls ( nausea , relative risk increase [ RRI ] 192 % , 95 % CI 102

to act as competitive alternative substrate inhibitors of virally encoded polymerasesdesignedto act as competitive alternative substrate inhibitors of virally encoded polymerases

AD pathogenic mechanisms through pathways specifically related to the pharmacodynamics of the GLP-1 analogues , even in non - diabetic patientscan influenceAD pathogenic mechanisms through pathways specifically related to the pharmacodynamics of the GLP-1 analogues , even in non - diabetic patients

side effects such as loss of sexual desire , impotence , hot flashes and the development of osteoporosis , which increases the risk of bone fracturescan causeside effects such as loss of sexual desire , impotence , hot flashes and the development of osteoporosis , which increases the risk of bone fractures

increased and prolonged cellular activityprovokeincreased and prolonged cellular activity

for structure - activity relationshipsdesignedfor structure - activity relationships

to the discovery ofleadingto the discovery of

alsomay ... to can ... causealso

to weight loss in patientscan leadto weight loss in patients

red cellscan causered cells

adverse health effectscould causeadverse health effects

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