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Qaagi - Book of Why

Causes

Effects

Strongyloides stercoraliscan causehyperinfection syndrome

Strongyloides stercoraliscan causehyperinfection syndrome

mutations in the LPIN2 gene(passive) is caused byMajeed syndrome

heterozygous missense mutations in the SAM domain of p63(passive) is caused byHay?Wells syndrome

a cystic duct remnant calculuscausingMirizzi syndrome

a deletion on Chromosome 21q11(passive) is caused byCardiovelofacial syndrome

Mycoplasma pneumonia infection in Japan(passive) caused byStevenseJohnson syndrome

filariform larvaecausinghyperinfection syndrome

Were Foundcould resultin combination syndrome

residual thrombuscausingpostphlebitic syndrome

the disease ... the mutated genescauseMajeed Syndrome

although the SMAD4 mutations in JP - HHT patients do show a tendency to cluster in the MH2 domaincausethe combined syndrome

Mutations in the PTEN genecan causeCowden syndrome

by mutations in the PTEN gene(passive) is caused byCowden syndrome

mutations in the PTEN gene(passive) is caused byCowden syndrome

Mutations of the PTEN gene , a tumor suppressor genecauseCowden syndrome

mutation in the PTEN gene(passive) is caused byCowden syndrome

a mutation in the PTEN gene(passive) is caused byCowden syndrome

may fuse to the extrahepatic biliary treecausingMirizzi syndrome

by germline mutations in PTEN(passive) is causedCowden syndrome

by germline mutations in PTEN(passive) is caused byCowden syndrome

a mutation in the PTEN gene , which is normally a tumour suppressor gene(passive) is caused byCowden syndrome

Dr. Mary Claire KingdiscoveredBRCA1 syndrome

These mutations ... mutationscausecardiofaciocutaneous syndrome

mutationscausecardiofaciocutaneous syndrome

by mutations in the PTEN(passive) is ... caused byCowden syndrome

mutations in a gene on chromosome 10 known as PTEN(passive) is caused byCowden syndrome

the PTEN genecauseCowden syndrome

PTEN ) genecausingCowden syndrome

the PTEN genecausesCowden syndrome

mutations in several genes(passive) can be caused byCardiofaciocutaneous syndrome

a mutation in the SMAD4 gene(passive) is caused byMyhre syndrome

mutations in the SMAD4 gene(passive) is caused byMyhre syndrome

Novel SMAD4 mutationcausingMyhre syndrome

by faults in the PTEN gene(passive) caused byCowden syndrome

a single shared homozygous founder mutation in SGOL1 , a component of the cohesin complexcausesCAID syndrome

genecauseCowden syndrome

a novel mutation(passive) caused byCowden syndrome

Inherited mutations On this genemight causeCowden syndrome

Inherited mutations With this genecan causeCowden syndrome

and dyed textile of various cultures worldwidepaintedand dyed textile of various cultures worldwide

vinyl stickers and waterslide decalspaintedvinyl stickers and waterslide decals

to a greater blood pressure reduction and faster blood pressure lowering to target levels , prompter response in a larger number of patients , lower probability of discouraging patient adherence with many treatment changes and reduced risk of hospitalization due to cerebrovascular and coronary events in about 25 %leadsto a greater blood pressure reduction and faster blood pressure lowering to target levels , prompter response in a larger number of patients , lower probability of discouraging patient adherence with many treatment changes and reduced risk of hospitalization due to cerebrovascular and coronary events in about 25 %

in higher Erk1/2 inhibition and in increased induction of apoptosisresultedin higher Erk1/2 inhibition and in increased induction of apoptosis

prominent and durable tumor regression compared to single agent therapycausesprominent and durable tumor regression compared to single agent therapy

in longer and better management of symptomscan resultin longer and better management of symptoms

in a reduction of tumor volume by 78 % ( p < 0.001 ) compared with the control groupresultedin a reduction of tumor volume by 78 % ( p < 0.001 ) compared with the control group

in better symptom control than an increased dosage of ICS alone [ 27may resultin better symptom control than an increased dosage of ICS alone [ 27

in maximum antitumor effects in the second model , where precancerous cells were already presentalso resultedin maximum antitumor effects in the second model , where precancerous cells were already present

to superior outcomesledto superior outcomes

alsoledalso

to more superior outcomemay leadto more superior outcome

in message levels similar to that seen with RAresultedin message levels similar to that seen with RA

reductions in tissue infarction and vascular injurycausesreductions in tissue infarction and vascular injury

tumor regression but was not well tolerated and decreased survival , suggesting that artemisinins should not be used in therapeutic strategiescausedtumor regression but was not well tolerated and decreased survival , suggesting that artemisinins should not be used in therapeutic strategies

of ingredients of plant and synthetic origincomposedof ingredients of plant and synthetic origin

in a > 2-log reduction for rifampin , compared to antimicrobial treatment aloneresultedin a > 2-log reduction for rifampin , compared to antimicrobial treatment alone

in statistically significant enhanced induction of MCL cell deathresultedin statistically significant enhanced induction of MCL cell death

to more significant improvements assigned to applications for drugsledto more significant improvements assigned to applications for drugs

in complete clearance of vessels and diffuse rednessresultedin complete clearance of vessels and diffuse redness

to an average survival of 15 - 17 months ... compared with 10 - 12 months for 5FU treatment aloneleadsto an average survival of 15 - 17 months ... compared with 10 - 12 months for 5FU treatment alone

in significantly higher sustained virological responses ( 53 %resultedin significantly higher sustained virological responses ( 53 %

to decreased Arg1-positivity compared to anti - CTLA-4 aloneledto decreased Arg1-positivity compared to anti - CTLA-4 alone

in no significant differencesresultedin no significant differences

to PUMA induction , acute apoptosis , and autophagyleadingto PUMA induction , acute apoptosis , and autophagy

to any sensitization of cell linesdid ... leadto any sensitization of cell lines

in a significant reduction in the expression of cyclin D1 and c - Mycresultedin a significant reduction in the expression of cyclin D1 and c - Myc

the accumulation of cells at G1 phase with the increases in the sub - G0 / G1 peak , DNA ladder , nuclear fragmentation , and caspase-3/7 activitysignificantly causedthe accumulation of cells at G1 phase with the increases in the sub - G0 / G1 peak , DNA ladder , nuclear fragmentation , and caspase-3/7 activity

rashes and skin reactionsmay causerashes and skin reactions

most significant ( P<0.001 ) reduction in body weight ... fasting blood glucose , serum levels of cholesterol , triglyceride , LDL , VLDL and increase levels of HDLcausedmost significant ( P<0.001 ) reduction in body weight ... fasting blood glucose , serum levels of cholesterol , triglyceride , LDL , VLDL and increase levels of HDL

rashes and skin reactions to sunlightmay causerashes and skin reactions to sunlight

in apoptosis through the formation of tBid , mitochondrial membrane depolarizationresultedin apoptosis through the formation of tBid , mitochondrial membrane depolarization

caspase - dependent apoptosis , PARP cleavage and Annexin Vcausescaspase - dependent apoptosis , PARP cleavage and Annexin V

in broadly effective cell kill of p53 WT and p53-negative cancer cellsresultedin broadly effective cell kill of p53 WT and p53-negative cancer cells

to increased IOP or initiation of antihypertensive eyedrops in 19 ( 29 % ) eyesledto increased IOP or initiation of antihypertensive eyedrops in 19 ( 29 % ) eyes

to a shift from T reg to T eff cells within the tumorleadsto a shift from T reg to T eff cells within the tumor

to greater clinical improvements for children with ADHDcould leadto greater clinical improvements for children with ADHD

in improved inhibition or delay the development of resistance in vitrowould resultin improved inhibition or delay the development of resistance in vitro

in increased clinical benefitmay resultin increased clinical benefit

to faster improvements ( without significantly affecting magnitudeledto faster improvements ( without significantly affecting magnitude

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