Loading ...

Blob

Smart Reasoning:

C&E

See more*

Qaagi - Book of Why

Causes

Effects

the insertion(passive) caused byan MLL / LAF4 fusion gene

by t(1;19)(q23;p13(passive) caused byE2A - PBX1 fusion gene

A translocationcausinga fusion of the C8orf34 gene

mutation ... <causinggene fusion " EXACT

by t(1;19)(q23;p13(passive) caused byPBX1 fusion gene

by a reciprocal translocation between chromosomes 9 and 22 ( the Philadelphia ( Ph ) chromosome(passive) caused bythe fusion gene

Drs(passive) was designed byThe GCaMP6f fusion gene

the t(9;22)(q34;q11 ) chromosomal translocation(passive) caused bythe fusion gene

by a reciprocal translocation between chromosomes 9 and 22(passive) caused bythe fusion gene

the balanced translocation t(9;22)(q34;q11resultsin the fusion gene

in NSCLC(passive) was discoveredEML4-ALK ) fusion gene

a t(12;22 ) translocation(passive) caused bygene fusion

a little inversion in chromosome 2leadsto a fusion gene

common rearrangementsresultingfrom gene fusion

the genescomposingthe fusion gene

a novel toxin genesresultingfrom gene fusion

a translocationleadingto the fusion gene

The translocationleadsto the ETV6-PDGFRB fusion gene

a chromosomal event called chromothripsis(passive) caused bygene fusion

by a chromosomal event called chromothripsis(passive) caused bya gene fusion

by a chromosomal event called chromothripsis(passive) caused bygene fusion

mutationcausinggene fusion

A mutationcausinggene fusion

DNA damage which results in parts from two separate genes to merge together(passive) is caused byA fusion gene

The translocation involves the PML and RARa ( retinoic acid receptor ) genesresultingin a PMLRARa fusion gene

ABL1 genesleadingto a fusion gene Fusion gene

and ' ' ABL1 ' ' genesleadingto a [ [ fusion gene

by t(9;22)(q34;q11)is(passive) caused bya fusion gene

by a t(7;17)(p15;q21 ) translocation(passive) caused bythe fusion gene

patients and their medical teamsdiscoverthe NTRK - fusion gene

a viral insertion rather thancausesthe gene fusion

Eventsleadingto a fusion gene

by t(9;22)(q34;q11)is thought to have a cooperative effect with EVI1 during the progression of AML and CML.[20(passive) caused bya fusion gene

Numerous studiesdiscoveredgene fusion

by t(9;22)(q34;q11)is thought to have a cooperative effect with EVI1 during the progression of AML and CML(passive) caused bya fusion gene

t(9;22)(q34;q11)is thought to have a cooperative effect with EVI1 during the progression of AML and CML(passive) caused bya fusion gene

co -(passive) was ... discoveredThe fusion gene

by t(9;22)(q34;q11)is thought to have a cooperative effect with EVI1 during the progression of AML and CML.[24(passive) caused bya fusion gene

the MLL rearrangementleadingto the fusion gene

Strand NGS between ALK and EML4 genes(passive) discovered byGene Fusion

from t ( 6;22)(p21;q12resultingfrom t ( 6;22)(p21;q12

to improved clinical outcomes in patients with lung cancerledto improved clinical outcomes in patients with lung cancer

from a mutationresultingfrom a mutation

the production of TRK , a family of proteins that drives tumour growthcausesthe production of TRK , a family of proteins that drives tumour growth

in dominant oncogenic activityresultingin dominant oncogenic activity

the production of TRK , a familycausesthe production of TRK , a family

to the development of solid tumorscan leadto the development of solid tumors

to the development of solid tumors in a variety of tissue typescan leadto the development of solid tumors in a variety of tissue types

from the Philadelphia chromosome rearrangement tresultingfrom the Philadelphia chromosome rearrangement t

to ERG over expressionleadingto ERG over expression

problems in the cell leading to cancercausesproblems in the cell leading to cancer

in measurable fusion protein productiondid ... resultin measurable fusion protein production

to ERG overexpressionleadingto ERG overexpression

ERG overexpression precedes chromosome copy number changes in prostate carcinomascausingERG overexpression precedes chromosome copy number changes in prostate carcinomas

ERG overexpression precedes chromosome copy number changes in prostate carcinomas andcausingERG overexpression precedes chromosome copy number changes in prostate carcinomas and

to ERGleadingto ERG

from the head - to - tail fusion of the Bcr and Abl genes[1resultsfrom the head - to - tail fusion of the Bcr and Abl genes[1

to over - expression of full length ERGleadingto over - expression of full length ERG

Erg Overexpression PrecedesCausingErg Overexpression Precedes

to changes in kinase activityleadingto changes in kinase activity

of a resistance and reporter genecomposedof a resistance and reporter gene

of HSP70 gene and an antigen protein genecomposedof HSP70 gene and an antigen protein gene

to tumor formationcan contributeto tumor formation

of native genetic sequence from two different genescomposedof native genetic sequence from two different genes

to an active enzyme with conserved type IB enzyme functionleadsto an active enzyme with conserved type IB enzyme function

constitutive activation of the tyrosine kinase , which is implicated in uncontrolled cell growth and proliferationcausesconstitutive activation of the tyrosine kinase , which is implicated in uncontrolled cell growth and proliferation

from a specific chromosomal translocationresultingfrom a specific chromosomal translocation

of a 5 sequence from the BCR region and 3 sequence from ABLcomposedof a 5 sequence from the BCR region and 3 sequence from ABL

to constitutive activation of the tyrosine kinaseleadsto constitutive activation of the tyrosine kinase

of a 5 sequence from the BCR regioncomposedof a 5 sequence from the BCR region

from a chromosomal translocation between chromosomes 9 and 12 observed in human leukemiaresultingfrom a chromosomal translocation between chromosomes 9 and 12 observed in human leukemia

from rearrangement of chromosome 4 that has been identified in many cancers including those of the urinary bladderresultingfrom rearrangement of chromosome 4 that has been identified in many cancers including those of the urinary bladder

to deletion ofleadingto deletion of

leukemia in humanscausesleukemia in humans

of human MIS transcriptional regulatory sequences linked to the SV40 T - antigen genecomposedof human MIS transcriptional regulatory sequences linked to the SV40 T - antigen gene

from genomic rearrangements of protein kinasesresultingfrom genomic rearrangements of protein kinases

of parts of two different genescomposedof parts of two different genes

cancers(passive) caused bycancers

in effective expression , processing and stability of messenger RNAresultsin effective expression , processing and stability of messenger RNA

the same pathway [ 1leadsthe same pathway [ 1

Blob

Smart Reasoning:

C&E

See more*