Loading ...

Blob

Smart Reasoning:

C&E

See more*

Qaagi - Book of Why

Causes

Effects

for students who have taken(passive) is designedgap course

the stable teethcausinggap teeth

to accommodate various product sizes(passive) can be designedGap size

first(passive) were ... discoveredThe gap genes

directly(passive) are ... influencedThe gap genes

directly(passive) are ... influencedThe ' ' ' gap genes '

at 25 microns(passive) is usually setGap size

to cover the difference in the vehicle value and the balance of your loan(passive) is designedGAP Advantage

to eliminate your unpaid auto loan balance in the event your vehicle is stolen or damaged beyond repair ( totaled(passive) is designedGAP Advantage

issued in sequences of the M1 cellular body , dephosphorylation , function and syndrome(passive) are composedS33 genes

for use in(passive) can be designedChimeric genes

by infection of chronic viruses(passive) caused bychimeric genes

Inherited mutations in the BRCA1 andleadBRCA2 genes

Mutations in the BRCA1 andresultBRCA2 genes

Mutations in the BRCA1 andcauseBRCA2 genes

Certain mutations in BRCA1 orcan leadBRCA2 genes

of aggregates of intercellular channels that connect the cytoplasm of two cells(passive) are composedGap junctions

Pathogenic mutations in BRCA1 andresultsBRCA2 genes

of intercellular channels formed by connexins ( Cx ) , which allow the direct exchange of ions , small metabolites and other second messenger molecules between adjacent cells(passive) are composedGap junctions

the gut microbiotainfluencesproinflammatory genes

More women with defects in BRCA1 andsetBRCA2 genes

hyperoxic extrauterine conditions(passive) caused bygap junctions

which either results in down regulation of tumor suppressor genes or upregulation of cancercausinggenes

A treatment procedure that targets the affectedmay leadgene(s

of exons , genomic regions with information that encode for proteins , and long stretches of DNA found between exons(passive) are mainly composedGenes

Cancer is caused by somatic mutations in specific cancercausinggenes

by various regulatory chromatin - associated factors(passive) influenced bygenes

Two gene variantshave discoveredgenes

the cost of genetic screening for cancer / diseasecausinggenes

by the lack of an enzyme due to a single abnormal gene(passive) is caused bygenes

by DNA methylation and/or histone modifications during plant development(passive) caused bygenes

of specific segments or regions of the DNA molecule(passive) are composedGenes

Mutational analysis of disease ... Genome wide scanning for disease predisposition genescausinggenes

sequenced Establishment of databases for cDNA annotation , expression , and analysis Antisense strands ... regulatory mechanismsinfluencesgenes

The insertedleadsgene(s

Genetic factors and interaction with the environment For many traitscontributegenes

to cover the difference between the insurance settlement and the loan balance(passive) is designedGAP

by a transcription factor Nrf2 and the translocation of the same factor into the cellular nucleus Nrf2(passive) influenced bygenes

to eliminate your unpaid net loan / lease balance in the event your vehicle is stolen or damaged beyond repair ( totaled(passive) is designedGAP

of molecules carrying the body s genetic information known as deoxyribonucleic acid ( DNA(passive) are composedGenes

the loss of contiguous body segmentscausesthe loss of contiguous body segments

the loss of contiguous body segments ... resembling a gap in the normal body plancausesthe loss of contiguous body segments ... resembling a gap in the normal body plan

the loss of contiguous body segments ... resembling a gap in the normal body plan ... s and pair - rule genescausesthe loss of contiguous body segments ... resembling a gap in the normal body plan ... s and pair - rule genes

different but partially overlapping defectscausedifferent but partially overlapping defects

in brittle cornea syndromeresultin brittle cornea syndrome

up the boundaries between the different segmentssetup the boundaries between the different segments

cilia to malfunctioncausecilia to malfunction

hereditary breast - ovarian cancer syndrome , where carriers have a substantially increased risk of developing breast and ovarian cancers , though their risk of breast cancer is higher than for ovarian cancercausehereditary breast - ovarian cancer syndrome , where carriers have a substantially increased risk of developing breast and ovarian cancers , though their risk of breast cancer is higher than for ovarian cancer

in 100 % recovery of annotated Core Eukaryotic Genes Mapping Approach ( CEGMA ) genes which is a benchmark for a high quality genome assembly ( Text S1resultingin 100 % recovery of annotated Core Eukaryotic Genes Mapping Approach ( CEGMA ) genes which is a benchmark for a high quality genome assembly ( Text S1

to brain tumorsmay contributeto brain tumors

from aquatic microorganismsare originatedfrom aquatic microorganisms

from a gene duplication eventoriginatingfrom a gene duplication event

from gene duplication within a populationresultingfrom gene duplication within a population

glaucomacauseglaucoma

from gene duplicationresultfrom gene duplication

from gene duplicationresultingfrom gene duplication

from gene duplicationresultfrom gene duplication

not only to breast cancercontributenot only to breast cancer

breast cancerusually causebreast cancer

an increase in the risk of breast cancercausean increase in the risk of breast cancer

the disorder refocuses attention on how a defect in the motor nerve , not the muscle , may be contributing to the diseasecan causethe disorder refocuses attention on how a defect in the motor nerve , not the muscle , may be contributing to the disease

in families that had a high incidence of breast cancerwere discoveredin families that had a high incidence of breast cancer

mutations in BRCA1 and(passive) were discoveredmutations in BRCA1 and

the expressioninfluencingthe expression

of sequencescomposedof sequences

of human and rat cDNAs , two strong translational suppression regionscomposedof human and rat cDNAs , two strong translational suppression regions

from a duplication of an ancestral gene after sorghum and maize lineages diverged from a common ancestororiginatedfrom a duplication of an ancestral gene after sorghum and maize lineages diverged from a common ancestor

from tandem duplication eventsresultingfrom tandem duplication events

from duplicationoriginatingfrom duplication

from a duplication event in the conifer lineageoriginatingfrom a duplication event in the conifer lineage

from multiple parental locioriginatefrom multiple parental loci

in increased vascularityresultin increased vascularity

substantially to genomic noveltycontributesubstantially to genomic novelty

of portions of gamma and betacomposedof portions of gamma and beta

of dextran binding domain DBD2composedof dextran binding domain DBD2

several new traits in modern humans(passive) are influenced byseveral new traits in modern humans

health problems that compromise the capacity of afflicted individualscan causehealth problems that compromise the capacity of afflicted individuals

of a serum - inducible Fos promoter , GH - coding sequences , andcomposedof a serum - inducible Fos promoter , GH - coding sequences , and

false positives(passive) caused byfalse positives

breast cancer incidence in families diagnosed with hereditary nonpolyposis colorectal cancerinfluencingbreast cancer incidence in families diagnosed with hereditary nonpolyposis colorectal cancer

Blob

Smart Reasoning:

C&E

See more*