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
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