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As a start , using GBS , we genotyped a USDA kabuli mini - core collection of 88 accessionsdiscovering174,040 variants
a diseasecausingallelic variant
non coding transcript splice regionresultsvariant
the obesitycausingFTO variant
by malware researchers from kaspersky(passive) discovered byVariant
by malware researchers(passive) discovered byVariant
by eating meat products from infected animals(passive) caused byvariant
by part of DNA usually including a gene(passive) caused byvariant
a non - coding diseasecausingvariant
Mutations detected in patients with unknown diseasecausingvariant
3 genecontributesvariant
any diseasecausingpredisposing variant
a disease ... that was quite exclusive to Indian population groupcausingvariant
in the course of a so - called genome - wide association study , in which the researchers scanned individual genomes for variations that were correlated with sleep patterns(passive) was discoveredThe variant
a rare non - diseasecausingvariant
Common geneinfluencesvariant
for small helicopter application(passive) is designedturboshaft variant
i.e. a non - diseasecausingvariant
a known diseasecausingvariant
the possible diseasecausingvariant
a non diseasecausingvariant
just a non diseasecausingvariant
to operate from austere , short - field bases and a range of air - capable ships operating near front - line combat zones(passive) is designedSTOVL ) variant
Whole exome sequencing was usedto discoverthe variant
incomplete transcript splice regionresultsvariant
the expected frequency of diseasecausingvariant
Geneinfluencesvariant
could known snpbe ... causingvariant
by a spasm of a coronary artery - rare(passive) caused byvariant
Bioinformatics > could known snpbe ... causingvariant
A whole exome variant filtering software for identification of diseasecausingvariants
online website diseasecausingvariant
by scientists in India(passive) first discovered byThe variant
The larger variant(passive) is designedVariant
a pathogenic or diseasecausingvariant
splice donor regionresultsvariant
More Nutrition Common geneinfluencesvariant
No potential diseasecausingvariant
Standard J - first Standarddesignedvariant
Microsoft security engineersdiscoveredthe variant
severe hemolytic anemiacausingsevere hemolytic anemia
axonal Charcot - Marie - Tooth diseasecausesaxonal Charcot - Marie - Tooth disease
in partial rescueresultedin partial rescue
an EDNRA gain of function in the developing upper jawcausesan EDNRA gain of function in the developing upper jaw
infantile neuroaxonal dystrophy " plus " syndromecausesinfantile neuroaxonal dystrophy " plus " syndrome
breast cancerto causebreast cancer
in increased protein stability and reduced TRAF2resultingin increased protein stability and reduced TRAF2
to partial exon skippingleadsto partial exon skipping
from the interpretation of corneal erosions at a stage where lattice lines are not easily detectable during slit - lamp examinationcould resultfrom the interpretation of corneal erosions at a stage where lattice lines are not easily detectable during slit - lamp examination
its reduced expression levelscausesits reduced expression levels
in increased cytotoxicityresultedin increased cytotoxicity
built by two industry teams , respectively led by Lockheed Martin and General Dynamicsdesignedbuilt by two industry teams , respectively led by Lockheed Martin and General Dynamics
a distinctive facial appearance , short stature and a mild biochemical and clinical phenotypecausesa distinctive facial appearance , short stature and a mild biochemical and clinical phenotype
to a frameshift that results in a premature stop codonleadingto a frameshift that results in a premature stop codon
a mild SMA phenotype with no myoclonic epilepsy : a clinical , biochemical and molecular studycausinga mild SMA phenotype with no myoclonic epilepsy : a clinical , biochemical and molecular study
in increased protein stabilityresultingin increased protein stability
a distinctive facial appearance , short stature and a mild biochemical and clinical phenotype Sharecausesa distinctive facial appearance , short stature and a mild biochemical and clinical phenotype Share
a distinctive facial appearance , short stature and a mild biochemical and clinical phenotype ( 22 August , 2016causesa distinctive facial appearance , short stature and a mild biochemical and clinical phenotype ( 22 August , 2016
the disease coursemay influencethe disease course
to low activityleadsto low activity
to low activityleadsto low activity
for use from aircraft carriersdesignedfor use from aircraft carriers
hemorrhagic diseasecausinghemorrhagic disease
to the diseaseis contributingto the disease
a change in the splicing pattern of BRCA1 10causesa change in the splicing pattern of BRCA1 10
the splice site of intron 3influencingthe splice site of intron 3
in the following : standard price controlresultsin the following : standard price control
re - infection in patientcausedre - infection in patient
the parameters of this variantSetsthe parameters of this variant
a mild SMA phenotype with nocausinga mild SMA phenotype with no
as a launch platform for twodesignedas a launch platform for two
in decreased whole - cell currentmight resultin decreased whole - cell current
more cases of viruscausingmore cases of virus
schizophrenia riskinfluencingschizophrenia risk
# 1(passive) is painted# 1
a mild SMA phenotype with no myoclonic epilepsycausinga mild SMA phenotype with no myoclonic epilepsy
2.result2.
for improved enzymatic activitydesignedfor improved enzymatic activity
at riskwill leadat risk
record casescausesrecord cases