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a base substitution for T with A in intron 16 , 1037 bases following exon 16(passive) caused bya single nucleotide polymorphism ( SNP
a recently available studydiscovereda single - nucleotide polymorphism of ( rs3219151
In the present study , next - generation sequencing ( NGS ) technology was usedto discoversingle nucleotide polymorphism ( SNP
likely ) non - diseasecausingSingle Nucleotide Polymorphism ( SNP
a substitution of valine ( val ) with methionine ( met ) in the 158 codon of the Catechol - o - Methyltransferase gene ( COMT - val158met(passive) caused bythe single nucleotide polymorphism
William E.R. The studyresultsfrom a single - nucleotide polymorphism
Variation or mutation in a single base paircreatesa single nucleotide polymorphism ( SNP
after sequencing 5547 base pairs in seven noncoding regions of cpDNA(passive) was discoveredOnly a single nucleotide polymorphism
Sequence changestypically causeSNPs , single nucleotide polymorphism
customdesigninga SNP ( Single Nucleotide Polymorphism
primersdesignedfor a single nucleotide polymorphism
a comprehensive genetic mapcomposedof 381 single nucleotide polymorphism
an amino acid changeresultsfrom a single nucleotide polymorphism
in the SU resistant sunflower(passive) was discoveredA single nucleotide polymorphism ( SNP
in exon 12(passive) was discoveredA single - nucleotide polymorphism ( SNP
orderto createan SNP ( single nucleotide polymorphism
in the small subunit of the starch biosynthesis rate - controlling enzyme ADP - glucose pyrophosphorylase , which resulted in the introduction of a STOP codon in the messenger RNA of the enzyme(passive) was discoveredA single nucleotide polymorphism ( SNP
nucleotide substitutions(passive) caused bythe single nucleotide polymorphism
Often tripletscausingsingle nucleotide polymorphism
the topic of my diploma and PhD thesis(passive) Triggered bysingle nucleotide polymorphism
AID - catalyzed deamination of deoxycytidinecreatesa single nucleotide polymorphism ( SNP
Genotype to Phenotype studiesHave discovereda single nucleotide polymorphism ( SNP
The G – C substitution in intron 3 of the IGF1 genemight influencesingle nucleotide polymorphism ( snp ) rs1520220
structural variants and their impact on detecting meiotic recombination events(passive) caused bysingle - nucleotide polymorphism calling
algorithmsdesignedto deconvolute single nucleotide polymorphism
CYP2B6resultingfrom a single nucleotide polymorphism
a minor structural changeresultingfrom a single - nucleotide polymorphism
the variability of rosuvastatin PKresultingfrom a single nucleotide polymorphism of ABCG2
a standard quantitative PCR assaydesignedfor a biallelic single nucleotide polymorphism
Neil Aronin and Philip Zamore of the University of Massachusetts Medical School in Worcesterhave discovereda single nucleotide polymorphism ( SNP
what ’s called a random point mutationresultingin a single - nucleotide polymorphism
on chromosome 19(passive) has been discoveredThis single nucleotide polymorphism
A latest genome - wide association research in prostate cancersdiscovereda single - nucleotide polymorphism
SNP ) marker discovery effort(passive) was ledThe single nucleotide polymorphism
for genomic studies [ 237(passive) is discoveredSingle nucleotide polymorphism
Aronin and Zamorehave discovereda single nucleotide polymorphism ( SNP
The Y. pestismight cause1.ORI3-k single - nucleotide polymorphism genotype
riskcausingSingle Nucleotide Polymorphism
The HIF1A C85InfluencesT Single Nucleotide Polymorphism
scientistshave discoveredsingle nucleotide polymorphism named rs12970134s
to an amino acid substitution ( Ala80Pro ) ( 5leadingto an amino acid substitution ( Ala80Pro ) ( 5
to false allelic fraction by droplet digital PCR ' , Clinical Chemistryleadingto false allelic fraction by droplet digital PCR ' , Clinical Chemistry
to a single amino acid substitution ( Y402H ) in CFHleadingto a single amino acid substitution ( Y402H ) in CFH
smaller grain size and loss of seed shattering during African rice domestication ' Nature Plants , vol 3 , 17064causessmaller grain size and loss of seed shattering during African rice domestication ' Nature Plants , vol 3 , 17064
Zanger U.M. Aberrant splicing(passive) caused byZanger U.M. Aberrant splicing
in an amino acid substitution at position 219 from serine to leucineresultsin an amino acid substitution at position 219 from serine to leucine
a valine to methionine exchange at position 129causesa valine to methionine exchange at position 129
an amino acid substitution within the 11th of 12 ankyrin repeats of ANKK1causesan amino acid substitution within the 11th of 12 ankyrin repeats of ANKK1
to a Pro-106-Ser amino acid substitution in the enzyme from the GR biotypeledto a Pro-106-Ser amino acid substitution in the enzyme from the GR biotype
a non - synonymous amino acid substitution in the functionally essential GAF domaincausesa non - synonymous amino acid substitution in the functionally essential GAF domain
to False Allelic Fraction by Droplet Digital PCR | Clinical Chemistry Eric S. Christenson , Brian W. Dalton , David Chu , Ian Waters , Karen Cravero , Daniel J. Zabransky , Amy E. DeZern , Ben Ho Park DOILeadingto False Allelic Fraction by Droplet Digital PCR | Clinical Chemistry Eric S. Christenson , Brian W. Dalton , David Chu , Ian Waters , Karen Cravero , Daniel J. Zabransky , Amy E. DeZern , Ben Ho Park DOI
in the production of an additional , longer isoform ( p26resultsin the production of an additional , longer isoform ( p26
Epub 2008 Jan 2.Aberrant splicing(passive) caused byEpub 2008 Jan 2.Aberrant splicing
smaller grain size and loss of seed shattering during African rice domestication Wenguang Wu1 n1 , Xiaoyun Liu1 n1 , Muhua Wang2 n1 , n2 , Rachel S. Meyer3 , Xiaojin Luo4 , Marie - Noelle Ndjiondjop5causessmaller grain size and loss of seed shattering during African rice domestication Wenguang Wu1 n1 , Xiaoyun Liu1 n1 , Muhua Wang2 n1 , n2 , Rachel S. Meyer3 , Xiaojin Luo4 , Marie - Noelle Ndjiondjop5
to a glutamine ( Gln ) by arginine ( Arg ) substitution at codon 460 of the purinergic P2X7 receptor ( P2X7Rleadingto a glutamine ( Gln ) by arginine ( Arg ) substitution at codon 460 of the purinergic P2X7 receptor ( P2X7R
in a silent mutation ( I219Imay resultin a silent mutation ( I219I
in the mutation of Cys211 to Argwould resultin the mutation of Cys211 to Arg
in the Arg753Gln mutation in TLR2resultedin the Arg753Gln mutation in TLR2
in the mutation of cysteine 211would resultin the mutation of cysteine 211
Gln488His mutation abrogatescausingGln488His mutation abrogates
brain morphology in drug - näve patients with major depressive disorder ' , Neuropsychiatric Disease and Treatmentinfluencesbrain morphology in drug - näve patients with major depressive disorder ' , Neuropsychiatric Disease and Treatment
for paternal identification to reduce the costs of trait recording in commercial pig breeding Harlizius , B. , Lopes , M. S. , Duijvesteijn , N. , van der Goor , L. H. P. V. , van Haeringen , W. A. , Panneman , H. , Guimaraes , S. E. F. , Merks , J. W. M. & Knol , E. F. , 2011setfor paternal identification to reduce the costs of trait recording in commercial pig breeding Harlizius , B. , Lopes , M. S. , Duijvesteijn , N. , van der Goor , L. H. P. V. , van Haeringen , W. A. , Panneman , H. , Guimaraes , S. E. F. , Merks , J. W. M. & Knol , E. F. , 2011
in a loss of body odor in people who are specifically homozygous for body odorresultingin a loss of body odor in people who are specifically homozygous for body odor
in a loss of body odor in people who are specifically homozygous for it.[22][23resultingin a loss of body odor in people who are specifically homozygous for it.[22][23
a variable upstream open reading frame regulates glucocorticoid receptor expression Gene 563 ( 1creatinga variable upstream open reading frame regulates glucocorticoid receptor expression Gene 563 ( 1
in a serine to gly- cine amino acid substitution ( Ser9Gly ) in the N terminal and gives rise to allelic differences in dopamine affinityresultsin a serine to gly- cine amino acid substitution ( Ser9Gly ) in the N terminal and gives rise to allelic differences in dopamine affinity
to an amino acid substitution of Gly16Arg segregates with hypertension and asthma ( Zaugg and Schaub , 2005 ; Sayers , 2013 ) and homozygote Gly16 subjectsleadingto an amino acid substitution of Gly16Arg segregates with hypertension and asthma ( Zaugg and Schaub , 2005 ; Sayers , 2013 ) and homozygote Gly16 subjects
in a nonsynonymous coding change , rs2071203 ( SEMA3B ) and rs1046956 ( SEMA3Fresultsin a nonsynonymous coding change , rs2071203 ( SEMA3B ) and rs1046956 ( SEMA3F
from a nucleotide substitution at codon 399 with an amino acid change from arginine ( Argresultingfrom a nucleotide substitution at codon 399 with an amino acid change from arginine ( Arg
BP response measured by office , home , ambulatory daytime and nighttime blood pressure 12967_2011_1033_MOESM1_ESM.DOC Additional file 1influencingBP response measured by office , home , ambulatory daytime and nighttime blood pressure 12967_2011_1033_MOESM1_ESM.DOC Additional file 1
the most common genetic mutation in humancausesthe most common genetic mutation in human
in a missense mutation in the DELLA motifresultingin a missense mutation in the DELLA motif
in the substitution M541Lresultingin the substitution M541L
in the Arg753Gln substitutionresultedin the Arg753Gln substitution
a nonsynonymous amino acid substitution of phenylalanine at position 380 by serine in the functionally essential GAF ( 39 , 59-cyclic - GMP phosphodiesterase , adenylate cyclasecauseda nonsynonymous amino acid substitution of phenylalanine at position 380 by serine in the functionally essential GAF ( 39 , 59-cyclic - GMP phosphodiesterase , adenylate cyclase
in a valine to methionine substitution ( Val66Metresultingin a valine to methionine substitution ( Val66Met
to allele dropout during validation of a CDH1 sequencing assayleadingto allele dropout during validation of a CDH1 sequencing assay
in a premature stop codon and led to small seeds and loss of seed shattering during African rice domesticationresultedin a premature stop codon and led to small seeds and loss of seed shattering during African rice domestication
to mutation F96L in the encoded calpain - like proteaseleadsto mutation F96L in the encoded calpain - like protease
a nonsynonymous amino acid substitution of phenylalanine at position 380 by serine in the functionally essential GAF ( 3′ , 5′-cyclic - GMP phosphodiesterase , adenylate cyclase ... formate hydrogen lyase activator protein ) domaincauseda nonsynonymous amino acid substitution of phenylalanine at position 380 by serine in the functionally essential GAF ( 3′ , 5′-cyclic - GMP phosphodiesterase , adenylate cyclase ... formate hydrogen lyase activator protein ) domain