Individuals Homozygous for the V Allele of FcγRIIIa May Have Increased Risk of HIV Infection Following Vaccination with Recombinant gp120D. ForthalIdsa
待解决 悬赏分:1 - 离问题结束还有 individuals homozygous for the G allele of rs53576问题补充:匿名 2013-05-23 12:21:38 rs53576的G等位基因纯合子的个体 匿名 2013-05-23 12:23:18 纯个人的G显性的 RS 53576 匿名 2013-05-23 12:24:58 个体同质接合为rs53576 G等位基因 匿名 2013-...
Briefly, we extracted DNA from whole peripheral blood of the patients and sequenced with the MGISEQ-2000 platform. The data were mapped to the hg19 and GATK were used to call genetic variants. We annotated variants using allele frequency databases (the 1000 Genomes Project, gnomAD, and ExAC) ...
Both variants are heterozygous in eight FH2-carriers and homozygous for the reference allele in all other sequenced Fleckvieh animals. Moreover, both variants are homozygous for the reference allele in 1007 non-Fleckvieh animals that have been sequenced for the 1000 bull genomes project [2]. ...
Filtering of variants for pathogenicity was performed with an in-house tool (MS, unpublished). Calls with an allele frequency ≥ 1% in the 1000 Genomes, ExAC or Kaviar databases were excluded. In addition, frequently observed variants in our in-house database (≥ 20x) were removed. All ...
(F) The construct without the X11a similar Bar 50 μm. FIG. 6 . Genetic interaction between loeand Appl. (A) A 4 d old Appl d mutant reveals no vacuolization, whereas The loe mutant not onlyinfluences APPL processing but also interacts genetically with the Appl d null allele. doi...
Patients Homozygous for the T435N Mutation of Succinyl-CoA:3-Ketoacid CoA Transferase (SCOT) Do Not Show Permanent Ketosis TOSHIYUKI FUKAO, HARUO SHINTAKU, RYOU KUSUBAE, GAI X. ZHANG, KOZUE NAKAMURA, MASASHI KONDO, AND NAOMI KONDO Department of Pediatrics [T.F., G.X.Z., K.N., M.K....
NKX2–5 gene and the carrier status of the other family members were shown in the fig. (N: Normal, +: Mutant allele, −: Normal allele) (b) DNA sequencing image for KCNQ1 mutation (c) DNA sequencing image for RYR2 variant (d) DNA sequencing image for NKX2–5 variant (...
The same variant has been reported in a heterozygous patient affected by adult-onset DCM [26], and it has also been found in multiple apparently healthy heterozygous carriers according to the gnomAD 2.1 database (minor allele frequency in the non-Finnish European population = 1/9187). It has...
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