ライフサイエンスコーパス: polymorphism

1 gous for the TSLPrs1898671 single-nucleotide polymorphism.

2 entration, TPPII has a distinct tendency for polymorphism.

3 tion of a conditional strategy and a genetic polymorphism.

4 those prime candidates for phenotype-causal polymorphisms.

5 ximately 9 000 000 imputed single-nucleotide polymorphisms.

6 using 45,608 high-quality single-nucleotide polymorphisms.

7 s for future studies of cancer mutations and polymorphisms.

8 enotyped with 2.5 million single-nucleotide polymorphisms.

9 clade distinguished by 93 single-nucleotide polymorphisms.

10 84 different genes and 147 single nucleotide polymorphisms.

11 h microsatellites and 9230 single-nucleotide polymorphisms.

12 daily dose groups regardless of baseline Gag polymorphisms.

13 on quantitative trait loci single nucleotide polymorphisms.

14 tion due to disease-associated mutations and polymorphisms.

15 The low activity allele of the maternal polymorphism, 5HTTLPR, in the serotonin transporter, SLC

16 The human AE3 polymorphism A867D is associated with idiopathic general

17 opulations, but the mechanisms by which this polymorphism affects TLR2 signaling are unclear.

18 ion, as in Gilbert's Syndrome (GS; UGT1A1*28 polymorphism), aggravated health effects have been deter

19 h HCV genotype 4a or 4d infections with NS5A polymorphisms, all 26 who received the elbasvir and graz

20 65 NF-kappaB, suggesting that the R753Q TLR2 polymorphism alters the functions of the myeloid differe

21 ed by recent TE activity leads to regulatory polymorphisms among populations has yet to be thoroughly

22 Genetic polymorphism analysis of the three key resistance genes,

23 sequencing and chromosome single-nucleotide polymorphism analysis.

24 IL-1 polymorphism and generalized reinfection are associated

25 lo simulations, we demonstrate that balanced polymorphism and recombination evolve between a target l

26 s highly sensitive to the common MTHFR C677T polymorphism and that the effect of the polymorphism on

27 -gene interactions between the missense APOE polymorphisms and FA status on metabolic markers in MetS

28 by sequencing identified 14,059 segregating polymorphisms and genome-wide association studies reveal

29 ly reported CKD-associated single-nucleotide polymorphisms and provided evidence for interaction betw

30 port a clinically meaningful role of CYP2C19 polymorphisms and response to tamoxifen in breast cancer

31 ished associations between single nucleotide polymorphisms and threat-related amygdala reactivity, wh

32 s, loss of STOP codons and single nucleotide polymorphisms, and short in-frame insertions and deletio

33 suggests that the conditions for multilocus polymorphism are restrictive.

34 ar to-date what the molecular causes of this polymorphism are.

35 re, these results suggest that most observed polymorphisms are likely nearly neutral with regard to f

36 cal illness, and several natural erythrocyte polymorphisms are protective against severe malaria.

37 ively, these results establish mitochondrial polymorphisms as quantitative trait loci in mammary carc

38 ted a total of 3.8 million single nucleotide polymorphisms, as well as imputed HLA alleles and amino

39 s72820264, an intragenetic single-nucleotide polymorphism associated with LVOTDs (P=2.1x10(-8)).

40 modified by the S357N mutation, a VWA domain polymorphism associated with more severe meconium ileus

41 c risk score comprising 93 single-nucleotide polymorphisms associated with BMI from previous genome-w

42 g populations were specifically enriched for polymorphisms associated with drought tolerance.

43 Genetic polymorphisms associated with drusenoid lesions in rhesu

44 ociation study to identify single-nucleotide polymorphisms associated with genetic susceptibility to

45 nsgenes heterozygous for the HD mutation and polymorphisms associated with HD in populations of East

46 election on G x E variation and characterize polymorphisms associated with plasticity.

47 PRNP in elk is highly conserved and a single polymorphism at codon 132 can markedly extend CWD latenc

48 o suggested association of otitis media with polymorphism at FBX011, but this is the first study to r

49 .) and oral routes, exploring the effects of polymorphisms at codon 146 of the goat PRNP gene on resi

50 ations, much of it in the associations among polymorphisms at different loci.

51 that could be used to detect and quantitate polymorphisms at positions 136, 154, and 171 of sheep Pr

52 ute kidney injury and four single-nucleotide polymorphisms at two independent loci on metaanalysis of

53 o-date and complete database on avian colour polymorphism based on the examination of available data

54 We found a significant single nucleotide polymorphism-based genetic correlation between ADHD and

55 species may be due to retention of ancestral polymorphisms because of incomplete lineage sorting (ILS

56 Inversion polymorphisms between low-copy repeats (LCRs) might pred

57 h also suggests that common and rare genetic polymorphisms can influence risk of more common causes o

58 trophoresis-based single-strand conformation polymorphism (CE-SSCP).

59 le read fractions at known single-nucleotide polymorphisms, considering depth-dependent behavior of s

60 in characterizing human history from genetic polymorphism data, progress in identifying genetic signa

61 variable analysis based on single nucleotide polymorphisms determining birth weight combined with res

62 ransmission (five or fewer single nucleotide polymorphisms different and with identical resistance-en

63 on studies reveal that the cancer-associated polymorphism does not abolish the interaction with p73al

64 hods By using an algorithm that was based on polymorphism-driven expression levels and specificities,

65 and the maintenance of neutral rearrangement polymorphism due to balancing selection on sexes and mat

66 We hypothesized that NTPDase1 polymorphisms exist and that they regulate this pathway.

67 Common single nucleotide polymorphisms explained 5.8% (95% CI: 4.5%-7.2%; P=1.00

68 identified 10 significant single-nucleotide polymorphisms (false discovery rate, 15%) in 4 quantitat

69 ther the addition of novel single-nucleotide polymorphisms for blood lipid levels enhances the predic

70 ome-wide association study single nucleotide polymorphisms for nevus count, at PLA2G6 (P = 1.7 x 10(-

71 ent analysis of 25 historical candidate gene polymorphisms for schizophrenia in the largest genome-wi

72 ce explained by all common single-nucleotide polymorphisms for this tiredness question was 8.4% (s.e.

73 lling is the complex task of separating real polymorphisms from errors.

74 umulation experiments and (2) extremely rare polymorphisms from natural populations.

75 sk score (PRS) composed of single nucleotide polymorphisms from the pathway most consistently associa

76 Using single-nucleotide polymorphism genotypes, we measured population diversity

77 he G allele of the TCN2 c.776G>C (rs1801198) polymorphism has been associated with a lower plasma con

78 STATEMENT The integrin beta3 Leu33Pro coding polymorphism has been associated with autism spectrum di

79 The R753Q TLR2 polymorphism has been associated with increased incidenc

80 ionally, catechol-O-methyltransferase (COMT) polymorphism has been reported to be associated with exe

81 nclusion, SCD patients with the FCGR2Cnc-ORF polymorphism have over a 3-fold lower risk for RBC alloi

82 Colour polymorphisms have played a major role in enhancing curr

83 if these differences are due to cryptic wSuz polymorphism, host background, geographical factors or a

84 The CNTNAP2 polymorphism identified in this population, hence, is no

85 on, INS gene (rs1004446_A), and non-HLA gene polymorphisms identified by the Type 1 Diabetes Genetics

86 Thus, polymorphism in certain plant NLR genes might be influen

87 A polymorphism in human APOBEC3C (A3C) that encodes an S18

88 PTGS2-765G>C polymorphism in humans, associated with reduced COX-2 ex

89 Together, our data suggest that polymorphism in the CagA C-terminus is responsible for d

90 alter the expression of cytolytic toxins, a polymorphism in the cyoE gene, which encodes a protoheme

91 tly, three groups independently identified a polymorphism in the Ebola glycoprotein (I544) that enhan

92 Genotyping of the rs660895 polymorphism in the HLA-DRB1 region was based on saliva

93 A single-nucleotide polymorphism in the human arylamine N-acetyltransferase

94 eport protective association of a functional polymorphism in the miR-146a precursor (rs2910164).

95 s for meta-analysis, involving a total of 53 polymorphisms in 28 genes/loci.

96 lence of 3 malaria-protective red blood cell polymorphisms in BWF cases vs both trial (non-BWF) and p

97 We suggest the polymorphisms in GAL3ST4 in different population are ass

98 pulations, and showed that single nucleotide polymorphisms in gene 3UTRs at the miRNA seed binding re

99 The existence of specific polymorphisms in genes of key hormones of the energy hom

100 Polymorphisms in HBGA genes, and in particular a nonsens

101 iscovery and genotyping of single-nucleotide polymorphisms in hundreds of individuals at a time in mo

102 Five polymorphisms in HvP5CS1 were significantly (P < 0.001)

103 Mutations and common polymorphisms in interferon regulatory factor 6 ( IRF6)

104 An assessment of polymorphisms in SLCO1A2 revealed that four variants wer

105 gests important roles of specific amino acid polymorphisms in the antigen-binding clefts.

106 CCR5 is the major co-receptor for HIV and polymorphisms in the CCR5 gene as well as promoter regio

107 at blood protein expression is influenced by polymorphisms in the corresponding gene, but also that t

108 Our data suggest that polymorphisms in the CYP2R1 and GC gene may contribute t

109 icated and relevant genetic variants include polymorphisms in the genes for interleukin (IL)-1beta, I

110 Polymorphisms in the genome that redistribute CTCF/cohes

111 We suggest that the complex polymorphisms in these animals are probably maintained b

112 Nine polymorphisms in VDR, CYP24A, CYP27B1, GC, and RXRA were

113 dation of 234,452 putative single nucleotide polymorphisms in-silico, of which 8,967 high value SNPs

114 ss was successful for five single-nucleotide polymorphisms in/near HSD17B11, VCAN, ADAMTSL3, IRS1, an

115 an body mass and for three single-nucleotide polymorphisms in/near VCAN, ADAMTSL3, and IRS1 for appen

116 ee species, the density of single nucleotide polymorphisms increases as one approaches a mobile intro

117 This mutation- and single nucleotide polymorphism-independent method could be crucial in domi

118 cific genetic mutations or single nucleotide polymorphisms influence the onset of disease, prognosis,

119 nsmembrane 6 superfamily member 2 rs58542926 polymorphisms influenced disease severity.

120 The high Polymorphism Information Content (PIC) index values (ran

121 haliana reproduction using single nucleotide polymorphism-informed RNA-sequencing analysis.

122 a possible mechanism, we observed that this polymorphism is an expression quantitative trait locus m

123 selection is expected to reduce variability, polymorphism is common in nature even under strong selec

124 tive effect of sexual trimorphism and colour polymorphism is unexplored.

125 Additionally, we find that a subset of these polymorphisms is linked to genome-wide association study

126 The ITGB3 coding polymorphism Leu33Pro (rs5918, Pl(A2)) produces hyperact

127 c diversity of the VGSC gene revealed a high polymorphism level of this gene across Africa with no ev

128 l variation, genomic background, and private polymorphisms) likely contribute to heterogeneity.

129 Outside the HLA region, only one polymorphism located nearby the IL12B gene surpassed the

130 Polymorphisms located within the MHC have been linked to

131 efficients based on 37 037 single-nucleotide polymorphism loci, and population density as an axis of

132 The DHCR7 polymorphism may be a pre-treatment predictive marker fo

133 These polymorphisms may be critical for the development of spe

134 We tested the hypothesis that the Sl and McC polymorphisms might influence CR1 clustering on erythroc

135 Polymorphism observed within the aggregation end product

136 acts of CerC16 (up to 20 mol %) on the lipid polymorphism of 1-palmitoyl-2-oleoyl-sn-glycero-3-phosph

137 al homogeneity, while relatively small-scale polymorphism of ITS copies within individuals has often

138 Finally, C/T polymorphism of MMP-9 gene at position -1562, which upre

139 We defined polymorphism of Papa-B, the bonobo ortholog of HLA-B, fo

140 ersus NS differentiation was observed in DNA polymorphism of two genes putatively involved in adaptat

141 te PSS1 genes by comparing single-nucleotide polymorphisms of (1) the bulked DNA sample of seven F2:3

142 his study aimed to determine whether genetic polymorphisms of genes in the vitamin D pathway are asso

143 Single nucleotide polymorphisms of genes involved in GC signaling (GR, GLC

144 Polymorphisms of rs182420 within the SULT2A1 gene were n

145 Likewise, polymorphisms of the IL-12A gene (IL12A), which encodes

146 Moreover, the observed polymorphism on amino acid 186 between H3N8 and H3N2 CIV

147 677T polymorphism and that the effect of the polymorphism on FOCM is greater in folate deficiency.

148 analysis included the effect of the at-risk polymorphism on postbronchodilator lung function.

149 nding neural correlates, and LMX1A-rs4657412 polymorphism on the adaptive WMT, in human immunodeficie

150 these mutations with the effects of 30 PTDH3 polymorphisms on expression plasticity in the same envir

151 myeloperoxidase elevating single nucleotide polymorphisms on stroke risk per risk allele, correspond

152 significant differences in single-nucleotide polymorphisms or copy number variants, respectively, for

153 f MHC alleles into 'supertypes' explains how polymorphisms persist during rapid host-parasite co-evol

154 Patterns of natural Tgr locus sequence polymorphisms predict partner-specific patterns of coope

155 attention and working memory, whereas NR3C2 polymorphisms predicted memory performance.

156 Further, we show that an rpsA polymorphism previously identified in a PZA resistant st

157 pfkelch13 propeller domain polymorphisms previously associated with artemisinin res

158 table change in expansions, suggesting these polymorphisms primarily affect Msh3 protein stability, n

159 ndividuals with AUD were genotyped for these polymorphisms, randomized to APZ (titrated to 15 mg) or

160 found no discernable effect of the missense polymorphism resulting in the amino acid substitution Gl

161 e, analysis of 176 amplified fragment length polymorphisms revealed significant genome-wide different

162 ation of the CRF1 receptor single nucleotide polymorphism rs110402 found that response to GSK561679 a

163 seline serum 25(OH)D concentration, and that polymorphism rs11185644 may contribute to variation in 2

164 The single nucleotide polymorphism rs1143678 substitutes Pro(1146) for Ser in

165 ge with the CKD-associated single-nucleotide polymorphism rs11959928 were shown to affect DRE functio

166 Four common single-nucleotide polymorphisms (rs1205, rs1130864, rs1800947, and rs30930

167 The lead single-nucleotide polymorphism (rs12445022) was also associated with cereb

168 ssociated with a genotyped single-nucleotide polymorphism (rs12519770, P=2.98x10(-)(8)) in an intron

169 erance, whereas patients with the ZnT8 R325W polymorphism (rs13266634) have decreased proinsulin stai

170 A widely prevalent single nucleotide polymorphism, rs13266634 in the SLC30A8 gene encoding th

171 -DISC1 noncoding RNA, lead single-nucleotide polymorphism: rs149133391, minor allele [C] frequency =

172 A single nucleotide polymorphism (rs16260) linked to increased cancer risk a

173 nment) and genetic background (i.e. TMEM106B polymorphism, rs1990622 T/C) on grey matter volume in a

174 eover, the GA haplotype of single-nucleotide polymorphisms rs2070951 and rs5522 in NR3C2 conferred ri

175 Single-nucleotide polymorphism rs2572886 in the LY6 family protein locus h

176 ified that the T allele in single-nucleotide polymorphism rs41269979 in the class II human leukocyte

177 ted whether the functional single nucleotide polymorphism rs4523957, which is an expression quantitat

178 o demonstrate that the SRR single nucleotide polymorphism, rs4523957, is associated with posttraumati

179 the allele of a functional single nucleotide polymorphism rs4988235, which has been previously associ

180 enhancer, we identified a single-nucleotide polymorphism, rs577676, which alters enhancer activity i

181 gands are sensitive to the single nucleotide polymorphism rs6971; however, this is probably not the c

182 es were tagged by a nearby single-nucleotide polymorphism (rs7570903), which also associated with HDA

183 complement factor H (lead single nucleotide polymorphism: rs800292; P=2.4x10(-35)).

184 riation because of the high degree of worker polymorphism seen in many taxa.

185 ers of strongly associated single nucleotide polymorphisms, selected on the basis of their strength o

186 ct of HLA in autoimmune disease, whereby HLA polymorphism shapes the relative abundance of self-epito

187 Single-single nucleotide polymorphism (SNP) and haplotype-based association tests

188 Single nucleotide polymorphism (SNP) associations were stratified by study

189 d asthma using genome-wide single-nucleotide polymorphism (SNP) data and air pollution exposure.

190 a genome-wide analysis of single-nucleotide polymorphism (SNP) data for Spanish teosinte, sympatric

191 bines a multiplex PCR with single nucleotide polymorphism (SNP) detection using highly selective BiDz

192 This strategy included a single nucleotide polymorphism (SNP) genome-wide association study (GWAS),

193 ype studies based first on single nucleotide polymorphism (SNP) genotyping and then with whole-genome

194 assessed by a high density single nucleotide polymorphism (SNP) genotyping array (Illumina MegaEx).

195 ional effect of a promoter single-nucleotide polymorphism (SNP) in IL32 on lipid profiles in RA patie

196 The lead single nucleotide polymorphism (SNP) in TRACK-HD (rs557874766) was genome-

197 atherosclerosis-associated single-nucleotide polymorphism (SNP) located in the intron of the long non

198 Our data show that a single-nucleotide polymorphism (SNP) mutation in the GL4 gene resulted in

199 ity AICE2 motif at a human single-nucleotide polymorphism (SNP) of the gene encoding the immunomodula

200 pecific variant type (e.g. single nucleotide polymorphism (SNP) or indel) within a broader set of var

201 VScore aggregates per-base single nucleotide polymorphism (SNP) pathogenicity scores across relevant

202 Orange gene (CmOr) golden single-nucleotide polymorphism (SNP) through a yet to be discovered mechan

203 nstraining the effect of a single-nucleotide polymorphism (SNP) to be equal across all families in wh

204 x monoclonal isolates, and single nucleotide polymorphism (SNP) variants emerging over time were dete

205 repeat (VNTR) allele and a single-nucleotide polymorphism (SNP), are associated with diurnal preferen

206 Genome-wide single nucleotide polymorphism (SNP)-based haplotyping has been used to de

207 Single nucleotide polymorphism (SNP)-based heritability and genetic correl

208 DABF is more powerful than single-nucleotide polymorphism (SNP)-set kernel association tests and burd

209 pathway-level somatic mutations, or germline polymorphisms (SNP) are associated with immune metagene

210 e study was to investigate single nucleotide polymorphisms (SNP) located in genes encoding interactin

211 rsity was high with a mean single nucleotide polymorphisms (SNP) rate of approximately 1 per 50 bases

212 total, 24,710 high-quality Single Nucleotide Polymorphisms (SNP) were identified.

213 Ten correlated single-nucleotide polymorphisms (SNPs) (r(2)>0.9) located in an intergenic

214 nificant fraction of human single-nucleotide polymorphisms (SNPs) alter pri-miRNA processing, and con

215 tified approximately 7.4 M single nucleotide polymorphisms (SNPs) and 1.9 M indels.

216 ationship of 11 630 exonic single-nucleotide polymorphisms (SNPs) and 43 copy number variations (CNVs

217 ating prior information of single nucleotide polymorphisms (SNPs) and combining two relevant existing

218 for an association between single nucleotide polymorphisms (SNPs) and expression under an additive mo

219 published type 2 diabetes single nucleotide polymorphisms (SNPs) and genome-wide methylation (methyl

220 Furthermore, single-nucleotide polymorphisms (SNPs) and insertions/deletions (indels) c

221 ciation studies of non-HLA single-nucleotide polymorphisms (SNPs) and outcomes after blood or marrow

222 we genotyped the 10 novel single nucleotide polymorphisms (SNPs) and performed an association study.

223 bes overlapping repeats or single nucleotide polymorphisms (SNPs) are based largely on ad hoc assumpt

224 ow-up study to examine the single nucleotide polymorphisms (SNPs) associated with family history (FH)

225 stics for four independent single nucleotide polymorphisms (SNPs) associated with isoleucine levels a

226 NA) by taking advantage of single-nucleotide polymorphisms (SNPs) distributed across the genome to di

227 No single-nucleotide polymorphisms (SNPs) exceeded genome-wide significance i

228 In aggregate, common single-nucleotide polymorphisms (SNPs) explained between 20% and 29% of th

229 ces of three nonsynonymous single nucleotide polymorphisms (SNPs) for the high affinity receptor for

230 cases and controls for 93 single nucleotide polymorphisms (SNPs) from 7 genes.

231 ry statistics obtained for single-nucleotide polymorphisms (SNPs) identified from a genome-wide assoc

232 ociations of 19,830 common single-nucleotide polymorphisms (SNPs) in 151 Wnt pathway autosomal genes

233 89 new highly informative single nucleotide polymorphisms (SNPs) in 305 individuals with Haplogroup

234 s the relationship between single nucleotide polymorphisms (SNPs) in nonsteroidal anti-inflammatory d

235 ide variants (SNVs) due to single nucleotide polymorphisms (SNPs) in the genome, or RNA editing event

236 ree major variants through single-nucleotide polymorphisms (SNPs) in the primary miRNA outside the ma

237 al analysis on known index single nucleotide polymorphisms (SNPs) indicated an additional independent

238 (2) Single nucleotide polymorphisms (SNPs) known to be involved in human eye c

239 for sensitive detection of single nucleotide polymorphisms (SNPs) on a surface plasmon resonance imag

240 By using the 2,271,584 single nucleotide polymorphisms (SNPs) on the panel from previous studies,

241 ng potentially pleiotropic single nucleotide polymorphisms (SNPs) possibly acting via obesity-related

242 through the genotyping of single nucleotide polymorphisms (SNPs) representing linkage blocks of the

243 ficant association between single nucleotide polymorphisms (SNPs) rs1800544 ADRA2A (odds ratio: 1.69;

244 Single-nucleotide polymorphisms (SNPs) that surpassed a significance thres

245 genome wide set of 14 559 single-nucleotide polymorphisms (SNPs) to identify the likely source popul

246 ed GWAS to explore whether single nucleotide polymorphisms (SNPs) were associated with functional and

247 -sequenced and genome-wide single nucleotide polymorphisms (SNPs) were selected to develop a large-sc

248 aluated the association of single nucleotide polymorphisms (SNPs) with natural log-transformed PTH co

249 en genetic variants (e.g., single nucleotide polymorphisms (SNPs)) and quantitative traits (QTs) such

250 between IA development and single nucleotide polymorphisms (SNPs), but many SNPs have not been replic

251 Single nucleotide polymorphisms (SNPs), the most common genetic markers in

252 ost potentially associated single-nucleotide polymorphisms (SNPs), whereas the markers on the other c

253 equence repeats (SSRs) and single nucleotide polymorphisms (SNPs).

254 th between two consecutive single-nucleotide polymorphisms (SNPs).

255 e identified more than 300 single-nucleotide polymorphisms (SNPs).

256 of millions of documented single nucleotide polymorphisms (SNPs).

257 o pinpoint disease-causing single nucleotide polymorphisms (SNPs).

258 s among ST382 strains were single nucleotide polymorphisms (SNPs).

259 significant (P<5 x 10(-8)) single-nucleotide polymorphisms (SNPs): 19 novel, 15 previously identified

260 ion (n = 769) yielded nine single-nucleotide polymorphisms (SNPs): G-1106A, A-1018T, T-1014C, T-988G,

261 tion in plasma and two LPA single-nucleotide polymorphisms ([SNPs] rs10455872 and rs3798220) with all

262 genotyped nine IL13 "tag" single nucleotide polymorphisms (tag SNPs) in 367 challenge-proven food al

263 omal copy number variation (CNV) refers to a polymorphism that a DNA segment presents deletion or dup

264 he largest effect is caused by an amino acid polymorphism that arose when an ancestral threonine was

265 el, and weight gain data to identify genetic polymorphisms that are associated with variation in inte

266 mputation revealed 660,238 single nucleotide polymorphisms that are rare (<1%) or absent in European

267 of LOX-1 have also uncovered various genetic polymorphisms that could modulate the risk of atheroscle

268 Incorporating knowledge of polymorphisms that occur before the emergence of multidr

269 We then evaluated polymorphisms that showed the strongest association with

270 Notably, for both individual and combined polymorphisms, the above similar recurrence risks were p

271 Two common polymorphisms, the c. 1298A > C, of the methylene-tetrah

272 utation rate and conserved single-nucleotide polymorphisms to identify discrete transmission chains,

273 additive effects of all 11 single-nucleotide polymorphisms to provide a prediction of the responsiven

274 genetically related (</=2 single-nucleotide polymorphisms) to >/=1 previous TS+/FT+ case or TS+/FT-

275 metabolic interactions and single-nucleotide polymorphism-trait associations not identified by the fo

276 ion by using clustering of single nucleotide polymorphisms' trajectories and (ii) use quantitative po

277 ents on fat crystallization was analyzed for polymorphism using powder X-ray diffraction, solid fat c

278 Patients were genotyped for the following polymorphisms: VKORC1-1639G>A, CYP2C9*2, CYP2C9*3, and C

279 The single nucleotide polymorphism was examined in the key genes of the folate

280 olate levels among tomato accessions, little polymorphism was found in folate biosynthesis genes.

281 phenotype based on 645 714 single-nucleotide polymorphisms was associated with atrial fibrillation (o

282 genomes to weight the GWAS single-nucleotide polymorphisms, we improve the statistical power of the g

283 , those with the rs1898671 single-nucleotide polymorphism were more likely to have stopped all other

284 A few new highly prevalent amino acid polymorphisms were also identified.

285 Here we investigated whether UBAC2 polymorphisms were associated with BD in a Japanese popu

286 In valproate subjects, no common polymorphisms were associated with seizure status.

287 ds ratio and 95% confidence intervals of all polymorphisms were estimated using the random-effect mod

288 nd patatin-like phospholipase-3 rs738409 C>G polymorphisms were genotyped; and IFN-stimulated gene he

289 Twenty-one single-nucleotide polymorphisms were significantly associated with lean bo

290 onset cutoffs; significant single nucleotide polymorphisms were tested in nine independent replicatio

291 Many CPPs exhibit some sort of structural polymorphism, where the secondary structure of the pepti

292 We also examined the LTA4H promoter polymorphism, which predicted cerebrospinal fluid (CSF)

293 curring alterations, including mutations and polymorphisms, which profoundly affect the cells in whic

294 We examined the association of the polymorphism with asthma and airway obstruction within a

295 s the association of EFNB3 single nucleotide polymorphisms with human hypertension risks, using 3,448

296 Single-nucleotide polymorphisms with P <5x10(-)(5) were prioritized accord

297 cific origin of HBB is confirmed by sequence polymorphisms within human xenograft-derived CTCs in mou

298 Single nucleotide polymorphisms within the prion protein gene have been li

299 Putative loss-of-function polymorphisms within the START domain protein were assoc

300 ronment interaction between EoE-predisposing polymorphisms (within TSLP, LOC283710/KLF13, CAPN14, CCL

301 g Y-STRs and Y-chromosomal single nucleotide polymorphisms (Y-SNPs).