ライフサイエンスコーパス: polymorphism

1 cal structural changes and single nucleotide polymorphism.

2 tissue samples were screened for the rs6971 polymorphism.

3 tiation, accelerated evolution, and balanced polymorphism.

4 l characteristics associated with the UNC13A polymorphism.

5 nd in the level of intraspecific cocoon-type polymorphism.

6 and swimming pattern, and lack of flagellar polymorphism.

7 thyl-oxobutyrate, and the PTPN22 (rs2476601) polymorphism.

8 expected PCR amplicon and 101 primers showed polymorphism.

9 mechanisms of cell encapsulation and mineral polymorphism.

10 s of native (WT) and p.P888L SAP97, a common polymorphism.

11 drogens and has a germline missense-encoding polymorphism.

12 reater effect on protein stability than gene polymorphisms.

13 ygenic risk score with 313 single nucleotide polymorphisms.

14 copy-number and, therefore, expression-level polymorphisms.

15 enic mice expressing different cervid PrP(C) polymorphisms.

16 otation data to prioritize likely functional polymorphisms.

17 ic information from 86 613 single-nucleotide polymorphisms.

18 associated with different single nucleotide polymorphisms.

19 y in C57BL/6J congenic mice harboring DBA/2J polymorphisms.

20 udies using 1000-G imputed single-nucleotide polymorphisms.

21 including a rich and poorly understood solid polymorphism(1,3-5), an anomalous melting line(6) and th

22 n white-tailed deer found significantly less polymorphism (11 alleles), as was expected of a non-clas

23 out in 30 knock-in mice with the FAAH C385A polymorphism (20/30 AC + AA).

24 human subjects genotyped for the FAAH C385A polymorphism (36/79 AC + AA).

25 plexity of the molecular mechanisms by which polymorphisms affect diseases.

26 The manner in which these polymorphisms alter function varies from conserving norm

27 However, higher 52-single nucleotide polymorphism AMD genetic risk score was not associated w

28 n in the soybean genome and haplotype block, polymorphism among accessions and genotyping quality.

29 We examined polymorphisms among the 1,135 sequenced accessions of Ar

30 whole-genome high-quality single-nucleotide polymorphism analysis.

31 Here, combining rare polymorphism and base-resolution methylation data in hum

32 mplete and unrepresentative of the degree of polymorphism and diversity in human and animal populatio

33 Because both this polymorphism and early-life stress alter serotonin level

34 remains challenging given the high level of polymorphism and homology between HLA genes.

35 The structural polymorphism and physicochemical properties of these non

36 APIs predominantly exhibit polymorphism and the propensity to form solvates and hyd

37 tal, we analyzed 8,582,968 single-nucleotide polymorphisms and conducted a meta-analysis of the two c

38 iation between vitamin D receptor (VDR) gene polymorphisms and diabetes has also been described.

39 ression while haplotype analyses assessed B1 polymorphisms and genetic variation.

40 the state of the knowledge regarding genetic polymorphisms and SARS-CoV-2 and COVID-19.

41 strict filtering to exclude common germline polymorphisms and sites with poor coverage or mappabilit

42 Single-nucleotide polymorphisms and structural variants including deletion

43 The genome-wide DNA polymorphisms and the promising candidate genes identifi

44 CD39 is regulated via single-nucleotide-polymorphisms and upon activation of aryl-hydrocarbon-re

45 olygenic risk score (N=929 single-nucleotide polymorphisms) and tested for an association with clinic

46 D for nonsynonymous mutations, an excess of polymorphism, and a spike in the levels of silent polymo

47 as a model ternary nitride, with controlled polymorphism, and for device applications, enabled by co

48 o reduced antioxidant function in particular polymorphisms, and possible impact on lung function, hav

49 us, phenotypic diversity and neutral genetic polymorphism are decoupled: trophic diversity being grea

50 evidence suggests that gene transcriptional polymorphisms are a strategy deployed by pathogens to ev

51 ic mapping population in which all molecular polymorphisms are known and for which molecular endophen

52 PEX glaucoma-associated single-nucleotide polymorphisms are located in and affect activity of the

53 oth gene flow and selection-mediated ancient polymorphisms are prevalent in the genus Populus.

54 Single nucleotide polymorphisms are widely associated with disease, but th

55 These polymorphisms, Arg111Cys, Arg111His, Phe112Tyr, and Ala1

56 se origin, the actual incidence of oncogenic polymorphisms arising in naive pluripotent stem cells is

57 Polymorphism around ompA gene was associated with villag

58 Single nucleotide polymorphism array analysis revealed there was no haplot

59 mparing CNV Radar calls to single nucleotide polymorphism array results from acute myeloid leukemia a

60 tients with IBD carrying a single-nucleotide polymorphism associated with the disease (PTPN2 rs189321

61 We genotyped 21 single-nucleotide polymorphisms associated with atrial fibrillation in amb

62 net state of immunosuppression," and genetic polymorphisms associated with poor fungal immunity could

63 Eleven of these genes harbor polymorphisms associated with the precipitation gradient

64 this issue by aggregating single nucleotide polymorphism associations to nearest genes.

65 A common polymorphism at the haptoglobin (Hp) genetic locus is as

66 The latter display polymorphism at the microscopic level, both in cerebral

67 By single nucleotide polymorphism-based and sib-pair analysis, we show that t

68 We developed a polygenic single nucleotide polymorphism-based predictor of LV mass in 7,601 individ

69 which enable the analysis of not only small polymorphisms, but also complex, large-scale structural

70 a prevalent nonsynonymous single-nucleotide polymorphism (C/T, rs2034310) of the human CD300f recept

71 Such polymorphism can dramatically influence cytotoxicity, le

72 ng, it has been shown that single nucleotide polymorphisms can affect RNA secondary structure, and he

73 ure, and here we show that single nucleotide polymorphisms can affect RNA-protein interactions from o

74 Different polymorphisms can also induce different amounts of patho

75 Interhomolog polymorphism causes mismatches in recombining molecules,

76 PNPLA3 polymorphism (CC vs. CG/GG) did not reveal any significa

77 Six puberty-related single-nucleotide polymorphisms (combined into a weighted allelic score) w

78 The G(96) polymorphism comprised 75 +/- 5% of the total PrP from t

79 One way in which non-coding polymorphisms could cause disease is by affecting crucia

80 Single nucleotide polymorphism data were produced from a restriction site-

81 Single-nucleotide polymorphisms-dense regions support a hypothesis that th

82 otide polymorphisms where frequencies of the polymorphisms differed between resistant and susceptible

83 adolescence, growth impairment, NOD2/CARD15 polymorphisms, disease behavior, and positive anti-Sacch

84 ndividuals, and decomposes single-nucleotide polymorphism effects as either additive, partial dominan

85 ng landmark features of these genes: extreme polymorphism, excess of nonsynonymous changes in peptide

86 major conduit through which OA genetic risk polymorphisms exert their functional effects.

87 ential methylation or with single nucleotide polymorphisms exhibiting significant inter-population di

88 ploidy is the likely result of an autosomal polymorphism, for which the BALB/cByJ allele is recessiv

89 Increasing evidence suggests that amyloid polymorphism gives rise to different strains of amyloids

90 diometabolic disease, a 32-single-nucleotide polymorphism GRS was a strong, independent predictor of

91 The Hp genetic polymorphism has an intriguing effect on the quaternary

92 or gene, notably the A118G single nucleotide polymorphism, have been linked to individual differences

93 autophagy gene Atg16L1 and its T300A coding polymorphism identified by genome-wide association studi

94 Single nucleotide polymorphisms identified by whole genome sequencing were

95 n significantly associated single nucleotide polymorphisms identified from literature.

96 tion summaries out to 1000 single-nucleotide polymorphisms identified optimal prediction with a 44 si

97 ls more evidence for adaptive maintenance of polymorphism in AMP genes than has previously been appre

98 phages are controlled by the natural genetic polymorphism in an outbred population.

99 PO was not susceptible to the rs6971 genetic polymorphism in human brain and heart samples.

100 w for the direct characterization of amyloid polymorphism in hydrated and complex biological samples.

101 223 is not susceptible to the rs6971 genetic polymorphism in in vitro assays, has favorable in vivo c

102 ern is the recurrence of the same phenotypic polymorphism in many species of a clade.

103 A polymorphism in SLC44A2 (rs2288904-A) present in 22% of

104 t we sequenced has maintained high levels of polymorphism in some regions of its genome.

105 It is also shown that polymorphism in specific genes, NOTCH4 and CAT, is signi

106 identified a rare missense single nucleotide polymorphism in the BMP type 1 receptor ALK6 (rs34970181

107 influenza virus inoculum containing an A388V polymorphism in the HA stalk (45% wild type and 55% muta

108 ling responses, including a known functional polymorphism in the self-binding domain of the candidate

109 We found extensive polymorphism in the size and sequence of motifs.

110 The rs12608932 single nucleotide polymorphism in UNC13A is associated with amyotrophic la

111 We examine conditions that govern HttEx1 polymorphism in vitro, including concentration and the r

112 Employing in silico analyses, we ranked polymorphisms in C57Bl/6N substrain and selected genes C

113 Loss-of-function polymorphisms in CYP2B6 result in higher efavirenz conce

114 Sequence polymorphisms in enhancer DNAs are a major source of pop

115 Here we interrogate LOH of polymorphisms in essential genes as a novel class of the

116 -bp open reading frame that exhibits genetic polymorphisms in human populations.

117 We identified polymorphisms in inflammasome genes interferon gamma ind

118 y, we investigated whether single nucleotide polymorphisms in MHCII-DRB regulatory gene may be associ

119 these mutations are nonsynonymous SNPs, but polymorphisms in more than one codon or entire codon del

120 from different mouse strains and identified polymorphisms in murine CD300LF which are critical for i

121 py and temporally varying selection maintain polymorphisms in natural populations; and provided impor

122 Supergenes underlie striking polymorphisms in nature, yet the evolutionary mechanisms

123 Polymorphisms in NLRP1 are linked to asthma; however, th

124 Polymorphisms in regulatory regions of the CCL2 promoter

125 It is proposed that polymorphisms in RIN4 from distantly related plant speci

126 (TB), but the relevance of inflammasome gene polymorphisms in TB-associated pulmonary damage is unkno

127 Single-nucleotide polymorphisms in the capsule biosynthesis gene wzc lead

128 genome-wide association studies have linked polymorphisms in the CHRNA5-CHRNA3-CHRNB4 gene cluster,

129 of understanding the role of strain-specific polymorphisms in the context of this specific NS1 functi

130 esistance gene Rps1b through transcriptional polymorphisms in the effector gene Avr1b that occur in t

131 equency <0.1, and five of the most prevalent polymorphisms in the guide RNA target site in collection

132 Finally, single nucleotide polymorphisms in the human genome that occur near the re

133 ese results further implicate common genetic polymorphisms in the pathogenesis of DCM.

134 tracking of low levels of single-nucleotide polymorphisms in the population over time.

135 wn and new, non-synonymous single nucleotide polymorphisms in the propeller region of the kelch 13 ge

136 Genetic polymorphisms in the region of the trimeric serine hydro

137 100 a priori candidate seed size genes with polymorphisms in the top 1% of seed mass association, re

138 modifications by selected single nucleotide polymorphisms in vitamin D-related genes.

139 ping of 33 risk-associated single nucleotide polymorphisms) in addition to the standard PSA test that

140 ariants (SNVs) and 50,000 insertion-deletion polymorphisms (indels) for association to AD, using mult

141 The integration of genome-wide polymorphism information with the QTL mapping and expres

142 ls facilitate conversion of different PrP(C) polymorphisms into PrP(Sc).

143 quencing analyses reveal a single nucleotide polymorphism introducing a premature stop codon in the l

144 these results, we concluded that a flagellar polymorphism is essential for spreading in structured en

145 This spectral site polymorphism is expected to confer expanded "UV-blue" sp

146 Six correlated single nucleotide polymorphisms located in a brain-expressed lincRNA (ENSG

147 e distance of 8 (IQR 4-13) single nucleotide polymorphisms; low diversity between clusters of the sam

148 e identified 45 candidate genes with ancient polymorphisms maintained by balancing selection.

149 ncient haplotypes bear insertion or deletion polymorphisms, many of which are associated with specifi

150 Identification of this MIF gene polymorphism may help for predicting the risk of ACS.

151 , we hypothesized that certain immune-escape polymorphisms may impair Nef's ability to antagonize SER

152 s of BDNF availability, such as the Val66Met polymorphism, may orchestrate sensitivity to stress, tra

153 ied on methylation amplified fragment length polymorphism (metAFLP)-derived TTCIV characteristics, wh

154 ence, we hypothesized that DRB gene promoter polymorphism might lead to altered DRB gene expression,

155 e most strongly associated single-nucleotide polymorphism minor allele with increased BCL2 gene and p

156 Indeed, height-associated single nucleotide polymorphisms near genes encoding other proteins in this

157 y be due to non-synonymous single nucleotide polymorphisms (nsSNPs) within the AT1R gene.

158 re genotyped for rs4680, a single nucleotide polymorphism of COMT, and randomly allocated to either p

159 The polymorphism of MIF gene (rs755622, rs1007888 and rs2096

160 An association between a polymorphism of the adenosine A(2A) receptor (A(2A)R) en

161 oth the re-entrant melting behaviour and the polymorphism of the solid phase.

162 odialysis with rs855791, a single nucleotide polymorphism of the TMPRSS6 gene that is hypothesized to

163 hared ancestry results from either ancestral polymorphism or introgression among taxa.

164 ns to assess the effects of disease, genetic polymorphisms, or concomitant drug intake on pulmonary A

165 ne flow and the presence of shared ancestral polymorphisms, particularly those maintained by balancin

166 ibody, antiflagellin, and OmpC), NOD2/CARD15 polymorphisms, perianal disease, and ethnicity were risk

167 An A1d1a control region polymorphism predicted to influence transcription is fix

168 Remarkably, single nucleotide polymorphisms present at nearly 20% in East Asian popula

169 ed to quantitate the relative amounts of the polymorphisms present in other animal species and even h

170 es were found in individuals with a germline polymorphism preventing transcription of ENTPD1, encodin

171 Genotypes of 33 single nucleotide polymorphisms previously assigned to the complement, lip

172 Our results suggest that these gene polymorphisms provide further genetic evidence for the p

173 e homozygous for these two single-nucleotide polymorphisms, Rabl2L119F (rs80006029) and Rabl2V158F (r

174 This pattern of vast allelic polymorphism raises several questions-How do different s

175 d in most psychiatric disorders, and genetic polymorphisms reducing expression of the dopamine transp

176 h high-density genome-wide single nucleotide polymorphisms, reflecting a comprehensive and dynamic ge

177 orphism, and a spike in the levels of silent polymorphism relative to silent divergence, as well as a

178 NAs and miRNA-targets underlying shell color polymorphism remain largely unknown in mollusca.

179 comprising 65, 43, and 13 single nucleotide polymorphisms, respectively.

180 in interspecific hybrids, and/or high-impact polymorphisms resulted in a set of 43 candidate speciati

181 is group was likely facilitated by ancestral polymorphism resulting from early co-option of dsx as a

182 tigated the evolutionary history of a common polymorphism resulting in a Y529 versus C529 change in t

183 Analysis of the DNA polymorphisms revealed that 2347 nonsynonymous SNPs and

184 re, n = 20), showing putative association of polymorphisms rs13900(C/T) and rs2857656(G/C) with treat

185 cent evidence associates a single nucleotide polymorphism rs174547 within the FADS1 gene, encoding FA

186 upstream of ATP8B1 (index single nucleotide polymorphism rs2571244, minor allele frequency = 0.08, P

187 reviously, we discovered a single nucleotide polymorphism (rs2869462) associated with absolute abunda

188 database, in which donor and recipient IFNL4 polymorphisms (rs368234815, rs12979860, and rs117648444)

189 ent manner, using the TLR1 single-nucleotide polymorphism rs5743618 (1805G/T) as a marker for TLR2/1

190 timal prediction with a 44 single-nucleotide polymorphism score and cutoff at the 30th percentile.

191 se subtilisin/kexin type 9 single-nucleotide polymorphisms, serum proprotein convertase subtilisin/ke

192 ir success, the individual single-nucleotide polymorphism (SNP) analysis approach adopted in most cur

193 veraged exome-sequence and single nucleotide polymorphism (SNP) array data from 29,358 individuals in

194 The lead single nucleotide polymorphism (SNP) at 16p12.3 is rs78193826 (odds ratio

195 imating heritability using single-nucleotide polymorphism (SNP) data.

196 normal pairs (n = 135) and single-nucleotide polymorphism (SNP) genotyping of primary tumors (n = 914

197 score analyses, as well as single-nucleotide polymorphism (SNP) heritability and genetic correlation

198 ellite markers and > 9,000 single nucleotide polymorphism (SNP) markers generated using the 2bRAD app

199 ct and position sex-linked single nucleotide polymorphism (SNP) markers in 19 families from the GIFT

200 fferences in the degree of single-nucleotide polymorphism (SNP) occurring in cells cultured at three

201 ed that the rs73185306 C/T single-nucleotide polymorphism (SNP) represents a favorable predisposing f

202 y FADS genotype at the key single-nucleotide polymorphism (SNP) rs174537, to metabolize 18-carbon ome

203 G allele of the lead risk single nucleotide polymorphism (SNP) rs67180937 was associated with lower

204 ciation study identified a single-nucleotide polymorphism (SNP) signal across the glutamate-rich 3 (E

205 isolated an OsPIP1;3 gene single-nucleotide polymorphism (SNP) that is mostly expressed in rice root

206 of the genetic effect of a single nucleotide polymorphism (SNP), as well as non-genetic influences on

207 and the common MTNR1B risk single nucleotide polymorphism (SNP), rs10830963, associate with type 2 di

208 We further calculated the single-nucleotide polymorphism (SNP)-based heritability of 12 subfields, a

209 e it practical to estimate single-nucleotide polymorphism (SNP)-heritability among distantly related

210 rage to detect significant single nucleotide polymorphism (SNP)-trait associations, which leads to hi

211 etection of the BRAF V600E single-nucleotide polymorphism (SNP).

212 associated with the UNC13A single nucleotide polymorphism (SNP; p = 0.045 and p = 0.036).

213 evolution with over 10,000 single nucleotide polymorphisms (SNP) variants in many subtypes.

214 omprehensively analyse the single nucleotide polymorphism (SNPs) of the BLM gene.

215 thousands and thousands of single-nucleotide polymorphisms (SNPs) (big p) genotyped on tens of thousa

216 ciation studies-identified single-nucleotide polymorphisms (SNPs) affect remote genes remains unknown

217 s (TFs) and a total of 514 single nucleotide polymorphisms (SNPs) among the identified DEGs.

218 351,824 Single-Nucleotide Polymorphisms (SNPs) and 38 imputed Human Leukocyte Anti

219 ed transient variations in single-nucleotide polymorphisms (SNPs) and constant turnover of minor popu

220 hypothesis that individual single nucleotide polymorphisms (SNPs) and gene-level variants are associa

221 The integration between single nucleotide polymorphisms (SNPs) and miRNAs has been associated with

222 e thousands of genome-wide single-nucleotide polymorphisms (SNPs) and mitochondrial DNA to provide th

223 richment of SSc-associated single-nucleotide polymorphisms (SNPs) and predict the degrees of skin fib

224 The functional genes or single nucleotide polymorphisms (SNPs) are not obvious due to linkage dise

225 he primary data for AdaPT; single-nucleotide polymorphisms (SNPs) are selected because they are gene

226 (GWAS) have identified 14 single nucleotide polymorphisms (SNPs) associated with cutaneous SCC.

227 sortium to examine whether single nucleotide polymorphisms (SNPs) associated with GDF-15 levels with

228 ehensive identification of single nucleotide polymorphisms (SNPs) associated with periodontitis in di

229 Many single nucleotide polymorphisms (SNPs) associated with type 2 diabetes ove

230 previously identified five single nucleotide polymorphisms (SNPs) at four susceptibility loci for dif

231 res comprising millions of single-nucleotide polymorphisms (SNPs) could be useful for population-wide

232 btain 925,854 high-quality single-nucleotide polymorphisms (SNPs) enabling the refined grouping of th

233 FMD were genotyped for 18 single-nucleotide polymorphisms (SNPs) from 14 candidate genes.

234 The assay includes 5000 single nucleotide polymorphisms (SNPs) from euchromatic and 1000 from hete

235 (NGS) approach to examine single nucleotide polymorphisms (SNPs) from virus passaged in dose escalat

236 IL33 single nucleotide polymorphisms (SNPs) have been reproducibly associated w

237 We assessed germline single-nucleotide polymorphisms (SNPs) in 180 mCRC patients (Angiopredict

238 Single nucleotide polymorphisms (SNPs) in Apolipoprotein E (APOE) are know

239 SETTING, AND PARTICIPANTS: Single-nucleotide polymorphisms (SNPs) in HMGCR, NPC1L1, and PCSK9 associa

240 ge of more than 45 million single-nucleotide polymorphisms (SNPs) in the human genome and release the

241 allow for the detection of single-nucleotide polymorphisms (SNPs) in the pathogen genomes sourced fro

242 arental inbred lines using single nucleotide polymorphisms (SNPs) markers obtained via genotyping-by-

243 ence were genotyped for 95 single nucleotide polymorphisms (SNPs) related to energy homeostasis.

244 88% of disease-associated single-nucleotide polymorphisms (SNPs) reside in noncoding regions.

245 e, we use 3057 genome-wide single-nucleotide polymorphisms (SNPs) to evaluate population genetic stru

246 ed with 46,818 polymorphic single nucleotide polymorphisms (SNPs) using DArTseq.

247 Single nucleotide polymorphisms (SNPs) were assessed using the Illumina Hu

248 8%) or blood (~62%) and 24 single-nucleotide polymorphisms (SNPs) were genotyped.

249 Strongly associated single nucleotide polymorphisms (SNPs) were located in regulatory regions

250 ty control, association of single nucleotide polymorphisms (SNPs) with log-transformed FGF21 and FGF2

251 (GWAS) have linked IGF2BP2 single-nucleotide polymorphisms (SNPs) with type 2 diabetes (T2D).

252 ositional distributions of single-nucleotide polymorphisms (SNPs) within and outside essential splice

253 studies (GWAS) to identify single nucleotide polymorphisms (SNPs), associated with agronomic traits i

254 , including 1) deleterious single-nucleotide polymorphisms (SNPs), in-frame indels, and deletions; 2)

255 ic distance was 5 or fewer single-nucleotide polymorphisms (SNPs), whereas reinfection with a differe

256 The 8 PACG-associated single nucleotide polymorphisms (SNPs; rs11024102 at PLEKHA7, rs3753841 at

257 etes, based on independent single nucleotide polymorphisms strongly associated (p = 5 x 10(-6)) with

258 that has been observed with other protective polymorphisms, such as hemoglobin C.

259 ct on the human genome, with many protective polymorphisms-such as the sickle-cell trait-having been

260 ene sequences identified a single-nucleotide polymorphism that results in a premature stop in transla

261 o detection of informative single nucleotide polymorphisms that are linked to the trait.

262 We also identified Vpu polymorphisms that associate with functional differences

263 ther, downstream of inflammasome activation, polymorphisms that cause loss of gasdermin D function co

264 human history, selecting for red blood cell polymorphisms that confer innate protection against seve

265 -modulating roles of three common human MLKL polymorphisms that encode amino acid substitutions withi

266 most frequently the derived state for human polymorphisms that predispose to recurrent copy number v

267 o test this hypothesis, we identified 58 Nef polymorphisms that were overrepresented in HIV-infected

268 using a 10 non-recombinant single nucleotide polymorphism threshold, tested for clustering of demogra

269 We investigated KIR-allelic polymorphism to interrogate the role of NK cells in PD.

270 Upon repair of this polymorphism to the sequence present in Ypt and Ye, lipi

271 xtraordinarily diverse in sequence, and this polymorphism underpins an important mechanism of self/no

272 node is one specific SNP (Single Nucleotide Polymorphism) variant and the end is disease outcome.

273 nel, we identified 355 050 single nucleotide polymorphism variants and quantified the abundance of 93

274 n-level surveys of transposable element (TE) polymorphism via split alignment approaches, which has p

275 This single nucleotide polymorphism was expressed in human embryonic kidney cel

276 argeting outbreak-specific single nucleotide polymorphisms was applied to 290 isolates, which allowed

277 arly, the presence of FcyR single nucleotide polymorphisms was unimpactful.

278 ing 956 candidate EoE risk single-nucleotide polymorphisms was used to genotype 627 cases and 365 con

279 nalyses of the key drug resistance-mediating polymorphisms were analyzed in a cross-sectional survey

280 Six polymorphisms were associated with stroke recurrence and

281 779 subjects and 1,192,414 single-nucleotide polymorphisms were available for PRS-analyses.

282 Atomic models of 103 of the known human AT1R polymorphisms were constructed using the molecular dynam

283 his active loop of AgRP, four human missense polymorphisms were deposited into the NIH Variation View

284 arge repeat sequences, and single nucleotide polymorphisms were identified, which are valuable for st

285 Genetic polymorphisms were obtained from ImmunoChip analysis.

286 Genetic polymorphisms were obtained from Immunochip analysis.

287 Coding single nucleotide polymorphisms were sequenced in candidate genetic modifi

288 Up to 94 single-nucleotide polymorphisms were used as instrumental variables for al

289 identified as clusters of single nucleotide polymorphisms where frequencies of the polymorphisms dif

290 ed allele of the rs1800407 single nucleotide polymorphism, which produces a hypomorphic protein, may

291 200466 is a TLR2 promoter insertion/deletion polymorphism with contradictory data about its role in h

292 to explain the association of PACRG and PRKN polymorphisms with an increased susceptibility to intrac

293 garding the association of single nucleotide polymorphisms with AVNFH, transcriptomics, proteomics, m

294 etic architecture, consisting of many common polymorphisms with small individual effects.

295 A single non-synonymous polymorphism within a protein synthesis gene (RARS) is a

296 A common polymorphism within human BSND significantly associates

297 Polyglutamine (polyQ) tract polymorphism within the human androgen receptor (AR) sho

298 Polymorphisms within and around Toll interacting protein

299 COMT modulates catecholamine metabolism, and polymorphisms within the rs4680 allele result in variabl

300 well as dairy cows carrying the ABCG2 Y581S polymorphism (Y/S) and noncarrier animals (Y/Y).