ライフサイエンスコーパス: genetic analyses

1 me (~32 Gb) presents a formidable barrier to genetic analyses.

2 e letters was evaluated as a new endpoint in genetic analyses.

3 importance of accounting for environment in genetic analyses.

4 ttern of calcifications to better target the genetic analyses.

5 s, MMA, and DMA and were also phenotypes for genetic analyses.

6 o growing interest in performing multi-trait genetic analyses.

7 bservational and 162 124 participants in the genetic analyses.

8 markers that facilitate powerful population genetic analyses.

9 ges in live-cell imaging and high-throughput genetic analyses.

10 Specimens with MSI were identified by genetic analyses.

11 y powerful strategy to facilitate systematic genetic analyses.

12 , flow cytometry, cytogenetic, and molecular genetic analyses.

13 s was demonstrated in vivo by phenotypic and genetic analyses.

14 er incorporating them into future population genetic analyses.

15 ed cell sorting (BONCAT-FACS) for subsequent genetic analyses.

16 ndividuals with T2D who provided consent for genetic analyses.

17 omy, stable isotopes, radiocarbon dating and genetic analyses.

18 study and underwent clinical evaluation and genetic analyses.

19 ipolar disorder cases and 5,000 controls for genetic analyses.

20 rease the accuracy and power of quantitative genetic analyses.

21 nting to rituximab (375 mg/m(2)) therapy and genetic analyses.

22 eactive protein levels were not mediators in genetic analyses.

23 xaminations; and laboratory tests, including genetic analyses.

24 prostate cancer with multiple metastases for genetic analyses.

25 and highlight the importance of sex-specific genetic analyses.

26 ic recording at rest and during exercise and genetic analyses.

27 based on these data and inference from human genetic analyses.

28 f identity by descent (IBD) are used in many genetic analyses.

29 Psks) have been identified through classical genetic analyses.

30 ese Japanese subpopulations using population genetics analyses.

31 In causal, genetic analyses, a 0.5-mmol/l (19.4-mg/dl) lower LDL ch

32 erform univariate and bivariate quantitative genetic analyses adjusting for age, age(2), sex, their i

33 Reverse genetic analyses also show that phy mutants of the moss

34 Using genetic analyses and 44 years of data from Camp Leakey,

35 Genetic analyses and a carotenoid cleavage inhibitor ind

36 We performed genetic analyses and an exhaustive phenotypic and functi

37 d genomes sometimes complicate developmental genetic analyses and comparisons to humans.

38 Using high-resolution genetic analyses and fate-mapping studies, three main mo

39 incorporating high-dimensional phenotypes in genetic analyses and in breeding schemes poses important

40 We performed detailed genetic analyses and intracellular flow cytometry to det

41 sociations with ICH, which were confirmed by genetic analyses and LDL-C-lowering trials.

42 diction, in vivo protein-DNA binding assays, genetic analyses and monitoring of epigenetic amino acid

43 haploid genome of C. reinhardtii facilitates genetic analyses and offers many of the advantages of mi

44 Genetic analyses and randomized trials suggest that low-

45 Genetic analyses and shipping records show that this obs

46 Genetic analyses and systematic mutagenesis have reveale

47 electron microscopy, immunofluorescence and genetic analyses, and high-speed video microscopy.

48 undergone some form of spatial or population genetics analyses, and this has revealed striking differ

49 lular [CO2 ] (Ci ) remains controversial and genetic analyses are needed.

50 Recent advances in imaging and molecular and genetic analyses are postulated as promising strategies

51 kthrough has been a focus on families, where genetic analyses are strongest, versus large-scale, case

52 Genetic analyses, based on mitochondrial DNA and microsa

53 Here, by performing chemical genetic analyses, biochemical assays, structural modelin

54 In this study, genetic analyses, biochemical characterizations, and phy

55 Here we combined complex genetic analyses, biochemical studies and pharmacologica

56 henotype/genotype correlations, we performed genetic analyses by direct sequencing and multiplex liga

57 ere was no evidence for confounding of these genetic analyses by horizontal pleiotropy.

58 e freshwater populations, despite population genetic analyses clearly supporting their young age, hav

59 Population-level genetic analyses combined with experiments in cellular m

60 Molecular genetic analyses confirmed that these animals expressed

61 Genetic analyses confirmed the pathogenic expansion in 1

62 ormation will likely be available from tumor genetic analyses, creating an efficient opportunity to i

63 We used a combination of genetic analyses, cytology and immunolocalisation to def

64 In summary, our systems genetics analyses defined the effect of T1D risk alleles

65 Observational and genetic analyses demonstrate a concordant, positive and

66 Our genetic analyses demonstrate that in stigmas, five MAPK

67 Genetic analyses demonstrate that the PPKs are collectiv

68 Further, genetic analyses demonstrate that the protein products o

69 ChIP-seq and genetic analyses demonstrate the importance of these int

70 uaranjavirus genus, additional antigenic and genetic analyses demonstrated that it is closely related

71 Genetic analyses demonstrated that the defective embryog

72 Genetic analyses demonstrated that Top1cc-dependent larg

73 High-resolution genetic analyses detected long-term temporal stability a

74 These genetic analyses determine the roles of starch biosynthe

75 thiazide responsiveness was not blunted, and genetic analyses did not show mutations in genes associa

76 Further genetic analyses discovered a tight linkage of the Htg9.

77 Completing the puzzle, population genetic analyses discriminated Corsica as the origin of

78 r, about 25% of all samples are rejected for genetic analyses for reasons that include too little tis

79 tudy highlights the importance of functional genetic analyses for the identification of new concepts

80 In this study, we performed genetic analyses for three Lebanese families with ARCI,

81 of face recognition (61%), and multivariate genetic analyses found that most of this genetic influen

82 collection of programs to perform population genetics analyses from next-generation sequencing data.

83 Genetic analyses further confirmed this metabolic hetero

84 Genetic analyses further show that 31 infiltration-relat

85 Our genetic analyses further support the conclusion that CRL

86 In exploratory genetic analyses, GNB3 single-nucleotide polymorphism rs

87 nrelated, could restore viability.IMPORTANCE Genetic analyses have been instrumental in deciphering t

88 While epidemiological data and viral genetic analyses have both independently shed light on t

89 Biochemical and genetic analyses have confirmed that six viral proteins

90 Although genetic analyses have demonstrated partially overlapping

91 ntified by in silico structural predictions, genetic analyses have demonstrated that the ompA RNA the

92 Moreover, until now, genetic analyses have not been applied to biparentally i

93 Biochemical and genetic analyses have previously identified caffeoyl shi

94 Biochemical and genetic analyses have recently demonstrated that counter

95 Genetic analyses have shown that these cleavage events a

96 Recent advances in genetic analyses have significantly refined human type 1

97 tive protein acetylation studies and forward genetic analyses identified a JmjC domain-containing pro

98 Additional biochemical and genetic analyses identified Nfu as an Fe-S cluster carri

99 Population genetic analyses identified significant population struc

100 Indeed, chemical and genetic analyses identified the lipopeptide fengycin as

101 Mass spectral and genetic analyses identified the major chloroplast galact

102 Coalescence-based multi-locus and population genetic analyses identify at least four separate and mon

103 Genetic analyses implicate both proteins as critical for

104 Our genetic analyses implied that BCL9 necessitates other in

105 rating hypotheses and facilitate comparative genetic analyses in future P. acnes research.

106 es the importance of comparative genomic and genetic analyses in future research.

107 We performed genetic analyses in individuals with available genomic d

108 Our genetic analyses in M. tuberculosis showed that nonfunct

109 Here we identify, through molecular and genetic analyses in mice, lipocalin 2 (LCN2) as an osteo

110 ting Wnt signaling, we performed an array of genetic analyses in murine tooth development, where Lrp4

111 g time has been a major focus of comparative genetic analyses in plant development.

112 post-mortem blood has not been subjected to genetic analyses in relation to cancer.

113 Through genetic analyses in Schizosaccharomyces pombe, we found

114 ccuracy, reliability, and reproducibility of genetic analyses in various applications require optimiz

115 movements have been investigated by reverse genetics analyses in Arabidopsis (Arabidopsis thaliana),

116 Genetic analyses included 120 white AREDS2 participants

117 Genetic analyses included homozygosity mapping and exome

118 Genetic analyses including AMOVA (F(RT) = 0.200), Barrie

119 Genetic analyses including FISH confirmed a loss of the

120 as food web structure analysis, also rely on genetic analyses including the DNA barcoding technology.

121 l and genetic maps, making novel genomic and genetic analyses, including map-based cloning, feasible.

122 ich is used as the basis for a wide range of genetic analyses, including studies of variation within

123 Genetic analyses indicate roles for plant-specific DNA-d

124 Genetic analyses indicate that eno exhibits synergistic

125 Transcriptomic and genetic analyses indicate that insect killing occurs as

126 Indeed, our genetic analyses indicate that muscles send inductive dI

127 Our evolutionary genetic analyses indicate that new species in this genus

128 Genetic analyses indicate that these B-GATAs act upstrea

129 Our genetics analyses indicate that plants with a hypomorphi

130 t Arabidopsis mutant (gre1) was isolated and genetic analyses indicated that a dysfunctional red (R)

131 Further genetic analyses indicated that dElys depletion re-activ

132 Quantitative genetic analyses indicated that overall CS surface area

133 Genetic analyses indicated that the P0(Br) -SKP1 interac

134 pelagic environment was further supported by genetic analyses, indicating a transportation of methano

135 Genetic analyses, live-cell microscopy, and simulations

136 Population genetic analyses of 150 individuals sampled in Korea, Ne

137 Genetic analyses of 151 patients defined pathogenic muta

138 Family-based genetic analyses of 838 individuals (372 affected and 46

139 We performed genetic analyses of a multiethnic cohort of patients wit

140 Genetic analyses of a newly developing ECD lesion reveal

141 Genetic analyses of a subset of these isolates identifie

142 Genetic analyses of Arabidopsis UMP1 revealed that, unli

143 Molecular genetic analyses of both point mutants reveal an importa

144 Genetic analyses of brain measures from tens of thousand

145 High-resolution genetic analyses of carriage and disease isolates can es

146 We used quantitative genetic analyses of data from living nonhuman primates a

147 bium legume symbiosis (RLS)(8) or by reverse genetic analyses of differentially expressed candidate g

148 Combinatorial loss- and gain-of-function genetic analyses of Eve target genes indicate that the i

149 Genetic analyses of fish brpf1 and mouse Brpf1 have unco

150 As the first series of genetic analyses of gut microbiome composition in humans

151 Detailed genetic analyses of HGT1 bladder tumors identify feature

152 expression in expanding leaves, and reverse genetic analyses of homologous NS1 target genes in Arabi

153 Genetic analyses of inbred mouse strains identified loci

154 We also combine quantitative genetic analyses of interacting sex-specific traits in D

155 udy aims to resolve this controversy through genetic analyses of Isla Mocha camelid remains dating fr

156 Recent genetic analyses of large populations have revealed that

157 Quantitative genetic analyses of life span and the micro-environmenta

158 Genetic analyses of liver tissues from patients have pro

159 r study warrant further evaluation in future genetic analyses of melanoma.

160 Genetic analyses of MGUS cells have provided evidence th

161 This emerging field encompasses detailed genetic analyses of natural populations, comparative gen

162 Genetic analyses of patients with MEHMO syndrome, an X-l

163 Genetic analyses of patients with severe spine segmentat

164 etic architecture of autism and suggest that genetic analyses of phenotypic extremes, such as female-

165 Computational genetic analyses of physical dependence on morphine acro

166 nsider recent comparative studies, including genetic analyses of plant mating events, population stru

167 Phenotypic and genetic analyses of TF mutants enable the organization o

168 Moreover, molecular and genetic analyses of the co-regulation by GAs and BRs of

169 ual Aux/IAA genes have specialized function, genetic analyses of the family have been limited by the

170 We performed genetic analyses of the HLA complex in patients with PSC

171 Population genetic analyses of the key drug resistance-mediating po

172 Genetic analyses of the new virus genome revealed a clas

173 In-depth genetic analyses of the oral microbiome through metageno

174 Biochemical and genetic analyses of the paralogs within Sulfolobus islan

175 Cell biological and genetic analyses of these SH3 partners implicate them in

176 microfluidic compact disc (CD) to perform 30 genetic analyses of three different species of foodborne

177 ameters and have revolutionized quantitative genetic analyses of wild populations.

178 report detailed morphometric, isotopic, and genetic analyses of Zhur that reveal details of her appe

179 Reverse genetics analyses of PA-X substitutions conserved in hum

180 Population genetics analyses of the focal editing sites further rev

181 ed comparative developmental, expression and genetic analyses on single and double vrs mutants to lea

182 ed comprehensive evolutionary and population genetics analyses on over 18 million DHSs discovered in

183 Combined with previous structural and genetic analyses, our results strongly suggest that Scm

184 an effectively prioritize causal variants in genetic analyses, particularly highly penetrant contribu

185 provide an overview of the primary types of genetic analyses performed for atrial fibrillation, incl

186 Previous genetic analyses predicted Pericarp Color1 (P1; R2R3-MYB

187 Genetic analyses prioritized rs11263763 and four other S

188 In this work, our genetic analyses prove that P4H5, and to a lesser extent

189 Genetic analyses provided conclusive evidence that fitne

190 ombination of cell-type-specific genomic and genetic analyses provides a means to dissect cellular an

191 The genetic analyses refine the oceanographic model indicati

192 with an emphasis on the immunophenotypic and genetic analyses required to assign prognosis, risk stra

193 Our biochemical, structural, and genetic analyses reveal a complex signaling network by w

194 Consistent with this mechanism, genetic analyses reveal that IME4 functions upstream of

195 Cellular and genetic analyses reveal that injury induces blastema for

196 Our genetic analyses reveal that Lats1/2 kinases suppress ex

197 Genetic analyses reveal that phyB1 phyB2 double mutants

198 Further genetic analyses reveal that translational errors upregu

199 Biochemical and genetic analyses revealed a drought stress-activated mit

200 Our genetic analyses revealed a function of dynamin in prope

201 Genetic analyses revealed an overrepresentation of antib

202 Genetic analyses revealed association of intronic PCSK6

203 Genetic analyses revealed discordance between the mitoch

204 . spindale and S. indicum were assembled and genetic analyses revealed high levels of diversity withi

205 Genetic analyses revealed MEcPP-mediated COI1-dependent

206 Genetic analyses revealed recurrent somatic inactivation

207 Transcriptome-instructed genetic analyses revealed that (1) one broadly expressed

208 inctive morphology sampled from the volcano, genetic analyses revealed that 65 had C. elephantopus an

209 Our genetic analyses revealed that CD4(+) effector memory T

210 Genetic analyses revealed that four pairs of genes were

211 Structure-guided molecular genetic analyses revealed that it has distinct and well-

212 Both phylogenetic and population genetic analyses revealed that J. microsperma diverged f

213 Proteomic and genetic analyses revealed that multiple IFN-I-stimulated

214 Transcriptomic and genetic analyses revealed that neurons positive for the

215 Genetic analyses revealed that PITG_04584, which lacks c

216 Protein interaction and genetic analyses revealed that PRDM9 interacts with STAG

217 Chromatin immunoprecipitation (ChIP)-Seq and genetic analyses revealed that PvrA directly regulates g

218 In Arabidopsis, genetic analyses revealed that response to these stresse

219 Biochemical and genetic analyses revealed that SLB1 controls M. truncatu

220 Pharmacological and genetic analyses revealed that the necrotic cell death i

221 Genetic analyses revealed that the Piezo and Pain ion ch

222 Genetic analyses revealed that the sfps-2 rrc1-3 phenoty

223 Refined genetic analyses revealed unique haplotype blocks confer

224 In genetic analyses, rs10493380 in LEPR was associated with

225 ncreasing ambient temperature and population genetic analyses show little evidence of differential su

226 Our genetic analyses show M. guttatus is highly dispersive a

227 Structural and genetic analyses show MglA-SspA facilitates sigma(70) bi

228 Extensive live imaging and genetic analyses show that abscission failure is due to

229 Genetic analyses show that the mutant locus is dominant

230 Population genetic analyses show that the segment ratio at this equ

231 Genetic analyses showed that all subtypes had an excess

232 Genetic analyses showed that AtPTPN is required for HSFA

233 Genetic analyses showed that the BN-J phenotype results

234 Genetic analyses showed that the neoplastic epithelium a

235 Pharmacological and genetic analyses showed that the NMDA-triggered microgli

236 Population genetic analyses showed that ZmMADS69 was a target of se

237 Reverse genetics analyses showed that the ability to induce a ro

238 Population genetic analyses, Statistical Parsimony, and Bayesian me

239 Accordingly, cytogenetic and molecular genetic analyses, such as conventional karyotyping, fluo

240 utilized to convey a Hh morphogen gradient, genetic analyses suggest craniofacial development does n

241 Genetic analyses suggest that APM-2/mu2 acts upstream of

242 However, molecular genetic analyses suggest that autosomal common variants

243 Genetic analyses suggest that Ccr4-Not acts upstream of

244 Genetic analyses suggest that conventional associations

245 d results and initial field-based population genetic analyses suggest that despite reductions in dive

246 Imaging of junctional components and genetic analyses suggest that epidermal microtubules fun

247 Cell-type-specific expression and genetic analyses suggest that Fili sends a transsynaptic

248 mutants even in the absence of H2O2 Further genetic analyses suggest that OxyR2-activated AhpC modul

249 In addition, genetic analyses suggest that some comorbidities may be

250 Biochemical and genetic analyses suggest that the derivative compounds i

251 Further genetic analyses suggest that UNC-104 functions downstre

252 Our findings support previous genetic analyses suggesting that long-term use of PCSK9

253 bining these maps and models with functional genetic analyses suggests that distinct DNA-protein inte

254 have been dissected through a combination of genetic analyses, superresolution microscopy, and electr

255 Genetic analyses supported coordinated regulation of c-d

256 We performed a series of genetic analyses, taking into account the parent-of-orig

257 review the hormonal assessments and specific genetic analyses that are useful additional tests, and d

258 The data presented here support the genetic analyses that mutations in SLC24A4 and SLC24A5 a

259 We hypothesize, guided by structural and genetic analyses, that a unique hydrophobic environment

260 ough unbiased genetic screens and systematic genetic analyses, that autophagy is required cell autono

261 Although blood is preferable for genetic analyses, this study offers an alternative when

262 We undertook large-scale human genetic analyses to address this question.

263 c sampling and individual-based conservation genetic analyses to assess genetic diversity and levels

264 nuclear magnetic resonance spectroscopy, and genetic analyses to characterize this trimolecular event

265 ive ability) are highly heritable, molecular genetic analyses to date have had limited success in ide

266 ere, we use a combination of biochemical and genetic analyses to demonstrate that the ability of the

267 We performed genetic analyses to determine whether hedgehog signaling

268 rrying out antigenic analyses in addition to genetic analyses to evaluate control measures such as va

269 attery [13] in conjunction with quantitative genetic analyses to examine whether cognitive performanc

270 Our findings have utility in the design of genetic analyses to identify such novel CRC risk genes.

271 Here, we use comprehensive genetic analyses to identify the pathway required for C.

272 his question, we applied cell biological and genetic analyses to investigate guard cell walls and the

273 used ex vivo invasion assays and population genetic analyses to investigate the involvement of compl

274 we combine crystallographic, biochemical and genetic analyses to show that two dsDNA binding sites se

275 raction screen, a CIF peptide antagonist and genetic analyses together implicate SERK proteins as ess

276 Our genetic analyses uncover the in vivo context-dependence

277 Genetic analyses used Mendelian randomization (MR) and d

278 Genetic analyses using ATG7-deficient cells indicate tha

279 We performed genetic analyses using data on the genotype-tissue expre

280 We also performed population genetic analyses using genome-wide SNPs.

281 Further genetic analyses using loss-of-function and gain-of-func

282 Genetic analyses using mutants in ABA synthesis (aba1 an

283 Genetic analyses utilising r(2) information will become

284 primers will be a useful resource for future genetic analyses, walnut breeding programs, high-level t

285 Using genetic analyses we identify Hipk as a repressor of both

286 Through functional and genetic analyses, we demonstrated that miR-125b induces

287 Through loss-of-function genetic analyses, we identified LOX3 and LOX4 as the pri

288 Using population genetic analyses, we show that most testis-specific para

289 Combining structural, biochemical, and genetic analyses, we show that pppGpp and ppGpp, as well

290 Genetic analyses were conducted with PLINK We found a si

291 Biochemical and genetic analyses were conducted with two closely related

292 Spatial and population genetic analyses were employed to examine the distributi

293 all available worldwide data were used, the genetic analyses were not powered for an effect size as

294 Genetic analyses were performed at the Center for Famili

295 Genetic analyses were performed in 23 patients.

296 obtained using FreeSurfer, and quantitative genetic analyses were performed in SOLAR.

297 Genetic analyses were reported combined across four race

298 derstand this difference better, we combined genetic analyses with electron cryo-tomography subtomogr

299 We combined high-throughput genetic analyses with mass spectrometry to systematicall

300 Systematic genetic analyses with retrograde signaling mutants revea