ライフサイエンスコーパス: genetic analysis

1 rdalis Linnaeus 1758 [5], were included in a genetic analysis.

2 to deduce the minimum cellularity needed for genetic analysis.

3 tion, and their correlations using bivariate genetic analysis.

4 rom those reported for patients referred for genetic analysis.

5 recovery and near 100% purity), followed by genetic analysis.

6 and global level, providing a framework for genetic analysis.

7 tion and have also been subjected to reverse genetic analysis.

8 strum is a valuable new tool for genetic analysis.

9 acilitate the development of rapid tools for genetic analysis.

10 14,348 patients were included in the genetic analysis.

11 ing high-resolution live cell microscopy and genetic analysis.

12 d all eleven FgRabs by live cell imaging and genetic analysis.

13 the need of a suitable SEM software tool for genetic analysis.

14 , protein products can perdure, complicating genetic analysis.

15 to the zebrafish, a tool for high-throughput genetic analysis.

16 iregion and longitudinal tumour sampling and genetic analysis.

17 ; 78%), including patients with inconclusive genetic analysis.

18 significant new opportunities for functional genetic analysis.

19 ir subcellular localization and, critically, genetic analysis.

20 had potential to benefit from more extensive genetic analysis.

21 Fragman is a valuable new tool for genetic analysis.

22 accuracy of the predictions through reverse genetics analysis.

23 Genetic analysis allowed us to assign most of the new mo

24 Our population genetic analysis also enabled us to differentiate select

25 Through in vivo genetic analysis and culture studies we show that inhibi

26 cal interpretation of the genome, population genetic analysis and functional genomic analysis of alle

27 p of patients was included in a prespecified genetic analysis and genotyped for variants in CYP2C9 an

28 Using genetic analysis and high-resolution imaging, we found t

29 This model agrees with our previous genetic analysis and highlights the consequences of redu

30 ctions and may serve as the basis for highly genetic analysis and immunoassays.

31 Using a combination of genetic analysis and in vivo localization of fluorescent

32 ction of blood samples, which will allow for genetic analysis and interrogation of gene-environment i

33 Using genetic analysis and live imaging, we show that exc-6 re

34 The genetic analysis and manipulation of medfly has been sub

35 flower and leaf development, with classical genetic analysis and next-generation sequencing to addre

36 has been designed and synthesised for use in genetic analysis and RNA detection.

37 nted here will act as a resource for reverse genetic analysis and will be useful in deciphering molec

38 Here, using genetic analysis and X-ray crystallography, we show that

39 treous hemorrhage, biopsy yield was 100% for genetic analysis, and no patients showed recurrence or i

40 ilage include those previously identified by genetic analysis, and several mucilage proteins are redu

41 est level of genome coverage for genomic and genetic analysis because of their abundance and relative

42 Genetic analysis between TWD40-2 and AP2M of the AP2 com

43 howed evidence of intracellular storage, and genetic analysis confirmed a GLA A gene mutation (p.Asn2

44 Importantly, genetic analysis confirms that the F1 generation from po

45 Genetic analysis, conformational studies, in vitro assay

46 Curiously, this is consistent with previous genetic analysis defining MYB33 and MYB65 as the major f

47 Genetic analysis demonstrated that spontaneous arsenate-

48 Genetic analysis demonstrates that all three SEIPINs con

49 Finally, genetic analysis demonstrates that GmSNAP11 contributes

50 Population genetics analysis demonstrates that the Korean populatio

51 Thus, our chemical genetics analysis demonstrates the utility of the HCV ce

52 The genetic analysis favors a predominantly dominant-negativ

53 We then carried out a genetic analysis, focusing on major genes of the IL-2 pa

54 For this purpose, we carried out a genetic analysis for En and TE in grapevine, a major cro

55 Addition of a genetic analysis for one of the most prevalent amino aci

56 Genetic analysis generated many polymorphic alleles and

57 Including the genetic-analysis group as a covariate accounted for sign

58 Furthermore, fitting an LMM that utilized a genetic-analysis group rather than a self-identified bac

59 i-dimensional clustering method to define a "genetic-analysis group" variable that retains many prope

60 familial relatedness, PCs for ancestry, and genetic-analysis groups for additional group-associated

61 Additionally, genetic-analysis groups had significant heterogeneity of

62 Reverse genetic analysis has failed to reveal abnormal phenotype

63 Synthetic lethal genetic analysis has identified MAT2A as an anticancer t

64 Genetic analysis has identified PyST mutants defective i

65 Genetic analysis has now shown that, surprisingly, mimic

66 Genetic analysis has revealed that the dual specificity

67 Genetic analysis has revealed two sigma-1R mutants invol

68 first discovered, technological advances in genetic analysis have made finding genomic variation a m

69 Genetic analysis highlighted that Italian swine IDVs are

70 identified through sequence alignment and/or genetic analysis; however, few have been studied in vitr

71 g relatedness among samples is essential for genetic analysis; however, managing sample records and p

72 The subsequent genetic analysis identified ACS-4, an acyl-CoA synthetas

73 The genetic analysis identified an MLL2 gene mutation.

74 Genetic analysis identified differences in cpsM, cpsO, a

75 Synthetic genetic analysis identified mutations that exhibit a ful

76 Recent genetic analysis identified the functional domains of th

77 Genetic analysis identified the Srs2 helicase as a prime

78 Genetic analysis in 96 patients suspected of having keto

79 G modules and their regulators, validated by genetic analysis in both species.

80 rive array' platform to facilitate efficient genetic analysis in C. albicans.

81 An exploratory genetic analysis in Cpc-PH identified genes and biologic

82 Genetic analysis in Drosophila demonstrated the function

83 Genetic analysis in haploids provides unconventional yet

84 Here, we show by grafting and genetic analysis in Medicago truncatula that, in the AON

85 Genetic analysis in mice has revealed an essential role

86 The method described here permits forward genetic analysis in mice, limited only by the rates of m

87 A retrospective genetic analysis in our aHUS cohort (n=513) using multip

88 use results of forward genetic screening and genetic analysis in our new model to demonstrate that al

89 mbine molecular mapping, lineage tracing and genetic analysis in the adult fruit fly to gain new insi

90 Our recent genetic analysis in the mouse identified the kynurenine

91 ions and conduct a comprehensive genome-wide genetic analysis in these groups.

92 Genetic analysis in this study reveals that two calcineu

93 Genetic analysis in transplantation, when linked to demo

94 nd biochemical analysis in vitro and initial genetic analysis in vivo, prior studies implicated a pat

95 Here we use in vivo imaging and genetic analysis in zebrafish to show that Plxnd1 regula

96 nalysis of the PCSK6 locus combining further genetic analysis, in silico predictions and molecular as

97 Genetic analysis included linkage analysis (n = 17) with

98 Molecular genetic analysis included sequencing of BEST1 and co-seg

99 In addition, genetic analysis (including gene disruption and mutation

100 ples were obtained from all participants for genetic analysis, including whole-exome sequencing and m

101 Electron tomography and genetic analysis indicate that ECV biogenesis occurs via

102 Remarkably, population genetic analysis indicated that CREB1 displayed striking

103 Genetic analysis indicated that HemH induction is needed

104 Finally, a genetic analysis indicated that SECE2 plays an essential

105 Lastly, genetic analysis indicated that the type I secretion sys

106 Genetic analysis indicated that this improvement origina

107 Genetic analysis indicates that family 5 UDGb can also a

108 Genetic analysis indicates that TGD4 is epistatic to TGD

109 Genetic analysis indicates that the inhibition of cell p

110 Genetic analysis indicates the gain of function for A/U

111 ns for downstream histologic, molecular, and genetic analysis is hindered by low tumor yield due to i

112 Germline RB1 genetic analysis is important to identify heritable reti

113 issue, Siroy et al. demonstrate how clinical genetic analysis is moving from a single-gene Sanger-seq

114 Genetic analysis is required to identify the cause of th

115 tive complex (CSC) of the fungal retromer by genetic analysis, live cell imaging and immunological as

116 has been used as a quantitative phenotype in genetic analysis looking for Huntington's disease modifi

117 Genetic analysis made using random amplification of poly

118 s appears to be highly heritable and further genetic analysis may help identify new biological pathwa

119 tudied using both quantitative and molecular genetic analysis methods, both approaches lack studies s

120 LMNA-related cardiomyopathy, suggesting that genetic analysis might be useful for diagnosis and risk

121 This protocol can be combined with genetic analysis, molecular-activity probes and optogene

122 We performed a genetic analysis of 2 siblings with infant-onset achalas

123 Genetic analysis of 22 subjects was performed in a secon

124 In a genetic analysis of 3308 AA IBD cases and controls, we f

125 Here we present a comprehensive genetic analysis of 35 orphan transport proteins of Plas

126 and evolutionary history of this lineage by genetic analysis of 4,987 isolates from 99 countries and

127 emerging technique which enables systematic genetic analysis of a cellular or molecular phenotype in

128 This article reports the genetic analysis of a female with features of asthma and

129 In first step, sequence homology-based genetic analysis of a set of 50 coding SNPs associated w

130 thermore, by combining the genomic data with genetic analysis of an additional 800 isolates and envir

131 Genetic analysis of an Australian family with three male

132 stent silencing enables a detailed molecular genetic analysis of an inherited epigenetic state.

133 In a genetic analysis of Ashkenazi Jewish individuals, we ass

134 Genetic analysis of both mitochondrial (cox1) and nuclea

135 Detailed genetic analysis of C. muridarum passages revealed a tru

136 vances in our ability to perform a molecular genetic analysis of Chlamydia species.

137 lly for the accumulation of PSI in a forward genetic analysis of chloroplast biogenesis in maize.

138 However, these have been based on the genetic analysis of clinical case-control series.

139 of ophthalmologic examination and molecular genetic analysis of CNGB1.

140 quired for plant viability, facilitating the genetic analysis of color and pattern mutants.

141 Two bottlenecks impeding the genetic analysis of complex traits in rodents are access

142 Genetic analysis of DNA methyltransferase deletion mutan

143 Patients underwent genetic analysis of DNMT1 gene, neurophysiological tests

144 Genetic analysis of double, triple, and quadruple mutant

145 Selection and genetic analysis of drug resistant viruses revealed that

146 the degree of EGFR-signaling inhibition nor genetic analysis of EGFR was sufficient to predict sensi

147 We performed a genetic analysis of families with small intestinal carci

148 report on HistoMosaic, a novel technique for genetic analysis of formalin-fixed, paraffin-embedded ti

149 rphic mutations are a valuable tool for both genetic analysis of gene function and for synthetic biol

150 Forward genetic analysis of genetic crosses between different li

151 evidence of an exoticN. bombiorigin based on genetic analysis of globalNosemapopulations; the widespr

152 ebrafish is emerging as a powerful model for genetic analysis of hair cell development and function b

153 obtained their shopping information, and did genetic analysis of hepatitis A virus recovered from pat

154 make use of genealogic information can favor genetic analysis of highly polygenic traits, but not gen

155 Genetic analysis of host species determinants in the bla

156 transplantation may contribute to tools for genetic analysis of human germ cell development.

157 This is the largest genetic analysis of IRDs in the Israeli and Palestinian

158 g and is computationally efficient, enabling genetic analysis of large cohorts (up to 500,000 individ

159 odifiers, supporting expanded, comprehensive genetic analysis of larger HD datasets.

160 Large-scale genetic analysis of lethal phenotypes has elucidated the

161 Exploit genetic analysis of long living individuals to reveal ma

162 Genetic analysis of molecular markers is critical in tra

163 Genetic analysis of mutant phenotypes suggests that RecG

164 e now describe the first detailed population genetic analysis of P. acnes isolates recovered from pai

165 Genetic analysis of patients revealed several different

166 IGNIFICANCE STATEMENT This report provides a genetic analysis of primary nociceptive neuron mechanism

167 Combining proteomics, in vivo imaging and genetic analysis of proteins linked to planar cell polar

168 ause AGD is related to weight, we included a genetic analysis of pup weight at birth and weaning.

169 In conclusion, we report the first detailed genetic analysis of RCCs in TSC patients.

170 secondary pathway is a phosphorelay based on genetic analysis of receptor histidine kinase activity a

171 etics and three-point crosses with molecular genetic analysis of recombinants to generate the map.

172 Here, we combine genetic analysis of rib development with agent-based sim

173 s of pathogenic bacteria will permit forward genetic analysis of Rickettsia pathogenesis.

174 Reverse genetic analysis of several candidates identified new Pr

175 Genetic analysis of sporozoite factors reveals the 6-cys

176 w comparative genome analysis and a thorough genetic analysis of SSV1 using both specific and random

177 neurotransmitter, is a widely used model for genetic analysis of synapse function and development.

178 We conducted a genetic analysis of the A. aegypti chromosome region tig

179 mulation in plants and describe a population-genetic analysis of the Alyssum serpyllifolium (Brassica

180 Genetic analysis of the AnR subclones versus parental ce

181 validated by several methods that include a genetic analysis of the conserved PACT domain that recru

182 e DA D2/3-receptor antagonist sulpiride with genetic analysis of the DA D2 receptor in a behavioral s

183 ed on available samples followed by detailed genetic analysis of the entire sHGG cohort.

184 at the University of Washington launched the genetic analysis of the eukaryotic cell cycle and set th

185 candidate disease modifiers, we completed a genetic analysis of the family and conducted statistical

186 Through reverse genetic analysis of the functions of four ripening-relat

187 Retrospective genetic analysis of the FZD4 gene was performed (Sanger

188 In contrast, genetic analysis of the HAMP domain from the Tsr methyl-

189 Genetic analysis of the hemagglutinin (HA) and neuramini

190 e we report the biochemical, structural, and genetic analysis of the Mycobacterium tuberculosis homol

191 Large-scale genetic analysis of the native inhabitants of Rapa Nui (

192 Genetic analysis of the outer core in a temperature-sens

193 Oakleaf provides a new phenotypic marker for genetic analysis of the Primula S locus.

194 the MHC, discuss some of the challenges for genetic analysis of the region, and provide an update on

195 Molecular genetic analysis of the RS1 was performed and the c.288G

196 Molecular genetic analysis of the switch-like regulation of daf-7

197 has sufficient tumor-derived DNA to perform genetic analysis of the tumor, including DNA copy number

198 We present the first population genetic analysis of the wild population as well as of ca

199 ve next-generation (Next-Gen) transcript and genetic analysis of this class of tumor-inducing herpesv

200 Biochemical and genetic analysis of this RNA reveals that SAM binding in

201 Genetic analysis of three carcinomas and five adenomas f

202 portant to cancer will soon be identified by genetic analysis of tumours.

203 e paradigm of what is possible in functional genetic analysis of wheat.

204 erlying ecological isolation, and population genetic analysis of wild populations, we set out to dete

205 sor tRNAs have played important roles in the genetic analysis of yeast and worms.

206 canned twice with the same task; and imaging genetics analysis of the control group.

207 We conducted a large-scale genetic analysis on a case-control cohort comprising 537

208 We conducted a large-scale genetic analysis on giant cell arteritis (GCA), a polyge

209 To address this, we performed a quantitative genetic analysis on the reproductive history of 16,268 S

210 anced microarray detection system for either genetic analysis or other diagnostic assays.

211 In this study, we use lineage and genetic analysis, pharmacological inhibition, explant cu

212 Using genetic analysis, photo-cross-linking, and structural mo

213 Further population genetics analysis provided strong evidence of balancing

214 Genetic analysis revealed a canine rabies virus variant

215 Genetic analysis revealed a different TRI1 allele in the

216 Genetic analysis revealed a homozygous deletion at the D

217 Genetic analysis revealed a novel heterozygous mutation

218 Genetic analysis revealed a separate, undescribed hetero

219 Genetic analysis revealed neither germ line nor somatic

220 Population genetic analysis revealed significant genetic differenti

221 The genetic analysis revealed significant heritability of bo

222 Genetic analysis revealed that ALA1 and ALA2 acted to en

223 Our genetic analysis revealed that BAM1 functions together w

224 Genetic analysis revealed that CDK-8 most likely promote

225 Genetic analysis revealed that more than 80% of proviral

226 Genetic analysis revealed that rtel1 mutant plants show

227 Genetic analysis revealed that this novel disorder is ca

228 However, molecular and genetic analysis revealed that Tmeff2 is a weak binder o

229 Genetic analysis revealed that zebrafish hnf4a activates

230 Genetic analysis reveals interactions that are largely c

231 Genetic analysis reveals that a combination of mutations

232 Consistent with this activity, genetic analysis reveals that Mte1 functions with Mph1 a

233 between APC and the Hippo signaling pathway, genetic analysis reveals that YAP is absolutely required

234 ncurrent copy-number data, our comprehensive genetic analysis reveals the primacy of NF1 loss as the

235 Consistently, genetic analysis showed COOLAIR and Polycomb complexes w

236 Genetic analysis showed that organoids reflect the metas

237 Furthermore, genetic analysis showed that the orthologue of IME2, a '

238 Multivariate genetic analysis showed that, although some genetic and

239 Genetic analysis showed truncation mutations in 58 patie

240 ll divisions, combined with marker lines and genetic analysis, showed that the spch-5 leaf phenotype

241 Genetic analysis shows that all cells near the Upd sourc

242 Genetic analysis shows that BOP2 promotes photo-morphoge

243 Genetic analysis shows that Notch signaling controls the

244 nisms of gating has advanced rapidly through genetic analysis, structural biology and electrophysiolo

245 Genetic analysis suggested that BoNT/H has a hybrid-like

246 Further genetic analysis suggested that c-di-AMP was essential b

247 Genetic analysis suggested that CTR truncation disrupts

248 RNA profiling and genetic analysis suggested that the ZmARGOS1 transgene a

249 Genetic analysis suggests that Snf1 negatively regulates

250 Genetic analysis suggests that the HDAC protein HDA17 pl

251 Our genetic analysis suggests that tubulointerstitial cellul

252 erapy was successful, and histopathology and genetic analysis supported a diagnosis of extraocular uv

253 is of ethylene-dependent gene expression and genetic analysis supports SHORT HYPOCOTYL2, a repressor

254 Genetic analysis supports the model that EepR is in a co

255 However, we show by genetic analysis that the effect of SVP cannot be fully

256 signaling, we conducted a systematic forward genetic analysis through reporter-based screens in haplo

257 will allow the extensive infrastructure for genetic analysis to be applied to proteomic assays, whic

258 n=12) and isolates (n=10) were found through genetic analysis to be susceptible to macrolide antibiot

259 ed chemical fingerprinting of skin swabs and genetic analysis to explore the chemical cues that may u

260 Genetic analysis to identify the mutation was performed

261 genetic HoFH, highlighting the importance of genetic analysis to improve familial hypercholesterolemi

262 We combined imaging and genetic analysis to track melanoma-derived vesicles at o

263 The iBAC library represents an important new genetic analysis tool openly available to the research c

264 Molecular and genetic analysis uncovered a two-step mechanism, where r

265 Genetic analysis using biofilm formation-related Pseudom

266 quaternary structures made it amenable to a genetic analysis using in-frame insertions and deletions

267 A genetic analysis using mutants in the ABA signaling path

268 informatic techniques have been proposed for genetic analysis using networks, based on random walks,

269 ional tests of association, and classic twin genetic analysis using results of telephone interviews c

270 Genetic analysis was performed by whole-exome sequencing

271 Genetic analysis was performed in 17 of 22, confirming d

272 Genetic analysis was performed in 464 kidney transplanta

273 Genetic analysis was performed using SOLiD sequencing fo

274 Genome-wide genetic analysis was undertaken in 1263 Aboriginal Austr

275 Guided by the mouse genetic analysis, we demonstrate that genetic variation

276 Here, using genetic analysis, we demonstrate that mamK-like has an i

277 Using genetic analysis, we determined that the serine protease

278 In a genetic analysis, we identified loss of function mutatio

279 n hemiganglia of the same individual and, by genetic analysis, we identify the bithorax-complex genes

280 Through genetic analysis, we place Knk1 into a novel pathway con

281 Using genetic analysis, we show that loss of CIZ1 or deletion

282 ing polysomnography (PSG), brain imaging and genetic analysis, were used.

283 The GWAS data were used to guide reverse genetic analysis, which found effectors of ABA accumulat

284 ations include the small sample size for the genetic analysis, which was underpowered to detect genom

285 ic susceptibilities in individual disorders, genetic analysis with increased numbers of variants and

286 However, approaches for synthetic genetic analysis with null-alleles in metazoans have not

287 Based on Genetic Analysis Workshop (GAW) 19 data, this article di

288 n data from 20 pedigrees, the members of our Genetic Analysis Workshop (GAW) 19 gene expression group

289 sults and application to gene DNAH9 from the Genetic Analysis Workshop 16 for associated with Anti-cy

290 sed method is demonstrated by applying it to Genetic Analysis Workshop 16 rheumatoid arthritis GWAS d

291 posed GCP method is applied to data from the Genetic Analysis Workshop 16.

292 on studies and applications to data from the Genetic Analysis Workshop 17 and the Ocular Hypertension

293 d by using whole genome sequencing data from genetic analysis workshop 18 (GAW18).

294 pplied the method to a real dataset from the Genetic Analysis Workshop 18 (GAW18).

295 The Pathway-based Analyses Group of the Genetic Analysis Workshop 19 (GAW19) sought reduction of

296 longitudinal analytical approaches from the Genetic Analysis Workshop 19 (GAW19).

297 ipants in the family-based analysis group at Genetic Analysis Workshop 19 addressed diverse topics, a

298 As part of the Genetic Analysis Workshop 19, approaches from this domai

299 current literature and developments from the Genetics Analysis Workshop 19 (GAW19) Collapsing Rare Va

300 Genetic analysis would be expected to identify functiona