ライフサイエンスコーパス: gene map

1 ha-glucosidase (designated GANC on the human gene map).

2 The results added 12 new loci to the horse gene map.

3 the chromosome-specific markers in the human gene map.

4 This shows the utility of such cellular gene maps.

5 lightly different ways, as a methodology for gene mapping.

6 complex diseases and strategies for disease gene mapping.

7 cted to provide the best-possible guides for gene mapping.

8 ng loci, and be an important tool in disease gene mapping.

9 a prerequisite for population-based disease gene mapping.

10 rate (FDR) controlling procedure in disease gene mapping.

11 brium has become important in the context of gene mapping.

12 neglected topics, given their importance in gene mapping.

13 large-scale association analysis for disease-gene mapping.

14 sociation methods are crucial for successful gene mapping.

15 gnificant practical implications for disease-gene mapping.

16 well to expectations of current methods for gene mapping.

17 and 2 polymorphic SINE insertions within the genes mapped.

18 In conclusion, gene mapping, allele sequence data, expression profile a

19 int sequencing, population screening, online gene mapping, allelic discrimination of tumor-associated

20 recurrent positive selection in the bat ACE2 gene map almost perfectly to known SARS-CoV interaction

21 litate rapid targeted expansion of the horse gene map and consequently, mapping and positional clonin

22 The compilation of a dense gene map and eventually a whole genome sequence (WGS) of

23 genetic markers that may be most useful for gene mapping and association studies.

24 hese influences is increasingly important as gene mapping and case-control studies are initiated in S

25 ges offered by reciprocal translocations for gene mapping and cloning, T(2;10)67Gso should prove a va

26 d application of molecular marker assays for gene mapping and discovery in field crops and trees.

27 AB-NAM an important tool for high-resolution gene mapping and discovery of novel allelic variation us

28 Integrated maps are useful for gene mapping and establishing the relationship between r

29 The results presented are useful for gene mapping and evolutionary and comparative genomics o

30 d that they may be most promising for future gene mapping and for extending pedigrees by phenotyping

31 rtant implications for strategies of disease-gene mapping and for understanding human evolutionary hi

32 enetic background interactions, we integrate gene mapping and gene mRNA expression data in segregatin

33 s have been due to technological advances in gene mapping and in statistical methods that relate gene

34 molecules opens new possibilities in optical gene mapping and in the fundamental study of DNA-protein

35 vent of sophisticated genomic techniques for gene mapping and microarray analysis has provided opport

36 of the longSAGE retina tags enhanced tag-to-gene mapping and revealed alternatively spliced genes.

37 Gene mapping and sequencing data lead to the generalizat

38 ted to a specific gene and require laborious gene mapping and sequencing.

39 e data is an important task for both disease-gene mapping and studies of human evolution.

40 Although analysis of gene maps and exon structures allows tentative assignmen

41 ore the relationship between similarities of gene maps and gene functions.

42 Gene maps and spatial autocorrelation analyses suggest t

43 n humans of the homologues of susceptibility genes mapped and identified in murine models.

44 butes to the expansion of the existing BTA18 gene map, and provides new information about the chromos

45 escribed on the basis of chromosome studies, gene mapping, and DNA sequencing.

46 Clinical diagnosis of CORD, disease gene mapping, and mutation identification.

47 Thus, comparative gene mapping appears to be an efficient strategy for ide

48 linkage analysis (LDLA) is a high-resolution gene mapping approach based on sophisticated mixed linea

49 e data show the power of an integrated human gene-mapping approach for heritable molecular phenotypes

50 computational method, CEGMA (Core Eukaryotic Genes Mapping Approach), for building a highly reliable

51 oth for successful implementation of disease-gene mapping approaches and for inferences about human d

52 l power and resolution compared to classical gene-mapping approaches.

53 ng widely recognized as the new currency for gene mapping as increasing numbers are discovered.

54 build a subnetwork of Gc signaling, with 54 genes mapping as nodes, and 6 non-Gc regulated genes inf

55 These genes map at loci in chromosomes 1(7H), 2 (2H), 3(3H), 4

56 egulators are the products of two paralogous genes mapping at positions adjacent to the corresponding

57 Effective gene mapping based on genetic association data will requ

58 methods offer a powerful approach to disease gene mapping, based on the association between causal mu

59 a candidate prostate cancer tumor suppressor gene maps between markers D16S3096 and D16S516.

60 apparent transcription start sites for each gene mapped by primer extension analysis.

61 Genes mapped by CpGs in these two modules were enriched

62 Software to perform the gene-mapping calculations, "MALDsoft," is freely availab

63 gene for transferrin and a transferrin-like gene map close to the QTL on chromosome 9.

64 In barley, more than 13 HvCBF genes map coincident with the major QTL FR-H2 suggesting

65 interactions connected functionally related genes, mapped core bioprocesses, and identified pleiotro

66 NA and protein sequence data, polymorphisms, gene mapping data and genome coordinates, and comparativ

67 The comparative gene mapping data on ECA14 and ECA21 finely align the ch

68 statistics and basic quality assessments for gene-mapping data, accommodating either pedigree or case

69 arnivore, cetartiodactyl, and rodent-ordered gene maps demonstrate that chromosome breakpoints, previ

70 Our comparative gene map demonstrates that the only regional gene in com

71 Using gene mapping, direct genomic sequencing, and extended ha

72 Gene mapping efforts are now focussing on linkage disequ

73 practical implications of these results for gene mapping efforts.

74 a marker for a disease subtype suitable for gene mapping efforts.

75 human traits thus far and will guide future gene-mapping efforts.

76 ding of genetic variation will help to guide gene-mapping efforts.

77 ovel chromosome 21 genes and four paralogous genes mapping elsewhere in the human genome.

78 evaluation, immunologic assays, homozygosity gene mapping, exome sequencing, Sanger sequencing, and f

79 Gene mapping experiments including transfections of UGT1

80 algorithm to define the asthma phenotype in gene mapping family-based studies.

81 A preliminary gene map for the VWS critical region is as follows: [see

82 The current gene mapping for complex diseases is heavily weighted by

83 High-resolution physically ordered gene maps for equine homologs of human chromosome 5 (HSA

84 The availability of gene maps for multiple organisms provides the foundation

85 pproach yields high confidence ranked target gene maps for TP53, DREAM, MMB-FOXM1 and RB-E2F and enab

86 Developing ordered gene maps from multiple mammalian species coupled with c

87 These include studies in gene mapping, functional characterization of previously

88 esource utilization given a set of SNP-based gene-mapping goals.

89 Because a high-density gene map has been constructed for maize inbred B73, all

90 Gene mapping has identified OS mutations within a protei

91 The ESTs and genes mapped here join 748 SSLp markers and 459 previous

92 A whole brain immediate early gene mapping highlighted the dorsolateral bed nucleus of

93 standardized gene list and a fully traceable gene mapping history for each gene from the original tra

94 Gene mapping identified a single base pair deletion in m

95 t serve as a leverage tool for complex trait gene mapping if genomes are screened with the appropriat

96 tSB not only is the first major Al tolerance gene mapped in a grass species that does not belong to t

97 chromosome 19 and found that the LKB1/STK11 gene mapped in the minimal-deleted region.

98 aphids, and the results indicate that target gene mapping in aphids is feasible.

99 In nature, gene mapping in field pedigrees is required to study soc

100 Exome sequencing is a promising tool for gene mapping in Mendelian disorders.

101 s provide a new genomic tool for comparative gene mapping in the cat and related Felidae, and provide

102 d as a backbone for the rapid development of gene maps in domesticated animals.

103 e sequence repeat (SSR)-based map, while 111 genes mapped in 19 of the 26 gaps >10 cM.

104 Sequence analysis of zebrafish genes mapped in this study and in prior work identified

105 omparison of the physical location of the 16 genes mapped in this study with the human genome reveals

106 Cell wall related genes mapping in genomic regions involved into tomato bi

107 Transcription of the acrABDEF genes, mapping in three widely spaced loci, was elevated

108 ry maintenance using ex vivo immediate-early gene mapping, in vivo neuronal recordings and viral-medi

109 By examining differentially expressed genes, mapping information, and genome resequencing, we

110 ized the murine neutral ceramidase (N-CDase) gene, mapped its chromosomal location and determined its

111 kage disequilibrium (MALD) is a whole genome gene mapping method that uses LD from extended blocks of

112 ics packages that provide a full spectrum of gene mapping methods, ranging from parametric linkage in

113 The KOS3 gene mapped near HMR, and its expression was regulated b

114 Genomes can be browsed visually on a gene map of each chromosome or plasmid.

115 We herein report a high-resolution gene map of the horse (Equus caballus) X chromosome (ECA

116 oviding what is, to our knowledge, the first gene map of the IFN region of any bat species.

117 red to construct a comprehensive comparative gene map of the mouse and human Lgn1/SMA intervals in th

118 To increase the density of a gene map of the zebrafish, Danio rerio, we have placed 3

119 netic association studies the mainstream for gene mapping of complex human diseases.

120 lected at the molecular level by comparative gene mapping of SSC12 and HSA17.

121 A21 finely align the chromosomes to sequence/gene maps of a range of evolutionarily distantly related

122 High-resolution gene maps of individual equine chromosomes are essential

123 Ordered gene maps of mammalian species are becoming increasingly

124 enetic studies, the high-resolution (gene-by-gene) mapping of amplicon boundaries and the quantitativ

125 to improved biolabeling experiments, such as gene mapping on a nanometer scale or multicolor microarr

126 nes mapped onto 1, 12, and 15; and the TRAP1 gene mapped onto 16.

127 genes mapped onto 3, 4, 6, 13 and 15; HSP90B genes mapped onto 1, 12, and 15; and the TRAP1 gene mapp

128 AraCyc currently features 1,418 unique genes mapped onto 204 pathways with 1,156 literature cit

129 ed onto chromosomes 1, 3, 4, and 11; HSP90AB genes mapped onto 3, 4, 6, 13 and 15; HSP90B genes mappe

130 HSP90AA genes mapped onto chromosomes 1, 3, 4, and 11; HSP90AB g

131 68, with a limited number of CG8486-specific genes mapping outside the hypervariable carbohydrate bio

132 ver risk alleles and complements established gene-mapping paradigms in neuropsychiatric disease.

133 egion on chromosome 12 containing the MODY 3 gene (map position 132 cM) and between the X-chromosome

134 These genes map primarily to four blocks in two chromosomes.

135 These data demonstrate that ordered RH-based gene maps provide the most precise assessment of compari

136 y patterns across ethnic groups may increase gene-mapping resolution.

137 six orders of placental mammals, confirm the gene-mapping results and indicate that the multiple huma

138 The structural gene maps revealed that the order of the head and tail g

139 lar mapping, and the positions of resistance genes mapped so far are listed.

140 A analyses, construction of genetic maps and gene mapping studies aiming to link phenotype and genoty

141 ch for mapped BAC clones that can be used in gene mapping studies and chromosomal mutation analysis p

142 Gene mapping studies in animal mutants with anaemia due

143 gnificant heritability supports their use in gene mapping studies of AgP susceptibility.

144 Phenotype assessment is a crucial issue in gene mapping studies of asthma.

145 aluable strategy for increasing the power of gene mapping studies of complex diseases.

146 human identification and parentage testing, gene mapping studies, cancer diagnostics, and diagnosis

147 Moreover, they show that, in gene mapping studies, genetic data from both parents and

148 ar families commonly used in complex disease gene mapping studies.

149 ey are not directly observed in most current gene mapping studies.

150 approach for improving power complex traits gene mapping studies.

151 pring trios are widely collected for disease gene-mapping studies and are being extensively genotyped

152 t genotyping errors lead to loss of power in gene-mapping studies and underestimation of the strength

153 Many gene-mapping studies for healing ability have been perfo

154 t assessment of glucose metabolism, enabling gene-mapping studies in large population samples.

155 These results suggest that future gene-mapping studies may identify pleiotropic genetic va

156 riation in molecular population genetics and gene-mapping studies of diseases with complex inheritanc

157 Gene-mapping studies routinely rely on checking for Mend

158 However, despite converging evidence from gene-mapping studies, aspects of the genetic contributio

159 ype imputation is necessary for facilitating gene-mapping studies, especially with the ever increasin

160 They show potential for gene-mapping studies.

161 genetic markers or functional candidates in gene-mapping studies.

162 is mouse model of childhood cancer, we did a gene mapping study with the SWXJ-9 recombinant inbred st

163 Existing methods for orthologous gene mapping suffer from two general problems: (i) they

164 technologies in combination with traditional gene mapping techniques, such as linkage analysis, can h

165 Our approach unifies two main goals of gene mapping that have generally been treated separately

166 ents from the Medicare database with disease-gene maps that we derived from several resources includi

167 ptimization Strategy (GOST), for orthologous gene mapping through combining sequence similarity and c

168 or receptor superfamily of proteins, and the gene mapped to 19q13.33, near the PLAUR locus for uPAR a

169 NKX3.1, a gene mapped to 8p21, is a member of the NK class of home

170 The disease gene mapped to a less than 2-megabase recessive locus at

171 PDXK, whose orthologue is the most proximal gene mapped to mouse chromosome 10.

172 TMPRSS2, whose orthologue is the most distal gene mapped to mouse chromosome 16, and PDXK, whose orth

173 The gene mapped to the ov-serpin cluster at 18q21 and reside

174 carboxypeptidase M (CPM)--another candidate gene mapped to this region.

175 We identified RIL, a LIM domain gene mapping to 5q31, a region frequently deleted in acu

176 s a candidate prostate cancer aggressiveness gene mapping to 7q32-q33.

177 ndidate prostate cancer tumor aggressiveness gene mapping to chromosome 7q32-q33.

178 en described as a single-locus multi-allelic gene mapping to molecular linkage group (MLG) F.

179 es is useful in studies ranging from disease gene mapping to speciation genetics.

180 o adult-onset ataxia pedigree, the causative gene maps to 19q13, overlapping the SCA13 disease locus

181 The human LMX1A gene maps to 1q22-q23, a region identified as a putative

182 Of note, Nek4 gene maps to a commonly deleted locus in non-small cell

183 The human IGRP gene maps to a diabetes susceptibility locus, suggesting

184 old allele of the P2X7 receptor and the P2X7 gene maps to a locus associated with disease, P2X7 is a

185 The LARG gene maps to a region on chromosome 11q23-24 that shows

186 For example, the human CAV-1 gene maps to a suspected tumor suppressor locus (D7S522/

187 The gene maps to chromosomal location Xp22.

188 The murine Rad51l2 gene maps to chromosome 11 and is located in the synteni

189 The nel-like1 (NELL1) gene maps to chromosome 11p15, which frequently undergoe

190 DECTIN-1 gene maps to chromosome 12, between p13.2 and p12.3, clo

191 The SCA2 gene maps to chromosome 12q24 and the causative mutation

192 The gene maps to chromosome 19p13.2-p13.3 and spans approxim

193 s highly restricted to immune cells, and its gene maps to chromosome 19q13.4, a locus that contains a

194 The human AP-2 epsilon gene maps to chromosome 1p42, consists of seven exons sp

195 s highly restricted to immune cells, and its gene maps to chromosome 1q44, a locus that is associated

196 The RINX gene maps to chromosome 20p11.2 to which no retinal dise

197 The h-l(3)mbt gene maps to chromosome 20q12, within a common deleted r

198 The human gene maps to chromosome 2q34-q36, and the mouse gene is

199 The gene maps to chromosome 3 at position 84C6.

200 the mouse genome showed that the basonuclin2 gene maps to chromosome 4 and consists of six exons span

201 The Zfp319 gene maps to chromosome 8, in a region of conserved synt

202 The FEZ1/LZTS1 gene maps to chromosome 8p22, a region that is frequentl

203 The GLIS2 gene maps to human chromosome 16p13.3, a locus implicate

204 The GIGYF2 gene maps to human chromosome 2q37 within a region linke

205 The NKX-3.1 homeobox gene maps to human chromosome 8p21, a region that underg

206 The zfAHR1 gene maps to linkage group 16 in a region that shares co

207 The zinfandel gene maps to linkage group 3 near the major globin gene

208 dentity with the Fla10 motor subunit and the gene maps to linkage group XII/XIII near RPL9.

209 The Gatm gene maps to mouse chromosome 2 in a region not previous

210 user to rapidly inspect and compare multiple gene maps to regions of genomic sequences.

211 The human CCDC88B gene maps to the 11q13 locus that is associated with sus

212 The DLX4 homeobox gene maps to the 17q21.3-q22 region that is amplified in

213 The cyclin D1 gene maps to the amplicon core, as do two new expressed

214 Since the Fus-2 gene maps to the chromosomal region 3p21.3, which contai

215 (DOCK4) is a GTPase exchange factor, and its gene maps to the commonly deleted 7q region.

216 The gene maps to the critical human tumor suppressor gene re

217 The causative gene maps to the long arm of chromosome 15 but has not y

218 The gene maps to the same chromosomal region as the maximum

219 The espin gene maps to the same region of mouse chromosome 4 as je

220 , suggesting that a second haploinsufficient gene maps to this interval.

221 s, in the present study we examined the GCMB gene, mapped to 6p23-24, as a candidate for isolated hyp

222 Identification of the causal gene, mapped to chromosome 5p15, will advance our unders

223 viously identified as a metastasis-promoting gene, mapped to the center of our 1.6-Mb target region.

224 Remarkably, these genes map to a single chromosome domain (18B3), and by q

225 In mice, the homologs of these genes map to chromosome 5 in a region of conserved synte

226 Seven of these genes map to confirmed diabetes susceptibility regions.

227 molecular level, mutations in key autophagy genes map to different stages of this highly conserved p

228 Several of the MRP genes map to loci associated with disorders consistent w

229 Murine mXCP1, mXCP2 and mXCP3 genes map to murine chromosome 16 and mXCP4 is positione

230 R on chromosome 2, NOR2, whereas active rRNA genes map to NOR4, on chromosome 4.

231 The gl8a and gl8b genes map to syntenic chromosomal regions, have similar,

232 Both genes map to syntenic regions of chromosome 1 and contai

233 Three potential candidate genes map to these regions: the beta subunit of the musc

234 Several candidate genes map to this region of the genome including a numbe

235 One of these genes mapped to 5q31-33.

236 rcent of the BAC clones containing duplicate genes mapped to a single chromosomal location, suggestin

237 EQTL for 195 genes mapped to both parental maps, the majority of whic

238 mapped to chromosome 1q, and down-regulated genes mapped to chromosome 1p.

239 Importantly, most up-regulated genes mapped to chromosome 1q, and down-regulated genes

240 Seven antixenobiotic genes mapped to chromosome I, six to chromosome II, and

241 view results from searches graphically (i.e. genes mapped to chromosomes or isolates displayed on a m

242 ridization (FISH) with BAC probes containing genes mapped to each linkage group.

243 brary sequences revealed that several of the genes mapped to known regions of deletion in ovarian can

244 d-largest number of differentially expressed genes mapped to mitochondrial enzyme inhibition.

245 ng pathway was the top gene set enriched for genes mapped to moderately AS-associated single-nucleoti

246 Three mouse ABC genes mapped to regions implicated in cholesterol gallst

247 2% of down-regulated and 51% of up-regulated genes mapped to regions present in decreased or increase

248 The largest number of genes mapped to ribosomal proteins, a signature hitherto

249 he lack of any known major RA susceptibility genes mapped to sex chromosomes.

250 Database searches for genes mapped to the critical region identified a gene kn

251 mutations in CASP10, BARD1, XRCC5, or PPP1R7 genes mapped to the deleted regions.

252 epigenetic analyses of a number of candidate genes mapped to the deleted regions.

253 Two of these candidate genes mapped to the site of translocation on chromosome

254 the basis of the observed overexpression of genes mapped to this region involved in maintenance of p

255 These genes mapped to two adjacent operons that we designated

256 expression of 122 (61%) and 88 (27%) of the genes mapping to 1p35-36 and all of 11q, respectively, s

257 To facilitate the identification of genes mapping to amplified regions, we have used a techn

258 nd frequency of gene amplification affecting genes mapping to ch13q34 in human breast cancer.

259 t that altered transcriptional regulation of genes mapping to chromosome 1 may contribute to disease

260 ing in a haploinsufficiency of RB1 and other genes mapping to chromosome 13, as well as activation of

261 aracterized by significant overexpression of genes mapping to chromosome 1q, and both exhibited a poo

262 impairs gene transcription, particularly at genes mapping to clusters such as HOX and PCDHB.

263 ic regions containing the orthologs of human genes mapping to human chromosome 20q.

264 ster of genes to be flanked predominantly by genes mapping to human chromosomes 7 and 19.

265 is analysis revealed 44 highly overexpressed genes mapping to localized amplicons on chromosome 13, g

266 t been analyzed in detail; to date, only VZV genes mapping to open reading frames (ORFs) 4, 21, 29, 6

267 hnologs are significantly overrepresented in genes mapping to pathogenic CNVs, irrespective of how CN

268 26 genes mapping to the 1q arm show highly significant (P</

269 er of candidate genes was reduced, and a few genes mapping to the BBS3 interval emerged as the best c

270 ohn's disease (CD), showed associations with genes mapping to the cytokine gene cluster on 5q31.

271 Twelve genes mapping to the deleted region were reliably identi

272 rs at the same rate as that observed between genes mapping to the distal portion of the circular chro

273 -mb region that included RUNX1, miR-802, and genes mapping to the Down syndrome critical region.

274 rt-range linkage with five orthologous human genes mapping to the Major Histocompatibility Complex (M

275 Transcripts for genes mapping to the p38 mitogen-activated protein kinas

276 Additionally, the expression of genes mapping to the Saltol region of chromosome 1 were

277 the positional cloning of candidate disease genes mapping to Xp22.1 and is therefore of value for th

278 vivo-induced (ivi) proteins, encoded by ivi genes, mapped to the backbone, O islands (OIs), and pO15

279 ohnologs between these gene sets and control genes, mapping to CNVs not known to be disease associate

280 Gene expression profiling and gene mapping using 500K single-nucleotide polymorphism (

281 method for fine-scale linkage-disequilibrium gene mapping using high-density marker maps.

282 Immediate early gene mapping using zif268 in situ hybridization revealed

283 For disease gene mapping, using both simulated and real data sets on

284 ed information on GBD occurrence and a 10-cM gene map, we performed multipoint variance-components an

285 ds mainly rely on sequence-based orthologous gene mapping, which often leads to suboptimal mapping re

286 logistic regression in case-control disease gene mapping with a large number of SNPs (single nucleot

287 eexamine the role of random effect models in gene mapping with inbred strains.

288 Gene mapping with recombinant inbred BXD strains reveale

289 TGFB1, a candidate gene mapped within this region, was excluded.

290 Overexpression of CKS1B, a gene mapping within a minimally amplified region between

291 e microrchidia CW-type zinc finger 2 (MORC2) gene mapping within the linkage region.

292 This gene maps within a subregion of human chromosome 10q24.3

293 The gene maps within the pgs 1 QTL interval and is expressed

294 The CTSB gene maps within this region.

295 The DC-SIGN and DC-SIGNR genes map within a 30-kb region on chromosome 19p13.2-3.

296 Investigators targeting 129/Sv genes mapping within chromosomal regions reported herein

297 Genes mapping within rare CNVs in TS showed significant

298 implicated in copy number pathogenicity: (i) genes mapping within rare disease-associated CNVs, (ii)

299 Key genes mapping within these deleted regions include PTEN,

300 Key amplified genes mapping within these regions include SKP2, FOXA1,