ライフサイエンスコーパス: chromosome 1

1 repair fidelity and cause damage to healthy chromosomes(1).

2 d more than a decade ago to a 2-Mb region on chromosome 1.

3 -wide significant p value of 1.7 x 10(-8) on chromosome 1.

4 rococcus and rs561177583 within LINC01787 on chromosome 1.

5 esidues and is encoded by a 34.5-kb locus on chromosome 1.

6 l functions and pathogenicity are located on chromosome 1.

7 nnis and mapped to an 0.9 megabase region of chromosome 1.

8 he NRT1.1 (CHL1) nitrate transporter gene on chromosome 1.

9 significant linkage (LOD 5.2) identified on chromosome 1.

10 chromosome 8 and two beta-globin paralogs on chromosome 1.

11 the TAR DNA-binding protein gene (TARDBP) on chromosome 1.

12 ect on blood pressure (BP) is located on rat chromosome 1.

13 ations of 17 mapped loci on tomato pachytene chromosome 1.

14 nterval spans a 7-Mb region on distal murine chromosome 1.

15 to malignancy through two genomic regions on chromosome 1.

16 ent the major Al tolerance QTL also found on chromosome 1.

17 implicating a novel susceptibility locus on chromosome 1.

18 ied rice homologs, of which 54% were on rice chromosome 1.

19 the 1-LOD interval of the linkage signal on chromosome 1.

20 any as were statistically expected mapped to chromosome 1.

21 sequence and biological annotation of human chromosome 1.

22 1000 nt and greater that cover 80% of human chromosome 1.

23 a highly repetitive satellite DNA element on chromosome 1.

24 s 12 exons, spanning a 40-kb region in mouse chromosome 1.

25 ith a uniparental disomy (UPD) of the entire chromosome 1.

26 nce in bottle gourd, to a 317.8-kb region on chromosome 1.

27 omparing to the average GC-content of 40% on chromosome 1.

28 s to a 30-centimorgan (cM) region located on chromosome 1.

29 on chromosome 20 and CTSK, CTSS and ARNT on chromosome 1.

30 s with a gene-rich region on the long arm of chromosome 1.

31 r of CB-dependent gene-positioning events on chromosome 1.

32 cts amplified from a polymorphic sequence on chromosome 1.

33 ed the Tsk2 gene mutation to <3 megabases on chromosome 1.

34 transcriptional regulator flanking abcR2 on chromosome 1.

35 y unmapped origin toward the 5' extremity of chromosome 1.

36 uction of Striga germination was detected on chromosome 1.

37 its reside within a syntenic region of mouse chromosome 1.

38 hopalosiphum maidis) susceptibility to maize Chromosome 1.

39 ne to the complex Gli-1 plus Glu-3 region on chromosome 1.

40 des a 25.5 kDa LOB domain protein located on chromosome 1S.

41 c 5S rDNA loci and were designated as marker chromosomes 1.

42 ificant peaks for aortic arch lesion size on chromosome 1 (105 Mb, LOD=5.0, and 163 Mb, LOD=6.8), and

43 variants related to culture were observed on chromosomes 1, 12 and 17, but a minimal amplicon in chro

44 ges on prolonged culture, commonly affecting chromosomes 1, 12, 17 and 20.

45 nt QTL that affects curvature of the arch on chromosome 1 (121 Mb, LOD=5.6) and a suggestive QTL on c

46 se embryonic fibroblasts (MEFs) trisomic for chromosome 1, 13, 16, or 19.

47 ximum disease severity was linked to QTLs on chromosomes 1, 15, and 19.

48 .7x10(-7)), and tsc0057290 (P=5.2x10(-7)) on chromosomes 1, 16, 18, and 18, respectively.

49 Loss of the short arm of chromosome 1 (1p) is the second most frequent chromosoma

50 splicing of pre-mRNA, is encoded by genes on chromosome 1 (1p36).

51 lation of the distal end of the short arm of chromosome 1 [1p36 deletion syndrome (1p36DS)] is one of

52 ies of these U1 snRNA genes, also located on chromosome 1 (1q12-21), were thought to be pseudogenes.

53 nt quality traits indicated QTL clustered on chromosome 1, 2, 4 and 6 for the AE population and chrom

54 some 1, 2, 4 and 6 for the AE population and chromosome 1, 2, 5 and 6 for the IA population.

55 Significant QTLs are present on chromosomes 1, 2, 3, 4, 6, and 10.

56 genotyped across eight chromosomal regions (chromosomes 1, 2, 3, 5, 14, 18, 20 and 21) in the sires

57 We mapped regions on chromosomes 1, 2, 4, 6, 7, and 15 that contain quantitat

58 identified quantitative trait loci (QTLs) on chromosomes 1, 2, 4, 6, and 7.

59 n the stroma and tumor grade (P = .0013), on chromosomes 1, 2, 5, 18, 20, and 22 in the stroma and re

60 observed suggestive evidence for linkage on chromosomes 1, 2, 5, 8, 14, 17, and 19.

61 ons with the largest effects were located on chromosomes 1, 2, 6, 7, and 9 and explained 55% of the p

62 TPS genes are found in clusters, notably on chromosomes 1, 2, 6, 8, and 10.

63 However chromosomes 1, 2, 9, 12 and 14 have a relatively high pr

64 An analysis of polymorphisms on chromosomes 1, 2, and R excluded meiosis as a mechanism

65 egregation in cells with improperly attached chromosomes [1, 2 and 3].

66 onal genes from non-recombining sex-specific chromosomes [1, 2], such as the Y chromosomes in mammals

67 namic changes to the number and structure of chromosomes(1,2).

68 tral loss of heterozygosity (CN-LOH)) on all chromosomes(1,2,5,6,9), but the sources of selective adv

69 to evaluate the independent contributions of chromosome 1, 3, 6, and 8 abnormalities for prognosticat

70 A series of 320 UM were analyzed for chromosome 1, 3, 6, and 8 abnormalities using whole geno

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

72 ere analyzed with MLPA evaluating 31 loci on chromosomes 1, 3, 6 and 8, and the results were correlat

73 eterogeneity of chromosomal abnormalities of chromosomes 1, 3, 6, and 8 is present in most UMs.

74 Thirty-one loci on chromosomes 1, 3, 6, and 8 were tested with MLPA for cop

75 Inversions on chromosomes 1-3 affecting diapause traits adapting flies

76 utgroup sequence than nine genes residing on chromosomes 1-3.

77 h reciprocal monosomy-trisomy of homeologous chromosomes (1:3 copies) or nullisomy-tetrasomy (0:4 cop

78 Tumors frequently carried extra copies of chromosomes 1, 3q, 5p, and 6 and lost chromosomes 3p, 4,

79 hromosomal organization of a subset of human chromosomes (#1, 4, 11, 12, 16, 17, and 18) was examined

80 the examined druggable genome, three loci on chromosomes 1, 4 and 12 revealed significant association

81 mapped to three CNVs in the genome, in mouse chromosomes 1, 4 and 17.

82 Three regions on chromosomes 1, 4 and 18 exhibited moderate haplotype eff

83 ociated SNPs mapped to intergenic regions on chromosomes 1, 4, 11, and 12.

84 , 15%) in 4 quantitative trait loci on mouse chromosomes 1, 4, 15, and 18, and Nedd4l (neural precurs

85 ant quantitative trait loci (QTL) for HDL on chromosomes 1, 4, 8, 15, 17, 18, and 19.

86 action (59%) of hypothetical genes than does chromosome 1 (42%).

87 for rMBP, to chromosome 16 for rSBP, and to chromosomes 1, 5, 6, 7, and 21 for the single-time-point

88 ametric analysis gave evidence of linkage on chromosomes 1, 5, 7, and 12.

89 ed a uniform pattern of insertion in all the chromosomes (1-5) without any preference for a particula

90 , have been reported to have fewer kMTs than chromosomes [1-5].

91 elomere reserve generates unstable dicentric chromosomes(1-5).

92 nalyzed the contribution of gene families in chromosomes 1, 6, 12, and 19, which encode key regulator

93 To characterize Mo2s, we map QTLs to chromosomes 1, 6, 7, and 9 using an F(2) population deri

94 ion approach to compare aneuploidy levels of chromosomes 1, 7, 14, 15, 16, 18, 19 and Y in the cerebr

95 Most correlated genes are located on chromosomes 1, 7, 9, 10, 13, 14, 19, 20, and 22, chromos

96 e previously reported the linkage signals on chromosomes 1, 7, and 17 in Caucasian families with gene

97 s that range in size from kilobases to whole chromosomes(1-7).

98 Loss of chromosome 1 (78.2-79.1 Mbp) was predictive of good outc

99 uired uniparental disomy, were detectable on chromosomes 1, 8, 9, 17, 19, and 22.

100 The heteromorphic regions of chromosomes 1, 9, 15, 16, and Y, which consist of highly

101 , logarithm of odds ratio (OR)(LOD) 4.1], on chromosome 1 and a suggestive QTL on chromosome 9 (38 cM

102 The gene for this protein is located on chromosome 1 and corresponds to the open reading frame E

103 of association based upon earlier linkage to chromosome 1 and enrichment for vesicle-related transpor

104 ce, we mapped the locus in three families to chromosome 1 and identified mutations in ALX3, which is

105 to a approximately 900 kb interval on mouse chromosome 1 and identify the transcription factor, Usf1

106 A genomic region on distal mouse chromosome 1 and its syntenic human counterpart 1q23-42

107 ed 24 LexA1 binding sites located throughout chromosome 1 and one binding site in chromosome 2.

108 heep map with the exception of one region on chromosome 1 and one on chromosome 12.

109 Sle1 on chromosome 1 and Sle3/5 on chromosome 7 are two of the m

110 and 2 recessive SWR contributions (Swrl-1 on chromosome 1 and Swrl-4 on chromosome 10).

111 n; (b) the combined loss of the short arm of chromosome 1 and the long arm of chromosome 19, or 1p19q

112 he murine lupus susceptibility locus Nba2 on chromosome 1 and the syntenic human locus are associated

113 B. mallei possesses two glmS genes on chromosome 1 and Tn7 transposes to both sites, although

114 ormation of a specific locus engineered into chromosome-1 and cleaved.

115 c regions containing copy number variants on chromosomes 1 and 10 were associated with the outcome of

116 mpartment size were previously identified in chromosomes 1 and 10, respectively.

117 r most shape and size-related traits, QTL on chromosomes 1 and 12.

118 evidence of linkage for 2 additional loci on chromosomes 1 and 13.

119 expression and DNAm levels in fetal brain at chromosomes 1 and 17 that were associated with ADHD and

120 We find that Neandertal alleles on chromosomes 1 and 18 are associated with reduced endocra

121 resenting increased nucleotide diversity, on chromosomes 1 and 2 in cultivated G. hirsutum as compare

122 h energy-dependent quenching 1) and HQE2, on chromosomes 1 and 2, and the phenotype of HQE2 was valid

123 ng around transcription start sites in human chromosomes 1 and 2, we predicted 16 novel p53 binding s

124 n (FISH) to differentiate individual meiotic chromosomes 1 and 2.

125 re consists of the structural maintenance of chromosomes 1 and 3 (Smc1-Smc3) heterodimeric ATPase, th

126 were located in the introgressed regions on chromosomes 1 and 3, validating our initial hypothesis.

127 d that at least three new QTL were mapped on chromosomes 1 and 3.

128 e used genotype data for 959 and 398 SNPs on chromosomes 1 and 4 on 179-244 individuals from each of

129 on mouse chromosome 17 and potential loci on chromosomes 1 and 4.

130 ZMM4 and ZMM15 map to duplicated regions on chromosomes 1 and 5 and are linked to neighboring MADS-b

131 Specifically, regions on chromosomes 1 and 5 appear to harbor genetic modifiers o

132 known genes, with significant enrichment on chromosomes 1 and 6.

133 l homolog of macaque chromosome 5 to macaque chromosomes 1 and 6.

134 ped ultraviolet damage hotspots across human chromosomes 1 and 6.

135 owth and host mortality to two major loci on chromosomes 1 and 7 with LOD (logarithm of the odds) sco

136 hromosome instability, particularly gains of chromosomes 1 and 7.

137 loci with smaller effects were identified on chromosomes 1 and 9.

138 At PMC meiosis, two marker chromosomes 1 and two marker chromosomes 2 formed bivale

139 gions, which include four large stretches on chromosomes 1 and X, containing genes of biomedical rele

140 on quantitative trait loci (QTLs), Rf-1 (rat chromosome 1) and Rf-4 (rat chromosome 14), from the Faw

141 A major modifier locus was identified on chromosome 1, and a paralogous ClpP5 gene was isolated a

142 s2773080 and rs3922812 in or near RALGPS2 on chromosome 1, and rs1509957 near EGR2 on chromosome 10.

143 cus within a small genomic region on soybean chromosome 1, and validated one of the candidate genes a

144 Another QTL on chromosome 1 approached significance (LOD score, 2.72; g

145 and loss of all or part of the short arm of chromosome #1 are both associated with a poor prognosis.

146 gnz1 and Agnz1 on the distal region of mouse chromosome 1 are associated with chronic glomerulonephri

147 within a syntenic region of human and mouse chromosome 1 are associated with predisposition to syste

148 of human biology and disease encoded within chromosome 1 are made possible with the highly accurate

149 Rearrangements and mutations of chromosome 1 are prevalent in cancer and many other dise

150 at loci on murine chromosome 6, and possibly chromosome 1, are involved in regulating susceptibility.

151 287 women identified LOC401937 (rs966321) on chromosome 1 as a novel locus highly associated with tan

152 to have been added to the ancestor of human chromosome 1 as a single block that was subsequently dis

153 omosome 2 and rs6669072 near LOC105378853 on chromosome 1) associated with cognitive performance at t

154 rovided modest evidence for linkage included chromosome 1 at 167.5 cM (LOD 1.51) and chromosome 3 at

155 estive linkage for mean arterial pressure on chromosome 1 at 192 cM (LOD=2.18).

156 One hot spot, located centrally on chromosome 1, behaved similarly in male and female meios

157 crosatellite mapping placed the No3 locus on chromosome 1 between D1Mit480 (32cM) and D1Mit7 (41cM),

158 w that transgene integration has occurred on chromosome 1, between D1Mit365 and D1Mit191.

159 hese elements, the Mo17-specific helitron on chromosome 1 (bin 1.07), is transcriptionally active, pr

160 DISC1) is one of two genes that straddle the chromosome 1 breakpoint of a translocation associated wi

161 This number of chromosome 1D breaks is eight times higher than the numb

162 o, termination is not at a fixed location in chromosome 1, but is rather variable.

163 0.43-cM, 43.2-Mbp interval at the S-locus on chromosome 1, but positional cloning was hampered by low

164 acted pairwise with two Ter sites located on chromosome 1 by chromosome kissing.

165 osomal RNA gene is excised from micronuclear chromosome 1 by site-specific cleavage at chromosome bre

166 fforts to identify the BMD candidate gene in chromosome 1 (Chr 1) QTL that was detected from a cross

167 e, are variants associated with CFH-CFHR5 on chromosome 1 (Chr1) and ARMS2/HTRA1 on chromosome 10 (Ch

168 olonies as well as in relapse isolates, with chromosome 1 (Chr1) disomy predominating.

169 s of heterozygosity for the entire length of chromosome 1 (Chr1), indicating that disease was caused

170 zed by loss of a portion of the short arm of chromosome 1, clustered with malignant leiomyosarcomas.

171 The Sle1c subinterval on distal murine chromosome 1 confers loss of tolerance to chromatin.

172 In GHS chromosome 1 congenic lines bred onto a WKY genomic back

173 of obesity traits in humans to the region on chromosome 1 containing the MAGP-1 gene.

174 igh-resolution radiation hybrid map of wheat chromosome 1D (D genome) in a tetraploid durum wheat (T.

175 ents (1 of which had add 7p in the remaining chromosome); 1 del 7q; and 1 der 7.

176 ously we mapped a new genetic locus on mouse chromosome 1, designated sst1 (for supersusceptibility t

177 nation rates across two genetic intervals on chromosome 1 did not exhibit the same relationships amon

178 ded by FCGR3A and FCGR2A-C, respectively, on chromosome 1), display polymorphisms that could affect t

179 e the DeltaRFB allele and distal left arm of chromosome 1 during vegetative propagation.

180 na) encodes two such genes in tandem loci on chromosome 1, EIF4E1B (At1g29550) and EIF4E1C (At1g29590

181 in the epidermal differentiation complex on chromosome 1, encode a family of 18 proteins of unknown

182 nic lines (NILs) for the Eps gene located in chromosome 1D (Eps-D1) at 6, 9, 12, 15, 18, 21 and 24 de

183 3 (Ept2 and Ept6), chromosome 10 (Ept9), and chromosome 1 (Ept10 and Ept13).

184 ied an oncogene, focally amplified lncRNA on chromosome 1 (FAL1), whose copy number and expression ar

185 bes at the AGTRAP-MTHFR-NPPA/B gene locus on chromosome 1 (FDR = 1.3E-04), with additional probes on

186 events at the Hlx1 hotspot located on mouse chromosome 1, finding that the results agree well with a

187 genomewide maximum LOD of 3.39 at 153 cM on chromosome 1 for Lp-PLA(2).

188 t genes in a recurrently amplified region of chromosome 1 for the ability to cooperate with BRAF(V600

189 -bacterial artificial chromosome interval on chromosome 1 from genetic analysis of a cross between th

190 data, and we applied EWT to the analysis of chromosome 1 from paired-end shotgun sequence data (30x)

191 alternative splice variants, encoded by the chromosome 1 gene, produce a family of transcripts compo

192 r alkaline phosphatase (ALP) levels (ALPL on chromosome 1, GPLD1 on chromosome 6, and JMJD1C-REEP3 on

193 loci included interesting candidate genes on chromosome 1 (GRIK3 (glutamate receptor ionotropic kaina

194 he exception of a small congenic interval on chromosome 1 harboring an alternative CD45/Ly-5 alloanti

195 Human chromosome 1 has been claimed to be a conserved ancestra

196 insulin-dependent diabetes (Idd) regions on chromosomes 1 (Idd5) and 3 (Idd3) derived from the nondi

197 The CFH gene is located on chromosome 1 in a region repeatedly linked to AMD in fam

198 iling suggests that loss of the short arm of chromosome 1 in cellular leiomyomata, an uncommon histol

199 approach for the recurrent MCL1 amplicon at chromosome 1 in human tumor cells.

200 tive-hypnotics, have been detected on distal chromosome 1 in mice, and as many as four QTLs on human

201 replication dynamics of a central region of chromosome 1 in procyclic forms.

202 pneumococcal meningitis were rs139064549 on chromosome 1 in the COL11A1 gene (p = 1.51 x 10(-6); G a

203 RFB region prevents spontaneous breakage of chromosome 1 in the diploid micronucleus.

204 ements are inserted at the maize p1 locus on chromosome 1s in the same orientation; the adjacent ends

205 Genes such as ELTD1 on chromosome 1, in addition to genes on chromosomes 4 (eg,

206 ng >15 mg/kg CQ identifies a 76 kb region in chromosome 1 including pvcrt, an ortholog of the Plasmod

207 tudies of a nuclease that targets a locus in chromosome-1 indeed show that constricted migration dela

208 tative trait locus (QTL) for Al tolerance on chromosome 1 indicated that AtALMT1 is located proximal

209 evious studies have shown that a 129-derived chromosome 1 interval (Sle16) on the C57BL/6 (B6) backgr

210 re sub-phenotyping shows that a new locus in chromosome 1 is associated with left ventricular adverse

211 The q arm of chromosome 1 is frequently amplified at the gene level i

212 Chromosome 1 is gene-dense, with 3,141 genes and 991 pse

213 nstrate that SMC1 (structural maintenance of chromosomes 1) is the key regulator of the intra-S-phase

214 , as well as SMC1 (structural maintenance of chromosome 1), is maintained upon Nbs1 knockdown in diff

215 ents of the genome of European ancestry at a chromosome 1 locus are at increased risk for MS [logarit

216 ing of a subset of 83 families linked to the chromosome 1 locus identified only two genes significant

217 receptor (IL-6 SR) with European ancestry on chromosome 1 (LOD 4.59), in a region that includes the g

218 osses identified highly significant peaks on chromosome 1 (LOD 9.7) for systolic blood pressure and o

219 anscriptional regulation of genes mapping to chromosome 1 may contribute to disease progression, and

220 We propose that an area on chromosome 1 may harbor a gene or genes conferring susce

221 erved in mice with targeted genes located on chromosome 1 may simply arise from epistatic interaction

222 The Sle1ab genomic interval on murine chromosome 1 mediates the loss of immune tolerance to ch

223 hich specifically suppress the anti-invasion chromosome 1 miR-200a/200b/429 cluster.

224 in MYL12A (rs1662342, P = 4.9 x 10(-8)) and chromosome 1 near CD1E and SPTA1 (rs7547997, P = 7.9 x 1

225 patibility on allotriploid hybrids: ui1.1 on chromosome 1 (near the S locus), and ui6.1 on chromosome

226 The most significant peak was found on chromosome 1, near complement factor H (CFH), with P= 6.

227 ed on the single-copy subtelomeric region of chromosome 1 north (approximately 3.5 kb), which represe

228 18 annotated genes and a syntenic region in chromosome 1 of B. distachyon.

229 and AtCK2 genes are head-to-head oriented on chromosome 1 of the Arabidopsis genome.

230 a 2-cM overlapping region of the long arm of chromosome 1 of tomato, a region not previously linked t

231 analysis identified eight genomic islands in chromosome 1 of V. anguillarum 775(pJM1) and two in chro

232 t of the transcription factor IIA located on chromosome 1 (OsTFIIAgamma1).

233 pression quartiles, 70 genes, 30% mapping to chromosome 1 (P < .001), were linked to early disease-re

234 anine aminotransferase included rs2499604 on chromosome 1 (P = 2.2 x 10(-6)), rs6487679 on chromosome

235 s, including an intergenic SNP, rs476141, on chromosome 1 (P-value 1.2 x 10(-7)).

236 th regional lymph node metastasis: ATA42G12 (chromosome 1, P = .00095), D5S1457 (P = .00095), D5S1501

237 ome 11; P = 6.7 x 10(-7)) and ENO1 and RERE (chromosome 1; P = 8.8 x 10(-7)).

238 Four suggestive loci were mapped: Swrl-5 on chromosome 1 (peak at 106 cM), linked to hypergammaglobu

239 ore shown that microhomology in this area of chromosome 1 predisposes to disease associated genomic d

240 a NZB-derived susceptibility locus on distal chromosome 1, produce autoantibodies to nuclear Ags, but

241 kcrossed to breed for congenic rats with the chromosome 1 QTL HC1 on a normocalciuric WKY background.

242 ant in the complement factor H (CFH) gene on chromosome 1, recent evidence of the existence of protec

243 The rice chromosome 1 region collinear with the two wheat regions

244 1.54 x 10(-11)) covered a large, gene-dense chromosome 1 region that has previously been linked to c

245 4 and related NOD ABD strains is caused by a chromosome 1 region that includes a novel mutation in po

246 d to CFA7 in a region corresponding to human chromosome 1, region q32.1-q32.2.

247 A region on chromosome 1 regulates both the fluorescence shift indic

248 located at 1q41, 36 kb upstream of PROX1 on chromosome 1 (relative hazard ratio, 0.69; Fisher's comb

249 Chromosome 1 results (ZLR=2.92) were similar to those re

250 ed genes in this region of cultivated tomato chromosome 1 revealed three candidate acyltransferases t

251 pulation with 39 molecular markers mapped on chromosome 1D revealed 88 radiation-induced breaks in th

252 iations were found (8535 female individuals, chromosome 1: rs2764450, chromosome 11: rs11215217; 7772

253 A locus on chromosome 1, rs7533564 (P = 1.9 x 10(-9)), was associat

254 um genome, ranging from approximately 60% of chromosome 1 (SBI-01) to approximately 33% of chromosome

255 5'-flanking region was amplified from human chromosome 1, sequentially deleted, and cloned into a lu

256 ivation of the major interacting Ter site on chromosome 1 significantly reduced fork arrest at the Te

257 s for the autoimmune disease lupus on murine chromosome 1, Sle1z/Sle1bz, and the orthologous human lo

258 Cohesin's structural maintenance of chromosome 1 (Smc1) and Smc3 are rod-shaped proteins wit

259 Structure maintenance of chromosome 1 (SMC1) is phosphorylated by ataxia telangie

260 phosphorylation of structural maintenance of chromosomes 1 (Smc1), which acts within chromatin to ens

261 One region on chromosome 1 (spanning approximately 5.8 cM) and another

262 f 4 SWR loci (H2 on chromosome 17, Swrl-1 on chromosome 1, Swrl-2 on chromosome 14, and Swrl-3 on chr

263 l) withdrawal to a 0.44 Mb interval of mouse chromosome 1 syntenic with human 1q23.2.

264 A study of the Chromosome 1 TaCLPB in four wheat genotypes demonstrated

265 p-value = 3.49 x 10(-8)) and for FEV1/FVC on chromosome 1 [TGFB2] (p-value = 8.99 x 10(-9)), 4 [FAM13

266 ant associations were identified for FEV1 on chromosome 1 [TGFB2] (p-value = 8.99 x 10(-9)), 9 [DBH]

267 ation co-segregates with a linkage region on chromosome 1 that associates with the emergence of sever

268 The bm2 gene was mapped to a small region of chromosome 1 that contains a putative methylenetetrahydr

269 apply the method to a 4.8-Mb region on mouse chromosome 1 that contains a QTL influencing anxiety seg

270 hree, and four doses of a 14.6-Mb segment of chromosome 1 that contains approximately 300 genes.

271 s mapping identified a large region on mouse Chromosome 1 that controls both hair and eccrine gland d

272 mapped one major QTL to the upper portion of chromosome 1 that explains 1/3 of the difference in flow

273 can American controls, and report a locus on chromosome 1 that is significantly associated with multi

274 Ath1 is a quantitative trait locus on mouse chromosome 1 that renders C57BL/6 mice susceptible and C

275 scovered a quantitative trait locus (QTL) on chromosome 1 that was linked to mean arterial pressure (

276 Using a chromosome 1 tile path array, we investigated 108 adult

277 esolved a quantitative trait locus on canine chromosome 1 to a 188-kb critical interval that encompas

278 complex length and crossover positions along chromosome 1 using a novel automated approach also revea

279 within the IL-10 cytokine family cluster on chromosome 1 using linkage disequilibrium (LD)-tagging s

280 ion of channel catfish (Ictalurus punctatus) chromosome 1 using two different donor templates (synthe

281 , a novel HDL association with cg17901584 in chromosome 1 was identified (P = 7.81 x 10(-8)).

282 ressure (BP) quantitative trait locus on rat Chromosome 1 was isolated in a short congenic segment sp

283 e is located within the 129chr1b interval on chromosome 1, was also performed.

284 dition to providing evidence for linkage for chromosome 1, we also identified a proband with a unipar

285 ion of genes mapping to the Saltol region of chromosome 1 were examined in both genotypes.

286 Our top 2 hits on chromosome 1 were functionally associated with variabili

287 the greatest differential RNA expression on chromosome 1 were those encoding decay-accelerating fact

288 proximately 50-Mb region on the short arm of chromosome 1 where patterns of polymorphism are highly c

289 We find that human chromosome 1 (which does not contain BRCA1) contains ove

290 One significant QTL on distal chromosome 1, which accounted for major variations in pl

291 ave identified a genetic locus sst1 on mouse chromosome 1, which controls progression of pulmonary tu

292 Arabidopsis has three, tandemly arranged on chromosome 1, which encode proteins with predicted secre

293 cate a substantial probability of linkage to chromosome 1, which had been previously overlooked; our

294 is of an unremarkable 206-kb region on human chromosome 1, which identified localized regions of link

295 opulation was used to detect a major peak on chromosome 1, which is designated gip-1 (geminivirus imm

296 A QTL-based genetic scan of chromosome 1 with 35 infected F(1) backcrossed mice reve

297 strains associate genes in a DNA segment on chromosome 1 with a genetic predisposition for this dise

298 c genomic position (e.g., position 11,272 on chromosome 1)?"--with either "yes" or "no." Here, we sho

299 n shared a 4.76 Mb region of homozygosity on chromosome 1, with an identical haplotype.

300 96% of core genes were located on the larger chromosome 1, with growth-neutral duplicates of core gen