ライフサイエンスコーパス: chromosome 1

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

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

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

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

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

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

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

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

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

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

11 to malignancy through two genomic regions on chromosome 1.

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

13 implicating a novel susceptibility locus on chromosome 1.

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

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

16 any as were statistically expected mapped to chromosome 1.

17 sequence and biological annotation of human chromosome 1.

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

19 1000 nt and greater that cover 80% of human chromosome 1.

20 a highly repetitive satellite DNA element on chromosome 1.

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

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

23 CAI-4 and SGY-243, can carry three copies of chromosome 1.

24 ZB contribution comes from the Nba2 locus on chromosome 1.

25 ipoprotein cholesterol (HDL) levels on mouse chromosome 1.

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

27 cessive spermatogenic defect mapped to mouse chromosome 1.

28 osely related strains carrying two copies of chromosome 1.

29 cts amplified from a polymorphic sequence on chromosome 1.

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

31 transcriptional regulator flanking abcR2 on chromosome 1.

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

33 uction of Striga germination was detected on chromosome 1.

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

35 hopalosiphum maidis) susceptibility to maize Chromosome 1.

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

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

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

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

40 l functions and pathogenicity are located on chromosome 1.

41 csae and 8 linked markers on the long arm of chromosome 1D.

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

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

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

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

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

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

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

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

50 .7x10(-7)), and tsc0057290 (P=5.2x10(-7)) on chromosomes 1, 16, 18, and 18, respectively.

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

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

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

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

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

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

57 These intervals are located on canine chromosomes 1, 2, 3, 34, and 37, and none is under obvio

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

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

60 ity with recurrent loss of heterozygosity at chromosomes 1, 2, 4, 6, 7, 9, 12, 14, and X and a low ra

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

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

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

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

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

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

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

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

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

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

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

72 tified four regions suggestive of linkage on chromosomes 1, 3, 11, and 18.

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

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

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

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

77 low-up genotyping showed that the regions on chromosomes 1, 3, and 18 are also suggestive of linkage

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

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

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

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

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

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

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

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

86 , 15%) in 4 quantitative trait loci on mouse chromosomes 1, 4, 15, and 18, and Nedd4l (neural precurs

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

88 reports of quantitative trait loci (QTL) on chromosomes 1, 4, and 15 and identified novel loci on ch

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

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

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

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

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

94 an and mouse for 24 imprinted genes on human chromosomes 1, 6, 7, 11, 13, 14, 15, 18, 19, and 20.

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

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

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

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 Only one-half of chromosome 1 and 11 translocation carriers developing di

102 uggestive linkage to a dominant CBA locus on chromosome 1 and a recessive CBA locus on chromosome 5;

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

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

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

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

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

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

109 isk of synechia was associated with paternal chromosome 1 and on both the maternal and paternally inh

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

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

112 l portion of the long arm of wheat consensus chromosome 1 and rice chromosome 10.

113 onservation occurred between wheat consensus chromosome 1 and rice chromosome 5 and between the proxi

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

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

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

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

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

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

120 Polymorphic markers from chromosomes 1 and 10 that are near important immunoregul

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

151 rivatives of CAI-4, carrying three copies of chromosome 1, are avirulent in the intravenously inocula

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

153 287 women identified LOC401937 (rs966321) on chromosome 1 as a novel locus highly associated with tan

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

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

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

157 m of odds [LOD] >0.59, P(pointwise) < 0.05): chromosome 1 at 173.9 cM (LOD = 3.09), chromosome 3 at 2

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

159 re, 2.16; empirical P = 0.0005) was found on chromosome 1 at 44 cM.

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

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

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

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

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

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

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

167 0.43-cM, 43.2-Mbp interval at the S-locus on chromosome 1, but positional cloning was hampered by low

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

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

170 We report a comparative map of canine chromosome 1 (CFA1) incorporating single nucleotide poly

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

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

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

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

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

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

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

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

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

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

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

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

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

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

185 ule (SLAM)/CD150 family includes a family of chromosome 1-encoded cell surface molecules with costimu

186 3 (Ept2 and Ept6), chromosome 10 (Ept9), and chromosome 1 (Ept10 and Ept13).

187 Seventy-five percent of wheat chromosome 1 ESTs had significant matches with rice sequ

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

205 a, lending further support to involvement of chromosome 1 in schizophrenia susceptibility in the Afri

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

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

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

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

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

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

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

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

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

215 uggest that a major Al tolerance QTL on rice chromosome 1 is likely to be orthologous to AltSB, where

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

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

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

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

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

221 For maize chromosome 1, mapping 45 simple-sequence repeat markers

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

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

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

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

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

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

228 GLI1 mapped to chromosome 1 near the putative glycerol kinase gene NHO1

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

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

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

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

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

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

235 m line [(lo) durum] has been identified with chromosome 1D of T. aestivum L.

236 The chromosome 1D of this line segregates as a whole without

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

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

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

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

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

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

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

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

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

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

247 The locus on chromosome 1 reached genomewide significance levels (non

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

249 wide significant evidence for linkage of the chromosome 1 region (P(genome-wide) = 0.036).

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

251 1.54 x 10(-11)) covered a large, gene-dense chromosome 1 region that has previously been linked to c

252 4 and related NOD ABD strains is caused by a chromosome 1 region that includes a novel mutation in po

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

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

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

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

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

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

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

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

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

262 5'-flanking region was amplified from human chromosome 1, sequentially deleted, and cloned into a lu

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

285 n lupus-prone NZM2328 mice, a locus Cgnz1 on chromosome 1 was linked to chronic glomerulonephritis, s

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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