ライフサイエンスコーパス: chromosome 3

1 and 6% were nonsyntenic (not located on rice chromosome 3).

2 miR-26a located in the locus 3p21.3 of human chromosome 3.

3 near-centromeric region of maize (Zea mays) chromosome 3.

4 ewide scan: two on chromosome 2 and three on chromosome 3.

5 iated with frontotemporal dementia linked to chromosome 3.

6 protein 100% identical with that encoded by chromosome 3.

7 HL tumor suppressor gene on the short arm of chromosome 3.

8 e complete centromere of rice (Oryza sativa) chromosome 3.

9 an absence of maternally imprinted genes on chromosome 3.

10 ficance, as well as a fifth epistatic QTL on chromosome 3.

11 families were found close to the telomer of chromosome 3.

12 emonstrating only trisomy of chromosome 7 or chromosome 3.

13 l alleles originating from a single maternal chromosome 3.

14 tellite markers all within a 10-Mb region on chromosome 3.

15 The Cmt1 locus is located on chromosome 3.

16 ive trait assigned to the Cdm locus on mouse chromosome 3.

17 around the VHL gene to complete loss of the chromosome 3.

18 um but rather mapped near the end of sorghum chromosome 3.

19 ed by a putative quantitative trait locus on chromosome 3.

20 henotype: DM1, on chromosome 19, and DM2, on chromosome 3.

21 hromosome 9, in a region homologous to human chromosome 3.

22 e: The QTL of greatest effect are located on chromosome 3.

23 nd 15 and suggestive evidence for a locus on chromosome 3.

24 is thaliana corresponds to gene At3g44880 on chromosome 3.

25 approximately 33 Mbp was anchored to sorghum chromosome 3.

26 2 and 85,000 base pairs of the 82F region of chromosome 3.

27 L tumour suppressor gene on the short arm of chromosome 3.

28 tely 59 cM block of the short arm of sorghum chromosome 3.

29 reveal additional copies of the long arm of chromosome 3.

30 ucture is also found in mouse genomic DNA in chromosome 3.

31 modifier gene to a 950-kb interval on mouse chromosome 3.

32 a 1.2-cM region near the centromere of mouse chromosome 3.

33 nt optic atrophy is the OPA1 gene located on chromosome 3.

34 tivation of the telomerase repressor gene on chromosome 3.

35 15 or 16 exons, and the gene is contained on chromosome 3.

36 and of 26.5 (LOD score approximately 5.7) on chromosome 3.

37 pp140 gene of Drosophila maps within 79A5 of chromosome 3.

38 on of chromosome 5 or 7, or abnormalities of chromosome 3.

39 on of GC-specific gene and enhancer loops on chromosome 3.

40 gous divergent haplotypes spanning 11 Mbp on chromosome 3.

41 e (C-C motif) receptor (CCR) gene cluster on chromosome 3.

42 ion of the VHL gene and loss of a segment of chromosome 3.

43 earby genes in a disease-associated locus on chromosome 3.

44 1) (P-value = 2.63x10(-16), beta = -0.23) on chromosome 3.

45 tive enzyme activity, and the restoration of chromosome 3.

46 exclusively with tumors showing monosomy of chromosome 3.

47 tic cross maps to a single parasite locus on chromosome 3.

48 r depressive disorder and the same region on chromosome 3.

49 ome 2 have been duplicated and inserted into chromosome 3.

50 nt loci of atherosclerosis susceptibility on chromosomes 3, 10, and 12.

51 omosome 16q and moderate linkage at sites on chromosomes 3, 10, and 19q, and a meta-analysis of studi

52 ound to be homoeologous to sequences on rice chromosome 3, 12% had matches with sequences on other ri

53 eterogeneity in the genome-wide analyses (on chromosomes 3, 12, 15, and 18) did not replicate.

54 ind genes, MBNL, MBLL and MBXL, which map to chromosomes 3, 13 and X, respectively, and which show ex

55 32%; and E, gain or loss of partial or whole chromosome 3, 18%.

56 ariate Cox analysis indicated that losses of chromosome 3, 1p, 6q, and 8p and gain of 8q, as well as

57 st LOD scores including all families were on chromosomes 3 (2.41 at 117 cM) and 12 (2.47 at 15.5).

58 This genome includes gapless assemblies of chromosome 3 (236 Mb) and chromosome 9 (162 Mb), and 53

59 showed abnormalities with loss of disomy of chromosomes 3 (35%/52%/65%), 6 (15%/34%/51%), and 8 (19%

60 ort here the complete nucleotide sequence of chromosome 3 (384 518 bp) and an analysis revealing 95 p

61 iated sequence, or TAS), on the right arm of chromosome 3 (3R-TAS).

62 also identified chromosome specific CAs for chromosomes 3, 4, 5, 8, 9, 10, 11, 12, 17, 19 that were

63 were not found in individual experiments, on chromosomes 3, 4, 9 and 11.

64 ied 4 new QTLs for the onset of arthritis on chromosomes 3, 4, and 11, and 1 new QTL for severity on

65 hin and across trait groups were detected at chromosomes 3, 4, and 7 through CIM.

66 gestive of linkage with ARM were observed on chromosomes 3, 5, 6, 12, 15, and 16.

67 oid tumors have multiple trisomies involving chromosomes 3, 5, 7, 9, 11, 15, 19, and 21, and infreque

68 oid and contain multiple trisomies involving chromosomes 3, 5, 7, 9, 11, 15, 19, and 21, but infreque

69 Our analysis reveals modifier loci on mouse chromosomes 3, 5, 8, 11 and 14 with distinct effects on

70 earrangements involving translocations among chromosomes 3, 5, and 9 were detected in comparison betw

71 even loci associated with prostate cancer on chromosomes 3, 6, 7, 10, 11, 19 and X (P = 2.7 x 10(-8)

72 sence variation, the most prominent found on chromosomes 3, 6, 7, 16, and 18.

73 d evidence for additional linkage regions on chromosomes 3, 6, 8, 12, 16, and X.

74 ve trait locus mapping identified regions on chromosomes 3, 6, 9, and 15 containing candidate genes a

75 Kaplan-Meier estimates ranging from 4% with chromosomes 3, 6, and 8 disomy up to 39% for 3 complete

76 risk melanoma who demonstrate alterations in chromosomes 3, 6, and 8 or those with class 2 on gene-ex

77 mes 3, 6, and 8, comparison (normal [disomy] chromosomes 3, 6, and 8 vs. any 3, 6, or 8 abnormality)

78 ts with uveal melanoma sampled for status of chromosomes 3, 6, and 8, comparison (normal [disomy] chr

79 y-based assay were performed for analysis of chromosomes 3, 6, and 8.

80 o the broad depression phenotype (rs9825823, chromosome 3: 61,082,153, p = 8.2 x 10(-9)) located in a

81 were female specific and were identified on chromosomes 3, 7, 10, 11, 13, and X.

82 tified, the coverage was extended for bovine chromosomes 3, 7, 15, and 29 compared with previously pu

83 ) is associated with trisomies especially of chromosomes 3, 7, 9, 11, 15, and 19, whereas the nonhype

84 sly reported obesity-susceptibility locus on chromosomes 3, 7, and 17 and (2) demonstrate that combin

85 itu hybridization with centromeric probes to chromosomes 3, 7, and 17.

86 The distal euchromatic regions of sorghum chromosomes 3-7 and 10 are approximately 1.8-fold larger

87 Cytogenetic maps of sorghum chromosomes 3-7, 9, and 10 were constructed on the basis

88 including Rec114 and Mer2, which assemble on chromosomes(3-7) and are nearly universal in eukaryotes(

89 different genomic regions: a broad region on chromosome 3 (70-160 cM; logarithm of odds [LOD] scores

90 Three of these loci on chromosomes 3, 8 and 11 do not coincide with previously

91 On chromosome 3, a maximal LOD score of 5.1 (D3Mit45, 79 cM

92 nt in the Mopti form, and microsatellites on chromosome 3, a region void of inversions.

93 , 3q26.2 rearrangements were the most common chromosome 3 abnormalities (50%, groups A-C).

94 Interestingly, although heterogeneous, chromosome 3 abnormalities involving non-3q26.2 loci (gr

95 Chromosome 3 abnormalities were observed in 116 (5.8%) o

96 f-3, a quantitative trait locus (QTL) on rat chromosome 3, affects the development of CKD in Fawn-Hoo

97 5701 carrier cases, rs10937275 in ST6GAL1 on chromosome 3 also showed genome-wide significance (OR =

98 w risk variants, rs2370964 and rs3093720, on chromosome 3 and 17, respectively.

99 In the multivariate analysis, loss of chromosome 3 and 8p remained significant after adjusting

100 5 ovarioles/ovary) identified a major QTL on chromosome 3 and a minor QTL on chromosome 2.

101 of the telomeric portion of the short arm of chromosome 3 and characterized by developmental delay, g

102 The major modifier for colitis was mapped on chromosome 3 and designated cytokine deficiency-induced

103 [lens opacity 10 (Lop10)] mutation to mouse chromosome 3 and identified a missense mutation (G-->C)

104 aberrations involving the long arm of human chromosome 3 and is thereby inactivated in most of the c

105 ent is due to complete maternal isodisomy of chromosome 3 and reduction to homozygosity of the mutant

106 on of gene content and order between sorghum chromosome 3 and the homeologous rice chromosome 1 was o

107 nificant clusters of down-regulated genes on chromosome 3 and up-regulated genes on chromosome 8q, wh

108 ophila melanogaster ClvR (tko) is located on chromosome 3 and uses Cas9 and four gRNAs to disrupt mel

109 s a de novo balanced translocation involving chromosomes 3 and 10.

110 ist2 and Hist3 clusters are present on mouse chromosomes 3 and 11, respectively.

111 influencing PON1 activity were localized to chromosomes 3 and 14.

112 2 genes are located at homologous regions of chromosomes 3 and 19.

113 ith specific IgA activity were identified in chromosomes 3 and 20, in regions close to IFNG (chromoso

114 Nematodirus Strongyle FEC were identified on chromosomes 3 and 20.

115 me 7, and two additional interacting loci on chromosomes 3 and 20.

116 loci supported by univariate QTLs such as on chromosomes 3 and 4 as well as at distinctly different l

117 breakpoints in the mouse genome occurred in chromosomes 3 and 4, each carrying a lacZ-reporter clust

118 B6- and B10-derived Idd-resistant alleles on chromosomes 3 and 4, respectively, is completely protect

119 ecurrent nonreciprocal translocation between chromosomes 3 and 5 in human renal cell carcinoma, facil

120 tic modifiers for TSC have been localized on chromosomes 3 and 5 of the rat genome.

121 g of many of these isolates by using loci on chromosomes 3 and 5.

122 ocations suggestive of linkage were found on chromosomes 3 and 6.

123 at sequences specific for the centromeres of chromosomes 3 and 7 as controls.

124 .2 M SNP dataset, major QTLs were located on chromosomes 3 and 7 for Mn containing six candidate gene

125 n revealed LOD scores of >2.5 for markers on chromosomes 3 and 9, and fine mapping was performed on 5

126 (EGF) and Tyk2 are encoded within the QTL on chromosomes 3 and 9, respectively.

127 lian loci on the long arms of Ae. speltoides chromosomes 3S and 7S.

128 Two distinct chromosomal loci, termed major (chromosome 3) and minor (chromosome 12), harbor the glob

129 We have also identified mouse (chromosome 3) and rat (chromosome 2) orthologues, as wel

130 omosomes 3 and 20, in regions close to IFNG (chromosome 3) and the MHC (chromosome 20).

131 female predominance, a splenomegaly, gain of chromosome 3, and CD27 expression.

132 and 81 on chromosome 2, between 0 and 30 on chromosome 3, and near locations 49 and 81 on chromosome

133 at this chromosome is orthologous to chicken chromosome 3, and that at a minimum, ZAL2 and ZAL2(m) di

134 ath if statistically insignificant losses of chromosome 3 are considered together with gains in 8q as

135 a surplus of polymorphic microsatellites on chromosome 3 as compared to chromosome 2 (P=0.0001).

136 pporting the use of rice and, in particular, chromosome 3, as a model for comparative studies among t

137 Analyses of copy number across chromosome 3, as well as expression data from pooled, pu

138 s, an expression quantitative trait locus on chromosome 3, associated with substantially higher expre

139 uded chromosome 1 at 167.5 cM (LOD 1.51) and chromosome 3 at 121.0 cM (LOD 1.61).

140 ore of 4.14 for major depressive disorder on chromosome 3 at 24.9 cM (3p26-3p25).

141 .05): chromosome 1 at 173.9 cM (LOD = 3.09), chromosome 3 at 26.3 cM (LOD = 1.27), chromosome 4 at 13

142 The hSEP1 gene is located in chromosome 3 at 3q25-26.1 between markers D3S1309 and D3

143 stronger evidence of linkage (e.g., CVD2 on chromosome 3 at 87 cM subsetting on low HDL with an init

144 g relatives, there was suggestive linkage to chromosome 3 at marker D3S2398 (KAC(all)=2.9).

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

146 % of WM patients, including 12% with gain on chromosome 3 at the 3p22 locus that included the MYD88 g

147 The cpfl3 mapped to mouse chromosome 3 at the same location as human GNAT2, known

148 dence of linkage (2 < or = MLS < 3), both on chromosome 3 (at 211 and 209 cM, respectively); however,

149 sly known as cirrin) was cloned from a human chromosome 3 BAC.

150 BCL6, a gene on chromosome 3 band q27, encodes a Kruppel-type zinc finge

151 The human BCL6 gene on chromosome 3 band q27, which encodes a transcriptional r

152 BCL6, a gene on chromosome 3, band q27, encodes a zinc finger transcript

153 The mutation was mapped to chromosome 3 between D3Mit221 and D3Mit224, a region tha

154 The Mrf1 gene was mapped to mouse chromosome 3, between markers D3Mit70 and D3Mit277.

155 some 8 (bin 8.05), with a duplicate locus on chromosome 3 (bin 3.09).

156 for association near neuroligin 1 (NLGN1) on chromosome 3, but did not support findings at BICC1.

157 BBS3 was previously mapped to chromosome 3 by linkage analysis in a large Israeli Bedo

158 oach, we demonstrated that the centromere of chromosome 3 (Cen3) contains approximately 441 kb of the

159 s trait did not map to the MHC, idd3, or the chromosome 3 (Chr3) regions that control clonal deletion

160 to all four trait groups were identified on chromosome 3 close to the qDTY 3.2 locus.

161 Chromosome 3 comprises just four contigs, one of which c

162 In reciprocal chromosome 3 congenic mice, introgressed D2 alleles incr

163 serum cholesterol trait to a 2-Mb region on chromosome 3 containing only 11 genes.

164 ocus was mapped to a 664-kb region of canine chromosome 3 containing regional candidate gene ADAMTS17

165 dd3 has been localized to a 650-kb region on chromosome 3 containing the IL-2 gene.

166 The 1.7-Mb congenic interval on chromosome 3, containing eight genes and five microRNAs,

167 A region on the right arm of chromosome 3 contains QTL that affect both traits, but o

168 these, affecting Ara + Gal and Ara on maize chromosome 3, could be aligned with a syntenic region on

169 transfectants, HCT116 cells transfected with chromosome 3 (designated HCT116Ch3), which bears the RII

170 at expansion in intron 1 of the ZNF9 gene on chromosome 3 (dystrophia myotonica type 2 [DM2]).

171 s a 294 nt single exon gene located on human chromosome 3 encoding a 97-aa protein with sequence and

172 A quantitative trait locus (QTL) on chromosome 3 epistatically affects nitrile formation in

173 6 [Estrogen-induced pituitary tumor (Ept)1], chromosome 3 (Ept2 and Ept6), chromosome 10 (Ept9), and

174 significant additive effects while those on chromosome 3 exhibited significant dominant effects.

175 strates that the translocation breakpoint on chromosome 3 falls within the recently identified minima

176 ried out a clonal screen on the right arm of chromosome 3 for female sterile mutations using the FLP-

177 nish pedigree, which is termed FTD linked to chromosome 3 (FTD-3), and also in an unrelated familial

178 ry, causes frontotemporal dementia linked to chromosome 3 (FTD3).

179 SCRT-III), are associated with FTD linked to chromosome 3 (FTD3).

180 iated with frontotemporal dementia linked to chromosome 3 (FTD3).

181 nant frontotemporal dementia (FTD) linked to chromosome 3 (FTD3).

182 guanylate binding proteins (GBPs) encoded on chromosome 3 (Gbp(Chr3) ), which respond to pathogen-ind

183 IFN-inducible Gbp proteins encoded on mouse chromosome 3 (Gbp(chr3)).

184 hromosome 3, and near locations 49 and 81 on chromosome 3 had the strongest support as locations of l

185 NOD mice with B6 resistance alleles only on chromosome 3 have lymphocytic liver infiltration without

186 Each tumor cell line contained multiple chromosome 3 homologues with variable deletion patterns,

187 er to isolate hybrid cell clones that retain chromosome 3 homologues with various deletions within FR

188 r epidermal differentiation complex on mouse chromosome 3, human chromosome 1q21.

189 In addition, support for an elevation on chromosome 3, identified in prior independent studies, w

190 to markers in the pericentrometric region of chromosome 3 in 77 families ascertained through a child

191 these QTL was mapped to the same location on chromosome 3 in both populations, reaching chromosome-wi

192 .4 kilobases (kb) and a homologous region on chromosome 3 in humans, greater apes, and lesser apes.

193 6 genes with loss of heterozygosity (LOH) on chromosome 3 in the disomy 3 metastasizing UMs that were

194 tatically interacting QTL of large effect on chromosome 3 into at least six QTL, and complementation

195 ss of heterozygosity within the short arm of chromosome 3 is a common molecular event in several type

196 Rice (Oryza sativa L.) chromosome 3 is evolutionarily conserved across the cult

197 logous to AltSB, whereas another rice QTL on chromosome 3 is likely to correspond to the Triticeae gr

198 were simultaneously impacted by introgressed chromosomes 3S(l)#2 and 6S(l)#3, which accounts for 41.2

199 shared by both introgression lines carrying chromosomes 3S(l)#2 and 6S(l)#3, which confer resistance

200 tiated by powdery mildew resistance genes in chromosomes 3S(l)#2 and 6S(l)#3.

201 Reciprocally, the presence of NOD-derived chromosome 3 loci shortens islet xenograft survival in t

202 in NOD Idd congenic mice bearing C57-derived chromosome 3 loci.

203 Linkage analysis in MF5L6 identified a chromosome 3 locus containing the tissue factor gene (F3

204 The chromosome 3 locus was also significantly linked to card

205 The chromosome 3S locus was designated Su1-Ph1 and the chrom

206 ive linkage was found near the p-terminus of chromosome 3 (lod score, 2.2) with evidence of an intera

207 One QTL (AS-1 on chromosome 3, LOD 4.3) was found to influence aortic str

208 Almost all uveal melanomas showing chromosome 3 loss (i.e., monosomy 3) are fatal.

209 mor thickness, TNM stage, epithelioid cells, chromosome 3 loss, and chromosome 8q gain.

210 osed connective tissue loops, mitotic count, chromosome 3 loss, chromosome 6p gain, chromosome 8q gai

211 In addition, chromosome 3-loss and 8p-loss were found to be independe

212 egions showed that six signatures, including chromosome 3-loss, 1p-loss, 8p-loss, and/or 8q-gain had

213 28 patients, correlating most strongly with chromosome 3 losses and gains on 8q (Cox univariate anal

214 death was improved by considering equivocal chromosome 3 losses as abnormal and by taking account of

215 s from the same patient using 10 polymorphic chromosome 3 markers.

216 Positions of QTL detected on chromosome 3 matched those for survival detected by othe

217 s, where SpoIIIE pumps three-quarters of the chromosome (>3 megabases) into one of the two daughter c

218 herwise high risk of metastasis conferred by chromosome 3 monosomy.

219 arkers AG2H135 and AG2H603 and the second on chromosome 3 near marker AG3H93.

220 These included SNPs on chromosome 3 near ZNF659, chromosome 11 near FANCF, chro

221 ome 12, near D12S1300 (P=.0159); a region on chromosome 3, near D3S1763, with a P value of.0062; and

222 rkers and of HapMap III data on 21,991 SNPs (chromosome 3) observed in 88 unrelated individuals from

223 Consistent deletion and LOH of genes on chromosome 3 occur in metastasizing disomy 3 UM and are

224 Deletions within the short arm of chromosome 3 occur very frequently in human carcinomas:

225 inocyte lineage-specific gene locus on mouse chromosome 3, occurs during epidermal morphogenesis.

226 tibility region 10 (Idd10) introgressed from chromosome 3 of C57BL/6 (B6) and A/J mice onto the NOD b

227 onal analysis of HMS1, a region of 9.2 kb in chromosome 3 of Drosophila mauritiana, which results in

228 in which mutations have been accumulated on chromosome 3 of Drosophila melanogaster by means of sing

229 otide polymorphisms (SNPs) from 204 genes on chromosome 3 of P. falciparum.

230 complex landscape of meiotic drive genes on chromosome 3 of the fission yeasts Schizosaccharomyces k

231 ysis revealed two small candidate regions on chromosome 3, one containing the USH3A gene CLRN1, which

232 escribe the sequencing and analysis of human chromosome 3, one of the largest human chromosomes.

233 insulin-dependent diabetes (Idd)10 locus on chromosome 3, originally identified by linkage analysis,

234 rrangements, 7%; D, rearrangements involving chromosome 3 other than 3q26.2 locus, 32%; and E, gain o

235 ied linkage of Crohn's disease to regions on chromosome 3 (P=0.0009) and X (P=0.001) in our cohort.

236 tions, risk for metastasis was increased for chromosome 3 partial monosomy (hazard ratio [HR], 2.84;

237 The short arm of human chromosome 3, particularly the region 3p14.2, is a major

238 na revealed putative homologs for 67% of the chromosome 3 proteins.

239 Two isolates of maize chromosome 3 proved to contain neocentromeres in the sen

240 counterpart containing a transferred, normal chromosome 3 (RCC23+3).

241 bset analysis (OSA) suggests that the linked chromosome 3 region consists of at least two separate lo

242 dization (FISH), we mapped the gene to mouse chromosome 3, region F2-F3.

243 idence of linkage was found for hyperopia on chromosome 3, region q26 (empiric P = 5.34 x 10(-4)), a

244 c lines in which a region located on soybean chromosome 3 required for iron efficiency was identified

245 78 cM on chromosome 4, and 1.91 at 103 cM on chromosome 3, respectively.

246 y cause increases in vein density, and maize chromosome 3 results in larger bundle sheath cells with

247 genitor species, Oryza nivara, with japonica chromosome 3 revealed a high degree of sequence identity

248 nd genotyping of 28 microsatellites spanning chromosome 3 revealed that the affected child was homozy

249 R-Edn3 rats located at the q terminus of rat chromosome 3 (RNO3).

250 The strongest were on chromosome 3 (rs4603973) near SATB1, a global regulator

251 four genomic regions (rs2929366/NM_144715 on chromosome 3, rs9127/Q7Z4C4 on chromosome 5, rs1445898/C

252 single-nucleotide polymorphisms were in the chromosome 3 SCN5A and SCN10A loci, where the most signi

253 idate regions for dyslexia, including one on chromosome 3 segregating in a large Finnish pedigree.

254 ling those in tumors by exposing human-mouse chromosome 3 somatic hybrid cells to aphidicolin-mediate

255 melanoma undergoing prognostic testing with chromosome 3 status by fluorescence in situ hybridizatio

256 .6% (n = 121) of the intraocular tumors, and chromosome 3 status could be determined in 97.3% (n = 11

257 Chromosome 3 status did not contribute additional progno

258 Chromosome 3 status did not provide prognostic informati

259 affin-embedded (FFPE) uveal melanomas, whose chromosome 3 status had been determined by multiplex lig

260 The first 260 samples were also analyzed for chromosome 3 status using a single nucleotide polymorphi

261 0 tumors (20.8%) were discordant for GEP and chromosome 3 status, among which GEP demonstrated superi

262 mor-Node-Metastasis (TNM) classification and chromosome 3 status.

263 s 0.43 (P = 0.001) and 0.38 (P = 0.004) over chromosome 3 status.

264 ccuracy over clinical TNM classification and chromosome 3 status.

265 tic structures may harbor entire loss of the chromosome 3, suggesting that loss of VHL gene function

266 ory demonstrated that an 80-kb P1 clone from chromosome 3 suppresses the tumorigenicity of the mouse

267 have involved, at a minimum, the deletion of chromosome 3 telomeric to the band 3p25.3.

268 ation mapping to identify at least 11 QTL on chromosome 3 that affect variation in life span between

269 he Def-1 gene to a region on the long arm of chromosome 3 that is genetically separable from the map

270 ontransposable element related proteins from chromosome 3 that lacked similarity to other known seque

271 d a single major quantitative trait locus on chromosome 3 that mapped to the Cdcs1 (cytokine deficien

272 sing CXM, we defined genetic variants on rat chromosome 3 that reduced relative tumor growth and hema

273 tions between specific chromatin regions and chromosomes; (3) the emergence, shape, and position of g

274 levels and two independent SNPs around TF on chromosome 3, the first report of a genome-wide signific

275 represents only the third example of UPD of chromosome 3 to be reported.

276 lysis, we narrowed candidate variants on rat chromosome 3 to six genes with a priority for future ana

277 Interestingly, chromosome 3 transfer into MSH3-null HCT116 cells activa

278 40 nonmetastasizing tumors were balanced for chromosome 3 (two copies).

279 ker on chromosome 2, two adjacent markers on chromosome 3, two adjacent markers on chromosome 6, and

280 rotein E) (rs429358, P=5.5 x 10(-14)) and on chromosome 3 upstream of BCHE (butyrylcholinesterase) (r

281 detected, the deduced size of the O. nivara chromosome 3 was 21% smaller than that of japonica.

282 The number of copies of chromosome 3 was assessed by chromosome in situ hybridiz

283 A single locus on chromosome 3 was associated with Cp levels but not with

284 One additional region on chromosome 3 was linked to these phenotypes at a lower l

285 A locus on the ceruloplasmin gene on chromosome 3 was significantly associated with Cp levels

286 A genomic region on chromosome 3 was strongly associated with the early grow

287 Focusing our efforts on the human X chromosome(3), we reconstructed the centromeric satellit

288 m channel genes SCN5A, SCN10A, and SCN12A on chromosome 3 were excluded as candidates (LOD scores < o

289 Two previous QTLs on chromosome 3 were identified across experiments, whereas

290 Gains of chromosome 3 were observed in four UMs, with three of th

291 No ubiquitous gene deletions of chromosome 3 were seen in the remaining 17 metastasizing

292 Using the LASSO model, we found that only chromosome 3, when trisomic, was associated with a longe

293 ation in cell ratio was mapped to a locus on chromosome 3, where Sex determining region Y box 2 (Sox2

294 ygotes were found to map to linkage group V (chromosome 3), which is known to form rod bivalents in t

295 ESTs spanned 29 cM on the short arm of rice chromosome 3, which is known to be syntenic to long arms

296 se strains and two QTL were detected: one on chromosome 3 with a LOD score of 9.3 and a second on chr

297 The strongest association was on chromosome 3 with rs6976 (odds ratio 1.12 [95% CI 1.08-1

298 9, P = 1.8 x 10(-7)) is in the ITIH1 gene on chromosome 3, with other strongly associated nonsynonymo

299 Mouse Tsrc1 was genetically mapped to chromosome 3 within the nonrecombinant region for the so

300 ew extended sequence of eIF4GI is located on chromosome 3, within two additional exons immediately up