ライフサイエンスコーパス: chromosome 2

1 exchange of DNA segments between homologous chromosomes(2).

2 te it to the area from megabases 48 to 75 on chromosome 2.

3 recessive gene located in a 1.1-Mb region on chromosome 2.

4 and mapping localized the critical region to Chromosome 2.

5 ome 1 of V. anguillarum 775(pJM1) and two in chromosome 2.

6 1 and found some evidence for another QTL on chromosome 2.

7 s) is linked to an inversion polymorphism on chromosome 2.

8 uplicates of core genes located primarily on chromosome 2.

9 ed by ref(2)P and is caused by other loci on chromosome 2.

10 syndrome (DRS) linked to the DURS2 locus on chromosome 2.

11 of five SCPL genes arranged in a cluster on chromosome 2.

12 us was minimally affected by the presence of chromosome 2.

13 major QTL on chromosome 3 and a minor QTL on chromosome 2.

14 ty 6 [MOB6]) and 84-180 Mb (MOB5) from mouse chromosome 2.

15 due to the presence of the SLC11A1 locus on chromosome 2.

16 linkage, for both CAD and MI, to a region on chromosome 2.

17 AML) is characterized by loss of one copy of chromosome 2.

18 e carriers to map ADANE to a 6.5Mb region on chromosome 2.

19 s spanning more than 55 kb of genomic DNA on Chromosome 2.

20 nt of DiGeorge syndrome, was mapped to mouse chromosome 2.

21 genes are contiguous and localized on mouse chromosome 2.

22 26 intergenes in a 68-kb region of S. pombe chromosome 2.

23 aturation is controlled by a separate QTL on chromosome 2.

24 luster of putative Eppin-like genes on mouse chromosome 2.

25 tion of AAGAG repeats near the distal tip of chromosome 2.

26 c contribution to variance in life span from chromosome 2.

27 nd resulted in a maximum LOD score of 3.4 on chromosome 2.

28 gulated principally by the Hc locus on mouse chromosome 2.

29 4% of the predicted genes and pseudogenes on chromosome 2.

30 converted to the corresponding sequences of chromosome 2.

31 oughout chromosome 1 and one binding site in chromosome 2.

32 whole genome resequencing focused on chicken chromosome 2.

33 and sheath blight disease resistance on rice chromosome 2.

34 f the causal mutations to a narrow region in chromosome 2.

35 ocated in one of the runs of homozygosity on chromosome 2.

36 lex rearrangement involving the short arm of chromosome 2.

37 etic analyses assigned the bs locus to mouse chromosome 2.

38 ) for rs9679290 in the EPAS1 (HIF2A) gene on chromosome 2.

39 s a mutant allele of the Gata3 gene on mouse Chromosome 2.

40 ta = -0.23) at the integrin, alpha 4 gene on chromosome 2.

41 of five microsatellite markers from proximal Chromosome 2.

42 around the site of ancestral fusion in human chromosome 2.

43 rg) within a shared haplotype of 2.93 Mbp on chromosome 2.

44 Snn2, which mapped to the short arm of wheat chromosome 2D.

45 ops tauschii contains W2 and Iw2 paralogs on chromosome 2D.

46 and three of these were designated as marker chromosomes 2.

47 speciation, and additional candidate loci on chromosomes 2 (079 and 175) and 3 (088) are discovered t

48 Nevertheless, the positive findings on chromosome 2, 10, and 22 should be pursued further.

49 ree novel genome-wide significant signals on chromosomes 2, 11, and 16.

50 or nine) IBK scores showed that locations on chromosomes 2, 12, 13 and 21 were associated with IBK di

51 may harbor genes influencing the latter, on chromosomes 2, 13, 16, and 19.

52 In addition, a region on chromosome 2 (193 cM) showed a significant increase in t

53 On multivariate analysis, loss of chromosomes 2 (2.4-4.1 Mbp) and 16 (33.8-35.6 Mbp) were

54 the tip with the centric heterochromatin of chromosome 2 (2h), which contains megabases of AAGAG rep

55 conducted for trisomics for the left arm of chromosome 2 (2L) and compared with the normal genotype.

56 of the Rf alleles mapped to the long arm of chromosome 2 (2L), and 5 of these were further mapped to

57 Alterations of the short arm of chromosome 2 (2p) have been of particular interest, sinc

58 /= 3) were detected at 33-42 centimorgans of chromosome 2 (2p24.3-2p24.1), with a maximum LOD score o

59 An intergenic region of human chromosome 2 (2p25.3) harbors genetic variants which are

60 solution deletion mapping of the long arm of chromosome 2 (2q) in invasive cervical carcinoma (CC).

61 inal evidence (P <.05) on several additional chromosomes (2, 3, 4, 10, 11, 12, 15, 18, and 20).

62 ated with Nematodirus FEC were identified on chromosomes 2, 3 and 14.

63 s found for quantitative trait loci (QTL) on chromosomes 2, 3, 14 and 20.

64 1 (FDR = 1.3E-04), with additional probes on chromosomes 2, 3, 4, 7, 12, 16, and 19.

65 al new significant or suggestive QTLs on rat chromosomes 2, 3, 7, 10, and 19 that control susceptibil

66 e also obtained other suggestive linkages on chromosomes 2, 3, 7, 8, 9, 12, 13, and 21.

67 g identified genome-wide significant QTLs on chromosomes 2, 3, 8, 10 (two QTLs), 15, and 18.

68 data suggest that quantitative trait loci on chromosomes 2, 3, 9, and 10 may influence circulating ad

69 he SR region spans more than half of the mat chromosome (>2.3 Mbp) and that it is of very recent orig

70 led 15 significant SNPs (P-value <10(-3)) on chromosomes 2D, 3B, 4D and 7B that were associated with

71 fresh market, and vintage), particularly on chromosomes 2, 4, 5, 6, and 11.

72 We identified six loci on chromosomes 2, 4, 7, 10, 11, and 18 that were linked to

73 n new prostate cancer susceptibility loci on chromosomes 2, 4, 8, 11 and 22 (with P = 1.6 x 10(-8) to

74 showed suggestive evidence of association at chromosomes 2, 4, and 10.

75 ur findings provide evidence that regions of chromosomes 2, 4, and 12 influence the development and p

76 tified four quantitative trait loci (QTL) on chromosomes 2, 4, and 8, with the QTL on chromosome 8 sh

77 o isolate large centromeric regions of human chromosomes 2, 5, 8, 11, 15, 19, 21 and 22 from human ce

78 trate the approach using root-growth QTLs on chromosomes 2, 5, and 9 of the Bala x Azucena rice mappi

79 support that boas and pythons possess ZW sex chromosomes [2, 5].

80 25-family data set, including two regions on chromosome 2 (57 Mb, NPL = 2.98; 145 Mb, NPL = 3.09), as

81 Association of 62 SSR loci on chromosomes 2D, 5A, and 5B with kernel morphology and mi

82 Four chromosomes (2, 6, 11, and 17) harbored loci contributin

83 with both length and weight were detected on chromosomes 2, 6 and 9 in multiple datasets.

84 Genetic association between SNPs on chromosomes 2, 6, 7, 9, 16 and 18 and CAC were detected

85 . C. thermophilum genome was composed of two chromosomes (2,683,362 bp and 1,012,010 bp), and both en

86 i for influenza virus resistance) located on chromosomes 2, 7, 11, 15, and 17 associated with resista

87 y traits were variously influenced by QTL on chromosomes 2, 7, 12, 15, and 16.

88 We find that all four HOX gene clusters on chromosomes 2, 7, 12, and 17 are preferential targets fo

89 ogous POTE family genes are found on 8 human chromosomes (2, 8, 13, 14, 15, 18, 21 and 22), which can

90 cortex gray matter volume were identified on chromosomes 2, 8, 16 and 19.

91 Locations on chromosomes 2, 9 and 10 remained significant after testi

92 ed recurrent alterations, including gains on chromosomes 2, 9p, 12p, and 21 and losses on 4q, 8p, 15,

93 ) and two QTLs (qSNAX.2 A.1, qSNAX.2 A.2) on chromosome 2 A coincided with a reported major NAX QTL (

94 The mouse L3mbtl gene is located on chromosome 2, a region of syntenic homology with human c

95 Chromosome 2 also harbors a superintegron, as well as ho

96 , all CAI-4 strains tested were trisomic for chromosome 2 although this trisomy appears to be unstabl

97 llion base pairs of the Adh-cactus region of chromosome 2 and 85,000 base pairs of the 82F region of

98 A significant, protective modifier locus on chromosome 2 and a suggestive locus on chromosome 13 tha

99 (Mcs1), is located on the centromeric end of chromosome 2 and appears to act in a semidominant fashio

100 admixture localized to discrete segments on chromosome 2 and at the HIVAN4 locus.

101 lacking one of two KRAB-ZFP gene clusters on chromosome 2 and chromosome 4 were nonetheless viable.

102 lines, we mapped Moo1 to an 8-Mb segment of chromosome 2 and demonstrated that Moo1 exerts its effec

103 ferase 1 (UGT1) locus spans nearly 200 kb on chromosome 2 and encodes nine UGT1A proteins that play a

104 allele at D2Mit29 on the centromeric end of chromosome 2 and extended distally to D2Rat201.

105 The diminutive mutation was mapped to chromosome 2 and fine mapped to scaffold 25.

106 located in intron 10 of Sfmbt2 gene on mouse chromosome 2 and has a pro-apoptotic role.

107 i (top SNPs: rs76114856 in the CENPO gene on chromosome 2 and rs6669072 near LOC105378853 on chromoso

108 P in each of these loci being rs187848990 on chromosome 2 and rs8100891 on chromosome 19.

109 t percent of these ESTs were present on rice chromosome 2 and the remaining were on other rice chromo

110 mum of five QTL in a genomewide scan: two on chromosome 2 and three on chromosome 3.

111 y conserved flanking Npdc1 and Abca2 loci on chromosome 2 and which contains the complete transcripti

112 he frequency of polymorphisms across the two chromosomes (2 and 3) examined most extensively, with an

113 ranscription factors ZmIDDveg9 and ZmIDD9 on chromosomes 2 and 10, respectively.

114 ) with chromosome 12 (LOD 5.03 at 35 cM) and chromosomes 2 and 12 for FEF(25-75%)/FVC (LOD 4.12 at 22

115 Interaction between genes on chromosomes 2 and 12 was present for all obesity traits,

116 OXO1, resulting from a translocation between chromosomes 2 and 13, is the most common genetic aberrat

117 ant (P < .01) polymorphic loci were found on chromosomes 2 and 16 for liver and on chromosomes 8 and

118 candidate genes for two sex-specific QTL on chromosomes 2 and 17.

119 al mapping identified new angiogenic QTLs on chromosomes 2 and 19, in addition to confirming our prev

120 For the learning disability subgroup, chromosomes 2 and 22 were most involved.

121 el' for the evolution of rice (Oryza sativa) chromosomes 2 and 3, implying that the grass common ance

122 identified 18 A. gambiae SRPN genes, all on chromosomes 2 and 3, through searches of genomic DNA and

123 vely, our students mapped 95 genetic loci on chromosomes 2 and 3.

124 inherited a reciprocal translocation between chromosomes 2 and 3.

125 three mRNA variants, encoded by two genes on chromosomes 2 and 3.

126 tenic with duplicated regions of Arabidopsis chromosomes 2 and 4, none of which harbor CLV1 or any ot

127 as well as near the nucleolus organizers on chromosomes 2 and 4.

128 ave identified two modifying loci on C57BL/6 chromosomes 2 and 5, which affect the penetrance of embr

129 with recessive D. virilis alleles at loci on chromosomes 2 and 5.

130 ); large regions that differed were found on chromosomes 2 and 6.

131 emonstrate consistent evidence of linkage to chromosomes 2 and X and also support the hypothesis that

132 Three QTL located on chromosomes 2 and X were identified to trigger significa

133 The extent of LD was estimated on chromosomes 2D and part of 5A, relative to the LD observ

134 HOSPHO1, SYNGAP1 and an intergenic region in chromosome 2) and triglycerides (MYLIP, TXNIP and SLC7A1

135 re linked to the X chromosome, 16 markers to chromosome 2, and 10 and 11 markers to chromosomal arms

136 ately 237 million base pairs of sequence for chromosome 2, and 186 million base pairs for chromosome

137 rotein-coding genes and 1,239 pseudogenes on chromosome 2, and 796 protein-coding genes and 778 pseud

138 onary TNF-alpha production was identified on chromosome 2, and a region affecting both polymorphonucl

139 Psl2 maps near D2Mit229 on distal chromosome 2, and inheritance of the dominant DBA/2 alle

140 nking radiation-sensitive fragile domains on chromosome 2, and subsequent R235 conversion are highly

141 ave suggested that polymorphisms in CASP8 on chromosome 2 are associated with breast cancer risk.

142 dicate at least 50% of hypothetical genes on chromosome 2 are expressed in the cDNA populations with

143 e-long region of the Drosophila melanogaster chromosome 2 as a model, we observed that the six gene-p

144 reased gene amplication in the distal arm of chromosome 2, as shown by comparative genomic hybridizat

145 We previously mapped a locus on BALB/c chromosome 2 associated with protection from leptin-defi

146 study (GWAS) detected a significant peak on chromosome 2 associated with the polygenic component of

147 The absence of a chromosome 2 association signal in this or previous asso

148 ral regions of suggestive linkage for CFPWV: chromosome 2 at 94 cM (LOD=2.46), chromosome 7 at 29 cM

149 subjects (logarithm of odds [LOD] = 3.4) on chromosome 2 at 95 cM (between GATA69E12 and GATA71G04)

150 l GWS association (1.17 x 10(-10)) mapped to chromosome 2 at rs1437396, between MTIF2 and CCDC88A, ac

151 sociations with homoarginine serum levels on chromosome 2 at the carbamoyl phosphate synthetase I loc

152 cting oocyst density were identified: one on chromosome 2 between markers AG2H135 and AG2H603 and the

153 nt in NCAM1 (chromosome 11) and a variant on chromosome 2 (between TEX41 and PABPC1P2) that has a tra

154 een recombination map positions 54 and 81 on chromosome 2, between 0 and 30 on chromosome 3, and near

155 iator protein of Vibrio cholerae specific to chromosome 2 (Chr2) also has single-strand binding activ

156 initiator of replication of Vibrio cholerae chromosome 2 (chr2), binds to the origin of replication

157 n chromosome 8, chr8-60.4 Mbp (LOD 3.8), and chromosome 2, chr2-243.5 Mbp (LOD 3.4).

158 QTL) regulating Scg5 expression in two mouse chromosome 2 congenic strains and three additional F2 in

159 iterpenoid phytoalexins, with the cluster on chromosome 2 containing four closely related/homologous

160 to possess crop haplotypes in the portion of chromosome 2 containing the ACETOLACTATE SYNTHASE gene,

161 The mouse ePAB gene on chromosome 2 contains 14 exons that specify an alternati

162 Our results demonstrate that mouse chromosome 2 contains a conserved linkage of Eppin-like

163 In contrast, chromosome 2 contains a larger fraction (59%) of hypothe

164 y QTL in the 36E;38B cytogenetic interval on chromosome 2 contains multiple closely linked QTLs, incl

165 These data support evidence for a gene on chromosome 2 contributing to risk of AutD, and they sugg

166 aps near a quantitative trait locus (QTL) on chromosome 2 controlling ear rank differences between ma

167 ven its strong effect, the linkage region on chromosome 2 could harbor a potentially important determ

168 gnificant linkage to glomerular crescents on chromosome 2 (Crgn8, LOD = 3.8).

169 to data from the Seattle SNP project and to Chromosome 2 data from the HapMap project.

170 n interstitial deletion of one copy of mouse chromosome 2 (del(2)).

171 The presence of chromosome 2 did not have consistent effects on the amou

172 t for the phytocassanes, is not found in the chromosome 2 diterpenoid biosynthetic gene cluster.

173 commonly acquire an interstitial deletion of chromosome 2 during progression.

174 because we could define a critical region in chromosome 2 encoding eight genes including BMP10 that c

175 ethod to a non-simulated dataset-a region on Chromosome 2 encompassing a short deletion.

176 In addition, BALB/c alleles on chromosome 2 exerted a cell-autonomous role in restraini

177 Only markers from the centromeric tip of Chromosome 2 failed to segregate independently from jal,

178 hromosomes 7, 8, 11, and 19 for liver and on chromosome 2 for spleen.

179 sis, two marker chromosomes 1 and two marker chromosomes 2 formed bivalents, whereas the others were

180 nzee pericentric inversion and the ancestral chromosome 2 fusion both predisposed and protected the c

181 The chromosome 2 gene is intronless and would encode a prote

182 c locus for isolated DRS, the DURS2 locus on chromosome 2, has been mapped to date.

183 sequences totalling approximately 2 Mb from chromosome 2 have been duplicated and inserted into chro

184 ells were previously stably transferred with chromosome 2 (HCT116+chr2), restoring a single regulated

185 linkage for the ratio FEV1/FVC was found on chromosome 2 (heterogeneity lod = 2.36, dominant model)

186 Previous characterization of mouse chromosome 2 identified genomic intervals that influence

187 d TMEM18 and regions downstream of TMEM18 on chromosome 2 in 3976 individuals of European ancestry fr

188 locus (QTL), Tmc1m1, for DPOAE amplitude on chromosome 2 in [(C/B)F1xC]N2-Tmc1Bth/+ backcross progen

189 he GRD3 family was acquired more recently on chromosome 2 in a lineage of N. tomentosiformis, the pat

190 The Gatm gene maps to mouse chromosome 2 in a region not previously shown to contain

191 of Iw1 has >94% identity to an IR region on chromosome 2 in Ae. tauschii that also produces miRW1 an

192 by alternative splicing of a gene located on chromosome 2 in humans, and orthologs of CRIP1a occur th

193 were mapped to the telomeric region of mouse chromosome 2 in independent founder families.

194 The strongest is located on chromosome 2, in an intergenic region 35- to 80-kb upstr

195 carry a nonreciprocal translocation on human chromosome 2, in which synchronized double stranded brea

196 ain 2 quantitative trait loci: the region on chromosome 2 included the C5 fraction of complement know

197 us work has shown that the presence of human chromosome 2 increases HIV-1 production in mouse cells.

198 A Ter site on chromosome 2 interacted pairwise with two Ter sites loca

199 enerated by an inversion on the short arm of chromosome 2: inv(2)(p21p23).

200 gene trees supports genetic introgression of chromosome 2 inversions between An. gambiae and An. arab

201 as been observed that a major QTL, se2.1, on chromosome 2 is responsible for a large portion of pheno

202 Human chromosome 2 is unique to the human lineage in being the

203 ncreased capsid production in the absence of chromosome 2, it did not result in a corresponding incre

204 wever, its effect requires a target locus on chromosome 2 known as Responder (Rsp).

205 led disruption of a single noncoding gene on chromosome 2, LINC00299, whose RNA product is expressed

206 yotyping shows gross abnormalities involving chromosome 2 (location of the FRZB gene) in five of twel

207 eterozygosity (LOH) was detected only at the chromosome 2 locus in all tumors from this family, consi

208 The chromosome 2 locus mapped near Mtap1a, which encodes a p

209 ranscription profiling and helped refine the chromosome 2 locus.

210 evidence for linkage of FEF(25-75%)/FVC with chromosome 2 (LOD 2.60 at 216 cM).

211 or linkage also was robust for FEV(1)/FVC on chromosome 2 (LOD 4.13 at 229 cM) and FEV(1) on chromoso

212 in addition to strong evidence of linkage to chromosome 2 (LOD=4.9), also produced a LOD of 2.4 on ch

213 We also found suggestive linkages on chromosomes 2 (LOD 1.58, 216 cM) and 7 (LOD 1.78, 163 cM

214 tative evidence of linkage was also found on chromosomes 2 (LOD = 1.7 at 89 cM), 3 (LOD = 1.9 at 124

215 e (LOD score 2.43) of opioid dependence with chromosome 2 markers for the AA subjects.

216 In summary, a genomic region on chromosome 2 may contain a pleiotropic locus contributin

217 construction for (1) genome-wide or multiple chromosomes, (2) multi-allelic and (3) extremely sparse

218 A genome scan revealed a locus on chromosome 2, named modifier of dw hearing, or Mdwh, tha

219 Fat-related loci occurring on mid-chromosome 2 near 60 cM, proximal chromosome 6, and mid-

220 ariants all map to a novel genetic region on chromosome 2 near the ASB3 gene, a region associated wit

221 CN and carrier FRE) mapped to the region of chromosome 2 near the candidate gene fruitless, identify

222 L1A and IL1B genes lie in close proximity on chromosome 2 near the gene for their natural inhibitor,

223 r CPO at or near genome-wide significance on chromosomes 2 (near CTNNA2) and 19 (near SULT2A1).

224 aches link VEGF responsiveness to regions on chromosomes 2 (near D2Mit6) and 10 (near D10Mit20).

225 d to the nucleolus organizer region (NOR) on chromosome 2 (NOR2).

226 velopment were recently mapped to the NOR on chromosome 2, NOR2, whereas active rRNA genes map to NOR

227 ease 2-like 1; P=5.7x10(-15)) and a locus on chromosome 2 (not near known genes) were associated with

228 n mutation in Ube2l6 that contributes to the chromosome 2 obesity quantitative trait locus.

229 as well as 163 other genes from one copy of chromosome 2 occurred in a hematopoietic stem cell (HSC)

230 howed that body weight (BW) loci on proximal chromosome 2 occurred in the same region as body length,

231 e cryptic (fla2) flagellar system encoded on chromosome 2 of B. thailandensis supported rapid intrace

232 The annotated sequence of chromosome 2 of Plasmodium falciparum was examined for g

233 It is located at the bottom of chromosome 2 of the Arabidopsis genome.

234 Finally, we ran IBIS on chromosome 2 of the UK Biobank dataset and estimate its

235 mpact imprinted Gnas cluster on distal mouse chromosome 2, one at exon 1A upstream of Gnas itself and

236 25% of the tumors displayed either a gain of chromosome 2 or loss of Y, the majority (75%) showed no

237 The region identified on chromosome 2 overlaps linked regions observed in two oth

238 5-5.02]) and rs9309464 in the EXOC6B gene on chromosome 2 (p = 6.01 x 10(-5); G allele OR 0.66 [95% C

239 crosatellites on chromosome 3 as compared to chromosome 2 (P=0.0001).

240 ith highly significant linkage were found on chromosomes 2 (Pgis2) and 18 (Pgis1) accounting for 40%

241 The chromosome 2 position effect is not explained by the NOR

242 ith C57BL/6J alleles, is a candidate for the chromosome 2 QTL for higher iron.

243 (positive) or chromosome 7 (negative); this chromosome 2 region has been implicated elsewhere in stu

244 ingle-nucleotide polymorphisms (SNPs) in the chromosome 2 region that included the Frizzled-related p

245 of 62 pheochromocytomas with LOH within the chromosome 2 region, which further narrowed down the loc

246 nstrated definitively that a locus on murine chromosome 2 regulates hematopoietic stem cell aging.

247 ABBR2, RUFY3, and in an intergenic region on chromosome 2 replicated with the same direction of effec

248 his system the presence of Sd on one copy of chromosome 2 results in dysfunction of the non-Sd-bearin

249 tified a major susceptibility locus on mouse chromosome 2 (rs27328255, P=6.68 x 10(-7)).

250 ase recruitment domain-containing 4) gene on chromosome 2 (rs385076; P=2.4 x 10(-45)).

251 Markers on chromosome 2 segregated with high tumor multiplicity in

252 omes 10, 11 and 14, and a re-analysis of the chromosome 2 sequence.

253 are referred to as "hypothetical genes." On chromosome 2, sequenced by The Institute for Genomic Res

254 In the other mutant, ife, chromosome 2 sequences totalling approximately 1.4 Mb ha

255 QTL on chromosome 2 showed significant additive effects while t

256 condensin subunit, structural maintenance of chromosomes 2 (SMC2), in unextracted metaphase chromosom

257 The admixture mapping signal identified on chromosome 2, spanning q11.2-14.1 and not previously rep

258 cating that selective rRNA gene silencing is chromosome 2-specific.

259 polar spindle structures around unreplicated chromosomes; 2) sperm nuclei added to extracts that cycl

260 Approximately 101 chromosome 2 substitution lines were scored for componen

261 ngs of nonrandom distribution of SNPs across chromosome 2, suggest that the Plasmodium falciparum gen

262 scriptional hotspot of vir genes observed on chromosome 2 suggests a potential active site modulating

263 ne integrations into the same locus on mouse chromosome 2 targeting a gene that is expressed in the n

264 genes in the 45A region on the right arm of chromosome 2 that are involved in oogenesis in Drosophil

265 The lack of a subtelomeric region of chromosome 2 that contains kahrp and pfemp3 causes reduc

266 th a large (>20 Mb) interstitial deletion of chromosome 2 that includes PU.1.

267 gs strongly suggest that there is a locus on chromosome 2 that influences coronary atherosclerosis ri

268 F in the rat is influenced by a locus on rat chromosome 2 that is also associated with cardiac capill

269 dominant suppressors, in the cases tested on chromosome 2 the suppressor mapped to the 2L telomere, r

270 uding (1) the folding patterns of individual chromosomes; (2) the highly enriched interactions betwee

271 In Chromosome 2, the most extreme signal is found in the la

272 antly reduced fork arrest at the Ter site on chromosome 2, thereby revealing a cooperative mechanism

273 rected by one or more genes present on human chromosome 2 to allow production of infectious HIV from

274 in by introgression of a segment of C57BL/6J chromosome 2 to the BALB/c background to confirm the gen

275 veying the panel of strains with substituted chromosomes; (2) to rapidly develop congenic strains ove

276 t linkage to AMD was found for one marker on chromosome 2, two adjacent markers on chromosome 3, two

277 d 2005 revealed that the V. parahaemolyticus chromosome 2 type III secretion system is not specifical

278 QTL) for fruit firmness was mapped to tomato chromosome 2 using the Zamir Solanum pennellii interspec

279 mosome 6q, as well as evidence of linkage on chromosome 2, using a dominant model.

280 single-nucleotide polymorphism (SNP) loci on chromosome 2 was common to all affected sheep and it was

281 A genetic linkage group on chromosome 2 was selected under artemisinin treatment.

282 Consistent LD on chromosome 2D was <1 cM, whereas in the centromeric regi

283 low frequency of an interstitial deletion of chromosome 2) was similar to that of the previous transg

284 3), which is 20 kb upstream of CXCR7 gene on chromosome 2, was associated with the total mean FA valu

285 rs from all of the 797 hypothetical genes on chromosome 2 were designed, and, through 5' and 3' RACE,

286 lymorphisms (SNPs) across STAT1 and STAT4 on chromosome 2 were genotyped using the Illumina platform,

287 Only those containing human chromosome 2 were permissive, which correlated with caps

288 Coat color maps to chromosome 2 where a strong candidate gene, tyrosinase-r

289 t (IL-1RN), are present at a single locus on chromosome 2, whereas IL-18 and IL-33 lie on chromosomes

290 Mutations on the right arm of chromosome 2 (which contains approximately 20% of the Dr

291 region exhibiting conserved synteny to human chromosome 2, which included one of the three dilute can

292 icrosatellite loci within the j inversion on chromosome 2, which is fixed in the Bamako form but abse

293 o the UBCS pattern found in all autosomes is chromosome 2, which shows a UBCS peak midchromosome, map

294 ed many associations with genomic regions in chromosome 2 with also the highest explained variation c

295 asis for association of the PARK11 region of chromosome 2 with familial Parkinson disease (PD) is unk

296 with a maximum model-free LOD score of 2.2; chromosome 2, with a LOD score of 2.1; chromosome 6, wit

297 e greatest evidence for linkage was found on chromosome 2, with a peak LOD of 3.34 at 240 cM.

298 ss a 40Kb region of Drosophila pseudoobscura chromosome 2, with one 20kb interval assayed every 5Kb a

299 ithm of odds [LOD] 4.53) was a broad peak on chromosome 2, with weaker linkage to age of type 2 diabe

300 We mapped Optn to chromosome 2, within a region that is syntenic to human