ライフサイエンスコーパス: chromosome 11

1 .86 x 10(-9)) (chromosome 13) and a locus on chromosome 11.

2 ybrid hamster cells (A(L)N) containing human chromosome 11.

3 4 patients demonstrated UPD for the whole of chromosome 11.

4 f BWS cases have uniparental disomy (UPD) of chromosome 11.

5 7 colocalized with one allele of Wsb1/Nf1 on chromosome 11.

6 b T-helper 2 (T(H)2) cytokine locus on mouse chromosome 11.

7 of 45 coding exons spanning 108 kb on mouse chromosome 11.

8 mapping entirely to the distal half of mouse chromosome 11.

9 us of chromosome 7 and the Wsb1-Nf1 locus of chromosome 11.

10 atory regions of the T(H)2 cytokine locus on chromosome 11.

11 a cell) that contains a single copy of human chromosome 11.

12 apped to the Ovum mutant (Om) locus on mouse chromosome 11.

13 r diabetes-resistant C57L (NOD.LC11) loci on chromosome 11.

14 KCNJ11) are adjacent to one another on human chromosome 11.

15 (Dup mutant) of the syntenic region on mouse chromosome 11.

16 tment and TNF-alpha levels was identified on chromosome 11.

17 stinct regions spanning approximately 40% of chromosome 11.

18 cated either loss or retention of the entire chromosome 11.

19 exons within a human genomic DNA fragment on chromosome 11.

20 linking to the EVR1 locus on the long arm of chromosome 11.

21 ets found at the functional mouse cluster on Chromosome 11.

22 lated gain involving the entire short arm of chromosome 11.

23 pe 2B (DA2B), the most common of the DAs, to chromosome 11.

24 lian fashion as a recessive gene residing on chromosome 11.

25 ific backcross panel places it at 63.0 cM on chromosome 11.

26 ecessive mouse mutations, 88 of which are on chromosome 11.

27 e family located on a small segment of mouse chromosome 11.

28 aled that 9 of 11 (82%) of CIS had losses on chromosome 11.

29 ed by a terminal deletion of the long arm of chromosome 11.

30 n that uses a balancer chromosome, inversion chromosome 11.

31 iously described H2a.X gene located on human chromosome 11.

32 on interval and its syntenic region on mouse chromosome 11.

33 d a tumor suppressor gene to the long arm of chromosome 11.

34 type, called Ltxs1, has been mapped to mouse chromosome 11.

35 ML, and apparent preferential methylation on chromosome 11.

36 ne Tbx21 gene, and its localization to mouse chromosome 11.

37 BQLN3 gene was mapped to the 11p15 region of chromosome 11.

38 (Csfgm or Csf2), are tightly linked on mouse chromosome 11.

39 metastasis suppressor genes encoded on human chromosome 11.

40 use of 22 STRP markers in a 55-cM region of chromosome 11.

41 nd NRH2 and NRH3 are less than 48kb apart on chromosome 11.

42 capture sequencing of the linked interval on chromosome 11.

43 on ratio distortion at the Om locus on mouse chromosome 11.

44 been physically mapped within 1 Mb of mouse chromosome 11.

45 1 has been mapped near the p53 gene on mouse chromosome 11.

46 d is located in the syntenic region of mouse chromosome 11.

47 and have mapped it as a single-copy gene on chromosome 11.

48 lysin genes in a repetitive region on cattle chromosome 11.

49 ion, resulting in paternal disomy of part of chromosome 11.

50 ther gene, Boymaw (also termed DISC1FP1), on chromosome 11.

51 nd was represented by copy gains of genes in chromosome 11.

52 which, assuming synteny, is located on avian chromosome 11.

53 Trp53 are both closely located on the mouse chromosome 11.

54 using a panel of microsatellite markers for chromosome 11.

55 lso exhibited a copy number loss of proximal chromosome 11 (11A-B), a region orthologous to human 17p

56 MPc3 maps to the distal arm of mouse chromosome 11 (11E2), a region that contains other known

57 ivity with the SPON1 variant at rs2618516 on chromosome 11 (11p15.2) reached connectome-wide, genome-

58 by the fatty acid desaturase (FADS) cluster (chromosome 11, 11q12.2-q13) and certain genetic variants

59 assification have led to linkage to sites on chromosomes 11, 13 and 16 and identification of the firs

60 Other loci on chromosomes 11, 14, and 16 were suggestive of linkage to

61 24/31) as being orthologous to three B. mori chromosomes (11, 23 and 24, respectively).

62 ies of mice with regional deletions on mouse chromosome 11 (33-80 cM) that can subsequently be subjec

63 We previously identified a 210 kb region on chromosome 11 (50.37-50.58 Mb, mm10) containing two prot

64 and STAT5b are encoded by adjacent genes on chromosome 11 (60.5 cM).

65 at3) gene and a 500-kb region spanning mouse chromosome 11, 60.5 cM containing three Stat genes (m-St

66 nine of 15 tumors exhibited a gain of distal chromosome 11, a region that is orthologous to human chr

67 Abca13 has been mapped to mouse chromosome 11.a2, revealing the human orthologue highly

68 ice carrying a duplication [Dp(11)17] in one chromosome 11 along with a null allele of Rai1 in the ot

69 leles at the Ovum mutant (Om) locus on mouse chromosome 11 among the offspring of (C57BL/6 x DDK) F(1

70 ghlighted a putative susceptibility locus on chromosome 11, among the later-onset families, with a LO

71 Chromosome 11 amplicons distal to Erbb2 arise in a model

72 mong the various models, including recurrent chromosome 11 amplifications and chromosome 4 deletions,

73 on results in the fusion of the API2 gene on chromosome 11 and a novel gene termed MALT1 on chromosom

74 egion near the CC16 coding gene (SCGB1A1) on chromosome 11 and another locus approximately 25 Mb away

75 Thus, the breakpoints on both chromosome 11 and chromosome 22 are clustered in multipl

76 gene: It spans at least 35 kilobases (kb) on chromosome 11 and contains five exons and four introns.

77 We identified one QTL on chromosome 11 and found some evidence for another QTL on

78 PSMA/GCPII is located on the short arm of chromosome 11 and functions as both a folate hydrolase a

79 d US differ considerably on the genome-wide, chromosome 11 and HbS mutation locus levels.

80 nnegan and defolliculated has been mapped to chromosome 11 and here we show that both mice harbor mut

81 lustered in 150-kb syntenic regions on mouse chromosome 11 and human chromosome 5q31.

82 c segment is syntenically conserved on mouse chromosome 11 and is bounded by the mouse homologs of th

83 o the interstitial deletion of band p11.2 of chromosome 11 and is characterized by multiple exostoses

84 The murine Rad51l2 gene maps to chromosome 11 and is located in the syntenic region of h

85 RAINB1 is present on chromosome 11 and is spread over 38 exons, resulting in

86 dearth of genes in the breakpoint region of chromosome 11 and it is therefore unlikely that the expr

87 tFL samples included gains of 3q27.3-q28 and chromosome 11 and losses of 9p21.3 and 15q.

88 urase genes reside in reverse orientation on chromosome 11 and that they are separated by <11,000 bas

89 re contained within a 140-kb region of mouse chromosome 11 and their expression is controlled by a lo

90 rid clones containing a single copy of human chromosome 11 and which were treated with 5-aza-2'-deoxy

91 Interestingly, the short arms of rice chromosomes 11 and 12 (and independently their homologs

92 ication of gene clusters as observed on rice chromosomes 11 and 12 and arabidopsis chromosome 5.

93 Based on detailed analysis of rice chromosomes 11 and 12 and their homologs in seven grass

94 8% of japonica paralogs produced 5-7 MYA on chromosomes 11 and 12 have been affected by gene convers

95 ce is exceptional regarding the evolution of chromosomes 11 and 12, inasmuch as in other species the

96 imilarity between the short arm ends of rice chromosomes 11 and 12.

97 at the distal ends of the short arms of rice chromosomes 11 and 12.

98 cells, single-copy GLTP genes were found in chromosomes 11 and 12.

99 reciprocal chromosome translocation between chromosomes 11 and 13 in two accessions of wild soybean.

100 Second, a translocation event between chromosomes 11 and 13 of some genotypes is shown to inte

101 subset of survivors that has lost fibroblast chromosomes 11 and 14 (tumor suppressor loci for this sy

102 four on chromosome 12 and additional two on chromosomes 11 and 15 were associated with flowering tim

103 associated with flowering time, and four on chromosomes 11 and 16 were associated with seed size.

104 affected, with most chromothriptic events on chromosomes 11 and 17 including, among other significant

105 mapping these regions (with the exception of chromosomes 11 and 17), most linkage peaks remained simi

106 male affected identified the same signals on chromosomes 11 and 17, as well as three other regions on

107 ess Scale genome scan identified two loci on chromosomes 11 and 17, with the highest score on chromos

108 an 16p13.3 switches in synteny between mouse Chromosomes 11 and 17.

109 will harbor a balanced translocation between chromosomes 11 and 18.

110 amilies), and fine mapping of the regions of chromosomes 11 and 20.

111 est the hypothesis that spatial proximity of chromosomes 11 and 22 in meiotic prophase oocytes and sp

112 have been mapped to specific Alu repeats on chromosomes 11 and 22, indicating that this event is due

113 events between similar AT-rich sequences on chromosomes 11 and 22, resulting in deletions and loss o

114 thin palindromic AT-rich repeats (PATRRs) on chromosomes 11 and 22, suggesting that hairpin/cruciform

115 strand breaks in AT-rich palindromes on both chromosomes 11 and 22.

116 gation event resulting in partial trisomy of chromosomes 11 and 22.

117 chromosome 2, whereas IL-18 and IL-33 lie on chromosomes 11 and 9, respectively.

118 on ratio distortion at loci on two different chromosomes, 11 and X.

119 ing behaviour, including a variant in NCAM1 (chromosome 11) and a variant on chromosome 2 (between TE

120 78% on the genomic level and 44% vs. 76% on chromosome 11) and presented a signature of positive sel

121 ss-of-function mutations in the MEN1 gene on chromosome 11, and endocrine tumors arising in these pat

122 hown that it maps near the mouse CD7 gene on chromosome 11, and established that the mouse K12 protei

123 Eleven IRs from Chromosome X, one from Chromosome 11, and seven already described from Chromoso

124 t susceptibility to astrocytoma is linked to chromosome 11, and that the modifier gene(s) responsible

125 ea locus on 14q; 10) the SCA type 5 locus on chromosome 11; and 11) the chromosome 19 region that con

126 ions from distal 1q (with orthology to mouse chromosome 11) appear to have a different history.

127 e translocated Cdkn1c, Slc22a1l and Tssc3 on chromosome 11 are affected, consistent with the hypothes

128 e X and show that it, and the Aanat locus on chromosome 11, are significantly associated with pineal

129 This approach uncovered a modifier locus on chromosome 11 associated with sarcolemmal membrane damag

130 one or more tumor suppressor genes (TSGs) on chromosome 11 at q13 and q22-24 regions.

131 Further, a sequenced chromosome 11 BAC clone, spanning the t(11;22) breakpoin

132 an approximate size of 20 kb and a second on chromosome 11 band 15.5-p15.4 that is the same size as t

133 Human chromosome-11 band-q23 translocations disrupting the MLL

134 age analysis reveals that elf3 maps to mouse chromosome 11 between D11Bir6 and D11Xrf477, a different

135 ) on mouse chromosome 4 (around 58.2 cM) and chromosome 11 (between 20-36 cM) that influence CARTta a

136 tail but little was known about genes in the chromosome 11 breakpoint region.

137 clone contig encompassing 2.51 Mb around the chromosome 11 breakpoint, which was constructed computat

138 acterized by a peculiar imbalance pattern on chromosome 11, but the landscape of mutations is not yet

139 phenotype, called Ltxs1, has been mapped to chromosome 11, but the responsible gene has not been ide

140 Although Par1 was previously mapped to mouse chromosome 11 by conventional linkage analyses, its cand

141 e mutation was mapped to the proximal end of chromosome 11 by genome-wide linkage analysis.

142 rint contig build) that maps proximal to the chromosome 11 centromere, a feature that interestingly c

143 Microcell-mediated transfer of normal chromosome 11 (chr 11) to a clonal derivative of the ova

144 We identified one DMR on chromosome 11 (chr11:2,322,050-2,323,247), annotated to

145 ovel spontaneous mouse mutation that maps to chromosome 11 close to the type I keratin locus.

146 hat the distortion maps to a single locus on chromosome 11, closely linked to Om, and that gene conve

147 ound minimal evidence of association for all chromosome 11 cluster SNPs (P >/= .01); a similar compar

148 Deletions in chromosome 11 consistent with CIN were verified in 80% o

149 A 2.3-centimorgan (cM) segment of rice chromosome 11 consisting of 340 kb of DNA sequence aroun

150 Idd4 on chromosome 11 consists of two subloci, Idd4.1 and Idd4.2

151 ocus on the tomato (Lycopersicon esculentum) chromosome 11 contained 15 putative genes.

152 A novel region on chromosome 11 containing olfactory receptor genes OR51B5

153 Both mutants were mapped to a region on chromosome 11 containing the peripheral myelin protein 2

154 e found a genomic signature for selection on chromosome 11 containing two closely linked loci.

155 artificial chromosome (BAC) clone mapping to chromosome 11, containing a region homologous to the hum

156 responsible, differential display comparing chromosome 11-containing (neo11/ 435) and parental, meta

157 Wnt3 demonstrates that this region of mouse chromosome 11 contains a large number of essential genes

158 obovoid and elongated shape, whereas sov2 on chromosome 11 controlled mainly elongated fruit shape.

159 sequenced 12 V. monoica bacterial artificial chromosomes, 11 corresponding to the papaya X-specific r

160 tic interaction was detected between loci on chromosome 11 (D11Mit39) and chromosome 18 (D18Mit64).

161 For example, on chromosome 11, decay occurred over 0.8 cM for processing

162 Selected tumors with localized gains of chromosome 11 delineate a 15-Mb region orthologous to hu

163 c lines carrying various segments of central chromosome 11 derived from LT-resistant DBA/2 mice on th

164 (LOD = 1.6) for a QTL for type 2 diabetes on chromosome 11 detected by Hanson and colleagues.

165 the fusion of DISC1 with a disrupted gene on chromosome 11 (DISC1FP1/Boymaw).

166 Thus chromosome loss or deletions within chromosome 11 do not account for the LOH observed by Sou

167 l DDK alleles in the central region of mouse chromosome 11 due to meiotic drive at the second meiotic

168 horses, the CXCL16 gene is located on equine chromosome 11 (ECA11) and encodes a glycosylated, type I

169 susceptible phenotype in a region of equine chromosome 11 (ECA11), positions 49572804 to 49643932.

170 opic endogenous retrovirus (eERV) located on chromosome 11 (Emv30) in the NOD genome, multiple de nov

171 single effector locus at a 1.5-Mbp region on chromosome 11 encoding a cluster of three p47 GTPases (I

172 among CTCF/cohesin sites over 2 Mb on human chromosome 11 encompassing the beta-globin locus and fla

173 rlapping deletions (SROs) were identified on chromosome 11 flanked by the markers D11S1338/D11S907 (1

174 We also obtained a unique QTL on chromosome 11 for collateral remodeling after middle cer

175 a portion of the orthologous region on mouse chromosome 11 for its tumorigenic potential using segmen

176 0)-GGFbeta3 MPNST cells (including universal chromosome 11 gains) and focal gains and losses affectin

177 provide further evidence of association for chromosome 11 gene cluster SNPs with substance dependenc

178 ent, respectively, of Il4 and Il13, adjacent chromosome 11 genes encoding the canonical T(H)2 cytokin

179 s versus heterozygous for B6 markers of this chromosome 11 genetic locus were, respectively, highly s

180 Human chromosome 11 has a VL30 retroelement, and a VL30 EST wa

181 LIPOPROTEIN (APO)A1/C3/A4/A5 gene cluster on chromosome 11 has been hypothesized to be a modifier of

182 Thus, the PATRRs from normal chromosomes 11 have been analyzed in detail.

183 C8 was characterized by copy losses on chromosome 11, having also the lowest lymphocytic infilt

184 m the normal allele but not from the deleted chromosome 11 homolog.

185 long with a null allele of Rai1 in the other chromosome 11 homologue [Dp(11)17/Rai1(-) mice] in order

186 tween 123.5 and 129.5 cM genetic distance on chromosome 11, identifying the site of a potential TSG i

187 The nob3 phenotype mapped to chromosome 11 in a region containing the metabotropic gl

188 the creation of a BAC clone contig on mouse chromosome 11 in a region showing conservation of synten

189 The distal region of chromosome 11 in B6 mice harbors a previously unrecogniz

190 some 7 in bands p12--p13 and Pkd1l1 to mouse chromosome 11 in band A2 by fluorescence in situ hybridi

191 4 introns, is single-copy, and is located on chromosome 11 in mice and 17 in humans, close to HER-2/n

192 t benzene induces a high frequency of LOH on chromosome 11 in p53+/- mice, likely mediated by aberran

193 The human MBP and MBPH genes localized to chromosome 11 in the centromere to 11q12 region.

194 1B (osteoprotegerin) gene, and rs3736228, on chromosome 11 in the LRP5 (lipoprotein-receptor-related

195 loss of heterozygosity/allelic imbalance on chromosome 11 in the stroma and tumor grade (P = .0013),

196 loss of heterozygosity/allelic imbalance on chromosome 11 in the stroma associated with tumor grade

197 A major locus on chromosome 11 in tight linkage with the marker D11Mit48

198 enome-wide study with particular emphasis on chromosome 11 in two SCA admixed cohorts obtained from u

199 to assemble a complete physical map of mouse chromosome 11 in which selection of clones containing sp

200 loss of the p53 gene, which resides on mouse chromosome 11, in four comparative genomic hybridization

201 stive linkage to a cluster of genes on mouse chromosome 11, including the genes for IL-4 and IL-13.

202 Thus, chromosome 11 is implicated but the breakpoints themselv

203 eviously using D11Mit markers, 36-40% of the chromosome 11 is now assembled into contigs, and these c

204 reported Trp53-Wnt3 balancer, most of mouse chromosome 11 is now available in balancer stocks.

205 restricted to female offspring while that on chromosome 11 is present in offspring of both sexes.

206 Equine chromosome 11 is shown to have an evolutionary new centr

207 trated that this region at the distal end of chromosome 11 is weakly linked to phenotypic markers of

208 eckstrin and the localization of the gene to chromosome 11, its expression in a nonhematopoetic cell

209 ation in the imprinted p15.5-p15.4 region of chromosome 11, known to be abnormally methylated in anot

210 ericans, the variant in a hypothetical gene (chromosome 11; LOC387761) was significantly associated w

211 Linkage to the chromosome 11 locus (D11Mit39) was confirmed in RA-treat

212 m pennellii introgression lines identified a chromosome 11 locus containing a cluster of BAHD acyltra

213 We conclude that a chromosome 11 locus derived from 129Sl/SvImJ essentially

214 time on chromosome 17 and also identified a chromosome 11 locus for lung pathogen burden.

215 e analysis revealed significant linkage to a chromosome 11 locus near D11Mit39 with a maximum LOD sco

216 there was evidence at GATA117D01 (140 cM) on chromosome 11 (LOD = 2.21).

217 , 7 cM of chromosome 9 (lod = 2.8), 12 cM of chromosome 11 (lod = 2.3), 27 cM of chromosome 12 (lod =

218 OD score for log(TG/HDL-C) = 1.8 at 140 cM], chromosome 11 [LOD score for log(TG/HDL-C) = 1.1 at 125

219 The second locus on chromosome 11, LOD = 5.6, named Blmpf2, is significant i

220 f the young (MODY2) homology region of mouse chromosome 11 (logarithm of odds 6.0).

221 wide significant quantitative trait locus on chromosome 11 (logarithm of the odds = 7.4) to a missens

222 3 (n = 14; 35% metastasized) were defined by chromosome 11 loss.

223 Our next largest MLS is for chromosome 11 (MLS = 1.75 at 84.0 cM), followed by chrom

224 es, three results were particularly notable: chromosome 11 (MLS = 2.98 at 82 cM), chromosome 14 (MLS

225 hived at the MRC Harwell Institute lacks the chromosome 11 modifier but instead harbors an ~37 Mb reg

226 ait difference has been mapped to a locus on chromosome 11 named Ltxs1.

227 e included SNPs on chromosome 3 near ZNF659, chromosome 11 near FANCF, chromosome 11 near ZBTB15, and

228 introns spanning roughly 4.5 kb and maps to chromosome 11 near the centromere.

229 The mouse Sebox gene was mapped to chromosome 11 near the Evi 2 locus.

230 Locus on chromosome 11 near the Stat3 and Stat5 genes controlled

231 ome 3 near ZNF659, chromosome 11 near FANCF, chromosome 11 near ZBTB15, and chromosome 12 near SENP1.

232 Losses on chromosome 11 occurred in only one of the 46 uremia-asso

233 Allelic loss at the MMP-1 locus on chromosome 11 occurs in many tumors including melanoma,

234 Jinx was mapped to mouse chromosome 11 on a total of 246 meioses and confined to

235 A single gene localized to chromosome 11 on the mouse genome encodes Pes1.

236 tein 24 (ARHGAP24), angiopoietin 4 (ANGPT4), chromosome 11 open reading frame (C11orf30/EMSY), and ex

237 articipant identified the novel ME3 locus on chromosome 11 (P = 2.18 x 10(-8)) at genome-wide signifi

238 in COL13A1 (P = 2.0 x 10(-7)), rs6591182 on chromosome 11 (P = 8.6 x 10(-7)), and rs887304 on chromo

239 ociations at several loci, including OR4C12 (chromosome 11; P = 6.7 x 10(-7)) and ENO1 and RERE (chro

240 Moreover, loci on either chromosome 11 (Pdcc2) or 9 (Pdcc3) modified the effect o

241 d that PHYA1 gene is located in A-sub-genome chromosome 11, PHYB gene is in A-sub-genome chromosome 1

242 r DNA from these mice reveals duplication of chromosome 11, potentially revealing regions of interest

243 d by a proximal deletion in the short arm of chromosome 11 (Potocki-Shaffer syndrome).

244 associated with allelic losses of the mouse chromosome 11 Prkar1a locus, an increase in total type I

245 The chromosome 11 QTL co-localizes with eae6b, and with Il12

246 e also present results from fine mapping the chromosome 11 QTL with use of SNP-association analysis w

247 roduction of a normal, neomycin-tagged human chromosome 11 reduces the metastatic capacity of MDA-MB-

248 breakpoints on chromosome 22 and a region of chromosome 11, refining the boundaries of many previousl

249 A number of genes located in this chromosome 11 region are discussed as potential candidat

250 Siberians have previously highlighted a 3 Mb chromosome 11 region containing 79 protein-coding genes

251 microsatellite and SNP markers identified a chromosome 11 region of 129 origin in C57BL/6J.129-YPOS

252 Csn3 (Cops3) maps to the mouse chromosome 11 region syntenic to the common deletion int

253 female individuals, chromosome 1: rs2764450, chromosome 11: rs11215217; 7772 male individuals, chromo

254 752 and rs10500641 near UBQLNL and OR52H1 on chromosome 11, rs2773080 and rs3922812 in or near RALGPS

255 ssociation at a nonsynonymous SNP in BDNF on chromosome 11 (rs6265[C], odds ratio (OR) = 1.06, 95% co

256 A region in chromosome 11 showed evidence of linkage in four familie

257 aining either the maternal or paternal human chromosome 11 showed that BORIS preferentially binds to

258 n loci at human Chromosome 16p13.3 and mouse Chromosome 11 shows that this segment of mouse Chromosom

259 Analysis of cervical cancer cell lines using chromosome 11 specific probes showed deletion and transl

260 s been shown to result in the fusion between chromosome 11 specific sequence and the switch gamma4 re

261 in MO7e cells was not random but tethered to chromosome 11, specifically to the globin LCR.

262 ps to the distal end of the short arm of pig chromosome 11 (SSC11).

263 ci, and 5 of these 30 (17%) are localized to chromosome 11, suggesting a trend toward overrepresentat

264 oma, specifically copy number gains at mouse chromosome 11, syntenic with gains on human chromosome 1

265 rom 11p15.5 frequently extends away from the chromosome 11 territory.

266 Kos1 is localized on mouse chromosome 11 that corresponds to human chromosome 17p13

267 ps to the imprinted region of proximal mouse chromosome 11 that demonstrates prenatal growth failure

268 fy a region of interest on the p-terminus of chromosome 11 that included gel-forming mucin genes.

269 es the Ppu020 and Faeder loci on a region of chromosome 11 that includes the Melanocortin-1 receptor

270 stive QTL near D11mit236 (20 cM, LOD 2.4) on chromosome 11 that influenced atherosclerotic lesion siz

271 as shown to carry a non-B6-derived region of chromosome 11 that protected against B6.Y (POS) sex reve

272 n [Dp(11)17] of the syntenic region on mouse chromosome 11 that spans the genomic interval commonly d

273 On chromosome 11 the translocation occurs within a short, p

274 parison with the finished sequence for mouse chromosome 11, the first finished mouse chromosome.

275 Located on chromosome 11, the transgene is transcriptionally silent

276 tumor suppressor gene(s) on the long arm of chromosome 11 through suppression of tumorigenicity assa

277 /+ backcross progeny, and three other QTL on chromosomes 11 (Tmc1m2), 12 (Tmc1m3), and 5 (Tmc1m4) in

278 translocated from its normal localization on chromosome 11 to chromosome 14.

279 Remarkably, two other unrelated chromosome 11 translocations discovered from the literat

280 ty (LOH) studies have implicated one or more chromosome 11 tumor-suppressor gene(s) in the developmen

281 The gene was localized to band B5 on Chromosome 11 using fluorescence in-situ hybridization (

282 haracterized loss of heterozygosity (LOH) on chromosome 11 using seven microsatellite markers in 27 b

283 ance of DDK alleles at the Om locus on mouse chromosome 11 was correlated with the X chromosome inact

284 nd ABCC8 genes and microsatellite markers on chromosome 11 were analyzed in DNA samples from the pati

285 annel subunits and microsatellite markers on chromosome 11 were analyzed in DNA samples from the pati

286 titative trait loci (QTL), eae6 and eae7, on chromosome 11 were identified by classical marker-specif

287 sis indicated that cells lacking one copy of chromosome 11 were present in all five mammary tumors an

288 analysis with double markers (MADM) to mouse chromosome 11 where Lis1, Ndel1, and 14-3-3varepsilon (e

289 ted a single linkage at the telomeric end of chromosome 11, where the Pdi gene itself resides (logari

290 on-recombining haplotypes of an inversion on chromosome 11, which contains 125 predicted genes.

291 and the ANO1 gene, lying 68 Mb away on human chromosome 11, which encodes a Ca(2+)-dependent chloride

292 ng between chromosome 22 and (in most cases) chromosome 11, which generates an aberrant transcription

293 al imbalance was partial or complete loss of chromosome 11, which harbors the p53 gene and is thus th

294 ing from telomeric segmental paternal UPD of chromosome 11, which unmasks a recessively acting gain-o

295 m response thresholds with a locus on distal chromosome 11, which we designate ahl8.

296 argeted deletion of a 450-kb region on mouse chromosome 11, which, based on computational analysis of

297 med previous findings of the FADS cluster on chromosome 11 with LA and arachidonic acid, and further

298 terminal deletion of part of the long arm of chromosome 11, with breakpoints in 11q23.3-11q24.2.

299 rt here a defective gene (Stat5b) located on chromosome 11 within a previously mapped T1D susceptibil

300 mosomes 11 and 17, with the highest score on chromosome 11 (z=3.22).