ライフサイエンスコーパス: chromosome 7

1 tation, MET [7q31] amplification, or gain of chromosome 7).

2 ntified a shared homozygous 4.7 Mb region on chromosome 7.

3 eptor (OR) genes, lies internally on macaque chromosome 7.

4 uch as the 67-kb Ifitm family locus on mouse chromosome 7.

5 genes identified FZD9 as a candidate TSG on chromosome 7.

6 human chromosome 19q13.4 and mouse proximal chromosome 7.

7 hly conserved gene, stumpy, located on mouse chromosome 7.

8 ensitive segments in the HOXA locus in human chromosome 7.

9 e of disease onset and confirmed two loci on chromosome 7.

10 near the protein structural locus (PON1) on chromosome 7.

11 ss of approximately 1.5-Mb pairs of DNA from chromosome 7.

12 me/Angelman syndrome (PWS/AS) locus on mouse chromosome 7.

13 genes tightly clustered in 0.85 Mb on mouse chromosome 7.

14 n of eight maternal-specific genes in distal chromosome 7.

15 ation revealed deletion of a small region on chromosome 7.

16 hin a genetic interval of 0.9 cM on proximal chromosome 7.

17 or susceptibility locus, Skts14, on proximal chromosome 7.

18 single IGFL family member that is located on chromosome 7.

19 CD38 on Chromosome 5 and the ART2 complex on Chromosome 7.

20 he M. spicilegus genome at the distal end of chromosome 7.

21 he previously hypothetical gene NM_026304 on chromosome 7.

22 tion of approximately 20 contiguous genes on chromosome 7.

23 der associated with a hemizygous deletion on chromosome 7.

24 le location in the pericentromeric region of chromosome 7.

25 derived lupus susceptibility locus on murine chromosome 7.

26 ependent of activating mutations in H-ras on chromosome 7.

27 expressed noncoding gene H19 on mouse distal chromosome 7.

28 physically linked on the distal end of mouse chromosome 7.

29 critical region of the l7Rn3 locus on mouse chromosome 7.

30 have demonstrated linkage on the long arm of chromosome 7.

31 enetic variation in the PON gene cluster, on chromosome 7.

32 man 11p15.5 and the syntenic region on mouse chromosome 7.

33 effect (P = 0.0083) at this peak at 7p13 on chromosome 7.

34 a gene cluster with CPA1, CPA2, and CPA4 on chromosome 7.

35 e strains being trisomic for Chromosome 4 or Chromosome 7.

36 The gene is located on the short arm of chromosome 7.

37 PCH1, to a 5.6-cM interval of region 7q31 on chromosome 7.

38 eptor gene at the syntenic location on human chromosome 7.

39 a region of shared synteny with distal mouse chromosome 7.

40 antitative trait locus is on the long arm of chromosome 7.

41 class II HDAC and its gene resides on human chromosome 7.

42 nd syntenic to the location of Prx on murine chromosome 7.

43 nce is obtained for linkage to the region on chromosome 7.

44 itative trait locus (QTL) was present on rat chromosome 7.

45 n found in close proximity on mouse proximal chromosome 7.

46 regulated Igf2-H19 imprinted domain on mouse chromosome 7.

47 rum genetic cross maps to a 36 kb segment of chromosome 7.

48 n inducing a frameshift mutation in STAG3 on chromosome 7.

49 within a cluster of IL-10 family members on chromosome 7.

50 y inherited allele located on proximal mouse chromosome 7.

51 s musculus, Clcn4-2 has been translocated to chromosome 7.

52 transcription from a single gene located on chromosome 7.

53 we have localized Mor1 to a 4.4-Mb region on chromosome 7.

54 our cells, such as amplification of EGFR and chromosome 7.

55 and was mapped to a 2.2-Mb interval on mouse chromosome 7.

56 is linked to the 27-kDa gamma-zein locus on chromosome 7S.

57 These SNPs were mainly enriched on chromosome 7, 1, 13, 14, 15 and 18.

58 on 14-wild-type NSCLCs (mean ratio of MET to chromosome 7, 1.2; P < .001; mean H score, 142; P < .001

59 exon 14-mutated NSCLCs (mean ratio of MET to chromosome 7, 1.4; P = .007; mean H score, 155; P = .002

60 In addition, loci on chromosomes 7, 10 (two loci) and 11 were highly signific

61 pistatic interactions among five regions, on chromosomes 7, 10, and 20, that have previously been lin

62 ive linkage was also observed for regions on chromosomes 7, 12, 14, and 15.

63 By contrast, large copy number gains of chromosomes 7, 12, 16 and 17 are usually early, monoclon

64 ciated with imprinting effects, but those on chromosomes 7, 12, and centromeric 18 lie in regions pre

65 Robertsonian translocation markers involving chromosomes 7, 14, and 17.

66 of the distal interphalangeal (DIP) joint on chromosome 7 (155 cM; LOD score 3.06) and a linkage regi

67 th age in a chromosome-specific manner, with chromosomes 7, 18 and Y most severely affected, i.e. up

68 d a 85-kilobase (kb) genomic region of mouse chromosome 7, 23.2 centimorgans analogous to human chrom

69 The linkage regions on chromosomes 7 (27-78 cM) and 18p overlap prior reports,

70 genomic amplification (mean ratio of MET to chromosome 7, 4.3) and strong c-Met immunohistochemical

71 my (40%) and trisomy (38%) for EGFR gene and chromosome 7 (40%), whereas balanced polysomy was seen i

72 age was then established to a novel locus on chromosome 7 (7p12.1-7q21).

73 Recurrent gain of chromosomes 7, 8, 10, and 15 and recurrent loss of chrom

74 sitive rats (DSS) replaced those of Lewis on chromosomes 7, 8, 10, and 17 on the Lewis background.

75 or suggestive (P < 0.1) QTL were detected on chromosomes 7, 8, 11, and 19 for liver and on chromosome

76 nd specific low-level copy number changes of chromosomes 7, 8, 13, 18, and 20, and unveiled additiona

77 This study identified regions on chromosomes 7, 8, 14, and 19 and 11 SNPs from the fine-m

78 ents derived from different regions of mouse chromosomes 7, 8, 9, 10, and 17.

79 A panel of six centromeric probes for chromosomes 7, 8, 9, 10, X, and Y, using a unique two-dy

80 Nine loci (mapped to chromosomes 7, 8, 9, 17, 21, and 22) were evaluated for

81 ed), chromosome 2 (53%), chromosome 6 (73%), chromosome 7 (80%), chromosome 12 (47%), and chromosome

82 73%) and partial loss of chromosome 4 (87%), chromosome 7 (80%), chromosome 8 (53%), chromosome 10 (3

83 adenomas were noted with CGH, i.e., gains on chromosomes 7 (9%) and 12 (11%).

84 ssed using chromosome enumeration probes for chromosomes 7, 9, 11, 12, 15, and 17 in 15 patients.

85 s with cytopenia, predisposition to MDS with chromosome 7 aberrations, immunodeficiency, and progress

86 Evolution of chromosome 7 abnormalities was seen most often in refrac

87 presence of at least three abnormalities, or chromosome 7 abnormalities, vs absence) and bone-marrow

88 ularity and a higher frequency of developing chromosome 7 abnormalities.

89 th numerical and structural abnormalities of chromosome 7 accounted for 40% of all cases followed by

90 and Klar suggested that segregation of mouse chromosome 7, after induction of a site-specific crossov

91 growth factor receptor (EGFR) gene locus on chromosome 7, an association for which the mechanism is

92 Recurring deletions of chromosome 7 and 7q [-7/del(7q)] occur in myelodysplasti

93 ations in the CR tumors, such as 8p loss and chromosome 7 and 8q gain.

94 assing the 27- and 50-kD gamma-zein genes on chromosome 7 and a deletion of at least 232 kb on chromo

95 We mapped mhyp to mouse chromosome 7 and cloned the underlying gene.

96 e changes are preferentially clustered along chromosome 7 and contain a significant enrichment of Gli

97 Kcnq1 imprinted domain is located on distal chromosome 7 and contains several imprinted genes that a

98 Loss of chromosome 7 and del(7q) [-7/del(7q)] are recurring cyto

99 haplotypes spanning a 153-Mb region of human chromosome 7 and found evidence of rare mitotic recombin

100 in the Prader-Willi syndrome (PWS) locus on chromosome 7 and genes from the protocadherin-alpha and

101 genes is Os07g37920 which is located on rice chromosome 7 and is colinear with GPC-B2.

102 mly and involve partner genes (sequences) on chromosome 7 and on chromosomes other than 7.

103 behavior and deafness to the same region on chromosome 7 and showed they are allelic by complementat

104 some candidate chromosome regions especially chromosome 7 and suggested five genes which may provide

105 ning an imprinted interval of proximal mouse chromosome 7 and the genomic sequence of the related int

106 ouse nuclei, the imprinted Igf2-H19 locus of chromosome 7 and the Wsb1-Nf1 locus of chromosome 11.

107 Trisomies of chromosome 7 and/or chromosome 20 were detected in 17 of

108 A genome scan identified QTL on chromosomes 7 and 11 controlling the sexual dimorphism a

109 ng receptor were localized to regions on rat chromosomes 7 and 11, respectively, but the suggestive q

110 association analysis, we detected linkage to chromosomes 7 and 17.

111 for a (7.18) Rb translocation and genotyped chromosomes 7 and 18 in 1812 individuals, 47% of which w

112 ng the frequency of nondisjunction involving chromosomes 7 and 18 were examined.

113 traits has been previously observed on both chromosomes 7 and 19 in several unrelated studies and, t

114 Regions on chromosomes 7 and 19 were recently reported to contain s

115 nked predominantly by genes mapping to human chromosomes 7 and 19.

116 F344 Cia4 and Cia6 regions of chromosomes 7 and 8 failed to significantly alter CIA se

117 These support the validity of the chromosomes 7 and 9 linkage/association signals and unde

118 al F(2) loci (Adip1-8), novel slQTL peaks on chromosomes 7 and 9, and several novel epistatic loci.

119 during post-harvest storage and two loci on chromosomes 7D and 7H(ch) are important for esterificati

120 omosome 5, Lbw4 on chromosome 6, and Nba5 on chromosome 7) and 2 recessive SWR contributions (Swrl-1

121 Only DA.F344(Cia4) (chromosome 7) and DA.F344(Cia6) (chromosome 8) congenics

122 ents developed a partial or complete loss of chromosome 7, and 9 patients manifested abnormalities of

123 lated", a novel class defined by polysomy of chromosome 7, and an unannotated class.

124 hromosome 10 and chromosome arm 10q, gain of chromosome 7, and hypermethylation of the promoter of MG

125 that stems from M. spretus, spans >10 Mb on chromosome 7, and includes the molecular target of antic

126 Mutations in IKZF1, a gene located on chromosome 7, and monosomy 7 are mutually exclusive in t

127 gressive origin (these cover about 13 Mbp of chromosome 7, and over 300 genes).

128 expected, of many genes and miRNAs mapped to chromosome 7, and overexpression of ID1, MECOM, and PTPR

129 , two separate male heterogametic XY loci on chromosome 7, and two additional interacting loci on chr

130 two autosomal SNPs that lie 16.4 kb apart on chromosome 7, and which influence an individual's suscep

131 , on distal chromosome 4 (Ap3q) and proximal chromosome 7 (Ap7q), strongly affected 10% ethanol intak

132 irst glimpses of genomic sequence from human chromosome 7 are directly facilitating these activities.

133 Heterozygous deletions of chromosome 7 are frequent in myelodysplastic syndrome (M

134 estimated that about 9% of all sites within chromosome 7 are of introgressive origin (these cover ab

135 During cell division, copies of mouse chromosome 7 are segregated selectively or randomly to d

136 Sle1 on chromosome 1 and Sle3/5 on chromosome 7 are two of the most critical lupus suscepti

137 GenBankTM indicated that mpao maps to murine chromosome 7 as seven exons.

138 e identified a significant modifier locus on chromosome 7, as well as a suggestive locus on chromosom

139 ntrast, sex-specific evidence for linkage on chromosome 7 at 153 cM in the male-only data subset (LOD

140 ion of linkage for forward wave amplitude on chromosome 7 at 174 cM (LOD=2.88, permuted P=0.017).

141 for CFPWV: chromosome 2 at 94 cM (LOD=2.46), chromosome 7 at 29 cM (LOD=2.50), chromosome 13 at 108 c

142 The largest multivariate linkage was on chromosome 7 at 69 cM (P = 0.0001).

143 3.7 related to hyperleptinemia is present on chromosome 7 at D12Mit38 (a marker previously assigned t

144 Proviral integrations on chromosome 7 at Evi24 are located 7.6-10.3 kb upstream o

145 d for both log(TG) and log(TG/HDL-C) were on chromosome 7 (at 155 cM), where the results for the two

146 to human chromosome 19q13.13-q13.2 and mouse chromosome 7, at 7.5 centimorgans.

147 romosome 21 syntenic with the area of murine chromosome 7 bearing the CHL2 gene.

148 luated for aneuploidy, including 3 mapped to chromosome 7 because of the specific relevance of monoso

149 A GWAS peak on chromosome 7 between LOC_Os07g11020 and LOC_Os07g11520 i

150 linkage of factor 3 to a genetic location on chromosome 7 between markers D7S479 and D7S471 (LOD = 3.

151 The mouse gene was mapped to chromosome 7 by fluorescence in situ hybridization.

152 quencing and identified a missense mutation (chromosome 7 c.74146970T>A) in GTF2I at high frequency i

153 was linked to a quantitative trait locus on chromosome 7 (Candq1).

154 vered at the fitness-1 (fit1) locus in mouse chromosome 7 cause hematopoietic abnormalities, growth r

155 e maternally or paternally duplicated distal chromosome 7 (Chr7) and Chr15 in mouse embryo fibroblast

156 ansmission and has been linked to the distal chromosome 7 cluster of imprinted genes.

157 Igf2)/H19 imprinting control region (ICR) on chromosome 7 colocalized with one allele of Wsb1/Nf1 on

158 Further analysis using mice congenic for chromosome 7 confirmed Pdcc1, demonstrating that variati

159 tant component scores identified a region on chromosome 7 consistent with a gene that broadly predisp

160 P=0.00002) and 290-kbp (P=0.0004) regions on chromosome 7 containing 2 and 7 candidate genes, respect

161 ci, CPLX1, GAK, and PCGF3 A second region on chromosome 7 containing REC8 and RNF212B explained 26.2%

162 logous to a segment of about 1.8 Mb on human chromosome 7 containing ten genes, including the gene mu

163 ion that shares conserved synteny with human chromosome 7 containing the human AHR, suggesting that t

164 Linkage results suggest that the region of chromosome 7 containing the leptin gene cosegregates wit

165 d gene cluster at the telomeric end of mouse chromosome 7 contains a differentially methylated CpG is

166 The imprinted gene cluster on mouse distal chromosome 7 contains a differentially methylated CpG is

167 The locus sun on the short arm of tomato chromosome 7 controls morphology of the fruit.

168 en PRCC was defined as any of the following: chromosome 7 copy gain, focal MET or HGF gene amplificat

169 Gene and chromosome 7 copy numbers were identified by fluorescent

170 identify several functional regions on mouse Chromosome 7 critical for differentiation of mesoderm (m

171 Mice homozygous for certain chromosome 7 deletions of the albino Tyr; c locus that a

172 non-autoimmune C57BL/6 (B6) background, the chromosome 7-derived lupus susceptibility loci Sle3 and

173 in an approximately 25-Mb interval on mouse chromosome 7 (designated SuprMam1).

174 tumor, increased copies of MET from gains of chromosome 7 did not result in increased MET activity an

175 with paternal duplication (PatDp) of distal chromosome 7 (dist7), a region replete with imprinted ge

176 e containing the 3-kb CEN7 locus on 69 kb of chromosome 7 DNA was stably and autonomously maintained

177 l of autism that duplicates 6.3 Mb region of chromosome 7 (Dp/+) corresponding to a region of chromos

178 an interaction between at least two genes on Chromosome 7-each of which has a very small effect on it

179 f self-nonself discrimination for the murine chromosome 7 encoded H47 histocompatibility locus, known

180 arithm of odds scores (MLS) were observed on chromosome 7 for log serum creatinine (MLS = 3.65, at 43

181 d 47 sequences from a 1.8-Mb region of human chromosome 7 for silencer and EB activities.

182 or 9 (Pdcc3) modified the effect of Pdcc1 on chromosome 7 for the proportion and absolute number of p

183 utation in the telomere shelterin gene POT1 (chromosome 7, g.124493086C>T; p.Ser270Asn) in five unrel

184 % v 9%, respectively) and lower frequency of chromosome 7 gain (13% v 74%, respectively) and 10q loss

185 the original C57BL/6 that differs in a small chromosome 7 genomic locus.

186 e mouse Hras gene, located close to Skts2 on chromosome 7, had specific activating mutations in the M

187 Human chromosome 7 has historically received prominent attenti

188 the putative myeloid tumor suppressor(s) on chromosome 7 has not yet been identified.We performed tr

189 riety of cytogenetic abnormalities involving chromosome 7 have been reported in endometrial stromal s

190 fically, gliomas with broad amplification of chromosome 7 have properties different from those with o

191 ve assigned PKD1L1 to the short arm of human chromosome 7 in bands p12--p13 and Pkd1l1 to mouse chrom

192 ably, Clcn4-2 introns have been truncated on chromosome 7 in M. musculus as compared with the X-linke

193 me 18 was significantly higher than that for chromosome 7 in males.

194 med sudden juvenile death syndrome (sjds) to chromosome 7 in mice.

195 ely to account for the blood pressure QTL on chromosome 7 in the Dahl rat model of hypertension.

196 lication of our model to variation data from chromosome 7 in the mouse (Mus musculus domesticus) geno

197 ox3, Obox4, Obox5, and Obox6 map to proximal chromosome 7 in the mouse.

198 b DNA fragment between MUC12 and SERPINE1 on chromosome 7 in the region q22.1.

199 d Kcnq1, imprinting of the genes retained on chromosome 7, including Kcnq1, Kcnq1ot1, Ascl2, H19 and

200 In EAs, one chromosome 7 intergenic region was genome-wide significa

201 ne with antiapoptotic activity; the locus on chromosome 7 is at JAZF1, a transcriptional repressor th

202 Loss or deletion of chromosome 7 is commonly seen in MDS and leads to a poor

203 he imprinting center 2 (IC2) on mouse distal chromosome 7 is flanked by several paternally repressed

204 Trisomy for chromosome 7 is frequently observed as an initiating eve

205 This suggests that at least one gene on chromosome 7 is imprinted and involved in the pathogenes

206 ISH experiments demonstrated that the top of chromosome 7 is inverted in L. pennellii accession LA716

207 he closely linked H19 gene located on distal chromosome 7 is regulated by a 2.4-kb imprinting control

208 strain, we demonstrate that C57BL/6-derived chromosome 7 is required for tissue preservation.

209 Monosomy of chromosome 7 is the most frequent autosomal monosomy in

210 cloned 5-HT(2C) receptor gene is located on chromosome 7, is approximately 202 kbp long, and contain

211 evelopment (mesd) deletion interval on mouse chromosome 7, is essential for specification of embryoni

212 chromosome 4, mouse chromosome 6, and human chromosome 7, is poorly characterized.

213 Igf2), which lie in close proximity on mouse chromosome 7, is regulated by methylation of a different

214 lying the cardiac K(+) current, I(Kr), cause chromosome 7-linked long QT syndrome (LQT2).

215 -related gene (HERG) K(+) channel gene cause chromosome 7-linked long QT syndrome type 2 (LQT2), whic

216 uman ether-a-go-go-related gene (hERG) cause chromosome 7-linked long QT syndrome type II (LQT2).

217 uman ether-a-go-go-related gene (HERG) cause chromosome 7-linked long-QT syndrome (LQTS), an inherite

218 iplex families, refining localization of the chromosome 7 locus and a locus on chromosome 9.

219 change of partial sequences of Pyheul in the chromosome 7 locus and modification of the gene expressi

220 A novel chromosome 7 locus is predicted to contribute with the p

221 A chromosome 7 locus was identified to be linked to lympho

222 with the latter trait being influenced by a chromosome 7 locus.

223 some 3S locus was designated Su1-Ph1 and the chromosome 7S locus was designated Su2-Ph1.

224 polymorphism data confirmed that polysomy of chromosome 7, locus of EGFR, was more frequent in males

225 o the strongest QTL for collateral number on chromosome 7 (logarithm of the odds [LOD]=29, effect siz

226 normalities on eltrombopag, including 5 with chromosome 7 loss or partial deletion.

227 ancestry association evidence were found on chromosomes 7 (low-density lipoprotein cholesterol), 8 (

228 ntified a quantitative trait locus on murine chromosome 7 (LSq-1) that is associated with the absence

229 mutations also showed specific imbalance of chromosome 7 markers that favored the chromosome carryin

230 The putative autism-susceptibility locus on chromosome 7 may be the result of separate QTLs for the

231 Chromosome 7 microsatellite markers were genotyped in al

232 le during steady-state HSC engraftment and a chromosome 7 modifier locus regulates this activity.

233 normalities involving chromosome 5 (n = 63), chromosome 7 (n = 85), chromosomes 5 and 7 (n = 66), rec

234 eceptor complex and syntenic region of mouse chromosome 7, named T cell-interacting, activating recep

235 itional on either chromosome 9 (positive) or chromosome 7 (negative); this chromosome 2 region has be

236 Comparison of the order of fosmid loci on chromosome 7 of cultivated and wild cucumbers, and the s

237 pus susceptibility locus identified on mouse chromosome 7 of the New Zealand Black/New Zealand White

238 s in metaphase positive for the Philadelphia chromosome); 7 of these patients had complete cytogeneti

239 to FISH values demonstrating only trisomy of chromosome 7 or chromosome 3.

240 n occurred in patients with abnormalities of chromosome 7 or complex cytogenetic alterations or both.

241 rican cohort, whereas rs11763963, located on chromosome 7 outside of a gene transcript, was the most

242 osis was associated with the SNP rs343062 on chromosome 7 (P = 2.7 x 10(-8)).

243 g inbred mouse strains identified a locus on chromosome 7 (Pdcc1) significantly linked to both the pr

244 cribed Idd7 locus on the proximal portion of Chromosome 7 predominantly, but not exclusively, determi

245 Association mapping within the chromosome 7 QTL interval using collateral traits measur

246 A screen for imprinted genes on mouse Chromosome 7 recently identified Inpp5f_v2, a paternally

247 performed a focused 5C analysis of a 2.8 Mb chromosome 7 region surrounding CFTR in a panel of cell

248 iglec genes and two pseudogenes in the mouse chromosome 7 region syntenic to the Siglec-3-related gen

249 IC (PWS-IC) on human chromosome 15 and mouse chromosome 7 regulates imprinted gene expression bidirec

250 uman chromosome 15 and the long arm of mouse chromosome 7, respectively, each having 11 exons and a C

251 gosity for large portions of the long arm of chromosome 7, resulting in retention of only the wild-ty

252 Deletion of the CaCse4p-binding region of chromosome 7 results in a high rate of loss of the alter

253 ained = 1.90%) and one over the CDK6 gene on chromosome 7 (rs445, p value = 6.03 x 10(-16), variance

254 MD (X chromosome), and a suggestive locus on chromosome 7 (rs73271865, P = 2.9 x 10(-7)) upstream of

255 hromosome 1 (SBI-01) to approximately 33% of chromosome 7 (SBI-07).

256 of 100 BP, corresponding to two sequences on chromosome 7, separated by a 22.6 kB intron.

257 systematically analyzing the evolving human chromosome 7 sequence for the presence of matching mouse

258 nd Ck1 homolog found on B. oleracea (BoCk1b) chromosome 7 served to define another orthologous segmen

259 Losses of 9p and 10 and simple gains of chromosome 7 showed at least trends toward increased fre

260 A locus on chromosome 7 (Skts1) showed a highly significant interac

261 significant three-way interaction effects of chromosome 7 SNP rs6960920, chromosome 9 SNP rs4744411,

262 ficant three-way interaction effects of both chromosome 7 SNPs and NLRP1 SNP rs6502867 on the vitilig

263 We identified a QTL of moderate effect on chromosome 7 that affected 2f1-f2 emissions intensities

264 DNA segments within a 66-Mb region of mouse chromosome 7 that are occupied by the erythroid transcri

265 ontrolled predominantly by a region of mouse chromosome 7 that contains the strain-specific Chrna7 al

266 reviously identified a locus on distal mouse chromosome 7 that contributes over 50% of the variation

267 ntified a single quantitative trait locus on chromosome 7 that exhibited significant linkage to both

268 scan, we identified a single strong locus on chromosome 7 that influenced two pathological features o

269 approaches used to identify risk variants on chromosome 7 that likely contribute to the etiology of a

270 -nucleotide polymorphism (SNP) rs10272438 on chromosome 7 that was significantly associated with AMD

271 senting 99.4% of the euchromatic sequence of chromosome 7, the first metacentric chromosome completed

272 Chromosome 7, the smallest of the eight chromosomes, has

273 ately 1-Mb imprinted genomic domain on mouse chromosome 7 to its orthologous region on human 11p15.5.

274 ranslocation of the inactive B centromere to chromosome 7 transferred the nondisjunction property to

275 We have identified and defined a chromosome 7 uniparental isodisomy and a 7p telomeric mi

276 p15 LOM) and maternal uniparental disomy for chromosome 7 [UPD(7)mat] explain 20-60% and 10% of the s

277 was fine-mapped to an 18.5-kb region on rice chromosome 7 using a cross between Oryza rufipogon (red

278 a cluster of imprinted genes on mouse distal chromosome 7 using the Cre/loxP recombination system.

279 The mapping of Xs(J) to chromosome 7 was confirmed, and the interval was narrowe

280 The centromeric region of chromosome 7 was identified as a lupus susceptibility lo

281 t the suggestive quantitative trait locus on chromosome 7 was not in the region of the VDR gene locus

282 On the other hand, gain on chromosome 7 was recognized almost exclusively in spinal

283 The frequency of nondisjunction for chromosome 7 was significantly higher in females than in

284 Monosomy of chromosome 7 was the most frequent cytogenetic abnormali

285 The murine H46 locus on chromosome 7 was thus found to encode the interleukin 4-

286 Fluorescence in situ hybridization (FISH) of chromosome 7 was used to identify small populations of a

287 A possible pericentric inversion in chromosome 7D was detected.

288 g only maternal or paternal copies of distal chromosome 7, we have identified five prominent footprin

289 Two linkage peaks on chromosome 7 were detected at 44-45 cM for type 2 diabet

290 The abnormalities of chromosome 7 were monosomy 7 in 4 patients (1 of which h

291 Abnormalities of chromosome 7 were present in 6 of the 8 patients, 3 of w

292 cs experiments focused on a 1.5 Mb region on chromosome 7 which is deleted in Williams-Beuren syndrom

293 an extended imprinted region of distal mouse chromosome 7, which also contains the Igf2 gene.

294 d to the isolation of the first such gene on chromosome 7, which encodes a transcription factor known

295 res conserved synteny with a region of mouse chromosome 7, which shares conserved synteny with human

296 Three studies have reported linkage on chromosome 7 with major depressive disorder (MDD) in or

297 ified gene locus, AKR1B15, which clusters on chromosome 7 with the other human AKR1B subfamily member

298 t on the allelic preference for imbalance on chromosome 7, with at least 90% of tumors from the conge

299 , conditional on the evidence for linkage at chromosome 7, with the location of the increased signal

300 ant distal to RET and a non-coding allele on chromosome 7 within the class 3 Semaphorin gene cluster.