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

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

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

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

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

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

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

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

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

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

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

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

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

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

16 ranging from 47.4 to 64.4 megabases (Mb) on chromosome 7.

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

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

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

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

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

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

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

24 he previously hypothetical gene NM_026304 on chromosome 7.

25 tion of approximately 20 contiguous genes on chromosome 7.

26 der associated with a hemizygous deletion on chromosome 7.

27 le location in the pericentromeric region of chromosome 7.

28 derived lupus susceptibility locus on murine chromosome 7.

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

30 expressed noncoding gene H19 on mouse distal chromosome 7.

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

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

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

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

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

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

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

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

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

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

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

42 mapping revealed a single critical locus on chromosome 7.

43 transcription from a single gene located on chromosome 7.

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

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

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

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

48 y inherited allele located on proximal mouse chromosome 7.

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

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

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

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

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

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

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

56 ns (sensitivity = 0.94, specificity = 0.92), chromosome 7/10 aneuploidies (sensitivity = 0.90, specif

57 9B, and MYD88), losses of 17p13 and gains of chromosome 7, 11q12.3-q25, whereas DLBCL, NOS was predom

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

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

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

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

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

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

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

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

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

67 multivalents, which varied by variety and by chromosome (7-48%).

68 , monosomal karyotypes, often with losses on chromosome 7, 5, or 17.

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

70 us deletion of ~1.6 Mb affecting 26 genes on chromosome 7 (7q11.23) and is clinically typified by two

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

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

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

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

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

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

77 ding isoform 12p (i12p) (10/10 samples), and chromosomes 7, 8, and 21 gains (7/10 samples).

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

79 73%) and partial loss of chromosome 4 (87%), chromosome 7 (80%), chromosome 8 (53%), chromosome 10 (3

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

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

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

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

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

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

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

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

88 d LGG include copy gain and amplification of chromosome 7, amplification, mutation, and overexpressio

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

90 d onto the same locations, i.e., 68-76 MB in chromosome 7 and 26-36 MB in chromosome 9.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

105 Four QTL (one on chromosome 7 and three on 10) were newly identified in t

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

140 3.7 related to hyperleptinemia is present on chromosome 7 at D12Mit38 (a marker previously assigned t

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

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

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

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

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

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

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

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

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

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

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

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

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

154 t a 17-Mb long 129P1 genomic region on mouse chromosome 7 conferred weight reduction and improved glu

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

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

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

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

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

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

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

162 nome-wide significant loci, the strongest on chromosome 7 containing tyrosinase (Tyr).

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

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

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

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

167 Gene and chromosome 7 copy numbers were identified by fluorescent

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

169 al activity of HMAs in AML/MDS patients with chromosome 7 deletions and other monosomal karyotypes.Se

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

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

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

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

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

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

176 KMT2C is a chromosome 7 epigenetic regulator implicated in developm

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

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

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

180 ing different lengths of genomic segments of chromosome 7 from the 129P1 donor strain in the B6 backg

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

182 % v 9%, respectively) and lower frequency of chromosome 7 gain (13% v 74%, respectively) and 10q loss

183 Sub-regions with chromosome 7 gain display a relative lack of leukocyte i

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

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

186 Human chromosome 7 has historically received prominent attenti

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

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

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

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

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

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

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

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

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

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

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

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

199 We describe a tomato gene cluster on chromosome 7 involved in medium chain acylsugar accumula

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

229 Chromosome 7 microsatellite markers were genotyped in al

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

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

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

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

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

235 ossessed 21 genes collinear with a region of chromosome 7 of grape.

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

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

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

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

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

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

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

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

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

245 onal criterion of MET/centromeric portion of chromosome 7 ratiomicron greater than or equal to 2 for

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

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

252 Outside of the APOE region, one locus on chromosome 7 (rs34331204) showed a sex-specific associat

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

254 The locus identified on chromosome 7 (rs56226325, MAF=0.17) near MAD1L1 was prev

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

278 The genetic segment for body weight on mouse chromosome 7 was investigated by newly created subcongen

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

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

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

282 Monosomy of chromosome 7 was the most frequent cytogenetic abnormali

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

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

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

286 such relationship, regulated by a variant on chromosome 7, was the association of Odoribacter (Bacter

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

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

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

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

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

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

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

294 entified a quantitative trait locus (QTL) on chromosome 7, which had a synergistic effect on body wei

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

296 icant locus was located in the FOXP2 gene in chromosome 7 with P = 2.38 x 10-10 for rs34291892.

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.