ライフサイエンスコーパス: chromosome 17

1 temporal dementia and parkinsonism linked to chromosome 17).

2 " that occupies approximately 40 cM of mouse chromosome 17.

3 genes found on human chromosome 6 and mouse chromosome 17.

4 untranslated region of erbB-2 gene on human chromosome 17.

5 u-negative frontotemporal dementia linked to chromosome 17.

6 ound a major SJL-derived suppressor locus on Chromosome 17.

7 al chromosomal rearrangements occur on human chromosome 17.

8 by a gene located on the short arm of human chromosome 17.

9 temporal dementia and parkinsonism linked to chromosome 17.

10 f a segment of chromosome 16 translocated to chromosome 17.

11 provides evidence of linkage of psoriasis to chromosome 17.

12 t to a approximately 956-kb segment of mouse chromosome 17.

13 mutation was localized to a 182-kb region of chromosome 17.

14 coding galactokinase in humans was mapped to chromosome 17.

15 LG 13 and localized them to the short arm of chromosome 17.

16 by a locus on human chromosome 19 and mouse chromosome 17.

17 compared with the 10% genome-wide and 18% on chromosome 17.

18 ociated with a deletion within band p11.2 of chromosome 17.

19 temporal dementia and parkinsonism linked to chromosome 17.

20 and its gene was mapped at the distal end of chromosome 17.

21 ha resulted from an interstitial deletion on chromosome 17.

22 a family of 5 receptors clustered on murine chromosome 17.

23 ion was detected for the ABCG5ABCG8 locus on chromosome 17.

24 ociated alternates of exon 1 of this gene on chromosome 17.

25 21-22, while the mouse Znt6 was localized to chromosome 17.

26 encoded by two genes closely linked on human chromosome 17.

27 that has a high degree of synteny with human Chromosome 17.

28 ation was seen with two loci flanking p53 on chromosome 17.

29 nal clathrin heavy chain (CHC17), encoded on chromosome 17.

30 prises 1,282 amino acids and is localized on chromosome 17.

31 ed fragment localizes to the q11.2 region of chromosome 17.

32 varian cancer susceptibility gene (BRCA1) on chromosome 17.

33 been mapped in mouse, and all are located on chromosome 17.

34 omplex region located at the proximal end of chromosome 17.

35 tumors with 17 markers from the long arm of chromosome 17.

36 by a 1.5 Mb duplication on the short arm of chromosome 17.

37 0, followed by a region of homology to mouse chromosome 17.

38 servation of synteny with sequences on human chromosome 17.

39 J mice carrying a 129/Sv-derived interval on chromosome 17.

40 spans 20 cM of the proximal region of mouse chromosome 17.

41 sides close by the H-2 complex (MHC gene) on chromosome 17.

42 European descent identifies a novel locus on chromosome 17.

43 temporal dementia and parkinsonism linked to chromosome 17.

44 ce for the involvement of the MAPT region on chromosome 17.

45 ne encoded by a cluster of eight paralogs on chromosome 17.

46 ur prior prostate cancer linkage evidence on chromosome 17.

47 with the major histocompatibility complex of chromosome 17.

48 ched contiguous genomic DNA sequences in rat chromosome 17.

49 E2C, which binds a unique sequence on human chromosome 17.

50 s infectivity controller 1 (vic1), mapped to chromosome 17.

51 6A4) and the integrin beta 3 gene (ITGB3) on chromosome 17.

52 ing two that are only 1.7 megabases apart on chromosome 17.

53 peak logarithm of odds ratio score on mouse chromosome 17 (10.9) was around marker D17Mit134 at 16.9

54 mapped the H-2Z1 transgene insertion site to chromosome 17, 100 and 460 kb away from Tbc1d5 and Satb1

55 protein p53, is located on the short arm of chromosome 17 (17p).

56 ocated in close proximity on the long arm of chromosome 17 (17q11-21).

57 On a whole-genome level (36,617 genes), chromosome 17 (19.2% in fetal, 16.5% in adult) contained

58 are located 7.8-8.8 Mb from the telomeres on chromosomes 17, 2, and 1, identified several orthologous

59 Three SNPs in the RANTES gene region on chromosome 17 (403A in the promoter, In1.1C in the first

60 s yielded suggestive evidence for linkage on chromosomes 17, 5, 11, 4, and 8 (listed in order by MLS)

61 r hUAT consists of 11 exons and is mapped to chromosome 17; a highly homologous gene, hUAT2, maps to

62 = 10%, platelets less than 50 x 10(9)/L, and chromosome 17 aberrations (median overall survival, 10,

63 = 10%, platelets less than 50 x 10(9)/L, and chromosome 17 aberrations defined AP in patients with MF

64 lities such as 11q deletion, trisomy 12, and chromosome 17 aberrations had a higher mean TNF-alpha le

65 ic phase, those who developed unfavorable or chromosome 17 abnormalities had median survivals of 18 a

66 ior rituximab exposure, and patients without chromosome 17 abnormalities.

67 lysis identified susceptibility intervals on chromosomes 17 (Alaa1) and 9 (Alaa2).

68 d oligonucleotide probes, specific for human chromosome 17 alpha satellite DNA sequence variants, tha

69 emporal dementia with parkinsonism linked to chromosome 17 also were n847-positive.

70 These 5q deletions often co-occur with chromosome 17 alterations involving the deletion of NF1

71 the genetic contribution to this trait with chromosome 17 and 1 accounting for 28 and 24%, respectiv

72 rax infection, locus 1) for survival time on chromosome 17 and also identified a chromosome 11 locus

73 d SNPs in the region between 34 and 36 Mb on chromosome 17 and early wheezing phenotypes, doctor-diag

74 gous gene, hUAT2, maps to a nearby region of chromosome 17 and is also likely to be a urate transport

75 pendent microcell hybrids contained a normal chromosome 17 and no other human chromosome on a mouse t

76 ic therapy were analyzed for the presence of chromosome 17 and p53 genes by fluorescent in situ hybri

77 This identified a primary locus on mouse chromosome 17 and potential loci on chromosomes 1 and 4.

78 ped the hea gene near the fsn locus on mouse chromosome 17 and show that the mutants are allelic.

79 region orthologous to a segment of silkworm chromosome 17 and show that there is only one core seque

80 Comparative analysis between human chromosome 17 and the orthologous chimpanzee chromosome

81 abnormal small ring chromosomes derived from chromosome 17 and the X chromosome also missegregate mor

82 list map near known hybrid sterility loci on chromosome 17 and the X chromosome, allowing us to nomin

83 noic Acid Receptor(alpha) (RARalpha) gene on chromosome 17 and variable partner genes (X genes) on di

84 inoic acid receptor alpha (RARalpha) gene on chromosome 17 and variable partner genes (X genes) on di

85 inoic Acid Receptor alpha (RARalpha) gene on chromosome 17 and variable partner genes (X genes) on di

86 une diseases and identified the risk loci of chromosomes 17 and 1 as NLRP1 (NALP1) and FOXD3, respect

87 nd resistant B6 mice identified two loci, on Chromosomes 17 and 1, that accounted for the high suscep

88 th inferior prognosis, including deletion of chromosomes 17 and 13 (Delta13) and t(4;14)(p16.3;q32).

89 ildren with hyperdiploid ALL without gain of chromosomes 17 and 18 had a poor prognosis.

90 NT FINDINGS: DFSP carries a translocation of chromosomes 17 and 22 leading to juxtaposition of the co

91 ibrids contained karyotypically normal human chromosomes 17 and a small number of other human chromos

92 The nmf223 locus was mapped to chromosome 17, and a missense mutation was identified in

93 e cell count 150 x 10(9)/L or more, abnormal chromosome 17, and lactate dehydrogenase 2N or more.

94 , heterozygous deletions of the short arm of chromosome 17, and mutations in IDH1/IDH2 and DNMT3A gen

95 e was confined to a critical region on mouse chromosome 17, and then ascribed to a C-->A transversion

96 within 20 kb of each other in region q21 of chromosome 17, and TUBG1P is on chromosome 7.

97 associated with reduced gene copy number and chromosome 17 aneusomy as observed in tumors from BRCA1

98 Concordance of chromosome 17 aneusomy between cancers and synchronous s

99 However, the clinical importance of chromosome 17 anomalies, in particular the effect on ERB

100 Allele losses from chromosome 17 are common in sporadic ovarian tumors.

101 Numerical aberrations of chromosome 17 are linked to breast-cancer initiation and

102 nomeric and higher-order alpha-satellites on chromosome 17 are phylogenetically distinct, consistent

103 nslocations involving the RAR alpha locus on chromosome 17 are the hallmark of acute promyelocytic le

104 tegrin gene within an asthma linkage peak on chromosome 17, as a candidate for susceptibility to asth

105 Here we report a finished sequence for human chromosome 17, as well as a structural comparison with t

106 amily with frontotemporal dementia linked to chromosome 17 associated with extensive tau pathology.

107 ch is located within a 1.4-Mb duplication on chromosome 17 associated with the most common form of Ch

108 Vs, CGRs and other structural aberrations of chromosome 17 at p13.3.

109 hat uncharacterized tryptase genes reside on chromosome 17 at the complex containing the three genes

110 Chromosome 17 at the p13.3 genomic region lacks extensiv

111 ficant linkage regions were also observed on chromosomes 17 at 86 cM (lod = 3.9) and 9 at 34 cM (lod

112 Ltbp-1 is a single copy gene that maps to chromosome 17, band E (1-3) and encompasses more than 21

113 Significant linkage was detected on chromosome 17 between single-nucleotide polymorphism mar

114 The chromosome 17 breakpoint maps approximately 932 kb upstr

115 A growing number of reports have implicated chromosome 17 breakpoints at a distance of up to 1 Mb fr

116 based on alpha-satellite (alphoid) DNA from chromosome 17 but not the Y chromosome regularly form HA

117 Allelic imbalance (AI) studies on chromosome 17 (C17) in Barrett's oesophageal adenocarcin

118 ch trio, the parent of origin of the deleted chromosome 17 carries at least one H2 chromosome.

119 n [defined as a ratio of HER-2/neu copies to chromosome 17 centromere (CEP17) copies > or = 2], 6 (15

120 ancer were analyzed by IHC and ISH; HER2 and chromosome 17 centromere (CEP17) counts were available i

121 R1-3 and Ki67 expression, and duplication of chromosome 17 centromere enumeration probe (Ch17CEP).

122 situ hybridization [ISH]-positive): HER2-to-chromosome 17 centromere ratio >/= 2.0, average HER2 cop

123 ween these two types, we have focused on the chromosome 17 centromeric region that has reached both h

124 stem, which includes Topo-IIalpha, HER2, and chromosome 17 (CEP17).

125 In view of the location of HER2/TOP2A on chromosome 17, Ch17CEP duplication might explain the inc

126 The chromosome 17/chromosome 10 breakpoint seems to have inv

127 volutionary conserved miR cluster located on chromosome 17 consisting of miR-99b, let-7e, and miR-125

128 d found a previously undescribed amplicon on chromosome 17 containing a novel overexpressed gene that

129 romosome 11 shows that this segment of mouse Chromosome 17 contains a group of three alpha-like pseud

130 These results show that a 140 kb fragment of chromosome 17 contains all elements necessary for the co

131 The interval on mouse Chromosome 17 contains several orthologous genes potenti

132 ively and significantly correlated with mean chromosome 17 copy number (r = 0.1, P: = 0.007).

133 tumors with polysomic (p17) or normal (n17) chromosome 17 copy number also benefited from trastuzuma

134 The largest mean value and variance for chromosome 17 copy number was identified in SCCs (2.4 +/

135 r 2 [HER2] protein expression, HER2 gene and chromosome 17 copy number, hormone receptor status) and

136 ulvar SCCs, we investigated abnormalities in chromosome 17 copy number.

137 independent of HER2/centromere 17 ratio and chromosome 17 copy number.

138 etastatic disease; however, a correction for chromosome 17 copy-number is necessary to completely dis

139 chromosome 4 (KLHL2 (Kelch-like protein 2)), chromosome 17 (CRHR1 (corticotropin-releasing hormone re

140 mmon variants to autism within the region on chromosome 17 defined in Stone et al., a dense panel of

141 ity for Tas, a gene located in the region of Chromosome 17 deleted in T(hp) and T(Orl), (2) homozygos

142 Here, we have created synthetic chromosome 17-derived alpha-satellite arrays, based on t

143 tion, the most significant being a region on chromosome 17 distal to H2 (Eae5).

144 ion (FISH) for the alpha satellite region of chromosome 17, DNA content by image analysis, and Ki-67

145 a detailed RH and comparative map for horse chromosome 17 (ECA17).

146 we observed a LOD score of 3.46 elsewhere on chromosome 17 (empirical pointwise P = .00002, uncorrect

147 cluster, we observed a LOD score of 3.06 on chromosome 17 (empirical pointwise P = .0002) for Europe

148 The mouse chromosome 16/chromosome 17 evolutionary breakpoint is between human g

149 uct revealed that mT4 is a new member of the chromosome 17 family of mouse tryptases.

150 t known previously to have illness linked to chromosome 17 for identified PGRN and MAPT mutations and

151 The QTL on chromosome 17 for radiation-induced lung fibrosis is wit

152 temporal dementia and Parkinsonism linked to chromosome 17 (FTDP-17) and Alzheimer's disease (AD).

153 emporal dementia with parkinsonism linked to chromosome 17 (FTDP-17) and Alzheimer's disease.

154 temporal dementia and Parkinsonism linked to chromosome 17 (FTDP-17) form filamentous structures.

155 emporal dementia with Parkinsonism linked to chromosome 17 (FTDP-17) is a group of related disorders

156 temporal dementia and Parkinsonism linked to chromosome 17 (FTDP-17) is an autosomal dominant neurode

157 emporal dementia with parkinsonism linked to chromosome 17 (FTDP-17) is caused by mutations in the MA

158 temporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) through comprehensive neurobehav

159 emporal dementia with parkinsonism linked to chromosome 17 (FTDP-17) unequivocally confirmed the cent

160 temporal dementia and Parkinsonism linked to chromosome 17 (FTDP-17), an autosomal dominant condition

161 emporal dementia with Parkinsonism linked to chromosome 17 (FTDP-17), an autosomal dominant neurodege

162 emporal dementia with parkinsonism linked to chromosome 17 (FTDP-17), and common variation in MAPT is

163 temporal dementia and parkinsonism linked to chromosome 17 (FTDP-17), and tau aggregates are present

164 l dementia (FTD) with parkinsonism linked to chromosome 17 (FTDP-17), but those in exon 10 (E10) or t

165 emporal dementia with Parkinsonism linked to chromosome 17 (FTDP-17), characterized by neuronal patho

166 emporal dementia with parkinsonism linked to chromosome 17 (FTDP-17), implying that tau abnormalities

167 emporal dementia with parkinsonism linked to chromosome 17 (FTDP-17), in order to study the neuroprot

168 temporal dementia and parkinsonism linked to chromosome 17 (FTDP-17), in which both RNA splicing and

169 temporal dementia and parkinsonism linked to chromosome 17 (FTDP-17), thereby proving that tau dysfun

170 emporal dementia with parkinsonism linked to chromosome 17 (FTDP-17), which has clinical and molecula

171 temporal dementia and parkinsonism linked to chromosome 17 (FTDP-17), which is caused by mutations in

172 temporal dementia and parkinsonism linked to chromosome 17 (FTDP-17), with filamentous tau aggregates

173 g hereditary FTD with Parkinsonism linked to chromosome 17 (FTDP-17).

174 temporal dementia and parkinsonism linked to chromosome 17 (FTDP-17).

175 emporal dementia with parkinsonism linked to chromosome 17 (FTDP-17).

176 emporal dementia with parkinsonism linked to chromosome 17 (FTDP-17).

177 in familial FTD with parkinsonism linked to chromosome 17 (FTDP-17).

178 temporal dementia and parkinsonism linked to chromosome 17 (FTDP-17).

179 al dementia and Parkinsonism associated with chromosome 17 (FTDP-17).

180 emporal dementia with parkinsonism linked to chromosome 17 (FTDP-17).

181 emporal dementia with Parkinsonism linked to chromosome 17 (FTDP-17).

182 temporal dementia and parkinsonism linked to chromosome-17 (FTDP-17), directly implicate tau abnormal

183 emporal dementia with parkinsonism linked to chromosome-17 (FTDP-17; n = 2; MAPT p.P301L and IVS10 +

184 temporal dementia and parkinsonism linked to chromosome 17 (FTDP17) causes aberrant microtubule bindi

185 emporal dementia with parkinsonism linked to chromosome 17 (FTDP17).

186 emporal dementia with parkinsonism linked to chromosome 17, giving tau a central role in the pathogen

187 Patients with abnormalities of chromosome 17 had a median survival of only 5 months.

188 congenic mice in which the linked region on chromosome 17 had been transferred onto a B6.AKR or a C3

189 A region on chromosome 17 has recently been highlighted as linked to

190 of BTA19 and the sequence-based map of human chromosome 17 [Homo sapiens, (HSA) 17] were found to be

191 istorted transmission (TRD) of the t-bearing chromosome 17 homolog to their offspring.

192 Homo sapiens chromosome 17 (HSA17) has two juxtaposed HOR arrays, D17

193 ween porcine chromosome 12 (SSC12) and human chromosome 17 (HSA17) is completely conserved.

194 e two alpha satellite arrays of Homo sapiens Chromosome 17 (HSA17), D17Z1 and D17Z1-B, behave as cent

195 previous study found significant linkage to chromosome 17 in a HDDD family (HDDD2), but no mutation

196 msk maps to the proximal end of mouse chromosome 17 in a region that is syntenic with human ch

197 A tandem duplication event, located on chromosome 17 in a second mutant, was found to cosegrega

198 The first locus on chromosome 17 in the major histocompatibility complex (M

199 ddition, we identified one genetic factor on chromosome 17 in the MHC region.

200 CYP39A1 locus) and in a syntenic position on chromosome 17 in the mouse (Cyp39a1 locus).

201 bridizes to a single DNA sequence present on chromosome 17 in the mouse genome.

202 it causes frontotemporal dementia linked to chromosome 17 in this pedigree by shifting tau transcrip

203 emporal dementia with parkinsonism linked to chromosome 17, in rTg4510 mice results in the formation

204 Changes of specific loci on chromosome 17 including ERBB2 amplification, P53 loss, B

205 fully annotated a 65,871-bp region of mouse Chromosome 17 including the Hba-ps4 alpha-globin pseudog

206 A locus on chromosome 17, including the H-2 complex, was significan

207 emporal dementia with parkinsonism linked to chromosome 17 is associated with either exonic or intron

208 Chromosome 17 is rich in protein-coding genes, having th

209 Chromosome 17 is unusual among the human chromosomes in

210 emporal dementia with Parkinsonism linked to chromosome 17) is directly linked genetically to mutatio

211 at the shk mutation, previously localized to chromosome 17, is a quaking (qk) allele consisting of a

212 ASPL maps to chromosome 17, is ubiquitously expressed, and matches nu

213 Recent advances in chromosome 17-linked dementias justify a rigorous search

214 nfirm and better define the influence of the chromosome 17-linked QTL on radiation sensitivity, we co

215 The chromosome 17-linked QTL was confirmed to influence the

216 argeting ERBB2 and other protein products of chromosome 17 loci.

217 The AKR/J chromosome 17 locus was not sufficient to increase HSC f

218 us (QTL) for RV weight was identified on rat chromosome 17 (lod score 6.5) that accounted for 22% of

219 29 mice, plus a suggestive modifier locus on chromosome 17 (LOD=3.7).

220 idence for quantitative trait locus (QTL) on chromosomes 17 (LOD = 4.2), 1 (LOD = 4.5), and 18 (LOD =

221 nkage of fasting insulin to the short arm of chromosome 17 (logarithm of odds [LOD] = 3.30; 54 cM bet

222 TP53 mutations and chromosome 17 LOH with selection against wild-type TP53

223 s for asthma, suggesting that this region of chromosome 17 may harbor a "universal" lung injury gene.

224 rs393152 within the extended MAPT region on chromosome 17 (meta analysis P-value across five indepen

225 ant locus associated with gallstone score on chromosome 17, named Lith9 (susceptibility allele confer

226 h 17 SNPs (all between KANSL1 and LRRC37A on chromosome 17 near MAPT) in a meta-analysis of the stage

227 2361; chromosome 5, near marker D5S1505; and chromosome 17, near marker D17S1301.

228 ions, including Igfals (previously placed on chromosome 17), Nubp2 (a fully characterized gene), Jsap

229 bility complex (MHC) class I region on mouse chromosome 17 of strain 129/SvJ (H2bc).

230 Analysis of the p arm of chromosome 17 of the focus-derived cell strains containi

231 d sequence data generated from re-sequencing chromosome 17 of the mouse strains A/J and CAST/EiJ with

232 t a model whereby a hot L1 source element on Chromosome 17 of the patient's genome evaded somatic rep

233 C17orf37 (chromosome 17 open reading frame 37), also known as C35/

234 ncoded by an uncharacterized gene (C17orf99; chromosome 17 open reading frame 99), that is expressed

235 r structurally similar HAC vectors, two with chromosome 17 or Y alphoid DNA (17alpha, Yalpha) and two

236 emporal dementia with Parkinsonism linked to chromosome 17 pathogenic mutations and develops a severe

237 The initial scan of chromosome 17 performed on two large pedigrees provided

238 Having previously shown that duplication of chromosome 17 pericentromeric alpha satellite as measure

239 Normal vulvar skin controls did not exhibit chromosome 17 polysomy (cells with more than four FISH s

240 ng regarding the association of copy gain of chromosome 17 (polysomy 17) with strong ERBB2 protein ex

241 ies (frontotemporal dementia associated with chromosome 17) presenting with an atypical parkinsonian

242 0, but < 6.0; AC2013), use of an alternative chromosome 17 probe reassigned 212 (7.4% overall) patien

243 temporal dementia and parkinsonism linked to chromosome 17, progressive supranuclear palsy, and corti

244 ght cluster, in the proximal region of mouse chromosome 17, providing a thus far unique example of a

245 Confirmation of the gene underlying the chromosome 17 QTL may reveal new strategies for influenz

246 segmental haploidy in the mouse t complex on chromosome 17, radiation-induced deletion complexes cent

247 loci was used to calculate a revised HER2-to-chromosome-17 ratio by using the eusomic gene locus as t

248 Abnormalities of chromosome 17, recognised over two decades ago to be imp

249 ere scored as amplified by using alternative chromosome 17 reference gene probes, and 13 (92.9%) of 1

250 s the hypothesis that the use of alternative chromosome 17 reference genes might more accurately asse

251 more,and defined the endpoints of the mouse chromosome 17 region.

252 ous deletion or duplication of band p11.2 of chromosome 17, respectively.

253 c into the second intron of the RARA gene on chromosome 17, resulting in a classic bcr3 PML-RARA fusi

254 onths later at relapse had loss of an entire chromosome 17, resulting in hemizygosity for the p53 loc

255 s of PMP22, as a 1.4 Mb duplication on human chromosome 17, resulting in three copies of PMP22, is th

256 The other (chromosome 17, rs1531554, OR = 0.68, P = 2.9 x 10(-8)) w

257 Copy-number anomalies in chromosome 17 seem to be common in tumours that show dis

258 To better define the chromosome 17 segment and the 16 to 17 transition, we us

259 e as few as 21 functional genes in the mouse chromosome 17 segment.

260 al dementia and parkinsonism associated with chromosome 17; several mutations causing this dementia l

261 al 50-Mb region of primarily the long arm of chromosome 17 showed LOH in 8 cases, whereas a less than

262 ucleus or a FISH ratio (HER2 gene signals to chromosome 17 signals) of more than 2.2; a negative resu

263 The close linkage of OVCA1 and p53 on human Chromosome 17 suggests that coordinated loss may be an i

264 revealed the existence of 4 SWR loci (H2 on chromosome 17, Swrl-1 on chromosome 1, Swrl-2 on chromos

265 The trac mutation maps to mouse chromosome 17, syntenic with human chromosome 2p21-22.

266 Previously a deletion in mouse chromosome 17, T(22H), was shown to behave like a t alle

267 temporal dementia and parkinsonism linked to chromosome 17," tau abnormalities are implicated directl

268 is a deletion of approximately 1 Mb on mouse chromosome 17 that alters the expression of the qk gene

269 of conserved synteny with a portion of mouse chromosome 17 that contains Fem1a.

270 wed to map belr1 to a 4-Mb interval on mouse chromosome 17 that contains the Trem2 gene.

271 pe is an ancestral version of proximal mouse chromosome 17 that has evolved mechanisms to persist as

272 We found an eQTL hotspot on rat chromosome 17 that is causally associated with multiple

273 inase A (PKA), is a tumor suppressor gene on chromosome 17 that is mutated in some CNC families.

274 neuropathy and results from a duplication on chromosome 17 that results in an extra copy and increase

275 At the proximal part of mouse chromosome 17 there are three well-defined genes affecti

276 l dementia with parkinsonism associated with chromosome 17, three unclassifiable tauopathy, and one a

277 s used as donor of the Ecogpt-carrying human chromosome 17 to 'tribrids' growing in suspension, made

278 DXZ1 (from the X chromosome) and D17Z1 (from chromosome 17), to generate human artificial chromosomes

279 temporal dementia and parkinsonism linked to chromosome 17 transiently respond to levodopa therapy.

280 ird tribrid had a portion of the long arm of chromosome 17 translocated to mouse as its only human ge

281 Frontotemporal dementia with parkinsonism chromosome 17 type (FTDP-17) is caused by mutations in M

282 e frontotemporal dementia with parkinsonism--chromosome 17 type (FTDP-17).

283 nt frontotemporal dementia with Parkinsonism-chromosome 17 type (FTDP-17).

284 se frontotemporal dementia with parkinsonism chromosome 17-type and by unknown mechanisms in other re

285 se frontotemporal dementia with parkinsonism chromosome 17-type by several mechanisms.

286 emporal dementia with parkinsonism linked to chromosome 17 was analyzed.

287 A positive lod score on chromosome 17 was calculated.

288 e, integration of these sequences into human chromosome 17 was demonstrated by the construction of hu

289 Loss of chromosome 17 was identified 5% of all samples and was s

290 In a detailed reconstruction of events on chromosome 17, we found large unpaired inversions and de

291 an inducible Xist transgene located on mouse chromosome 17, we show that 24 h after synchronous induc

292 This is a variant region of Chromosome 17 which exists as a polymorphism in wild mic

293 emporal dementias and Parkinsonism linked to chromosome 17), which are characterized by the formation

294 A locus on mouse chromosome 17, which controls activation of recombinatio

295 age to chromosome 8, we find that a locus on chromosome 17, which encompasses the MHC locus, impacts

296 ffort to restrict the wide linkage region on chromosome 17 with a dense set of 31 markers using multi

297 ge analysis identified a candidate region on chromosome 17 with a maximum multipoint logarithm of odd

298 temporal dementia and parkinsonism linked to chromosome 17 with mutations in Tau (FTDP-17T).

299 alysis, we identified a 13-Mb locus on mouse chromosome 17 with significant linkage to the developmen

300 of single-nucleotide polymorphisms (SNPs) on chromosome 17 within a chemokine gene cluster associated