ライフサイエンスコーパス: Tg

1 ized by droplets containing triacylglycerol (TG).

2 te in the vadose zone as 605-1814 Teragrams (Tg).

3 nal peptide (vip) in the trigeminal ganglia (TG).

4 tein cholesterol (LDL-C), and triglycerides (TG).

5 ering (SD-TIRS) with a transmission grating (TG).

6 e sensory neurons of the trigeminal ganglia (TG).

7 e activation energy becoming very large near Tg.

8 sensory neurons in all three branches of the TG.

9 ng towards the glass transition temperature, Tg.

10 ocked all of these changes in the cornea and TG.

11 ected to trigger the release of teragrams (1 Tg = 10(6) tons) of methane from thawing subsea permafro

12 in single phenotype rare variant analyses (P TG = 6.5 x 10(-8) and P FI = 0.27).

13 gion will triple to 2.6 Tg a(-1) SO2 and 2.6 Tg a(-1) NOx by 2030, with the largest increases occurri

14 s from coal in the region will triple to 2.6 Tg a(-1) SO2 and 2.6 Tg a(-1) NOx by 2030, with the larg

15 These results are consistent with TG accumulation in the Pnpla3(148M/M) mice being caused

16 Dga1p, a diacylglycerol acyltransferase, and TG accumulation were both 30-35% lower in the absence of

17 Single-cell analysis of DAM in Tg-AD and triggering receptor expressed on myeloid cells

18 or expressed on myeloid cells 2 (Trem2)(-/-) Tg-AD reveals that the DAM program is activated in a two

19 populations in wild-type and AD-transgenic (Tg-AD) mouse brains.

20 AHFAs) were increased and transplantation of Tg adipose tissue improved glucose tolerance in recipien

21 virus (AAV) vectors for gene delivery to the TG after intradermal whiskerpad delivery in mice.

22 hing depended on the wheat protein fraction, TG amount and its origin.

23 correlation between the abilities of Tg and Tg analogs to deplete ER Ca(2+) stores and their detrime

24 that low (0.1 mum) concentrations of Tg and Tg analogs with various long-chain substitutions at the

25 of apoptosis at low concentrations of Tg and Tg analogs, whereas high cytosolic Ca(2+) levels and SOC

26 stinct from that of SERCA1a, indicating that Tg analogues with a higher specificity for SPCA1a can pr

27 Between Tg and approximately 60 K, the nonexponential rebinding

28 In this time course study, cohorts of Tg and control mice were euthanized at defined intervals

29 Furthermore, both TG and DSC results support the formation of inclusion co

30 l properties of the CPCMs were determined by TG and DSC.

31 TG and HDL-C concentrations were not associated with ris

32 l role in preventing HSV-1 reactivation from TG and subsequent virus shedding in tears that trigger r

33 erved a correlation between the abilities of Tg and Tg analogs to deplete ER Ca(2+) stores and their

34 report that low (0.1 mum) concentrations of Tg and Tg analogs with various long-chain substitutions

35 iation of apoptosis at low concentrations of Tg and Tg analogs, whereas high cytosolic Ca(2+) levels

36 e current DOM C stock in China is 925 +/- 54 Tg and that it grew by 6.7 +/- 2.2 Tg C/yr over the past

37 We challenged juvenile Scnn1b-Tg and wild-type mice with Aspergillus fumigatus and hou

38 ino acid signature was associated with serum TG and with the risk of hypertriglyceridemia after 2 yea

39 all detected pathologic alterations between TG and WT mice, only (18)F-AV45 could detect an effect o

40 ression at the glass transition temperature (Tg) and ambient pressure sub-Tg annealing.

41 gered contact-dependent thrombin generation (TG) and amplified TG initiated by low concentrations of

42 l stability as analyzed by thermogravimetry (TG) and differential thermal analysis (DTA).

43 Both sensory trigeminal ganglion (TG) and sympathetic superior cervical ganglion (SCG) neu

44 ithin sensory neurons of trigeminal ganglia (TG), and TG-resident CD8(+) T cells play a critical role

45 c (Tg) mouse [synapsin-driven Cav-1 (SynCav1 Tg)] and subjected it to a controlled cortical impact mo

46 noted between PD and BOP, PD and TC, PD and TG, and CAL and TG in each group (P <0.01).

47 s-reactivity profile (IgE against CTX, Bos d TG, and HSA-alpha-Gal) was identified, which is associat

48 memory CD8(+) T cells (TCM), locally within TG, and improved protection against recurrent herpesviru

49 ermined how the CXCL10/CXCR3 pathway affects TG- and cornea-resident CD8(+) T cell responses to recur

50 lyses in other models of lipodystrophy, AZIP(tg/+) and Adipoq-Cre(tg/+)Pparg(fl/fl) mice, coupled wit

51 multiple low-dose streptozotocin (STZ), hep-tg animals developed less severe hyperglycemia compared

52 ocation induced by catecholamine injections, TG animals were resistant to triggered ventricular arrhy

53 that the effects of hot compression and sub-Tg annealing can be combined to access a "forbidden glas

54 licate glass at 1 GPa at Tg, followed by sub-Tg annealing in-situ at 1 GPa.

55 on temperature (Tg) and ambient pressure sub-Tg annealing.

56 es previously subjected to high-pressure sub-Tg annealing.

57 mples during subsequent ambient pressure sub-Tg annealing.

58 Above the solvent glass transition (Tg approximately 180 K), the rebinding progress slows as

59 on results from iodination of thyroglobulin (TG) at residues Tyr(5) and Tyr(130), whereas thyroidal T

60 nclusion, we uncovered here an active cornea-TG axis, driven by PEDF-R activation, that fosters axon

61 P = 3.84 x 10(-31)) and serum triglycerides (TG) (beta = 0.067, P = 4.5 x 10(-21)).

62 TG biosensors work ideally within 2.5-2700s, in pH range

63 operating principles, merits and demerits of TG biosensors, specifically nanomaterials based biosenso

64 Thapsigargin (Tg) blocks the sarco/endoplasmic reticulum (ER) Ca(2+)-A

65 d(TG(Br)GG(Br)GAC7) forms long linear quadruplex wires und

66 ctivation was induced from latently infected TG by UV-B light.

67 ree forms of unlabeled, human thyroglobulin (Tg) by bottom-up protein analysis.

68 The popularity of transglutaminase (TG) by the food industry and the variation in functional

69 K below their glass transition temperature (Tg), by subjecting them to active plastic deformation.

70 eliminated 4.0+/-0.9 Tmol per year (48+/-11 Tg C per year) or 13% of total organic carbon (OC) carri

71 uld rise to 6.9+/-1.5 Tmol per year (83+/-18 Tg C per year) or 19% by 2030.

72 into agricultural lands, which caused 10,607 Tg C release from land ecosystems to atmosphere.

73 ,325) muatm and a total FCO2 of 189 (74-347) Tg C year(-1) , and evaluate the corresponding uncertain

74 tration amount in surface soils reached 10.9 Tg C year(-1) , which contributed an estimated 43% of to

75 t a total sink of carbon at the rate of 1.26 Tg C yr(-1) .

76 global marine monoterpene emissions of 0.16 Tg C yr(-1), similar to a previous bottom-up estimate ba

77 er than a previous top-down estimate of 29.5 Tg C yr(-1).

78 s C removal (naive=0.42 Tg C, optimized=0.25 Tg C) to achieve the same treatment efficacy.

79 red significantly less C removal (naive=0.42 Tg C, optimized=0.25 Tg C) to achieve the same treatment

80 25 +/- 54 Tg and that it grew by 6.7 +/- 2.2 Tg C/yr over the past two decades primarily due to incre

81 usly demonstrated that RORgammat-transgenic (tg) C57BL/6 mice, which have Th17-biased responses due t

82 ction by Helicobacter species of transgenic (Tg) C57BL6 mice, ectopically expressing the human form o

83 er carbon stock has increased by 6.7 +/- 2.2 Tg carbon per year, primarily due to increasing forest a

84 cordingly, Ca(2+)-spark analysis in isolated TG cardiomyocytes revealed remarkably reduced Ca(2+) lea

85 Generation of Il5 (Tg) /Cd300f (-/-) mice revealed marked and distinct incr

86 optive-transfer approach, we show that naive Tg CD4 T cells become activated, proliferate, migrate to

87 issions of methane decreased by 3.7 (+/-1.4) Tg CH4 per year from the 2001-2007 to the 2008-2014 time

88 d that fossil fuels contribute between 12-19 Tg CH4 per year to the recent atmospheric methane increa

89 equivalent to net emissions increase of 25 Tg CH4 per year.

90 ould contribute significantly (0.61 +/- 0.18 Tg CH4/yr, 95% CL) to U.S. emissions.

91 L-1beta-positive astrocytes increased in the Tg(CJD) hippocampus, and blocking IL-1 receptor signalin

92 d of age, the magnitude of LTP increased in Tg(CJD) mice but decreased in PrP KO mice, indicating di

93 naptic plasticity in hippocampal slices from Tg(CJD) mice, which model a genetic form of CJD.

94 sions derived from 8.3% of PAs (112 +/- 49.5 Tg CO2 yr(-1); n = 171).

95 B deficient (ETB def) or transgenic control (TG-con) rats were used in the presence or absence of ETA

96 6.0-11.0, temperature 25-39.5 degrees C and TG concentration range, 0.001-100mM, the detection limit

97 Higher TG concentrations at baseline were associated with an in

98 s using the alpha-Gal analytes CTX and Bos d TG confirms the history of MA patients in 91% and 88% of

99 ynthesis pathway and resulted in high plasma TG content.

100 injection of ferumoxytol, and 18 Jax C57BL/6-Tg (Csf1r-EGFP-NGFR/FKBP1A/TNFRSF6) 2Bck/J mice received

101 mmonly used SERCA1a inhibitors thapsigargin (Tg), cyclopiazonic acid, and 2,5-di-tert-butylhydroquino

102 tiple ASYMP epitopes (prime) and neurotropic TG delivery of the T cell-attracting chemokine CXCL10 (p

103 Moreover, TG demonstrated improved cardiac function after myocardi

104 TG disposal and acylcarnitine production during lipid ov

105 s mainly associated with greater circulating TG disposal, lower systemic lipolysis, and better fatty

106 metry and differential scanning calorimetry (TG-DSC), evolved gas analysis (TG-DSC-FTIR) and High-res

107 calorimetry (TG-DSC), evolved gas analysis (TG-DSC-FTIR) and High-resolution mass spectra (HRMS).

108 hermogravimetry/derivative thermogravimetry (TG/DTG), differential scanning calorimetry coupled with

109 ture by different mechanisms, both 8oxoG and Tg enhance telomerase binding and extension activity to

110 ol compounds induced estrogenic responses in Tg(ERE:Gal4ff)(UAS:GFP) zebrafish that were inhibited by

111 which disrupts the telomeric DNA structure, Tg exhibits substantially reduced perturbation of G-quad

112 majority of filtered air (FA)-exposed Scnn1b-Tg(+) (FA-Tg(+)) mice successfully cleared spontaneous b

113 use of MARV with analysis of triglycerides (TG), fasting insulin (FI) and waist-to-hip ratio (WHR) i

114 provides stronger support for association (P TG+FI = 1.8 x 10(-9)) than observed in single phenotype

115 s developed using tryptic marker peptides of TG (five markers), and bovine and porcine fibrinogen (si

116 Q8 inhibits developmental angiogenesis in Tg(fli1:EGFP) zebrafish and inhibits human microvascular

117 -magnesium aluminosilicate glass at 1 GPa at Tg, followed by sub-Tg annealing in-situ at 1 GPa.

118 These differences define a SAR of Tg for SPCA1a distinct from that of SERCA1a, indicating

119 The glass transition temperature (Tg) for all of the powders significantly decreased at 45

120 obtained to produce 6.074+/-0.019UmL(-1) of TG from a novel source; Streptomyces sp.

121 of PNPLA3-148M and impaired mobilization of TG from LDs.

122 the detection of microbial transglutaminase (TG) from Streptomyces mobaraensis in different types of

123 ous detection of microbial transglutaminase (TG) from Streptomyces mobaraensis, and bovine and porcin

124 l exploitation was compared to commonly used TG, from Streptomyces mobaraensis.

125 tion polymer derived from 6-thioguanosine (6-TG-H), a sulfur-containing analog of a natural nucleosid

126 seen at temperatures below the bulk solvent Tg, has low activation energy, and is likely due to fast

127 he intermediate temperature range of 0.6-0.7 Tg However, most materials are expected to carry higher

128 to the ion source by using thermogravimetry (TG) hyphenated to REMPI time-of-flight mass spectrometry

129 The availability of Tg(igfbp5a:GFP) line provides a whole organism platform

130 development of a zebrafish transgenic line, Tg(igfbp5a:GFP), which faithfully reports the mitotic ac

131 D and BOP, PD and TC, PD and TG, and CAL and TG in each group (P <0.01).

132 combinant human histones H3 and H4 triggered TG in recalcified human plasma in a platelet-dependent m

133 PF) in stomach carcinoma, and thyroglobulin (TG) in thyroid carcinoma.

134 that this unexpected stimulation arises from Tg-induced conformational alterations and dynamics in te

135 ndent thrombin generation (TG) and amplified TG initiated by low concentrations of tissue factor.

136 through a similar mechanism as thapsigargin (TG), involving increased cytosolic calcium.

137 y affected double mutant embryos ( Irf6(+/-);Tg(KRT14::Spry4)).

138 xpress Spry4 in the basal epithelial layer ( Tg(KRT14::Spry4)).

139 isoform CREM-IbDeltaC-X in transgenic mice (TG) leads to spontaneous-onset AF preceded by atrial dil

140 Surprisingly, the Tg lesion stimulates telomerase loading and activity to

141 These biosensors measured TG level in fruit juices, beverages, sera and urine samp

142 TG level is below 150mg/dL in healthy persons.

143 e displayed decreased plasma cholesterol and TG levels and reduced atherosclerotic lesions.

144 variant in APOC3 causes reduced circulating TG levels and, hence, protects from CHD.

145 CIII (ApoC-III) is a key regulator of plasma TG levels through regulation of lipolysis and lipid synt

146 To identify novel regulators of TG levels, we carried out a high throughput screen (HTS)

147 ciation, if any, between serum triglyceride (TG) levels and gemfibrozil consumption with periodontal

148 Serum levels of total cholesterol (TC), TG, low-density lipoprotein, and high-density lipoprotei

149 gnificantly lower accumulation in CC10-IL-13 Tg lungs relative to the specific tracer.

150 P-13 were significantly higher in CC10-IL-13 Tg lungs.

151 PDGF-alpha-syn transgenic (tg) male and female mice were immunized with GP-alone, G

152 roducibility of tau prion formation in young Tg(MAPT*P301S+/+) mice establishes a rapid assay for com

153 measures of disease were more uniform in the Tg(MAPT*P301S+/+) mice.

154 ction, decreased TRPC1 expression, inhibited Tg-mediated STIM1-Cav1.3 interaction, and induced caspas

155 tected a significant age-related increase in TG mice (P < 0.0001) but did not detect the treatment-in

156 ccessfully purified from the saliva of these TG mice and its identity was verified.

157 slocation in WT mice was exacerbated in MIOX-TG mice but absent in MIOX(-/-) mice.

158 induced in another set of control and hREG3A-TG mice by administration of trinitrobenzene sulfonic ac

159 ted to the catastrophic loss of insulin, hep-tg mice continued to have significantly lower blood gluc

160 ted to a controlled cortical impact, SynCav1 Tg mice demonstrated preserved hippocampus-dependent fea

161 Regardless of treatment, TG mice demonstrated significantly lower (18)F-FDG uptak

162 CC10-IL-13 Tg mice developed considerable pulmonary tissue remodeli

163 REG3A TG mice developed only mild colonic inflammation after e

164 Unexpectedly, T-bet-tg mice died 2 to 3 weeks after infection due to failure

165 ion of collagen-induced arthritis (CIA), tau-tg mice displayed an increased incidence and an earlier

166 Already at steady-state conditions, tau-tg mice exhibit peripheral immune activation that is man

167 al microbiota from REG3A-TG mice protect non-TG mice from induction of colitis.

168 80 metabolites accurately discriminated UCP3 Tg mice from WT when modeled within a specific exercise

169 wild-type (WT) mice, cisplatin-treated MIOX-TG mice had even greater increases in urea, creatinine,

170 Fecal samples from REG3A-TG mice had lower levels of ROS than feces from control

171 Similarly, MIOX-TG mice had the highest and MIOX(-/-) mice had the lowes

172 al microbiota occurred after a few months in TG mice heterozygous for REG3A that harbored a wild-type

173 We believe that APRIL Tg mice infected by Helicobacter species may represent a

174 In this study, we found that aged Tg mice of both sexes expressing human tau proteins harb

175 Fecal microbiota from REG3A-TG mice protect non-TG mice from induction of colitis.

176 Wild-type (WT) and TG mice received vehicle or BACE inhibitor (60 mg/kg) st

177 Obese Tg mice remained insulin sensitive, had increased glucos

178 nificantly higher in the lungs of CC10-IL-13 Tg mice than wild-type animals.

179 146a-deficient mice with 2D2 T cell receptor-Tg mice to generate 2D2 CD4 T cells that are deficient i

180 hTNF-Tg mice treated with infliximab demonstrated significant

181 fore AF onset) and old (TGo, after AF onset) TG mice were investigated by mRNA microarray profiling i

182 ted, aggregated tau in brain tissue of P301S-tg mice, associated with a decrease in detergent-soluble

183 an the hindbrain across the life span of the Tg mice, suggesting that sortilin, at least in part, inh

184 s into different brain regions of female non-Tg mice, we demonstrated the induction and propagation o

185 let transcriptome was greatly altered in hep-tg mice, with >2,000 genes differentially expressed vers

186 between AD-tau, CBD-tau, and PSP-tau in non-Tg mice.

187 sufficient to rescue the memory deficits in Tg mice.

188 om db/db mice and normalized in db/dbhnRNP F-Tg mice.

189 ial remodeling and development of AF in CREM-TG mice.

190 uced allergen-induced inflammation in Scnn1b-Tg mice.

191 xpression in the airway epithelium of Scnn1b-Tg mice.

192 hages following infliximab treatment in hTNF-Tg mice.

193 ver, in contrast with FA-Tg(+) mice, the SHS-Tg(+) mice had pronounced epithelial necrosis, alveolar

194 However, in contrast with FA-Tg(+) mice, the SHS-Tg(+) mice had pronounced epithelial

195 by PND22, the SHS-exposed Scnn1b-Tg(+) (SHS-Tg(+)) mice failed to resolve these infections.

196 f filtered air (FA)-exposed Scnn1b-Tg(+) (FA-Tg(+)) mice successfully cleared spontaneous bacterial i

197 stions, we exposed Scnn1b transgenic (Scnn1b-Tg(+)) mice to SHS from postnatal day (PND) 3-21 and lun

198 itional MIOX-overexpressing transgenic (MIOX-TG) mice and MIOX-knockout (MIOX(-/-)) mice with tubule-

199 -related mutant human APP (hAPP) transgenic (Tg) mice and patient brains.

200 Tsc1 (tg) mice have less fibrosis and inflammation in aged as

201 art-specific phosphodiesterase 2-transgenic (TG) mice showed a marked reduction in resting and in max

202 were attenuated in db/dbhnRNP F-transgenic (Tg) mice specifically overexpressing hnRNP F in their RP

203 is article, we show that tau-transgenic (tau-tg) mice that develop neurodegenerative disease characte

204 Human TNF transgenic (hTNF-Tg) mice were treated with infliximab after development

205 ce, cardiac-specific SIRT2 transgenic (SIRT2-Tg) mice, and their respective littermates (8 to approxi

206 ent tau strains occurs in nontransgenic (non-Tg) mice, and to investigate whether there are strain-sp

207 span increased significantly in female Tsc1 (tg) mice, but not in male Tsc1 (tg) mice.

208 pithelial Na(+) channel (Scnn1b)-transgenic (Tg) mice.

209 scued NKT cell development in IkappaBDeltaN (tg) mice.

210 female Tsc1 (tg) mice, but not in male Tsc1 (tg) mice.

211 rast, mTORC2 signaling was enhanced in Tsc1 (tg) mice.

212 itracer PET imaging in transgenic APPPS1-21 (TG) mice.

213 By contrast, the higher Tg microsphere structures exhibit reduced compression se

214 Melanoma onset was accelerated in kit(lf); Tg(mitfa:BRAF(V600E)); p53(lf) fish.

215 troduced a kit(lf) mutation into a strain of Tg(mitfa:BRAF(V600E)); p53(lf) melanoma-prone zebrafish.

216 ef and pork were performed using a technical TG mixture (Activa, Ajinomoto), and bovine and porcine p

217 xperiments were performed with two technical TG mixtures with and without caseinate.

218 Male FVB/N-Tg(MMTVneu)202Mul/J (Her2) transgenic mice were bred to

219 Pnpla3(148M/M) mice being caused by impaired TG mobilization from LDs.

220 elf-assembly reaction is compatible with a 6-TG-modified DNA duplex and provides a straightforward me

221 that an 80-mer minicircle DNA using the same TG-motifs faithfully reproduces the CPD pattern in the n

222 orm of nitric oxide synthase (iNOS) from VCP TG mouse and by pharmacological inhibition of iNOS in is

223 no-associated virus particles in mutant hAPP Tg mouse brains decreases synaptic Abeta levels and amel

224 ed with green fluorescent protein (T40PL-GFP Tg mouse line) exhibited hyperphosphorylated tau misloca

225 on-targeted Cav-1-overexpressing transgenic (Tg) mouse [synapsin-driven Cav-1 (SynCav1 Tg)] and subje

226 Thorough assessment of transgenic (Tg) mouse lines that replicate this process is critical

227 human P301S tau-expressing transgenic (P301S-tg) mouse model of frontotemporal dementia/tauopathy.

228 storically used first-generation transgenic (Tg) mouse models that overexpress proteins linked to fam

229 ng CaMKIIdeltac-overexpressing (CaMKIIdeltac-Tg) mouse ventricles.

230 By using a transgenic (TG) mouse with cardiac-specific overexpression (3.5-fold

231 this problem by developing a TCR-transgenic (Tg) mouse with CD4 T cells that respond to a common Ag i

232 vivo, we generated an aP2-WISP2 transgenic (Tg) mouse.

233 In this study, we generated a new Tg(mrc1a:egfp)(y251) transgenic zebrafish that uses a ma

234 rial were carried out by Raman spectroscopy, TG-MS, UV/vis, and fluorescence spectroscopy.

235 h the amount of surface oxygen determined by TG-MS.

236 helical chains, characterized as {Au(I)(mu-6-TG)} n , extending many mum in length that are structura

237 x 10-8), and one novel locus associated with TG near WDR11-FGFR2 (P = 2.7 x 10-10).

238 y expressed in the same trigeminal ganglion (TG) neuron during reactivation and cooperatively stimula

239 8, and 9 trafficked from the whiskerpad into TG neurons and expressed transgenes within cell bodies a

240 hibition in vivo increases the percentage of TG neurons expressing deltaR on the surface and allows e

241 but no significant differences were found in TG neurons.

242 lized with these receptors in SCG but not in TG neurons.

243 n of viral progeny in SCG neurons but not in TG neurons.

244 genetically manipulate trigeminal ganglion (TG) neurons would be useful in the study of the craniofa

245 activity in dental pulp, trigeminal ganglia (TG) neurons, and their nerve fibers.

246 Conversely, the protein interaction of the Tg O-2 side chain with SPCA1a appears comparable with th

247 Approximately 500 Tg of 2-methyl-1,3-butadiene (isoprene) is emitted by de

248 in coastal marine ecosystems, fix up to 27.4 Tg of carbon per year, and provide important structural

249 e, delivery of exogenous CXCL10 chemokine in TG of CXCL10(-/-) mice, using the neurotropic adeno-asso

250 CD103(high)CD8(+) tissue-resident T cells in TG of latently infected HLA-A*0201-transgenic mice and r

251 CD8, IFN-gamma, and PD-1 transcripts in the TG of latently infected mice.

252 m(2) ) containing an estimated 128.2 +/- 9.1 Tg of peatland belowground soil C within the mapping are

253 ider injection into the atmosphere of 15,000 Tg of soot, the amount estimated to be present at the Cr

254 rocytes from a bitransgenic murine model (Bi-Tg) of thyroid-specific PBF and PTTG overexpression.

255 o evaluate the effect of shell stiffness and Tg on compressive behavior and compression set in siloxa

256 and doubled the median survival time of TCL1-Tg:p53(-/-) mice, which develop disease resembling human

257 present data suggesting that TSH-stimulated TG phosphorylation contributes to enhanced de novo T3 fo

258 f the fractured interfaces validated the sub-Tg, plasticity-induced, molecular mobilization causing b

259 t, narrow polydispersity, and amorphous, low Tg, poly(alpha-olefinate)s (xPAOs) as a new class of hyd

260 of lipodystrophy, AZIP(tg/+) and Adipoq-Cre(tg/+)Pparg(fl/fl) mice, coupled with skin graft experime

261 density lipoprotein (HDL) triglycerides (HDL-TG) predicted LVEF (beta=1.90 [95% confidence interval (

262 expressing the human COMT-Val gene (COMT-Val-tg) present exaggerated remote memories (>50 days) while

263 inflammasomes in microglial cells and in HIV-Tg rats administered lipopolysaccharide.

264 lipopolysaccharide (LPS) to HIV transgenic (Tg) rats followed by assessment of IL-1beta mRNA express

265 apparent feeble numbers of CD8(+) T cells in TG remains a challenge for immunotherapeutic strategies.

266 sory neurons of trigeminal ganglia (TG), and TG-resident CD8(+) T cells play a critical role in preve

267 t, 8oxoG induces high accessibility, whereas Tg retains limited accessibility, of telomeric G-quadrup

268 ith the tip generation/substrate collection (TG/SC) mode of scanning electrochemical microscopy (SECM

269 ovo T3 that can be formed upon iodination of TG secreted from PCCL3 (rat thyrocyte) cells was augment

270 V1 vectors are suitable for gene delivery to TG sensory neurons following intradermal whiskerpad inje

271 infections by PND22, the SHS-exposed Scnn1b-Tg(+) (SHS-Tg(+)) mice failed to resolve these infection

272 1(G93A) mice in the hybrid background (B6SJL-Tg(SOD1-G93A) have been criticized because of high noise

273 astic deformation in this newly reported sub-Tg solid-state bonding.

274 Here, we report a new phenomenon of sub-Tg, solid-state, plasticity-induced bonding; where amorp

275 d us to isolate and evaluate a high-yielding TG strain.

276 The present study used Tg-SwDI mice, which have extensive CAA.

277 CpG ODN in a triple transgenic mouse model, Tg-SwDI, with abundant vascular amyloid, in association

278 Hemizygous Tg-TBK1 mice (with one TBK1 transgene per genome) had a

279 BK1 mice had 7.6% fewer RGCs than hemizygous Tg-TBK1 mice and 20% fewer RGCs than wild-type mice (P =

280 n intraocular pressures was detected between Tg-TBK1 mice and wild-type littermates as they aged (P >

281 Tg-TBK1 mice exhibit the cardinal sign of glaucoma, a pr

282 Homozygous Tg-TBK1 mice had 7.6% fewer RGCs than hemizygous Tg-TBK1

283 cted in the retinal ganglion cells (RGCs) of Tg-TBK1 mice than in wild-type littermates.

284 -amplitude coupling (PAC) in stg/stg, stg/+, tg/tg and wild-type (+/+) mice.

285 nked patterns of aberrant PAC in stg/stg and tg/tg mice compared to +/+ and stg/+ mice.

286 ceptor defect, but not homozygous tottering (tg/tg) mice with a P/Q type calcium channel mutation.

287 azer (stg/stg) but not homozygous tottering (tg/tg) mice.

288 ed significant repression of DDR genes in Bi-Tg thyrocytes (P=2.4 x 10(-4)) compared with either PBF-

289 this, genetic instability was greatest in Bi-Tg thyrocytes with a mean genetic instability (GI) index

290 Additions of TG to wheat protein and flour based doughs revealed that

291 TgCRND8 (Tg) transgenic mice express human amyloid precursor prot

292 nstrated that Acot1 knockdown led to greater TG turnover and FA oxidation, suggesting that ACOT1 is i

293 mice globally overexpressing heparanase (hep-tg) was the discovery of improved glucose homeostasis.

294 ype of pre-treatment on the detectability of TG were found.

295 e, but not control sera, led to secretion of TG with an increased intrinsic ability to form T3 upon i

296 ell-tolerated phenotype persisted in elderly TG with no indications of cardiac pathology or premature

297 ock in the period of 2004-2008 is 925 +/- 54 Tg, with an average density of 5.95 +/- 0.35 Mg C ha(-1)

298 c methane, counterintuitively, involves a 25-Tg/y decrease in methane emissions from 2003 to 2016 tha

299 have not changed significantly (0.2 +/- 0.7 Tg yr(-1)) between 2010 and 2015, suggesting that major

300 y SO2 during passive degassing, or 23 +/- 2 Tg/yr.