ライフサイエンスコーパス: Tg

1 th the protozoan parasite Toxoplasma gondii (Tg).

2 itutive breast cancer mouse model (MMTV-PyMT-Tg).

3 precursor protein and presenilin 1 (APP/PS1-Tg).

4 d PG, HFD also enhanced thrombin generation (TG).

5 rally VZV-infected human trigeminal ganglia (TG).

6 included ceramides (Cer) and triglycerides (TG).

7 s sensory neurons within trigeminal ganglia (TG).

8 d ganglion types [DRG vs trigeminal ganglia (TG)].

9 espectively, indicating a higher rigidity of Tg.

10 put, resulting in the excess accumulation of TG.

11 ion with an efficiency comparable to that of TG.

12 e-damaging effects of IgG from patients with TG.

13 reased ROS and marginally decreased cellular TG.

14 ed for untargeted lipidomics and to quantify TG.

15 ne expression in the HSV-1 latently infected TG.

16 e neuro-inflammation severity, especially in TG.

17 d TG at 150 minutes as a function of fasting TG.

18 6, with a current annual surplus rate of 1.6 Tg.

19 uence contexts contained 85-90% AT and 5-10% TG.

20 ) after periodontal debridement (test group [TG]1), or omega-3 PUFA + ASA (3 g of fish oil/d + 100 mg

21 ion, myocyte hypertrophy (WT, 19.8 mum; CatA-TG, 21.9 mum), cellular apoptosis, and elevated mRNA exp

22 LV end diastolic volume (WT, 50.8 mul; CatA-TG, 61.9 mul).

23 radicals (WT, 4.54 mumol/mg tissue/min; CatA-TG, 8.62 mumol/mg tissue/min), increased inflammation, m

24 studies; 86,854 people], and triglycerides [TG; 84 studies; 121,009 people]) levels and prevalences

25 (high-density lipoprotein) subparticles (HDL-TG), a smaller decrease of HDL diameter and smaller incr

26 Hepatic TG production and intestinal TG absorption were unchanged in ppHF dams, but systemic

27 ective role for CC to limit ROS and cellular TG accumulation, and to alter hepatic energy metabolism

28 patomegaly due to glycogen and triglyceride (TG) accumulation in the liver.

29 enically express GFP on smooth muscle cells (Tg[acta2:GFP]), to visualize the beating heart.

30 ated risk of experiencing low HDL-C and high TG (all p < 0.05).

31 TG and AG can be further investigated as potential bioma

32 sported by both OATP1B1 and OATP1B3, whereas TG and AG were preferentially (>68%) transported by OATP

33 We observe that PRAP1 directly binds to TG and facilitates MTTP-mediated lipid transfer.

34 h the exceptions of human PG, baboon TG, rat TG and Guinea pig PG.

35 A 1 SD higher TG and LDL-C level caused a 0.062 (95% CI 0.040, 0.083)

36 AP1's ability to form a ternary complex with TG and MTTP, as well as impairs its ability to facilitat

37 In this study, we performed simultaneous TG and PG analysis in blood plasma samples from humans a

38 Integrating TG and PG measurements may define a prothrombotic risk f

39 TG and PG parameters from Guinea pig samples were extrem

40 TG and PG were investigated in male and female donor pla

41 les, which correlated negatively with plasma TG and positively correlated with bacterial genera enric

42 tions, resulting in smaller increases of HDL-TG and VLDL subparticles.

43 nt wild-type flank infection infiltrated the TG and were retained long term, suggesting that latent e

44 nd Rag1 (KO)/Tg(+) juveniles, the Il2rg (KO)/Tg(+) and Il2rg (KO)/Rag1 (KO)/Tg(+) juveniles exhibited

45 were comparable between the immunocompetent Tg(+) and Rag1 (KO)/Tg(+) juveniles, the Il2rg (KO)/Tg(+

46 en demonstrated for anti-thyroglobulin (anti-TG) and anti-thyroid peroxidase (anti-TPO) as models.

47 g acute infection in the trigeminal ganglia (TG) and brain stem compared to the control-vaccinated gr

48 ng MR, we inferred that higher triglyceride (TG) and LDL cholesterol (LDL-C) levels caused elevated A

49 M1 PUFA containing triglycerides (TG) and phospholipids were correlated with CB LysoPC and

50 of neutral lipids, such as triacylglycerol (TG) and sterol esters, surrounded by a phospholipid (PL)

51 V(cmax) accessed at growth temperature (R(d,tg) and V(cmax,tg) ) should increase by 3.7% and 5.5% pe

52 oxygen species (ROS), cellular triglyceride (TG), and glucose and B-hydroxybutyrate (BHB) export were

53 with total cholesterol (TC), triglycerides (TG), and lipoprotein concentrations is unknown.

54 low for EtioG (6.2 uM) as compared with AG, TG, and DHTG (46.2, 56.7, and 71.3 uM, respectively), wh

55 , sensory neurons within trigeminal ganglia (TG) are an important site for latency.

56 tercalate just into the PL tail region (CORE-TG) are disordered and increase the amount of PL packing

57 Those at the monolayer surface (SURF-TG) are ordered like PLs with the glycerol moiety expose

58 Simultaneously, the thrombin generation (TG) assay was used to assess their ability to initiate c

59 als of a nonlinear regression that predicted TG at 150 minutes as a function of fasting TG.

60 GWAS of fasting and postprandial serum TG at 150 minutes were performed.

61 fficiency of gB-CD8s and their levels in the TG at early times.

62 The partial molar volume changes of BSA and Tg at the maximal investigated pressure and minimal salt

63 , total riverine export amounts to 43 +/- 15 Tg BC year(-1) (12 +/- 5% of the OC flux).

64 4 is increased in podocytes of patients with TG but not in those without TG despite other forms of re

65 found that Valpha14 TCR transgenic (Valpha14(Tg)) but not Vbeta8 TCR congenic (Vbeta8(Cg)) NC mice ex

66 sociated with serum levels of TC, LDL-C, and TG, but inversely associated with serum levels of HDL-C

67 t IgG from kidney transplant recipients with TG, but not from those without TG, cause a reduction in

68 , swine and rat plasmas demonstrated similar TG, but swine plasmas did not generate plasmin.

69 me rate, soil legacy P may reach up to 106.5 Tg by 2050.

70 errestrial DOC inputs to river network of 35 Tg C year(-1) (14%) from 1860 to 2010.

71 PP from L. hyperborea is estimated at ~ 7.61 Tg C yr(-1).

72 askatchewan emitted a total of 36.3 +/- 15.0 Tg C, emphasizing the importance of southern boreal fire

73 the storms was estimated at 10.44 (+/-2.33) Tg, ca. 23% of island-wide pre-hurricane forest AGB.

74 Findings of this study indicate that TG can be used safely and the occurrence of hepatotoxici

75 Overall, application of TG can rationally modify the functionality and digestibi

76 cipients with TG, but not from those without TG, cause a reduction in the expression of nephrin, sign

77 km(2) and total CH(4) emission is 13.8-17.7 Tg CH(4) year(-1): 11.2-14.4 Tg via diffusion and ebulli

78 inventory estimates total emissions of 0.53 Tg CH(4)/yr [0.40-0.71 Tg CH(4)/yr, 95% CI] and correspo

79 tal emissions of 0.53 Tg CH(4)/yr [0.40-0.71 Tg CH(4)/yr, 95% CI] and corresponds to a loss rate of 2

80 l (CI): 0.46, 0.86) and 10 mg/dL increase in TG change associated with increased odds of LGA (OR = 1.

81 s increased, suggesting that increased blood TG clearance contributes to the decreased blood TG conce

82 lia, likely resulted in the release of 11-21 Tg CO(2) (-eq) since the 1950s, increasing cumulative CO

83 esulted in cumulative emissions of 0.06-0.14 Tg CO(2-eq) over the last 40 years in Cockburn Sound.

84 .34x10(-3)), mainly smaller increases of the TG-component in almost all HDL (high-density lipoprotein

85 total B-12 with serum TC, LDL-C, HDL-C, and TG concentrations across trimesters.

86 Obesity impairs the rise of maternal blood TG concentrations by reducing ANGPTL4 expression in mice

87 estingly, a lower increase in maternal blood TG concentrations has been observed in some obese mother

88 We found not only that maternal blood TG concentrations in ppHF dams were remarkably lower tha

89 clearance contributes to the decreased blood TG concentrations in ppHF dams.

90 xpression of ANGPTL4 restored maternal blood TG concentrations in ppHF dams.

91 ms, Ucp1 gene deletion did not restore blood TG concentrations in ppHF dams.

92 randial TG metabolism independent of fasting TG concentrations, resulting in smaller increases of HDL

93 l lipid supply, maternal blood triglyceride (TG) concentrations are robustly elevated during pregnanc

94 The increase in serum triglyceride (TG) concentrations in response to a meal is considered a

95 dominantly the strongly electron-withdrawing tg conformation of their side chains, which is reflected

96 digestion showed decreased digestibility of TG-crosslinked chickpea-stabilized emulsions, while prot

97 Tg-CX3CL1 mice exhibit enhanced neurogenesis in both sub

98 When Tg-CX3CL1 mice were crossed with Alzheimer's PS19 mice,

99 We estimate that rivers export 18 +/- 4 Tg DBC year(-1) globally and that, including particulate

100 of patients with TG but not in those without TG despite other forms of renal dysfunction.

101 minescence (PL) lifetime enables time-gated (TG) detection without autofluorescence background.

102 ficant age-related changes in triglycerides (TG), diglycerides (DG), phosphatidylcholine, phosphatidy

103 rt kinetics of glucuronides of testosterone (TG), dihydrotestosterone (DHTG), androsterone (AG), and

104 disease) were included, with a median daily TG dose of 20 mg (range: 20-40 mg), a median treatment d

105 vior on heating and cooling processes, using TG/DTG/DTA, TG-MS, DSC, hot stage microscopy and DRX ana

106 ul in identifying activated cells within the TG during HSV-1 infection.IMPORTANCE Without an effectiv

107 vitro hormone-production assays using human TG expressed in HEK293T cells.

108 including LDL cholesterol, triacylglycerol (TG), fasting glucose (FG), glycated hemoglobin (HbA1c),

109 e TG-PL overlap, whereas that caused by SURF-TG fluctuates and is highly correlated with the area per

110 o mCherry demonstrate the versatility of the TG-FRET nanoprobes and the possibility of in vivo biocon

111 Tg via diffusion and ebullition and 2.6-3.3 Tg from spring release of CH(4) stored in bubbles in win

112 otein cholesterol (HDL-c) and triglycerides (TG) from two independent GWAS datasets.

113 ters latency within the trigeminal ganglion (TG), from which it can reactivate throughout the life of

114 ing approaches were applied to the rat liver TG-GATEs dataset to develop feature selection and predic

115 GG/TG genotypes for rs7905446 and female gender were associ

116 The GG/TG genotypes were consistently associated with response

117 Compared to ST and TG groups, optimal neural vessel density and branching i

118 th in SU and STG groups compared with ST and TG groups.

119 the lack of a three-dimensional structure of TG has prevented mechanistic understanding(4).

120 -specific CD8(+) T cells within the infected TG have been shown to play a crucial role in inhibiting

121 No significant effects were observed for TG, HbA1c, CRP, ALT, and AST.

122 egrowth induced by lipin1 depletion required TG hydrolysis and PL synthesis.

123 tes an energy-consuming futile cycle between TG hydrolysis and resynthesis, leading to inhibition of

124 ue transglutaminase immunoglobulin A (anti-t-TG-IgA) titer was assessed.

125 signal-to-background ratios compared to non-TG imaging.

126 n inhibition alone was sufficient to abolish TG in FXII- or FXI-deficient plasma.

127 RBC-MVs initiated TG in normal pooled plasma and in FXII- or FXI-deficient

128 ikrein activated FIX in buffer and initiated TG in normal pooled plasma, as well as FXII- or FXI-defi

129 was necessary for abolishing RBC-MV-induced TG in normal pooled plasma, whereas kallikrein inhibitio

130 t that sustained Nur77 overexpression (Nur77(tg)) in mouse thymocytes abrogates iNKT cell development

131 rotein) cholesterol (LDL-C) or triglyceride (TG)-increasing variants associates with increased CAD ri

132 o identify genetic variation of postprandial TG independent of fasting TG, we calculated the TG respo

133 in-containing protein 3 (TIM-3) expressed by TG infiltrating gB-specific CD8(+) T cells from the HSV-

134 lin resistance, manifests when triglyceride (TG) input in the liver is greater than TG output, result

135 t contain shared and unique SNPs showed that TG is not a risk factor for CAD.

136 The degree of interdigitation caused by CORE-TG is stable and determines the width of the TG-PL overl

137 Tyrosine proximity within TG is thought to enable the coupling reaction but hormon

138 Transplant glomerulopathy (TG) is a major cause of late allograft loss.

139 Thioguanine (TG) is a thiopurine which has been used for patients wit

140 sory ganglia such as the trigeminal ganglia (TG) is influenced by virus-specific CD8(+) T cells that

141 Thyroglobulin (TG) is the protein precursor of thyroid hormones, which

142 From these results, it can be inferred that TG itself is not a causal risk factor for CAD, but it's

143 bacterial burden was increased in Il2rg (KO/)Tg(+) juveniles but returned to significantly lower leve

144 As previously reported, immunocompetent Tg(+) juveniles exhibited spontaneous neonatal bacterial

145 he Il2rg (KO)/Tg(+) and Il2rg (KO)/Rag1 (KO)/Tg(+) juveniles exhibited suppressed expression levels o

146 ween the immunocompetent Tg(+) and Rag1 (KO)/Tg(+) juveniles, the Il2rg (KO)/Tg(+) and Il2rg (KO)/Rag

147 icantly lower levels in Il2rg (KO)/Rag1 (KO)/Tg(+) juveniles.

148 Additionally, TG-LASSO identified genes associated with the drug respo

149 On the other hand, TG-LASSO improved the predictions and distinguished resi

150 Then, we developed a new algorithm called TG-LASSO that explicitly integrates information on sampl

151 An elevated TG level was not protective after adjustment.

152 n (AMI) patients, higher admission LDL-C and TG levels have been shown to be associated with better c

153 erexpression of ANGPTL8 resulted in elevated TG levels in lean mice.

154 ate if and how obesity alters maternal blood TG levels.

155 egnancy significantly reduces maternal blood TG levels.

156 Thyroglobulin (Tg) levels and/or neck ultrasounds were performed at 6 w

157 ensity lipoprotein (LDL-C) and triglyceride (TG) levels form the cornerstone approach of cardiovascul

158 tor of ATGL, the rate-limiting triglyceride (TG) lipase in many cell types.

159 pid groups, for example, in males, 17.04% of TG lipid species decline with age whilst 37.86% increase

160 d TT + pCND were equally likely to achieve a Tg < 0.2 (54.5% vs 66.7%, P = 0.54) and/or a stimulated

161 At 1 year, rates of Tg < 0.2 (88.9% vs 90.0%, P = 1.00) and sTg < 1 (93.8% v

162 hus, when the supply of PLs is limited, SURF-TG may reduce surface tension by behaving as a secondary

163 r LIPC as a main contributor to postprandial TG metabolism independent of fasting TG concentrations,

164 were entirely mimicked in young CaMKIIdelta TG mice (6-8 weeks) where no overt cardiac dysfunction w

165 depletion of C/EBPbeta from human alpha-Syn Tg mice abolishes rotenone-elicited PD pathologies and m

166 lm-grown rather than planktonic PAO1; Scnn1b-Tg mice also cleared infections more slowly than their w

167 We intranasally infected Scnn1b-Tg mice and wild-type littermates with the laboratory P.

168 er, these results show the promise of Scnn1b-Tg mice as models of early P. aeruginosa colonization in

169 antially reduced premature deaths of APP/PS1-Tg mice at a dose lowering brain 24S-hydroxycholesterol

170 Scnn1b-Tg mice carried higher bacterial burdens when infected w

171 that chromatin obtained from the adrenals of TG mice containing the intron conversion binds more stro

172 We found that TG mice containing the intron conversion have (a) increa

173 d (c) increased blood pressure compared with TG mice containing WT intron 2.

174 By 12 weeks, male Tg mice had 22.2% and female Tg mice had 29.6% reduced t

175 12 weeks, male Tg mice had 22.2% and female Tg mice had 29.6% reduced trabecular bone volume (BV) co

176 Osteogenic cultures from Tg mice had reduced differentiation and mineralization w

177 MIOX-TG mice had worsening renal functions with kidneys havin

178 In contrast, Scnn1b-Tg mice infected with a mucoid CF isolate carried high b

179 Scnn1b-Tg mice infected with nonmucoid early CF isolates mainta

180 CaMKIIdelta TG mice lacking deltaB exhibited more severe HF, eccentr

181 At longer times both TAC and TG mice progressed to overt HF (at 45 days and 11-13 wee

182 ohol Western diet-fed hepatitis C virus NS5A Tg mice with hepatocyte-specific TBC1D15 deficiency or e

183 in the distal intestine of VDR null mice (KO/TG mice) results in the normalization of serum calcium a

184 In CatA-TG mice, LV interstitial fibrosis formation was enhanced

185 lasts, osteoclasts, and marrow adipocytes in Tg mice, suggesting independence of EPO signaling in mat

186 ,25(OH)(2)D(3) in the distal intestine of KO/TG mice.

187 d trabecular bone in control mice but not in Tg mice.

188 ses similar to those of PAO1-infected Scnn1b-Tg mice.

189 Scnn1b transgenic (Scnn1b-Tg(+)) mice, which recapitulate cystic fibrosis-like muc

190 We generated humanized transgenic (TG) mice containing all the introns, exons, and 5'- and

191 ype (WT), Fgf15(-/-) , and Fgf15 transgenic (TG) mice with BA levels modulated by feeding cholestyram

192 iments with BAFF-deficient B6.Baff(-/-) Bcl2(Tg) mice, B cell-deficient B6.muMT mice, BAFF-overexpres

193 ment, were somewhat exaggerated in IL-33(KO)/Tg+ mice compared with IL-33(HET)/Tg+ mice.

194 compared with IL-33(HET)/Tg+ mice, IL-33(KO)/Tg+ mice had complete absence of bronchoalveolar lavage

195 IL-33(HET)/Tg+ mice, although the IL-33(KO)/Tg+ mice had significantly reduced levels of MUC5AC prot

196 compared with IL-33(HET)/Tg+ mice, IL-33(KO)/Tg+ mice had significantly reduced levels of Th2-associa

197 As compared with IL-33(HET)/Tg+ mice, although the IL-33(KO)/Tg+ mice had significan

198 As compared with IL-33(HET)/Tg+ mice, IL-33(KO)/Tg+ mice had complete absence of bro

199 As compared with IL-33(HET)/Tg+ mice, IL-33(KO)/Tg+ mice had significantly reduced l

200 IL-33(KO)/Tg+ mice compared with IL-33(HET)/Tg+ mice.

201 Two distinct classes of TG molecules that interact with the LD monolayer are fou

202 t that 5-8% of the LD surface is occupied by TG molecules, a number that exceeds the maximal solubili

203 ung disease model (i.e., Scnn1b-Tg-positive [Tg+]) mouse, remain unclear.

204 ing and cooling processes, using TG/DTG/DTA, TG-MS, DSC, hot stage microscopy and DRX analysis.

205 dditional water column denitrification of 38 Tg N/y, and the loss of fixed nitrogen and carbon produc

206 in 2014 were estimated to be 12.32 and 3.79 Tg N/year, respectively.

207 text]O flux ranges from a low of 3.3 +/- 1.3 Tg N[Formula: see text] in the boreal spring to a high o

208 n the boreal spring to a high of 5.5 +/- 2.0 Tg N[Formula: see text] in the boreal summer.

209 ean [Formula: see text]O flux of 4.2 +/- 1.0 Tg N[Formula: see text], 64% of which occurs in the trop

210 ive transfer of CD8(+) T cells from Valpha14(Tg) NC mice into AD-susceptible wild-type NC mice suppre

211 d may be considered as cell-free therapy for TG nerve repair.

212 Percoll-gradient enriched DRG and TG neuronal fractions produced distinct sex-dependent DE

213 For example, Akt3 is detected in more TG neurons during BoHV-1 latency than in reactivation an

214 emia zinc finger), and KLF15, are induced in TG neurons early during dexamethasone-induced reactivati

215 T-ORF63, but not RNA 63, expression in human TG neurons.

216 h LDL-C, 48% for low HDL-C, and 21% for high TG; no strong trends.

217 TC, 120 for LDL-C, 47 for HDL-C, and 139 for TG; no strong trends.

218 e charcoal industry in 2014 required 140-460 Tg of biomass and 260 tonnes of plastic and that industr

219 About 250 Tg of dissolved organic carbon are annually transported

220 manure applications have resulted in ~ 33.4 Tg of legacy P accumulated in the agricultural soils fro

221 odeling, we estimate that 18-27 of the 23-31 Tg of methane released at the seafloor could have reache

222 nput of fertilisers and thus save up to 31.8 Tg of P fertiliser use (US$ 20.8 billion) in the coming

223 gnite fires large enough to emit more than 5 Tg of soot into the stratosphere.

224 kout), CaMKIIdeltaC transgenic in wild-type (TG), or KO background, and wild-type mice exposed to TAC

225 ride (TG) input in the liver is greater than TG output, resulting in the excess accumulation of TG.

226 system (RAS) upregulated in the kidney of KS-tg/OVE mice compared to WT/OVE mice, suggesting a distur

227 d erythropoietin levels in the kidneys of KS-tg/OVE mice.

228 erexpressing kallistatin with OVE26 mice (KS-tg/OVE).

229 As a first step, we used Tg(Pcp2-L10a-Egfp) TRAP mice to profile actively transcr

230 lower than in control dams but also that the TG peak occurred earlier during gestation.

231 inetic parameters to calculate the metric of TG/PG ratio revealed a quantifiable net shift toward a p

232 TG is stable and determines the width of the TG-PL overlap, whereas that caused by SURF-TG fluctuates

233 brosis-like lung disease model (i.e., Scnn1b-Tg-positive [Tg+]) mouse, remain unclear.

234 Hepatic TG production and intestinal TG absorption were unchange

235 D development in GSD 1a by balancing hepatic TG production and secretion.

236 Pten-deficient mouse (Pten(Delta/Delta) BRF1(Tg)) prostate cancer model accelerated prostate carcinog

237 ] for LDL-C and 1.24 [95% CI, 1.13-1.36] for TG PRS).

238 L-C PRS and 1.31 (95% CI, 1.19-1.43) for the TG PRS.

239 to 1.55 (95% CI, 1.48-1.61) mmol/L with the TG PRS.

240 vity in the AD clinical spectrum and amyloid Tg rat model.

241 cant with the exceptions of human PG, baboon TG, rat TG and Guinea pig PG.

242 Congruently, Tg rats recapitulated and validated the association betw

243 activity in the LV of transgenic mice (CatA-TG) reduced EC-SOD protein levels by 43%.

244 e mechanisms that lead to podocyte injury in TG remain unclear.

245 1.7 IU/mL and 6 IU/mL for anti-TPO and anti-TG, respectively.

246 independent of fasting TG, we calculated the TG response at 150 minutes by the residuals of a nonline

247 GWAS of the TG response identified a variant near LIPC as a main con

248 o elucidate the genetics of the postprandial TG response through genome-wide association studies (GWA

249 the assembly and secretion of triglyceride (TG)-rich, apoB-containing lipoproteins.

250 suggest stratospheric injection of 14 +/- 2 Tg S associated with the TBJ eruption, exceeding those o

251 ysis and very low density lipoprotein (VLDL)-TG secretion assays revealed that hepatic ChREBP knockdo

252 e of "old fat." Interestingly, enhanced VLDL-TG secretion in shSCR-treated L-G6pc(-/-) mice associate

253 hniques and paves the way for further use of TG-SERS and SPR in EV studies.

254 ed at growth temperature (R(d,tg) and V(cmax,tg) ) should increase by 3.7% and 5.5% per degree increa

255 Increased urine podocin/creatinine ratio in TG signifies accelerated podocyte loss.

256 Transection (ST), Simple Transection & Glue (TG), Stepwise Transection and Sutures (SU), and Stepwise

257 4.5% vs 66.7%, P = 0.54) and/or a stimulated Tg (sTg) <1 (59.3% vs 64.0%, P = 0.78).

258 the CNS by favorably producing triglyceride (TG) storage lipids rather than phospholipid (PL) membran

259 nutes or pretreatment with trypsin abolished TG, suggesting the presence of MV-associated proteins th

260 exacerbated brain microvascular pathology in Tg-SwDI mice as observed by increased blood-brain barrie

261 To induce systemic overburden of ADMA, Tg-SwDI mice were treated with a daily dose of exogenous

262 evated ADMA levels in the blood and brain of Tg-SwDI mice.

263 Abeta deposition and cognitive impairment in Tg-SwDI mice.

264 uman beta-amyloid precursor protein Swedish (Tg-SwDI), a model of cerebrovascular beta-amyloidosis.

265 directing neuronal lipid synthesis away from TG synthesis and toward PL synthesis may promote axon re

266 Decreasing TG synthesis by deleting neuronal diglyceride acyltransf

267 on of gene modules involved in triglyceride (TG) synthesis and adipogenesis decreased, and this was a

268 observed dysbiosis in fecal samples from Hol(Tg/Tg) mice compared with feces from wild-type mice; fec

269 ) mice, Ednrb(s-l//s-l) mice, and male TashT(Tg/Tg) mice, compared with control mice, but not Ret(9/-

270 icantly prolonged mean survival times of Hol(Tg/Tg) mice, Ednrb(s-l//s-l) mice, and male TashT(Tg/Tg)

271 netrated aganglionic colon epithelium of Hol(Tg/Tg) mice, inducing production of endogenous GDNF, and

272 with human apoprotein A1-transgenic (APOA1 (tg/tg)) mice, which have elevated cholesterol-effluxing

273 or trisomy 21-associated HSCR), TashT (TashT(Tg/Tg), a model for male-biased HSCR), Piebald-lethal (E

274 ith four mouse models of HSCR: Holstein (Hol(Tg/Tg), a model for trisomy 21-associated HSCR), TashT (

275 Plaques of APOA1 (tg/tg)/Apoe (-/-) mice fed F1394 showed a 60% reduction

276 rticles, and subjected Apoe (-/-) and APOA1 (tg/tg)/Apoe (-/-) mice to an atherogenic diet to develop

277 iptome signature in the trigeminal ganglion (TG) that includes Rictor, the rapamycin-insensitive comp

278 he long-term efficacy and safety of low-dose TG therapy in IBD patients failing AZA and MP.

279 functional TRL2 (TLR2(+/+), C57BL/6-Tyrc-Brd-Tg(Tlr2-luc/gfp)Kri/Gaj;TLR2(-/-),C57BL/6-Tlr2tm1Kir).

280 We transferred the reaction sites from TG to an engineered tyrosine donor-acceptor pair in the

281 Serum triglyceride (TG), total cholesterol (TC), high-density lipoprotein ch

282 n of the VLDL lipidation proteins microsomal TG transfer protein and transmembrane 6 superfamily memb

283 rate at 12 months was 65 and 54% remained on TG until the end of follow-up.

284 on is 13.8-17.7 Tg CH(4) year(-1): 11.2-14.4 Tg via diffusion and ebullition and 2.6-3.3 Tg from spri

285 Median TG was 1.19 (95% CI, 1.18-1.20) mmol/L, ranging from 0.9

286 Cardiac remodeling in CatA-TG was accompanied by an increased LV weight/body weight

287 er, the pregnancy-induced elevation of blood TG was almost abolished in Angptl4 (-/-) dams.

288 on of postprandial TG independent of fasting TG, we calculated the TG response at 150 minutes by the

289 1B3-mediated uptake for EtioG, AG, DHTG, and TG were 19.8, 29.3, 69.6, and 110.4 uM, respectively.

290 ression, and the beneficial effects of Fat-1(tg) were abolished in the absence of ChemR23.

291 tein cholesterol (HDL-C), and triglycerides (TG) were evaluated preconception and throughout pregnanc

292 ild type and 8 McGill-R-Thy1-APP transgenic (Tg)) were examined.

293 myosin heavy chain) promoter (alpha MHC JunD(tg)) were protected against hyperglycemia-induced cardia

294 In case of TG, when using the full datasets, an increased risk for

295 ) with ~6M variants separately for LDL-C and TG with weights from a UK Biobank-based genome-wide asso

296 ow adipocytes; in contrast, transgenic mice (Tg) with osteoblastic-specific deletion of Epor exhibit

297 olated luteal LDs were composed primarily of TG, with lesser amounts of cholesteryl esters, diglyceri

298 B(high) T cells from CD83(flox/flox)/CD4-cre(tg) (/wt) mice into Rag2-deficient mice elicited more se

299 Tregs from CD83(flox/flox)/CD4-cre(tg/wt) mice had similar suppressive activity as Tregs fr

300 aenorhabditis elegans Fat-1 transgene (Fat-1(tg)xApoe(-/-)), which enables the endogenous synthesis o

301 ains, resulting in methane emissions of 0.69 Tg/year (95% cr int: 0.25, 1.23).