ライフサイエンスコーパス: gamma

1 uction of the cytokine interferon-gamma (IFN-gamma).

2 e/guanylate kinase, and human DNA polymerase gamma.

3 e peroxisome proliferator-activated receptor gamma.

4 and maintained their ability to produce IFN-gamma.

5 etry of the electronic bands surrounding the Gamma = (0, 0) and X = (pi/aFe, 0) points of FeSe and to

6 ies between affecteds and controls (C/TTCTG: gamma(2) value = 0.014; p = 0.904).

7 Consistent with the notion that gamma-2 is associated with surface AMPARs, CNQX, a parti

8 ut such currents were severely attenuated in gamma-2-lacking stargazer (stg/stg) mice.

9 theta 3-7 Hz, alpha 7-13 Hz, beta 13-30 Hz, gamma 30-90 Hz and high frequency 90-350 Hz) that were a

10 In the absence of T-bet, IFN-gamma aberrantly induced a type I IFN transcriptomic pro

11 ionship affects information encoding in high-gamma activity (HGA) in cortical areas where neurons are

12 opmental disorders are characterized by weak gamma activity despite showing normal blood flow.

13 owing question onset; at the same time, high-gamma activity was attenuated in the left orbitofrontal

14 In particular, gamma activity was modulated by the phase of the alpha o

15 strength, and its relationship to broadband gamma activity.

16 s activated in such a context are mainly IFN-gamma(+), adhere to CFB, and induce their transition int

17 PPAR-gamma agonists, like pioglitazone, appear antiproteinuri

18 ng (57)Fe(II) to (56)Fe-labeled goethite and gamma-Al2O3 and characterized the resulting solids using

19 ation of Fe(II)(aq) alone, both goethite and gamma-Al2O3 surfaces increased Fe(II) oxidation rates re

20 the heat capacity, including a high value of gamma, along with a deviation from a Curie-Weiss law obs

21 hierarchical copper- and zinc- buds dressing gamma-AlOOH mesostrands, which are oriented in randomly

22 CPP-115, a next-generation gamma-amino butyric acid (GABA)-aminotransferase (AT) in

23 vice is characterized in vitro by delivering gamma-amino butyric acid to a target solution, and demon

24 nia, the density of cartridges detectable by gamma-aminobutyric acid (GABA) membrane transporter 1 im

25 netic stimulation of mouse zona incerta (ZI) gamma-aminobutyric acid (GABA) neurons or their axonal p

26 d c-fos expression in VTA 5-HT2CR expressing gamma-aminobutyric acid (GABA) neurons, but not 5-HT2CR

27 se and nitrate stimulated PGC1alpha-mediated gamma-aminobutyric acid (GABA) secretion from muscle.

28 differentially methylated probes implicated gamma-aminobutyric acid (GABA), dopamine and serotonin n

29 cell types (cholinergic, glutamatergic, and gamma-aminobutyric acid (GABA)ergic neurons) across its

30 elective action on the omega1 subtype of the gamma-aminobutyric acid A receptor, zolpidem tartrate pr

31 cotransporter expression and impaired spinal gamma-aminobutyric acid type A receptor function, indica

32 tivated by l-glutamate (l-Glu), l-aspartate, gamma-aminobutyric acid, and acetylcholine, with l-Glu e

33 during real-time-corrected three-dimensional gamma-aminobutyric acid-edited magnetic resonance (MR) s

34 xcitatory circuits, an abnormal depolarizing gamma-aminobutyric acidergic (GABAergic) drive has been

35 bination to create conditional Oprm1 mice in gamma-aminobutyric acidergic forebrain neurons.

36 a selective enhancement of synaptogenesis in gamma-aminobutyric acidergic interneurons.

37 ting cell types include hypocretin and GABA (gamma-aminobutyric-acid)-releasing neurons of the latera

38 ike cells present in the liver expresses IFN-gamma and can confer protection against M. avium infecti

39 O2 with different morphologies (alpha, beta, gamma and delta) was investigated using flow tube reacto

40 specific IgE, cytokine levels, and IL-4, INF-gamma and Foxp3 gene promoter DNA methylation status, an

41 SCFAs inhibited IFN-gamma and IL-17A production in peripheral blood mononucl

42 ofile, as reflected by heightened interferon gamma and interleukin 17 (IL-17) production as well as b

43 rent study, we examined DNA polymerase (pol) gamma and pol beta as possible complementing enzymes in

44 DPSCs treated with IFN-gamma and supplemented with pyrrolidine dithiocarbamate

45 ting: (i) early correlated inhibition of IFN-gamma and TNF-alpha production, along IL-10 increase, (i

46 duced by T cells upon activation through IFN-gamma and TNF-alpha.

47 nds (theta, alpha, beta, low gamma, and high gamma) and the dynamics of these features over time.

48 ive frequency bands (theta, alpha, beta, low gamma, and high gamma) and the dynamics of these feature

49 ction of three key cytokines: TNF-alpha, IFN-gamma, and IL-2.

50 se in tumor necrosis factor-beta, interferon-gamma, and monocyte chemoattractant protein-1.

51 wer amyloid-beta in a preventive mode, i.e., gamma- and beta-secretase; the rationale behind these tw

52 on led to a decrease in the concentration of gamma- and delta-tocopherol, as well as in the IP.

53 -4, IL-10, IL-17A, and gamma interferon [IFN-gamma]) and rendered T cells refractory to mitogen for a

54 Rats receiving PPAR-gamma antagonists displayed proteinuria and increased po

55 , effects abrogated by neutralizing anti-IFN-gamma antibodies.

56 n mice with MAS, treatment with the anti-IFN-gamma antibody significantly decreased circulating level

57 IL-21 and IFN-gamma are coexpressed by Tfh cells during viral infectio

58 /-) mice, whereas Rag2(-/-) mice lacking IFN-gamma are more susceptible than either Rag2(-/-) or Rag2

59 We propose hepatic PTPR-gamma as a link between obesity-induced inflammation and

60 Thus, glutamine may enhance the IFN-gamma-associated immune response and reduce the rate of

61 On electrocorticography analysis, high-gamma augmentation involved the bilateral superior-tempo

62 -band influences directly modulate bottom-up gamma band influences via cross-frequency interaction.

63 Gamma band rhythms may synchronize distributed cell asse

64 c to the hippocampus, most pronounced in the gamma band, and not explained by spatial movement or anx

65 mates have demonstrated an important role of gamma-band activity (40-100 Hz) in the feedforward flow

66 h the flow of visual information mediated by gamma-band activity.

67 ion task preceded subsequent stimulus-driven gamma-band activity.

68 These data support the use of gamma-band ASSR as a translational end point in pro-cogn

69 attention covaried positively with occipital gamma-band EEG, consistent with activation of cortical r

70 maturation, restored a functional balance of gamma-band network oscillations, and allowed treated eFS

71 at piriform cortex is an important driver of gamma-band oscillations in the vStr and associated limbi

72 l, synchronous oscillations in the theta and gamma bands between the BLA and interconnected structure

73 We have also found that gamma-, beta-, homoallylic, and allylic fluorination are

74 IFN-gamma blocking antibody administered to Sphk2(-/-) mice

75 inhibitory efficacy of alpha/beta and alpha/gamma BSBHps, but not of alpha/delta analogues.

76 re-property relations is crucial to optimize gamma but requires state of the art measurement techniqu

77 clopropyl carbinols to form alpha-alkylidene-gamma-butyrolactones (ABLs) is reported.

78 bet and GATA3, and reduced production of IFN-gamma by CD8(+) T cells.

79 reaction period to 48-70 h led to successive gamma-C(sp(3))-H arylation/intramolecular amidation and

80 essive arylation/intramolecular amidation of gamma-C(sp(3))-H bonds.

81 This study addresses how IFN-gamma can suppress activation of diabetogenic CD8(+) T c

82 atment combining alpha-amylase, protease and gamma-carboxy peptidase allowing complete sample prepara

83 ed glutamates, CCP5 uniquely metabolizes the gamma-carboxyl linked, branch point glutamate.

84 adherin-based complexes, including beta- and gamma-catenin and actin, components of adherens junction

85 CD-IC-NF (2:1) than zein-THY-NF and zein-THY/gamma-CD-IC-NF (1:1).

86 re, much more THY was released from zein-THY/gamma-CD-IC-NF (2:1) than zein-THY-NF and zein-THY/gamma

87 entified distinct alpha, beta, delta, and PP/gamma cell-type signatures.

88 unological imbalance of Tregs and CD4(+) IFN-gamma(+) cells in the lacrimal gland.

89 betic severe combined immunodeficient common gamma chain-deficient stem cell factor (huNSG) mice exhi

90 in mice lacking both the Rag2 and the common gamma-chain (gammac) genes (Rag2(-/-)gammac(-/-)), indic

91 ptide, which is a product of both alpha- and gamma-cleavage events, could also induce TrkB phosphoryl

92 d peroxisome proliferator-activated receptor gamma coactivator (PGC)-1alpha as well as attenuated for

93 Peroxisome proliferator-activated gamma coactivator 1-alpha (PGC1alpha) regulates energy m

94 Peroxisome proliferator-activated receptor gamma coactivator 1alpha (PGC1alpha) controls BAT-mediat

95 e peroxisome proliferator-activated receptor gamma coactivator 1alpha.

96 f peroxisome proliferator-activated receptor gamma coactivator-1alpha expression.

97 tween somatic and visual effects, and higher gamma connectivity along the dorsal visual pathways when

98 ivers of C57BL/6 mice, gamma interferon (IFN-gamma) controls intracellular Leishmania donovani infect

99 turation of Th17 cells into inflammatory IFN-gamma-coproducing effector cells.

100 Disease-protective IFN-gamma could be derived from any lymphocyte source and su

101 ology of aggregates formed by the P23T human gammaD-crystallin mutant associated with congenital cata

102 control experiments on in vitro alphaB- and gammaD-crystallin, 2D IR spectroscopy can identify the h

103 the bronchoalveolar fluid, and IL-2 and IFN-gamma cytokines in restimulated splenocyte cultures.

104 beta- and gamma-cytoplasmic actin are nearly indistinguishable in

105 ethyl-2,4-nonanedione, gamma-nonalactone and gamma-decalactone, whereas herbaceous and green aromas w

106 asis and s.c. tumor growth, and this was IFN-gamma dependent.

107 sian model selection between exponential and gamma distributions for these time periods gives support

108 ice were injected with gamma interferon (IFN-gamma) DNA or colony-stimulating factor 1 (CSF-1) DNA pr

109 We investigated the role of gamma during fast stopping and recorded scalp electroenc

110 Mutants of gamma-ECS and PCS1 were hypersensitive to As and had hig

111 (HAC1), gamma-glutamyl-cysteine synthetase (gamma-ECS), phytochelatin synthase (PCS1) and phosphate

112 val [CI], 1.4,1.7], P value < .0001) and IFN-gamma ELISPOT (estimated GMFR = 2.0 [95% CI, 1.6,2.6], P

113 The half-life and confounding gamma emissions of (52g)Mn are prohibitive to clinical t

114 ace NHE3, NKCC2, NCC, alpha-ENaC and cleaved gamma-ENaC compared to NSD.

115 -gamma or with conditioned media-derived IFN-gamma exhibited low levels of Cathepsin K, TRAP, RANK, a

116 Importantly, IFN-gamma exposure during activation reduced the cytotoxicit

117 T cells were then analyzed for IL-13 and IFN-gamma expression.

118 premature induction of interferon-gamma (IFN-gamma) expression in T cells and to generate pathogenic

119 d theta bands, whereas this property in high-gamma fluctuations mirrors speech rate.

120 ifferent visual stimulation showed different gamma frequencies.

121 Gamma frequency activity can be recorded directly from t

122 reviously to regulate PCDH-alpha, -beta and -gamma gene expression.

123 ction with specific antibodies for gliadins, gamma-gliadins, LMW subunits and antigenic epitopes to g

124 trates its role in developmentally regulated gamma-globin gene expression and the ability to control

125 microbial, tryptophan, plant component, and gamma-glutamyl amino acid-related metabolites.

126 ryotes lack homologs of this enzyme (and the gamma-glutamyl cycle) but are predicted to have some way

127 ) and S-4-mercapto-4-methylpentan-2-one-N-(l-gamma-glutamyl)-l-cysteine (gammaGluCys-4MMP) but at too

128 ockout, including arsenate reductase (HAC1), gamma-glutamyl-cysteine synthetase (gamma-ECS), phytoche

129 cumulation of glutathione and its precursor, gamma-glutamylcysteine, and significant depletion of 1 o

130 ith long-acting pasireotide monotherapy were gamma-glutamyltransferase increased (four [10%] of 41 pa

131 primary cilia(+) LPCs, and increased active gamma-glutamyltranspeptidase enzyme secretion.

132 keratin 19, connexin 43, integrin beta4, and gamma-glutamyltranspeptidase), whereas the hepatocyte sp

133 Yeast lacking SGS1 accumulate R-loops and gamma-H2A at sites of Sgs1 binding, replication pausing

134 Expression of the DNA damage/repair marker, gamma-H2AX and DNA damage response marker, phosphorylate

135 The gamma-H2AX foci decay ratio correlated negatively with t

136 on, MCL-1-depleted cells exhibited decreased gamma-H2AX foci, decreased phosphorylation of ATR, and h

137 mers: alpha-HBCD (10%), beta-HBCD (10%), and gamma-HBCD (80%).

138 d amidoalkylation reaction involving various gamma-hydroxy lactams and C/O/S nucleophiles at room tem

139 to prevent premature induction of interferon-gamma (IFN-gamma) expression in T cells and to generate

140 at Ct growth inhibition occurs by interferon-gamma (IFN-gamma)-mediated depletion of intracellular tr

141 as low production of the cytokine interferon-gamma (IFN-gamma).

142 Here we show that human peripheral blood IFN-gamma(+)IL-17(+) (TH1/17) and IFN-gamma(-)IL-17(+) (TH17

143 blood IFN-gamma(+)IL-17(+) (TH1/17) and IFN-gamma(-)IL-17(+) (TH17) CD4(+) T cells display distinct

144 Flow cytometry was used to measure IFN-gamma, IL-13, IL-9, IL-17, and IL-22 cytokines in CD4(+)

145 s and output of cytokines, such as IL-4, IFN-gamma, IL-17, and IL-10.

146 ession of inflammatory genes (TNF-alpha, IFN-gamma, IL-1beta, IL-6, and CCL2 mRNAs), and attenuated t

147 his correlated with lower frequencies of IFN-gamma-, IL-5-, and IL-13-producing CD4(+) T cells, reduc

148 cells (cDC1) promoted ILC1 production of IFN-gamma in a STAT4-dependent manner to limit early viral b

149 rferon (IFN)-gamma or epithelial-derived IFN-gamma in constitutively released or Porphyromonas gingiv

150 dition, CD4 T cells produced less interferon-gamma in response to T-cell stimulation.

151 ctivation in oligodendrocytes aggravated IFN-gamma-induced remyelinating oligodendrocyte death and re

152 Mechanistic analyses reveal that IFN-gamma induces CD70 expression in T cells, and CD70 limit

153 otoxic T lymphocyte-associated genes and IFN-gamma-inducible chemokines, including CXCL10, in IDH-mut

154 d WT mice showed upregulation of several IFN-gamma-inducible genes.

155 family, such as absent in melanoma-2 and IFN-gamma-inducible protein (IFI)16, bind dsDNA and form cas

156 ivation associated with increased interferon-gamma-inducible protein 10, interleukin (IL)-6, IL-8, va

157 IFN-gamma-inducible protein 16 (IFI16) is an immunological D

158 In the livers of C57BL/6 mice, gamma interferon (IFN-gamma) controls intracellular Leis

159 s in vivo, wild-type mice were injected with gamma interferon (IFN-gamma) DNA or colony-stimulating f

160 evident, while decreased mitogen-stimulated gamma interferon (IFN-gamma) production suggested immuno

161 In this study, we report that gamma interferon (IFN-gamma) treatment, but not IFN-alph

162 terleukin 2 [IL-2], IL-4, IL-10, IL-17A, and gamma interferon [IFN-gamma]) and rendered T cells refra

163 eptides from rDEN2Delta30 and used them in a gamma interferon enzyme-linked immunosorbent spot assay

164 everal candidate miRNA-deletion mutants post gamma-irradiation and identified cel-mir-237 as a miRNA

165 g, hsa-miR-125b, functions as sensitizers to gamma-irradiation in both a nematode in vivo model and b

166 gamma-Irradiation led to a decrease in the concentration

167 ockout mouse prostate was also sensitized to gamma-irradiation.

168 expression levels of IL-32 alpha, beta, and gamma isoforms, IL1a, IL1b, IL6, IL8, TNFA, PTGS2, CXCR1

169 a single procedure using the 4C or Perfexion Gamma Knife.

170 C6 expression, as did podocyte-specific PPAR-gamma knockout mice, which were more sensitive to adriam

171 Furthermore, neonatal and interferon gamma knockout mouse models of C. parvum infection ident

172 yptophan levels and trended toward lower IFN-gamma levels compared to women with persisting infection

173 eveal the extent of the spin correlations in gamma-lithium iridate.

174 PTPR-gamma loss-of-function lowers glycemia and insulinemia b

175 pants by quantitative QFT result (interferon-gamma <0.35 IU/mL, 0.35-4.00 IU/mL, and >4.00 IU/mL) at

176 rexpressing Brevibacterium linens methionine-gamma-lyase (BlMGL) produced the sulfur volatile compoun

177 h Na2S or by overexpression of cystathionine gamma-lyase (CSE).

178 h inhibition occurs by interferon-gamma (IFN-gamma)-mediated depletion of intracellular tryptophan, a

179 rdinates F(-) through its partially positive gamma-methylene in mimicry of phenylalanine's quadrupola

180 calculations, we show that, for ringwoodite (gamma-Mg2SiO4), additionally, Si(4+) vacancies are forme

181 reached at 25% RH and 45% for delta-MnO2 and gamma-MnO2, respectively, possibly due to their differen

182 or innervation of intrafusal fibers by human gamma-MNs and demonstrated by morphological and immunocy

183 Using gamma-MSH as a template, we developed a peptide, [Leu(3)

184 eveloped a peptide, [Leu(3), Leu(7), Phe(8)]-gamma-MSH-NH2 (compound 5), which is 16-fold selective f

185 Here we report that gamma networks desynchronize and theta networks synchron

186 alyzed reactions enables one-pot assembly of gamma-nitroketones from three simpler building blocks.

187 were identified as 3-methyl-2,4-nonanedione, gamma-nonalactone and gamma-decalactone, whereas herbace

188 The surface tension (gamma) of xylem sap plays a key role in stabilizing air-

189 ts, our study revealed that higher levels of gamma-OHPdG are strongly associated with low survival (P

190 eaphenon E treatment significantly decreased gamma-OHPdG levels in the liver DNA of xeroderma pigment

191 Effect of recombinant human interferon (IFN)-gamma or epithelial-derived IFN-gamma in constitutively

192 IFN-gamma or lipopolysaccharide (LPS) polarizes macrophages

193 es treated either with recombinant human IFN-gamma or with conditioned media-derived IFN-gamma exhibi

194 SSC provides an increase in the gamma-oryzanol recovery followed by improving of the fun

195 e investigated the sources of the narrowband gamma oscillation, the factors modulating its strength,

196 Gamma oscillations are associated with enhanced attentio

197 Gamma oscillations arise in the subthalamic-globus palli

198 chanism accounts for the graded emergence of gamma oscillations at the stimulation site while retaini

199 type of image that elicits larger narrowband gamma oscillations in healthy visual cortex is also more

200 on site while retaining propagating waves of gamma oscillations in the non-stimulated tissue.

201 ocal circuitry is not a major contributor to gamma oscillations in the vStr LFP and that piriform cor

202 ence gaps, LRTC in the delta, theta, and low-gamma oscillations resumed the low levels observed for i

203 Cortical cognitive processing involves gamma oscillations, which support memory, attention, cog

204 critical to allow for development of robust gamma oscillations.

205 is engagement of the circuitry that produces gamma oscillations.

206 radiolabels into product from both alpha and gamma phosphates of donor molecules.

207 causality correlate with heightened frontal gamma power, they also correlated with increased severit

208 d peroxisome proliferator-activated receptor gamma (PPARgamma) in the early phase of differentiation.

209 Peroxisome proliferator-activated receptor gamma (PPARgamma), PPARgamma coactivator 1beta (PGC1beta

210 y peroxisome proliferator activated receptor-gamma (PPARgamma).

211 IFN-gamma-primed MCs guide activation of T cells by Staphylo

212 o transition of pathogenic Th17 cells to IFN-gamma producers.

213 r adults, can further differentiate into IFN-gamma-producing CD4(+) T cells.

214 ng a potential protective role for these IFN-gamma-producing cells.

215 was confirmed by in vitro measurement of IFN-gamma production by activated T cells.

216 Identification of excessive IFN-gamma production by blood and lymph node-derived T cells

217 When activated in vitro, however, IFN-gamma production by naive wild type and tristetraprolin-

218 18 and are unable to optimally stimulate IFN-gamma production by NK cells.

219 IFN-gamma production by these lymphocytes likely plays a key

220 PC-NK killing, proliferation, and interferon gamma production capacity, whereas AZA diminished their

221 The mTORC1 and IFN-gamma production defects were partially rescued by suppl

222 AT4, nuclear translocation, and impaired IFN-gamma production.

223 by activating NK cells and facilitating IFN-gamma production.

224 sed mitogen-stimulated gamma interferon (IFN-gamma) production suggested immunomodulation, which was

225 Rok, an analog of H-NS from gamma-proteobacteria that affects chromosome architectur

226 The growth of acid-tolerant gamma-proteobacterial AOB should be prevented, by keepin

227 e hydrogen concentrations observed by Dawn's Gamma Ray and Neutron Detector to assess potential volat

228 ed rebrightening in the afterglow of a short gamma-ray burst at redshift z = 0.356, although findings

229 f and intense flashes of gamma-rays known as gamma-ray bursts (GRBs), followed by longer-lived afterg

230 opose an all-optical scheme for ultra-bright gamma-ray emission and dense positron production with la

231 he extremely energetic and long-lived prompt gamma-ray emission from GRB 160625B.

232 e demonstrated by reconstructing neutron and gamma-ray images.

233 s power prompt, brief and intense flashes of gamma-rays known as gamma-ray bursts (GRBs), followed by

234 to IL-2 and shares with it the IL-2 beta and gamma receptor (R) subunits.

235 ed enhancement of IFN production required Fc gamma receptor engagement, bypassed fusion, and initiate

236 at broadly reactive antibodies require Fc-Fc gamma receptor interactions for optimal protection; howe

237 or functions, through engagement of their Fc-gamma receptors.

238 unstimulated organoid cultures, elevated IFN-gamma reduced the mRNAs encoding for RANKL, TRAP, and Ca

239 ways are both involved in the process of IFN-gamma-regulated odonto/osteogenic differentiation of DPS

240 ating CAVD microenvironment, resulted in IFN-gamma release.

241 IFN-gamma repressed genes by suppressing the function of enh

242 Distributions of IFN-gamma response levels were analyzed in healthy adolescen

243 rom Salmonella infection by priming host IFN-gamma responses.

244 Primary visual cortex exhibits two types of gamma rhythm: broadband activity in the 30-90 Hz range a

245 ndependently predicts that context-dependent gamma rhythms depend critically on SOM interneurons.

246 o address the frequency of susceptibility to gamma-secretase cleavage among human RTKs.

247 degradation of the mutant APP, and inhibited gamma-secretase cleavage of the mutant C99 to generate A

248 Because this residue is just before the gamma-secretase cleavage site, we then investigated whet

249 weak hydrogen bonds are at or near preferred gamma-secretase cleavage sites, suggesting that the sequ

250 Recent determination of intact human gamma-secretase cryo-electron microscopy structure has o

251 lease of soluble BCMA (sBCMA); inhibition of gamma-secretase enhanced surface expression of BCMA and

252 armacologic blockage of Notch activation via gamma-secretase inhibition.

253 F [99-residue CTF (C99)]- and Notch-specific gamma-secretase interaction assays identified a unique E

254 gamma-Secretase is an intramembranous protein complex co

255 In contrast, E-Abetan stabilizers increase gamma-secretase processivity.

256 response, it augmented the frequency of IFN-gamma secreting total T cells, T-helper and CTLs against

257 to control the viral infection involving IFN-gamma secretion.

258 t IFN-gamma stimulation, suggesting that IFN-gamma sensitizes these leukemias to T cell killing by me

259 Microbiota-induced PPAR-gamma signaling also limits the luminal bioavailability

260 physiological role of these proteins in IFN-gamma signaling has not been clarified.

261 s, because topical therapies that target IFN-gamma signaling in keratinocytes could be safe and effec

262 index), with secondary outcomes of beta and gamma Simpson's and Shannon's diversities.

263 This need to control gamma-static fusimotor drive explicitly as a function of

264 ning phagosomes and identified an interferon-gamma-stimulated and Rab20-dependent membrane traffickin

265 and BC-CML stem cells were MHCI+ without IFN-gamma stimulation, suggesting that IFN-gamma sensitizes

266 This method opens a rapid access to gamma-substituted propyl-1,1-diesters, ketoesters, cyano

267 Furthermore, gamma subunit palmitoylation had a dominant role over be

268 ENaC activation by DHHCs was lost when gamma subunit palmitoylation sites were mutated, whereas

269 ouse models containing either isoform of the gamma-subunit in the heart.

270 ential for ATP synthesis, and cannot convert gamma-subunit rotation into the conformational changes i

271 lower transcript expression of CYSTATHIONINE gamma-SYNTHASE (AtCGS), Met's main regulatory enzyme.

272 ivated CD4(+) Foxp3(-) (forkhead box P3) IFN-gamma(+) T cells in the heart-draining lymph nodes.

273 One of the crucial IFN-gamma target genes required for control of M. tuberculos

274 ymyl-compounds, mainly carvacrol, thymol and gamma-terpinene.

275 We discovered a significant IL-17A(+)IFN-gamma(+) (Th17/1) population and determined that these c

276 eased production of protective cytokines IFN-gamma, TNF-alpha, and IL-12, as well as recruitment of N

277 ammatory cytokines and chemokines (IL-6, IFN-gamma, TNF-alpha, CXCL1, and CCL2) and extensive splenic

278 ession of the pro-inflammatory cytokines IFN-gamma, TNF-alpha, IL-1beta and RANTES and activation of

279 ucted by measuring granulysin and interferon-gamma to confirm the causalities.

280 mma-tocopherol methyl transferase converting gamma-tocopherol into alpha-tocopherol) associated with

281 gamma-Tocopherol is effective scavengers of reactive nit

282 70.1, an orthologue of VTE4 (which encodes a gamma-tocopherol methyl transferase converting gamma-toc

283 ds and monounsaturated fatty acids and serum gamma-tocopherol were weakly associated with intake (R(2

284 ed Flow-FISH for single-tube analysis of IFN-gamma transcript and protein profile to simultaneously s

285 IFN-gamma treatment to GCSCs induced ZEB1 expression, attenu

286 study, we report that gamma interferon (IFN-gamma) treatment, but not IFN-alpha, -beta, or -lambda t

287 chondrial surface, recruits the MT nucleator gamma-tubulin ring complex (gamma-TuRC), and is sufficie

288 the purported functional differences between gamma-tubulins is unknown.

289 sequence" present in all alpha-, beta-, and gamma-tubulins.

290 y originate in the C-terminal regions of the gamma-tubulins.

291 b mRNA levels and decreased interferon (IFN)-gamma, tumor necrosis factor (TNF)-alpha and IL-1beta pr

292 the MT nucleator gamma-tubulin ring complex (gamma-TuRC), and is sufficient to convert mitochondria t

293 ic sulfamidate imines with a variety of beta,gamma-unsaturated alpha-ketocarbonyls in neat conditions

294 olv cosolvent systems (acetone, ethanol, and gamma-valerolactone) exhibit phase separation at cellulo

295 ms in the order of THF > acetone > ethanol > gamma-valerolactone.

296 , and compared with children with interferon-gamma values between 0.35-4.00 IU/mL (IRR 11.4 [95% CI 2

297 duals who had a change in QuantiFERON-TB IFN-gamma values from less than 0.2 to greater than 0.7 IU/m

298 However, QFT conversion at interferon-gamma values higher than 4.00 IU/mL was associated with

299 (TEM) cells that secrete IL-17A, but not IFN-gamma, was responsible for early IL-17A production.

300 All of the SLNs defined by the ex vivo gamma-well assay of (99m)Tc activity were detected by fl