ライフサイエンスコーパス: gamma

1 ome 15, encodes the DNA polymerase gamma(Pol gamma).

2 ms would be unstable if not for variation in gamma.

3 was reversed by therapeutic blockade of IFN-gamma.

4 recognition repeats termed alpha, beta, and gamma.

5 in lungs including TNF, IL-6, IL-10, and IFN-gamma.

6 ed with mice deficient in all sources of IFN-gamma.

7 t when the human host cell is exposed to IFN-gamma.

8 IRF8 that was further induced by interferon-gamma.

9 inhibit STAT1 phosphorylation induced by IFN-gamma.

10 eukin-4 and reduced production of interferon-gamma.

11 tralized interferon (IFN)-alpha, but not IFN-gamma.

12 At 6 hpi, Pol II increased on gamma(1) and gamma(2) genes while Pol II pausing remaine

13 At 6 hpi, Pol II increased on gamma(1) and gamma(2) genes while Pol II pausing remained prominent o

14 ith tissue remodeling, such as COL8A1, actin gamma-2 (ACTG2), and tetraspanin 12 (TSPAN12).

15 It was noted that these 1:1 alpha/Sulfono-gamma-AA peptides were completely resistant to proteolyt

16 The homogeneous right-handed d-sulfono-gamma-AApeptides represent a new generation of unnatural

17 odel application, the right-handed d-sulfono-gamma-AApeptides reveal much-enhanced binding affinity c

18 d peroxisome proliferator-activated receptor gamma activity and reduced proliferation.

19 the digestion of PNNs induces a decrease in gamma activity, an oscillation dependent on PV+ cells, i

20 signaling pathways to optimize antiviral IFN-gamma activity.

21 lve aberrant increases in cortical broadband gamma activity.

22 tional link between selective processing and gamma-activity.SIGNIFICANCE STATEMENT The ability to foc

23 Previous studies have implicated a role for gamma-adducin (ADD3), a cytoskeletal protein encoded by

24 (peroxisome proliferator-activated receptor gamma) agonist that stimulates mitochondrial activity, a

25 etailed anchoring mechanism of Ag species on gamma-Al(2)O(3) remains largely unknown.

26 granular supports such as carbon materials, gamma-Al(2)O(3), and zeolite, which is vital to their pr

27 non-random distribution of oxygen species in gamma-Al(2)O(3).

28 The gamma aminobutyric acid (GABA) neurotransmission system

29 Glutamate (GLU) and gamma-aminobutyric acid (GABA) are the major excitatory

30 that release the inhibitory neurotransmitter gamma-aminobutyric acid (GABA) at non-image-forming brai

31 -fat milk and regular-fat cheese enriched in gamma-aminobutyric acid (GABA) influences daytime ambula

32 xylase enzyme GAD67, a critical actor of the gamma-aminobutyric acid (GABA) metabolism as it catalyse

33 tion of the metabotropic GABA(B) receptor by gamma-aminobutyric acid (GABA) results in prolonged inhi

34 ors (HA) exhibited a significant increase in gamma-aminobutyric acid (GABA) transmission compared wit

35 o find the relative quantity of glutamate to gamma-aminobutyric acid (GABA), DA, and glutamate neuron

36 lase 2 but not the parvalbumin subset of SNr gamma-aminobutyric acid (GABA)-releasing (GABAergic) neu

37 ions due to significant, tonic inhibition by gamma-aminobutyric acid (GABA).

38 drugs that inhibit alpha5 subunit-containing gamma-aminobutyric acid type A receptor function improve

39 ed that inhibiting alpha5 subunit-containing gamma-aminobutyric acid type A receptors would improve c

40 Long-term neuronal adaptations of gamma-aminobutyric acidergic striatal projection neurons

41 t it penetrates the membrane deeply, whereas gamma-aminobutyric is excluded from the bilayer.

42 The values of the parameters gamma and beta of the model were validated in continuous

43 ic host cell reservoir via regulation of IFN-gamma and IL-10.

44 ory inflammatory cytokines, for example, IFN-gamma and IL-12, in CCR2i- versus vehicle-treated mice.

45 on of T cell-derived IL-10 increased the IFN-gamma and IL-17A response to HDM, reducing IL-13 levels

46 that this depends on PLP-CD8 elaborating IFN-gamma and perforin in a coordinated suppression program

47 associated with feedforward processing than gamma and pose limits on the proposed role of gamma as a

48 scence-based assay was developed against IFN-gamma and provided an optimized, physiologically relevan

49 n the spleens and livers of STm-infected IFN-gamma(-/-) and T-bet(-/-) mice.

50 n-induced microstructure bands of austenite (gamma) and martensite (alpha' ) phases on the partitioni

51 namics in the theta (around 4-8 Hz) and beta-gamma (around 15-40 Hz) ranges.

52 materials to produce a range of multifaceted gamma-aryl tertiary alkylamines and can be rendered enan

53 amma and pose limits on the proposed role of gamma as a feedforward mechanism.

54 associated with increases in spiking and in gamma-band (40 to 90 Hz) power/connectivity that fed for

55 understand the neural mechanisms underlying gamma-band ASSR network abnormalities in schizophrenia.

56 e) and 16 unexposed donors, using interferon-gamma-based assays with peptides spanning SARS-CoV-2 exc

57 The oxidized Pol gamma becomes editing-deficient, displaying a 20-fold el

58 ncludes parameters for Signal Amplification (gamma), Binding affinity (K(d)), Receptor activation Eff

59 IFN-gamma binds to its receptor on Leishmania-infected macro

60 of l-carnitine and, to a much lesser extent, gamma-butyrobetaine.

61 mic acid, hydroxymethylfurfural, lipids, and gamma-butyrolactone also contributed to score and sensor

62 enantioselective allylic alkylation using a gamma-butyrolactone-derived silyl ketene acetal.

63 meric receptor complex (IL-2Ralpha/IL-2Rbeta/gamma(c)).

64 ages, most genes belong to an avian-specific gamma-c clade, within which sequences cluster by species

65 elling experiments, which indicated that the gamma-C(sp(3) )-H bond cleavage is the rate-limiting ste

66 octadecanedioate and vitamin E metabolites (gamma-CEHC and gamma-CEHC glucuronide); MR analysis show

67 te and vitamin E metabolites (gamma-CEHC and gamma-CEHC glucuronide); MR analysis showed that genetic

68 the regions between CDR2 and CDR3 of the TCR gamma chain and modulated by the affinity of the CDR3 re

69 We generated immunodeficient Rat Rag-/- Gamma chain-/- human signal regulatory protein alpha-pos

70 roxidase, MBP, and fibrin alpha-, beta-, and gamma-chains.

71 those of other sauropsid species in a gamma (gamma) clade that predates the divergence of different a

72 ine influenza viruses isolated in 2009-2016, gamma-clade viruses had less stable HA proteins (activat

73 Peroxisome proliferator activated receptor gamma coactivator (PGC)-1alpha, has been proposed as a m

74 (peroxisome proliferator-activated receptor-gamma coactivator 1), a Parkin downstream target that ca

75 e peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1alpha) is a transcriptio

76 t peroxisome proliferator-activated receptor gamma coactivator 1-alpha and oxidative phosphorylation

77 isome proliferator-activated receptor (PPAR) gamma-coactivator 1alpha], PPARalpha, and catalase as ke

78 wakefulness was not restored, the functional gamma connectivity remained reduced, but there was a sig

79 % from blood samples counted on a calibrated gamma-counter.

80 We found that cortical theta-gamma coupling was reduced in both male and female juven

81 The methodology provides a short route to gamma-cyanoesters that can be useful synthetic intermedi

82 ter-soluble azobenzene and alpha-, beta-, or gamma-cyclodextrins, have been proposed as a model to st

83 ions of curcumin/HP-beta-CyD and curcumin/HP-gamma-CyD were yielded uniform fiber morphology with ~20

84 cells, respectively, restored IL-12 and IFN-gamma cytokine levels and BMM -T cell interaction.

85 n 6 of C8A as a predominant cause of C8alpha-gamma deficiency in African Americans.

86 Both delta-azaproline and gamma,delta-dehydro-delta-azaproline exhibit strong tran

87 Subsets of gamma-delta T cells (CD3(+)TCRgd(+)), CD8(+) T cells (CD

88 Most notable is a trans-acting gamma/delta' hydroxyl group that 99% of other AAA+ prote

89 of small-ranged species reduce biome-scale (gamma) diversity.

90 lating Il-18bp is induced in response to Ifn-gamma during CpG-induced macrophage activation syndrome

91 Neutralization of IFN-gamma during infection abrogated Ido1 expression and was

92 carriers that recruit GGA (Golgi-localized, gamma-ear-containing, ARF-binding protein), clathrin ada

93 CD8(+) T-cell clones was measured using IFN-gamma ELIspot.

94 y the presence of concomitant and dominating gamma emitters, primarily (137)Cs, which results in incr

95 ever, the detection of minute amounts of the gamma-emitting radiosilver isotopes is often thwarted by

96 idues in the cytosolic portions of beta- and gamma-ENaC subunits as being important for PIP(2)-ENaC i

97 rements for IFN-gamma production and how IFN-gamma enhances local immune responses to prevent Bp-medi

98 hose driven by sensory experience, to induce gamma entrainment.

99 rophage) M1-like polarization and interferon-gamma-expressing T-helper type 1 (Th1) cells but increas

100 ed leptin sensitivity via reduced interferon-gamma expression and induced adipose leptin expression v

101 There was also a protective effect of higher gamma' fibrinogen levels on cardioembolic and large arte

102 n of ischaemic stroke, while factor VIII and gamma' fibrinogen require further population-based studi

103 two ionic reactants, affords enantioenriched gamma-fluoroamines in high yields.

104 ipsilesional M1 to contralesional M1 within gamma frequencies during motor preparation for hand open

105 These interactions occurred in beta and gamma frequency bands depending on the area contributing

106 and 1440 mg) on NMDAR engagement measured by gamma-frequency band auditory steady-state response (40

107 is important for synchronization across the gamma-frequency range, the role of distinct interneurona

108 r with those of other sauropsid species in a gamma (gamma) clade that predates the divergence of diff

109 e P2 and P3 peptides derived from alpha- and gamma-gliadins.

110 naling pathway from HRI to ATF4 to BCL11A to gamma-globin and illustrate potential limits of murine m

111 actor 4 (ATF4) as a novel regulator of fetal gamma-globin gene expression in human cells by repressin

112 llele copy, P = 0.046-0.002), including five gamma-glutamyl amino acids, beta-citryl-glutamate, N-ace

113 lele in HUVECs, including impairments of the gamma-glutamyl cycle and methylglyoxal detoxification.

114 artyl-glutamate, and ophthalmate-a marker of gamma-glutamyl cycle malfunction.

115 ohort, adults with Pi*MZ had lower levels of gamma-glutamyl transferase in serum and lower LSMs than

116 ecular-weight thiol-containing tripeptide (l-gamma-glutamyl-l-cysteinyl-glycine) that can function as

117 common grade 3-4 adverse events were raised gamma-glutamyltransferase (13 [16%] of 80 patients; coho

118 With either kinase, gamma-H2AX spreads as far as ~50 kb on both sides of the

119 ing phosphorylation of histone-variant H2AX (gamma-H2AX) to mark radiation-induced foci (RIFs).

120 This approach yielded the first structure of gamma-herpesviral core NEC, namely the 1.56 angstrom str

121 stein-Barr virus (EBV) is a ubiquitous human gamma-herpesvirus that establishes life-long infection a

122 ted CAR-T cell activation through interferon gamma (IFN-gamma) production and CD107a membrane accumul

123 find that T cell infiltration and interferon-gamma (IFN-gamma) signaling signatures correspond most h

124 monstrate a role for the cytokine interferon-gamma (IFNgamma) and the enzyme transglutaminase 2 (TG2)

125 ng cell fitness after exposure to interferon-gamma (IFNgamma).

126 hich was enhanced by priming with interferon gamma (IFNgamma).

127 blast expansion and cytokine production (IFN-gamma, IL-2, and TNF), with the highest median magnitude

128 However, the percentage of IFN-gamma(+) ILCs in infected colons was 5- to 10-fold highe

129 te T-bet and coexpress IL-17, IL-22, and IFN-gamma in a STAT3- and retinoic acid-dependent manner.

130 learance, we found that increased plasma IFN-gamma in early clinical sepsis was associated with the l

131 37 cells, enhanced induced production of IFN-gamma in human PBMC culture, and increased survival of i

132 gher (p < 0.01) concentrations of interferon-gamma in plasma of low responders compared to high respo

133 NK cells are likely key sources of IFN-gamma in this model.

134 (13,14), and are controlled by IFN-I and IFN-gamma in vivo(15-17).

135 As expected, IFN-gamma induced genes involved in Ag presentation and anti

136 ein, as evidenced by an observed hd-anti-IFN-gamma-induced increase in the specific binding of IFN-ga

137 ported by the interaction between excitatory gamma inputs and local inhibition.

138 els of chemokines KC and monokine induced by gamma interferon.

139 pleckstrin homology (PH) domains 2 (ADAP2), gamma-interferon-inducible lysosome/endosome-localized t

140 zing) and CD4+ T-cell (expressing interferon-gamma, interleukin-2, and CD40 ligand) responses were ev

141 has been developed, wherein a beta amine and gamma iodide are incorporated onto an aliphatic alcohol

142 Gamma irradiation showed >98% active structures of melat

143 xposure to desiccation, heavy metals, UV and Gamma irradiation.

144 2 receptor activation prevents and mitigates gamma-irradiation-induced colonic mucosal barrier dysfun

145 Superior Gamma is achieved through a combination of extraordinari

146 ng in isolated human HDL either by synthetic gamma-ketoalkenal phospholipids or by oxPLs generated du

147 1960, and Feb 1, 2020, reporting the use of gamma knife radiosurgery as primary treatment for uveal

148 the efficacy, outcomes, and complications of gamma knife radiosurgery for uveal melanomas and metasta

149 Gamma knife radiosurgery is regarded as the gold-standar

150 RNA sequence analysis of pn-csERRalpha/gamma knockdown hearts at 5 weeks of age combined with c

151 at ERR (estrogen-related receptor) alpha and gamma, known transcriptional regulators of postnatal mit

152 e reaction provides enol- or enamine-derived gamma-lactams.

153 myrocin G (4) to the corresponding 5-hydroxy-gamma-lactone isomer myrocin C (1) are also detailed.

154 failure of the polymerisation of alpha/beta/gamma laminin trimers.

155 Interferon-gamma levels of endotoxin-stimulated PBMCs from children

156 Circulating plasma IFN-gamma levels were also assayed in 400 patients with CL a

157 with decreased articular IL-12/23p40 and IFN-gamma levels.

158 pt durations have DF-dependent means and are gamma-like distributed.

159 selected Mertensia species were analyzed for gamma-linolenic acid-rich oils and minor functional comp

160 en category is encoded via broadband and sub-gamma (<30 Hz) power variations, while the attended cate

161 ls, cysteine metabolism by the cystathionine gamma lyase (CSE), generates hydrogen sulfide-related su

162 lfide (H(2)S) by inhibition of cystathionine gamma-lyase (CSE) increases sFlt-1 and soluble endoglin

163 the canonical definition of temperature and Gamma(mag); and iii) possibility of performing adiabatic

164 Tax(+) and Tax(+)/interferon-gamma(-/-) malignancies of the ear, tail, and foot compr

165 RNA decay pathways, the PABPN1- and PAPalpha/gamma-mediated RNA decay (PPD) pathway and an ARS2-media

166 In IFN-gamma(-/-) mice, there is deficient granuloma formation

167 ated by the dynamic expression in remodeling gamma-neurons, we focus here on the role of actin elonga

168 DNA copies, and surges in granzyme B and IFN-gamma occurred within the early hours after reactivation

169 Here I vary the component response rates (gamma) of randomly generated complex systems.

170 rthermore, the combination of MTP-PE and IFN-gamma on AML blasts generated an inflammatory cytokine p

171 xes (RW) or a mixture of beta-sitosterol and gamma-oryzanol (PS).

172 Studies have shown that gamma oscillations (30-100 Hz) are relevant for neurocir

173 r GSK3beta inhibition reverses both abnormal gamma oscillations and behavioral deficits with high cor

174 not GSK3A knockdown, also reversed abnormal gamma oscillations and behavioral deficits.

175 rogression whereas the induction of cortical gamma oscillations can reduce amyloid load and improve c

176 With intact cortex, theta and gamma oscillations could be reliably elicited in V1 and

177 Gamma oscillations have been argued to support visual pe

178 eposition and increases the power of ex vivo gamma oscillations in conventionally housed mice.

179 nced the firing rate of cortical neurons and gamma oscillations, as well as improved cognition.

180 of ring conformation, while a novel residue, gamma-oxo-delta-azaproline, features rapid amide isomeri

181 Activation of PPAR-gamma partially restored mitochondrial membrane potentia

182 major phospholipase in mitochondria, iPLA(2)gamma (patatin-like phospholipase domain containing 8 (P

183 iated inflammatory process driven by the IFN-gamma pathway.

184 ithelium with 5-amino salicylic acid, a PPAR-gamma (peroxisome proliferator-activated receptor gamma)

185 n the receiving population's activity by its gamma phase and amplitude.

186 e preceded by enhanced STN spike-to-cortical gamma phase coupling, indicating a role in motor prepara

187 Because the gamma phase has a large Young's modulus (ca. 26 GPa), a

188 temporal and frontal brain regions supports gamma phase synchronization.

189 The OER-active gamma-phases are characterized by about 8% contraction o

190 ignaling also induced an anergic T-bet(-)IFN-gamma(-) phenotype in CD8(+) T cells and was equally sup

191 system (the TriPPPro approach), in which the gamma-phosphate is covalently modified by two different

192 T calculations show that a degeneracy at the Gamma point of the energy bands of the high-temperature

193 ar chromosome 15, encodes the DNA polymerase gamma(Pol gamma).

194 Fmr1-KO rats showed gamma power abnormalities and behavioral hyperactivity t

195 These results suggest that gamma power abnormalities are a translatable biomarker a

196 ical response, psychotomimetic symptoms, and gamma power changes in 34 individuals (ages 18-65) with

197 ons partially rescued the elevated broadband gamma power elicited by subanesthetic doses of ketamine.

198 minated V4 theta, it had little effect on V4 gamma power except for delaying its emergence by >100 ms

199 elease, synchronous spike firing, and evoked-gamma power increase with lowered baseline power.

200 re robustly diminished, whereas the baseline gamma power is enhanced in schizophrenia.

201 gamma power is increased with pyramidal cell disinhibiti

202 bited reduced basal alpha power and enhanced gamma power, and these rats showed enhanced locomotor ac

203 a peroxisome proliferator-activated receptor gamma (PPARgamma) antagonist.

204 ion of peroxisome protein activator receptor gamma (PPARgamma), a nuclear receptor involved in inflam

205 pes, induced HSV-specific polyfunctional IFN-gamma-producing CD107(ab+) CD4(+) T cells associated wit

206 eradication related to the activation of IFN-gamma-producing CD8 T cells.

207 It will be worth investigating whether IFN-gamma-producing ILCs also improve endometrial resistance

208 on by them, with mycobacterium-specific, IFN-gamma-producing, purely adaptive CD8(+) alphabeta T, and

209 rovide insight into the requirements for IFN-gamma production and how IFN-gamma enhances local immune

210 lls in Rag-deficient mice both prevented IFN-gamma production and rescued mutant colonization.

211 sequencing, we found that in GA lesions IFN-gamma production by CD4(+) T cells is upregulated and is

212 , and Vdelta2(+) gammadelta T cells) and IFN-gamma production by them, with mycobacterium-specific, I

213 (antigen-specific antibody responses and IFN-gamma production) and biodistribution (antigen and adjuv

214 cellular responses, as characterized by IFN-gamma production, upon re-stimulation with SARS-CoV-2 pe

215 NK cells were the main source of IFN-gamma production, which was enhanced by IL-15.

216 factors, but these cells showed impaired IFN-gamma production.

217 red mitochondrial membrane potential and IFN-gamma production.

218 ell activation through interferon gamma (IFN-gamma) production and CD107a membrane accumulation by fl

219 utilizes accessible carbamate esters bearing gamma-propargylic C-H bonds and furnishes versatile prod

220 alizing antibodies against TNF-alpha and IFN-gamma protected mice from mortality during SARS-CoV-2 in

221 oflexi, and classes Anaerolineae, Delta- and Gamma- Proteobacteria than the deeper sections, indicati

222 many bacterial species but not in beta- and gamma-proteobacteria.

223 Here, we show that loss of clustered gamma protocadherins (Pcdhg), but not of genes in the al

224 ient olefins for the generation of unnatural gamma-quaternary amino acids and other valuable syntheti

225 was also carried out using 0, 1, 5 and 10 Gy gamma radiation.

226 nt of resistance of E. dermatitidis to acute gamma-radiation exposure and the major mechanisms it use

227 eutron backscatter and the Compton-scattered gamma radiations, simultaneously.

228 category is most robustly encoded in the sub-gamma range.

229 then used to reconstruct the spectrum of the gamma-ray beam.

230 a-ray repeater (SGR) bursts were detected in gamma-ray energies.

231 During the third session, 29 soft-gamma-ray repeater (SGR) bursts were detected in gamma-r

232 testing identified the same T-cell receptor gamma rearrangement present in the gastric biopsies.

233 the loss of virus-infected cells through Fc gamma receptor (FcgammaR)-mediated effector functions, w

234 zation of its putative protein substrate IFN-gamma receptor 1 (IFNGR1) at the protein level in TNBC.

235 -2 had significantly more C1q binding and Fc gamma receptor activation, a surrogate for ADCC function

236 ng, TLR9-driven fatality is dependent on IFN-gamma receptor signaling.

237 of autoantibodies to fragment cystallizable gamma receptors (Fcgamma receptors).

238 monoclonal antibodies require binding to Fc gamma receptors (FcgammaRs) for full effect and increasi

239 By comparison, peripheral blood interferon gamma release assays in the same cohort achieved a PPV o

240 atently infected humans, as evidenced by IFN-gamma release upon peptide stimulation.

241 In turn, IFN-gamma released by Vdelta2(+) cells upregulates IL-12 sec

242 s to suppress an atypical and pathogenic IFN-gamma response to inhaled HDM.

243 In contrast, IFN-gamma response via TCR and plasma IgG specific for Bp we

244 Augmented IFN-gamma responses in the HDM allergic airway disease model

245 The provision of a source of IFN-gamma reverses this, coincident with subsequent granulom

246 s to act as excitatory pacemakers for the V1 gamma rhythm.

247 visual signals should be transferred through gamma-rhythmic bursts of information, resulting in a mod

248 f generating delta/theta (ie, 2 to 6 Hz) and gamma rhythms.

249 ts in 3D-printed anatomic replicas using the gamma scintigraphy technique.

250 Furthermore, knockout of IFITM3 reduces gamma-secretase activity and the formation of amyloid pl

251 M3 in neurons and astrocytes, which binds to gamma-secretase and upregulates its activity, thereby in

252 mature form and impairs the integrity of the gamma-secretase complex as well as its catalytic activit

253 ptors, their ligands (Jagged 1-2, DLL1,3,4), gamma-secretase complex proteins (Presenilin 1, Nicastri

254 Impaired gamma-secretase function is associated with the developm

255 ne tissues from mice given injections of the gamma-secretase inhibitor dibenzazepine, and mice with i

256 nyl]-S-phenylglucine t-butyl ester (DAPT), a gamma-secretase inhibitor, which inhibits Notch signalin

257 gamma-Secretase is a multi-subunit enzyme whose aberrant

258 These findings reveal a mechanism in which gamma-secretase is modulated by neuroinflammation via IF

259 e disclose three structurally differentiated gamma-secretase modulators (GSMs) based on an oxadiazine

260 ld type APH-1B or the APH-1B T27I variant on gamma-secretase processing of human APP, the murine Notc

261 esenilin 1 (PS1) is the catalytic subunit of gamma-secretase, an enzyme complex responsible for the m

262 MVA-NP+M1 activated a marked interferon gamma-secreting T-cell response to M1 peptides.

263 edian frequency of RSV-F-specific interferon gamma-secreting T-cells after a ChAd155-RSV high dose wa

264 SG3 autoantibodies stimulated DSG3-CAART IFN-gamma secretion and homotypic clustering, consistent wit

265 chronic Chagas' disease patients, using IFN-gamma secretion as a readout.

266 re dependent on IL-18 and IL-12, whereas IFN-gamma secretion was restricted by high concentrations of

267 ed products in up to 91 % yield, >98:2 alpha:gamma selectivity, >98:2 Z:E selectivity, and >99:1 enan

268 Blockade of IFN-gamma signaling in mice increases lesion size and parasi

269 unication between the IFN-alpha/beta and IFN-gamma signaling pathways to optimize antiviral IFN-gamma

270 on of the IL-2/STAT5, TNF/NF-kappaB, and IFN-gamma signaling pathways.

271 and ultimately requires tumor-intrinsic IFN-gamma signaling, via a mechanism that is distinct from o

272 cell infiltration and interferon-gamma (IFN-gamma) signaling signatures correspond most highly with

273 l as TNF-alpha, IL-6, or IL-17A, but not IFN-gamma, similarly induced sHLH in SIRPalpha(-/-) mice but

274 ntioselectivity and dictates the outstanding gamma site-selectivity.

275 results in increased detection limits in the gamma spectra.

276 rneuronal subtypes in slow (<60 Hz) and fast gamma states remains unclear.

277 Here, we show that both IFN-gamma stimulation and murine norovirus (MNV) infection i

278 d by our data showing mislocalization of the gamma subunit.

279 ta reveal the specific coupling between ENaC gamma-subunit and claudin-8 expression.

280 Conditional kidney tubule-specific ENaC gamma-subunit knockout mice displayed decreased claudin-

281 nduction in macrophages & STAT4-mediated IFN-gamma synthesis in T cells.

282 The iTBS-gamma tACS approach may be potentially useful in rehabil

283 (HSs) underwent iTBS during gamma-tACS (iTBS-gamma tACS) and during sham-tACS (iTBS-sham tACS) in two

284 healthy subjects (HSs) underwent iTBS during gamma-tACS (iTBS-gamma tACS) and during sham-tACS (iTBS-

285 a non-hydrolyzable ATP analog, adenosine 5'-(gamma-thio)-triphosphate (ATPgammaS) added intravenously

286 uced increase in the specific binding of IFN-gamma to its receptor in U937 cells, enhanced induced pr

287 ive of CEBPB, miR-520G overexpression or IFN-gamma treatment.

288 accumulation and asymmetric distribution of gamma-tubulin during mitosis.

289 Finally, we show that XMAP215 and gamma-tubulin promote alphabeta-tubulin assembly in an a

290 While the MT nucleator, gamma-tubulin ring complex (gamma-TuRC) has been identif

291 ly by correctly localising the MT nucleator, gamma-Tubulin Ring Complex (gamma-TuRC), within the cell

292 metric architecture, the gamma-TuRC arranges gamma-tubulins into a helical geometry poised to nucleat

293 Despite its asymmetric architecture, the gamma-TuRC arranges gamma-tubulins into a helical geomet

294 mma-TuRC) has been identified, precisely how gamma-TuRC nucleates a MT remains poorly understood.

295 associated protein complex, Augmin, recruits gamma-TuRC to pre-existing spindle MTs, amplifying their

296 he MT nucleator, gamma-tubulin ring complex (gamma-TuRC) has been identified, precisely how gamma-TuR

297 he MT nucleator, gamma-Tubulin Ring Complex (gamma-TuRC), within the cell.

298 Although IFN-gamma typically helps microbial clearance, we found that

299 r peroxisome proliferator-activated receptor gamma was associated with accumulation of lipid vacuoles

300 We report the first example of a statistical gamma work distribution applied to single molecule pulli