ライフサイエンスコーパス: infiltration

1 on, mesoappendiceal invasion, lymphovascular infiltration).

2 otein repression along with decreased T-cell infiltration.

3 use alveolar damage with perivascular T-cell infiltration.

4 ells, which resulted in decreased macrophage infiltration.

5 ited autoimmune phenotypes, including T cell infiltration.

6 e correlated with intratumoral CD8(+) T-cell infiltration.

7 tural sediment and compared to fine sediment infiltration.

8 ld serve as a viable basis for combating GBM infiltration.

9 with patient survival and tumor immune cell infiltration.

10 ocytes with moderate perivascular lymphocyte infiltration.

11 f tumor-residing cDC1s overcomes poor T-cell infiltration.

12 mouse cancer model boosted cytotoxic T cell infiltration.

13 cells, inducing immune and inflammatory cell infiltration.

14 aining microthrombi with neutrophil-platelet infiltration.

15 lly dependent on local EpAT accumulation and infiltration.

16 d intestinal damage and increased neutrophil infiltration.

17 sis, reactive oxygen species, and neutrophil infiltration.

18 patially selective delignification and epoxy infiltration.

19 mage, LPS-induced weight loss, and leukocyte infiltration.

20 enefit and positively correlated with T cell infiltration.

21 mmatory cytokine expression and myeloid cell infiltration.

22 patterns is an effective way to inhibit the infiltration.

23 disease mediated by pulmonary CD8(+) T cell infiltration.

24 rties, and dysfunctional intratumoral immune infiltration.

25 hrough of B cells and their aggressive graft infiltration.

26 ing step to improve intratumoral immune cell infiltration.

27 lowed with much delay by reduction in T cell infiltration.

28 a subgroup characterized by distinct stromal infiltration.

29 cating ubiquitous variability in immune cell infiltration.

30 40%) and commence runoff (-33%), and reduced infiltration (-34%) and sediment production (-68%).

31 a (40%), and the right atrium pseudo-tumoral infiltration (36%).

32 100% showed regional fatty infiltration, 98% included foreign body, 45% had mural t

33 nd 1 (CXCL1), a key chemokine for neutrophil infiltration (a hallmark of NASH), is highly elevated in

34 ugh it did not alter the level of macrophage infiltration after axotomy.

35 tochemistry confirmed enhanced CD8(+) T cell infiltration and accumulation by R848-TSLs.

36 recruited in vivo) induces local immune-cell infiltration and activated dendritic cells, evoking a po

37 rrelation between Arf1 expression and T-cell infiltration and activation along with patient survival

38 Poor intratumoral T cell infiltration and activation are major barriers that prev

39 sensor pathway, which results in macrophage infiltration and activation during Kras-driven PDAC in m

40 ciated with better immune control: increased infiltration and activation of cytotoxic T lymphocytes (

41 PD-1/PD-L1 T cell checkpoint induces T cell infiltration and anticancer responses in murine and huma

42 Most breast cancers exhibit low immune infiltration and are unresponsive to immunotherapy.

43 tem is activated with subsequent immune cell infiltration and cytokine production.

44 atory responses in the lungs with neutrophil infiltration and edema, further confirmed as consolidati

45 We studied i) mortality, ii) macrophage infiltration and expression of markers of alternative ac

46 oning in HFD tumors, impairing CD8(+) T cell infiltration and function.

47 In the DTH model, assessment of T cell infiltration and gene expression profile at the DTH biop

48 ts hallmark manifestations are attributed to infiltration and inflammation by macrophages.

49 We find that T cell infiltration and interferon-gamma (IFN-gamma) signaling

50 erize the microstructural effects of amyloid infiltration and is a contrast-free method to identify t

51 ry response is associated with higher immune infiltration and leads to enrichment of pre-existing ICB

52 ic, and, in the VP, there was massive immune infiltration and massive desquamation of the luminal epi

53 ificantly reduced lymphocytic and neutrophil infiltration and mast cells degranulation (p < 0.05).

54 ing NACT, increased natural killer (NK) cell infiltration and oligoclonal expansion of T cells were d

55 gnaling independently orchestrates leukocyte infiltration and organ fibrosis.

56 or Notch3 deficiency protects from leukocyte infiltration and organ fibrosis.

57 lation and increased Treg frequency in islet infiltration and pancreatic lymph nodes.

58 and as a negative regulator of T-cell tumor infiltration and patient survival in diverse human cance

59 lar subtype and share a high level of immune infiltration and PD-L1 expression, similar to basal tumo

60 B HR(+)HER2(-) BC, including limited immune infiltration and poor sensitivity to ICBs.

61 ivKO mice showed increased inflammatory cell infiltration and proinflammatory gene expression in the

62 tic combination partners that augment T-cell infiltration and proliferation in so-called immune cold

63 e of NTS in C57BL/6 mice by decreasing renal infiltration and proliferation of T cells, which resulte

64 emic EP2 antagonism prevented monocyte brain infiltration and provided broader rescue of SE-induced e

65 helial barrier permeability, lower leukocyte infiltration and reduced activation of the endothelial b

66 iR-149 expression correlated with macrophage infiltration and reduced patient survival.

67 artificial microenvironments to promote cell infiltration and reprogramming are discussed.

68 To understand factors driving the infiltration and retention of ganglionic CD8s, we examin

69 tional role for csMHCII in regulating T cell infiltration and sensitivity to anti-PD-1.

70 nforced expression of CIITA increased T cell infiltration and sensitized tumors to anti-PD-1 therapy.

71 Gal-3 markedly attenuated F4/80+ macrophage infiltration and significantly increased the expression

72 we find that Cxcr4 promotes initial monocyte infiltration and subsequent territorial restriction of m

73 d by significant weight loss and immune cell infiltration and the expression of early inflammatory ma

74 lls displayed reduced cerebral CD4(+) T-cell infiltration and thrombotic activity following experimen

75 Human NASH features hepatic neutrophil infiltration and up-regulation of major neutrophil-recru

76 ix metalloproteinases and reduction in MDSCs infiltration, and all these contributed to inhibit pulmo

77 a, tubular injury, neutrophil and macrophage infiltration, and complement activation (plasma C5a) and

78 xazolone with increased ear swelling, T-cell infiltration, and expression of Ifng.

79 polarization to M2 phenotype, prevented Th1 infiltration, and increased Th2 and Treg levels.

80 ifested by increased weight loss, macrophage infiltration, and inflammatory cytokines in the colon ti

81 ial chemotactic ability is a major player in infiltration, and plant stomatal defense in closing the

82 of sterile kidney injury, reduced neutrophil infiltration, and serum creatinine levels were apparent.

83 id biosynthesis, neutrophils and macrophages infiltration, and STAT3 and MAPK signaling in the liver.

84 asured via CT, alveolar wall thickness, cell infiltration, and surfactant protein A concentration in

85 nced vascular permeability, increased T cell infiltration, and tumor growth suppression.

86 is characterized by inflammation, leukocyte infiltration, and vascular remodeling.

87 largely intact genome integrity, high immune infiltration, and younger patient age.

88 ng disrupted tissue structures, inflammatory infiltrations, and oral microbiome, whereby several mast

89 ommon types (n = 16 each), followed by local infiltration around the lids and facial nerve (n = 6), t

90 s correlated with increased Foxp3(+) T cells infiltration as well as CXCR-2 expression.

91 e collagen content and attenuated muscle fat infiltration as well as pathogenetic molecular pathways

92 croenvironment to promote robust immune cell infiltration at the expense of lung function.

93 ovel MRI-based techniques to assess cellular infiltration beyond the macroscopic tumor margins and to

94 ranasal delivery of CXCL10 siRNA blocked Th1 infiltration but did not fully rescue microglial activat

95 is debate: rocks that experience significant infiltration by a water-bearing fluid may release orders

96 ontacts and is required to restrict neuropil infiltration by astrocytic processes.

97 nor T cells, corresponding with robust tumor infiltration by donor effector over regulatory cells for

98 cells to directly react to pathogenic T cell infiltration by engulfing living T cells.

99 Diffuse brain infiltration by glioma cells causes detrimental disease

100 ow-grade inflammation and progressive tissue infiltration by immune cells and increased expression of

101 anes with pore sizes <0.8 um prevented their infiltration by immune cells.

102 changes in intestinal microbiota, diminished infiltration by myeloid cells, and an accumulation of in

103 in barrier permeability, and increased brain infiltration by myeloid cells.

104 lex coacervate treatment displayed increased infiltration by natural killer (NK) cells and CD8alpha(+

105 n of resident mononuclear phagocytes, tissue infiltration by non-resident inflammatory cells, and the

106 reted CXCL10, in turn, stimulated the T-cell infiltration by serving as the ligand and chemoattractan

107 ehavioral parameters without affecting tumor infiltration by T cells or neutrophils.

108 ha-smooth muscle actin, and mononuclear cell infiltration (CD11b(+) Ly-6c(hi) monocytes and CD11b(+)

109 2, RANTES, and TNF-alpha), inflammatory cell infiltration (CD3 + T cells, macrophages, and neutrophil

110 ISO-mediated increases in inflammatory cell infiltration, collagen deposition and fibrosis.

111 results suggest that increased myeloid cell infiltration contributes to autoreactive CD4 T cell-medi

112 At ratios of d(MP)/d(GS) > 0.32, hardly any infiltration could be observed.

113 Visible absorption spectra across a range of infiltration cycles.

114 Infiltration declined most (-56%) at fine scales, and mo

115 -8040 increased CD8(+) effector T cell tumor infiltration, decreased myeloid-derived suppressor cells

116 The infiltration depth of the microplastic particles increas

117 ging methods for the detection of myocardial infiltration, device infection, and cardiovascular infla

118 ntified the extent of inflammatory leukocyte infiltration early in pressure overload.

119 analyzed histologically to characterize EpAT infiltration, fibrosis, and gap junction localization.

120 usion captured the spatiotemporal dynamic of infiltration for each molecule into the brain parenchyma

121 Evidence of P. gingivalis infiltration has been detected in autopsy specimens from

122 nds showed significantly greater lymphocytic infiltration, higher levels of MHC II, IFN-gamma, IL-1be

123 ll types to estimate relative proportions of infiltration in a panCNS tumor cohort spanning 80 subtyp

124 d enhanced tumor formation and hepatosplenic infiltration in a tail-vein-injected mouse model.

125 ficantly inhibited macrophage and neutrophil infiltration in both models.

126 in particulate form and improved immune cell infiltration in draining lymph nodes.

127 The investigation of myeloid cell infiltration in HCC, NET and intrahepatic CCA tumors fur

128 with FOLR1-TCB induced strong CD8(+) T-cell infiltration in HeLa tumors, where (89)Zr-Df-IAB22M2C ag

129 re were higher lymphocytes and M1 macrophage infiltration in high mutation BCs.

130 TH-MYCN tumors were found to resemble immune infiltration in human tumors more closely than the subcu

131 ment (defined as the composite of neutrophil infiltration in less than 5% of crypts and no crypt dest

132 eficiency causes pro-inflammatory macrophage infiltration in metabolic tissues and is linked to renin

133 the intraocular inflammation and reduced PMN infiltration in mouse eyes, but, increased the bacterial

134 h decreased IFNgamma response and lymphocyte infiltration in patient tumors.

135 (BBB) disruption and peripheral immune cell infiltration in the cerebellum following blast exposure.

136 bacterial penetration and denser neutrophil infiltration in the dermis.

137 ibrin depositions, macrophage and neutrophil infiltration in the placenta did not differ between heal

138 evel, abundance of IgG4 enhanced plasma cell infiltration in the portal region of the liver, and sati

139 ace hepatitis with IgG4 positive plasma cell infiltration in the portal region, without evidence of b

140 By introducing Ni by successive infiltration in the solid template, the CeO(2) crystal s

141 SA-IL-4 fusion protein prevents immune-cell infiltration in the spinal cord, decreases integrin expr

142 imals, with two also displaying eosinophilic infiltration in the stomach.

143 be associated with type and degree of immune infiltration in the tumor microenvironment.

144 or combined with anti-PD-1 augmented T cell infiltration in tumor-draining lymph nodes.

145 redirecting TAM activation and T cell tumor infiltration in vivo.

146 enotype in mice by inducing immune cell lung infiltration, including eosinophils, increasing cytokine

147 er levels of Th1 cytokines, decreased T cell infiltration, increased B cell numbers, and decreased ma

148 etroperitoneal lymph nodes, and immune cells infiltration, indicating that blocking VEGF-C signaling

149 mas were accompanied by increased macrophage infiltration, inflammatory activation and oxidative stre

150 w)Ly6g(high) cells, but only minor leukocyte infiltration into acutely ischemic-reperfused cortex and

151 evere toxicities, restricted trafficking to, infiltration into and activation within tumours, subopti

152 he factors that can play a role in bacterial infiltration into leafy greens by keeping stomata open a

153 avascular albumin leakage or major leukocyte infiltration into the brain.

154 fatal cerebral edema associated with T cell infiltration into the brain.

155 n mice, TFH cells accordingly promote B cell infiltration into the CNS and the severity of MS animal

156 Leukocyte infiltration into the CNS was inhibited in cortactin-def

157 leakage, microglial activation, and antibody infiltration into the CNS, and have their olfactory func

158 eased leukocytosis in the CSF and blood, but infiltration into the cortex remained low over time.

159 mice fed a high-fat diet exhibit macrophage infiltration into the hypothalamus, whereas females were

160 duced more C. jejuni invasion and neutrophil infiltration into the Il10(-/-) mouse colon tissue compa

161 T-cell infiltration into the ileum was increased; epithelial pr

162 lower F4/80- and CX3CR1-positive macrophage infiltration into the liver in parallel with lower Ly6C(

163 Immune cell infiltration into the lung in the rat OVA model of asthm

164 myopathy, characterized by inflammatory cell infiltration into the myocardium and a high risk of dete

165 rovascular leakage, fibrosis and immune cell infiltration into the myocardium.

166 ll activation and markedly reduced mast cell infiltration into the small intestine.

167 th chronic EAE, SA-IL-4 inhibits immune-cell infiltration into the spinal cord and completely abrogat

168 egulatory polarization of myeloid cells upon infiltration into tumors remain largely unexplored.

169 ithin previous continuum models of microbead infiltration into tumour spheroids as they rely on resol

170 Neutrophil infiltration is a hallmark of nonalcoholic steatohepatit

171 Therefore, if fatty infiltration is seen in isolation radiologist should loo

172 Fatty infiltration is the feature more common.

173 n early hypoxia response and high lymphocyte infiltration levels exhibiting significantly improved LR

174 k mapped the distribution of neck muscle fat infiltration (MFI) in the deep cervical extensor muscles

175 in myeloid cells is essential for leukocyte infiltration, neuroinflammation, and demyelination in ex

176 properties such as soil water content, water infiltration, nutrient status, and pH.

177 vo approaches showed that increased cerebral infiltration of ACE10 as compared to wild-type monocytes

178 Infiltration of activated PECs may disrupt ECM remodelin

179 e of protumoral M2 macrophages and increased infiltration of antitumor CD8+ effector and memory T-cel

180 We found a marked infiltration of autoreactive CD4 T cells, macrophages, a

181 rmation of inflammatory cytokines, and brain infiltration of blood-borne monocytes.

182 We found increased infiltration of both surrogate tumor antigen- and oHSV a

183 oma (GBM) is characterized by rapid cellular infiltration of brain tissue, raising the possibility th

184 of serum IL-6, which activates STAT3 and the infiltration of CD11b+ myeloid cells into the lung.

185 ibitor reduced skin phenotypes and decreased infiltration of CD4 T cells, macrophages, and neutrophil

186 nockout (KO) in breast cancer cells promoted infiltration of CD4(+) and CD8(+) T cells, leading to tu

187 IL-4 treatment markedly reduced the infiltration of CD8(+) T cells and brain pathology.

188 -PD-1 and was accompanied by increased tumor infiltration of CD8(+) T cells.

189 Infiltration of CD8(+) T-cells into the placental villou

190 ed that AA strikingly increased intratumoral infiltration of CD8+ T cells and macrophages, suggesting

191 nsive remodeling of the ECM and an increased infiltration of CD8+ T cells.

192 All patients were treated with local infiltration of corticosteroid.

193 a cells, correlating with an increase in the infiltration of cytotoxic CD8(+) T cells.

194 promoted cell cycle progression, suppressed infiltration of cytotoxic T cells, and accelerated SCLC.

195 e-anchored systemic immunotherapy led to the infiltration of effector immune cells into the lungs, in

196 is suggested by the presence of IL-13, with infiltration of eosinophils and IgE-coated mast cells in

197 fect bone marrow-derived expansion and local infiltration of eosinophils, but markedly decreased M2 m

198 n inflammation along with a reduction in the infiltration of gammadelta T cells and the expression of

199 sequelae of eosinophil-dependent downstream infiltration of IL33-producing M2 macrophages leading to

200 clones, accumulation of somatic aberrations, infiltration of immune and stromal cells in proportions

201 yte hyperproliferation and a disease-related infiltration of immune cells.

202 e dysfunction in large part by eliciting the infiltration of immune-inhibitory cells, such as regulat

203 f BBB tight junction proteins, reduced brain infiltration of immunoglobulin, and attenuated neuroinfl

204 anoscale materials can improve targeting and infiltration of immunomodulatory payloads into tissues a

205 Histology showed infiltration of inflammatory cells including neutrophils

206 model, we show that JAK3 inhibition enhances infiltration of inflammatory cells, reduces expression o

207 sion of established lesions and inhibits the infiltration of inflammatory cells.

208 in cardiac inflammatory neutrophils and the infiltration of inflammatory monocytes.

209 ic activation of trypsinogen and more edema, infiltration of lung and pancreas by inflammatory cells,

210 ression inversely correlates with the immune infiltration of lung squamous tumors, while tumors with

211 an 11.5-fold increase of dendritic cells and infiltration of lymphocytes throughout the pancreatic tu

212 es from HFD-treated KO mice showed increased infiltration of M1 type inflammatory macrophages.

213 patocytes (Shp (Hep-/-)) resulted in massive infiltration of macrophages and CD4(+) T cells in the li

214 ion treatment markedly enhanced intratumoral infiltration of macrophages and CD8+ T lymphocytes, gran

215 ry gland and caused severe inflammation with infiltration of macrophages and neutrophils and upregula

216 Thus, our findings reveal that the combined infiltration of macrophages and neutrophils is required

217 In addition, infiltration of macrophages was decreased by treatment (

218 (lymph)angiogenic VEGF-A, VEGF-C, VEGF-D and infiltration of macrophages.

219 prognostically favorable association between infiltration of mast cells and less aggressive tumor cel

220 inflammatory condition characterized by the infiltration of maternal CD8(+) T cells into the placent

221 cervical LNs had a greater tumor burden and infiltration of MDSC and M2 macrophages compared with LN

222 These changes result from an infiltration of mesenchymal cells, an important cell typ

223 status, and attenuates proliferation and/or infiltration of microglia to the region thereby curtaili

224 s after peak viral titer and correlates with infiltration of monocytes, neutrophils and activated T c

225 The GI mucosa showed eosinophil infiltration of more than 40/high-power field in the sto

226 Glp1r(-/-) mice displayed increased renal infiltration of neutrophils and T cells after induction

227 from Cl66-Dox and Cl66-Pac cells had higher infiltration of neutrophils and T helper 17 cells.

228 We show lung infiltration of neutrophils in an autopsy specimen from

229 e of S100A8 and S100A9, as well as increased infiltration of neutrophils in the skin.

230 ses, and cholesterol biosynthesis, increased infiltration of neutrophils, inflammatory monocytes, and

231 t resistance, unfavorable prognosis, and the infiltration of pro-tumorigenic macrophages.

232 immediately before and during the eruption, infiltration of rainfall into Kilauea Volcano's subsurfa

233 We demonstrate infiltration of recipient leukocytes, regardless of reje

234 mors blunted the immune response by inducing infiltration of regulatory T cells and expression of imm

235 tumors with ALAL-1 amplification show lower infiltration of several types of immune cells.

236 Infiltration of solutions with such low tension could le

237 distributions of SARS-CoV-2 RNA and massive infiltration of T cells and macrophages.

238 neous inflammatory lesions accompanied by an infiltration of T cells and myeloid cells.

239 at the epidermis promotes the activation and infiltration of T cells into the skin, and provides a di

240 Infiltration of T lymphocytes, activation of microglia,

241 t elicited antitumour immunity and increased infiltration of T lymphocytes, resulting in highly poten

242 duced intratumor CCR2 expression and altered infiltration of TAMs and CTLs as evidenced by immunohist

243 The activation of microglial cells and infiltration of Th1 cells resulted in white matter injur

244 educed cyst burden, it resulted in a massive infiltration of the cystic kidneys by macrophages and T

245 howed a big mass of soft tissue with diffuse infiltration of the gallbladder, displacement of the tra

246 ound that acute DSS colitis-induced enhanced infiltration of the hippocampus with macrophages and inf

247 d significant loss of BMAT with myeloma cell infiltration of the marrow, whereas BMAT was restored af

248 and pre-eclampsia are associated with T-cell infiltration of the placenta and placental pathological

249 s was associated with impaired M2 macrophage infiltration of the primary tumors.

250 mucus layer of the gut provides a barrier to infiltration of the underlying epithelia by both the nor

251 nin-dependent hypertension due to macrophage infiltration of the vasculature and direct activation of

252 hester disease (ECD) is characterized by the infiltration of tissues by foamy CD68+CD1a- histiocytes,

253 tasis, and immunosuppression, which inhibits infiltration of tumor-specific cytotoxic CD8+ T cells.

254 ed with T cells, suggesting increased T cell infiltration of tumors.

255 ure of mice to thermoneutrality promotes the infiltration of white adipose tissue with mast cells tha

256 oopaque foreign body, mural thickness, fatty infiltration or extraluminal air bubbles.

257 alysis, grading G2 (OR 6.98), lymphovascular infiltration (OR 8.63), and size >15.5 mm (OR 35.28) wer

258 type and promoted intratumoral CD8(+) T-cell infiltration, overcoming the exclusion effect; TGFbeta1

259 gnificant levels of oesophageal eosinophilic infiltration (P < .05) in 4/6 of these animals, with two

260 YT/ICGscore had significantly increased CD8+ infiltration (p < 0.001), as expected, and worse surviva

261 se aggressiveness in GBM, particularly tumor infiltration (P = .0044) and hyperplastic blood vessels

262 ), CCL2/IL13 expression (p<10(-109)) and TAM infiltration (p<10(-96)).

263 Cationic interfaces elicit stromal cell infiltration, peripherally derived inflammation, neural

264 s, CD4, CD8A, CD8B, and the tumor-lymphocyte infiltration phenotype.

265 MRI of the leg muscles showed fibrofatty infiltration predominating in the posterior thigh and th

266 signature analysis confirmed the lymphocyte infiltration profile consistent with the histomorphology

267 ause it regulates the dynamics of macrophage infiltration, proinflammatory and anti-inflammatory cyto

268 This hinders effector T-cell infiltration, proliferation and immune reactivity, there

269 C6 had the lowest natural killer infiltration rate and was represented by copy gains of g

270 osome 11, having also the lowest lymphocytic infiltration rate.

271 LRG1 deletion causes impaired immune cell infiltration, reepithelialization, and angiogenesis.

272 We discover that 49 of 189 infiltration-related phenotypes are associated with eith

273 Genetic analyses further show that 31 infiltration-related phenotypes have genome-wide signifi

274 then used in Soil Water Balance groundwater infiltration simulations to understand the state-of-the-

275 l analysis revealed microglial or macrophage infiltration, suggesting activation in brain regions con

276 d inversely correlated with cytotoxic T cell infiltration, suggesting that HE4 may cause deregulated

277 Here, we demonstrate how sequential infiltration synthesis (SIS) of alumina, a simple solven

278 revealed significantly decreased immune cell infiltration, synthesis of reactive oxygen species, infl

279 minants in both natural soils and artificial infiltration systems.

280 MCC950 significantly reduced neutrophil infiltration, T-cell activation, and disease severity in

281 xpression pattern that indicated immune cell infiltration; this tumor type was associated with the sh

282 within the aquifer are, in part, created by infiltration through the vadose zone, illustrating the c

283 -2 immune activation, inflammation, cellular infiltration, tissue repair enzymes, pathways of oxidati

284 In addition, the resins' infiltration to dentin tubules, mechanical performance,

285 make the catalyst synthesized by successive infiltration to have higher catalytic activity for soot

286 Tumor lymphocyte infiltration was 0.17%.

287 Leukocyte infiltration was elevated in the prostates harvested fro

288 rophils (e.g. CXCL5, CXCL8) and neutrophilic infiltration was followed with much delay by reduction i

289 In stress models, inflammatory cell infiltration was initially lower in knockout mice but la

290 +/- 0.1 vs 7.8 +/- 0.2 um; p < 0.0001), cell infiltration was lower (20 +/- 2 vs 32 +/- 2 n/field; p

291 d pre-eclampsia, whereas CD79alpha(+) B-cell infiltration was only apparent with reduced fetal growth

292 ntigen load) and the degree of CD8(+) T cell infiltration were not associated with clinical response,

293 gh reliability and exhibit rapid, aggressive infiltration when transplanted into adult rodent brains.

294 infiltration system in hemp utilizing vacuum infiltration, which is an alternative method to stable t

295 E is driven predominantly by maternal T cell infiltration, which is significantly different from cont

296 dermal disorganization and inflammatory cell infiltration, which were improved in the 3 treated group

297 ivo treatments modifying apoplastic pH (stem infiltration with a pH buffer) or reducing stem metaboli

298 levels of viral genomes in blood and tissue infiltration with Epstein-Barr virus (EBV)-positive lymp

299 itored cortical epileptogenesis during tumor infiltration with in vivo electrophysiology and GCAMP7 c

300 al nitric oxide synthase, and vascular/brain infiltration with inflammatory cells.

301 buffer) or reducing stem metabolic activity (infiltration with sodium vanadate and sodium cyanide; pl