ライフサイエンスコーパス: draining

1 pipes experience regular flow restarting and draining.

2 of the presence of tumor in the lymph nodes draining a tumor, providing the ability to achieve the r

3 others, were exclusively identified in skin-draining and mesenteric LNs, respectively.

4 The diameters of lymphatic vessels draining Ang-4- or VEGF-C (positive control)-expressing

5 he number and diameter of all feeding and/or draining arteries were measured, and endoleaks were clas

6 d the diameter of the largest feeding and/or draining artery (OR = 4.55, P = .013).

7 endoleak in whom the largest feeding and/or draining artery was larger than 2.2 mm were at high risk

8 endoleak in whom the largest feeding and/or draining artery was larger than 3.8 mm and patients with

9 d the diameter of the largest feeding and/or draining artery.

10 on (closure of all treated external openings draining at baseline with absence of collections >2 cm,

11 e of all treated external openings that were draining at baseline, and absence of collections >2 cm o

12 amer that packs ("creams") assay droplets by draining away excess oil through microfabricated drain c

13 Free-draining biofilters remained aerobic with negligible gre

14 ctive immune cells entering the CNS from the draining cervical lymph node.

15 fic Tregs were progressively enriched in the draining cervical lymph nodes and CNS as compared with s

16 with reduced lymphocyte proliferation in the draining cervical lymph nodes, decreased leukocyte infil

17 ls which specifically accumulated in the CNS-draining cervical lymph nodes.

18 th Crohn's disease and treatment-refractory, draining complex perianal fistulas were randomly assigne

19 th Crohn's disease and treatment-refractory, draining, complex perianal fistulas.

20 from the central nervous system (CNS) to the draining deep cervical lymph nodes.

21 onal lymphatic capillaries are necessary for draining excess fluid after inflammation; however, Nrp2-

22 entral reader) or development of a new or re-draining fistula or abscess, before or at week 76.

23 nodule count, with no increase in abscess or draining-fistula counts, at week 12.

24 imaging) and clinical remission (absence of draining fistulas).

25 he Gulf of Alaska originates from landscapes draining glacier runoff, but the influence of the influx

26 f new surface-to-bed conduits caused by lake-draining hydro-fractures may be limited.

27 ecific CD4 T cell responses within the local draining iliac lymph nodes, yet robust Th1 and Th17 resp

28 Surprisingly, second-tier tumor-draining inguinal LNs exhibited reduced uptake, indicati

29 pillaries that are functionally incapable of draining interstitial fluid.

30 In 4% of subjects, RPSD was draining into the common hepatic duct (CHD) and in 0.8%

31 nt, habitable lake environment fed by rivers draining into the crater.

32 ant was right posterior sectoral duct (RPSD) draining into the left hepatic duct (LHD) in 27.6% of su

33 strated arterio-portal-venous shunting, with draining into the TIPS.

34 Skin culture of one of the draining lesions was performed at this time, but there w

35 Nitrate concentrations in rivers draining Leverett Glacier in southwest Greenland and Kia

36 ntation and four isolates in the recipients' draining liquid at the Kidney Disease Center, The First

37 in IFN-gamma ELISPOT counts was seen in the draining LN but not in PBMCs.

38 ination of intradermal Ag administration and draining LN sampling can be used as a sensitive method t

39 o allograft, then via afferent lymphatics to draining LN to protect allografts.

40 oxin (LT) during migration from allograft to draining LN, and that LT deficiency or blockade prevents

41 cumulation of dermal dendritic cells in skin-draining LN.

42 TDLNs (+1 cmH2O) relative to both non-tumor-draining LNs (-1 cmH2O) and LNs from naive animals (-1 t

43 on to the evolving microenvironment of tumor-draining LNs (TDLNs) remains poorly understood.

44 s of long-lived memory B cells (Bmem) in the draining LNs and plasma cells (PCs) in the bone marrow (

45 rease in Treg percentages in aorta and aorta-draining LNs and reduced atherosclerosis.

46 Comparison of non-draining LNs and spleens of tumor-bearing mice with LNs

47 ve transcriptional analysis of FRCs from non-draining LNs and TDLNs demonstrated reprogramming of key

48 uptake of nanoparticle contrasts into tumor-draining LNs could also allow selective targeting of the

49 Mature cDC2 in mucosal-draining LNs expressed tissue-specific markers derived f

50 s that the self-drainage of OVA+CAF09 to the draining LNs is required for the activation of CD8alpha(

51 pact of adjuvants on Ag retention within the draining LNs is unknown.

52 . rodentium activated DC especially in colon-draining LNs, and gene expression changed in pDC more pr

53 from that of the small intestine in terms of draining LNs, and identify pDC as active sentinels of co

54 he skin with their migratory counterparts in draining LNs, we have identified a novel NF-kappaB-regul

55 d medullary macrophage compartments of mouse draining LNs, where it persists for at least 2 wk.

56 subsets, both in small intestinal and colon-draining LNs.

57 ow selective targeting of therapies to tumor-draining LNs.

58 evealed by pentamer staining in the skin and draining LNs.

59 le they were restricted to the cortex of non-draining LNs.

60 et in LNs with the highest frequency in lung-draining LNs.

61 ity to prime CD8(+) T cell responses in skin-draining LNs.

62 nce requires effector T-cell egress from the draining lymph node (dLN).

63 ment of inflammatory monocytes (iMos) to the draining lymph node (dLN).

64 on to, and localization with, T cells in the draining lymph node (dLN).

65 ing of these antigen-presenting cells to the draining lymph node (LN), it was shown that the iron oxi

66 lts indicate that tumor growth reduces tumor-draining lymph node accumulation and alters the distribu

67 s to a delay in CD8 T cell activation in the draining lymph node and hinders the timely appearance of

68 IL-1beta production by myeloid cells in the draining lymph node and served as a strong stimulus for

69 of IFNgamma-producing CD8(+) T cells in the draining lymph node and spleen.

70 bserved Th1/Th17 effector cells in the tumor draining lymph node and tumors.

71 In addition, draining lymph node cells from FHL2-KO mice show reduced

72 reduced IFN-gamma and IL-17 were detected in draining lymph node cells from P2rx7(-/-) mice.

73 re found in bronchoalveolar lavage fluid and draining lymph node cells of Nur77-KO mice, as well as i

74 led to a similar bias in CD4(+) T cells from draining lymph node cells toward IL-17A and away from IF

75 sue, bronchoalveolar lavage fluid (BALF) and draining lymph node cells were analysed for inflammation

76 served both full-length and cleaved SIRT1 in draining lymph node cells.

77 mune disease by regulating SIRT1 cleavage in draining lymph node effector cells.

78 and alloantigen-induced T cell expansion in draining lymph node experiments.

79 r, the severe loss of dendritic cells in the draining lymph node had no impact on viral replication i

80 tion of dendritic cells and T cells into the draining lymph node immediately following infection and

81 causes retention of effector T cells in the draining lymph node in a neuroinflammatory autoimmunity

82 However, we show that draining lymph node macrophages, but not macrophages at

83 Interestingly, tumor-infiltrating and tumor-draining lymph node NK cells displayed an upregulated ex

84 gammadelta T cells in the infected foot and draining lymph node that was associated with the product

85 r phenotype that allows trafficking from the draining lymph node to the lungs and, thereby, prevented

86 Both VLPs efficiently reached the same draining lymph node where they were taken up and process

87 e identified in the porcine-NICC xenografts, draining lymph node, and spleen.

88 +) and CD103(+) dendritic cells, in the lung-draining lymph node, as well as increased expression of

89 Here we report that macrophages in the draining lymph node, but not in the tissue at the site o

90 ime dependent changes in RNA profiles of the draining lymph node, suggesting a change in cell profile

91 ency of T cells and myeloid cells within the draining lymph node.

92 ent passive diffusion of the nanogels to the draining lymph node.

93 tion of renal antigens to CD8 T cells in the draining lymph node.

94 g parenchyma independently of priming in the draining lymph node.

95 ell (DC) Ag presentation in the local muscle-draining lymph node.

96 he MHC II(high) mature DCs were found in the draining lymph node.

97 iling of innate immune response genes in the draining lymph node.

98 increased emm1 GAS dissemination locally to draining lymph nodes (controls median 183 CFU per node [

99 required CCR2 expression to traffic between draining lymph nodes (dLN) and the tumor.

100 n vitro but failed to home from the graft to draining lymph nodes (dLN) as efficiently as wild type.

101 antigen capture and subsequent migration to draining lymph nodes (DLN).

102 cells and T cells to lymphatics and then to draining lymph nodes (dLN).

103 ed s.c. shows minimal uptake into lymphatics/draining lymph nodes (dLNs) and instead is rapidly distr

104 d with a lack of iNKT cell activation in the draining lymph nodes (dLNs) and prevented the protective

105 nfection, CD4(+) T cells are expanded in the draining lymph nodes (DLNs) and restimulated in the infe

106 raction of the vaccine dose localized in the draining lymph nodes (dLNs) and the spleen 6h after i.p.

107 igated virus-host interactions in the rectal draining lymph nodes (dLNs) of rhesus macaques at differ

108 ry changes either in the lung or in the lung draining lymph nodes (LDLN), pretreatment of blood eosin

109 ans cells are APCs that migrate from skin to draining lymph nodes (LN) to drive peripheral tolerance

110 pecific cells underwent several divisions in draining lymph nodes (LN; DLNs) while maintaining expres

111 d presentation of antigen to T cells in skin draining lymph nodes (LNs) both 3 and 10days after admin

112 ent increase in size and cellularity of skin-draining lymph nodes (LNs) in mice.

113 rease in Treg percentages in aorta and aorta-draining lymph nodes (LNs) of these mice compared with a

114 cells and germinal center (GC) B cells from draining lymph nodes (LNs) than the parent virus rLBNSE.

115 f natural and peripheral Tregs in spleen and draining lymph nodes (LNs), elevated IL-10 and TGF-beta

116 e generation of cellular immune responses in draining lymph nodes (LNs).

117 45(+) leukocytes present in tumor tissue and draining lymph nodes (LNs).

118 duce IL-17 in the skin and expand rapidly in draining lymph nodes (LNs).

119 otein expression were higher in T cells from draining lymph nodes (P = 0.03 and P = 0.04, respectivel

120 und in histopathologically negative prostate draining lymph nodes (PDLN) in mice harboring oncogene-d

121 om peripheral blood (PB) and from pancreatic draining lymph nodes (PLN) of T1D patients and non-diabe

122 4+ T cell hyporesponsiveness within the skin-draining lymph nodes (sdLN), manifested as reduced CD4+

123 under steady-state conditions, ILCs in skin-draining lymph nodes (sLNs) were continuously activated

124 Although STING also induced IDO in tumor-draining lymph nodes (TDLN) during EL4 thymoma growth, t

125 sophils expressing IL4 are enriched in tumor-draining lymph nodes (TDLN) of PDAC patients.

126 g responses, which quickly manifest in tumor-draining lymph nodes (TDLNs) after tumor inoculation and

127 ar sinus (SCS) CD169(+) macrophages in tumor-draining lymph nodes (tdLNs) in mice and humans.

128 AM did not prevent lymphocyte recruitment to draining lymph nodes 24 h after transfer, but it was req

129 of IL-4-producing TFH cells and TH2 cells in draining lymph nodes after airway exposure to IL-1 famil

130 a necessary step for virus dissemination via draining lymph nodes and blood.

131 ntional DCs that transport tumor antigens to draining lymph nodes and cross-present antigen to activa

132 on significantly increased Foxp3(+) Tregs in draining lymph nodes and in the spleen but failed to red

133 en caused homing of tumor-infiltrating DC to draining lymph nodes and increased infiltration of T cel

134 complex class II molecules, migrated to the draining lymph nodes and induced an increase in Treg cel

135 ired the emigration of XCR1(+) dermal DCs to draining lymph nodes and occurred irrespective of TLR si

136 gulatory T cells at the graft site and graft-draining lymph nodes and preventing T-cell infiltration.

137 rentially retained at the injection site and draining lymph nodes and produced fewer systemic inflamm

138 immune responses was analyzed by collecting draining lymph nodes and sera and by challenging the ani

139 nt CD11b(+) DCs, which enhances migration to draining lymph nodes and Th2 priming capacity.

140 ion by plasmacytoid DC (pDC) from skin/tumor draining lymph nodes and the cross-priming of Ag-specifi

141 of CCR6(+) Treg cells was also found in the draining lymph nodes and tumor-infiltrating lymphocytes

142 oducing CD4(+) T cells in muscle tissues and draining lymph nodes as well as reduced parasite burden

143 reduced CD40 expression in DCs isolated from draining lymph nodes at 2 days post infection (dpi).

144 CD11b(-) cDCs from the gut-draining lymph nodes efficiently induced pT(reg) cells a

145 o showed suppressed T cell activation in the draining lymph nodes following challenge.

146 of CD4(+) central-memory T cells within the draining lymph nodes following induction of contact hype

147 ed to support a role of macrophage efflux to draining lymph nodes following treatment with infliximab

148 Cells in draining lymph nodes from BALB/c-CXCR3(Tg) mice showed e

149 Neutrophils sorted from vaccine-draining lymph nodes from rhesus macaques also showed ex

150 on of dermal mast cells from the skin to the draining lymph nodes has a prominent role in activating

151 T cells into the lung lumen, parenchyma, and draining lymph nodes in HDM-sensitized mice.

152 ro and in vivo, trafficking through lymph to draining lymph nodes in mice.

153 dies have highlighted the importance of lung-draining lymph nodes in the respiratory allergic immune

154 n by Ag-specific T cells upon stimulation of draining lymph nodes in vitro.

155 +) pulmonary dendritic cells in the lung and draining lymph nodes in wild-type BALB/c mice after RSV

156 lated from tumor-infiltrating lymphocytes or draining lymph nodes maintained similar phenotypic and s

157 t of SIV from penile mucosal surfaces to the draining lymph nodes may allow an HIV vaccine that produ

158 r helper T (Tfh) cells were also detected in draining lymph nodes of allergic mice.

159 ntional effector T cells were collected from draining lymph nodes of allogeneic or syngeneic corneal

160 onstrate that although lymphocytes from skin-draining lymph nodes of autoimmune-prone MRL/MpJ-Fas(lpr

161 solated CD4(+) T cells from the upper airway draining lymph nodes of both OVA323-339- and MPO409-428-

162 B cells were induced at higher levels in the draining lymph nodes of CD47KO mice compared to those in

163 xtended monitoring of IDO(+) DC in the tumor-draining lymph nodes of IL-12 plus GM-CSF-treated tumor-

164 CXCL13 levels correlated with GC activity in draining lymph nodes of immunized mice, immunized macaqu

165 Furthermore, skin-draining lymph nodes of LC-ablated MRL-lpr mice had sign

166 Upon analysis of microRNA (miR) profile in draining lymph nodes of mice with DTH, treatment with I3

167 clinical-grade adjuvants in whole blood and draining lymph nodes of mice.

168 -secreting virus-specific CD4 T cells in the draining lymph nodes of NK1R(-/-) mice was much higher t

169 In uterus-draining lymph nodes of pregnant dams, the frequencies o

170 ion of MOG35-55-specific T cells in the skin draining lymph nodes of primed mice, but it is not requi

171 CD103(+) DC from the skin/tumor draining lymph nodes of the immunized mice appeared resp

172 mal mast cell migration from the skin to the draining lymph nodes plays a prominent role in activatin

173 g RPM we find that high endothelial cells in draining lymph nodes rapidly increase translation in the

174 g kinetics in IL-12-treated tumors and tumor-draining lymph nodes revealed a transient loss followed

175 is of CD11c(+)MHC-II(hi) DCs in the lung and draining lymph nodes revealed that allergen exposure inc

176 differential distribution of exosomes in the draining lymph nodes that is dependent on the lymphatic

177 lung during inflammation and migrated to the draining lymph nodes to boost TH2-mediated effector resp

178 ouse MB49 bladder tumors, spleens, and tumor-draining lymph nodes to identify patterns of anti-tumor

179 dendritic cells (DCs) mature and migrate to draining lymph nodes to induce immune responses.

180 nd migrate out of the skin and mucosa to the draining lymph nodes to present antigens to T and B cell

181 Thus, ILC populations traffic to draining lymph nodes using different mechanisms.

182 ith pBCG or rBCG, and gene expression in the draining lymph nodes was analyzed by microarray at day 1

183 Furthermore, HIV-1 dissemination to draining lymph nodes was detected only in HSV-2-coinfect

184 wing TNF inhibition, positing that efflux to draining lymph nodes was involved.

185 lymphocytes expressing RANKL in the cervical draining lymph nodes were higher in IL-33-treated P. gin

186 nced suppressive capacity of Tregs from skin-draining lymph nodes when compared with Tregs from the l

187 s) are professional APCs that traffic to the draining lymph nodes where they present processed antige

188 focused the in vivo immune activation on the draining lymph nodes while dramatically reducing systemi

189 lungs (including the major blood vessels and draining lymph nodes) obtained en bloc from 72 individua

190 ent in ApoE(-/-)Irf5(-/-) mice in the aorta, draining lymph nodes, and bone marrow cell cultures, ind

191 antigen presenting cell (APC) trafficking to draining lymph nodes, and enhances antigen cross-present

192 tracting chemokines, migration of DCs to the draining lymph nodes, and priming of allergen-specific T

193 +)CD80(-) GC B cells in proximal- and distal-draining lymph nodes, and promoted the persistence of GC

194 Treg cells remained unchanged in the lungs, draining lymph nodes, and spleens of infected mice.

195 enous and exogenous DCs, migration of DCs to draining lymph nodes, and tumor infiltration of CD4(+) a

196 cific CD4(+) T cells proliferated in the eye draining lymph nodes, but did not induce uveitis.

197 cer cells tend to metastasize first to tumor-draining lymph nodes, but the mechanisms mediating cance

198 mour antigens to antigen-presenting cells in draining lymph nodes, leading to increased surface prese

199 by myeloid-derived suppressor cells in tumor-draining lymph nodes, leading to T cell responses skewed

200 es of CD4(+)Foxp3(+) T cells in the pancreas-draining lymph nodes, pancreas, and peripheral blood of

201 ased numbers of migratory dendritic cells in draining lymph nodes, specifically dendritic cells with

202 ficant reductions in bacterial burden in the draining lymph nodes, spleen, and liver were observed.

203 to secondary sites of infection, mainly the draining lymph nodes, spleen, gastrointestinal tract, an

204 skin infection by restoring DC migration to draining lymph nodes, Th17 differentiation, and increase

205 th appropriate Ag specificity are present in draining lymph nodes, they are conspicuously absent from

206 gene-expressing melanocytes localize to skin-draining lymph nodes, where they induce T-cell prolifera

207 s in the paws and in Th17 lymphocytes in the draining lymph nodes, whereas T-regulatory cells were da

208 leukocytes found in primary tumors or tumor-draining lymph nodes, which included mainly CD14(+) mono

209 eased lymphatic flow from the donor graft to draining lymph nodes, which may be a factor in promoting

210 inhibited Th1 and Th17 and amplified Treg in draining lymph nodes, while reducing dry eye pathogenesi

211 fibroblastic reticular cell networks in the draining lymph nodes.

212 ad box P3) IFN-gamma(+) T cells in the heart-draining lymph nodes.

213 o t 5, that targets the lung rather than the draining lymph nodes.

214 , and eosinophil infiltration in the stomach-draining lymph nodes.

215 e immune responses at the injection site and draining lymph nodes.

216 from whole nondiseased human lungs and lung-draining lymph nodes.

217 s was isolated from tonsils, gut mucosa, and draining lymph nodes.

218 of organ-specific Treg cells in the prostate-draining lymph nodes.

219 significantly attenuated niT cell numbers in draining lymph nodes.

220 he rationale for surgical resection of tumor-draining lymph nodes.

221 and kinetics, TFH and GC B cell responses in draining lymph nodes.

222 riven recruitment of T-cell oral tissues and draining lymph nodes.

223 ) T cell priming in both the spleen and skin-draining lymph nodes.

224 CD4(+) T cells and plasmablasts in the joint-draining lymph nodes.

225 injection) trafficking of both cell types to draining lymph nodes.

226 gene expression in vivo, particularly within draining lymph nodes.

227 nodes when compared with Tregs from the lung-draining lymph nodes.

228 elevated Th1 and Th17 cell reactivity in the draining lymph nodes.

229 se in the effector CD4(+) T cell response in draining lymph nodes.

230 ion and impaired effector T-cell egress from draining lymph nodes.

231 vant distribution and prolonging activity in draining lymph nodes.

232 tory T cell response in the cornea and local draining lymph nodes.

233 gnificant reduction in IL-17(+) cells in the draining lymph nodes.

234 the initiation of the immune response in the draining lymph nodes.

235 R T cells occurred only in the regional skin-draining lymph nodes.

236 nary MCs before leaving the inflamed skin to draining lymph nodes.

237 the vaccine injection site, but not vaccine-draining lymph nodes.

238 tivate antigen-specific CD8 T cells in renal draining lymph nodes.

239 upregulation of T cell activation markers in draining lymph nodes.

240 g trafficking of antigen-presenting cells to draining lymph nodes.

241 response on the malignancy and the affected draining lymph nodes.

242 he kidney and T cell activation in the renal draining lymph nodes.

243 2L(hi)CD44(lo)Foxp3(+) central Treg cells in draining lymph nodes.

244 in tissue, and migrate through lymphatics to draining lymph nodes.

245 cific B cells were detected in local genital draining lymph nodes.

246 f specific B cells to the mesenteric but not draining lymph nodes.

247 IL-1beta expression by myeloid cells in the draining lymph nodes.

248 n increase in donor cells in the mediastinal draining lymph nodes; increased lymphatic vessel area; a

249 the CNS and meninges to the peripheral (CNS-draining) lymph nodes.

250 enic cellular signature within the blood and draining lymphatics following both immunization routes.

251 al lamina propria dendritic cells (DCs) into draining mesenteric lymph nodes (MLN).

252 Naive lymphocytes traffic to the gut-draining mesenteric lymph nodes where they undergo antig

253 orland streams, and lowest of all in streams draining non-native conifers.

254 omplex OM including recurrent, spontaneously-draining, non-responsive, and chronic cases) was monitor

255 harynx with initial prion replication in the draining oropharyngeal lymphoid tissues, rapidly followe

256 at the CD8alpha(+) DCs are activated by self-draining OVA+CAF09 in the lymphoid organs, whereas the C

257 hils traffic from the airway lumen into lung-draining paratracheal lymph nodes.

258 These DCs capture draining particles and present associated antigens to T

259 xposure impacts microbial respiration of DOC draining permafrost soils.

260 pening when calcium chloride is added or the draining pH altered.

261 addition can be used, together with a lower draining pH, to alter the manufacturing process without

262 alterations in lymph drainage through tumor-draining popliteal and inguinal LNs versus contralateral

263 foci around the cortex and medulla of tumor-draining popliteal LNs, while they were restricted to th

264 re encoded by highly expanded B cells in the draining popliteal lymph node (PLN).

265 uces marked B cell accumulation within tumor-draining popliteal lymph nodes (TDLN).

266 ion of the inguinal and popliteal nodes with draining popliteal lymphatic vessel significantly decrea

267 In the current study, we harness the draining properties of the lymphatic system and show tha

268 led several small fluctuant masses that were draining purulent material.

269 correlated with soil texture or with wetland draining-reflooding frequency.

270 33 Gy over 11 days to the chest wall and the draining regional lymph nodes, followed by an optional m

271 catchment and coastal plume of a small peat-draining river over a seasonal cycle.

272 ating naive Ag-specific B cells arrive in Ag-draining secondary lymphoid organs, they may join the on

273 their mucosal and peripheral sites to local draining secondary lymphoid tissues.

274 us infections, but these infections lack the draining sinuses and fungal grains characteristic of eum

275 d by abscess formation, tissue fibrosis, and draining sinuses.

276 saturated sites ("Wet Basins") and two quick draining sites ("Dry Basins"), were monitored over a app

277 mically peripheral dendritic cells from skin-draining sites.

278 ening in the posterior hyaloids membrane for draining subhyaloid hemorrhage.

279 ccasional first flush occurring at a subsite draining suburban land.

280 In recent decades, hundreds of glaciers draining the Antarctic Peninsula (63 degrees to 70 degre

281 We find that the gravel fluxes from rivers draining the central Himalayan mountains, with upstream

282 isorders, the presence of a lymphatic system draining the CNS potentially offers a new player and a n

283 series from two proglacial meltwater rivers draining the Greenland Ice Sheet, using a recently devel

284 in IL-4 production by cells from lymph nodes draining the infection site.

285 Lymph-borne Th1 and Th17 cells draining the inflamed skin of sheep migrated toward the

286 Nevertheless, streams draining the most extensive deciduous woodland had the g

287 model that directly collects lymphatic fluid draining the muscle, and 3) to investigate the function

288 aining the vaccination site and in distal LN draining the respiratory mucosa, although in lower numbe

289 ic ASC were detected in all lymphoid tissues draining the respiratory tract, mostly as IgM-secreting

290 gap, we quantified the susceptibility of DOM draining the shallow organic mat and the deeper permafro

291 ed by environmental cues in lymphoid tissues draining the site of infection.

292 divisions during TFH differentiation in LNs draining the site of initial infection.

293 l to be operational within lymph nodes (LNs) draining the tumor interstitium.

294 at 7 dpv in the prescapular lymph node (LN) draining the vaccination site and in distal LN draining

295 crofluidic channels required for filling and draining them with readout and cleaning solutions, thus

296 selenium concentrations reported for streams draining these fills.

297 of spontaneous cholecysto-cutaneous fistula draining through an old surgical scar have been reported

298 AVF draining vein diameter and blood flow rate were assessed

299 es to IgG1 were observed, particularly in LN-draining virus replication sites already described.

300 Streams draining watersheds with stormwater ponds had consistent