ライフサイエンスコーパス: draining

1 pipes experience regular flow restarting and draining.

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

3 e liquid layer remains on it upon cyclically draining and replenishing the sample solution, ensuring

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

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

6 activation in both peripheral blood and the draining axillary lymph node, indicating significant BCG

7 e oval fossa and right upper pulmonary veins draining beyond the cavoatrial junction on transesophage

8 Free-draining biofilters remained aerobic with negligible gre

9 itre in tumour-draining lymph than in tumour-draining blood.

10 t the filling, to ~2 m depth, and subsequent draining, by overflow and channel incision, of four surf

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

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

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

14 NS-draining lymph nodes, sparing their liver-draining counterparts.

15 motes enhanced priming of CD8 T cells in the draining deep cervical lymph nodes, migration of CD8 T c

16 h splanchnic venous blood bypasses the liver draining directly into systemic circulation through a co

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

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

19 ols on temperature sensitivity; R in streams draining flat watersheds was up to six times more temper

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

21 ween gLNs, with the proximal small intestine-draining gLNs preferentially giving rise to tolerogenic

22 nts draining <200 km(2) or from large rivers draining >100,000 km(2).

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

24 pillaries that are functionally incapable of draining interstitial fluid.

25 venous drainage pattern as anterior (A-CCF: draining into ophthalmic veins) and posterior (P-CCF: no

26 ophthalmic veins) and posterior (P-CCF: not draining into ophthalmic veins).

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

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

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

30 ickpoints in eleven separate channel systems draining into the Martian Northern lowlands.

31 niotomy/craniectomy and external ventricular draining/intracranial pressure monitoring.

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

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

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

35 er within seconds into the parenchyma of the draining LN in an intact form.

36 Cells within the draining LN retained canonical markers of lung TRM, incl

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

38 ommitted to the residency program within the draining LN, where they provide longer-lived regional me

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

40 efficiently, than their counterparts in the draining LNs (TLN cells).

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

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

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

44 borne molecules from the periphery enter the draining LNs via a reticular conduit system.

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

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

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

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

49 mmune response at secondary lymphoid tissues draining local gut and systemic circulation.

50 emistry are from small, headwater catchments draining <200 km(2) or from large rivers draining >100,0

51 Bacteria then traffic to the draining lymph node (dLN) where they replicate to large

52 T cell migration from the dermis to the skin draining lymph node (dLN).

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

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

55 induce the migration of CD301b(+) DCs to the draining lymph node (dLN).

56 ype 1 dendritic cell IL-27 production in the draining lymph node 12 h after s.c. vaccination directly

57 8+ cells are likewise elevated in the tumour draining lymph node and activated to a greater extent th

58 B cells and follicular helper T cells in the draining lymph node and Ag-specific Th1 and Th17 cells i

59 istant tumors, while sparing the intervening draining lymph node and spleen.

60 alloantigen-induced immune responses in the draining lymph node at lower doses and reduced administr

61 Within the draining lymph node CD4(+) T-cell population, 30% expres

62 Gene set enrichment analysis of draining lymph node cells from day 1 after immunization

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

64 ic CD4 T cells in the CNS during disease and draining lymph node during priming.

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

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

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

68 robust activation of dendritic cells in the draining lymph node in vivo.

69 infection, we find that while CD169 promoted draining lymph node infection, it limited systemic sprea

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

71 rment at entering or distributing within the draining lymph node of ectromelia virus (ECTV)-infected

72 tion, and migration of immune cells to local draining lymph node or to an anatomically distant tumor.

73 OTAP results in an IFN-dependent increase in draining lymph node size and a concomitant increase in C

74 xogenous tumor Ags, and migrate to the tumor draining lymph node to initiate cross-priming of tumor-r

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

76 ualization of the potential metastatic tumor-draining lymph node(s) for their needed surgical biopsy

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

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

79 ) T cells were also suppressed in pancreatic draining lymph node, demonstrating bystander tolerance a

80 -L1 inhibition specifically within the tumor-draining lymph node, identifying a potential role for PD

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

82 tor T cell responses, from activation in the draining lymph node, to the execution of effector functi

83 by increasing local HA concentration in the draining lymph node.

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

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

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

87 he tumor suppresses T cell activation in the draining lymph node.

88 ent of neutrophils to the ear dermis and ear draining lymph nodes (dLN) as early as 6-18 h after immu

89 cation of intravaginally administered DCs to draining lymph nodes (dLNs) and stimulate in vivo prolif

90 n of multiple T cell subsets to the skin and draining lymph nodes (DLNs) during dengue virus (DENV) i

91 ice and for lifelong parasite persistence in draining lymph nodes (dLNs) of healed mice.

92 terestingly, the environmental milieu of the draining lymph nodes (DLNs) of the mice implanted with t

93 flammatory factors in the grafted cornea and draining lymph nodes (dLNs) were evaluated with slit-lam

94 gens that are regionally drained and through draining lymph nodes (DLNs).

95 The gut-draining lymph nodes (gLNs) are key sites for orchestrat

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

97 as well as a decreased number of LC in skin-draining lymph nodes (LN).

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

99 ls in mouse skin and colon, their respective draining lymph nodes (LNs) and spleen.

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

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

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

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

104 une responses at peripheral sites and within draining lymph nodes (LNs).

105 s (P = .086 and .006, respectively), and the draining lymph nodes (P = .02).

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

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

108 s, resulting in reduced LC migration to skin-draining lymph nodes (sdLNs) and defective skin toleranc

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

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

111 nsively characterized myeloid cells in tumor draining lymph nodes (tdLN) of mice and identified two s

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

113 g nanoparticles that are rapidly conveyed to draining lymph nodes after administration in peripheral

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

115 However, colonization of neither draining lymph nodes after IN infection nor the spleen a

116 erized by an early burst transit through the draining lymph nodes and a relatively limited overall sy

117 oid dendritic cells migrating to mediastinal draining lymph nodes and bearing migratory and immunoreg

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

119 of programmed-death-ligand-1) in spinal cord-draining lymph nodes and decreases the number of T helpe

120 engulfed MCGs are actively shuttled to skin-draining lymph nodes and finally degraded inside DCs wit

121 nhibited fever-induced T cell trafficking to draining lymph nodes and impaired the clearance of bacte

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

123 ine needle aspiration to serially sample the draining lymph nodes and investigate the dynamics and sp

124 ls and subsequent dissemination to the tumor-draining lymph nodes and lungs.

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

126 follicular helper (Tfh) cells in their lung draining lymph nodes and produced IgE Abs to peanuts.

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

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

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

130 T(FH) were first observed in the lung-draining lymph nodes and with further exposure were also

131 antigen-specific CD8(+) T cells in the skin draining lymph nodes compared to a conventional intrader

132 stimulator (ICOS), in the skin allograft and draining lymph nodes compared to endogenous and polyclon

133 antigen specific T cell proliferation in the draining lymph nodes during EAE.

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

135 cells found in the infected liver and liver-draining lymph nodes exhibited transcriptionally and phe

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

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

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

139 IFN-gamma and IL-2-producing T cells in skin draining lymph nodes in a cell-intrinsic fashion.

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

141 te a massive B cell response in the abomasal draining lymph nodes in Ostertagia ostertagi (OO)-infect

142 Tregs were examined in the uterus and uterus-draining lymph nodes in virgin estrus mice and 3.5 d pos

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

144 igen transfer into and presentation in tumor-draining lymph nodes induce activation of tumor-specific

145 gest that the presence of TPO in the thyroid draining lymph nodes induces the activation of T(eff) an

146 cited a Th1 response that was primed in skin-draining lymph nodes involving Ag presentation by migrat

147 Tumor metastasis to the draining lymph nodes is critical in patient prognosis an

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

149 gus macaques, of the trafficking dynamics to draining lymph nodes of a model messenger RNA vaccine la

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

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

152 m cells leads to maturation and migration to draining lymph nodes of cross-presenting dermal DCs.

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

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

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

156 MC-derived IL-13 acted on DCs from draining lymph nodes of OVA-sensitized skin to selective

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

158 cal animal models, ss-CyFaP is visualized in draining lymph nodes of rats through 3.1 cm of overlaid

159 ion, dendritic cells (DCs) purified from the draining lymph nodes of tape-stripped and ovalbumin (OVA

160 pPD-1(+) T cells were also detected in tumor-draining lymph nodes of tumor bearing mice and in biopsi

161 and maintenance and maturation of GCs in the draining lymph nodes of vaccinated mice.

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

163 antly, we found that the signal in the tumor-draining lymph nodes provides key information about resp

164 gher frequencies of memory Th17 cells in the draining lymph nodes relative to young mice.

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

166 cumulation, although Bmem outnumbered ASC in draining lymph nodes throughout infection.

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

168 mechanistic studies at site of injection and draining lymph nodes to directly address the question of

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

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

171 liposome and protein retention at the local draining lymph nodes was demonstrated with the liposome-

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

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

174 oscopic examination of the primary tumor and draining lymph nodes) require the infrastructure and exp

175 they are rare, including adipose, lung, skin-draining lymph nodes, and a previously undescribed popul

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

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

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

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

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

181 ited T(H) cell TGF-beta signalling in tumour-draining lymph nodes, causing reorganization of tumour v

182 y extensive Treg proliferation in the uterus-draining lymph nodes, comprising 70% neuropilin 1(+) tTr

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

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

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

186 promotes DC maturation and migration to skin-draining lymph nodes, partially through MC-derived TNF,

187 RNA vaccine at the injection site and in the draining lymph nodes, performed cellular analyses of the

188 sed migration of lung dendritic cells to the draining lymph nodes, resulting in greater numbers of vi

189 e TR1 cells and their recruitment to the CNS-draining lymph nodes, sparing their liver-draining count

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

191 e maturation of dendritic cells in the tumor-draining lymph nodes, subsequently initiating T cell-med

192 mice, ARG1-containing EVs are transported to draining lymph nodes, taken up by dendritic cells and in

193 In draining lymph nodes, tdTomato-positive (tdTomato(+)) AS

194 also induce germinal centre reactions in the draining lymph nodes, where diversification and maturati

195 he interfollicular regions of the intestinal draining lymph nodes, where they act to limit TfH respon

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

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

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

199 ce including blood, bone marrow, spleen, and draining lymph nodes.

200 of dendritic cells and T-cell priming in the draining lymph nodes.

201 oid organs with the exception of the thyroid-draining lymph nodes.

202 DC differentiation in the brain and in tumor-draining lymph nodes.

203 cell function within the TME but not in the draining lymph nodes.

204 en-primed dendritic cell numbers in the skin-draining lymph nodes.

205 ruitment of activated dendritic cells to the draining lymph nodes.

206 odes, which are known to accumulate in joint-draining lymph nodes.

207 prime parasite-specific CD8 T cells in liver-draining lymph nodes.

208 orm and improved immune cell infiltration in draining lymph nodes.

209 2L(hi)CD44(lo)Foxp3(+) central Treg cells in draining lymph nodes.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

224 , and BAFF(+) CD11b(hi) NK cells expanded in draining lymph nodes.

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

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

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

228 fibroblastic reticular cell networks in the draining lymph nodes.

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

230 ferentiation in the lung, independent of the draining lymph nodes.

231 T cell subtype interacting with DCs in mouse draining lymph nodes.

232 s that carry the bacteria through successive draining lymph nodes.

233 TB(4) receptors (R) in vitro and in inflamed draining lymph nodes.

234 -PD-1 augmented T cell infiltration in tumor-draining lymph nodes.

235 pe 2 conventional dendritic cells (cDC2s) in draining lymph nodes.

236 es which also depend upon T cell egress from draining lymph nodes.

237 lariae migrated through lymphatic vessels to draining lymph nodes.

238 uce migration of Th2-skewing CD301b(+) DC to draining lymph nodes.

239 eficient Th2 cells were retained in the lung-draining lymph nodes.

240 ed inflammatory Th1 populations in allograft draining lymph nodes.

241 to persistence at the injection site and in draining lymph nodes.

242 monocytes and then delivered to mediastinal draining lymph nodes.

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

244 s circulating between parenchymal organs and draining lymph nodes; injection of known amounts of mole

245 ation on T cells population in the wound and draining lymph nodes; on day 14, these mice also display

246 more melanoma cells per microlitre in tumour-draining lymph than in tumour-draining blood.

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

248 th IL-15 and CpG DNA are elevated in microbe-draining lymphatic tissues, and unraveling the basis for

249 s three factors: efficient antigen uptake in draining lymphatics from the site of injection, protecti

250 omes offered the most rapid clearance to the draining lymphatics with cationic liposomes forming a de

251 ote longer retention of the liposomes at the draining lymphatics.

252 eron expression at the injection site and in draining lymphoid tissue compared to a nonamphiphilic co

253 itization and the generation of Th1 cells in draining lymphoid tissues; (c) decreases graft infiltrat

254 r SAH, while suggesting that modulating this draining may offer therapeutic approaches to alleviate S

255 h egress of CD69+/CD103+ CD8+ T cells to the draining mediastinal LN via the lymphatic vessels, which

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

257 ietary Ags preferentially in lymphoid organs draining mucosal barriers, likely as a result of dysregu

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

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

260 dera at Kilauea Volcano in 2018 included the draining of an active lava lake, which provided a window

261 e show that this transition corresponds to a draining of the interface inducing a local dehydration o

262 ubsidence of Ambrym's caldera and concurrent draining of the lava lakes.

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

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

265 xposure impacts microbial respiration of DOC draining permafrost soils.

266 LV) exploits the sentinel macrophages in the draining popliteal lymph node (pLN) to infect highly per

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

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

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

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

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

274 mically peripheral dendritic cells from skin-draining sites.

275 imes more temperature sensitive than streams draining steeper watersheds.

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

277 e grounding line ice discharge of 176 basins draining the Antarctic Ice Sheet from 1979 to 2017.

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

279 export occur following wildfires in streams draining the Central Siberian Plateau.

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

281 racterization of meningeal lymphatic vessels draining the CNS.

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

283 ite was involved and behaved as parasitoids, draining the host of its internal fluids and killing it.

284 ke into both lymphatic and blood capillaries draining the injection site.

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

286 moving into warm, low-elevation tributaries draining the same bedrock lithology.

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

288 tive downregulation of LXA(4) in lymph nodes draining the site of immunization, while at the same tim

289 s in naive, unchallenged mice, including LNs draining the skin, lungs, and gastrointestinal tract.

290 selenium concentrations reported for streams draining these fills.

291 idespread access to the microvasculature and draining to the APC-rich perivasculature.

292 oid space, and space surrounding large veins draining toward the dural sinuses on fluid-attenuated in

293 rting, gushing, sloshing, soaking, dripping, draining, trickling, pooling, and pouring-despite tremen

294 AVF draining vein diameter and blood flow rate were assessed

295 n CT and MRI in AVM size, feeding artery and draining vein diameter, and artifact score (P >.05 for a

296 fundamentally limited by effects from large draining veins.

297 Absence of feeding and/or draining vessel was predictive of good VA (P = 0.004).

298 Our results further indicate that large draining vessels, prominently residing in proximity of t

299 y of ecosystem respiration (R) among streams draining watersheds with different geomorphic characteri

300 Streams draining watersheds with stormwater ponds had consistent