ライフサイエンスコーパス: lymphatic vessel

1 , it is unknown whether the SC is a blood or lymphatic vessel.

2 irregular, enlarged and excessively branched lymphatic vessels.

3 ndothelial growth factor receptor 3-positive lymphatic vessels.

4 larly distinct from those found in veins and lymphatic vessels.

5 ial cells, where it regulates development of lymphatic vessels.

6 es, such as lymphangiogenesis and obstructed lymphatic vessels.

7 oincidentally steering cell collectives into lymphatic vessels.

8 inhibition because it is highly expressed in lymphatic vessels.

9 valve (LVV) prevents backflow of blood into lymphatic vessels.

10 ity, to developing, resting and regenerating lymphatic vessels.

11 bioactive material to blood capillaries and lymphatic vessels.

12 s in the control of growth and remodeling of lymphatic vessels.

13 oietin 2 (Ang2) deficiency leads to abnormal lymphatic vessels.

14 recirculate to secondary lymphoid organs via lymphatic vessels.

15 ading to incomplete separation of venous and lymphatic vessels.

16 ssing Cyp26b1 had hypoplastic lymph sacs and lymphatic vessels.

17 e involved in lymphocyte trafficking via the lymphatic vessels.

18 nce of blood endothelial cells in peripheral lymphatic vessels.

19 od filled lymph sacs and hyperplastic dermal lymphatic vessels.

20 c process of intraluminal valve formation in lymphatic vessels.

21 levated tumor Adm expression led to enlarged lymphatic vessels.

22 ed macrophages upstream of blocked or absent lymphatic vessels.

23 e semipermeable barrier in blood vessels and lymphatic vessels.

24 r the remodeling and maturation of blood and lymphatic vessels.

25 rent molecular signature from blood and true lymphatic vessels.

26 he endothelial cells that line the blood and lymphatic vessels.

27 lve the dynamic pulsatile flow in collecting lymphatic vessels.

28 e as well as enlarged jugular lymph sacs and lymphatic vessels.

29 Gy radiation, popliteal lymphadenectomy, and lymphatic vessel ablation.

30 latures, the lack of functional intratumoral lymphatic vessels, abnormal tumor microenvironment, and

31 We show that dural lymphatic vessels absorb CSF from the adjacent subarachn

32 there is a marked decline in the density of lymphatic vessels, accompanied by accumulation of low-MW

33 manner; and induces ICAM-1 up-regulation on lymphatic vessels, allowing neutrophils to crawl along t

34 the tenet that orbital adipose tissue lacks lymphatic vessels and analyzed the clinicopathologic dif

35 (+/-) mice spontaneously develop corneal and lymphatic vessels and are deficient in sVEGFR-3.

36 rast agents to target cellular biomarkers in lymphatic vessels and can be detected by OCT using a pha

37 itiate sprouting or differentiation of trunk lymphatic vessels and did not form a thoracic duct.

38 ntial differences between peripheral and CNS lymphatic vessels and examine the purported mechanisms o

39 hich directs egress from the skin via dermal lymphatic vessels and extravasation into the LN parenchy

40 ctor administration induced robust growth of lymphatic vessels and helped to preserve the structure o

41 xpressing the cognate chemokine receptors to lymphatic vessels and LEC permeability by inducing the d

42 ervations suggest that downstream mesenteric lymphatic vessels and lymph drainage into mesenteric lym

43 deficient mice develop dilated, blood-filled lymphatic vessels and lymphatic capillaries that are ect

44 e causes defects in maturation of collecting lymphatic vessels and lymphatic valve formation, uncover

45 nt, treatment with DMH1 altered fibroblasts, lymphatic vessels and macrophages to be less tumor promo

46 s been widely used to conveniently visualize lymphatic vessels and other Prox1-expressing tissues suc

47 entry of tissue-infiltrated neutrophils into lymphatic vessels and subsequent crawling along the lumi

48 escribe the recently characterized meningeal lymphatic vessels and their role in drainage of the brai

49 hat DCs docked to the basolateral surface of lymphatic vessels and transited to the lumen through hya

50 uable tool for intravital imaging of corneal lymphatic vessels and valves and can be used to study pa

51 ins tissue fluid balance, and dysfunction of lymphatic vessels and valves causes human lymphedema syn

52 ef episode of initial inflammation regressed lymphatic vessels, and a significant increase in CD11b(+

53 ted in increased LEC proliferation, enlarged lymphatic vessels, and abnormal lymphatic vessel morphog

54 d a pure committed LEC phenotype, formed new lymphatic vessels, and expressed lymphangiogenic factors

55 e amount of the inoculum within the lumen of lymphatic vessels, and the timing of the transport indic

56 ria for distinguishing the DT from blood and lymphatic vessels; and (c) presence of a DT wall organiz

57 Thus, facial lymphatic vessels appear to be the first functional lymp

58 Our results show that major trunk lymphatic vessels are conserved in the zebrafish, and pr

59 Lymphatic vessels are critical for the maintenance of ti

60 We conclude that human lymphatic vessels are highly sensitive to nifedipine in

61 Levels of VEGFC and markers of lymphatic vessels are increased in CRC tissues from pati

62 These findings suggest that lymphatic vessels are intimately linked with the de novo

63 Donor lymphatic vessels are not anastomosed to that of the rec

64 k corneal transplantation in which blood and lymphatic vessels are present and treatment begins at th

65 Primitive lymphatic vessels are remodeled into functionally specia

66 iated with increased immune suppression, yet lymphatic vessels are required for fluid drainage and im

67 Lymphatic vessels are thought to arise from PROX1-positi

68 Lymphatic vessels are thought to contribute to metastasi

69 mediastinal draining lymph nodes; increased lymphatic vessel area; and graft infiltration of CD4(+),

70 Here, we identified LECs, which line the lymphatic vessels, as a niche for Mycobacterium tubercul

71 a thorough and complete description of trunk lymphatic vessel assembly.

72 promoter to drive strong EGFP expression in lymphatic vessels at all stages of development and in ad

73 pressed throughout the developing mesenteric lymphatic vessels at E16.5, and that, by E18.5, Notch1 e

74 the arrest of tumor cells in the collecting lymphatic vessels at the junction with the lymph node su

75 ransit of leukocytes and tumor cells through lymphatic vessels based largely onin vitrostudies with r

76 promise as a molecule to control and regress lymphatic-vessel-based dysfunction.

77 mary endothelial cells from dermal blood and lymphatic vessels (blood vascular endothelial cells and

78 Given new evidence that lymphatic vessels both correlate with intratumoral lymph

79 r LNs of OVA/CFA-immunized mice not only via lymphatic vessels but also from blood, across high endot

80 issue or invade distant organs via blood and lymphatic vessels, but the role of lymphangiogenesis in

81 Instead, each collecting lymphatic vessel can individually contract and dilate pr

82 Collecting lymphatic vessels (CLVs), surrounded by fat and endowed

83 Moreover, lymphatic vessels collapse and become dysfunctional as m

84 EMT cells preferentially migrated toward lymphatic vessels compared with blood vessels, both in v

85 Lymphatic vessels constitute a ubiquitous countercurrent

86 to elevated downstream pressure, collecting lymphatic vessels containing one valve (incomplete lymph

87 , double-blinded clinical trial: conversely, lymphatic vessel contraction frequency was increased and

88 Lymphatic vessel density (LVD) was determined by immunoh

89 g rate (r = -0.9812, P < 0.0005) and initial lymphatic vessel density (r = -0.9449, P < 0.005).

90 GFC from the adenoviral vector had increased lymphatic vessel density and more metastases in lymph no

91 luded paw thickness, lymphatic drainage, and lymphatic vessel density as measured by podoplanin immun

92 by indocyanine green clearance and increased lymphatic vessel density as measured by podoplanin immun

93 Lymphatic vessel density did not impact the time to deve

94 cavenging receptor, ACKR2, display increased lymphatic vessel density in a range of tissues under res

95 Lymphatic vessel density in CLAD patients did not differ

96 ination of embryonic skin revealed that this lymphatic vessel density phenotype is developmentally es

97 rtum breast cancers have increased peritumor lymphatic vessel density that correlates with increased

98 Moreover, lymphatic vessel density was increased in normal postpar

99 The dermis revealed enhanced lymphatic vessel density, and transcriptional profiling

100 ion in obesity is characterized by decreased lymphatic vessel density, decreased collecting lymphatic

101 lymphatic vessel pumping capacity, decreased lymphatic vessel density, decreased lymphatic migration

102 duces lymphatic leakiness, decreases initial lymphatic vessel density, impairs collecting vessel pump

103 EPR effect were evaluated, such as blood and lymphatic vessel density, intratumoral hypoxia, and the

104 us lymphatic collecting vessel pumping rate, lymphatic vessel density, lymphatic leakiness, and lymph

105 displayed a reciprocal phenotype of reduced lymphatic vessel density.

106 er, we have recently discovered that corneal lymphatic vessels develop luminal valves as lymphangioge

107 t begin to address how fluid flow influences lymphatic vessel development and function.

108 teraction represents a critical regulator of lymphatic vessel development and the transcriptional net

109 ledge of the molecular mechanisms underlying lymphatic vessel development is still limited.

110 owerful model organism that enables study of lymphatic vessel development using high-resolution imagi

111 investigated the functional role of flow in lymphatic vessel development using mice deficient for th

112 evelopment, arterial mural cell coating, and lymphatic vessel development, required sphingosine 1-pho

113 ation but also plays a central role in blood-lymphatic vessel development, tumor metastasis, and prev

114 enzyme contributes to later blood vessel or lymphatic vessel development.

115 kinase 5 (Cdk5) is an essential regulator of lymphatic vessel development.

116 t ACKR2 regulates macrophage dynamics during lymphatic vessel development.

117 through cell-type-specific networks and that lymphatic vessel dilation occurs secondarily to increase

118 Surprising recent evidence suggests that lymphatic vessels do not merely represent passive channe

119 In most tissues, lymphatic vessels drain excess interstitial fluid back t

120 ased blood vessel permeability and decreased lymphatic vessel drainage during inflammation, highlight

121 The diameters of lymphatic vessels draining Ang-4- or VEGF-C (positive co

122 Mice lacking lymphatic vessels, due either to loss of the lymphangiog

123 ilizing the endothelium of microvascular and lymphatic vessels during ANDV infection.

124 latelet CLEC-2 signaling in the formation of lymphatic vessels during development.

125 nk to form an intricate, branched network of lymphatic vessels during embryogenesis.

126 blation of Hdac3 in mice led to blood-filled lymphatic vessels, edema, defective lymphovenous valve m

127 onstitute the luminal layer of all blood and lymphatic vessels, emerge de novo from the mesoderm in a

128 uding blood vessel endothelial cells (BECs), lymphatic vessel endothelial cells (LECs), bone marrow-d

129 milar to lymphatic regression, the number of lymphatic vessel endothelial hyaluronan receptor 1 (LYVE

130 and lymphatic markers including podoplanin, lymphatic vessel endothelial hyaluronan receptor 1 (LYVE

131 atic endothelial cell markers podoplanin and lymphatic vessel endothelial hyaluronan receptor 1 (LYVE

132 n vivo imaging of the expression profiles of lymphatic vessel endothelial hyaluronan receptor 1 (LYVE

133 n of Chd4 specifically in cells that express lymphatic vessel endothelial hyaluronan receptor 1 (LYVE

134 al sodium channel gamma expression, and more lymphatic vessel endothelial hyaluronan receptor 1-posit

135 LYVE-1 (lymphatic vessel endothelial hyaluronan receptor-1) is a

136 Immunohistochemistry was performed with lymphatic vessel endothelial hyaluronate receptor 1 (LYV

137 2-FLAIR and T1-weighted black-blood imaging, lymphatic vessels enhance with gadobutrol, a gadolinium-

138 onstrates definitively that mouse collecting lymphatic vessels exhibit autonomous, large-amplitude co

139 Hdac3-deficient lymphovenous valves and lymphatic vessels exhibited reduced expression of the tr

140 ease growth factors such as VEGF-C to induce lymphatic vessel expansion (lymphangiogenesis) in primar

141 Lymphatic vessel expansion occurs in two distinct phases

142 reater than that of arterioles or collecting lymphatic vessels exposed to uniform increases in pressu

143 Lymphatic vessels facilitate fluid homeostasis, immune c

144 and the spatial distribution of specialized lymphatic vessel features.

145 ross the nasal mucosa and enter the lumen of lymphatic vessels following inhalation.

146 cessary to match a unique need of intestinal lymphatic vessels for both continuous maintenance, due t

147 ector CD8(+) T cells accumulated at efferent lymphatic vessels for egress, whereas high affinity-stim

148 w is essential for the remodeling of primary lymphatic vessels, for ensuring the proper distribution

149 Taken together, these results indicate that lymphatic vessel formation after lung transplantation me

150 Cui et al. provide compelling evidence that lymphatic vessel formation improves lung allograft survi

151 g hPSCs, and that these cells are potent for lymphatic vessel formation in vivo and wound healing.

152 underlying molecular mediators of blood and lymphatic vessel formation within the orbital fat also w

153 portunity to study the mechanisms underlying lymphatic vessel formation, remodeling and function in a

154 lls is sufficient to inhibit tumor blood and lymphatic vessel formation, thus leading to a significan

155 of sunitinib-treated patients and increased lymphatic vessels found in 70% of neoadjuvant treated pa

156 ctly by isolating and cannulating collecting lymphatic vessels from genetically modified mice for ex

157 Mesenteric lymphatic vessels from MetSyn or LPS-injected rats exhib

158 e next addressed whether RCT was mediated by lymphatic vessels from the aortic wall by loading the ao

159 lymphatic endothelium, we excised collecting lymphatic vessels from the popliteal fossa of mice and r

160 hether CCB treatment is detrimental to human lymphatic vessel function and thereby exacerbates oedema

161 when extrapolating in vitro observations of lymphatic vessel function to the clinical situation, as

162 1 (-/-) Apoe (-/-) mice showed impairment of lymphatic vessel function with decreased drainage of int

163 +) cells, which have been linked to impaired lymphatic vessel function.

164 ular network affecting valve development and lymphatic vessel function.

165 RATIONALE: Lymphatic vessels function to drain interstitial fluid f

166 Collecting lymphatic vessels generate pressure to transport lymph d

167 lpha (TNF-alpha) coupled with VEGFA elicited lymphatic vessel genesis significantly above either fact

168 Inflammation stimulates new lymphatic vessel growth (inflammatory lymphangiogenesis)

169 pes simplex virus type-1 (HSV-1) induces new lymphatic vessel growth (lymphangiogenesis) in the corne

170 The secreted protein CCBE1 is required for lymphatic vessel growth in fish and mice, and mutations

171 endothelial cell tips are a prerequisite for lymphatic vessel growth in vivo, and a VEGFR3 blockade c

172 ch FOXC1 and FOXC2 regulate ERK signaling in lymphatic vessel growth.

173 ways for the specific growth of arteries and lymphatic vessels have been identified, but the mechanis

174 es of the glymphatic system and of meningeal lymphatic vessels have generated a lot of excitement, al

175 entery, TLOs are positioned along collecting lymphatic vessels in a manner expected to affect deliver

176 primes directly the neutrophils to enter the lymphatic vessels in a strictly CCR7-dependent manner; a

177 In addition to a loss of lymphatic vessels in CD118(-/-) mice, HSV-1 infection re

178 Anti-VEGFR3 antibody reduced numbers of lymphatic vessels in colons and prevented metastasis.

179 Although histological analysis of lymphatic vessels in donor grafts can yield information

180 stimulated a VEGFC-dependent development of lymphatic vessels in experimental tumors.

181 n in utero abolished the abnormally enlarged lymphatic vessels in FOXC-deficient embryos.

182 Here, we report the existence of meningeal lymphatic vessels in human and nonhuman primates (common

183 ata that directly address the exact roles of lymphatic vessels in lung allograft function and surviva

184 n of vascular endothelial cadherin (CDH5) on lymphatic vessels in mice and in human intestinal lympha

185 gans with the proposed function of meningeal lymphatic vessels in neurological disorders, specificall

186 intrinsic, active contractions of collecting lymphatic vessels in relation to their ability to active

187 tery (DM) is the major conduit for blood and lymphatic vessels in the gut.

188 ively transferred lymphocytes accumulated at lymphatic vessels in the lymph nodes of ADAP-deficient m

189 Endothelial cells line the lymphatic vessels in the lymphoid tissues and have frequ

190 locally that are involved in the genesis of lymphatic vessels in the normally avascular cornea in re

191 es, we performed a comprehensive analysis of lymphatic vessels in the skin of type 2 diabetic versus

192 s study provide new insight into the role of lymphatic vessels in transplant tolerance.

193 tion along with a subsequent constriction of lymphatic vessels in tumors.

194 fied an important role for disturbed flow in lymphatic vessels, in which it cooperates with the trans

195 nd allowed a convenient visualization of all lymphatic vessels, including those in the central nervou

196 ogical detection of tumor cells in blood and lymphatic vessels indicated both hematogenous and lympha

197 ing depth of tumor infiltration (P = 0.004), lymphatic vessel infiltration (P = 0.002), tumor differe

198 Here, we have analysed neutrophil-lymphatic vessel interactions in real time and in vivo u

199 trast, there was an initial robust growth of lymphatic vessels into the cornea of HSV-1-infected CD11

200 usly shown that HSV-1 elicits the genesis of lymphatic vessels into the cornea proper through epithel

201 te from the injection site, via the afferent lymphatic vessels, into the local lymph node.

202 ltration of the submucosa (P=0.002) but also lymphatic vessel invasion (P<0.001), multifocal tumor gr

203 sport of interstitial fluid and solutes into lymphatic vessels is important for maintaining interstit

204 Lymphangiogenesis, the growth of lymphatic vessels, is essential in embryonic development

205 mplex, consisting of fin muscles, bones, and lymphatic vessels, is involved in the hydraulic control

206 munity using a mouse model that lacks dermal lymphatic vessels (K14-VEGFR3-Ig mice).

207 hatic trafficking of immune cells, increased lymphatic vessel leakiness and changes in the gene expre

208 mphatic migration of immune cells, increased lymphatic vessel leakiness and decreased expression of l

209 terstitial hypertension collapsing blood and lymphatic vessels, limiting drug delivery.

210 ut of the meninges, we discovered functional lymphatic vessels lining the dural sinuses.

211 Lacteals are lymphatic vessels located at the center of each intestin

212 y found in the exocrine pancreas, with small lymphatic vessels located close to and around acini.

213 ovenous malformation (CM-AVM) is a blood and lymphatic vessel (LV) disorder that is caused by inherit

214 One of the main tasks of the lymphatic vessel (LV) system is the promotion of immune

215 Tumor lymphatic vessels (LV) serve as a conduit of tumor cell

216 Lymphatic vessels (LVs) are critical for immune surveill

217 The recent discovery of meningeal lymphatic vessels (LVs) has raised interest in their pos

218 Although stromal lymphatic vessels (LVs) serve as initial metastatic rout

219 Whereas in IL-7Ralpha(-/-) mice, dermal lymphatic vessels (LVs) were abnormally organized and ly

220 organization, high endothelial venules, and lymphatic vessels (LVs).

221 and displaying complete aplasia of the dural lymphatic vessels, macromolecule clearance from the brai

222 ffusion (chylothorax) frequently accompanies lymphatic vessel malformations and other conditions with

223 egulates many of the key steps in collecting lymphatic vessel maturation and development.

224 of lymphovenous hemostasis and its effect on lymphatic vessel maturation and synthesizes the outstand

225 cillatory shear stress (OSS), which promotes lymphatic vessel maturation, triggers Wnt/beta-catenin s

226 mphangiogenesis and identifies a property of lymphatic vessel memory in response to recurrent inflamm

227 Surprisingly, we found that the lymphatic vessel memory response did not depend on the v

228 er a priming mechanism to facilitate a rapid lymphatic vessel memory response: a potential important

229 ages were associated with the development of lymphatic vessel memory.

230 regulate inflammatory lymphangiogenesis and lymphatic vessel memory.

231 on, enlarged lymphatic vessels, and abnormal lymphatic vessel morphogenesis.

232 Here we report the surprising finding of a lymphatic vessel network in the dura mater of the mouse

233 uently influences lymphocyte trafficking and lymphatic vessel network organization.

234 ion accelerated the development a functional lymphatic vessel network.

235 rom embryonic lymphangiogenesis or quiescent lymphatic vessels observed in other tissues.

236 Cholangioscopy revealed dilated lymphatic vessels obstructing the bile duct and compound

237 Although lymphatic vessels of cervical and thoracic skin develop

238 mock-infected inoculum was identified within lymphatic vessels of the lamina propria and in spaces of

239 tubes freshly isolated from mouse collecting lymphatic vessels of the popliteal fossa.

240 ss immune function, I reevaluate the passive lymphatic vessel paradigm and discuss its relevance to a

241 dysfunction and lymphedema due to defective lymphatic vessel patterning and valve formation.

242 Importantly, FOXC2 completely rescues the lymphatic vessel patterning defects in mice lacking beta

243 Additionally, lymphatic vessel patterning is defective in these mice,

244 s with progression and metastasis, and local lymphatic vessels play complex and poorly understood rol

245 Blood and lymphatic vessels provide nutrients for the skin and ful

246 obese mice had markedly decreased collecting lymphatic vessel pumping capacity, decreased lymphatic v

247 mphatic vessel density, decreased collecting lymphatic vessel pumping frequency, decreased lymphatic

248 Lymphangiogenic growth factors improve lymphatic vessel regeneration and lymph node function af

249 es regulate the formation and maintenance of lymphatic vessels remain largely uncharacterized.

250 lammation and immunity critically depends on lymphatic vessel remodeling and drainage.

251 Lymphangiogenesis and lymphatic vessel remodeling are complex biological proce

252 Pecam1 deletion in mice results in impaired lymphatic vessel remodeling, including abnormal valve mo

253 d sets functionally related to inflammation, lymphatic vessel remodeling, lymphangiogenesis, and lipi

254 tion, a common clinical condition, regulates lymphatic vessel remodeling.

255 leads to the question of how each segment of lymphatic vessel responds to local signals that can cont

256 Our work reveals how lymphatic vessel responses are shaped by tissue speciali

257 Morphological analysis of the lymphatic vessels revealed a dramatic expansion during t

258 ester human skin, the phenotype of blood and lymphatic vessels roughly resembles the one in adult ski

259 Their results support the concept that the lymphatic vessel route is critical for RCT from atherosc

260 Thus, the lymphatic vessel route is critical for RCT from multiple

261 constriction was transmitted to the upstream lymphatic vessel segment even though it was protected fr

262 Lymphatic vessels serve as conduits for immune cell traf

263 ear the surgery site, whereas the collecting lymphatic vessels showed a gradually decreasing contract

264 and popliteal nodes with draining popliteal lymphatic vessel significantly decreased the presence of

265 ntal and/or functional defects affecting the lymphatic vessels: sporadic and familial forms of primar

266 in a collagen matrix in vitro, as well as in lymphatic vessel sprouting assayed ex vivo.

267 cells (LECs), consistent with an increase in lymphatic vessel sprouting in a three-dimensional lympha

268 TGFBIp-induced lymphatic vessel sprouting was inhibited by addition of

269 lar marker expression, pericyte changes, and lymphatic vessel sprouting were assessed.

270 mal epithelial cells, fibroblasts, blood and lymphatic vessels, structural components, and infiltrati

271 sity, suggesting neovascularization and rare lymphatic vessels suggestive of limited lymphangiogenesi

272 ro-lymphangiogenic macrophages to developing lymphatic vessel surfaces is increased in ACKR2-deficien

273 Lymphatic vessels surround follicles within the ovary, b

274 E-1), and podoplanin mRNA and contained more lymphatic vessels than tissue from patients without UFF.

275 However, cellular and Ag trafficking in the lymphatic vessels that connect an i.m. injection site wi

276 uced de novo generation of deep intratumoral lymphatic vessels that were highly permissive to invasio

277 s then leave the lymph node via the efferent lymphatic vessel to perform their systemic function.

278 the resulting fluid shear stress causes the lymphatic vessel to relax locally.

279 )(-/-) and inducible NO synthase (iNOS)(-/-) lymphatic vessels to controlled pressure steps followed

280 We have directly cannulated the ovine lymphatic vessels to detail the in vivo innate and adapt

281 Like many cancers, mammary carcinomas use lymphatic vessels to disseminate, and numerous clinical

282 of fluid pressure environments, allowing the lymphatic vessels to provide pumping when needed but rem

283 The contribution of lymphatic vessels to transplant pathophysiology remains

284 drenaline did not elicit normal increases in lymphatic vessel tone when maximal constriction was redu

285 Dural lymphatic vessels transport fluid into deep cervical LNs

286 ranscription of genes that are important for lymphatic vessel valve development.

287 elopment and maintenance of lymphovenous and lymphatic vessel valves.

288 Levels of podoplanin (a marker of lymphatic vessels), VEGFC, and VEGFR3 were increased in

289 t innate lymphoid cells that had invaded the lymphatic vessel wall, suggesting these cells may be med

290 l coverage (SMC coverage) of CLEC2-deficient lymphatic vessels was both premature and excessive, a ph

291 crofluorometric technique adapted to in vivo lymphatic vessels, we determined that rat mesenteric col

292 mune cells from the lymphoid organs into the lymphatic vessels; we investigated its role in the respo

293 Larger collecting lymphatic vessels were located in fibrotic septa between

294 nd in turn relies on an absence of blood and lymphatic vessels, which is remarkable given the cornea'

295 xistence of 'suction pressure' in collecting lymphatic vessels, which manifests as a transient drop i

296 mor blood vessels induced the development of lymphatic vessels, which may have contributed to the tre

297 the proliferation of LECs and the number of lymphatic vessels, while elevated tumor Adm expression l

298 easurement of the function of tumor-draining lymphatic vessels, with potential applications in the de

299 well as rare staining of podoplanin-positive lymphatic vessels within acutely inflamed orbital fat ti

300 Recent rediscoveries of lymphatic vessels within the dura mater surrounding the