ライフサイエンスコーパス: lymphatic vessel

1 egrin and thus ensures proper development of lymphatic vessels.

2 d co-localization with tumor macrophages and lymphatic vessels.

3 e occur along cranial nerves to extracranial lymphatic vessels.

4 mphovenous valves, and for the patterning of lymphatic vessels.

5 ction molecules VE-cadherin and claudin 5 in lymphatic vessels.

6 rent molecular signature from blood and true lymphatic vessels.

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

8 es, such as lymphangiogenesis and obstructed lymphatic vessels.

9 e semipermeable barrier in blood vessels and lymphatic vessels.

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

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

12 lve the dynamic pulsatile flow in collecting lymphatic vessels.

13 reast cancer metastasis occurs via blood and lymphatic vessels.

14 irregular, enlarged and excessively branched lymphatic vessels.

15 ndothelial growth factor receptor 3-positive lymphatic vessels.

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

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

18 roy and regress pathologic corneal blood and lymphatic vessels.

19 ndary antibody to quantify corneal blood and lymphatic vessels.

20 essurized, single-valve segments of isolated lymphatic vessels.

21 of the heart after an injury is supported by lymphatic vessels.

22 e chemokines to enable formation of coherent lymphatic vessels.

23 and it directly depends on tumor-associated lymphatic vessels.

24 ignaling that fail to develop intact cardiac lymphatic vessels.

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

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

27 present on cancer-associated macrophages and lymphatic vessels; activation of VEGFR3 signaling foster

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

29 lattice Boltzmann model includes an initial lymphatic vessel and a collecting lymphangion embedded i

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

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

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

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

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

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

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

37 to highlight and contextualize the roles of lymphatic vessels and lymphangiogenesis in immunobiology

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

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

40 d requires an intricate network of blood and lymphatic vessels and nerves to provide nutrients and el

41 the entry and transport of tumor cells into lymphatic vessels and on to distant organs.

42 bust, spontaneous contractions of collecting lymphatic vessels and one-way secondary lymphatic valves

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

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

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

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

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

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

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

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

51 ry of transplanted lungs demonstrated robust lymphatic vessels, and functional assays demonstrated ly

52 structure composed of fibroblasts, blood and lymphatic vessels, and immune cells.

53 roblasts, extracellular matrix, vascular and lymphatic vessels, and nerves.

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

55 to immune cells to help them find blood and lymphatic vessels, and to endothelial cells to stabilize

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 Herein, we use the lymphatic vessel architecture at the limbal border of th

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

60 Lymphatic vessels are important for these functions in o

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 to determine whether and where intracranial lymphatic vessels are present.

65 Finally, we show that lymphatic vessels are required for cardiac regeneration

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

67 Additionally, liver lymphatic vessels are thought to drain to perihepatic ly

68 easurements suggest that rat tail collecting lymphatic vessels are under an axial stretch of ~1.24 un

69 It is likely that collecting lymphatic vessels are under axial strain in vivo and tha

70 ndothelial cells (ECs), which line blood and lymphatic vessels, are generally described to come from

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

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

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

74 ificantly better regressed corneal blood and lymphatic vessels at 1 week after the treatment compared

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

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

77 use secreted factors preferentially drain to lymphatic vessels before dilution in the blood, we hypot

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

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

80 s control maintenance of established corneal lymphatic vessels, but not blood vessels.

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

82 red lymphatic contractile activity in MetSyn lymphatic vessel by increasing phasic contractile freque

83 eeper that maintains separation of blood and lymphatic vessels by limiting the plasticity of committe

84 f wound healing, including the growth of new lymphatic vessels by which immune cells, protein, and fl

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

86 Moreover, lymphatic vessels collapse and become dysfunctional as m

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

88 Peritumoral lymphatic vessels connect the primary tumor to lymph nod

89 n lymphatic muscle influences the diminished lymphatic vessel contractions in MetSyn animals.

90 on and formed physical connections with host lymphatic vessels, demonstrating a mechanism by which ly

91 Lymphatic vessel density (LVD) was determined by immunoh

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

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

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

95 Lymphatic vessel density did not impact the time to deve

96 Lymphatic vessel density in CLAD patients did not differ

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

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

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

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

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

102 We here demonstrate that cardiac lymphatic vessels develop in young adult zebrafish, usin

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

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

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

106 sly shown that TBX1 is required for systemic lymphatic vessel development in prenatal mice and it is

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

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

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

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

111 t ACKR2 regulates macrophage dynamics during lymphatic vessel development.

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

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

114 show that this lineage is indispensable for lymphatic vessel development.

115 lenvatinib treatment abrogated the increased lymphatic vessels development in the endometriotic lesio

116 We show that the remodelled lymphatic vessel displayed increasing intrinsic contract

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

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

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

120 t owing to the characterization of meningeal lymphatic vessels draining the CNS.

121 Heterogeneity of lymphatic vessels during embryogenesis is critical for o

122 However, the role of these lymphatic vessels during neuroinflammation is not well u

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

124 lymph vascularized areas, a higher number of lymphatic vessel end points, and branching points and in

125 Lymphatic vessel endothelial hyaluronan receptor 1 (LYVE

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

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

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

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

130 ons with diaphragms) associated with LYVE-1 (lymphatic vessel endothelial hyaluronan receptor 1), neu

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

132 ifferentiation and function markers (LYVE-1 [lymphatic vessel endothelial hyaluronan receptor 1]: p <

133 Macrophages expressing lymphatic vessel endothelial hyaluronan receptor-1 were

134 2-FLAIR and T1-weighted black-blood imaging, lymphatic vessels enhance with gadobutrol, a gadolinium-

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

136 Lymphatic vessel expansion occurs in two distinct phases

137 Lymphatic vessels facilitate fluid homeostasis, immune c

138 fective coronary artery development, cardiac lymphatic vessels fail to expand onto the ventricle.

139 In a microfluidic maze mimicking lymphatic vessels, filariae follow the direction of the

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

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

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

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

144 Lymphatic vessels form a critical component in the regul

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

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

147 ed three-dimensional imaging to characterize lymphatic vessel formation in the mammalian embryonic ki

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

149 est that the blockade of pathways regulating lymphatic vessel formation shapes an inflammatory respon

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

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

152 helial overproduction of miR-204 accelerates lymphatic vessel formation, suggesting a critical positi

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

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

155 Using mesenteric lymphatic vessels from C57BL/6J, Ub-CreER(T2) ;Rasa1(fx/

156 Mesenteric lymphatic vessels from high-fructose diet-induced metabo

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

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

159 1 (-/-) Apoe (-/-) mice showed impairment of lymphatic vessel function with decreased drainage of int

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

161 RATIONALE: Lymphatic vessels function to drain interstitial fluid f

162 Conversely, tumor blood and lymphatic vessel growth is in part regulated by the immu

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

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

165 via crosstalk with surrounding renal cells, lymphatic vessels have been implicated in the progressio

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

167 oncept along with the discovery of meningeal lymphatic vessels have, in recent years, highlighted tha

168 regulate contractile function in collecting lymphatic vessels; however, less is known about the role

169 ardinal marker for lymphatic endothelium-the lymphatic vessel hyaluronan receptor-1 (Lyve-1).

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

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

172 The study shows that the remodeling of lymphatic vessels in cancer is influenced by CCL27 and C

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

174 nsion of high endothelial venules (HEVs) and lymphatic vessels in comparison to the TPLNs.

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

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

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

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

179 Lymphatic vessels in meninges drain interstitial fluid i

180 pressor, leads to misconnection of blood and lymphatic vessels in mice and humans.

181 eal the major spinal pathways for outflow to lymphatic vessels in mice.

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

183 Peripheral lymphatic vessels in patients with HFpEF exhibit structu

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

185 We did not observe any lymphatic vessels in spinal dura mater.

186 evidence of organ-specific heterogeneity of lymphatic vessels in the context of solid organ transpla

187 Lymphatic vessels in the donor lung exhibited active spr

188 the development, structure, and function of lymphatic vessels in the healthy adult kidney.

189 based on the ligation of one of two parallel lymphatic vessels in the hind limb of sheep and the eval

190 The functional state of lymphatic vessels in the lower extremities of patients w

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

192 e recently emerged controversial role of the lymphatic vessels in tumor dissemination and cancer immu

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 d enhanced expression of CXCR3 and increased lymphatic vessel infiltration.

197 Although lymphatic vessels initially arise from embryonic veins,

198 ritical homeostatic regulators of collecting lymphatic vessel integrity.

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

200 culature, the barrier function of collecting lymphatic vessels is also important by ensuring efficien

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

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

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

204 ntravertebral regions of the sacral spine to lymphatic vessels, leading to sacral and iliac LNs.

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

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

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

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

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

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

211 and is associated with increased numbers of lymphatic vessels (LV) and tumor-associated macrophages

212 Cranial lymphatic vessels (LVs) are involved in the transport of

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

214 The formation of new lymphatic vessels (lymphangiogenesis), or remodeling of

215 or PROX1 is necessary for the development of lymphatic vessels, lymphatic valves (LVs) and lymphoveno

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

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

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

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

220 Clearance of CSF from the spine to lymphatic vessels may have significance for many conditi

221 Recent work has shown that meningeal lymphatic vessels (mLVs), mainly in the dorsal part of t

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

223 ession was significantly decreased in MetSyn lymphatic vessels, myosin light chain 20, MLC(20) phosph

224 We report that lymphatic vessels near the cribriform plate undergo lymp

225 els drains through the interstitium into the lymphatic vessel network and this drainage is different

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

227 tly the peripheral immune system through the lymphatic vessel network is a question of significant cl

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

229 Although lymphatic vessels of cervical and thoracic skin develop

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

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

232 A new study shows that in addition, lymphatic vessels of the skin are intimately associated

233 unctional changes in the intact, remodelling lymphatic vessel over a 42-day period.

234 HFpEF showed rarefaction of small blood and lymphatic vessels (p = 0.003 and p = 0.012, respectively

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

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

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

238 in a CCR10-dependent manner, while abnormal lymphatic vessel patterning in CCR10-deficient mice conf

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

240 The gut-brain axis formed by blood and lymphatic vessels paves the way for microbiota to impact

241 nents, including cancer-associated blood and lymphatic vessels, pericytes, cancer associated fibrobla

242 l therapeutic target to selectively modulate lymphatic vessel permeability and function.

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

244 Lymphatic vessels play important roles in coordinating f

245 Loss of popliteal lymphatic vessel (PLV) contractions, which is associated

246 Moreover, the density of M-LECPs and lymphatic vessels positive for myeloid marker proteins s

247 Lymphatic vessels provide a route of fluid, macromolecul

248 The spontaneous contractions of collecting lymphatic vessels provide an essential propulsive force

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

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

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

252 In addition, the presence of functional lymphatic vessels regulates the formation of tumor infla

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

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

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

256 itatively assessed the development of kidney lymphatic vessels, remodeling from a ring-like anastomos

257 and Ca(v)3.1(-/-); 3.2(-/-) double knock-out lymphatic vessels responded similarly to mibefradil and

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

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

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

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

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

263 and refill time after manual emptying of the lymphatic vessels showed no differences between the 2 gr

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

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

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

267 Blood and lymphatic vessels structurally bear a strong resemblance

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

269 The kidney contains a network of lymphatic vessels that clear fluid, small molecules, and

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

271 cells including high endothelial venules and lymphatic vessels that resemble secondary lymphoid organ

272 dipose hypertrophy, dysfunction of blood and lymphatic vessels, the overall oestrogen dependence and

273 the docking and entry of dendritic cells to lymphatic vessels through selective adhesion to its liga

274 nd skin-inoculated filariae migrated through lymphatic vessels to draining lymph nodes.

275 through sequential lymph nodes and efferent lymphatic vessels to enter the bloodstream.

276 port that Streptococcus pyogenes also hijack lymphatic vessels to escape a local infection site, tran

277 We then highlight the contributions of lymphatic vessels to multiple forms of renal pathology,

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

279 surgery, and its rapid transport through the lymphatic vessels to the SLN is then visualized with dyn

280 is established by active sprouting of donor lymphatic vessels towards the host and the formation of

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

282 ntial for the development and maintenance of lymphatic vessel valves.

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

284 , which permits in vivo imaging of blood and lymphatic vessels via fluorescence microscopy.

285 es on orchestrated contraction of collecting lymphatic vessels, via lymphatic muscle cells and one-wa

286 Lymphatic vessel volume fraction and fractal dimension s

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

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

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

290 Larger collecting lymphatic vessels were located in fibrotic septa between

291 Donor lymphatic vessels were numerous at the site of anastomos

292 These valves are present in the collecting lymphatic vessels, which generally have lymphatic muscle

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

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

295 cells to the draining mediastinal LN via the lymphatic vessels, which we term retrograde migration.

296 Suppressing miR-204 leads to loss of lymphatic vessels while endothelial overproduction of mi

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

298 The function of lymphatic vessels within tertiary lymphoid organs remain

299 There are no conventional lymphatic vessels within the CNS parenchyma, although it

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