ライフサイエンスコーパス: interstitial cell

1 gnaling pathways in glomerular, tubular, and interstitial cells.

2 valve by Lp(a) and is also secreted by valve interstitial cells.

3 y play a role in the mineralization of valve interstitial cells.

4 plays a role in the mineralization of valve interstitial cells.

5 with a transient decline on P8 primarily in interstitial cells.

6 cells, immune cells, and various classes of interstitial cells.

7 ne TGF-beta signaling between epithelial and interstitial cells.

8 GFRalpha(+) cells are distinct from c-Kit(+) interstitial cells.

9 tissue constructs seeded with porcine valve interstitial cells.

10 ific protein-1-expressing (FSP-1-expressing) interstitial cells.

11 tor IL-13ralpha2 in close proximity to valve interstitial cells.

12 onad that also gives rise to uncharacterised interstitial cells.

13 helium contributes only to non-steroidogenic interstitial cells.

14 s, 10.6% were glomerular cells, and 81% were interstitial cells.

15 ng primarily in CD45-positive leukocytes and interstitial cells.

16 some bronchial epithelial, endothelial, and interstitial cells.

17 gnals to cardiomyocytes, vascular cells, and interstitial cells.

18 ed the effects of Lp(a) and OxPL on valvular interstitial cells.

19 signalling and lysosomal homeostasis within interstitial cells.

20 dence, in the case of heart valves, as valve interstitial cells.

21 ling is activated in both cardiomyocytes and interstitial cells.

22 tedly induced via Rag1-Cre expression in CNS interstitial cells.

23 protein kinase 1) in cultured porcine valve interstitial cells.

24 ctor receptor-alpha positive (PDGFRalpha(+)) interstitial cells.

25 revented H19-induced mineralization of valve interstitial cells.

26 duced renal Epo in a limited number of renal interstitial cells.

27 duction in the number of EPO-producing renal interstitial cells.

28 reased the REPC fraction among Phd2-/- renal interstitial cells.

29 d DCN produced by prematurely differentiated interstitial cells accumulates in the extracellular matr

30 1) to be a mediator of Aldo-induced valvular interstitial cell activation and proteoglycan secretion

31 ation at the neonatal stage and varied valve interstitial cell activation at early and late stages.

32 dothelial injury and a cascade of immune and interstitial cell activation in the kidney lead to AKI.

33 Aldo enhanced valvular interstitial cell activation markers and induced endothe

34 Foxd1 is expressed in interstitial cells adjacent to nephron progenitor cells,

35 -derived cells to the expanded population of interstitial cells after kidney damage in animals and hu

36 aling is activated in tubular epithelial and interstitial cells after renal injury, and recombinant s

37 -catenin signaling in tubular epithelial and interstitial cells, along with increased expression of m

38 Moreover, we documented that valve interstitial cells also expressed ATX in CAVD.

39 hat reorganization of the vasculature and of interstitial cells also play critical roles in testis co

40 the native thymus, when combined with thymic interstitial cells and a natural decellularised extracel

41 ed expression of COX-2 in WT renal medullary interstitial cells and again the increase in formation o

42 HIF-2/EPO axis in FOXD1 stroma-derived renal interstitial cells and examined the role of individual P

43 acid in the mineralization of isolated valve interstitial cells and in a mouse model of CAVD.

44 rogenesis and osteogenesis of cultured valve interstitial cells and is downregulated in stenotic aort

45 transvalvular pressure can activate valvular interstitial cells and latent paracrine signaling cytoki

46 ) derived from smooth muscle cells, valvular interstitial cells and macrophages as the mediators of c

47 nd vascular smooth muscle cells, but also of interstitial cells and matrix.

48 appaB-dependent communication between NG2(+) interstitial cells and myoblasts.

49 s-attenuating role for Mrc2-expressing renal interstitial cells and suggest the involvement of a lyso

50 ecular, and histological changes of valvular interstitial cells and valvular endothelial cells associ

51 The proliferation of valve interstitial cells and ventricular valve endothelial cel

52 terogeneous enteric neuronal, smooth muscle, interstitial cell, and inflammatory abnormalities.

53 s) produces the acid-secreting copper cells, interstitial cells, and enteroendocrine cells of the sto

54 d by immunohistochemistry within epithelium, interstitial cells, and macrophages in the distal renal

55 67 labeling, rare positive COX-2 staining of interstitial cells, and negative or mild staining for p5

56 ecting duct, proximal tubule, distal tubule, interstitial cells, and rarely glomerular cells followin

57 expression in cultured mouse renal medullary interstitial cells, and Sirt1+/- mice displayed reduced

58 ng osteoblast differentiation in human valve interstitial cells, and that this can be a potential tar

59 orin (DCN) is repressed by FOXD1 in cortical interstitial cells, and we show that compound genetic in

60 r epithelial cells and macrophages and a few interstitial cells are the source of the cytokines and c

61 findings have pointed to the urothelium and interstitial cells as key participants in the transducti

62 The accumulation of these interstitial cells associated with collagen deposition a

63 ever, UUO induces RGC-32 expression in renal interstitial cells at the early stage of kidney injury,

64 of fibroblast activation, is limited to the interstitial cells at the early stage, and became appare

65 ronic inflammatory disease, and aortic valve interstitial cells (AVIC) play an important role in valv

66 ur aim was to determine whether aortic valve interstitial cells (AVICs) and pulmonary valve interstit

67 retch and inflammation in human aortic valve interstitial cells (AVICs).

68 derations, development, endothelial cell and interstitial cell biology, extracellular matrix biology,

69 In GFP chimeras, some interstitial cells but not tubular cells expressed GFP a

70 nduced COX2 expression in cultured medullary interstitial cells by immunoblot analysis.

71 systemic growth from a subset of enterocytes-interstitial cells-by promoting food intake and insulin/

72 RNA interference reduced primary human valve interstitial cell calcification.

73 progenitor cells (EPCs) and c-Kit(+) cardiac interstitial cells (cCICs) when cultured together sponta

74 vis-kidney junction regions whereas c-Kit(+) interstitial cells (CD117(+) /CD45(-) ) are found predom

75 At P30, four interstitial cell clusters are apparent with leaflet spe

76 t collagen- and glycosaminoglycan-expressing interstitial cell clusters, and prevalent ECM gene expre

77 METHODS AND In cultured porcine valve interstitial cells, CNP inhibited pathological different

78 We propose that FOXD1 lineage renal interstitial cells consist of distinct subpopulations th

79 , Sirt1 activation increased renal medullary interstitial cell COX2 expression both in vitro and in v

80 as documented on the mineralization of valve interstitial cell cultures.

81 However, conditional deletion of Wnt4 in interstitial cells did not reduce myofibroblast prolifer

82 These results indicate that BM-derived interstitial cells do not make a significant contributio

83 provide a molecular link between tubular and interstitial cells during CKD progression and identify S

84 The GLI1(+) interstitial cells eventually develop into two cell line

85 titial pericytes, and these FoxD1-derivative interstitial cells expand and differentiate into smooth

86 We establish that interstitial cells express Vegfa and respond, by prolife

87 eased proliferation of endothelial cells and interstitial cells expressing platelet-derived growth fa

88 protective factor for mouse renal medullary interstitial cells following oxidative stress and sugges

89 apoptosis in Sirt1-deficient renal medullary interstitial cells following oxidative stress.

90 did not calcify, whereas sheep aortic valve interstitial cells grown on control substrates calcified

91 Sheep aortic valve interstitial cells grown on TGA-pretreated collagen did

92 TGF-beta1-treated valvular interstitial cells had higher pre-stress (1100 nN) and e

93 lar cells, smooth muscle cells, and valvular interstitial cells, have also been shown to exhibit mult

94 ch suggests that impaired bladder Cajal-like interstitial cells (ICCs) are a important component in t

95 rn of expression of beta2-ARs in human valve interstitial cells (ICs) and assess their influence on d

96 Most smooth muscle tissues contain interstitial cells (ICs) in addition to contractile smoo

97 Interstitial cells (ICs) in close proximity to ASMCs and

98 and Results- Primary cultures of human valve interstitial cells (ICs) treated for 21 days with osteog

99 the presence and functional contribution of interstitial cells (ICs).

100 We recently reported a new class of interstitial cells in detrusor muscles and showed that t

101 To better understand how cortical interstitial cells in general, and FOXD1 in particular,

102 alveolar macrophages in lung, and epithelial/interstitial cells in other organs, including the reprod

103 The surviving cohort forms interstitial cells in the white matter (WM) and a band o

104 l changes of PV leaflets and passage zero PV interstitial cells in their protein and gene levels.

105 n of 5-HT(2B) receptors on human heart valve interstitial cells in vitro induces a proliferative resp

106 bundantly expressed in mouse renal medullary interstitial cells in vivo.

107 es, including endothelial, smooth muscle and interstitial cells, in the remodelled pulmonary arteriol

108 ther the mutant oncogene is expressed in CNS interstitial cells, including neuronal cells and progeny

109 Thus, VEGF-A, whether expressed by interstitial cells infected with an adenoviral vector or

110 ight Adamts19 as a novel marker for valvular interstitial cells; inference of gene regulatory network

111 was arbitrarily set at "i2t2": a mononuclear interstitial cell infiltrate present in at least 25% of

112 l segmental glomerulosclerosis together with interstitial cell infiltrates, upregulated gene expressi

113 eration of both tubular epithelial cells and interstitial cells is reduced by NS8593 treatment in UUO

114 flets from the same heart were collected and interstitial cells isolated.

115 Interstitial cells, known as platelet derived growth fac

116 However, bronchiolar epithelial cell and interstitial cell labeling was diminished at 40 days (p

117 rogenesis and inflammation in glomerular and interstitial cells, likely as the result of enhanced PPA

118 Both supporting and interstitial cell lineages arise from WT1(+) somatic pro

119 ditional CE cells and to both supporting and interstitial cell lineages, implying that cells in the C

120 but is dispensable for the smooth muscle and interstitial cell lineages.

121 Recent evidence suggests that interstitial cells may also play a role in determining t

122 duced osteogenic differentiation of valvular interstitial cells, mediated by OxPL and inhibited with

123 Thereby, interstitial cell migration and adhesion events, influen

124 he knee meniscus as a model system, we query interstitial cell migration in the context of migratory

125 ding of the fundamental mechanisms governing interstitial cell migration might lead to interventions

126 The limits of interstitial cell migration thus depend upon scaffold po

127 hypothesis that Fen may disrupt mitral valve interstitial cell (MVIC) homeostasis through its effects

128 cultured cells and, notably, in mitral valve interstitial cells (MVICs) obtained during mitral valve

129 In addition to scattered endothelial and interstitial cells, Notch-activated (EGFP(+)) cells unex

130 however, ongoing apoptosis of epithelial and interstitial cells occurred in lungs of SFTPC-/- mice, b

131 Its cellular origin from the interstitial cell of Cajal and distinctness from smooth

132 69I/+) mice than in single-mutant mice, both interstitial cell of Cajal hyperplasia and mast cell hyp

133 ;T669I/+) mice developed gastric and colonic interstitial cell of Cajal hyperplasia as well as cecal

134 The differential conduction pattern in the interstitial cell of Cajal is responsible for the genera

135 ar pathways downstream of KIT, expression of Interstitial Cell of Cajal-like markers, and release of

136 mal endocardial cushions (EC), and activated interstitial cells of adult diseased valves share charac

137 estinal stromal tumors (GIST) are related to interstitial cells of Cajal (ICC) and often contain acti

138 ated because SMC are electrically coupled to interstitial cells of Cajal (ICC) and PDGFRalpha(+) cell

139 be expressed in smooth muscle cells (SMCs), interstitial cells of Cajal (ICC) and platelet-derived g

140 Specialized cells known as interstitial cells of Cajal (ICC) are distributed in spe

141 Interstitial cells of Cajal (ICC) are pacemaker cells th

142 hysiological approaches to determine whether interstitial cells of Cajal (ICC) are present in the gui

143 Interstitial cells of Cajal (ICC) are putative pacemaker

144 Interstitial cells of Cajal (ICC) are required for norma

145 Interstitial cells of Cajal (ICC) are unique cells that

146 Ano1 channels are expressed by interstitial cells of Cajal (ICC) but not by smooth musc

147 Interstitial cells of Cajal (ICC) control intestinal smo

148 Two distinct populations of interstitial cells of Cajal (ICC) exist within the tunic

149 Interstitial cells of Cajal (ICC) express c-kit; however

150 Interstitial cells of Cajal (ICC) express the receptor t

151 KEY POINTS: Interstitial cells of Cajal (ICC) from murine colonic mu

152 Interstitial cells of Cajal (ICC) generate pacemaker act

153 Interstitial cells of Cajal (ICC) generate slow waves an

154 Interstitial cells of Cajal (ICC) generate slow waves.

155 Disruptions in interstitial cells of Cajal (ICC) have also been reporte

156 Interstitial cells of Cajal (ICC) have been identified i

157 Nitrergic nerves and interstitial cells of Cajal (ICC) have been implicated i

158 r activity, contractions and distribution of interstitial cells of Cajal (ICC) in human gastric muscl

159 The morphological features of interstitial cells of Cajal (ICC) in the gastrointestina

160 It has been generally assumed that interstitial cells of Cajal (ICC) in the human gastroint

161 Maintaining the integrity of networks of interstitial cells of Cajal (ICC) is essential to preser

162 gastrointestinal obstruction by hyperplastic interstitial cells of Cajal (ICC) or GISTs.

163 ffecting the vagus, muscle, enteric neurons, interstitial cells of Cajal (ICC) or other cellular comp

164 Interstitial cells of Cajal (ICC) provide important regu

165 Interstitial cells of Cajal (ICC) provide pacemaker acti

166 ver the past two decades has determined that interstitial cells of Cajal (ICC) serve as pacemaker cel

167 nsiderable speculation about the function of interstitial cells of Cajal (ICC) since their discovery

168 Slow waves (SWs) produced by interstitial cells of Cajal (ICC) underlie phasic contra

169 Interstitial cells of Cajal (ICC) were described more th

170 Interstitial cells of Cajal (ICC) were proposed as poten

171 ytium, including smooth muscle cells (SMCs), interstitial cells of Cajal (ICC), and cells expressing

172 ytium, including smooth muscle cells (SMCs), interstitial cells of Cajal (ICC), and cells expressing

173 omes from primary smooth muscle cells (SMC), interstitial cells of Cajal (ICC), and PDGFRalpha(+) cel

174 strointestinal (GI) muscles are generated by interstitial cells of Cajal (ICC), and these events acti

175 quantify nerves, S100beta for glia, Kit for interstitial cells of Cajal (ICC), CD45 and CD68 for imm

176 Klotho expression, enteric neurons, interstitial cells of Cajal (ICC), smooth muscle cells a

177 ice prevented GIST development, although the interstitial cells of Cajal (ICC), the cells of origin o

178 Altered number and function of interstitial cells of Cajal (ICC), the gastrointestinal

179 from smooth muscle cells, but present in the interstitial cells of Cajal (ICC), the pacemaker cells t

180 ker cells of the gastrointestinal tract, the interstitial cells of Cajal (ICC), where activation trig

181 es inflammatory responses leading to loss of interstitial cells of Cajal (ICC), which generate intest

182 olves neuropathy, myopathy, and depletion of interstitial cells of Cajal (ICC), which may cause dysrh

183 ought to originate in pacemaker cells termed interstitial cells of Cajal (ICC).

184 ves are generated and actively propagated by interstitial cells of Cajal (ICC).

185 channels, which are expressed exclusively in interstitial cells of Cajal (ICC).

186 Colonic intramuscular interstitial cells of Cajal (ICC-IM) are associated with

187 Intramuscular interstitial cells of Cajal (ICC-IM) are closely associa

188 slow waves (SWs) initiated in intramuscular interstitial cells of Cajal (ICC-IM) by activation of Ca

189 slow waves (SWs) initiated in intramuscular interstitial cells of Cajal (ICC-IM) by activation of Ca

190 Colonic intramuscular interstitial cells of Cajal (ICC-IM) exhibit spontaneous

191 ion between enteric nerves and intramuscular interstitial cells of Cajal (ICC-IM) in the stomach and

192 Intramuscular interstitial cells of Cajal (ICC-IM) play a critical rol

193 y in the colon is the intramuscular class of interstitial cells of Cajal (ICC-IM).

194 Intramuscular interstitial cells of Cajal (ICC-IMs) and cholinesterase

195 lls surrounding the myenteric plexus, called interstitial cells of Cajal (ICC-MY).

196 or is present in pacemaker cells such as the interstitial cells of Cajal (ICCs) and atypical SMCs tha

197 this hypothesis by quantifying densities of interstitial cells of Cajal (ICCs) and mapping slow-wave

198 e used Ca(2+) imaging to investigate whether interstitial cells of Cajal (ICCs) at these borders gene

199 patially to ETV1(+) cells, which include the interstitial cells of Cajal (ICCs) from which GISTs pres

200 BACKGROUND & AIMS: Depletion of interstitial cells of Cajal (ICCs) is common in diabetic

201 transplantation, murine stem cells (SCs) for interstitial cells of Cajal (ICCs), electrical pacemaker

202 ternatively, intermediate cells, such as the interstitial cells of Cajal (ICCs), might detect nitrerg

203 KIT is highly expressed in interstitial cells of Cajal (ICCs)-the presumed cell of

204 dent on release of carbon monoxide (CO) from interstitial cells of Cajal (ICCs).

205 nteric and submucosal plexus, had functional interstitial cells of Cajal and had an electromechanical

206 sis, but new information points to a role of interstitial cells of Cajal and mast cells.

207 Intramuscular interstitial cells of Cajal and platelet-derived growth

208 At a more basic level, the importance of interstitial cells of Cajal as pacemakers, neuromodulato

209 Interstitial cells of Cajal at the level of the deep mus

210 SMCs), circular smooth muscle cells (CSMCs), interstitial cells of Cajal distributed in the myenteric

211 ce demonstrating a mechanosensitive role for interstitial cells of Cajal in smooth muscle tissues.

212 Interstitial cells of Cajal in the deep muscular plexus

213 omach, but like Kit(W/W-v) mice, they lacked interstitial cells of Cajal in the gut and exhibited bil

214 the interactions between myenteric neurons, interstitial cells of Cajal in the myenteric region (ICC

215 autonomous mechanisms restore the numbers of interstitial cells of Cajal that are reduced in the nNOS

216 testinal muscles is generated by specialized interstitial cells of Cajal that produce the patterns of

217 Since the first description of 'interstitial cells of Cajal' in the mammalian gut in 191

218 astic transformation of gut pacemaker cells (interstitial cells of Cajal).

219 ies that bind to molecules in neurons, glia, interstitial cells of Cajal, and muscularis macrophages.

220 les of W/W(V) mice, which lack intramuscular interstitial cells of Cajal, did not affect membrane dep

221 ucosal > myenteric) and is not seen in glia, interstitial cells of Cajal, or smooth muscle.

222 astrointestinal muscles, and specifically in interstitial cells of Cajal, provides a means of transmi

223 Interstitial cells of Cajal, which express the calcium-a

224 Interstitial cells of Cajal, which express the receptor

225 no defects were found in enteric neurons or interstitial cells of Cajal.

226 immunoreactivity was located on non-neuronal interstitial cells of Cajal.

227 e gastrointestinal tract and arises from the interstitial cells of Cajal.

228 dgfralpha and were located near Kit-positive interstitial cells of Cajal.

229 Hand1 expression is restricted to muscle and interstitial cells of Cajal.

230 sis, melanogenesis, and gametogenesis and in interstitial cells of Cajal.

231 nd the enteric nervous system, including the interstitial cells of Cajal.

232 muscles that is mediated by mechanosensitive interstitial cells of Cajal.

233 pposition with, bundles of muscle fibers and interstitial cells of Cajal.

234 luding defects in neurons, smooth muscle, or interstitial cells of Cajal.

235 ymal transition and express markers of valve interstitial cells of different valvular layers, demonst

236 t predominantly in nuclei of endothelial and interstitial cells of mitral valves in mouse.

237 to differentiate into either endothelial or interstitial cells of the valve leaflet.

238 showed by immunofluorescence that the target interstitial cells of Wnt7b/canonical Wnt signaling are

239 In response to equibiaxial stretch, valvular interstitial cells on stiff substrates decreased their t

240 ing nodule formation in porcine aortic valve interstitial cells (PAVICs) cultured in osteogenic (OST)

241 ionic conductances in a novel population of interstitial cells (PDGFRalpha(+) cells) in murine bladd

242 +) cells, which include pericytes and PW1(+) interstitial cells (PICs), play a dual role in muscular

243 process, but growing evidence suggests that interstitial cells play an essential role during testis

244 Valve interstitial cells populate aortic valve cusps and have

245 udy highlights the cellular diversity of the interstitial cell population and suggests that complex c

246 ds, suggesting that regulation of the Leydig/interstitial cell population is important for male germ

247 By contrast, interstitial cell populations are different from P7 to P

248 tures were identified in the nephron, kidney interstitial cell populations, vascular endothelium, and

249 ence of gene regulatory networks in valvular interstitial cells positions Adamts19 in a highly discri

250 tive CITED1-expressing compartment, cortical interstitial cells prematurely differentiate.

251 phron progenitor cells by repressing a renal interstitial cell program.

252 yofibroblasts (2.8 times decreased), reduced interstitial cell proliferation (2.6 times decreased), b

253 Eln(+/-) mice demonstrated increased valve interstitial cell proliferation at the neonatal stage an

254 terstitial cells (AVICs) and pulmonary valve interstitial cells (PVICs) differ in expression of Toll-

255 One type of interstitial cell, referred to as 'fibroblast-like cells

256 mediating COX2 expression in renal medullary interstitial cells (RMICs).

257 Ca(2+) transients were observed in c-Kit(+) interstitial cells, smMHC(+) PDGFRalpha cells and smMHC(

258 nstant throughout postnatal development, but interstitial cell subpopulations undergo changes in gene

259 expression in primary mouse renal medullary interstitial cells substantially reduced cellular resist

260 ts a new decisive immunological role of lung interstitial cells such as SMC in promoting acute pulmon

261 epends on the immunological function of lung interstitial cells such as smooth muscle cells (SMC).

262 esults from 15-PGDH-expressing myofibers and interstitial cells, such as macrophages, within muscle.

263 ily during fetal development in myocytes and interstitial cells suggesting a role for this protein du

264 mediators colocalized primarily to valvular interstitial cells suggesting autocrine/paracrine activa

265 he gills and fins, as well as in clusters of interstitial cells surrounding the kidney tubules.

266 A focal increase in tubular and interstitial cell TGF-beta1 expression starting at 20 wk

267 e TLR2 and TLR4, in both tissue and isolated interstitial cells, than pulmonary valves.

268 activation in renal tubular epithelia and in interstitial cells that peaked 2-3 days after injury.

269 at line the leaflet surface and the valvular interstitial cells that populate the valve extracellular

270 Vascular Endothelial Growth Factor (VEGF) in interstitial cells, the local overexpression of the corr

271 1 expression, as shown by He et al., enabled interstitial cells to withstand the oxidizing medullary

272 expansion of three distinct cardiac-derived interstitial cell types from human heart tissue, previou

273 iomyocytes (CM), the heart contains numerous interstitial cell types which play key roles in heart re

274 Hh-responsive Gli1-positive interstitial cells underwent 11-fold proliferative expan

275 rozygous knock-out of Phd2 in renal cortical interstitial cells using a Pax3-Cre transgene or by homo

276 plays a role in maintaining renal medullary interstitial cell viability in the hypertonic environmen

277 lular matrix (ECM) organization and valvular interstitial cell (VIC) distribution that characterize t

278 ndothelial cells (VEC) regulate aortic valve interstitial cell (VIC) phenotype and matrix calcificati

279 otypic changes occurring in the aortic valve interstitial cells (VICs) during osteogenic differentiat

280 lmark of early CAVD, but culture of valvular interstitial cells (VICs) in biomaterial environments co

281 Treatment of E14 aortic valve interstitial cells (VICs) in culture with osteogenic med

282 A knockdown of H19 in valve interstitial cells (VICs) increased the expression of NO

283 rix elasticity, we cultured primary valvular interstitial cells (VICs) isolated from porcine aortic v

284 Using valvular interstitial cells (VICs) isolated from porcine aortic v

285 alves affects the biology of aortic valvular interstitial cells (VICs) remains to be elucidated.

286 ganized extracellular matrix (ECM) and valve interstitial cells (VICs) surrounded by an endothelial c

287 fects of TNF-alpha on murine aortic valvular interstitial cells (VICs) within three-dimensional, free

288 trioventricular valve, we focus on the valve interstitial cells (VICs), which confer biomechanical st

289 nt on Mef2c expression in fetal mitral valve interstitial cells (VICs).

290 lular matrix production in cultured valvular interstitial cells was dependent on SMAD2/3 and p38 sign

291 Alveolar and interstitial cells were isolated from lung resection tis

292 More than 99% of those GFP interstitial cells were leukocytes.

293 ultured valve tissues, and cultured valvular interstitial cells were obtained from patients with mitr

294 mean of 8.6% of smooth muscle actin-positive interstitial cells were Y chromosome positive.

295 Gremlin is expressed by mature myofibers and interstitial cells, which are separate from BMP4-express

296 Renal interstitial cells with EPO-producing capacity are poorl

297 Renal interstitial cells with EPO-producing capacity were enti

298 In vitro treatment of mitral valve interstitial cells with TGF-beta2 increased beta-catenin

299 rtical white matter neurons, or white matter interstitial cells (WMICs), are found within the subcort

300 euronal population, also termed white matter interstitial cells (WMICs), in the brain of a lesser ape