ライフサイエンスコーパス: interstitial cell

1 matrix and myofibroblasts (a mesenchyme-like interstitial cell).

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

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

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

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

6 tissue constructs seeded with porcine valve interstitial cells.

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

8 onad that also gives rise to uncharacterised interstitial cells.

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

10 helium contributes only to non-steroidogenic interstitial cells.

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

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

13 some bronchial epithelial, endothelial, and interstitial cells.

14 revented H19-induced mineralization of valve interstitial cells.

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

16 E showed early signs of proliferation in the interstitial cells.

17 tol, and betaine in cultured mouse medullary interstitial cells.

18 biopsies showed granular antigen-staining in interstitial cells.

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

20 ling is activated in both cardiomyocytes and interstitial cells.

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

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

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

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

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

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

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

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

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

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

31 d -Rbeta protein expression was increased in interstitial cells after day 4 and reached maximal expre

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

33 o-TRH gene expression was induced in cardiac interstitial cells after MI, and this effect was restric

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

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

36 r source of tTg; however, both mesangial and interstitial cells also contributed to elevated levels i

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

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

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

40 as limited to cardiac myocytes and absent in interstitial cells and coronary vessels.

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

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

43 Increased expression of PDGF-B by interstitial cells and in some tubules was observed afte

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 The proliferation of valve interstitial cells and ventricular valve endothelial cel

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

52 s/macrophages, subepithelial fibroblast-like interstitial cells, and additionally type I alveolar epi

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 de novo expression of PDGF-D was detected in interstitial cells at day 4, which increased to maximal

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

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

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

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

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

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

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

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

72 RNA interference reduced primary human valve interstitial cell calcification.

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

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

75 ated similar de novo expression of PDGF-D in interstitial cells, correlating with expression of PDGF-

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

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

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

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

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

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

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

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

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

85 d valve disease because serotonin can induce interstitial cell expression of tumor growth factor beta

86 and norfenfluramine in vivo (i.e., valvular interstitial cell fibroplasia) predict that long-term MD

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

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

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

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

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

92 Interstitial cells have been implicated in the pathogene

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

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

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

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

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

102 buted substantially to blood, lymphatic, and interstitial cells in the pancreas.

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

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

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

106 rotein in glomerular epithelial cells and in interstitial cells, in comparison with nondiabetic WT mi

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

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

112 Interstitial cells, known as platelet derived growth fac

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

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

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

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

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

118 regulation of the phenotypic composition of interstitial cells (macrophages, myofibroblasts, capilla

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

120 opmental induction that specifies primordial interstitial cells (mesenchymal cells), requires vascula

121 Thereby, interstitial cell migration and adhesion events, influen

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

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

124 edulla and in cultured mouse renal medullary interstitial cells (MMICs) and its role in facilitating

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

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

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

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

129 immunohistochemistry revealed disruption in interstitial cell of Cajal (ICC) networks at the level o

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

131 69I/+) mice than in single-mutant mice, both interstitial cell of Cajal hyperplasia and mast cell hyp

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

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

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

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

136 dus of W/W(V) mice, which lack intramuscular interstitial cells of Cajal (ICC(IM)) lacked the dischar

137 ne of W/Wv mutant mice, which lack pacemaker interstitial cells of Cajal (ICC) and electrical slow wa

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

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

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

141 Interstitial cells of Cajal (ICC) are a fundamental comp

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

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

144 studies have demonstrated that intramuscular interstitial cells of Cajal (ICC) are preferential targe

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

146 Interstitial cells of Cajal (ICC) are putative pacemaker

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

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

149 Interstitial cells of Cajal (ICC) control intestinal smo

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

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

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

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

154 Interstitial cells of Cajal (ICC) generate pacemaker act

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

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 Interstitial cells of Cajal (ICC) were described more th

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

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

171 Slow waves are generated by the interstitial cells of Cajal (ICC), and these events acti

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

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

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

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

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

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

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

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

180 Arterial interstitial cells of Cajal (ICC)-like cells (AIL cells)

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

182 ow waves are generated and propagated by the interstitial cells of Cajal (ICC).

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

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

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

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

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

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

189 t in W/W(V) mutants which lack intramuscular interstitial cells of Cajal (ICC-IM).

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

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

192 waves originate from a myenteric network of interstitial cells of Cajal (ICC-MY).

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

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

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

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

197 Interstitial cells of Cajal (ICCs) were identified in th

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

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

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

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

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

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

204 Intramuscular interstitial cells of Cajal and platelet-derived growth

205 ight regulation of ion channels expressed in interstitial cells of Cajal and smooth muscle.

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

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

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

209 Interstitial cells of Cajal generate the slow wave and a

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

211 Interstitial cells of Cajal in the deep muscular plexus

212 eactive fibers formed a dense network around 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 scular plexus in very close association with interstitial cells of Cajal visualized by c-kit immunost

217 and 3) muOR immunoreactivity is localized to interstitial cells of Cajal visualized by c-kit.

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

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

220 d to secondary Ca(2+) waves in intramuscular interstitial cells of Cajal, ICC-IM, and smooth muscle c

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

222 Interstitial cells of Cajal, which express the receptor

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

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

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

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

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

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

229 d a normal complement of enteric neurons and interstitial cells of Cajal.

230 ent for induction of GIST and hyperplasia of interstitial cells of Cajal.

231 of hematopoietic cells, germ cells, and the interstitial cells of Cajal.

232 cted in neurons containing calbindin, nor in interstitial cells of Cajal.

233 dogenous opioid ENK, and is not expressed by interstitial cells of Cajal.

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

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

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

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

238 nd interstitial cells of the myocardium, and interstitial cells of the conduction tissue.

239 l cells of the aortic root, perivascular and interstitial cells of the myocardium, and interstitial c

240 anscripts were detected in renal tubules and interstitial cells of the obstructed uPAR+/+ kidneys.

241 in adrenal cortical cells, spermatocytes and interstitial cells of the testis, theca cells of the ova

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

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

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

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

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

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

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

249 Valve interstitial cells populate aortic valve cusps and have

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

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

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

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

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

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

256 uscles of intact rats, stimulation increased interstitial cell proliferation and capillary swelling,

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

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

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

260 The survival of renal medullary interstitial cells (RMICs) requires their adaptation to

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

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

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

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

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

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

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

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

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

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

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

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

273 1 expression, as shown by He et al., enabled interstitial cells to withstand the oxidizing medullary

274 pts found in cultures enriched in Sertoli or interstitial cells to yield a germ cell-enriched transcr

275 but from cells also able to give rise to an interstitial cell type.

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

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

278 longed mitogenic responses in human valvular interstitial cells via activation of 5-HT2B receptors.

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

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

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

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

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

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

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

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

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

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

289 are believed to differentiate from valvular interstitial cells (VICs).

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

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

292 Alveolar and interstitial cells were isolated from lung resection tis

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

294 aining revealed that the endothelium and the interstitial cells were most intensely stained with anti

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

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

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

298 Renal interstitial cells with EPO-producing capacity are poorl

299 Renal interstitial cells with EPO-producing capacity were enti

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