ライフサイエンスコーパス: mesenchymal cell

1 dinated signals from adjacent epithelial and mesenchymal cells.

2 oing a phenotypic change to become more like mesenchymal cells.

3 of MC lineage cells from naive pdgfrb (low) mesenchymal cells.

4 (FLCN) is highly expressed in neonatal lung mesenchymal cells.

5 ofibroblasts (SCMF), a subpopulation of lung mesenchymal cells.

6 -mesenchymal transition and proliferation of mesenchymal cells.

7 ssing phenotypic markers for endothelial and mesenchymal cells.

8 tors are required to activate Hoxd13 in limb mesenchymal cells.

9 prominent clustering of the adjacent dermal mesenchymal cells.

10 iferation, migration, and differentiation of mesenchymal cells.

11 secretion by osteoblasts, chondrocytes, and mesenchymal cells.

12 parative processes, and serve as pluripotent mesenchymal cells.

13 dependent set of sorted, primary MDS-derived mesenchymal cells.

14 ls into the front-rear polarity of migrating mesenchymal cells.

15 dipogenic differentiation in the pluripotent mesenchymal cells.

16 riptional program, and transdifferentiate to mesenchymal cells.

17 g DLX5, DLX6 and HAND2, were also reduced in mesenchymal cells.

18 mp1 gene expressions in mouse dental papilla mesenchymal cells.

19 ltered differentiation outcomes specified by mesenchymal cells.

20 ce mineral formation of mouse dental papilla mesenchymal cells.

21 e tooth development and mouse dental papilla mesenchymal cells.

22 ose tissue and primarily in undifferentiated mesenchymal cells.

23 independent endothelial marker expression in mesenchymal cells.

24 that restores a mucociliated epithelium from mesenchymal cells.

25 differentiation and mineralization of dental mesenchymal cells.

26 ogenitor cells, mature neurons or epithelial-mesenchymal cells.

27 as up-regulated by DSP (aa183-219) in dental mesenchymal cells.

28 s expression of CD31, VeCadherin, or Tie2 in mesenchymal cells.

29 1 expression was induced in nonproliferative mesenchymal cells.

30 yllium, it did disrupt cell proliferation in mesenchymal cells.

31 eas others reflect the phenotypes of stem or mesenchymal cells.

32 uired for digit identity in a subset of limb mesenchymal cells.

33 orming growth factor (TGF)-beta signaling in mesenchymal cells.

34 chondrogenic cells, and ITGA7+ smooth muscle-mesenchymal cells.

35 lammation by inducing cytokine production by mesenchymal cells.

36 notypic conversion of endothelial cells into mesenchymal cells.

37 o the effect of co-culturing with immune and mesenchymal cells.

38 and increased the proliferation of handplate mesenchymal cells.

39 cluding the basement membrane and underlying mesenchymal cells.

40 ellular matrix and, only to a lesser extent, mesenchymal cells.

41 distinct from, but closely related to, lung mesenchymal cells.

42 m cells and receive signals from surrounding mesenchymal cells.

43 s (BASCs) upon co-culture with lung-resident mesenchymal cells.

44 t molecular and cellular analyses of cryptal mesenchymal cells.

45 e of IDH mutations in the differentiation of mesenchymal cells.

46 types, including epithelial, endothelial and mesenchymal cells.

47 d the transition from endothelial cells into mesenchymal cells, a critical step in heart valve develo

48 duced canonical WNT signaling in neighboring mesenchymal cells, a phenotype reproduced by endocardial

49 -Os), a surrogate marker of undifferentiated mesenchymal cells able to differentiate to osteoblasts,

50 By contrast, tissue specific deletion in cap mesenchymal cells abolishes mesenchyme to epithelial tra

51 xpression of growth factors (Nrg2, Rspo3) by mesenchymal cells acting in a paracrine fashion on lumin

52 senescent cholangiocytes promoted quiescent mesenchymal cell activation in a platelet-derived growth

53 WNT5A, which is secreted by surrounding mesenchymal cells, acts as a guidance cue to orchestrate

54 axillin is a well-characterized regulator of mesenchymal cell adhesion signaling, F-actin cytoskeleto

55 ochemical properties as force transducers in mesenchymal cell aggregates, we show that the magnitude

56 to uncover spatially zonated populations of mesenchymal cells along the crypt-villus axis.

57 Gorab-deficient dermal mesenchymal cells also displayed a significantly reduced

58 posttranslational change in microtubules in mesenchymal cells alters the mesenchymal microenvironmen

59 to an extracellular matrix containing amnion mesenchymal cells (AMCs) through a basement membrane.

60 rse transition, MET, in primary human amnion mesenchymal cells (AMCs) through progesterone receptor m

61 These changes result from an infiltration of mesenchymal cells, an important cell type in the pathoge

62 Importantly, expression of mesenchymal cell and cholangiocyte marker was significan

63 f FZHY's role is to inhibit the formation of mesenchymal cells and cholangiocytes.

64 ine the age-dependent contribution of native mesenchymal cells and circulating factors on in vivo bon

65 g is recovered as inflammation resolves, and mesenchymal cells and collagen fibers align.

66 full EMT, but rather adopt some qualities of mesenchymal cells and maintain some epithelial character

67 ity resulted in premature differentiation of mesenchymal cells and reduced vasculogenesis of the sple

68 propriate nature of the interactions between mesenchymal cells and surrounding/underlying matrix/subs

69 for osteochondroprogenitors within CD105(+) mesenchymal cells and that these cells readily form bone

70 leukocytes, extracellular matrix components, mesenchymal cells, and a collection of nerves, blood, an

71 sarcoma subtypes compared with non-malignant mesenchymal cells, and knockdown of DDX3 by RNA interfer

72 llular injury, activation/differentiation of mesenchymal cells, and morphological/biological changes

73 th often predominant expression of p120-1 in mesenchymal cells, and p120-3 generally prevalent in epi

74 Pro-fibrotic mesenchymal cells are known to be the key effector cells

75 Our results indicate that CD34(+) Gp38(+) mesenchymal cells are programmed to develop in the intes

76 mechanism is only present in non-transformed mesenchymal cells as collagen-induced MT1-MMP activation

77 Wall degradation of mesenchymal cells, as well as motility of both types of

78 Alveolar fibrocytes are monocyte-derived mesenchymal cells associated with poor prognosis in pati

79 cephalic roof plate is pioneered by distinct mesenchymal cells at the dorsal midline of the neural tu

80 tion of the interzone, a region of condensed mesenchymal cells at the site of the prospective joint.

81 t restores an epithelium, transitioning from mesenchymal cells at the surface of the aggregate.

82 pithelial cells into multipolar and invasive mesenchymal cells before differentiating into nonmyocyte

83 al Hh ligands not only regulate a variety of mesenchymal cell behaviors, but they also direct these m

84 w increasing our understanding of intestinal mesenchymal cell biology and function could lead to new

85 ritical for supporting cell proliferation in mesenchymal cells both in vivo and in vitro beta1 integr

86 that TACC2 can promote MT polymerization in mesenchymal cells but not neuronal growth cones, thus di

87 -term viral replication in hematopoietic and mesenchymal cells, but not epithelial cells (IECs), in t

88 Increased HA levels and mesenchymal cells, but not vascular endothelial growth f

89 ling the organized proliferation of adjacent mesenchymal cells by regulating proper Wnt4 expression d

90 esists physical forces, with tendon-specific mesenchymal cells called tenocytes orchestrating extrace

91 make to become sensory, glial, autonomic, or mesenchymal cells can be formalized as a series of seque

92 of the hGH minigene in CollagenVI expressing mesenchymal cells can lead through local and/or systemic

93 . (2017) show that exosomal miRs secreted by mesenchymal cells can regulate epithelial KIT(+) progeni

94 hesions and under conditions of confinement, mesenchymal cells can spontaneously switch to a fast amo

95 Although impaired interdigital cell death of mesenchymal cells causes syndactyly in multiple genetic

96 tify pericryptal CD34(+) Gp38(+) alphaSMA(-) mesenchymal cells closely associated with Lgr5(+) IESCs.

97 th smooth-muscle-induced physical forces and mesenchymal cell clustering beneath emerging villi are i

98 allel to the core-Vangl2 PCP axis to control mesenchymal cell clustering.

99 Although cardiac mesenchymal cell (CMC) therapy mitigates post-infarct ca

100 m rapidly adhering (RA) fractions of cardiac mesenchymal cells (CMCs) are effective in preserving lef

101 ar matrix (ECM) constructed by AKAP12+ colon mesenchymal cells (CMCs) generated M2 macrophages by reg

102 RATIONALE: Human cardiac mesenchymal cells (CMSCs) are a therapeutically relevant

103 RV fibrotic regions were populated with mesenchymal cells coexpressing vimentin and PDGFRalpha (

104 CUX1 to Snail and the E-cadherin promoter in mesenchymal cells compared to epithelial prostate and br

105 Using time-lapse imaging, we find that mesenchymal cell condensation at hair follicles is local

106 ning subsets of hematopoietic cells, and how mesenchymal cells contribute to other stem cell niches.

107 herogenesis, but it is unclear whether other mesenchymal cells contribute to this process.

108 reveals that Bmp signaling in Hh-responsive mesenchymal cells controls cluster pattern.

109 Mesenchymal cell crawling is a critical process in norma

110 n the CompuCell3D simulation environment) of mesenchymal cells crawling on a two-dimensional substrat

111 cooperation emerges in mid-level energy, as mesenchymal cells create paths that are used by amoeboid

112 repertoire of HLA class I-bound peptides in mesenchymal cells deficient in immunoproteasome componen

113 e perform an unbiased interrogation of tumor mesenchymal cells, delineating the co-existence of disti

114 The EDA wave spreads across a mesenchymal cell density gradient, triggering pattern fo

115 In the mouse, mesenchymal cells differentiate into airway smooth muscl

116 This DSP domain facilitates dental mesenchymal cell differentiation and mineralization.

117 ver, mechanisms of DSP in controlling dental mesenchymal cell differentiation are unknown.

118 cific expression analyses revealed that Cpdm mesenchymal cells display increased responsiveness towar

119 Mesenchymal cells displayed distinct molecular profiles

120 Fbeta playing key roles in the regulation of mesenchymal cells during simple repair.

121 DSP, occludin and FAK was detected in dental mesenchymal cells during tooth development.

122 that lead to a change in phenotype toward a mesenchymal cell (e.g., myofibroblast, smooth muscle cel

123 Lung mesenchymal cells elicit this process through repressing

124 ing about the cellular origin (epithelial or mesenchymal cells) essential for root cementum growth.

125 ct was attributed primarily to inhibition of mesenchymal cell expansion.

126 In the fetal pancreas, peripheral mesenchymal cells expressed Sema3a, while central nascen

127 ensity in the interstitial area of Nestin(+) mesenchymal cells expressing CXCL12 and myeloid cells ex

128 This process is driven by subluminal mesenchymal cells expressing Misr2, which trigger the re

129 Mesenchymal cells expressing platelet-derived growth fac

130 of a potent epigenetic switch that controls mesenchymal cell fate into myogenic and osteogenic linea

131 trial epithelial cell identity by repressing mesenchymal cell fates, and that coexistent ARID1A and P

132 Mesenchymal cells formed separate, well-defined clusters

133 ther extracellular matrix gene production by mesenchymal cells from both murine and human fibrotic lu

134 ormal regulatory mechanism that prevents the mesenchymal cells from differentiating.

135 rospectively identified, sorted and expanded mesenchymal cells from human primary NSCLC samples based

136 changes such as loss of 10p in disseminated mesenchymal cells generate epithelial variants, which ca

137 Although mesenchymal cells have been successfully induced into LC

138 production of stem cell niche factors by the mesenchymal cells have not been well elucidated, due to

139 gical importance is undisputed, the level of mesenchymal cell heterogeneity within and between organs

140 iated by immune cell function independent of mesenchymal cell Hox5 family function.

141 This analysis identifies a mesenchymal cell hub coordinating the LAM disease phenot

142 l cancer, we show that IKKbeta in intestinal mesenchymal cells (IMCs) is critically involved in colit

143 cess is operational in airway epithelial and mesenchymal cells in asthma.

144 hat WT1 is expressed by both mesothelial and mesenchymal cells in idiopathic pulmonary fibrosis lungs

145 The importance of mesenchymal cells in inflammation and/or neoplastic tran

146 t2a1 in mice showed expression of SULT2A1 in mesenchymal cells in palate, palatal rugae and palatal e

147 These secreted factors are upregulated in mesenchymal cells in response to serum withdrawal, and o

148 cells in epithelial tissues, are markers of mesenchymal cells in the adult lung.

149 Mesenchymal cells in the crypt play indispensable roles

150 hair follicle relies on signals derived from mesenchymal cells in the dermis during skin morphogenesi

151 Mesenchymal cells in the intestine comprise a variety of

152 oregulatory circuits engaging epithelial and mesenchymal cells in the intestine, airways, and skin an

153 ities and functions of the innate immune and mesenchymal cells in the microenvironment of tumors shou

154 eutral lipids upon interaction with resident mesenchymal cells in the premetastatic lung.

155 Mesenchymal cells in tumors, called cancer-associated fi

156 ive inhibition of RANKL in hematopoietic vs. mesenchymal cells, in conjunction with in situ expressio

157 Importantly, mesenchymal cells including fibroblasts are prominent in

158 icroenvironmental characteristics of colonic mesenchymal cells, including the intrinsic involvement o

159 whereas the numbers of both endothelial and mesenchymal cells increase substantially from birth to e

160 ort that hyperacetylation of microtubules in mesenchymal cells increased cytokeratin 14-positive (K14

161 type, whereas knocking down the ZEB1 gene in mesenchymal cells induced an epithelial phenotype, demon

162 that NO66 overexpression in Prx1-expressing mesenchymal cells inhibited skeletal growth and bone for

163 Here we show that 3D mesenchymal cell intercalations are essential to shape t

164 lic calcium transients that orient and drive mesenchymal cell intercalations.

165 el, Klar et al. incorporated adipose-derived mesenchymal cells into skin substitutes and found that a

166 pathology demonstrated migration of resident mesenchymal cells into the scaffold and trilaminar ECM o

167 epithelial to mesenchymal transition (EMT), mesenchymal cells invade the myocardium to form coronary

168 d for 2D cell migration but is essential for mesenchymal cell invasion in 3D culture and in a mouse c

169 Chemotaxis of fibroblasts and other mesenchymal cells is critical for embryonic development

170 e that high Notch activity in the unmodified mesenchymal cells is driven by ligands produced by the c

171 of TGF-beta1 to modulate DNA methylation in mesenchymal cells is less clear.

172 nd found that co-targeting of epithelial and mesenchymal cells is likely to be the most effective str

173 ransdifferentiation of epithelial cells into mesenchymal cells, is critical for embryonic development

174 senchymal transition, resulting in increased mesenchymal cells, is the likely cause of morphological

175 anoids co-cultured with immortalized stomach mesenchymal cells (ISMCs).

176 mma that drives expression of B7-H1 on graft mesenchymal cells leading to Tef cell apoptosis.

177 epithelial cell-restricted miR-200 family in mesenchymal cells limited mTOR signaling and sensitized

178 ased number of peptides are detected for the mesenchymal cell line relative to the epithelial cell in

179 bryonic mouse lung at E16.5 to identify lung mesenchymal cell lineage relationships that currently re

180 It is involved in dental mesenchymal cell lineages and dentin formation through r

181 hymal stem cells differentiate into distinct mesenchymal cell lineages and regulate the immune respon

182 ple subpopulations of immune, epithelial and mesenchymal cell lineages.

183 Cs contribute to incisor MTACs and the other mesenchymal cell lineages.

184 Using mesenchymal cell lines derived from biopsies of patients

185 Here we established one epithelial and two mesenchymal cell lines from ascites of a bladder cancer

186 their upregulation in metastatic tumors and mesenchymal cell lines is coordinated to that of collage

187 been characterized primarily in nonmalignant mesenchymal cells, little is known about its role in can

188 To evaluate the function of mesenchymal cells located at the large intestinal crypt,

189 (>15% per year) and more limited renewal of mesenchymal cells (<4% per year in adulthood).

190 Genetic loss of Hif1alpha in mesenchymal cells marked by Prx-cre prevents the formati

191 The cells also expressed known mesenchymal cell markers and promoted new bone formation

192 ithelial marker expression and downregulated mesenchymal cell markers at RNA and protein level in BEA

193 Fibrotic diseases display mesenchymal cell (MC) activation with pathologic deposit

194 ng hepatocytes, endothelial cells (ECs), and mesenchymal cells (MCs) and recently reported the mass p

195 Mesenchymal cells (MCs) derived from fibrotic lung allog

196 In order to understand the role of mesenchymal cells (MCs) in the adult thymus, we performe

197 root formation is a dynamic process in which mesenchymal cells migrate toward the site of the future

198 sively rather than instructively in directed mesenchymal cell migration during gastrulation.

199 ctive activity is also critical for directed mesenchymal cell migration.

200 netic protein (BMP) signalling together with mesenchymal cell movement, acting in a coordinated react

201 t is differentially up-regulated in alveolar mesenchymal cells of human subjects with rapidly progres

202 Leydig cells (LCs), proposed to derive from mesenchymal cells of mesonephric origin.

203 The mesenchymal cells on the other hand, exhibited constitut

204 ut (CKO) of Notch1 in collagen I-expressing (mesenchymal) cells on treatment with tamoxifen (Notch1 C

205 A may be a better choice in situations where mesenchymal cells or inflammatory cells are significantl

206 ic ablation of alpha6 in collagen-expressing mesenchymal cells or pharmacological blockade of matrix

207 Our results supported a resident liver mesenchymal cell origin of the TDFSM cells, which were n

208 mors induced by MPyV from an epithelial to a mesenchymal cell origin.

209 t cell count (P = 0.04); 2) lower density of mesenchymal cells (P = 0.05); and 3) more diffuse, non-l

210 Mesenchymal cells, Paneth cells, immune cells, endotheli

211 and nonprofessional APCs (eg, epithelial and mesenchymal cells), particularly within the gastrointest

212 tify the key players establishing epithelial-mesenchymal cell plasticity during reversible and irreve

213 alcium from its body cavity into the primary mesenchymal cells (PMCs) that are responsible for spicul

214 iments to determine the fates of peribiliary mesenchymal cells (PMCs) that surround the bile duct aft

215 in mouse, the transition of a PDGFRalpha(+) mesenchymal cell population into mammary epithelial prog

216 ibroblasts, arise via activation of resident mesenchymal cell populations and the recruitment of bone

217 These closely related mesenchymal cell populations form extensive connections

218 tified as distinct pluripotent stem cells in mesenchymal cell populations in humans.

219 y refers to the pairing of hematopoietic and mesenchymal cell populations that regulate HSC self-rene

220 e marrow stromal cells (BMSCs) are versatile mesenchymal cell populations underpinning the major func

221 to proliferation and migration of endogenous mesenchymal cell populations, as well as invasion of the

222 n to be important in lung development within mesenchymal cell populations.

223 lex extracellular matrix as well as multiple mesenchymal cell populations.

224 ith the submandibular gland, focusing on the mesenchymal cell populations.

225 endothelial, smooth muscle, hematopoietic or mesenchymal cell progeny.

226 found them linked to positive regulation of mesenchymal cell proliferation in LNCaP and C4-2B, and s

227 Interestingly, we found increased pulpal mesenchymal cell proliferation in the presumptive root f

228 is DSP domain induces endogenous dental pulp mesenchymal cell proliferation, differentiation and migr

229 es on the interaction between epithelial and mesenchymal cells, providing a simple system to investig

230 ditional genetic loss of Ezh2 in uncommitted mesenchymal cells (Prrx1-Cre) results in multiple defect

231 DGFRalpha, a potent activator of AKT in lung mesenchymal cells, recapitulated the alveolar phenotypes

232 We show here that CAFs and other mesenchymal cells rely much more on glutamine than epith

233 h in vitro cell expansion of embryonic tooth mesenchymal cells renders them unable to induce tooth fo

234 ttern formation by lowering the threshold of mesenchymal cells required to begin to form a feather bu

235 hat ITGB4(+) cancer stem cell (CSC)-enriched mesenchymal cells reside in an intermediate epithelial/m

236 equired in endocardial cells to regulate the mesenchymal cell responses that remodel cardiac cushions

237 ependent Collagen I production in intestinal mesenchymal cells result in fibrosis in patients with Mo

238 lead to persistent inflammation and loss of mesenchymal cells, resulting in minimal tissue repair.

239 l cells and PDGFRalpha(+) collagen-producing mesenchymal cells reveals intra-scar activity of several

240 By using an inducible Cre model to mark mesenchymal cells (Scx-creERT/tdTomato + ) prior to inju

241 n substitutes and found that adipose-derived mesenchymal cells secreted high levels of transforming g

242 phe inhibition by SLAIN2 and CLASP1 supports mesenchymal cell shape in soft 3D matrices by enabling m

243 The gene expression pattern in the cryptal mesenchymal cells showed that receptors of the hormone/c

244 ess the human TNFR1 under the control of the mesenchymal cell-specific CollagenVI promoter.

245 AP) has been established as an inducible and mesenchymal cell-specific mediator of disease progressio

246 We review the intestinal mesenchymal cell-specific pathways that regulate these p

247 rly characterize this therapy-resistant high-mesenchymal cell state in human cancer cell lines and or

248 A high-mesenchymal cell state observed in human tumours and can

249 r stem cells (CSCs) as well as of epithelial/mesenchymal cell state transitions.

250 herapy-resistant cancer cells across diverse mesenchymal cell-state contexts.

251 ication of mechanical stretch to multipotent mesenchymal cells stimulated the nuclear translocation o

252 olling the directed migration of slow-moving mesenchymal cells such as fibroblasts are not well under

253 Mesenchymal cells such as fibroblasts are weakly polariz

254 rement in pdgfrb expression in peri-arterial mesenchymal cells, suggesting that these transcriptional

255 sts (CAFs) are a heterogeneous population of mesenchymal cells supporting tumor progression, whose or

256 work integrating beta-catenin/SHH signals in mesenchymal cell survival and outgrowth of the mandible

257 , but not in the poorly differentiated quasi-mesenchymal cells that coexist in the same tumor.

258 ately reprogrammed stem cells (iRSCs), human mesenchymal cells that express exogenous Oct4, Sox2, Klf

259 +) cells indigenous to the ovary and Gli1(+) mesenchymal cells that migrate from the mesonephros.

260 helial tumor cells into quasi-mesenchymal or mesenchymal cells that possess cancer stem cell properti

261 en receptor (Ar) identify a subpopulation of mesenchymal cells that regulate sinus ridge morphogenesi

262 2 processes, providing a source for diverse mesenchymal cells that support formation of the highly f

263 Gli1 was a marker of mesenchymal cells that surround the biliary tree but not

264 Osteoblasts are specialized mesenchymal cells that synthesize bone matrix and coordi

265 In spiders, a group of BMP secreting mesenchymal cells (the cumulus) functions as an organize

266 s, including IL-6, are produced by activated mesenchymal cells themselves and activate STAT3.

267 that the transformed epithelium hijacks the mesenchymal cells through Notch signaling, which prevent

268 l cell behaviors, but they also direct these mesenchymal cells to secrete additional soluble factors

269 n of histone marks during differentiation of mesenchymal cells to the osteogenic and myoblastic linea

270 l migration, reminiscent of an epithelial-to-mesenchymal cell transition, potentially contributing to

271 ctivation of NLRP3 in myeloid cells, but not mesenchymal cells triggers chronic inflammation, which u

272 When Notch or zfh1 are depleted in the mesenchymal cells, tumor growth is compromised.

273 The diversity of mesenchymal cell types in the lung that influence epithe

274 ostasis, proliferation of all epithelial and mesenchymal cell types remained low but intermediate cel

275 f adipocyte progenitors consists of distinct mesenchymal cell types that are present in both mouse an

276 diverse but poorly characterized network of mesenchymal cell types(2,3).

277 Contrary to that observed in mesenchymal cell types, here NOX4 suppresses Rho and Cdc

278 NA-seq) to identify three distinct PDGFRA(+) mesenchymal cell types.

279 Crosstalk between epithelial and mesenchymal cells underlies formation of the face and pa

280 crosstalk between epithelium and neighboring mesenchymal cells underpin the generation of different p

281 ization at cellular protrusions of migrating mesenchymal cells, using as a model the RAB13 RNA, which

282 understand the role of Vhl in the biology of mesenchymal cells, we analyzed mutant mice lacking Vhl i

283 The mesenchymal cells were considerably more heterogeneous b

284 Exosomes derived from normal fibroblast-like mesenchymal cells were engineered to carry short interfe

285 Bone-derived mesenchymal cells were introduced into the organofiber s

286 zed by histology and immunofluorescence, and mesenchymal cells were isolated.

287 brocytes-circulating and bone marrow-derived mesenchymal cells-were also detectable.

288 ta-catenin signaling is activated in cushion mesenchymal cells where it supports FGF-driven expansion

289 A-expressing cells were identified as FN1(+) mesenchymal cells which are responsible for the precocio

290 row derived mononuclear cells, or autogenous mesenchymal cells, which can be administered as cryopres

291 nsion coincides with deformation of adjacent mesenchymal cells, which correlates with an increase in

292 some SCPs detach from nerve fibers to become mesenchymal cells, which differentiate further into chon

293 riched with highly plastic hybrid epithelial/mesenchymal cells, which display invasive features and a

294 tumors and identified new subsets of stromal mesenchymal cells with distinct transcriptional profiles

295 d mono-unsaturation within de-differentiated mesenchymal cells with innate resistance to BRAF inhibit

296 Mesenchymal cells with properties of activated repair ce

297 and increasing BMP4 production by patients' mesenchymal cells with resistance.

298 Treatment of mesenchymal cells with the Cat L inhibitor Z-FY-CHO led

299 ibute to osteoblasts, marrow adipocytes, and mesenchymal cells within adult bones.

300 Prominent accumulation of mesenchymal cells within tumors has long been appreciate