ライフサイエンスコーパス: stromal cell

1 is complex (TSC) genes, and recruit abundant stromal cells.

2 ntified CD40L as a novel GLI2 target gene in stromal cells.

3 upon decidualization of primary endometrial stromal cells.

4 ell types, including epithelial, immune, and stromal cells.

5 sistant disease in cocultures of bone marrow stromal cells.

6 ack of growth factors secreted from adjacent stromal cells.

7 by coculture with developmentally supportive stromal cells.

8 e repertoire of genes specifically in thymic stromal cells.

9 l activation of CD40L in bone marrow-derived stromal cells.

10 d disease and in the presence of bone marrow stromal cells.

11 in vivo is TLR independent and emanates from stromal cells.

12 ow toxicity to normal lymphocytes and normal stromal cells.

13 gnaling within both tumor cells and adjacent stromal cells.

14 mice developed into tumors containing green stromal cells.

15 previously demonstrated in human bone marrow stromal cells.

16 ed extensively in human pancreatic tumor and stromal cells.

17 HIF-1alpha, and aromatase expression in LFS stromal cells.

18 itochondria from murine or human bone marrow stromal cells.

19 2D)) also regulates tumor cell signaling via stromal cells.

20 PKM2 suppressed aromatase expression in LFS stromal cells.

21 ne evasion, and co-option of other tumor and stromal cells.

22 mune cells that also localize near senescent stromal cells.

23 progenitors, osteocytes and CXCL12-producing stromal cells.

24 cose media increased adhesion to bone marrow stromal cells.

25 oncomitant knockdown of Atg7 in both AML and stromal cells.

26 e and hyaluronic acid) and mouse bone marrow stromal cells.

27 ion of ANG-2 expression from macrophages and stromal cells.

28 gration, localization, and interactions with stromal cells.

29 ct contact between the malignant B cells and stromal cells.

30 t C3aR expression and function in immune and stromal cells.

31 l role in the decidualization of endometrial stromal cells.

32 en deposition in the bone marrow mesenchymal stromal cells.

33 ant B cells cocultured with CD40L-expressing stromal cells.

34 by a subpopulation of ICAM1(+) perivascular stromal cells.

35 ent cytolysin, pyolysin (PLO), which targets stromal cells.

36 n of IL-17RA-expressing podoplanin(+)CD31(-) stromal cells, a profile associated with fibroblastic re

37 , these data suggest that CXCL12 secreted by stromal cells activates invasiveness of prostate cancer

38 tissue contains adipose-derived mesenchymal stromal cells (ADSCs) that have regenerative and reparat

39 d by genetic deletion ofCcl19 Thus, ACKR4 on stromal cells aids the egress of APCs from mouse skin, a

40 t trans-cellular regulation originating from stromal cells and affect tumour cells, highlighting the

41 MI-2 abrogated survival signals provided by stromal cells and BCR cross-linking and was effective ag

42 nship between a subpopulation of mesenchymal stromal cells and cancer cells in the bone marrow.

43 che that is composed of hematopoietic cells, stromal cells and extracellular matrix (ECM).

44 and breast cancer clusters recruit activated stromal cells and guide the sprouting of endothelial cel

45 pathways mediated by factors secreted by BM stromal cells and involved a switch from BCL2 to BCLXL-d

46 ne CXCL13 is expressed by FDC and follicular stromal cells and modulates the homing of CXCR5-expressi

47 Thus the interplay between stromal cells and myeloid cells in the myeloma microenvi

48 Bone marrow stromal cells and osteoblasts derived from these mice sh

49 on upregulates Tgfbeta signaling in prostate stromal cells and promotes progression of a reactive str

50 l migration toward CXCL12 and beneath marrow stromal cells and reduced CD44 expression.

51 th decreases MM cell adhesion to bone marrow stromal cells and reduces MM cell homing to the bone mar

52 t, which contains adjacent epithelial cells, stromal cells and smooth muscle cells, and soluble and c

53 ofibroblasts derive from Gli1(+) mesenchymal stromal cells and that a Gli inhibitor targets them for

54 s showed that the expression of caldesmon in stromal cells and the expression of osteopontin in both

55 our microenvironment ('host', which includes stromal cells and the immune system).

56 repressor, is down-modulated in skin cancer stromal cells, and Atf3 knockout mice develop aggressive

57 ation through endothelial cells, adhesion to stromal cells, and cell proliferation and display an inc

58 interactions between breast cancer cells and stromal cells, and iii) cancer-regulated angiogenesis.

59 The complex interplay between cancer cells, stromal cells, and immune cells in the tumor microenviro

60 of the ectonucleotidase CD73 by tumor cells, stromal cells, and immune cells is associated in cancer

61 and gradually degrade endosteal endothelium, stromal cells, and osteoblastic cells, whereas central m

62 ntiation and expansion of immune-suppressive stromal cells, and remodels the metabolic landscape to s

63 ce partial reprogramming of tumor-associated stromal cells, and respond to therapy.

64 interactions with developmentally supportive stromal cells, and that the relative motility of NK cell

65 ensional culture, with or without supporting stromal cells, and under these conditions they give rise

66 requirement maps to IL-4Ralpha expression by stromal cells, and we provide evidence that it regulates

67 PDGFRalpha+ stromal cells are major producers of IL-33 in adipose ti

68 xtensively, the contribution of fibroblastic stromal cells as portals of entry into the CNS was only

69 L12 axis was amplified in activated lymphoid stromal cells as shown in our in vitro model of human ly

70 like phenotype, including haematopoietic and stromal cells as well as a neuronal niche.

71 uingly, increased expression of Arf in tumor stromal cells, as in tumor keratinocytes themselves, con

72 port the application of adipose-derived stem/stromal cells (ASCs) for engineering the pulmonary vascu

73 w that MDM cells contribute to the postnatal stromal cells at the dorsal aspect of the prostatic uret

74 y, tolerability, and efficacy of mesenchymal stromal cell-based therapy in pilot clinical trials, inc

75 Uncovering new mechanisms that control stromal cell behavior and their accumulation within tumo

76 Genetic lineage tracing indicated that stromal cells blocking the ureteropelvic junction were d

77 dies have shown that bone marrow mesenchymal stromal cells (BM-MSC) protect AML blasts from spontaneo

78 Previously, we demonstrated that bone marrow stromal cell (BMSC) and CB-BF pellet cultures make carti

79 tes superoxide, which stimulates bone marrow stromal cells (BMSC) to AML blast transfer of mitochondr

80 ifference in the metabolomics of bone marrow stromal cells (BMSCs) derived from hyperglycaemic (type

81 ed osteogenic differentiation of bone marrow stromal cells (BMSCs) of Bag-1(+/-) (heterozygous) femal

82 Systemic infusion of bone marrow stromal cells (BMSCs), a major type of multipotent strom

83 and capacity to transfect human bone marrow stromal cells (BMSCs).

84 Human bone marrow stromal cells (BMSCs, also known as bone marrow-derived

85 Cancer cells need to communicate with stromal cells by humoral factors such as VEGF, FGFs, and

86 n cancer cells themselves and between cancer-stromal cells by secreted signaling molecules (ligands)

87 selectively autoamplify its own synthesis in stromal cells by signaling transcriptional repression of

88 nvincingly in rodent models that mesenchymal stromal cells can prolong solid organ graft survival and

89 1+/-0.002; P<0.001), multipotent mesenchymal stromal cell colony maximum (estimate+/-SE, 0.01+/-0.002

90 .01+/-0.002; P=0.002) in BM, and mesenchymal stromal cell colony maximum in PB (estimate+/-SE, 0.02+/

91 l layers were significantly reduced, and the stromal cell compartment did not expand and became atrop

92 Recapitulating tissue ECM composition and stromal cell composition enhanced cancer cell invasion.

93 Mesenchymal stromal cells, mesenchymal stromal cells-conditioned with carbon monoxide, fibrobla

94 ion, maintenance, and metastatic progression.Stromal cells contribute to tumor development but the me

95 ocytes, mucosal endothelium, epithelium, and stromal cells controls leukocyte recruitment and microen

96 We showed that mesenchymal stromal cells, cortical bone stem cells, and tail-tip fi

97 in PDAC tissues both expressed LIF, but only stromal cells could secrete it.

98 eciprocal interactions between malignant and stromal cells create a local microenvironment that foste

99 cale cell assemblages of encapsulated marrow stromal cells cultured in microwells, osteogenic differe

100 portant roles in blastocyst implantation and stromal cell decidualization.

101 se of defects in blastocyst implantation and stromal cell decidualization.

102 In the case of cancerous tissue, stromal cell-derived differentiation signals in particul

103 ered chemokine receptor CXCR7 and its ligand stromal cell-derived factor (SDF)-1 are known to be invo

104 (P = 0.04), stem cell factor (P = 0.05), and stromal cell-derived factor 1 (P = 0.03) compared to tho

105 In addition, the angiogenic factors stromal cell-derived factor 1 (SDF-1alpha), vascular end

106 nly in muscles atrophying because of cancer: stromal cell-derived factor 1 (SDF1), adenylate cyclase

107 on 1 (PLCepsilon1) as a crucial regulator of stromal cell-derived factor 1 alpha (SDF-1alpha)-induced

108 ling induced by the chemokine ligand CXCL12 (stromal cell-derived factor 1).

109 <em>CXCL12</em>, which encodes a chemokine, stromal cell-derived factor 1, that is expressed in card

110 Stromal cell-derived factor 1/CXCR4 inhibition impaired

111 r adhesion molecule 1; interleukin 6 [IL-6]; stromal cell-derived factor 1; tissue inhibitor of metal

112 of vascular endothelial growth factor D and stromal cell-derived factor 1alpha (P = .037 and .025, r

113 gration toward formyl-Met-Leu-Phe (fMLP) and stromal cell-derived factor 1alpha (SDF-1alpha) as well

114 In addition, median stromal cell-derived factor-1 (SDF-1) levels were 43% hi

115 r pathway may participate, together with the stromal cell-derived factor-1 (SDF-1)/C-X-C chemokine re

116 L5551 inhibited CXCR4 binding to its ligand, stromal cell-derived factor-1alpha, and reduced hypoxia-

117 ived factor-1alpha, and reduced hypoxia- and stromal cell-derived factor-1alpha-mediated migration do

118 ly replication of certain prion strains upon stromal cell-derived follicular dendritic cells (FDC) in

119 histone H3 lysine 27 (H3K27me3) in decidual stromal cells dictate both elements of pregnancy success

120 ritic cells (DCs), rather than TECs or other stromal cells, disrupts the S1P gradient, preventing egr

121 In addition, Meflin is found on stromal cells distributed throughout the BM, and on peri

122 ection of cytokines that improve mesenchymal stromal cell engraftment into the heart both in normal c

123 In series 2, umbilical cord-mesenchymal stem/stromal cells enhanced animal survival and decreased alv

124 Successful implantation requires endometrial stromal cell (ESC) decidualisation.

125 signaling mediated IL-4-induced endometrial stromal cell (ESC) proliferation ex vivo, and that genit

126 t IRF-1 restricts CHIKV and RRV infection in stromal cells, especially muscle cells, and that this co

127 nsduction of bone marrow-derived mesenchymal stromal cells ex vivo, followed by intramyocardial cell

128 rties in an in vivo model of squamous cancer-stromal cell expansion.

129 Mesenchymal stromal cells exposed to carbon monoxide, with docosahex

130 We found that, in vitro, bone marrow stromal cells exposed to IR enter DNA replication follow

131 efficacy of >98% in pre-purified mesenchymal stromal cells, extracted from human dental pulp, with no

132 emonstrate that EAV has specific tropism for stromal cells (fibrocytes and possibly tissue macrophage

133 We show that SerpinB2 is required by stromal cells for normal collagen remodelling in vitro,

134 l for the decidualization of the endometrial stromal cells for successful pregnancy.

135 ps have observed increased nuclear CTNNB1 in stromal cells from a high frequency of MDS/AML patients,

136 Bone marrow stromal cells from Clec11a-deficient mice showed impaire

137 xeno-free conditions, with mesenchymal stem/stromal cells from human bone marrow, in a rat model of

138 We wished to compare mesenchymal stem/stromal cells from human umbilical cord, grown in xeno-f

139 rotein 1 (HAPLN1) is produced in bone marrow stromal cells from MM patients, is detected in patients'

140 NA methylome analysis of bone marrow-derived stromal cells from myelodysplastic syndrome (MDS) patien

141 We isolated human endometrial stromal cells from nonpregnant donors with a previous pr

142 on of SOD3 in tumor stroma, we characterized stromal cells from the thyroid.

143 n of biallelic RELA expression in protecting stromal cells from TNF-mediated cell death, thus delinea

144 that mature hematopoietic cells regulate BM stromal-cell function.

145 The secretome of cancer and stromal cells generates a microenvironment that contribu

146 Moreover, primary splenic stromal cells grown in the presence of IL-17 enhanced th

147 who received umbilical cord-mesenchymal stem/stromal cells had improvements in oxygenation, respirato

148 llicular helper (TFH) cells and infiltrating stromal cells have been shown to favor FL B-cell growth,

149 l line M2-10B4 and human primary bone marrow stromal cells have confirmed that NELL-1 enhances BMP2-i

150 Mesenchymal stromal cells have emerged as potential candidates for c

151 Activated meningeal fibroblastic stromal cells have the capacity to rapidly elaborate an

152 of GPR64 was increased in human endometrial stromal cells (hESCs) during in vitro decidualization.

153 ecidual gene expression in human endometrial stromal cells (HESCs).

154 Scaffolds coated with human mesenchymal stromal cells (hMSCs) proved to be superior in terms of

155 ere we discuss how EVs released by cancer or stromal cells impact the proliferation, differentiation,

156 logue octreotide induces apoptosis in VHL-HB stromal cells in a dose-dependent fashion by BAX - caspa

157 te responses in lymph nodes, but the role of stromal cells in adipose tissue inflammation is unknown.

158 vered a pathogenic function for fibroblastic stromal cells in alloimmune reactivity that can be disso

159 e of Notch ligands expressed by fibroblastic stromal cells in alloimmunity.

160 -related with IL-6 and HGF overexpression in stromal cells in human gastric cancer tissues.

161 tly augmented in macrophages and mesenchymal stromal cells in inflamed human pulp tissues.

162 llular communication between tumor cells and stromal cells in local and distant microenvironments.

163 ectin stimulation of alpha5beta1 integrin on stromal cells in PDA results in reduced angiogenesis and

164 Cancer cells and stromal cells in PDAC tissues both expressed LIF, but on

165 Stromal cells in the bone marrow secrete a variety of cy

166 el function for podoplanin on periarteriolar stromal cells in the bone marrow: promoting megakaryocyt

167 Recent research has highlighted the role of stromal cells in the generation and persistence of chron

168 unofluorescence indicated that podoplanin(+) stromal cells in the red pulp were the primary producers

169 resent over 90% of CRC, RSPO3 is produced by stromal cells in the tumor microenvironment and the acti

170 aging the Shh-IL6-RANKL signaling network in stromal cells in the tumor microenvironment.

171 CXCL12 and reducing adhesion to mesenchymal stromal cells in vitro We also found that HIF-2alpha str

172 evaluate the effect of CXL on human corneal stromal cells in vitro, we developed a 3-D in vitro CXL

173 also give rise to bone marrow adipocytes and stromal cells in vivo.

174 and other molecules between transformed and stromal cells, including fibroblasts, endothelial and im

175 Interestingly, coculture of AML cells with stromal cells increased autophagy and chemoresistance in

176 Interactions between MM and stromal cells increased IL-8 secretion by stromal cells

177 utilize pH modulation to recruit associated stromal cells, induce partial reprogramming of tumor-ass

178 tumour tissue, independent of proliferation, stromal cell infiltration and tumour characteristics.

179 , such as cancer-immune system interactions, stromal cell interactions, oncoviruses, and sensitivity

180 amic scaffolds coated with human mesenchymal stromal cells into immune-deficient mice, we were able t

181 nous injection of singly encapsulated marrow stromal cells into mice delays clearance kinetics and su

182 ed mice receiving human amniotic mesenchymal stromal cells intravenously or intracerebroventricularly

183 The decidualization of uterine stromal cells is a key event in implantation.

184 pproach in a 3D carrier scaffold seeded with stromal cells is an effective in vivo niche model for st

185 ion of the Hh effector Smoothened (Smo) from stromal cells is associated with the loss of osteoblasto

186 pid mediator (LM) profiles of tendon-derived stromal cells isolated from healthy donors and patients

187 d the number of bone marrow mesenchymal stem/stromal cells, likely due to decreased expression of PDG

188 In vitro studies using the mouse bone marrow stromal cell line M2-10B4 and human primary bone marrow

189 ls was reduced in the presence of lymph node stromal cells (LNSCs) from NOD mice but not from mice la

190 Stromal cell (macrophage) gene regulation and signalling

191 The percentage of stromal cells, macrophages, hematopoietic stem cells and

192 Mesenchymal stromal cells, mesenchymal stromal cells-conditioned wit

193 depends upon continuous guidance from thymus stromal cell microenvironments.

194 tentially unfavorable effects of mesenchymal stromal cell (MSC) activation on the heart.

195 e been investigated for inducing mesenchymal stromal cell (MSC) differentiation towards the smooth mu

196 Human mesenchymal stromal cell (MSC) lines can vary significantly in their

197 echanisms underlying OA-mediated mesenchymal stromal cell (MSC) osteogenic differentiation are not kn

198 Mesenchymal stromal cell (MSC) therapy demands the attention of clin

199 both ex vivo bone marrow-derived mesenchymal stromal cells (MSC) and in vitro 3T3-L1 preadipocytes si

200 Mesenchymal stromal cells (MSC) are potential renal therapeutics.

201 c niche by examining the role of mesenchymal stromal cells (MSC) in cancer cell homing.

202 Autologous mesenchymal stromal cells (MSC) treatments have shown feasibility, s

203 been suggested to originate from mesenchymal stromal cells (MSC), but their relationship with MSCs is

204 including immune cells and mesenchymal stem/stromal cells (MSC).

205 Mesenchymal stromal cells (MSCs) are a promising candidate for a cel

206 As mesenchymal stromal cells (MSCs) are continuously exposed in vivo to

207 Mesenchymal stromal cells (MSCs) are one of major components of the

208 RATIONALE: Mesenchymal stromal cells (MSCs) are promising therapeutic strategie

209 urine models of BMF that Gli1(+) mesenchymal stromal cells (MSCs) are recruited from the endosteal an

210 Mesenchymal stromal cells (MSCs) are strongly immunosuppressive via

211 esicles (EVs) isolated from mesenchymal stem/stromal cells (MSCs) contribute to recovery of damaged t

212 -term passaged (P10) aging human mesenchymal stromal cells (MSCs) could be used for bone tissue regen

213 ed that coculture of islets with mesenchymal stromal cells (MSCs) enhanced islet insulin secretory ca

214 on for a first-in-human trial of mesenchymal stromal cells (MSCs) for septic shock, we applied system

215 cell-based therapy options, mesenchymal stem/stromal cells (MSCs) from bone marrow, adipose tissue, a

216 the presence of multipotent mesenchymal stem/stromal cells (MSCs) in non-carcinogenic thyroids and pa

217 ThPO, and IL-6) from bone marrow mesenchymal stromal cells (MSCs) in vitro.

218 Mesenchymal stem/stromal cells (MSCs) play crucial roles in maintaining t

219 Mesenchymal stem/stromal cells (MSCs) possess osteogenic potential and pr

220 Mesenchymal stromal cells (MSCs) present in the bone marrow microenv

221 Mesenchymal stromal cells (MSCs) tend to infiltrate into tumors and

222 these issues by using human mesenchymal stem/stromal cells (MSCs) that produce EVs when incubated in

223 tu differentiation of BM-derived mesenchymal stromal cells (MSCs).

224 creas, colon, and prostate-appears rooted in stromal cell niche activity.

225 Such stromal cell niches can ultimately foster the establishm

226 zed Notch-mediated immunopathogenic role for stromal cell niches in secondary lymphoid organs after a

227 Since in patient-derived xenografts (PDXs) stromal cells of the human tumour are substituted by mur

228 duced GPR64 expression in the epithelial and stromal cells of the uterus in ovariectomized wild-type

229 epithelial cells, not in basal epithelial or stromal cells, of BRCA1 mutation carriers.

230 and hypoxic signaling pathways in tumor and stromal cells on each step of the metastatic cascade.

231 omal cells with bone marrow-mesenchymal stem/stromal cells on physiologic indices of lung injury, cel

232 ryopreserved umbilical cord-mesenchymal stem/stromal cells on survival, as well as measures of injury

233 , and no antigen was seen in fetal placental stromal cells or fetal organs.

234 ion at all gestational ages, associated with stromal cells or near blood vessels, but was absent in t

235 ion and reduced G-CSF expression in CRTC2/3m stromal cells, our results demonstrate how cross-couplin

236 nstrated here that FL-infiltrating LN and BM stromal cells overexpressed CXCL12 in situ.

237 Evidence suggests that stromal cells play critical roles in tumor growth.

238 ed a range of ECM densities, composition and stromal cell populations.

239 lves, triggered CXCL12 upregulation in human stromal cell precursors.

240 COX-2 is localised to stromal cells (predominantly macrophages) in human and m

241 l cells (BMSCs), a major type of multipotent stromal cells, produces pain relief (antihyperalgesia) t

242 ance on bovine serum during mesenchymal stem/stromal cell proliferation.

243 o-free human umbilical cord-mesenchymal stem/stromal cells reduce the severity of rodent E. coli-indu

244 Stromal cells regulate leukocyte responses in lymph node

245 Although mesenchymal stem/stromal cells represent a promising therapeutic strategy

246 des evidence that inhibiting FDFT1 increases stromal cell resilience to a cholesterol-dependent cytol

247 Thus, understanding how tumor and stromal cells respond to hypoxia will allow for the desi

248 s underlying the crosstalk between tumor and stromal cells revealed that melanoma cells produced PDGF

249 the functional capacity of tumor-associated stromal cells revealed that myeloid cells, primarily DCs

250 at present with highly vascular tumours with stromal cells similar to human haemangioblastomas.

251 ic commitment, and the LepR(+)Runx2-GFP(low) stromal cells sit atop the BM stromal hierarchy.

252 ibrosis thought to be induced by mesenchymal stromal cells stimulated by overproduced growth factors.

253 ailable data on culture-expanded mesenchymal stromal cells tested in renal transplantation, AKI, and

254 us hiPSCs as source and generates a range of stromal cells that co-develop with parenchymal cells to

255 is study, we investigate whether mesenchymal stromal cells that constitute a supportive microenvironm

256 itioning within the tissue are controlled by stromal cells that construct the barriers of the CNS.

257 r and molecular specialization within thymic stromal cells that enables their regulation of specific

258 mus, Nes expression was restricted to thymic stromal cells that expressed cerebellar degeneration-rel

259 -chip" platform incorporates human tumor and stromal cells that grow in a 3D extracellular matrix and

260 ntly, 17f had minimal effects on bone marrow stromal cells that play vital functions in the microenvi

261 ic function for secretory autophagy in HNSCC stromal cells that promotes malignant progression.

262 of Dll1 and Dll4 in subsets of fibroblastic stromal cells that were derived from chemokine Ccl19-exp

263 In the absence of stromal cells, the stepwise order of rearrangements is b

264 nt of the safety and efficacy of mesenchymal stromal cell therapies to allow the translation of this

265 d promising results for HSCT and mesenchymal stromal cell therapy as alternatives to systemic therapi

266 Umbilical cord-mesenchymal stem/stromal cell therapy decreased nicotinamide adenine dinu

267 or patients with fistulizing CD, mesenchymal stromal cell therapy deposits MSCs locally, into fistuli

268 cell transplantation (HSCT) and mesenchymal stromal cell therapy have been proposed for patients wit

269 Umbilical cord-mesenchymal stem/stromal cells, therefore, represent an attractive option

270 nd stromal cells increased IL-8 secretion by stromal cells through cell-cell adhesion and soluble fac

271 ontal transfer of genetic material from host stromal cells to cancer cells triggers the evolution of

272 ommunication bridges between tumor cells and stromal cells to create a permissive microenvironment fo

273 iptional effector, acts within mouse mammary stromal cells to direct a hormone-responsive niche signa

274 ular cholesterol increases the resilience of stromal cells to PLO.

275 eta-cyclodextrin increased the resilience of stromal cells to PLO.

276 otential for umbilical cord-mesenchymal stem/stromal cells to reduce E. coli-induced oxidant injury.

277 Intracardiac injection of mesenchymal stromal cells transiently preconditioned with cardiotrop

278 s comparable to bone marrow-mesenchymal stem/stromal cell treatment.

279 nt, endothelial cells (ECs) are an important stromal cell type interacting with malignant cells to fa

280 affolds, we tested the capacity of different stromal cell types to support human HSCs.

281 ontent of many tumours associated immune and stromal cell types, their therapeutically relevant ratio

282 ed method, and use it to infer 64 immune and stromal cell types.

283 e separation of viable from non-viable human stromal cells using remote dielectrophoresis, in which a

284 l trophoblast cells and maternal endometrial stromal cells, using single-cell transcriptomics.

285 ted that regulated activation of TGF-beta by stromal cells was able to directly control epithelial re

286 This imbalance between adipocytes and stromal cells was accompanied by overexpression of the c

287 Loss of Lkb1 in stromal cells was associated with induction of an inflam

288 tment of cardiotrophin-1-treated mesenchymal stromal cells was consequent to signal transducer and ac

289 r, we found that expression of Hsp70 in host stromal cells was essential to support tumor growth.

290 Furthermore, podoplanin staining on stromal cells was more diffuse, and CXCL12 staining was

291 Carbon monoxide preconditioned mesenchymal stromal cells were also able to alleviate organ injury,

292 gen receptor alpha (Esr1) from mouse uterine stromal cells, where the embryo is implanted during preg

293 alized channels lined with human bone marrow stromal cells, which adopt a mural cell-like phenotype t

294 imulated the production of the CXCL13 by TME stromal cells, which in turn promoted ILC3-stromal inter

295 n nonhematopoietic, nonepithelial intestinal stromal cells, which respond to OSM by producing various

296 of a synapse between developing NK cells and stromal cells, which we term the developmental synapse.

297 rgeted disruption of both CRTC2 and CRTC3 in stromal cells with a mesenchymal Prx1-Cre transgene also

298 ryopreserved umbilical cord-mesenchymal stem/stromal cells with bone marrow-mesenchymal stem/stromal

299 , Chung and colleagues present evidence that stromal cells within lymphoid tissue express the Notch l

300 esident B cells account for more than 20% of stromal cells within visceral adipose tissues; however,