ライフサイエンスコーパス: stromal

1 oto-oncogene c-Myb and conclude that loss of stromal 5-LO expression favors tumor progression.

2 70) that lung adenocarcinomas increase bone stromal activity in the absence of bone metastasis.

3 s in survival and mutational load as well as stromal and immune cell composition.

4 a) signaling through IL-1R and MyD88 in both stromal and immune cells drive inflammation in Ptpn6(spi

5 Stromal and immune cells had consistent expression progr

6 geneous tumour cells along with neighbouring stromal and immune cells.

7 ls that separate HER2+ cancer cells from the stromal and immune microenvironment in HER2+ invasive br

8 utions of multiple tumor clones and assorted stromal and infiltrating cell populations to pooled geno

9 Patched 1 (Ptch1) has epithelial, stromal and systemic roles in murine mammary gland organ

10 secreted by cancer cells, is abundant in the stromal and tumour compartments of aggressive ovarian ca

11 is associated with the reduction in both its stromal and vascular components.

12 The diverse malignant, stromal, and immune cells in tumors affect growth, metas

13 parated gene expression profiles from tumor, stromal, and immune cells using a non-negative matrix fa

14 icantly lower (vascular area: beta = -0.306, stromal area: beta = -0.377, both P < .001) than control

15 er adjusting for age, choroidal vascular and stromal areas were significantly lower (vascular area: b

16 ss, choroidal volume, choroidal vascular and stromal areas within the macular (6 mm) and foveal (1.5

17 Iris stromal atrophy was noted in 26 patients (52%), progress

18 We identified four stromal axes enriched for T cells (T), B cells (B), epit

19 method (STROMA4) assigns a score along each stromal axis for each patient and then combined the axis

20 Stromal, but not hematopoietic, cells were the essential

21 d can be tissue-engineered onto thin corneal stromal carriers.

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

23 Stromal cell (macrophage) gene regulation and signalling

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

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

26 portant roles in blastocyst implantation and stromal cell decidualization.

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

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

29 depends upon continuous guidance from thymus stromal cell microenvironments.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

90 Mesenchymal stromal cells have emerged as potential candidates for c

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

109 Stromal cells regulate leukocyte responses in lymph node

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

141 gration, localization, and interactions with stromal cells.

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

143 l role in the decidualization of endometrial stromal cells.

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

145 en deposition in the bone marrow mesenchymal stromal cells.

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

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

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

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

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

151 upon decidualization of primary endometrial stromal cells.

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

153 sistant disease in cocultures of bone marrow stromal cells.

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

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

156 PU-H71 induced apoptosis in the presence of stromal co-culture or cytoprotective survival signals.

157 Stromal coculture did not prevent leukemia cell cycle ac

158 Tumor-stromal communications impact tumorigenesis in ways that

159 c mice revealed high levels of CXCL12 in the stromal compartment as well as high staining for CXCR4 a

160 cant gene-expression changes in the proximal stromal compartment, and estrogen treatment uniquely aff

161 SerpinB2 expression, particularly in the stromal compartment, is associated with reduced metastas

162 cuss the implications for the development of stromal compartment-specific therapies.

163 ymic dendritic cells (DCs) and, in these two stromal compartments, TSSP edits the peptide repertoire

164 rthritis but in any disease with a prominent stromal component.

165 efined HNSCC subtypes by their malignant and stromal composition and established p-EMT as an independ

166 ay improve our understanding of how specific stromal composition could impact T-cell activity, with p

167 Stromal content heavily impacts the transcriptional clas

168 aring these alternative collagen sources for stromal contributions to stiffness, organization and ult

169 iR-221(hi) CAF microvesicles and established stromal CSC niches in experimental and patient-derived b

170 Here we show that stromal cues elicit an adaptive response in the cancer c

171 vation is the consequence of mutant Kras and stromal cues, providing insight into the role of the tum

172 the bone marrow retention signal provided by stromal-derived CXCL12, thereby enabling dissemination o

173 ed ROCK in LSK cells and sensitized them for stromal-derived factor-1alpha (SDF)-induced migration.

174 Stromal-derived intratumoural heterogeneity (ITH) has be

175 maintain HSPCs ex vivo, we demonstrate that stromal EVs play a critical role in the regulation of HS

176 h SRP9/14 and generates unshielded RN7SL1 in stromal exosomes.

177 , two pathologies characterized by excessive stromal expansion, we used mouse models to characterize

178 r outlet obstruction, most likely because of stromal expansion.

179 The remodeling of the stromal extracellular matrix (ECM) has a crucial, but in

180 s process can expose epithelial cells to the stromal extracellular matrix (ECM), which is distinct fr

181 show that mesenchymal cadherin-11 modulates stromal fibroblast function.

182 sforming growth factor beta, which activates stromal fibroblast markers.

183 Stromal fibroblast-specific deletion of mouse orthologs

184 paired normal and prostate cancer-associated stromal fibroblasts (CAFs) derived from a coculture cell

185 Our study identifies a crosstalk between stromal fibroblasts and epithelial cells under starvatio

186 cies in the switching expression of MMP-3 in stromal fibroblasts and prostate cancer cells during tum

187 These results suggest that stromal fibroblasts expressing cadherin-11 regulate adip

188 bligate component of the matrix assembled by stromal fibroblasts from head and neck squamous cell car

189 e precursors while favoring the formation of stromal fibroblasts.

190 eal epithelium underlying the stimulation of stromal fibrosis and myofibroblast formation in corneal

191 ADCDTI and FA showed correlation only with stromal fraction (r = 0.512 and -0.413, respectively; P

192 lectron microscopy analysis of ADHE-enriched stromal fractions revealed fine spiral structures, simil

193 0.485, -0.422 for cytoplasmic, cellular, and stromal fractions, respectively; P < .040).

194 ssion profiles in the prostate and show that stromal gene signature changes ahead of the epithelial g

195 A stromal gene signature reflecting bone remodeling and im

196 Runx2-GFP(low) stromal cells sit atop the BM stromal hierarchy.

197 e of Notch signaling in regulating prostatic stromal homeostasis.

198 Using mouse models, we show that stromal insufficiency limits the number of donor-derived

199 e human CRAC channel Orai1 by its activator, stromal interacting molecule 1 (STIM1).

200 In this study, we use mice deficient in stromal interacting molecules 1 and 2, which are require

201 , ORAI2, and ORAI3 proteins and activated by stromal interaction molecule (STIM) 1 and STIM2.

202 Ca(2+) (CRAC) channels that are activated by stromal interaction molecule (STIM) 1 and STIM2.

203 We studied the role of stromal interaction molecule 1 (STIM1) in coupling store

204 re fully reconstituted via two proteins, the stromal interaction molecule 1 (STIM1), a Ca(2+) sensor

205 amines this issue by focusing on the role of stromal interaction molecule 1 (STIM1), an endo/sarcopla

206 STIM1 (stromal interaction molecule 1) regulates Ca(2+) signali

207 n the molecular machinery that mediate SOCE: stromal interaction molecule-1 (STIM1), which functions

208 Stromal-interaction molecule 1 (STIM1), upon sensing the

209 insight into the HNSCC ecosystem and define stromal interactions and a p-EMT program associated with

210 E stromal cells, which in turn promoted ILC3-stromal interactions and production of the cancer cell m

211 reduce SOX11-enhanced MCL cell migration and stromal interactions and revert cell adhesion-mediated d

212 represents a central node in mediating tumor-stromal interactions that promote osteolytic bone metast

213 Taken together, our results illuminate tumor-stromal interactions, which drive metastasis, and provid

214 activating paracrine Shh signaling in tumor-stromal interactions.

215 The stromal intermediate of TIC40 integrated into the envelo

216 ancer patients whose tumors express both low stromal JAG1 and low stromal PTEN exhibit a shorter time

217 forming activity implying a direct role for stromal JAGGED-1 in regulation of MaSC properties.

218 also found in the stroma following anterior stromal keratectomy, in which surgical removal of the ep

219 1-infected mice prevented the development of stromal keratitis lesions more effectively than did cont

220 t herpes epithelial keratitis without herpes stromal keratitis sequelae, possessed a significant leuk

221 to be highly plastic and capable of inducing stromal keratitis when adoptively transferred into Rag1(

222 pical corticosteroids and oral acyclovir for stromal keratitis.

223 ight foreshadow the partitioning of PSI into stromal lamellae in plants, similarly sustained by long-

224 Decellularized human corneal stromal laminas transplantation seems safe and moderatel

225 strongly supporting the concept of targeting stromal LDH-A as an effective strategy to blunt tumoral

226 terogeneity in their adhesion strength under stromal-like conditions, unlike their nonmetastatic coun

227 taking advantage of two fetal liver-derived stromal lines with widely differing abilities to maintai

228 Together, our findings demonstrate that stromal lumican restrains PDAC cell growth through media

229 parameters (nuclear, cytoplasmic, cellular, stromal, luminal fractions) were determined.

230 e to a chemoattractant gradient created from stromal, lymphoid, or antigen presenting cell interactio

231 Thymic stromal lymphopoietin (TSLP) and IL-7 are related cytoki

232 e pro-TH2 cytokines IL-25, IL-33, and thymic stromal lymphopoietin (TSLP) are associated with FA, and

233 RATIONALE: Thymic stromal lymphopoietin (TSLP) is known to be elevated and

234 red by an increased expression of the thymic stromal lymphopoietin (TSLP) proinflammatory cytokine.

235 n ILC2s were stimulated with IL-7 and thymic stromal lymphopoietin (TSLP), 2 ligands of IL-7 receptor

236 helial cell-derived cytokines such as thymic stromal lymphopoietin (TSLP), IL-33, and IL-25 may drive

237 ociated with an increase in levels of thymic stromal lymphopoietin (TSLP), IL-9, and IL-13, but not I

238 the epithelial-cell-derived cytokine thymic stromal lymphopoietin (TSLP), in patients whose asthma r

239 ytes is the pro-inflammatory cytokine thymic stromal lymphopoietin (TSLP).

240 se dust mite (HDM)-induced release of thymic stromal lymphopoietin and GM-CSF from tracheal epithelia

241 e expression in response to IL-33 and thymic stromal lymphopoietin in vitro.

242 markers (CCL2, CCL5, CCL11, IL-3, and thymic stromal lymphopoietin) at 3 time points (ie, during the

243 kines (interleukin [IL] 25, IL33, and thymic stromal lymphopoietin) by colon tissues, which activated

244 s, with an emphasis on the actions of thymic stromal lymphopoietin, IL-25, and IL-33 at the epithelia

245 gics similarly inhibit TH2 cytokines (thymic stromal lymphopoietin, IL-4, IL-5, IL-13, and the itch-s

246 iated cytokines (interleukin (IL)-33, thymic stromal lymphopoietin, IL-5 and IL-13), serum immunoglob

247 matory markers IL-1, IL-4, IL-13, and thymic stromal lymphopoietin.

248 cells and promotes progression of a reactive stromal microenvironment in the Pten null prostate cance

249 myofibroblast differentiation in the mammary stromal microenvironment.

250 se to multiagent chemotherapy, we found that stromal Nf1 status had no effect.

251 The ability of stromal niche cells to control and adapt epithelial stem

252 During normal tissue repair, stromal niche signals, often Hedgehog-induced, promote e

253 We show that triggering of stromal NOTCH-MYC by breast cancer cells results in a PO

254 stromal opacities persisting after DSAEK and stromal opacities occurring secondarily in post-DSAEK co

255 dications for DALK after DSAEK included both stromal opacities persisting after DSAEK and stromal opa

256 forkhead box FOXD1 cell lineage, from which stromal progenitors arise.

257 suggesting that chronic activity of HIF2 in stromal progenitors impairs kidney development.

258 ubtypes are largely re-capitulated using non-stromal protein markers.

259 stic2 locus identified a previously unknown stromal protein that interacts physically with both ALB4

260 tumors express both low stromal JAG1 and low stromal PTEN exhibit a shorter time to recurrence than t

261 mammary epithelium of mice with and without stromal PTEN expression.

262 Combined, these results unveil a novel stromal PTEN-to-JAGGED-1 axis in maintaining the MaSC ni

263 feration, epithelial-mesenchymal transition, stromal reaction, and angiogenesis through autocrine and

264 OSDI score, basal epithelial cells density, stromal reflectivity and sub-basal nerve tortuosity (p =

265 OSDI score, basal epithelial cells density, stromal reflectivity, sub-basal nerves tortuosity (p = 0

266 -23 as the principal instructing signals for stromal reprogramming.

267 imilar to native PanINs, including prominent stromal responses.

268 n all cells (Sharpin(cpdm)), and mice with a stromal (S100a4-Cre) deletion of Sharpin, have reduced m

269 80 consecutive keratoconic eyes without deep stromal scarring, with at least 1 postoperative examinat

270 ded of a direct interaction with Stt7 on the stromal side of the membrane.

271 ow levels of either alone suggesting similar stromal signaling in advanced disease.

272 in A2 (AnxA2) at Y23 and Y333 in response to stromal signals HGF and IGF-1, respectively, and IGF-1 e

273 The stromal signals that promote B lymphopoiesis remain poor

274 Stromal SOD3 had a stimulatory effect on cancer cell gro

275 Mesenchymal stromal stem cells (MSCs) isolated from adult tissues of

276 al metabolic environment affects mesenchymal stromal/stem cells (MSCs) from umbilical cord's Wharton'

277 ed cell death protein 1 (PD-1) expression on stromal (sTILs) and intratumoral TILs.

278 ry MCL tumors overexpress cell migration and stromal stimulation gene signatures compared with their

279 tissues of living animals, such as the inner stromal structure of a live mouse cornea, the fine struc

280 The peripheral stromal structure of the cyt b6f complex had, until now,

281 -thickness recipient cornea (up to the DSAEK stromal surface),7.0 mm in diameter, with a donor lamell

282 alized biomimetic colorectal tumouroids with stromal surrounds that comprised a range of ECM densitie

283 h multivariate Cox regression models fitting stromal TILs as a continuous variable (per 10% increment

284 icant loss of cells invading the surrounding stromal tissue and reduced HepG2 colonization into lung

285 d with an impaired early vascularization and stromal tissue growth as well as reduced glandular secre

286 Tumor invasion into surrounding stromal tissue is a hallmark of high grade, metastatic c

287 Gastrointestinal stromal tumor (GIST) is the most common subtype of sarco

288 , we reported that estrogen signaling in the stromal tumor microenvironment is associated with cervic

289 geted for cancer therapy in gastrointestinal stromal tumors (GISTs) and chronic myelogenous leukemia

290 GI stromal tumors (GISTs) are neoplasms with a varying mali

291 ival (RFS) in patients with gastrointestinal stromal tumors (GISTs) treated with surgery and adjuvant

292 adult (AYA) population with gastrointestinal stromal tumors (GISTs).

293 s, fostering hyperplasia in gastrointestinal stromal tumours (GISTs), and additional genetic alterati

294 grate the complexities of lymphatic biology, stromal variability, chemoattractant distribution, and f

295 Analysis of the stromal vascular fraction from periprostatic white adipo

296 In WAT, Id1 is mainly localized in the stromal vascular fraction, where the adipose progenitor/

297 lated miRNAs targeting growth factors in the stromal-vascular fraction (SVF) under conditions that pr

298 r data highlight the importance of balancing stromal versus adipogenic cell expansion during white ad

299 bit reduced thylakoid contents and increased stromal volume, indicative of defective development.

300 The impact of stromal WNT2 on carcinoma formation or progression was n