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1 last differentiation and bone formation from mesenchymal stem cells.
2 e formed through adipogenesis from precursor mesenchymal stem cells.
3 ) were recently identified as liver-resident mesenchymal stem cells.
4 -1beta in micromass pellet cultures of human mesenchymal stem cells.
5 me of Ewing sarcoma compared with progenitor mesenchymal stem cells.
6 are the mesodermal lineage that derives from mesenchymal stem cells.
7 aling at endoplasmic reticulum (ER) in human mesenchymal stem cells.
8 n of human neural stem cells (NSCs), but not mesenchymal stem cells.
9 support mechanosensitive differentiation of mesenchymal stem cells.
10 dated in experiments using human bone marrow mesenchymal stem cells.
11 s such as dermal fibroblasts and endometrial mesenchymal stem cells.
12 outperform bone marrow-mononuclear cells and mesenchymal stem cells.
13 to adhered cells was demonstrated with human mesenchymal stem cells.
14 PCR in human synovial fibroblasts and murine mesenchymal stem cells.
15 define populations of incisor epithelial and mesenchymal stem cells.
17 ey repair achieved by adipose tissue-derived mesenchymal stem cells (ad-MSCs) is associated with rest
18 intraperitoneal injection of human amniotic mesenchymal stem cells (AFSCs) into a mouse model of OI
22 ypes of bone marrow mononuclear cells: CD90+ mesenchymal stem cells and CD45+ CD14+ auto-fluorescent+
23 y also promoted the differentiation of human mesenchymal stem cells and diminished clonogenic surviva
25 ctivity in primary human bone marrow-derived mesenchymal stem cells and human osteosarcoma-derived ce
26 osteoclasts can be differentiated from hiPSC-mesenchymal stem cells and macrophages when co-cultured
28 ified histone signature in lineage-committed mesenchymal stem cells and preadipocytes that pairs H3K4
29 ed osteogenesis of mouse bone marrow-derived mesenchymal stem cells and promotes myogenic induction o
30 review directions and advances in the use of mesenchymal stem cells and their derived hepatocytes for
31 differences in terms of attachment of human mesenchymal stem cells, and allow their differentiation
32 ed SNPs were enriched in enhancers active in mesenchymal stem cells, and analysis of annotated genes
33 he fibrotic liver, human bone marrow-derived mesenchymal stem cells, and human hepatogenic profibroti
35 Similar findings were obtained with human mesenchymal stem cells, and results were confirmed by ta
36 resident fibroblasts, identified a subset of mesenchymal stem cells, and shown these populations to b
37 ineage commitment of primary mouse and human mesenchymal stem cells, and support the growth of a broa
38 hase 1 trial to determine whether autologous mesenchymal stem cells, applied in a bioabsorbable matri
42 ng the cell types under investigation, adult mesenchymal stem cells are widely studied, and in early
43 ls (BMSCs, also known as bone marrow-derived mesenchymal stem cells) are manufactured using many diff
44 allow enzyme-free passaging and expansion of mesenchymal stem cells, as well as isolation of cells po
46 n of osterix, collagen I, and osteocalcin by mesenchymal stem cells at 7 and 14 d of stimulation and
48 We recently identified CD271(+) bone marrow-mesenchymal stem cells (BM-MSCs) as a potential site of
50 osteogenic potential and senescence of bone mesenchymal stem cells (BMSCs) isolated from a TDO patie
51 ic effect of injections of local bone marrow mesenchymal stem cells (BMSCs) on osteoarthritis (OA) of
52 ce has demonstrated that bone marrow-derived mesenchymal stem cells (BMSCs) showed great potential in
53 ve target cells, such as bone marrow-derived mesenchymal stem cells (BMSCs), remains challenging.
54 tor cells, endothelial progenitor cells, and mesenchymal stem cells can be successfully concurrently
55 global view of phenotypic diversification of mesenchymal stem cell-cardiomyocyte hybrids and associat
57 ting of mature white adipocytes, multipotent mesenchymal stem cells, committed progenitor cells, fibr
58 mouse embryonic fibroblasts and bone marrow mesenchymal stem cells compared with wild-type counterpa
59 We evaluated the therapeutic potential of mesenchymal stem cell-conditioned medium (CM-MSC) as an
61 tential biomarkers for potency prediction of mesenchymal stem cell-derived and pluripotent stem cell-
62 low extracorporeal CO2 removal technique and mesenchymal stem cell-derived microparticles, have also
63 lance between bone formation, carried out by mesenchymal stem cell-derived osteoblasts, and bone reso
64 ogels, Alakpa et al. (2016) demonstrate that mesenchymal stem cell differentiation is paired to deple
66 in vitro, compared with bone marrow-derived mesenchymal stem cells, displayed a 55-fold increase in
67 rmation, demonstrating that mechanosensitive mesenchymal stem cells drive condensation of heterotypic
68 tissue-engineered cultures comprised of rat mesenchymal stem cells dynamically seeded on 85% porous
69 lly or physiologically related cells, namely mesenchymal stem cells, endothelial cells or granulocyte
70 are actively incorporated by endothelial and mesenchymal stem cells ex vivo and in vivo and that the
73 We here test whether a new population of mesenchymal stem cells from human gingiva (GMSCs), which
77 dons differentiated from bone marrow derived mesenchymal stem cells from young (20-24 years) and old
78 Here, we show that glioma-associated human mesenchymal stem cells (GA-hMSC), a newly identified str
79 d repair to allow for the selection of human mesenchymal stem cells harboring the oncogenic transloca
82 ajor factor VIII (FVIII) synthesis site, and mesenchymal stem cells have been shown to control joint
83 LI by injection of human bone marrow derived mesenchymal stem cells (hBD-MSCs) with or without solubl
87 s been described to differently affect human mesenchymal stem cell (hMSC) and mouse mesenchymal stem
88 rs have demonstrated that PEDF directs human mesenchymal stem cell (hMSC) commitment to the osteoblas
90 the physiological role of succinate on human mesenchymal stem cell (hMSC) migration by regulating the
91 Promoting the paracrine effects of human mesenchymal stem cell (hMSC) therapy may contribute to i
95 llular matrix mechanical properties on human mesenchymal stem cell (hMSCs) function was investigated.
96 l mechanism licensing transcription in human mesenchymal stem cells (hMSCs) adipogenically primed by
97 ic and vasculogenic differentiation of human mesenchymal stem cells (hMSCs) and endothelial colony-fo
98 y coprinting multiple inks composed of human mesenchymal stem cells (hMSCs) and human neonatal dermal
101 ty in both the nematode C. elegans and human mesenchymal stem cells (hMSCs) by disrupting the SKN-1/N
102 elease/recovery of 3T3 fibroblasts and human mesenchymal stem cells (hMSCs) from 3D cultures while ma
105 on and chondrogenic differentiation of human mesenchymal stem cells (hMSCs) in a 3D printed poly-(eth
106 ding and osteogenic differentiation of human mesenchymal stem cells (hMSCs) into complex tissue-like
107 RATIONALE: Myocardial delivery of human mesenchymal stem cells (hMSCs) is an emerging therapy fo
109 ructs seeded with porcine AF cells and human mesenchymal stem cells (hMSCs) showed approximately 2.2-
110 potential of adipose tissue - derived human mesenchymal stem cells (hMSCs) was evaluated in vitro.
111 protein corona on stem cell labeling, human mesenchymal stem cells (hMSCs) were labeled with the abo
116 suggest that mutations in Evc2 affect dental mesenchymal stem cell homeostasis, which further leads t
118 oses of allogeneic bone marrow-derived human mesenchymal stem cells identically delivered in patients
120 ion in the synovial fibroblasts or in murine mesenchymal stem cells in a dose- and time-dependent man
122 coordinated manner, including recruitment of mesenchymal stem cells, induction of immune response, in
123 ges in conventional cell culture systems and mesenchymal stem cells inside biomimetic hydrogels that
125 vation of FFA4 expressed by murine C3H10T1/2 mesenchymal stem cells is required for induced different
130 in TNBC, specifically within mesenchymal and mesenchymal stem cell-like subtypes, whereas expression
132 ofibroblast differentiation of lung resident mesenchymal stem cells (LR-MSC) plays an important role
133 ofibroblast differentiation of lung resident mesenchymal stem cells (LR-MSCs) and in the lung tissues
134 nally, the effect of FGF-10 on lung-resident mesenchymal stem cells (LR-MSCs) has not been studied.
135 their number by symmetric division, express mesenchymal stem cell markers, and generate chondrocytes
136 so expressed a similar phenotypic profile of mesenchymal stem cell markers, except a relatively highe
138 population (BMSCs, also known as BM-derived mesenchymal stem cells), may contribute to the hematolog
139 preadipocytes and mouse bone marrow-derived mesenchymal stem cells (mBMSCs) to evaluate the adipogen
140 and Msx2 genes in mouse bone marrow-derived mesenchymal stem cells (mBMSCs) to regenerate a proximal
141 human mesenchymal stem cell (hMSC) and mouse mesenchymal stem cell (mMSC) immunomodulation and differ
142 igates the efficacy of local and intravenous mesenchymal stem cell (MSC) administration to augment ne
144 oblasts (MO-EVs) to induce mineralisation in mesenchymal stem cell (MSC) cultures and delineate the u
146 ption factor 2 (RUNX2) are key regulators of mesenchymal stem cell (MSC) differentiation toward adipo
147 tion of a bare 3D gelatin scaffold, to human mesenchymal stem cell (MSC) encapsulation and proliferat
148 ich is non-myogenic, Pax7(-) and express the mesenchymal stem cell (MSC) marker platelet-derived grow
149 ro or in vivo, how they converge to regulate mesenchymal stem cell (MSC) mechanosensing is not fully
150 pore formation from elasticity, we show that mesenchymal stem cell (MSC) osteogenesis in vitro, and c
154 The role of patient age in the efficacy of mesenchymal stem cell (MSC) therapy in ischemic cardiomy
155 mulating data support a therapeutic role for mesenchymal stem cell (MSC) therapy; however, there is n
156 mulating data support a therapeutic role for mesenchymal stem cell (MSC) therapy; however, there is n
157 plicated diverse organ-resident perivascular mesenchymal stem cell (MSC)-like cells and bone marrow-M
161 ponse to chemical stimuli from cancer cells, mesenchymal stem cells (MSC) can differentiate into canc
162 graft comprised of human bone marrow-derived mesenchymal stem cells (MSC) combined with CD34+ hematop
171 ted the ability of human bone derived marrow mesenchymal stem cells (MSC), and human adipose derived
172 res the generation of signals that stimulate mesenchymal stem cells (MSC), myofibroblasts and fibrobl
176 ccumulated evidence supports the notion that mesenchymal stem cells (MSCs) act in a paracrine manner,
177 tes suppresses fibrogenesis and desensitizes mesenchymal stem cells (MSCs) against subsequent mechani
178 to evaluate the neuroprotective potential of mesenchymal stem cells (MSCs) against the deleterious im
182 mitigate RIPF once it occurs, but recently, mesenchymal stem cells (MSCs) and a drug treatment stimu
185 uman induced pluripotent stem cells (iPSCs), mesenchymal stem cells (MSCs) and human umbilical vein e
186 gth 20nt sgRNAs in stem cells, such as human mesenchymal stem cells (MSCs) and induced pluripotent st
192 iferation, and osteogenic differentiation of mesenchymal stem cells (MSCs) are all enhanced in cells
197 ponse to tissue injury, both macrophages and mesenchymal stem cells (MSCs) are recruited to the site
200 ts own strengths and weaknesses, we utilized mesenchymal stem cells (MSCs) as a medium to perform for
202 ic gene to PDGFB, another potent mitogen for mesenchymal stem cells (MSCs) but potentially safer than
205 study, we investigated the potential role of mesenchymal stem cells (MSCs) derived from human MT in t
206 3R(hDM/hDM) bone- and adipose tissue-derived mesenchymal stem cells (MSCs) differentiate into adipocy
209 Although accumulating data support that mesenchymal stem cells (MSCs) enhance the efficacy of ca
215 investigated the potential involvement of BM mesenchymal stem cells (MSCs) from ISM patients by the K
220 s in endodontic regeneration based on pulpal mesenchymal stem cells (MSCs) have demonstrated promisin
223 the safety and efficacy of allogeneic human mesenchymal stem cells (MSCs) in reducing the time to re
224 We have previously shown that endogenous mesenchymal stem cells (MSCs) in the aged heart are mark
225 is mediated through TKI-mediated priming of mesenchymal stem cells (MSCs) in the bone marrow (BM).
226 n of two human cancer cell types and primary mesenchymal stem cells (MSCs) increases DNA breaks throu
227 Extracellular matrix (ECM) of the human Mesenchymal Stem Cells (MSCs) influences intracellular t
228 factors, on the availability and delivery of mesenchymal stem cells (MSCs) into the root canal system
230 EVs) secreted from human bone marrow-derived mesenchymal stem cells (MSCs) on SE-induced adverse chan
235 eveloped a culture-based method for inducing mesenchymal stem cells (MSCs) to secrete neurotrophic fa
237 we analyzed the role of the lncRNA HOTAIR in mesenchymal stem cells (MSCs) with particular focus on s
238 Pericytes are widely believed to function as mesenchymal stem cells (MSCs), multipotent tissue-reside
239 h factor-beta that increase proliferation of mesenchymal stem cells (MSCs), whereas bone morphogeneti
240 ic of bone marrow- and other non-gut-derived mesenchymal stem cells (MSCs), which are emerging as pot
256 nt (PDL) has been reported to be a source of mesenchymal stem cells (MSCs).New vascular networks from
257 rthermore, IL-3 enhances RANKL expression in mesenchymal stem cells of wild-type mice but not in STAT
258 Human embryonic kidney (HEK) cells and ovine mesenchymal stem cells (oMSCs) were printed at tissue-re
259 uld be detected in human bone marrow-derived mesenchymal stem cells or human hepatogenic profibrotic
261 e differentiation and mechanotransduction of mesenchymal stem cells, osteoblasts, osteocytes, and cho
267 animal due to the presence of epithelial and mesenchymal stem cells-provides a model for the study of
269 te (HCCS-PDA) were examined by culturing rat mesenchymal stem cells (rMSCs) on HCCS-PDA and HCCS coat
271 e (>15) showed significantly decreased HSCs, mesenchymal stem cells, Schwann cells, and neural fibers
272 tem cells (HSCs) and associated niche cells, mesenchymal stem cells, Schwann cells, neural fibers, an
274 stiffness of flat hydrogel surfaces induced mesenchymal stem cell spreading and proliferation; howev
275 culture conditions and during coculture with mesenchymal stem cells that mimic the AML microenvironme
277 m, including bone marrow transplantation and mesenchymal stem cell therapy, have entered into early c
278 er of fibronectin (FN), we were able to grow mesenchymal stem cells to densities comparable to those
280 ifferential short- and long-term response of mesenchymal stem cells to dynamic tensile loading based
282 oblasts and adipose- and bone marrow-derived mesenchymal stem cells to obtain cancer-associated fibro
283 mplished reversible differentiation of human mesenchymal stem cells to osteoblasts in a spatially def
284 own about the molecular events that initiate mesenchymal stem cells to proliferate and differentiate
286 hase 2A clinical trial of ischaemia-tolerant mesenchymal stem cells to treat Alzheimer's disease in t
287 itive method was developed to evaluate human mesenchymal stem cells trans-differentiation to endothel
291 n=15) or 100 million (n=15) allogeneic human mesenchymal stem cells via transendocardial injection (0
297 ne knockdown efficiencies in adipose derived mesenchymal stem cells with minimal cytotoxicity compare
298 -derived neural stem cells (hNSCs) and human mesenchymal stem cells with neurogenic potential from um
300 Treatment of isolated bone marrow-derived mesenchymal stem cells with SR2595 promotes induction of
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