Mesenchymal stem cells: biology and potential clinical uses.
By R. Deans, A. Moseley. Experimental Hematology, 2000
1,476 citations recorded by the source corpus.
Subfields: Genetics, Hematology, Pulmonary and Respiratory Medicine
View Paper: https://www.semanticscholar.org/paper/fdc796fa648af4e5b58dbb5af40c6df4807d80a7
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Citations in the corpus
- Mesenchymal stem cells suppress lymphocyte proliferation in vitro and prolong skin graft survival in vivo. (2002, background): “and Fas ligand; they do not express B7-1, B7-2, CD40, or CD40L [4,5,9].”
- T cell responses to allogeneic human mesenchymal stem cells: immunogenicity, tolerance, and suppression. (2005, background): “MSCs also express adhesion molecules such as ICAM-1/LFA-1 [4, 6] that have costimulatory properties [13] which could participate in T cell priming and interfere with the induction of tolerance.”
- Immunomodulatory effect of human adipose tissue‐derived adult stem cells: comparison with bone marrow mesenchymal stem cells (2005, positive): “Similar properties were previously reported for bone marrow mesenchymal stem cells (BM-MSCs), which have been extensively studied (Lazarus et al, 1995; Pittenger et al, 1999; Deans & Moseley, 2000; Jorgensen et al, 2003).”
- Long-term cultures of bone marrow-derived human mesenchymal stem cells frequently undergo spontaneous malignant transformation. (2009, result): “These observations are in line with recently published phenotypic expression patterns of hMSC (29, 30).”
- Retention of multilineage differentiation potential of mesenchymal cells during proliferation in response to FGF. (2001, methodology): “Thus transplantation of bone marrow MSC may provide a new method for treatment of osteoporosis, arthritis, periodontal diseases, intrinsic muscular dystrophies, cardiac diseases, and degenerative nerve diseases (5).”
- HLA expression and immunologic properties of differentiated and undifferentiated mesenchymal stem cells. (2003, background): “1016/S0301-472X(03)00110-3 MSC express intermediate levels of human leukocyte antigen (HLA) major histocompatibility complex (MHC) class I molecules and negligibly low levels of HLA class II and Fas ligand; they do not express the costimulatory molecules B7-1, B7-2, CD40, or CD40L [3,9,10].”