Page last updated: 2024-08-24

plerixafor and Myocardial Ischemia

plerixafor has been researched along with Myocardial Ischemia in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's4 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Cheng, M; Huang, K; Kishore, R; Losordo, DW; Miller, RJ; Qin, G; Tang, YL; Yan, D; Zhao, TC; Zhou, J1
Kim, BJ; Kim, DK; Kim, JH; Kim, KW; Lee, MS; Oh, BJ; Park, KS; Park, SG; Yoon, KS1
Chen, Y; Han, H; Hong, D; Qiao, H; Tong, Y; Wu, Y; Xu, W; Yang, J; Zhou, C1
Brunner, S; David, R; Fischer, R; Franz, WM; Gerbitz, A; Huber, BC; Nathan, P; Segeth, A; Theiss, HD; Vallaster, M; Zaruba, MM1

Other Studies

4 other study(ies) available for plerixafor and Myocardial Ischemia

ArticleYear
A critical role of Src family kinase in SDF-1/CXCR4-mediated bone-marrow progenitor cell recruitment to the ischemic heart.
    Journal of molecular and cellular cardiology, 2015, Volume: 81

    Topics: Animals; Benzylamines; Bone Marrow Cells; Chemokine CXCL12; Chemotaxis; Cyclams; Gene Expression Regulation; Genes, Reporter; Green Fluorescent Proteins; Heterocyclic Compounds; Indoles; Male; Mesenchymal Stem Cells; Mice; Mice, Knockout; Myocardial Ischemia; Myocardium; Proto-Oncogene Proteins c-kit; Receptors, CXCR4; Signal Transduction; src-Family Kinases; Sulfonamides

2015
Differences in donor CXCR4 expression levels are correlated with functional capacity and therapeutic outcome of angiogenic treatment with endothelial colony forming cells.
    Biochemical and biophysical research communications, 2010, Aug-06, Volume: 398, Issue:4

    Topics: Animals; Benzylamines; Cell Movement; Cells, Cultured; Chemokine CXCL12; Cyclams; Endothelium, Vascular; Heterocyclic Compounds; Humans; Living Donors; Male; Mice; Mice, Nude; Myocardial Ischemia; Neovascularization, Physiologic; Nitric Oxide Synthase Type III; Phosphatidylinositol 3-Kinases; Phosphorylation; Proto-Oncogene Proteins c-akt; Receptors, CXCR4; Stem Cell Transplantation; Stem Cells; Umbilical Cord

2010
Tanshinone IIA increases recruitment of bone marrow mesenchymal stem cells to infarct region via up-regulating stromal cell-derived factor-1/CXC chemokine receptor 4 axis in a myocardial ischemia model.
    Phytomedicine : international journal of phytotherapy and phytopharmacology, 2011, Apr-15, Volume: 18, Issue:6

    Topics: Abietanes; Animals; Benzylamines; Bone Marrow Cells; Cell Movement; Chemokine CXCL12; Cyclams; Disease Models, Animal; Drugs, Chinese Herbal; Female; Heterocyclic Compounds; Male; Mesenchymal Stem Cells; Myocardial Infarction; Myocardial Ischemia; Myocardium; Phytotherapy; Rats; Rats, Sprague-Dawley; Receptors, CXCR4; Salvia miltiorrhiza; Stem Cell Transplantation; Up-Regulation

2011
Parathyroid hormone is a DPP-IV inhibitor and increases SDF-1-driven homing of CXCR4(+) stem cells into the ischaemic heart.
    Cardiovascular research, 2011, Jun-01, Volume: 90, Issue:3

    Topics: Adult Stem Cells; Animals; Benzylamines; Cardiotonic Agents; Chemokine CXCL12; Cyclams; Dipeptidyl Peptidase 4; Hematopoietic Stem Cell Mobilization; Hematopoietic Stem Cells; Heterocyclic Compounds; Male; Mice; Mice, Inbred C57BL; Mice, Transgenic; Myocardial Ischemia; Parathyroid Hormone; Protease Inhibitors; Receptors, CXCR4; Regenerative Medicine

2011