Intracoronary Infusion of CD133 + and CD133 − CD34 + Selected Autologous Bone Marrow Progenitor Cells in Patients with Chronic Ischemic Cardiomyopathy: Cell Isolation, Adherence to the Infarcted Area, and Body Distribution-Reference-Cited by-同舟云学术

Intracoronary Infusion of CD133 + and CD133 − CD34 + Selected Autologous Bone Marrow Progenitor Cells in Patients with Chronic Ischemic Cardiomyopathy: Cell Isolation, Adherence to the Infarcted Area, and Body Distribution

Published:2006-10 Issue:10 Volume:24 Page:2279-2283
ISSN:1066-5099
Container-title:STEM CELLS
language:en
Short-container-title:STEM CELLS

Author:

Goussetis Evgenios¹,Manginas Athanassios²,Koutelou Maria³,Peristeri Ioulia¹,Theodosaki Maria¹,Kollaros Nikolaos³,Leontiadis Evangelos²,Theodorakos Athanasios³,Paterakis George⁴,Karatasakis George²,Cokkinos Dennis V.²,Graphakos Stelios¹

Affiliation:

1. Stem Cell Transplant Unit; “Aghia Sophia” Children's Hospital, Thivon and Levadias; “G. Genimmatas” General District Hospital, Athens, Greece

2. Department of Cardiology, Onassis Cardiac Surgery Center; “G. Genimmatas” General District Hospital, Athens, Greece

3. Department of Nuclear Medicine, Onassis Cardiac Surgery Center; “G. Genimmatas” General District Hospital, Athens, Greece

4. Immunology Department and National Histocompatibility Center; “G. Genimmatas” General District Hospital, Athens, Greece

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1634/stemcells.2005-0589

Reference27 articles.

1. Regeneration of ischemic cardiac muscle and vascular endothelium by adult stem cells

2. Neovascularization of ischemic myocardium by human bone-marrow–derived angioblasts prevents cardiomyocyte apoptosis, reduces remodeling and improves cardiac function

3. Myocardial regeneration by activation of multipotent cardiac stem cells in ischemic heart failure

4. Bone marrow cells regenerate infarcted myocardium

5. Comparison of human skeletal myoblasts and bone marrow-derived CD133+progenitors for the repair of infarcted myocardium

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