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Department of Physiology and Biophysics, The Centre for Clinical and Experimental Transplantation (CCET), Australian Islet Transplant Consortium, School of Medicine, Cooperative Research Centre for Cell Therapy Manufacturing (CRC-CTM), Mawson Institute, Gene Therapy and Autoimmunity Group, Centre for Stem Cell Research, University of Illinois at Chicago, Chicago, Illinois 60612, USA
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Department of Physiology and Biophysics, The Centre for Clinical and Experimental Transplantation (CCET), Australian Islet Transplant Consortium, School of Medicine, Cooperative Research Centre for Cell Therapy Manufacturing (CRC-CTM), Mawson Institute, Gene Therapy and Autoimmunity Group, Centre for Stem Cell Research, University of Illinois at Chicago, Chicago, Illinois 60612, USA
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Department of Physiology and Biophysics, The Centre for Clinical and Experimental Transplantation (CCET), Australian Islet Transplant Consortium, School of Medicine, Cooperative Research Centre for Cell Therapy Manufacturing (CRC-CTM), Mawson Institute, Gene Therapy and Autoimmunity Group, Centre for Stem Cell Research, University of Illinois at Chicago, Chicago, Illinois 60612, USA
Department of Physiology and Biophysics, The Centre for Clinical and Experimental Transplantation (CCET), Australian Islet Transplant Consortium, School of Medicine, Cooperative Research Centre for Cell Therapy Manufacturing (CRC-CTM), Mawson Institute, Gene Therapy and Autoimmunity Group, Centre for Stem Cell Research, University of Illinois at Chicago, Chicago, Illinois 60612, USA
Department of Physiology and Biophysics, The Centre for Clinical and Experimental Transplantation (CCET), Australian Islet Transplant Consortium, School of Medicine, Cooperative Research Centre for Cell Therapy Manufacturing (CRC-CTM), Mawson Institute, Gene Therapy and Autoimmunity Group, Centre for Stem Cell Research, University of Illinois at Chicago, Chicago, Illinois 60612, USA
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Department of Physiology and Biophysics, The Centre for Clinical and Experimental Transplantation (CCET), Australian Islet Transplant Consortium, School of Medicine, Cooperative Research Centre for Cell Therapy Manufacturing (CRC-CTM), Mawson Institute, Gene Therapy and Autoimmunity Group, Centre for Stem Cell Research, University of Illinois at Chicago, Chicago, Illinois 60612, USA
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Department of Physiology and Biophysics, The Centre for Clinical and Experimental Transplantation (CCET), Australian Islet Transplant Consortium, School of Medicine, Cooperative Research Centre for Cell Therapy Manufacturing (CRC-CTM), Mawson Institute, Gene Therapy and Autoimmunity Group, Centre for Stem Cell Research, University of Illinois at Chicago, Chicago, Illinois 60612, USA
Department of Physiology and Biophysics, The Centre for Clinical and Experimental Transplantation (CCET), Australian Islet Transplant Consortium, School of Medicine, Cooperative Research Centre for Cell Therapy Manufacturing (CRC-CTM), Mawson Institute, Gene Therapy and Autoimmunity Group, Centre for Stem Cell Research, University of Illinois at Chicago, Chicago, Illinois 60612, USA
Department of Physiology and Biophysics, The Centre for Clinical and Experimental Transplantation (CCET), Australian Islet Transplant Consortium, School of Medicine, Cooperative Research Centre for Cell Therapy Manufacturing (CRC-CTM), Mawson Institute, Gene Therapy and Autoimmunity Group, Centre for Stem Cell Research, University of Illinois at Chicago, Chicago, Illinois 60612, USA
Department of Physiology and Biophysics, The Centre for Clinical and Experimental Transplantation (CCET), Australian Islet Transplant Consortium, School of Medicine, Cooperative Research Centre for Cell Therapy Manufacturing (CRC-CTM), Mawson Institute, Gene Therapy and Autoimmunity Group, Centre for Stem Cell Research, University of Illinois at Chicago, Chicago, Illinois 60612, USA
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group showed that IGF1 releasing silk fibroin scaffolds initiated chondrogenesis from human mesenchymal stem cells in vitro ( Uebersax et al . 2008 ). Adsorbing IGF1 onto porous hydroxyapatite, or chitosan scaffolds, enhanced osseointegration in vivo
Department of Cell Physiology and Metabolism, Animal Biology and Physiology, Organic Chemistry, Faculty of Medicine, University of Geneva, 1 rue Michel-Servet, 1211 Geneva 4, Switzerland Departments of
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investigate putative direct effects of S. birrea on insulin-secreting cells. Regarding the in vivo hypoglycaemic effect of S. birrea stem-bark, chronic treatments have been reported only with organic extracts ( Dimo et al . 2007 , Gondwe et al . 2008
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Candido S Montalto G Cervello M Steelman L Abrams SL 2015 Roles of EGFR and KRAS and their downstream signaling pathways in pancreatic cancer and pancreatic cancer stem cells. Advances in Biological Regulation 59 65 – 81 . ( doi
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Cardiovascular Research Institute & Department of Physiology, University of California, San Francisco, San Francisco, California, USA
Eli and Edythe Broad Center for Regeneration Medicine and Stem Cell Research, University of California, San Francisco, San Francisco, California, USA
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Eli and Edythe Broad Center for Regeneration Medicine and Stem Cell Research, University of California, San Francisco, San Francisco, California, USA
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proliferation of pre-existing cardiomyocytes rather than expansion and differentiation of stem cell populations ( Jopling et al. 2010 , Kikuchi et al. 2010 , Porrello et al. 2011 , Xin et al. 2013 b ). Unfortunately, mammalian cardiomyocytes withdraw
State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China
Institute of Reproductive Sciences, Key Laboratory of Animal Reproduction and Germplasm Enhancement in Universities of Shandong, College of Animal Science and Technology, Qingdao Agricultural University, Qingdao, China
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Institute of Reproductive Sciences, Key Laboratory of Animal Reproduction and Germplasm Enhancement in Universities of Shandong, College of Animal Science and Technology, Qingdao Agricultural University, Qingdao, China
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State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China
Institute of Reproductive Sciences, Key Laboratory of Animal Reproduction and Germplasm Enhancement in Universities of Shandong, College of Animal Science and Technology, Qingdao Agricultural University, Qingdao, China
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State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China
Institute of Reproductive Sciences, Key Laboratory of Animal Reproduction and Germplasm Enhancement in Universities of Shandong, College of Animal Science and Technology, Qingdao Agricultural University, Qingdao, China
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5738 – 5753 . ( doi:10.18632/oncotarget.6792 ) Johnson J Canning J Kaneko T Pru JK Tilly JL 2004 Germline stem cells and follicular renewal in the postnatal mammalian ovary . Nature 428 145 – 150 . ( doi:10.1038/nature02316
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Department of Biological and Medical Sciences, Oxford Brookes University, Oxford, UK
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zur Nieden NI 2011 Hyperglycemia impairs skeletogenesis from embryonic stem cells by affecting osteoblast and osteoclast differentiation . Stem Cells and Development 20 465 – 474 . ( https://doi.org/10.1089/scd.2010.0205 ) 20939707 Ferron M Wei
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Introduction According to the migration theory, each zone of the adult adrenal cortex is derived from a common pool of stem cells located in the periphery of the cortex, which, for organ maintenance and replenishment, migrates centripetally and
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mutations more frequently ( Maier et al . 2006 ). Adult stem cells have been suggested as an alternative source of benign and malignant tumour formation ( Reya et al . 2001 , Fierabracci 2012 ). These cells reside in all tissues and organs and are capable
Department of Physiology, South Texas Veterans Health Care System, and Barshop Institute for Longevity and Aging Studies, University of Texas Health Science Center, 15355 Lambda Drive, San Antonio, Texas TX 78245, USA
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immunodeficient mice. Biology of adrenocortical stem/progenitor cells The nature of adrenocortical stem/progenitor cells remains relatively undefined in both primates and rodents, although dramatic progress has been made in the last decade. A recent review
Human and Animal Physiology Group, Department of Animal Sciences, Wageningen University, Marijkeweg 40, 6709 PG Wageningen, The Netherlands
Department of Internal Medicine, Erasmus Medical Centre, Erasmus University, Rotterdam, The Netherlands
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Human and Animal Physiology Group, Department of Animal Sciences, Wageningen University, Marijkeweg 40, 6709 PG Wageningen, The Netherlands
Department of Internal Medicine, Erasmus Medical Centre, Erasmus University, Rotterdam, The Netherlands
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Human and Animal Physiology Group, Department of Animal Sciences, Wageningen University, Marijkeweg 40, 6709 PG Wageningen, The Netherlands
Department of Internal Medicine, Erasmus Medical Centre, Erasmus University, Rotterdam, The Netherlands
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Human and Animal Physiology Group, Department of Animal Sciences, Wageningen University, Marijkeweg 40, 6709 PG Wageningen, The Netherlands
Department of Internal Medicine, Erasmus Medical Centre, Erasmus University, Rotterdam, The Netherlands
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Human and Animal Physiology Group, Department of Animal Sciences, Wageningen University, Marijkeweg 40, 6709 PG Wageningen, The Netherlands
Department of Internal Medicine, Erasmus Medical Centre, Erasmus University, Rotterdam, The Netherlands
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; 50–75% of the original foetal-type Leydig cell population present at birth persists in the adult testis ( Kerr & Knell 1988 ). The second generation of Leydig cells, the so-called adult-type Leydig cells, develops from stem Leydig cells through