Micromass Cell Culture System
Mostrando 1-4 de 4 artigos, teses e dissertações.
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1. Micromass cultures are effective for differentiation of human amniotic fluid stem cells into chondrocytes
OBJECTIVES: Articular cartilage is vulnerable to injuries and undergoes an irreversible degenerative process. The use of amniotic fluid mesenchymal stromal stem cells for the reconstruction of articular cartilage is a promising therapeutic alternative. The aim of this study was to investigate the chondrogenic potential of amniotic fluid mesenchymal stromal
Clinics. Publicado em: 05/04/2018
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2. Condrogênese a partir de células-tronco do líquido amniótico humano estimulado com TRF-ß3 em micromass / Chondrogenesis differentiation of mesenchymal stem cells from human amniotic fluid with TGF-beta3 in micromass culture system
Introduction: The use of mesenchymal stem cells (MSC) for reconstruction of articular cartilage, leads to a promising therapeutic alternative, due to the tissue vulnerability to injuries and irreversible degenerative process. The aim of this study was to investigate the chondrogenic potential of MSC from human amniotic fluid in Micromass system (high-density
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 30/08/2012
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3. Periosteum as a source of mesenchymal stem cells: the effects of TGF-β3 on chondrogenesis
INTRODUCTION: Numerous experimental efforts have been undertaken to induce the healing of lesions within articular cartilage by re-establishing competent repair tissue. Adult mesenchymal stem cells have attracted attention as a source of cells for cartilage tissue engineering. The purpose of this study was to investigate chondrogenesis employing periosteal m
Clinics. Publicado em: 2011
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4. Identification of a phenotype-specific enhancer in the first intron of the rat collagen II gene.
The regulation of the collagen II gene was investigated by transfecting plasmids containing potential regulatory sequences of this gene coupled to the gene for chloramphenicol acetyltransferase (CAT) into various cells. The 5' flanking region of this gene functioned as a weak promoter when transfected into chicken chondrocytes or fibroblasts. Inclusion of an