Results 51 to 60 of about 195,947 (391)

Adipogenesis, Osteogenesis, and Chondrogenesis of Human Mesenchymal Stem/Stromal Cells: A Comparative Transcriptome Approach

open access: yesFrontiers in Cell and Developmental Biology, 2020
Adipogenesis, osteogenesis and chondrogenesis of human mesenchymal stem/stromal cells (MSC) are complex and highly regulated processes. Over the years, several studies have focused on understanding the mechanisms involved in the MSC commitment to the ...
A. Robert   +3 more
semanticscholar   +1 more source

Osteogenesis imperfecta and potential therapies

open access: yesJournal of Education, Health and Sport, 2022
Background: Osteogenesis imperfecta (OI) is a genetically determined disorder of connective tissue. In this article we reviewed epidemiology, types of OI, pathophysiology, symptoms and potential therapies.
Mateusz Fabis   +6 more
doaj   +1 more source

Ptosis as a unique hallmark for autosomal recessive WNT1-associated osteogenesis imperfecta [PDF]

open access: yes, 2019
Osteogenesis imperfecta (OI) is a heritable connective tissue disorder, mainly characterized by bone fragility and low bone mass. Defects in the type I procollagen-encoding genes account for the majority of OI, but increasingly more rare autosomal ...
Elcioglu, Nursel   +8 more
core   +1 more source

CircRFWD2 Promotes Osteogenic Differentiation of human Dental Pulp Stem Cells by Targeting miR-6817-5p Through BMP-Smad and p38 MAPK Pathway

open access: yesCell Transplantation, 2021
Dental pulp stem cells (DPSCs) are one promising cell source of mesenchymal stem cells in bone tissue engineering. However, it remains unknown that the molecules and signaling pathways involved in osteogenesis of DPSCs. Hence, this study investigated the
Xinqi Huang   +6 more
doaj   +1 more source

Osteoclastogenesis and Osteogenesis

open access: yesInternational Journal of Molecular Sciences, 2022
Bone is a highly dynamic tissue that is continuously remodeled to attain and maintain optimal bone integrity, mass, and strength [...]
openaire   +2 more sources

Plastin 3 in X-Linked Osteoporosis: Imbalance of Ca2+-Dependent Regulation Is Equivalent to Protein Loss

open access: yesFrontiers in Cell and Developmental Biology, 2021
Osteogenesis imperfecta is a genetic disorder disrupting bone development and remodeling. The primary causes of osteogenesis imperfecta are pathogenic variants of collagen and collagen processing genes.
Christopher L. Schwebach   +2 more
doaj   +1 more source

A comparative study of mesoporous glass/silk and non-mesoporous glass/silk scaffolds: Physiochemistry and in vivo osteogenesis [PDF]

open access: yes, 2011
Mesoporous bioactive glass (MBG) is a new class of biomaterials with a well-ordered nanochannel structure, whose in vitro bioactivity is far superior than that of non-mesoporous bioactive glass (BG); the material's in vivo osteogenic properties are ...
Fan, Wei   +4 more
core   +2 more sources

Simultaneous elastic shape optimization for a domain splitting in bone tissue engineering [PDF]

open access: yes, 2018
This paper deals with the simulateneous optimization of a subset $\mathcal{O}_0$ of some domain $\Omega$ and its complement $\mathcal{O}_1 = \Omega \setminus \overline{\mathcal{O}}_0$ both considered as separate elastic objects subject to a set of loading scenarios.
arxiv   +1 more source

Serum creatine kinase isoenzymes in children with osteogenesis imperfecta [PDF]

open access: yes, 2017
This study evaluates serum creatine kinase isoenzyme activity in children with osteogenesis imperfecta to determine its usefulness as a biochemical marker during treatment with bisphosphonate.
Celli, L   +8 more
core   +1 more source

Association between spondylolisthesis and L5 fracture in patients with osteogenesis imperfecta [PDF]

open access: yes, 2017
To investigate if an association between spondylolisthesis and L5 fracture occurs in patients affected by Osteogenesis Imperfecta (O.I.). Methods Anteroposterior and lateral radiograms were performed on the sample (38 O.I.
Celli M   +5 more
core   +1 more source

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