Management of endocrine disease: Osteogenesis imperfecta: An update on clinical features and therapies

R Marom, BM Rabenhorst… - European journal of …, 2020 - academic.oup.com
Osteogenesis imperfecta (OI) is an inherited skeletal dysplasia characterized by bone
fragility and skeletal deformities. While the majority of cases are associated with pathogenic …

Fragility fractures: risk factors and management in the elderly

F Migliorini, R Giorgino, F Hildebrand, F Spiezia… - Medicina, 2021 - mdpi.com
Given the progressive ageing of Western populations, the fragility fractures market has a
growing socioeconomic impact. Fragility fractures are common in the elderly, negatively …

Osteogenesis imperfecta: new perspectives from clinical and translational research

JT Tauer, ME Robinson, F Rauch - Journal of Bone and Mineral …, 2019 - academic.oup.com
Osteogenesis imperfecta (OI) is a monogenic bone fragility disorder that usually is caused
by mutations in one of the two genes coding for collagen type I alpha chains, COL1A1 or …

Biology and biomechanics of the heart valve extracellular matrix

KM Kodigepalli, K Thatcher, T West… - Journal of …, 2020 - mdpi.com
Heart valves are dynamic structures that, in the average human, open and close over
100,000 times per day, and 3× 109 times per lifetime to maintain unidirectional blood flow …

Genetics and epigenetics of bone remodeling and metabolic bone diseases

L Oton-Gonzalez, C Mazziotta, MR Iaquinta… - International Journal of …, 2022 - mdpi.com
Bone metabolism consists of a balance between bone formation and bone resorption, which
is mediated by osteoblast and osteoclast activity, respectively. In order to ensure bone …

Mesenchymal stem cells in the treatment of osteogenesis imperfecta

E Lang, JA Semon - Cell Regeneration, 2023 - Springer
Osteogenesis imperfecta (OI) is a disease caused by mutations in different genes resulting
in mild, severe, or lethal forms. With no cure, researchers have investigated the use of cell …

AAV-based gene editing of type 1 collagen mutation to treat osteogenesis imperfecta

YS Yang, T Sato, S Chaugule, H Ma, J Xie… - … Therapy-Nucleic Acids, 2024 - cell.com
Osteogenesis imperfecta (OI) is a genetic disorder characterized by bone fragility, low bone
mass, fractures, and extraskeletal manifestations. Since OI is commonly caused by single …

Total flavonoids of Rhizoma Drynariae promotes differentiation of osteoblasts and growth of bone graft in induced membrane partly by activating Wnt/β-catenin …

S Li, H Zhou, C Hu, J Yang, J Ye, Y Zhou, Z Li… - Frontiers in …, 2021 - frontiersin.org
Total flavonoids of Rhizoma drynariae (TFRD), a Chinese medicine, is widely used in the
treatment of fracture, bone defect, osteoporosis and other orthopedic diseases, and has …

Fermented oyster extract promotes osteoblast differentiation by activating the Wnt/β-catenin signaling pathway, leading to bone formation

IMN Molagoda, WAHM Karunarathne, YH Choi… - Biomolecules, 2019 - mdpi.com
The Pacific oyster, Crassostrea gigas, is well-known as a nutritious food. Recently, we
revealed that fermented extract of C. gigas (FO) inhibited ovariectomy-induced osteoporosis …

The WNT1G177C mutation specifically affects skeletal integrity in a mouse model of osteogenesis imperfecta type XV

N Vollersen, W Zhao, T Rolvien, F Lange, FN Schmidt… - Bone research, 2021 - nature.com
The recent identification of homozygous WNT1 mutations in individuals with osteogenesis
imperfecta type XV (OI-XV) has suggested that WNT1 is a key ligand promoting the …