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Bone|March 10, 2018
Congenital disorders of bone and bloodAnna Teti, Steven L Teitelbaum
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 14, 2007
A new heterozygous mutation (R714C) of the osteopetrosis gene, pleckstrin homolog domain containing family M (with run domain) member 1 (PLEKHM1), impairs vesicular acidification and increases TRACP secretion in osteoclastsAndrea Del Fattore, Rachele Fornari, Liesbeth Van Wesenbeeck, et al.
The Journal of Biological Chemistry|January 14, 2016
Anabolic and Antiresorptive Modulation of Bone Homeostasis by the Epigenetic Modulator Sulforaphane, a Naturally Occurring IsothiocyanateRoman Thaler, Antonio Maurizi, Paul Roschger, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 22, 2011
Mechanisms inducing low bone density in Duchenne muscular dystrophy in mice and humansAnna Rufo, Andrea Del Fattore, Mattia Capulli, et al.
Molecular Biology of the Cell|April 13, 2012
NHERF1 acts as a molecular switch to program metastatic behavior and organotropism via its PDZ domainsRosa Angela Cardone, Maria Raffaella Greco, Mattia Capulli, et al.
World Journal of Clinical Oncology|August 13, 2014
Molecular pathogenesis of bone metastases in breast cancer: Proven and emerging therapeutic targetsNadia Rucci, Patrizia Sanità, Simona Delle Monache, et al.
Bone|October 16, 2007
Genetics, pathogenesis and complications of osteopetrosisAndrea Del Fattore, Alfredo Cappariello, Anna Teti
Journal of Cellular Physiology|September 2, 2018
Apoptosis-associated speck-like protein containing a caspase-1 recruitment domain (ASC) contributes to osteoblast differentiation and osteogenesisSuelen Sartoretto, Sara Gemini-Piperni, Rodrigo A da Silva, et al.
Life Sciences|July 9, 2026
Generation of a P4hbY393C mouse model of cole-carpenter syndrome and therapeutic proof-of-conceptAntonio Maurizi, Elisa Pucci, Piergiorgio Patrizii, et al.
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