Showing results (131-140 of 142) with videos related to
Sort By:
Pageof 15
Journal of Science and Medicine in Sport|August 10, 2019
Functional polymorphisms within the inflammatory pathway regulate expression of extracellular matrix components in a genetic risk dependent model for anterior cruciate ligament injuriesMathijs A M Suijkerbuijk, Marco Ponzetti, Masouda Rahim, et al.Orphanet Journal of Rare Diseases|January 25, 2012
Novel C16orf57 mutations in patients with Poikiloderma with Neutropenia: bioinformatic analysis of the protein and predicted effects of all reported mutationsElisa A Colombo, J Fernando Bazan, Gloria Negri, et al.Materials Science & Engineering. C, Materials for Biological Applications|May 16, 2020
The role of apoptosis associated speck-like protein containing a caspase-1 recruitment domain (ASC) in response to bone substitutesSuelen C Sartoretto, Monica D Calasans-Maia, Adriana T N N Alves, et al.Plos Medicine|October 14, 2015
P2RX7 purinoceptor: a therapeutic target for ameliorating the symptoms of duchenne muscular dystrophyAnthony Sinadinos, Christopher N J Young, Rasha Al-Khalidi, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 11, 2013
CLCN7 and TCIRG1 mutations differentially affect bone matrix mineralization in osteopetrotic individualsFlorian Barvencik, Ingo Kurth, Till Koehne, et al.Frontiers in Endocrinology|September 6, 2021
The "GEnomics of Musculo Skeletal Traits TranslatiOnal NEtwork": Origins, Rationale, Organization, and ProspectsFjorda Koromani, Nerea Alonso, Ines Alves, et al.The Journal of Clinical Investigation|April 4, 2007
Involvement of PLEKHM1 in osteoclastic vesicular transport and osteopetrosis in incisors absent rats and humansLiesbeth Van Wesenbeeck, Paul R Odgren, Fraser P Coxon, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 31, 2003
Chloride channel ClCN7 mutations are responsible for severe recessive, dominant, and intermediate osteopetrosisAnnalisa Frattini, Alessandra Pangrazio, Lucia Susani, et al.The American Journal of Pathology|January 1, 2003
Genotype-phenotype relationship in human ATP6i-dependent autosomal recessive osteopetrosisAnna Taranta, Silvia Migliaccio, Irene Recchia, et al.Nature Genetics|July 17, 2007
Osteoclast-poor human osteopetrosis due to mutations in the gene encoding RANKLCristina Sobacchi, Annalisa Frattini, Matteo M Guerrini, et al.Pageof 15