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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Bone Resorption and SQSTM1[original query]
Sequestosome 1 (SQSTM1) mutations in Paget's disease of bone from the United States.
Calcified tissue international 2008 Apr 82 (4): 271-7.
Rhodes Emily C, Johnson-Pais Teresa L, Singer Frederick R, Ankerst Donna P, Bruder Jan M, Wisdom Julie, Hoon Dave S B, Lin Emerald, Bone Henry G, Simcic Kenneth J, Leach Robin
Genetic variation in inflammatory and bone turnover pathways and risk of osteolytic responses to prosthetic materials.
Journal of orthopaedic research : official publication of the Orthopaedic Research Society 2015 Feb 33 (2): 193-8.
MacInnes Scott J, Del Vescovo Elena, Kiss-Toth Endre, Ollier William E R, Kay Peter R, Gordon Andrew, Greenfield Edward M, Wilkinson Mark
A mutation in p62 protein (p. R321C), associated to Paget's disease of bone, causes a blockade of autophagy and an activation of NF-kB pathway.
Bone 2020 2 133 115265.
Usategui-Martín Ricardo, Gestoso-Uzal Nerea, Calero-Paniagua Ismael, De Pereda José María, Del Pino-Montes Javier, González-Sarmiento Rogel
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