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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 - 4 (of 4 Records)

Query Trace: Metabolic Syndrome X and LRP6[original query]
Rare nonconservative LRP6 mutations are associated with metabolic syndrome.
Human mutation 2013 May .
Singh R, Smith E, Fathzadeh M, Liu W, Go GW, Subrahmanyan L, Faramarzi S, McKenna W, Mani A
LRP6 enhances glucose metabolism by promoting TCF7L2-dependent insulin receptor expression and IGF receptor stabilization in humans.
Cell metabolism 2013 Feb 17 (2): 2.
Singh R, De Aguiar RB, Naik S, Mani S, Ostadsharif K, Wencker D, Sotoudeh M, Malekzadeh R, Sherwin RS, Mani A
The association of LRP6 rs2302685 (V1062I) polymorphism with the risk of hyperlipidemia in Iranian children and adolescents.
Annals of human genetics 2018 Jul .
Montazeri-Najafabady Nima, Dabbaghmanesh Mohammad Hossein, Mohammadian Amiri Raje
An LRP6 mutation (Arg360His) associated with low bone mineral density but not cardiovascular events in a Caucasian family.
Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2022 7 33 (11): 2445-2448.
Puente Nuria, Vega Ana I, Hernandez José L, Fernandez-Luna Jose L, Riancho Jose
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