Publications by authors named "Maria Solanas-Barca"

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Genetic variants in CCNB1 associated with differential gene transcription and risk of coronary in-stent restenosis.
Carlos Silvestre-Roig, Patricia Fernández, María L Mansego, Claudia M van Tiel, Rosa Viana, María Solanas-Barca

Circ Cardiovasc Genet· February 2014

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Apolipoprotein E gene mutations in subjects with mixed hyperlipidemia and a clinical diagnosis of familial combined hyperlipidemia.
María Solanas-Barca, Isabel de Castro-Orós, Rocío Mateo-Gallego, Montserrat Cofán, Nuria Plana

Atherosclerosis· June 2012

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Iron deposits and dietary patterns in familial combined hyperlipidemia and familial hypertriglyceridemia.
Rocio Mateo-Gallego, Maria Solanas-Barca, Elena Burillo, Ana Cenarro, Iva Marques-Lopes

J Physiol Biochem· September 2010

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Mutations in HFE causing hemochromatosis are associated with primary hypertriglyceridemia.
María Solanas-Barca, Rocío Mateo-Gallego, Pilar Calmarza, Estíbaliz Jarauta, Ana M Bea

J Clin Endocrinol Metab· November 2009

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Overexpression of the CXCL3 gene in response to oxidized low-density lipoprotein is associated with the presence of tendon xanthomas in familial hypercholesterolemia.
Paula Martín-Fuentes, Fernando Civeira, María Solanas-Barca, Angel Luis García-Otín, Estíbaliz Jarauta

Biochem Cell Biol· June 2009

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