Genetic association study of dyslexia and ADHD candidate genes in a Spanish cohort: Implications of comorbid samples.

Autor: Mirian Sánchez-Morán, Juan Andrés Hernández, Jon Andoni Duñabeitia, Adelina Estévez, Laura Bárcena, Aintzane González-Lahera, María Teresa Bajo, Luis J Fuentes, Ana M Aransay, Manuel Carreiras

Publikováno v: PLoS ONE, Vol 13, Iss 10, p e0206431 (2018)

Dyslexia and attention deficit hyperactivity disorder (ADHD) are two complex neuro-behaviorally disorders that co-occur more often than expected, so that reading disability has been linked to inattention symptoms. We examined 4 SNPs located on genes

Externí odkaz: https://doaj.org/article/819c8fd2b66143429e7929c6765e96f1

The Expression of mir-19b-3p and HIPK3 is Highly Correlated in Patients with Precancerous Lesions of Gastric Cancer

Autor: Nuria Macias, Carles Pericay, Anna Brunet-Vega, María José Ramírez Lázaro, Ana M. Aransay, Aintzane González-Lahera, María Elisa Quílez, Juanjo Lozano, Lorena Garcia-Martinez, Antonia Montserrat, Mireia Miquel, Sergio Lario, Xavier Calvet, José Luis Lavín, Maria Vila-Casadesús

Publikováno v: ResearcherID

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0973825bcec8f11ed7e6a66cfd29b42
https://doi.org/10.1016/s0016-5085(17)32341-7

Inverse Correlation of Pleckstrin mRNA and miR-200a in the Antrum of Helicobacter Pylori Infected Patients

Autor: Sergio Lario, Maria Casadesus, Lorena Garcia-Martinez, Carles Pericay, Ana M. Aransay, Aintzane González-Lahera, Xavier Calvet, Juanjo Lozano, José Luis Lavín, Nuria Macias, María José Ramírez Lázaro, Anna Brunet-Vega, Mireia Miquel, María Elisa Quílez, Antonia Montserrat

Publikováno v: ResearcherID

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce6716805e1f32a62a7b7f703def0be9
https://doi.org/10.1016/s0016-5085(17)32342-9

Solute carrier family 2 member 1 is involved in the development of nonalcoholic fatty liver disease

Autor: Yannik Le Marchand-Brustel, Antonio Martín-Duce, Ibon Martínez-Arranz, Aintzane González-Lahera, Torben Hansen, Mercedes Vazquez-Chantada, Carmelo García-Monzón, Philippe Gual, José M. Mato, Johanne Marie Justesen, Karine Clément, Juan José Lozano, Karin Schlangen, Ana M. Aransay, Karina Banasik, Nicolas Veyrie, Daniel R. Witte, Juan L. García-Rodríguez, Maria Regueiro, Joan Caballería, Patricia Aspichueta, Torben Joergensen, María L. Martínez-Chantar, Jose J. Echevarria-Uraga, Albert Tran, Torsten Lauritzen, Joan Tordjman, Xabier Buqué, Naiara Rodríguez-Ezpeleta, Oluf Pedersen, Iñaki Mendibil, A. Castro

Publikováno v: Vazquez-Chantada, M, Gonzalez-Lahera, A, Martinez-Arranz, I, Garcia-Monzon, C, Regueiro, M M, Garcia-Rodriguez, J L, Schlangen, K A, Mendibil, I, Rodriguez-Ezpeleta, N, Lozano, J J, Banasik, K, Justesen, J M, Joergensen, T, Witte, D R, Lauritzen, T, Hansen, T, Pedersen, O, Veyrie, N, Clement, K, Tordjman, J, Tran, A, Le Marchand-Brustel, Y, Buque, X, Aspichueta, P, Echevarria-Uraga, J J, Martin-Duce, A, Caballeria, J, Gual, P, Castro, A, Mato, J M, Martinez-Chantar, M L & Aransay, A M 2013, ' Solute carrier family 2 member 1 is involved in the development of nonalcoholic fatty liver disease ', Hepatology, vol. 57, no. 2, pp. 505-514 . https://doi.org/10.1002/hep.26052, https://doi.org/10.1002/hep.26052
Hepatology

Susceptibility to develop nonalcoholic fatty liver disease (NAFLD) has genetic bases, but the associated variants are uncertain. The aim of the present study was to identify genetic variants that could help to prognose and further understand the gene

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96574a47047aa14d1fa2a5349ea4eddb
https://pure.au.dk/portal/da/publications/solute-carrier-family-2-member-1-is-involved-in-the-development-of-nonalcoholic-fatty-liver-disease(452ce038-0975-468a-9269-db146e863948).html

Impaired Function of Solute Carrier Family 19 Leads to Low Folate Levels and Lipid Droplet Accumulation in Hepatocytes

Autor: Ainara Cano, Mercedes Vazquez-Chantada, Javier Conde-Vancells, Aintzane Gonzalez-Lahera, David Mosen-Ansorena, Francisco J. Blanco, Karine Clément, Judith Aron-Wisnewsky, Albert Tran, Philippe Gual, Carmelo García-Monzón, Joan Caballería, Azucena Castro, María Luz Martínez-Chantar, José M. Mato, Huiping Zhu, Richard H. Finnell, Ana M. Aransay

Publikováno v: Biomedicines, Vol 11, Iss 2, p 337 (2023)

Low serum folate levels are inversely related to metabolic associated fatty liver disease (MAFLD). The role of the folate transporter gene (SLC19A1) was assessed to clarify its involvement in lipid accumulation during the onset of MAFLD in humans and

Externí odkaz: https://doaj.org/article/604e1f5cef3f4e0f877c63c8750f776b