Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Aintzane González-Lahera"'
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 12, p e0209718 (2018)
[This corrects the article DOI: 10.1371/journal.pone.0206431.].
Externí odkaz:
https://doaj.org/article/a566b005045c4b33a90c68d5094cff67
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
Autor:
Juan José Lozano, Xavier Calvet, José Luis Lavín, Maria Vila-Casadesús, María Elisa Quílez, Anna Brunet-Vega, María José Ramírez-Lázaro, Sergio Lario, Aintzane González-Lahera, Ana M. Aransay
Publikováno v:
Scientific Data, Vol 7, Iss 1, Pp 1-9 (2020)
Scientific Data
Scientific Data
Helicobacter pylori infects 4.4 billion individuals worldwide and is considered the most important etiologic agent for peptic ulcers and gastric cancer. Individual response to H. pylori infection is complex and depends on complex interactions between
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
Publikováno v:
Methods in Molecular Biology ISBN: 9781493925186
Single-cell genome and transcriptome characterizations will probe to be decisive within the stem cells research, especially to describe appropriately the genetic impact of the diverse stem cells populations that are present in each organism. In the p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ca320ddba4f8897be14686a30cfa239e
https://doi.org/10.1007/978-1-4939-2519-3_5
https://doi.org/10.1007/978-1-4939-2519-3_5
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
Autor:
Nuria Macias-Camara, Ana M. Aransay, Ramon M. Rodriguez, David Mosen-Ansorena, Patricia Fuentes, María J. García-León, María L. Toribio, Aintzane González-Lahera, Beatriz Suarez-Alvarez, Carlos López-Larrea, Marina García-Peydró
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
Nucleic Acids Research
instname
Nucleic Acids Research
© The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research. Thymocyte differentiation is a complex process involving well-defined sequential developmental stages that ultimately result in the generation of mature
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::461c6911174996abeccd0b4b4974d4bd
http://hdl.handle.net/10261/125392
http://hdl.handle.net/10261/125392
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
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
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
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
Autor:
Aintzane González Lahera, Sergio Lario, Xavier Calvet, Nuria Macias, Anna Brunet, María José Ramírez-Lázaro, José Luis Lavín, Juan José Lozano, M. Elisa Quílez, Mireia Miquel Planas, Carles Pericay Pijaume, Antonia Montserrat, Ana M. Aransay
Publikováno v:
Gastroenterology. 148:S-319