Zobrazeno 1 - 8
of 8
pro vyhledávání: '"J A G, Agúndez"'
Autor:
P. Ropero, O. Briceño, G. López Alonso, J. A. G.-Agúndez, F. A. González Fernández, F. García Hoz, A. Villegas Martínez, M. Díaz-Rubio, J. M. Ladero
Publikováno v:
Revista Espanola de Enfermedades Digestivas, Vol 99, Iss 7, Pp 376-381 (2007)
Objetivo: comprobar si las mutaciones del gen HFE, que pueden inducir sobrecarga hepática de hierro, guardan relación con el riesgo de desarrollar carcinoma hepatocelular (CHC) en sujetos predispuestos a sufrir este tumor. Material y métodos: se h
Externí odkaz:
https://doaj.org/article/cc534aa4cce14cb8b753cfdc2c87b00d
Autor:
J A G, Agúndez, J M, Ladero, M, Olivera, L, Lozano, M, Fernández-Arquero, E G, de laConcha, M, Díaz-Rubio, J, Benitez
Publikováno v:
Scandinavian Journal of Gastroenterology. 37:99-103
Ethanol abuse is the most prevalent cause of liver cirrhosis in Spain. Genetic polymorphisms affect the activity of the enzymes involved in ethanol metabolism and in processing the toxic by-products generated in the liver. N-acetyltransferase 2 (NAT2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4771575d44b4b45c563a63e9c63d4a72
https://doi.org/10.1080/003655202753387437
https://doi.org/10.1080/003655202753387437
Autor:
O, Lorenzo-Betancor, E, García-Martín, S, Cervantes, J A G, Agúndez, F J, Jiménez-Jiménez, H, Alonso-Navarro, A, Luengo, F, Coria, E, Lorenzo, J, Irigoyen, P, Pastor
Publikováno v:
European journal of neurology. 18(8)
Essential tremor (ET) is a frequent movement disorder with a substantial family aggregation. A genome-wide association study has recently shown that LINGO1 gene variants are associated with increased risk of ET. We intended to replicate these finding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::96b991ccc2322614067d9e404e2358e2
https://pubmed.ncbi.nlm.nih.gov/21219542
https://pubmed.ncbi.nlm.nih.gov/21219542
Autor:
G, Gervasini, J A G, Agúndez, J, García-Menaya, C, Martínez, C, Cordobés, P, Ayuso, J A, Cornejo, M, Blanca, E, García-Martín
Publikováno v:
Allergy. 65(12)
Nonsynonymous polymorphisms in genes coding for histamine-metabolizing enzymes, diamine oxidase and histamine N-methyltransferase are related to the risk of developing allergic diseases. The role of polymorphisms in the histidine decarboxylase gene r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::21fcb19995232450b06e555deb1cf4e7
https://pubmed.ncbi.nlm.nih.gov/20608921
https://pubmed.ncbi.nlm.nih.gov/20608921
Autor:
E, García-Martín, C, Martínez, H, Alonso-Navarro, J, Benito-León, I, Puertas, L, Rubio, T, López-Alburquerque, J A G, Agúndez, F J, Jiménez-Jiménez
Publikováno v:
European journal of neurology. 17(6)
The polymorphic enzyme human serum paraoxonase 1 (PON1), encoded by the gene PON1 (chromosome 7q21.3), plays a major role in the metabolism of organophosphorus compounds. We investigated the possible association between the PON1 genotype and allelic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9ee8f5b846f2414f4455612a6b86232e
https://pubmed.ncbi.nlm.nih.gov/20050883
https://pubmed.ncbi.nlm.nih.gov/20050883
Autor:
P, Ropero, O, Briceño, G, López-Alonso, J A G, Agúndez, F A, González Fernández, F, García-Hoz, A, Villegas Martínez, M, Díaz-Rubio, J M, Ladero
Publikováno v:
Revista espanola de enfermedades digestivas : organo oficial de la Sociedad Espanola de Patologia Digestiva. 99(7)
To disclose whether mutations in the HFE gene inducing liver iron overload are related to the risk of hepatocellular carcinoma (HCC) in otherwise predisposed patients.One hundred and ninety-six patients (161 males) diagnosed with HCC and 181 healthy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4b54dedeffd082db332aa140b958da97
https://pubmed.ncbi.nlm.nih.gov/17973580
https://pubmed.ncbi.nlm.nih.gov/17973580
Publikováno v:
Farmacia hospitalaria : organo oficial de expresion cientifica de la Sociedad Espanola de Farmacia Hospitalaria. 30(4)
To study the major mutations in genes CYP2C8 and CYP2C9, their frequency in populations of diverse ethnical descent, their analysis methods, and the major drugs with affected metabolism, with a special emphasis on NSAIDs.Repeated searches of Pubmed (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a5668069cea2e54ba218eddb78e0aecf
https://pubmed.ncbi.nlm.nih.gov/17022718
https://pubmed.ncbi.nlm.nih.gov/17022718
Autor:
M, Olivera, C, Martínez, J A, Molina, H, Alonso-Navarro, F J, Jiménez-Jiménez, E, García-Martín, J, Benítez, J A G, Agúndez
Publikováno v:
Acta neurologica Scandinavica. 113(5)
The arylamine N-acetyltransferase (NAT2) is a polymorphic enzyme involved in deactivation and activation of carcinogens through N- and O-acetylation. We investigated the association between the genetic NAT2 polymorphism and brain tumors by analysis o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::12fb41ce194a77bb6ab924f5ba162334
https://pubmed.ncbi.nlm.nih.gov/16629768
https://pubmed.ncbi.nlm.nih.gov/16629768