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1دورية أكاديمية
المؤلفون: Kent, L.N, Bae, S, Tsai, S.-Y, Tang, X, Srivastava, A, Koivisto, C, Martin, C.K, Ridolfi, E, Miller, G.C, Zorko, S.M, Plevris, E, Hadjiyannis, Y, Perez, M, Nolan, E, Kladney, R, Westendorp, B, De Bruin, A, Fernandez, S, Rosol, T.J, Pohar, K.S, Pipas, J.M, Leone, G
المساهمون: PHYSIOLOGY
المصدر: Unpaywall 20201031
مصطلحات موضوعية: transcription factor E2F1, transcription factor E2F3, transcriptome, E2f1 protein, mouse, E2f3 protein, tumor protein, animal model, animal tissue, Article, cancer incidence, cancer prognosis, cancer survival, chromatin, chromatin immunoprecipitation, controlled study, copy number variation, disease course, DNA microarray, e2f1 gene, e2f3 gene, epigenetics, female, gain of function mutation, gene, gene dosage, gene expression, gene locus, gene mapping, gene mutation
العلاقة: Kent, L.N, Bae, S, Tsai, S.-Y, Tang, X, Srivastava, A, Koivisto, C, Martin, C.K, Ridolfi, E, Miller, G.C, Zorko, S.M, Plevris, E, Hadjiyannis, Y, Perez, M, Nolan, E, Kladney, R, Westendorp, B, De Bruin, A, Fernandez, S, Rosol, T.J, Pohar, K.S, Pipas, J.M, Leone, G (2017). Dosage-dependent copy number gains in E2f1 and E2f3 drive hepatocellular carcinoma. Journal of Clinical Investigation 127 (3) : 830-842. ScholarBank@NUS Repository. https://doi.org/10.1172/JCI87583Test; https://scholarbank.nus.edu.sg/handle/10635/179227Test
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2Mitochondria function associated genes contribute to Parkinson’s Disease risk and later age at onset
المؤلفون: Billingsley K.J., Barbosa I.A., Bandrés-Ciga S., Quinn J.P., Bubb V.J., Deshpande C., Botia J.A., Reynolds R.H., Zhang D., Simpson M.A., Blauwendraat C., Gan-Or Z., Gibbs J.R., Nalls M.A., Singleton A., Noyce A., Tucci A., Middlehurst B., Kia D., Tan M., Houlden H., Morris H.R., Plun-Favreau H., Holmans P., Hardy J., Trabzuni D., Bras J., Mok K., Kinghorn K., Wood N., Lewis P., Guerreiro R., Lovering R., R’Bibo L., Rizig M., Escott-Price V., Chelban V., Foltynie T., Williams N., Brice A., Danjou F., Lesage S., Martinez M., Giri A., Schulte C., Brockmann K., Simón-Sánchez J., Heutink P., Rizzu P., Sharma M., Gasser T., Nicolas A., Cookson M., Faghri F., Hernandez D., Shulman J., Robak L., Lubbe S., Finkbeiner S., Mencacci N., Lungu C., Scholz S., Reed X., Leonard H., Rouleau G., Krohan L., van Hilten J., Marinus J., Adarmes-Gómez A., Aguilar M., Alvarez I., Alvarez V., Javier Barrero F., Bergareche Yarza J., Bernal-Bernal I., Blazquez M., Bernal M.B.-T., Boungiorno M., Buiza-Rueda D., Cámara A., Carcel M., Carrillo F., Carrión-Claro M., Cerdan D., Clarimón J., Compta Y., Diez-Fairen M., Dols-Icardo O., Duarte J., Duran R., Escamilla-Sevilla F., Ezquerra M., Fernández M., Fernández-Santiago R., Garcia C., García-Ruiz P., Gómez-Garre P., Heredia M.G., Gonzalez-Aramburu I., Pagola A.G., Hoenicka J., Infante J., Jesús S., Jimenez-Escrig A., Kulisevsky J., Labrador-Espinosa M., Lopez-Sendon J., de Munain Arregui A.L., Macias D., Torres I.M., Marín J., Marti M.J., Martínez-Castrillo J., Méndez-del-Barrio C., Menéndez González M., Mínguez A., Mir P., Rezola E.M., Muñoz E., Pagonabarraga J., Pastor P., Errazquin F.P., Periñán-Tocino T., Ruiz-Martínez J., Ruz C., Rodriguez A.S., Sierra M., Suarez-Sanmartin E., Tabernero C., Tartari J.P., Tejera-Parrado C., Tolosa E., Valldeoriola F., Vargas-González L., Vela L., Vives F., Zimprich A., Pihlstrom L., Taba P., Majamaa K., Siitonen A., Okubadejo N., Ojo O., Ryten M., Koks S.
المصدر: npj Parkinsons Disease
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instnameمصطلحات موضوعية: genotype, Mendelian randomization analysis, CLN8 gene, MUC1 gene, genetic analysis, bioenergy, genetic risk, genetic risk score, Article, ATG14 gene, disorders of mitochondrial functions, MRPS34 gene, degenerative disease, mitochondrial gene, EP300 gene, gene mutation, human, MPI gene, gene, molecular phylogeny, LMBRD1 gene, genome-wide association study, monogenic disorder, mitochondrial dynamics, Parkinson disease, E2F1 gene, mitophagy, CAPRIN2 gene, priority journal, risk factor, LGALS3 gene, disease exacerbation, gene expression, gene ontology, meta analysis
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::9375763f2b9ae8b0fc7b9fdef2856c1fTest
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=10173Test