Zobrazeno 1 - 10
of 283
pro vyhledávání: '"Vicente, AM"'
Autor:
González-Del-Alba A, Conde-Moreno AJ, García Vicente AM, González-Peramato P, Linares-Espinós E, Climent MÁ
Publikováno v:
Cancers
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Based on the discussion of current state of research of relevant topics of metastatic bladder cancer (mBC) among a group of experts of a Spanish Oncology Genitourinary (SOGUG) Working Group, a set of recommendations were proposed to overcome the chal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::3f3fb31b9e7a64162db428e7cec1c2d5
https://fundanet.iislafe.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=15570
https://fundanet.iislafe.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=15570
In diverse bacterial lineages, multienzyme assemblies have evolved that are central elements of RNA metabolism and RNA-mediated regulation. The aquatic Gram-negative bacterium $\textit{Caulobacter crescentus}$, which has been a model system for study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a56c4cd2f8fc38eac9d8fa51a76fb61b
Autor:
Anney, RJL, Ripke, S, Anttila, V, Grove, J, Holmans, P, Huang, H, Klei, L, Lee, PH, Medland, SE, Neale, B, Robinson, E, Weiss, LA, Zwaigenbaum, L, Yu, TW, Wittemeyer, K, Willsey, AJ, Wijsman, EM, Werge, T, Wassink, TH, Waltes, R, Walsh, CA, Wallace, S, Vorstman, JAS, Vieland, VJ, Vicente, AM, Vanengeland, H, Tsang, K, Thompson, AP, Szatmari, P, Svantesson, O, Steinberg, S, Stefansson, K, Stefansson, H, State, MW, Soorya, L, Silagadze, T, Scherer, SW, Schellenberg, GD, Sandin, S, Sanders, SJ, Saemundsen, E, Rouleau, GA, Rogé, B, Roeder, K, Roberts, W, Reichert, J, Reichenberg, A, Rehnström, K, Regan, R, Poustka, F, Poultney, CS, Piven, J, Pinto, D, Pericak-Vance, MA, Pejovic-Milovancevic, M, Pedersen, MG, Pedersen, CB, Paterson, AD, Parr, JR
Publikováno v:
Anney, RJL; Ripke, S; Anttila, V; Grove, J; Holmans, P; Huang, H; et al.(2017). Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. Molecular Autism, 8(1). doi: 10.1186/s13229-017-0137-9. UCSF: Retrieved from: http://www.escholarship.org/uc/item/9kd189vf
© 2017 The Author(s). Background: Over the past decade genome-wide association studies (GWAS) have been applied to aid in the understanding of the biology of traits. The success of this approach is governed by the underlying effect sizes carried by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::669870b3364dbdbb306a1a440276d3de
http://www.escholarship.org/uc/item/9kd189vf
http://www.escholarship.org/uc/item/9kd189vf
Autor:
Holmes, MV, Dale, CE, Zuccolo, L, Silverwood, RJ, Guo, Y, Ye, Z, Prieto-Merino, D, Dehghan, Abbas, Trompet, S, Wong, A, Cavadino, A, Drogan, D, Padmanabhan, S, Li, Shan, Yesupriya, A, Leusink, M, Sundstrom, J, Hubacek, JA, Pikhart, H, Swerdlow, DI, Panayiotou, AG, Borinskaya, SA, Finan, C, Shah, S, Kuchenbaecker, KB, Shah, T, Engmann, J, Folkersen, L, Eriksson, P, Ricceri, F, Melander, O, Sacerdote, C, Gamble, DM, Rayaprolu, S, Ross, OA, McLachlan, S, Vikhireva, O, Sluijs, Iris, Scott, RA, Adamkova, V, Flicker, L, van Bockxmeer, FM, Power, C, Marques-Vidal, P, Meade, T, Marmot, MG, Ferro, JM, Paulos-Pinheiro, S, Humphries, SE, Talmud, PJ, Leach, IM, Verweij, N (Niek), Linneberg, A, Skaaby, T, Doevendans, PA, Cramer, MJ, van der Harst, P, Klungel, OH, Dowling, NF, Dominiczak, AF, Kumari, M, Nicolaides, AN, Weikert, C, Boeing, H, Ebrahim, S, Gaunt, TR, Price, JF, Lannfelt, L, Peasey, A, Kubinova, R, Pajak, A, Malyutina, S, Voevoda, MI, Tamosiunas, A, Zee, AH, Norman, PE, Hankey, GJ, Bergmann, MM, Hofman, Bert, Franco Duran, OH, Cooper, J, Palmen, J, Spiering, W, Jong, PA, Kuh, D, Hardy, R, Uitterlinden, André, Ikram, Arfan, Ford, I, Hyppoenen, E, Almeida, OP, Wareham, NJ, Khaw, KT, Hamsten, A, Husemoen, LLN, Tjonneland, A, Tolstrup, JS, Rimm, E, Beulens, JWJ, Verschuren, WMM, Onland-Moret, NC, Hofker, MH, Wannamethee, SG, Whincup, PH, Morris, R, Vicente, AM, Watkins, H, Farrall, M, Jukema, JW, Meschia, J, Cupples, LA, Sharp, SJ, Fornage, M, Kooperberg, C, Lacroix, AZ, Dai, JY, Lanktree, MB, Siscovick, DS, Jorgenson, E, Spring, B, Coresh, J, Li, YR, Buxbaum, SG, Schreiner, PJ, Ellison, RC, Tsai, MY, Patel, SR, Redline, S, Johnson, AD, Hoogeveen, RC, Rotter, JI, Boerwinkle, E, de Bakker, PIW, Kivimaki, M, Asselbergs, FW, Sattar, N, Lawlor, DA, Whittaker, J, Smith, GD, Mukamal, K, Psaty, BM, Wilson, JG, Lange, LA, Hamidovic, A, Hingorani, AD, Nordestgaard, BG, Bobak, M, Leon, DA, Langenberg, C, Palmer, TM, Reiner, AP, Keating, BJ, Dudbridge, F, Casas, JP
Publikováno v:
BMJ-British medical journal, 349. BMJ Publishing Group
Objective: To use the rs1229984 variant in the alcohol dehydrogenase 1B gene (ADH1B) as an instrument to investigate the causal role of alcohol in cardiovascular disease. Design: Mendelian randomisation meta-analysis of 56 epidemiological studies. Pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::9bce34c69de0a3c4e83beb0ae8fc1f79
https://hdl.handle.net/20.500.14279/3672
https://hdl.handle.net/20.500.14279/3672
Autor:
Correia, CT, Conceição, IC, Oliveira, B, Coelho, J, Sousa, I, Sequeira, AF, Almeida, J, Café, C, Duque, F, Mouga, S, Roberts, W, Gao, K, Lowe, JK, Thiruvahindrapuram, B, Walker, S, Marshall, CR, Pinto, D, Geschwind, JI, Scherer, SW, Oliveira, G, Vicente, AM
BACKGROUND: Validating the potential pathogenicity of copy number variants (CNVs) identified in genome-wide studies of autism spectrum disorders (ASD) requires detailed assessment of case/control frequencies, inheritance patterns, clinical correlatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1504::20892f355d827ebfd2b3fd1d3b545c98
https://hdl.handle.net/10400.4/1713
https://hdl.handle.net/10400.4/1713
Autor:
Traylor, M, Farrall, M, Holliday, EG, Sudlow, C, Hopewell, JC, Cheng, YC, Fornage, M, Ikram, MA, Malik, R, Bevan, S, Thorsteinsdottir, U, Nalls, MA, Longstreth, WT, Wiggins, KL, Yadav, S, Parati, EA, DeStefano, AL, Worrall, BB, Kittner, SJ, Khan, MS, Reiner, AP, Helgadottir, A, Achterberg, S, Fernandez-Cadenas, I, Abboud, S, Schmidt, R, Walters, M, Chen, WM, Ringelstein, EB, O'Donnell, M, Ho, WK, Pera, J, Lemmens, R, Norrving, B, Higgins, P, Benn, M, Sale, M, Kuhlenbäumer, G, Doney, ASF, Vicente, AM, Delavaran, H, Algra, A, Davies, G, Oliveira, SA, Palmer, CNA, Deary, I, Schmidt, H, Pandolfo, M, Montaner, J, Carty, C, de Bakker, PIW, Kostulas, K, Ferro, JM, van Zuydam, NR, Valdimarsson, E, Nordestgaard, BG, Lindgren, A, Thijs, V, Slowik, A, Saleheen, D, Paré, G, Berger, K, Thorleifsson, G, Hofman, A, Mosley, TH, Mitchell, BD, Furie, K, Clarke, R, Levi, C, Seshadri, S, Gschwendtner, A, Boncoraglio, GB, Sharma, P, Bis, JC, Gretarsdottir, S, Psaty, BM, Rothwell, PM, Rosand, J
Publikováno v:
The Lancet Neurology
The Lancet Neurology, 11(11), 951-962
Traylor, M, Farrall, M, Holliday, E G, Sudlow, C, Hopewell, J C, Cheng, Y-C, Fornage, M, Ikram, M A, Malik, R, Bevan, S, Thorsteinsdottir, U, Nalls, M A, Longstreth, W, Wiggins, K L, Yadav, S, Parati, E A, Destefano, A L, Worrall, B B, Kittner, S J, Khan, M S, Reiner, A P, Helgadottir, A, Achterberg, S, Fernandez-Cadenas, I, Abboud, S, Schmidt, R, Walters, M, Chen, W-M, Ringelstein, E B, O'Donnell, M, Ho, W K, Pera, J, Lemmens, R, Norrving, B, Higgins, P, Benn, M, Sale, M, Kuhlenbäumer, G, Doney, A S F, Vicente, A M, Delavaran, H, Algra, A, Davies, G, Oliveira, S A, Palmer, C N A, Deary, I, Schmidt, H, Pandolfo, M & Montaner, J & Carty, C 2012, ' Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration) : a meta-analysis of genome-wide association studies ', Lancet Neurology, vol. 11, no. 11, pp. 951-62 . https://doi.org/10.1016/S1474-4422(12)70234-X
Lancet Neurology, 11(11), 951-962. Lancet Publishing Group
The Lancet. Neurology
The Lancet Neurology; Vol 11
The Lancet Neurology, 11(11), 951-962
Traylor, M, Farrall, M, Holliday, E G, Sudlow, C, Hopewell, J C, Cheng, Y-C, Fornage, M, Ikram, M A, Malik, R, Bevan, S, Thorsteinsdottir, U, Nalls, M A, Longstreth, W, Wiggins, K L, Yadav, S, Parati, E A, Destefano, A L, Worrall, B B, Kittner, S J, Khan, M S, Reiner, A P, Helgadottir, A, Achterberg, S, Fernandez-Cadenas, I, Abboud, S, Schmidt, R, Walters, M, Chen, W-M, Ringelstein, E B, O'Donnell, M, Ho, W K, Pera, J, Lemmens, R, Norrving, B, Higgins, P, Benn, M, Sale, M, Kuhlenbäumer, G, Doney, A S F, Vicente, A M, Delavaran, H, Algra, A, Davies, G, Oliveira, S A, Palmer, C N A, Deary, I, Schmidt, H, Pandolfo, M & Montaner, J & Carty, C 2012, ' Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration) : a meta-analysis of genome-wide association studies ', Lancet Neurology, vol. 11, no. 11, pp. 951-62 . https://doi.org/10.1016/S1474-4422(12)70234-X
Lancet Neurology, 11(11), 951-962. Lancet Publishing Group
The Lancet. Neurology
The Lancet Neurology; Vol 11
Background: Various genome-wide association studies (GWAS) have been done in ischaemic stroke, identifying a few loci associated with the disease, but sample sizes have been 3500 cases or less. We established the METASTROKE collaboration with the aim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::379db6159900ded79d8c403cab3986e0
https://openaccess.sgul.ac.uk/id/eprint/101492/1/mmc1.pdf
https://openaccess.sgul.ac.uk/id/eprint/101492/1/mmc1.pdf
Autor:
Rosa, A, Fonseca, BV, Krug, T, Manso, H, Gouveia, L, Albergaria, I, Gaspar, G, Correia, M, Viana-Baptista, M, Simões, RM, Pinto, AN, Taipa, R, Ferreira, C, Fontes, JR, Gabriel, JP, Matos, I, Lopes, G, Ferro, JM, Vicente, AM, Oliveira, SA
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
BACKGROUND: The genetic contribution to stroke is well established but it has proven difficult to identify the genes and the disease-associated alleles mediating this effect, possibly because only nuclear genes have been intensely investigated so far
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::959fc8c72319e0368fca8cd337db154d
https://hdl.handle.net/10400.23/300
https://hdl.handle.net/10400.23/300
Autor:
Barreto, M., Ferreira, RC., Lourenço, L., Moraes-Fontes, MF., Santos, E., Alves, M., Carvalho, C., Martins, B., Andreia, R., Viana, JF., Vasconcelos, C., Mota-Vieira, L., Ferreira, C., Demengeot, J., Vicente, AM.
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Background: CD4(+)CD25(+) regulatory T cells play an essential role in maintaining immune homeostasis and preventing autoimmunity. Therefore, defects in Treg development, maintenance or function have been associated with several human autoimmune dise
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::d90fed3502c84979ba07570d06a9770b
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