Mostrando resultados 5 a 11 de 11
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| Derechos | Preview | Fecha Public. | Título | Autor(es) | Tipo |
| closedAccess |  | 2004 | Mutation analysis in Spanish patients with hereditary hemorrhagic telangiectasia: Deficient endoglin up-regulation in activated monocytes | Sanz-Rodríguez, Francisco CSIC ORCID; Fernandez-Lopez, Africa CSIC; Zarrabeitia, Roberto; Pérez-Molino, Alfonso; Ramírez, José R.; Coto, Eliecer; Bernabéu, Carmelo CSIC ORCID ; Botella, Luisa María CSIC ORCID | artículo |
| closedAccess |  | mar-2006 | Mutation study of Spanish patients with hereditary hemorrhagic telangiectasia and expression analysis of Endoglin and ALK1 | Fernandez-Lopez, Africa CSIC; Sanz-Rodríguez, Francisco CSIC ORCID; Zarrabeitia, Roberto; Pérez-Molino, Alfonso; Morales, Carmelo; Restrepo, Carlos M.; Ramírez, José Ramón; Coto, Eliecer; Lenato, Gennaro M.; Bernabéu, Carmelo CSIC ORCID ; Botella, Luisa María CSIC ORCID | artículo |
| openAccess |  | mar-2007 | Role of the CDKN1A/p21, CDKN1C/p57, and CDKN2A/p16 Genes in the Risk of Atherosclerosis and Myocardial Infarction | Rodríguez, Isabel; Coto, Eliecer; Reguero, Julian R.; González, Pelayo; Andrés, Vicente CSIC ORCID; Lozano, Iñigo; Martín, María; Álvarez, Victoria; Morís, César | artículo |
| openAccess |  | 2-abr-2004 | A single-nucleotide polymorphism in the human p27kip1 gene (-838C>A) affects basal promoter activity and the risk of myocardial infarction | González, Pelayo; Díez-Juan, Antonio CSIC ORCID; Coto, Eliecer; Victoria, Álvarez; Reguero, Julian R.; Batalla, Alberto; Andrés, Vicente CSIC ORCID | artículo |
| closedAccess |  | abr-2022 | Smoking is associated with age at disease onset in Parkinson's disease | Pérez de la Rosa, Irene ; Morís, Germán; Coto, Eliecer; Blázquez-Estrada, Marta; Suárez, Esther; García-Fernández, Ciara; Martínez, Carmen; Duarte, Israel; Pérez-Oliveira, Sergio; Álvarez, Victoria; Menéndez-González, Manuel | artículo |
| openAccess |  | 23-abr-2019 | The epistasis project: A multi-cohort study of the effects of BDNF, DBH, and SORT1 epistasis on Alzheimer's disease risk | Belbin, Olivia CSIC; Morgan, Kevin; Medway, Chris; Warden, Donald; Cortina-Borja,Mario; Van Dujin, Cornelia, M; Adams, Heiab H.H.; Frank-García, Ana; Brookes, Keeley; Sánchez-Juan, Pascual; Álvarez, Victoria; Heun, Reinhard; Kölsch, Heike; Coto, Eliecer; Kehoe, Patrick G.; Rodríguez-Rodríguez, Eloy; Bullido, María Jesús CSIC ORCID; Ikram, M. Arfan; Smith A. David; Lehmann, Donald J. | artículo |
| openAccess |  | 2019 | Transethnic meta-analysis of rare coding variants in PLCG2, ABI3, and TREM2 supports their general contribution to Alzheimer’s disease | Dalmaso, M. Carolina; Brusco, Luís I.; Olivar, Natvidad; Muchnick, Carolina; Hanses, Claudia; Milz, Esther; Becker, Julian; Heilmann-Heimbach, Stefanie; Hoffmann, Per; Prestia, Federico A.; Galeano, Pablo; Sánchez-Avalos, M. Soledad; Martínez, Luis E.; Carulla, Mariana E.; Azurmendi Pablo J.; Liberczuk, Cynthia; Fezza, Cristina; Sampaño, Marcelo; Fierens, María; Jemar, Guillermo; Solis, Patricia; Medel, Nancy; Lisso, Julieta; Sevillano, Zulma; Bosco, Paolo; Bossu, Paola; Spalletta, Gianfranco; Galimberti, Daniela; Mancuso, Michelangelo; Nacmias, Benedetta; Sorbi, Sandro; Mecocci, Patrizia; Pilotto, Alberto; Caffarra, Paolo; Panza, Francesco; Bullido, María Jesús CSIC ORCID; Clarimón, Jordi; Sánchez-Juan, Pascual; Coto, Eliecer; Sánchez-García, Florentino; Graff, Caroline; Ingelsson, Martin; Bellenguez, Céline; Castaño, Eduardo M.; Kairiyama, Claudia; Politis, Daniel G.; Kochen, Silvia; Scaro, Horacio; Maier, Wolfgang; Jessen, Frank; Mangone, Carlos E.; Lambert, Jean-Charles; Morelli, Laura; Ramírez, Alfredo | artículo |
