Browsing by Author Nunes Martínez, Virginia
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| Issue Date | Title | Author(s) |
|---|---|---|
| 25-May-1990 | A polymorphic DNA probe from chromosome 7 (7q22) | Casals, T.; Nunes Martínez, Virginia; Estivill, Xavier, 1955- |
| 16-Dec-2004 | Análisis del DNA mitocondrial y de la actividad de la cadena respiratoria mitocondrial en la enfermedad de Alzheimer de tipo esporádico | Rodríguez Santiago, Benjamín |
| 1996 | Base genética de la cistinuria, heterogeneidad genética | Nunes Martínez, Virginia |
| 19-Sep-2014 | Bases moleculars de la Leucoeocefalopatia Megalencefàllca amb Quists subcorlicals. Utilització de models animals i cel·lulars | Sirisi Dolcet, Sònia |
| 5-May-2020 | Cerebellar astrocyte transduction as gene therapy for megalencephalic leukoencephalopathy | Sánchez, Ángela; García-Lareu, Belén; Puig, Meritxell; Prat, Esther; Ruberte, Jesús; Chillón, Miguel; Nunes Martínez, Virginia; Estevez, Raúl; Bosch, Assumpció |
| 21-Nov-2019 | Comparison of zebrafish and mice knockouts for Megalencephalic Leukoencephalopathy proteins indicates that GlialCAM/MLC1 forms a functional unit | Pérez Rius, Carla; Folgueira, Mónica; Elorza Vidal, Xabier; Alia, Alia; Hoegg-Beiler, Maja B.; Eeza, Muhamed N.H.; Díaz, María Luz; Nunes Martínez, Virginia; Barrallo-Gimeno, Alejandro; Estévez Povedano, Raúl |
| 2000 | Errors congènits del metabolisme (ECM). | Pàmpols i Ros, Teresa; Arranz, J. A.; Artuch Iriberri, Rafael; Baiget Bastús, Montserrat; Borja, F.; Briones, P.; Casals, T.; Chabás, A.; Coll, M. J.; Rio, E. del; Domínguez, C.; Estivill, Xavier, 1955-; Gallano, Pia; Giròs, Marisa; Martínez, M.; Maya, A.; Milà i Recasens, Montserrat; Margarit, E.; Nunes Martínez, Virginia; Oriola Ambrós, Josep |
| 19-Feb-2013 | Estudi de variants de significat desconegut en la síndrome de Lynch | Borràs Flores, Ester |
| 5-Dec-2023 | Exploring the Contribution of the Transporter AGT1/rBAT in Cystinuria Progression: Insights from Mouse Models and a Retrospective Cohort Study | Gràcia-Garcia, Silvia; Mayayo Vallverdú, Clara; Prat, Esther; Vecino-Pérez, Marta; González, Laura; San Miguel, Luz; Lopera, Noelia; Arias, Ángela; Artuch, Rafael; López de Heredia, Miguel; Torrecilla, Carlos; Rousaud-Barón, Ferran; Angerri, Oriol; Errasti-Murugarren, Ekaitz; Nunes Martínez, Virginia |
| 11-Jan-2008 | Genetic and genomic analysis modeling of germline c-MYC overexpression and cancer susceptibility | Solé Acha, Xavier; Hernández, Pilar; López de Heredia, Miguel; Armengol, Lluís; Rodríguez Santiago, Benjamín; Gómez, Laia; Maxwell, Christopher A.; Aguiló Lúcia, Fernando; Condom i Mundó, Enric; Abril, Jesús; Pérez Jurado, Luis; Estivill, Xavier, 1955-; Nunes Martínez, Virginia; Capellá, G. (Gabriel); Gruber, Stephen B.; Moreno Aguado, Víctor; Pujana Genestar, M. Ángel |
| 21-Feb-2013 | Genotypic classification of patients with Wolfram syndrome: insights into the natural history of the disease and correlation with phenotype | López de Heredia, Miguel; Clèries Soler, Ramon; Nunes Martínez, Virginia |
| 11-Apr-1991 | Mspl restriction fragment length polymorphism near exon 10 of cystic fibrosis (CFTR) gene. | Bosch, A.; Kruyer, H.; Nunes Martínez, Virginia; Estivill, Xavier, 1955- |
| 5-Jul-1990 | Mutation analysis in cystic fibrosis | Gasparini, Paolo; Pignatti, P. F.; Novelli, Giuseppe; Dallapiccola, B.; Nunes Martínez, Virginia; Casals, T.; Estivill, Xavier, 1955-; Fernández Muñoz, Esteve; Balassopoulou, A.; Loukopoulos, D.; Lavinha, J.; Simova, L.; Komel, R. |
| 1-Jun-1995 | Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens | Chillón, Miguel; Casals, T.; Mercier, Bernard; Bassas, Lluís; Lissens, Willy; Silber, Sherman; Romey, Marie Catherine; Ruiz Romero, Javier; Verlingue, Claudine; Claustres, Mireille; Nunes Martínez, Virginia; Férec, Claude; Estivill, Xavier, 1955- |
| 1996 | A nuclear defect in the 4p16 region predisposes to multiple mitochondrial DNA deletions in families with Wolfram syndrome. | Barrientos Rubio, Antoni; Volpini Bertrán, Víctor; Casademont i Pou, Jordi; Genís, David; Manzanares, Josep-Maria; Ferrer, Isidro (Ferrer Abizanda); Corral, Jordi; Cardellach, Francesc; Urbano Márquez, A. (Álvaro); Estivill, Xavier, 1955-; Nunes Martínez, Virginia |
| 25-Aug-1990 | PCR detection of the pKM.19/ScrfI RFLP (D7S23), a marker closely linked to the cystic fibrosis mutation | Nunes Martínez, Virginia; Chillón, Miguel; Lench, N.; Ramsay, M.; Estivill, Xavier, 1955- |
| 24-Feb-2005 | Reabsorció renal d'aminoàcids: anàlisi de mutacions de SLC7A9, el gen de cistinúria de tipus B, i generació d'un model murí "knockout" de Slc7a8 | Font i Llitjós, Mariona |
| 18-Aug-2000 | Respiratory chain dysfunction associated with multiple mitochondrial DNA deletions in antiretroviral therapy-related lipodystrophy. | Miró i Andreu, Òscar; Gómez, Montserrat; Pedrol, Enric; Cardellach, Francesc; Nunes Martínez, Virginia; Casademont i Pou, Jordi |
| Nov-2003 | Reversible mitochondrial respiratory chain impairment during symptomatic hyperlactatemia associated with antiretroviral therapy | Miró i Andreu, Òscar; López Moreno, Sònia; Martínez, Esteban; Rodríguez Santiago, Benjamín; Blanco, José L.; Milinkovic, Ana; Miró Meda, José M.; Nunes Martínez, Virginia; Casademont i Pou, Jordi; Gatell, José M.; Cardellach, Francesc |
| 11-Mar-1990 | Scrfl restriction fragment length polymorphism at the D7S23 locus (probe pKM.19), closely linked to cystic fibrosis | Nunes Martínez, Virginia; Ramsay, M.; Casals, T.; Chillón, Miguel; Lench, N.; Schwartz, Myron; Estivill, Xavier, 1955- |