Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Federico García-Bragado"'
Autor:
Blanca Gonzalez-Farre, Joan Enric Ramis-Zaldivar, Julia Salmeron-Villalobos, Olga Balagué, Verónica Celis, Jaime Verdu-Amoros, Ferran Nadeu, Constantino Sábado, Antonio Ferrández, Marta Garrido, Federico García-Bragado, María Dolores de la Maya, José Manuel Vagace, Carlos Manuel Panizo, Itziar Astigarraga, Mara Andrés, Elaine S. Jaffe, Elias Campo, Itziar Salaverria
Publikováno v:
Haematologica, Vol 104, Iss 9 (2019)
Burkitt-like lymphoma with 11q aberration is characterized by pathological features and gene expression profile resembling those of Burkitt lymphoma but lacks the MYC rearrangement and carries an 11q-arm aberration with proximal gains and telomeric l
Externí odkaz:
https://doaj.org/article/39ae097fcf364b2da034aa8f90e33ba8
Autor:
Rebeca Manso, Socorro M. Rodríguez-Pinilla, Julia González-Rincón, Sagrario Gómez, Silvia Monsalvo, Pilar Llamas, Federico Rojo, David Pérez-Callejo, Laura Cereceda, Miguel A. Limeres, Carmen Maeso, Lucía Ferrando, Carlos Pérez-Seoane, Guillermo Rodríguez, José M. Arrinda, Federico García-Bragado, Renato Franco, José L. Rodriguez-Peralto, Joaquin González-Carreró, Francisco Martín-Dávila, Miguel A. Piris, Margarita Sánchez-Beato
Publikováno v:
Haematologica, Vol 100, Iss 1 (2015)
Externí odkaz:
https://doaj.org/article/f8f1129976c34161bff15d311d282170
Autor:
Amets Sáenz, Margarita Azpitarte, Rubén Armañanzas, France Leturcq, Ainhoa Alzualde, Iñaki Inza, Federico García-Bragado, Gaspar De la Herran, Julián Corcuera, Ana Cabello, Carmen Navarro, Carolina De la Torre, Eduard Gallardo, Isabel Illa, Adolfo López de Munain
Publikováno v:
PLoS ONE, Vol 3, Iss 11, p e3750 (2008)
Limb-girdle muscular dystrophy type 2A (LGMD2A) is a recessive genetic disorder caused by mutations in calpain 3 (CAPN3). Calpain 3 plays different roles in muscular cells, but little is known about its functions or in vivo substrates. The aim of thi
Externí odkaz:
https://doaj.org/article/abc544911c5d412a9f1a888f30568023
Autor:
Miguel A. Piris, Purificación Domínguez Franjo, Federico García Bragado, Javier Menarguez Palanca, Teresa Flores, Rafael Ramos-Asensio, Juan Carlos Solera-Arroyo, Francisca Iniesta-Martínez, Socorro M. Rodríguez-Pinilla, Jose Rodriguez, Pablo L. Ortiz-Romero, Lydia Sánchez-Verde, Raquel Pajares, Esperanza Martín-Sánchez, Santiago Montes-Moreno, Margarita Sánchez-Beato, Lina Odqvist
Purpose: Peripheral T-cell lymphomas (PTCL) are a heterogeneous entity of neoplasms with poor prognosis, a lack of effective therapies, and a largely unknown molecular pathology. Deregulated NF-κB activity has been associated with several lymphoprol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03e9a57985d05def337772783222f710
https://doi.org/10.1158/1078-0432.c.6521891.v1
https://doi.org/10.1158/1078-0432.c.6521891.v1
Autor:
Miguel A. Piris, Purificación Domínguez Franjo, Federico García Bragado, Javier Menarguez Palanca, Teresa Flores, Rafael Ramos-Asensio, Juan Carlos Solera-Arroyo, Francisca Iniesta-Martínez, Socorro M. Rodríguez-Pinilla, Jose Rodriguez, Pablo L. Ortiz-Romero, Lydia Sánchez-Verde, Raquel Pajares, Esperanza Martín-Sánchez, Santiago Montes-Moreno, Margarita Sánchez-Beato, Lina Odqvist
PDF file - 1756K, Supplementary Materials and Methods; Table S1: Antibodies and conditions for immunohistochemistry; Table S2: Multivariate Cox analysis; Table S3: Immunohistochemical staining of NF-κB in T cell lymphoma cell lines; Table S4: Pathwa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::661624bd1f4855cf925f0a077fa3ff65
https://doi.org/10.1158/1078-0432.22450262.v1
https://doi.org/10.1158/1078-0432.22450262.v1
Autor:
Per Harald Jonson, Peter Hackman, Anna Vihola, Jaakko Sarparanta, Johanna Palmio, Jon Andoni Urtizberea, Jan Weinberg, Federico García-Bragado, Juan José Poza, Marco Savarese, Ana Maria Cobo, Montse Olivé, Bjarne Udd
Publikováno v:
Annals of Neurology. 85:899-906
Objective To clinically and pathologically characterize a cohort of patients presenting with a novel form of distal myopathy and to identify the genetic cause of this new muscular dystrophy. Methods We studied 4 families (3 from Spain and 1 from Swed
Autor:
Jon Andoni Urtizberea, Johanna Palmio, Per Harald Jonson, Montse Olivé, P. Hackman, A. Vihola, B. Udd, Federico García-Bragado, Cobo Am, Jaakko Sarparanta, Marco Savarese, J. Weinberg, J. J. Poza
Publikováno v:
Neuromuscular Disorders. 29:S120-S121
Autor:
Maria Cristina Caballero, Frans R.J. Verhey, Saartje Burgmans, Carmen Echavarri, Federico García-Bragado, Harry B.M. Uylings
Publikováno v:
Journal of Alzheimer's Disease, 30(4), 909-917. IOS Press
Echavarri, C, Burgmans, S, Caballero, M C, Garcia-Bragado, F, Verhey, F R J & Uylings, H B M 2012, ' Co-occurrence of Different Pathologies in Dementia: Implications for Dementia Diagnosis ', Journal of Alzheimer's Disease, vol. 30, no. 4, pp. 909-917 . https://doi.org/10.3233/JAD-2012-111400
Echavarri, C, Burgmans, S, Caballero, M C, Garcia-Bragado, F, Verhey, F R J & Uylings, H B M 2012, ' Co-occurrence of Different Pathologies in Dementia: Implications for Dementia Diagnosis ', Journal of Alzheimer's Disease, vol. 30, no. 4, pp. 909-917 . https://doi.org/10.3233/JAD-2012-111400
The standard for differentiating between dementia subtypes is currently based on neuropathological changes and follows traditional nosological classifications. However, the high incidence of comorbid neuropathologies complicates the differentiation b
Autor:
J.A. Lobrinus, Jon Andoni Urtizberea, M. Goicoechea, Murray Krahn, A. Lopez de Munain, Amets Sáenz, Marc Bartoli, Sébastien Jacquemont, Nicolas Lévy, F. Leturcq, E. Groen, Christophe Pécheux, Federico García-Bragado, Pierre-Yves Jeannet, K. Bushby, Frank Hanisch, Jonathan B. Strober
Publikováno v:
Clinical Genetics
Clinical Genetics, Wiley, 2011, 80 (4), pp.398-402. ⟨10.1111/j.1399-0004.2010.01620.x⟩
Clinical Genetics, 2011, 80 (4), pp.398-402. ⟨10.1111/j.1399-0004.2010.01620.x⟩
Clinical Genetics, Vol. 80, No 4 (2011) pp. 398-402
Clinical Genetics, Wiley, 2011, 80 (4), pp.398-402. ⟨10.1111/j.1399-0004.2010.01620.x⟩
Clinical Genetics, 2011, 80 (4), pp.398-402. ⟨10.1111/j.1399-0004.2010.01620.x⟩
Clinical Genetics, Vol. 80, No 4 (2011) pp. 398-402
International audience; no abstract
Publikováno v:
Arthritisrheumatology (Hoboken, N.J.). 67(9)