Suchergebnisse - Saida Ortolano
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New Insights in the Amyloid-Beta Interaction with Mitochondria von Carlos Spuch, Saida Ortolano, Carmen Navarro
Veröffentlicht 2012Artigo -
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Characterization of the defective interaction between a subset of natural killer cells and dendritic cells in HIV-1 infection von Domenico Mavilio, Gabriella Lombardo, Audrey Kinter, Manuela Fogli, Andrea Sala, Saida Ortolano, Annahita Farschi, Dean Follmann, Gregg Roby, Colin Kovacs, Emanuela Marcenaro, Daniela Pende, Alessandro Moretta, Anthony S. Fauci
Veröffentlicht 2006Artigo -
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ATP release through connexin hemichannels and gap junction transfer of second messengers propagate Ca <sup>2+</sup> signals across the inner ear von Fabio Anselmi, Victor H. Hernández, Giulia Crispino, Anke Seydel, Saida Ortolano, Stephen D. Roper, Nicoletta Kessaris, William D. Richardson, Gesa Rickheit, Mikhail A Filippov, Hannah Monyer, Fabio Mammano
Veröffentlicht 2008Artigo -
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The Novel Mouse Mutation Oblivion Inactivates the PMCA2 Pump and Causes Progressive Hearing Loss von Sarah L. Spiden, Mario Bortolozzi, Francesca Di Leva, Martin Hrabé de Angelis, Helmut Fuchs, Dmitry Lim, Saida Ortolano, Neil J. Ingham, Marisa Brini, Ernesto Carafoli, Fabio Mammano, Karen P. Steel
Veröffentlicht 2008Artigo -
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The Novel PMCA2 Pump Mutation Tommy Impairs Cytosolic Calcium Clearance in Hair Cells and Links to Deafness in Mice von Mario Bortolozzi, Marisa Brini, Nick Parkinson, Giulia Crispino, Pietro Scimemi, Romolo Daniele De Siati, Francesca Di Leva, Andrew Parker, Saida Ortolano, Edoardo Arslan, Steve D. M. Brown, Ernesto Carafoli, Fabio Mammano
Veröffentlicht 2010Artigo -
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A functional study of plasma-membrane calcium-pump isoform 2 mutants causing digenic deafness von Romina Ficarella, Francesca Di Leva, Mario Bortolozzi, Saida Ortolano, Francesca Donaudy, Marco Petrillo, Salvatore Melchionda, Andrea Lelli, Teuta Domi, Laura Fedrizzi, Dmitry Lim, G. E. Shull, Paolo Gasparini, Marisa Brini, Fabio Mammano, Ernesto Carafoli
Veröffentlicht 2007Artigo -
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Limb-girdle muscular dystrophy 1F is caused by a microdeletion in the transportin 3 gene von M Melia, Akatsuki Kubota, Saida Ortolano, Juan J. Vílchez, Josep Gámez, Kurenai Tanji, Eduardo Bonilla, Lluís Palenzuela, Israel Fernández‐Cadenas, Anna Přistoupilová, Elena García‐Arumí, Antoni L. Andreu, Carmen Navarro, Michio Hirano, Ramón Martí
Veröffentlicht 2013Artigo -
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Characterization of the plasma proteomic profile of Fabry disease: Potential sex- and clinical phenotype-specific biomarkers von Laura López-Valverde, M.E. Vázquez-Mosquera, Cristóbal Colón, Susana B. Bravo, Sofía Gouveia, J. Víctor Álvarez, Rosario Sánchez‐Martínez, Manuel López‐Mendoza, M. López Rodríguez, Eduardo Villacorta, M Goicoechea-Diezhandino, Francisco Guerrero-Márquez, Saida Ortolano, Elisa Leão Teles, Á. Hermida Ameijeiras, María L. Couce
Veröffentlicht 2024Artigo -
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Towards frailty biomarkers: Candidates from genes and pathways regulated in aging and age-related diseases von Ana L. Cardoso, Adelaide Fernandes, Juan Antonio Aguilar‐Pimentel, Martin Hrabě de Angelis, Joana R. Guedes, María Alexandra Brito, Saida Ortolano, Giovambattista Pani, Sophia Athanasopoulou, Efstathios S. Gonos, Markus Schosserer, Johannes Grillari, Pärt Peterson, Bilge Güvenç Tuna, Soner Doğan, Angelika Meyer, Ronald van Os, Anne‐Ulrike Trendelenburg
Veröffentlicht 2018Revisão
Suchwerkzeuge:
Ähnliche Schlagworte
Biology
Medicine
Cell biology
Biochemistry
Disease
Gene
Genetics
Anatomy
Pathology
Inner ear
Internal medicine
Chemistry
Computational biology
Environmental health
Hair cell
Intracellular
Molecular biology
Mutation
Neuroscience
Stereocilia (inner ear)
Bioinformatics
Cholesterol
Cochlea
Computer science
Connexin
Enzyme
Extracellular
Fabry disease
Gap junction
Gerontology