Arama Sonuçları - Marina Mora

Sonuçları Daraltın
  1. 1
    NMR metabolomics identifies over 60 biomarkers associated with Type II Diabetes impairment in db/db mice

    NMR metabolomics identifies over 60 biomarkers associated with Type II Diabetes impairment in db/db mice Yazar: Marina Mora-Ortiz, Patricia Nuñez Ramos, Alain Oregioni, Sandrine P. Claus

    Baskı/Yayın Bilgisi 2019
    Tam Metin Erişim Tam Metin Erişim
    Artigo
    Favorilerime ekle
    Kaydedildi:
  2. 2
    DNAJB6 Myopathies: Focused Review on an Emerging and Expanding Group of Myopathies

    DNAJB6 Myopathies: Focused Review on an Emerging and Expanding Group of Myopathies Yazar: Alessandra Ruggieri, S. Saredi, Simona Zanotti, Maria Barbara Pasanisi, Lorenzo Maggi, Marina Mora

    Baskı/Yayın Bilgisi 2016
    Tam Metin Erişim Tam Metin Erişim
    Revisão
    Favorilerime ekle
    Kaydedildi:
  3. 3
    Interaction between gut microbiota and sex hormones and their relation to sexual dimorphism in metabolic diseases

    Interaction between gut microbiota and sex hormones and their relation to sexual dimorphism in metabolic diseases Yazar: Jose Antonio Santos-Marcos, Marina Mora-Ortiz, Manuel Tena‐Sempere, José López‐Miranda, Antonio Camargo

    Baskı/Yayın Bilgisi 2023
    Tam Metin Erişim Tam Metin Erişim
    Revisão
    Favorilerime ekle
    Kaydedildi:
  4. 4
    Tackling muscle fibrosis: From molecular mechanisms to next generation engineered models to predict drug delivery

    Tackling muscle fibrosis: From molecular mechanisms to next generation engineered models to predict drug delivery Yazar: Simone Bersini, Mara Gilardi, Marina Mora, Silke Krol, Chiara Arrigoni, Christian Candrian, Simona Zanotti, Matteo Moretti

    Baskı/Yayın Bilgisi 2018
    Tam Metin Erişim
    Revisão
    Favorilerime ekle
    Kaydedildi:
  5. 5
    Opposing roles of miR-21 and miR-29 in the progression of fibrosis in Duchenne muscular dystrophy

    Opposing roles of miR-21 and miR-29 in the progression of fibrosis in Duchenne muscular dystrophy Yazar: Simona Zanotti, Sara Gibertini, Maurizio Curcio, Paolo Savadori, Barbara Pasanisi, Lucia Morandi, F. Cornelio, Renato Mantegazza, Marina Mora

    Baskı/Yayın Bilgisi 2015
    Tam Metin Erişim
    Artigo
    Favorilerime ekle
    Kaydedildi:
  6. 6
    Expression of transforming growth factor-beta 1 in dystrophic patient muscles correlates with fibrosis. Pathogenetic role of a fibrogenic cytokine.

    Expression of transforming growth factor-beta 1 in dystrophic patient muscles correlates with fibrosis. Pathogenetic role of a fibrogenic cytokine. Yazar: Pia Bernasconi, E Torchiana, Paolo Confalonieri, Raffaella Brugnoni, Rita Barresi, Marina Mora, F. Cornelio, Lucia Morandi, Renato Mantegazza

    Baskı/Yayın Bilgisi 1995
    Tam Metin Erişim Tam Metin Erişim
    Artigo
    Favorilerime ekle
    Kaydedildi:
  7. 7
    Analysis of T cell receptor repertoire of muscle-infiltrating T lymphocytes in polymyositis. Restricted V alpha/beta rearrangements may indicate antigen-driven selection.

    Analysis of T cell receptor repertoire of muscle-infiltrating T lymphocytes in polymyositis. Restricted V alpha/beta rearrangements may indicate antigen-driven selection. Yazar: Renato Mantegazza, Francesca Andreetta, Pia Bernasconi, Fulvio Baggi, Jorge R. Oksenberg, Ornella Simoncini, Marina Mora, F. Cornelio, Lawrence Steinman

    Baskı/Yayın Bilgisi 1993
    Tam Metin Erişim Tam Metin Erişim
    Artigo
    Favorilerime ekle
    Kaydedildi:
  8. 8
    Novel PTRF mutation in a child with mild myopathy and very mild congenital lipodystrophy

    Novel PTRF mutation in a child with mild myopathy and very mild congenital lipodystrophy Yazar: Anna Ardissone, Cinzia Bragato, Lorella Caffi, Flavia Blàsevich, Sabrina Maestrini, Maria Luisa Bianchi, Lucia Morandi, Isabella Moroni, Marina Mora

    Baskı/Yayın Bilgisi 2013
    Tam Metin Erişim Tam Metin Erişim
    Artigo
    Favorilerime ekle
    Kaydedildi:
  9. 9
    Early-onset liver mtDNA depletion and late-onset proteinuric nephropathy in Mpv17 knockout mice

    Early-onset liver mtDNA depletion and late-onset proteinuric nephropathy in Mpv17 knockout mice Yazar: Carlo Viscomi, Antonella Spinazzola, Marco Maggioni, Erika Fernández‐Vizarra, Valeria Massa, Claudio Pagano, Roberto Vettor, Marina Mora, Massimo Zeviani

    Baskı/Yayın Bilgisi 2008
    Tam Metin Erişim Tam Metin Erişim
    Artigo
    Favorilerime ekle
    Kaydedildi:
  10. 10
    Exosomes and exosomal miRNAs from muscle-derived fibroblasts promote skeletal muscle fibrosis

    Exosomes and exosomal miRNAs from muscle-derived fibroblasts promote skeletal muscle fibrosis Yazar: Simona Zanotti, Sara Gibertini, Flavia Blàsevich, Cinzia Bragato, Alessandra Ruggieri, S. Saredi, Marco Fabbri, Pia Bernasconi, Lorenzo Maggi, Renato Mantegazza, Marina Mora

    Baskı/Yayın Bilgisi 2018
    Tam Metin Erişim
    Artigo
    Favorilerime ekle
    Kaydedildi:
  11. 11
    Severe X-Linked Mitochondrial Encephalomyopathy Associated with a Mutation in Apoptosis-Inducing Factor

    Severe X-Linked Mitochondrial Encephalomyopathy Associated with a Mutation in Apoptosis-Inducing Factor Yazar: Daniele Ghezzi, Irina F. Sevrioukova, Federica Invernizzi, Costanza Lamperti, Marina Mora, Pio D’Adamo, Francesca Novara, Orsetta Zuffardi, Graziella Uziel, Massimo Zeviani

    Baskı/Yayın Bilgisi 2010
    Tam Metin Erişim
    Artigo
    Favorilerime ekle
    Kaydedildi:
  12. 12
    SUN-LB11 What Is the Value of Clinical Suspicion in Neonatal Screening for Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency (CAH 21OHD)?

    SUN-LB11 What Is the Value of Clinical Suspicion in Neonatal Screening for Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency (CAH 21OHD)? Yazar: Fernández, María Sanz, Sitja, Marina Mora, González-Pinto, Lucía L Carrascón, de León, Esther González Ruiz, Arnao, Dolores Rodríguez, Sánchez, Amparo Rodríguez

    Baskı/Yayın Bilgisi 2020
    Tam Metin Erişim Tam Metin Erişim
    Metin
    Favorilerime ekle
    Kaydedildi:
  13. 13
    Comparative proteomic analyses of Duchenne muscular dystrophy and Becker muscular dystrophy muscles: changes contributing to preserve muscle function in Becker muscular dystrophy patients

    Comparative proteomic analyses of Duchenne muscular dystrophy and Becker muscular dystrophy muscles: changes contributing to preserve muscle function in Becker muscular dystrophy p... Yazar: Daniele Capitanio, Manuela Moriggi, Enrica Torretta, Pietro Barbacini, Sara De Palma, Agnese Viganò, Hanns Lochmüller, Francesco Muntoni, Alessandra Ferlini, Marina Mora, Cecilia Gelfi

    Baskı/Yayın Bilgisi 2020
    Tam Metin Erişim Tam Metin Erişim
    Artigo
    Favorilerime ekle
    Kaydedildi:
  14. 14
    Relationship Between Voice Analysis and Functional Status in Patients with Amyotrophic Lateral Sclerosis

    Relationship Between Voice Analysis and Functional Status in Patients with Amyotrophic Lateral Sclerosis Yazar: Margarita Pérez-Bonilla, P. Díaz Borrego, Marina Mora-Ortiz, Roberto Fernández-Baíllo, María Nieves Muñoz-Alcaraz, Fernando Jesús Mayordomo-Riera, Eloy Girela-López

    Baskı/Yayın Bilgisi 2025
    Tam Metin Erişim
    Artigo
    Favorilerime ekle
    Kaydedildi:
  15. 15
    Telethon Network of Genetic Biobanks: a key service for diagnosis and research on rare diseases

    Telethon Network of Genetic Biobanks: a key service for diagnosis and research on rare diseases Yazar: Mirella Filocamo, Chiara Baldo, Stefano Goldwurm, Alessandra Renieri, C. Angelini, Maurizio Moggio, Marina Mora, Giuseppe Merla, Luisa Politano, Barbara Garavaglia, Lorena Casareto, Francesca Bricarelli

    Baskı/Yayın Bilgisi 2013
    Tam Metin Erişim Tam Metin Erişim
    Artigo
    Favorilerime ekle
    Kaydedildi:
  16. 16
    Remodeling of the chromatin structure of the facioscapulohumeral muscular dystrophy (FSHD) locus and upregulation of FSHD-related gene 1 (FRG1) expression during human myogenic differentiation

    Remodeling of the chromatin structure of the facioscapulohumeral muscular dystrophy (FSHD) locus and upregulation of FSHD-related gene 1 (FRG1) expression during human myogenic dif... Yazar: Beatrice Bodega, Gabriella Di Capua Ramírez, Florian Grasser, Stefania Cheli, Silvia Brunelli, Marina Mora, Raffaella Meneveri, Anna Marozzi, Stefan O. Mueller, Elena Battaglioli, Enrico Ginelli

    Baskı/Yayın Bilgisi 2009
    Tam Metin Erişim Tam Metin Erişim
    Artigo
    Favorilerime ekle
    Kaydedildi:
  17. 17
    Identification of novel mutations in five patients with mitochondrial encephalomyopathy

    Identification of novel mutations in five patients with mitochondrial encephalomyopathy Yazar: Lucia Valente, Daniela Piga, Eleonora Lamantea, Franco Carrara, Graziella Uziel, Paola Cudia, Anna Zani, Laura Farina, Lucia Morandi, Marina Mora, Antonella Spinazzola, Massimo Zeviani, Valeria Tiranti

    Baskı/Yayın Bilgisi 2008
    Tam Metin Erişim
    Artigo
    Favorilerime ekle
    Kaydedildi:
  18. 18
    Decorin and biglycan expression is differentially altered in several muscular dystrophies

    Decorin and biglycan expression is differentially altered in several muscular dystrophies Yazar: Simona Zanotti, Tiziana Negri, Cristina Cappelletti, Pia Bernasconi, Eleonora Canioni, Claudia Di Blasi, Elena Pegoraro, C. Angelini, Patrizia Ciscato, A. Prelle, Renato Mantegazza, Lucia Morandi, Marina Mora

    Baskı/Yayın Bilgisi 2005
    Tam Metin Erişim
    Artigo
    Favorilerime ekle
    Kaydedildi:
  19. 19
    Engineering an Environment for the Study of Fibrosis: A 3D Human Muscle Model with Endothelium Specificity and Endomysium

    Engineering an Environment for the Study of Fibrosis: A 3D Human Muscle Model with Endothelium Specificity and Endomysium Yazar: Simone Bersini, Mara Gilardi, Giovanni Stefano Ugolini, Veronica Sansoni, Giuseppe Talò, Silvia Perego, Simona Zanotti, Paola Ostano, Marina Mora, Monica Soncini, Marco Vanoni, Giovanni Lombardi, Matteo Moretti

    Baskı/Yayın Bilgisi 2018
    Tam Metin Erişim Tam Metin Erişim
    Artigo
    Favorilerime ekle
    Kaydedildi:
  20. 20
    Spastic Paraplegia and OXPHOS Impairment Caused by Mutations in Paraplegin, a Nuclear-Encoded Mitochondrial Metalloprotease

    Spastic Paraplegia and OXPHOS Impairment Caused by Mutations in Paraplegin, a Nuclear-Encoded Mitochondrial Metalloprotease Yazar: Giorgio Casari, Maurizio De Fusco, Sonia Ciarmatori, Massimo Zeviani, Marina Mora, Patricio Fernández‐Silva, Giuseppe De Michele, Alessandro Filla, Sergio Cocozza, R. Marconi, A. Dürr, Bertrand Fontaine, Andrea Ballabio

    Baskı/Yayın Bilgisi 1998
    Tam Metin Erişim Tam Metin Erişim
    Artigo
    Favorilerime ekle
    Kaydedildi:

Arama Araçları: