Torthaí cuardaigh - Giorgio Casari

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  1. 1
    Related polypeptides are encoded by Drosophila F elements, I factors, and mammalian L1 sequences.

    Related polypeptides are encoded by Drosophila F elements, I factors, and mammalian L1 sequences. de réir Pier Paolo Di Nocera, Giorgio Casari

    Foilsithe / Cruthaithe 1987
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  2. 2
    Endothelin-B receptor mutations in patients with isolated Hirschsprung disease from a non-inbred population

    Endothelin-B receptor mutations in patients with isolated Hirschsprung disease from a non-inbred population de réir Alberto Auricchio, Giorgio Casari, Annamaria Staiano, Andrea Ballabio

    Foilsithe / Cruthaithe 1996
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  3. 3
    Analysis of Uromodulin Polymerization Provides New Insights into the Mechanisms Regulating ZP Domain-mediated Protein Assembly

    Analysis of Uromodulin Polymerization Provides New Insights into the Mechanisms Regulating ZP Domain-mediated Protein Assembly de réir Céline Schaeffer, S Santambrogio, Simone Perucca, Giorgio Casari, Luca Rampoldi

    Foilsithe / Cruthaithe 2008
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  4. 4
    m-AAA and i-AAA complexes coordinate to regulate OMA1, the stress-activated supervisor of mitochondrial dynamics

    m-AAA and i-AAA complexes coordinate to regulate OMA1, the stress-activated supervisor of mitochondrial dynamics de réir Francesco Consolato, Francesca Maltecca, Susanna Tulli, Irene Sambri, Giorgio Casari

    Foilsithe / Cruthaithe 2018
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  5. 5
    Noncoding RNA synthesis and loss of Polycomb group repression accompanies the colinear activation of the human <i>HOXA</i> cluster

    Noncoding RNA synthesis and loss of Polycomb group repression accompanies the colinear activation of the human <i>HOXA</i> cluster de réir Luca Sessa, Achim Breiling, G Lavorgna, Laura Silvestri, Giorgio Casari, Valerio Orlando

    Foilsithe / Cruthaithe 2006
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  6. 6
    Variable and Tissue-Specific Subunit Composition of Mitochondrial <i>m</i>-AAA Protease Complexes Linked to Hereditary Spastic Paraplegia

    Variable and Tissue-Specific Subunit Composition of Mitochondrial <i>m</i>-AAA Protease Complexes Linked to Hereditary Spastic Paraplegia de réir Mirko Koppen, Metodi D. Metodiev, Giorgio Casari, Elena I. Rugarli, Thomas Langer

    Foilsithe / Cruthaithe 2006
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  7. 7
    Tissue-specific splicing pattern of fibronectin messenger RNA precursor during development and aging in rat.

    Tissue-specific splicing pattern of fibronectin messenger RNA precursor during development and aging in rat. de réir Franco Pagani, Laura Zagato, Carlo Vergani, Giorgio Casari, Alessandro Sidoli, Francisco E. Baralle

    Foilsithe / Cruthaithe 1991
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  8. 8
    Haploinsufficiency of<i>AFG3L2</i>, the Gene Responsible for Spinocerebellar Ataxia Type 28, Causes Mitochondria-Mediated Purkinje Cell Dark Degeneration

    Haploinsufficiency of<i>AFG3L2</i>, the Gene Responsible for Spinocerebellar Ataxia Type 28, Causes Mitochondria-Mediated Purkinje Cell Dark Degeneration de réir Francesca Maltecca, Raffaella Magnoni, Federica Cerri, Gregory A. Cox, Angelo Quattrini, Giorgio Casari

    Foilsithe / Cruthaithe 2009
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  9. 9
    Autosomal dominant restless legs syndrome maps on chromosome 14q

    Autosomal dominant restless legs syndrome maps on chromosome 14q de réir Maria Teresa Bonati, Luigi Ferini‐Strambi, Paolo Aridon, Alessandro Oldani, Marco Zucconi, Giorgio Casari

    Foilsithe / Cruthaithe 2003
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  10. 10
    Human tenascin: primary structure, pre-mRNA splicing patterns and localization of the epitopes recognized by two monoclonal antibodies

    Human tenascin: primary structure, pre-mRNA splicing patterns and localization of the epitopes recognized by two monoclonal antibodies de réir Annalisa Siri, Barbara Carnemolla, Marco Saginati, Alessandra Leprini, Giorgio Casari, Francisco E. Baralle, Luciano Zardi

    Foilsithe / Cruthaithe 1991
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  11. 11
    Mitochondria and Melanosomes Establish Physical Contacts Modulated by Mfn2 and Involved in Organelle Biogenesis

    Mitochondria and Melanosomes Establish Physical Contacts Modulated by Mfn2 and Involved in Organelle Biogenesis de réir Tiziana Daniele, Ilse Hurbain, Riccardo Vago, Giorgio Casari, Graça Raposo, Carlo Tacchetti, Maria Vittoria Schiaffino

    Foilsithe / Cruthaithe 2014
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  12. 12
    Increased Susceptibility to Cortical Spreading Depression in the Mouse Model of Familial Hemiplegic Migraine Type 2

    Increased Susceptibility to Cortical Spreading Depression in the Mouse Model of Familial Hemiplegic Migraine Type 2 de réir Loredana Leo, Lisa Gherardini, Virginia Barone, Maurizio De Fusco, Daniela Pietrobon, Tommaso Pizzorusso, Giorgio Casari

    Foilsithe / Cruthaithe 2011
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  13. 13
    Mitochondrial import and enzymatic activity of PINK1 mutants associated to recessive parkinsonism

    Mitochondrial import and enzymatic activity of PINK1 mutants associated to recessive parkinsonism de réir Laura Silvestri, Viviana Caputo, Emanuele Bellacchio, Luigia Atorino, Bruno Dallapiccola, Enza Maria Valente, Giorgio Casari

    Foilsithe / Cruthaithe 2005
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  14. 14
    Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia

    Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia de réir Luigia Atorino, Laura Silvestri, Mirko Koppen, Laura Cassina, Andrea Ballabio, R. Marconi, Thomas Langer, Giorgio Casari

    Foilsithe / Cruthaithe 2003
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  15. 15
    A novel bipartite splicing enhancer modulates the differential processing of the human fibronectin EDA exon

    A novel bipartite splicing enhancer modulates the differential processing of the human fibronectin EDA exon de réir Massimo Caputi, Giorgio Casari, Silvia Guenzi, R. Tagliabue, Alessandro Sidoli, Carlos A. Melo, Francisco E. Baralle

    Foilsithe / Cruthaithe 1994
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  16. 16
    Respiratory dysfunction by AFG3L2 deficiency causes decreased mitochondrial calcium uptake via organellar network fragmentation

    Respiratory dysfunction by AFG3L2 deficiency causes decreased mitochondrial calcium uptake via organellar network fragmentation de réir Francesca Maltecca, Diego De Stefani, Laura Cassina, Francesco Consolato, M Wasilewski, Luca Scorrano, Rosario Rizzuto, Giorgio Casari

    Foilsithe / Cruthaithe 2012
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  17. 17
    Defective glutamate and K <sup>+</sup> clearance by cortical astrocytes in familial hemiplegic migraine type 2

    Defective glutamate and K <sup>+</sup> clearance by cortical astrocytes in familial hemiplegic migraine type 2 de réir Clizia Capuani, Marcello Melone, Angelita Tottene, Luca Bragina, Giovanna Crivellaro, Mirko Santello, Giorgio Casari, Fiorenzo Conti, Daniela Pietrobon

    Foilsithe / Cruthaithe 2016
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  18. 18
    Uromodulin storage diseases: Clinical aspects and mechanisms

    Uromodulin storage diseases: Clinical aspects and mechanisms de réir Francesco Scolari, Gianluca Caridi, Luca Rampoldi, Regina Tardanico, Claudia Izzi, Doroti Pirulli, Antonio Amoroso, Giorgio Casari, Gian Marco Ghiggeri

    Foilsithe / Cruthaithe 2004
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  19. 19
    A Recessive Variant of the Romano-Ward Long-QT Syndrome?

    A Recessive Variant of the Romano-Ward Long-QT Syndrome? de réir Silvia G. Priori, Peter J. Schwartz, Carlo Napolitano, Laura Bianchi, Adrienne T. Dennis, Maurizio De Fusco, Arthur Brown, Giorgio Casari

    Foilsithe / Cruthaithe 1998
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  20. 20
    Linkage Analysis Identifies a Novel Locus for Restless Legs Syndrome on Chromosome 2q in a South Tyrolean Population Isolate

    Linkage Analysis Identifies a Novel Locus for Restless Legs Syndrome on Chromosome 2q in a South Tyrolean Population Isolate de réir Irene Pichler, Fabio Marroni, Cláudia B. Volpato, James F. Gusella, Christine Klein, Giorgio Casari, Alessandro De Grandi, Peter P. Pramstaller

    Foilsithe / Cruthaithe 2006
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