檢索結果 - Maria Teresa Bassi

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  1. 1
    Cloning of the Gene Encoding a Novel Integral Membrane Protein, Mucolipidin—and Identification of the Two Major Founder Mutations Causing Mucolipidosis Type IV

    Cloning of the Gene Encoding a Novel Integral Membrane Protein, Mucolipidin—and Identification of the Two Major Founder Mutations Causing Mucolipidosis Type IV 由 Maria Teresa Bassi, Marta Manzoni, Eugenio Monti, Maria Teresa Pizzo, Andrea Ballabio, Giuseppe Borsani

    出版 2000
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  2. 2
    Alternative splicing in the human gene for the core protein A1 generates another hnRNP protein.

    Alternative splicing in the human gene for the core protein A1 generates another hnRNP protein. 由 Massimo Buvoli, Fabio Cobianchi, Marco Bestagno, A. Mangiarotti, Maria Teresa Bassi, Giuseppe Biamonti, Silvano Riva

    出版 1990
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  3. 3
    Overexpression of wild‐type and mutant mucolipin proteins in mammalian cells: effects on the late endocytic compartment organization

    Overexpression of wild‐type and mutant mucolipin proteins in mammalian cells: effects on the late endocytic compartment organization 由 Marta Manzoni, Eugenio Monti, Roberto Bresciani, Andrea Bozzato, Sergio Barlati, Maria Teresa Bassi, Giuseppe Borsani

    出版 2004
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  4. 4
    cDNA cloning of human hnRNP protein Al reveals the existence of multiple mRNA isoforms

    cDNA cloning of human hnRNP protein Al reveals the existence of multiple mRNA isoforms 由 Massimo Buvoli, Giuseppe Biamonti, Pantelis Tsoulfas, Maria Teresa Bassi, A. Ghetti, Silvano Riva, Carlo Morandi

    出版 1988
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  5. 5
    Epilepsy in Tubulinopathy: Personal Series and Literature Review

    Epilepsy in Tubulinopathy: Personal Series and Literature Review 由 Romina Romaniello, Claudio Zucca, Filippo Arrigoni, Paolo Bonanni, Elena Panzeri, Maria Teresa Bassi, Renato Borgatti

    出版 2019
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  6. 6
    The Fine Tuning of Drp1-Dependent Mitochondrial Remodeling and Autophagy Controls Neuronal Differentiation

    The Fine Tuning of Drp1-Dependent Mitochondrial Remodeling and Autophagy Controls Neuronal Differentiation 由 Chiara Vantaggiato, Marianna Castelli, Matteo Giovarelli, Genny Orso, Maria Teresa Bassi, Emilio Clementi, Clara De Palma

    出版 2019
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  7. 7
    Charcot-Marie-Tooth disease with pyramidal features due to a new mutation of EGR2 gene

    Charcot-Marie-Tooth disease with pyramidal features due to a new mutation of EGR2 gene 由 Carlo, Fusco, Carlotta, Spagnoli, Grazia, Gabriella Salerno, Elena, Pavlidis, Daniele, Frattini, Francesco, Pisani, Maria, Teresa Bassi

    出版 2019
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  8. 8
    A novel mutation in the β‐tubulin gene <i>TUBB2B</i> associated with complex malformation of cortical development and deficits in axonal guidance

    A novel mutation in the β‐tubulin gene <i>TUBB2B</i> associated with complex malformation of cortical development and deficits in axonal guidance 由 Romina Romaniello, Alessandra Tonelli, Filippo Arrigoni, Cinzia Baschirotto, Fabio Triulzi, Nereo Bresolin, Maria Teresa Bassi, Renato Borgatti

    出版 2012
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  9. 9
    Brain malformations and mutations in <i>α</i>‐ and <i>β</i>‐tubulin genes: a review of the literature and description of two new cases

    Brain malformations and mutations in <i>α</i>‐ and <i>β</i>‐tubulin genes: a review of the literature and description of two new cases 由 Romina Romaniello, Filippo Arrigoni, Anna Cavallini, Erika Tenderini, Cinzia Baschirotto, Fabio Triulzi, Maria Teresa Bassi, Renato Borgatti

    出版 2014
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  10. 10
    Nitric Oxide Sustains Long-Term Skeletal Muscle Regeneration by Regulating Fate of Satellite Cells Via Signaling Pathways Requiring Vangl2 and Cyclic GMP

    Nitric Oxide Sustains Long-Term Skeletal Muscle Regeneration by Regulating Fate of Satellite Cells Via Signaling Pathways Requiring Vangl2 and Cyclic GMP 由 Roberta Buono, Chiara Vantaggiato, Viviana Pisa, Emanuele Azzoni, Maria Teresa Bassi, Silvia Brunelli, Clara Sciorati, Emilio Clementi

    出版 2011
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  11. 11
    Characterization and Mutation Analysis of Human LEFTY A and LEFTY B, Homologues of Murine Genes Implicated in Left-Right Axis Development

    Characterization and Mutation Analysis of Human LEFTY A and LEFTY B, Homologues of Murine Genes Implicated in Left-Right Axis Development 由 Kenjiro Kosaki, Rika Kosaki, Maria Teresa Bassi, Mark Lewin, John W. Belmont, Gail M. Schauer, Brett Casey

    出版 1999
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  12. 12
    Tubulin genes and malformations of cortical development

    Tubulin genes and malformations of cortical development 由 Romina Romaniello, Filippo Arrigoni, Andrew E. Fry, Maria Teresa Bassi, Mark I. Rees, Renato Borgatti, Daniela T. Pilz, Thomas D. Cushion

    出版 2018
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  13. 13
    Identification and expression of NEU3, a novel human sialidase associated to the plasma membrane

    Identification and expression of NEU3, a novel human sialidase associated to the plasma membrane 由 Eugenio Monti, Maria Teresa Bassi, Nadia Papini, Mirko Riboni, Marta Manzoni, Bruno Venerando, Gianluigi Croci, Augusto Preti, Andrea Ballabio, Guido Tettamanti, Giuseppe Borsani

    出版 2000
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  14. 14
    Syntaxin 4 Is Required for Acid Sphingomyelinase Activity and Apoptotic Function

    Syntaxin 4 Is Required for Acid Sphingomyelinase Activity and Apoptotic Function 由 Cristiana Perrotta, Laura Bizzozero, Denise Cazzato, Sara Morlacchi, Emma Assi, Fabio Simbari, Yang Zhang, Erich Gulbins, Maria Teresa Bassi, Patrizia Rosa, Emilio Clementi

    出版 2010
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  15. 15
    X-Linked Late-Onset Sensorineural Deafness Caused by a Deletion Involving OA1 and a Novel Gene Containing WD-40 Repeats

    X-Linked Late-Onset Sensorineural Deafness Caused by a Deletion Involving OA1 and a Novel Gene Containing WD-40 Repeats 由 Maria Teresa Bassi, Raj Ramesar, Barbara Caciotti, Ingrid Winship, Alessandro De Grandi, Mirko Riboni, Philip L. Townes, Peter Beighton, Andrea Ballabio, Giuseppe Borsani

    出版 1999
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  16. 16
    The Low-Affinity Receptor for Neurotrophins p75<sup>NTR</sup> Plays a Key Role for Satellite Cell Function in Muscle Repair Acting via RhoA

    The Low-Affinity Receptor for Neurotrophins p75<sup>NTR</sup> Plays a Key Role for Satellite Cell Function in Muscle Repair Acting via RhoA 由 Daniela Deponti, Roberta Buono, Giuseppina Catanzaro, Clara De Palma, Renato Longhi, Raffaella Meneveri, Nereo Bresolin, Maria Teresa Bassi, Giulio Cossu, Emilio Clementi, Silvia Brunelli

    出版 2009
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  17. 17
    A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhood

    A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhood 由 Maria Teresa Bassi, Nereo Bresolin, A. Tonelli, K. Nazos, Francesca Crippa, Cinzia Baschirotto, Claudio Zucca, Anna Bersano, Diego Dolcetta, Fm Boneschi, Virginia Barone, Giorgio Casari

    出版 2004
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  18. 18
    The first ALS2 missense mutation associated with JPLS reveals new aspects of alsin biological function

    The first ALS2 missense mutation associated with JPLS reveals new aspects of alsin biological function 由 Chris Panzeri, Clara De Palma, Andrea Martinuzzi, Andrea Daga, G. De Polo, Nereo Bresolin, Christopher C.J. Miller, Elizabeth L. Tudor, Emilio Clementi, Maria Teresa Bassi

    出版 2006
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  19. 19
    ZFYVE26/SPASTIZIN and SPG11/SPATACSIN mutations in hereditary spastic paraplegia types AR-SPG15 and AR-SPG11 have different effects on autophagy and endocytosis

    ZFYVE26/SPASTIZIN and SPG11/SPATACSIN mutations in hereditary spastic paraplegia types AR-SPG15 and AR-SPG11 have different effects on autophagy and endocytosis 由 Chiara Vantaggiato, Elena Panzeri, Marianna Castelli, Andrea Citterio, Alessia Arnoldi, Filippo M. Santorelli, Rocco Liguori, Marina Scarlato, Olimpia Musumeci, António Toscano, Emilio Clementi, Maria Teresa Bassi

    出版 2018
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  20. 20
    Cornelia de Lange syndrome mutations in SMC1A or SMC3 affect binding to DNA

    Cornelia de Lange syndrome mutations in SMC1A or SMC3 affect binding to DNA 由 Ekaterina Revenkova, Maria Luisa Focarelli, S. P. Lucia, Marianna Paulis, Maria Teresa Bassi, Linda Mannini, Annalisa Frattini, Domenico Delia, Ian D. Krantz, Paolo Vezzoni, Rolf Jessberger, Antonio Musio

    出版 2008
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