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Dysregulation of myelin synthesis and actomyosin function underlies aberrant myelin in CMT4B1 neuropathy.
Guerrero-Valero, Marta; Grandi, Federica; Cipriani, Silvia; Alberizzi, Valeria; Di Guardo, Roberta; Chicanne, Gaetan; Sawade, Linda; Bianchi, Francesca; Del Carro, Ubaldo; De Curtis, Ivan; Pareyson, Davide; Parman, Yesim; Schenone, Angelo; Haucke, Volker; Payrastre, Bernard; Bolino, Alessandra.
  • Guerrero-Valero M; Human Inherited Neuropathies Unit, Institute of Experimental Neurology (INSPE) and Division of Neuroscience, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Ospedale San Raffaele, 20132 Milan, Italy.
  • Grandi F; Human Inherited Neuropathies Unit, Institute of Experimental Neurology (INSPE) and Division of Neuroscience, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Ospedale San Raffaele, 20132 Milan, Italy.
  • Cipriani S; Human Inherited Neuropathies Unit, Institute of Experimental Neurology (INSPE) and Division of Neuroscience, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Ospedale San Raffaele, 20132 Milan, Italy.
  • Alberizzi V; Human Inherited Neuropathies Unit, Institute of Experimental Neurology (INSPE) and Division of Neuroscience, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Ospedale San Raffaele, 20132 Milan, Italy.
  • Di Guardo R; Human Inherited Neuropathies Unit, Institute of Experimental Neurology (INSPE) and Division of Neuroscience, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Ospedale San Raffaele, 20132 Milan, Italy.
  • Chicanne G; Inserm UMR-1048, I2MC, Université Toulouse 3 Paul Sabatier, 31432 Toulouse, France.
  • Sawade L; Department of Molecular Pharmacology and Cell Biology, Leibniz-Forschungsinstitut für Molekulare Pharmakologie, 13125 Berlin, Germany.
  • Bianchi F; Department of Neurology, IRCCS Ospedale San Raffaele, 20132 Milan, Italy.
  • Del Carro U; Department of Neurology, IRCCS Ospedale San Raffaele, 20132 Milan, Italy.
  • De Curtis I; Cell Adhesion Unit, Division of Neuroscience, IRCCS Ospedale San Raffaele, 20132 Milan, Italy.
  • Pareyson D; Unit of Rare Neurodegenerative and Neurometabolic Diseases, Department of Clinical Neurosciences, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milan, Italy.
  • Parman Y; Istanbul Faculty of Medicine, Neurology Department, Istanbul University, 34390 Istanbul, Turkey.
  • Schenone A; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetic and Maternal Infantile Sciences, IRCCS Policlinico San Martino, University of Genoa, 16132 Genoa, Italy.
  • Haucke V; Department of Molecular Pharmacology and Cell Biology, Leibniz-Forschungsinstitut für Molekulare Pharmakologie, 13125 Berlin, Germany.
  • Payrastre B; Inserm UMR-1048, I2MC, Université Toulouse 3 Paul Sabatier, 31432 Toulouse, France.
  • Bolino A; Human Inherited Neuropathies Unit, Institute of Experimental Neurology (INSPE) and Division of Neuroscience, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Ospedale San Raffaele, 20132 Milan, Italy; bolino.alessandra@hsr.it.
Proc Natl Acad Sci U S A ; 118(10)2021 03 09.
Article en En | MEDLINE | ID: mdl-33653949
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Transducción de Señal / Enfermedad de Charcot-Marie-Tooth / Fosfatos de Fosfatidilinositol / Proteínas Tirosina Fosfatasas no Receptoras / Vaina de Mielina Límite: Animals Idioma: En Año: 2021 Tipo del documento: Article
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Transducción de Señal / Enfermedad de Charcot-Marie-Tooth / Fosfatos de Fosfatidilinositol / Proteínas Tirosina Fosfatasas no Receptoras / Vaina de Mielina Límite: Animals Idioma: En Año: 2021 Tipo del documento: Article