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Generation of two hiPSC lines (UMILi027-A and UMILi028-A) from early and late-onset Congenital Central hypoventilation Syndrome (CCHS) patients carrying a polyalanine expansion mutation in the PHOX2B gene.
Cuadros Gamboa, Ana Lucia; Benfante, Roberta; Nizzardo, Monica; Bachetti, Tiziana; Pelucchi, Paride; Melzi, Valentina; Arzilli, Cinzia; Peruzzi, Marta; Reinbold, Rolland A; Cardani, Silvia; Morrone, Amelia; Guerrini, Renzo; Zucchi, Ileana; Corti, Stefania; Ceccherini, Isabella; Piumelli, Raffaele; Nassi, Niccolò; Di Lascio, Simona; Fornasari, Diego.
Afiliación
  • Cuadros Gamboa AL; Department of Medical Biotechnology and Translational Medicine (BIOMETRA), Università degli Studi di Milano, Milan, Italy.
  • Benfante R; Department of Medical Biotechnology and Translational Medicine (BIOMETRA), Università degli Studi di Milano, Milan, Italy; CNR - Institute of Neuroscience, Milan, Italy; NeuroMi-Milan Center for Neuroscience, University of Milano Bicocca, Milan, Italy.
  • Nizzardo M; Neurology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
  • Bachetti T; UOSD Laboratory of Genetics and Genomics of Rare Diseases, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
  • Pelucchi P; Institute for Biomedical Technologies, National Research Council, Milan, Italy.
  • Melzi V; Neurology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
  • Arzilli C; Sleep Disordered Breathing and SIDS Center, Meyer Children's Hospital, Florence, Italy.
  • Peruzzi M; Sleep Disordered Breathing and SIDS Center, Meyer Children's Hospital, Florence, Italy.
  • Reinbold RA; Institute for Biomedical Technologies, National Research Council, Milan, Italy.
  • Cardani S; Department of Medical Biotechnology and Translational Medicine (BIOMETRA), Università degli Studi di Milano, Milan, Italy.
  • Morrone A; Neuroscience Department, Meyer Children's Hospital, Florence, Italy; Department of Neurosciences, Psychology, Pharmacology and Child Health, University of Florence, Italy.
  • Guerrini R; Neuroscience Department, Meyer Children's Hospital, Florence, Italy; Department of Neurosciences, Psychology, Pharmacology and Child Health, University of Florence, Italy.
  • Zucchi I; Institute for Biomedical Technologies, National Research Council, Milan, Italy.
  • Corti S; Neurology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy; Dino Ferrari Centre, Neuroscience Section, Department of Pathophysiology and Transplantation (DEPT), Università degli Studi di Milano, Milan, Italy.
  • Ceccherini I; UOSD Laboratory of Genetics and Genomics of Rare Diseases, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
  • Piumelli R; Sleep Disordered Breathing and SIDS Center, Meyer Children's Hospital, Florence, Italy.
  • Nassi N; Sleep Disordered Breathing and SIDS Center, Meyer Children's Hospital, Florence, Italy.
  • Di Lascio S; Department of Medical Biotechnology and Translational Medicine (BIOMETRA), Università degli Studi di Milano, Milan, Italy. Electronic address: simona.dilascio@unimi.it.
  • Fornasari D; Department of Medical Biotechnology and Translational Medicine (BIOMETRA), Università degli Studi di Milano, Milan, Italy; CNR - Institute of Neuroscience, Milan, Italy. Electronic address: diego.fornasari@unimi.it.
Stem Cell Res ; 61: 102781, 2022 05.
Article en En | MEDLINE | ID: mdl-35421844
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Células Madre Pluripotentes Inducidas Límite: Female / Humans Idioma: En Revista: Stem Cell Res Año: 2022 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Reino Unido
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Células Madre Pluripotentes Inducidas Límite: Female / Humans Idioma: En Revista: Stem Cell Res Año: 2022 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Reino Unido