View in EDS

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.

Saved in:
Bibliographic Details
Title: 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.
Authors: 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.
Source: Stem cell research [Stem Cell Res] 2022 May; Vol. 61, pp. 102781. Date of Electronic Publication: 2022 Apr 07.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Elsevier Country of Publication: England NLM ID: 101316957 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1876-7753 (Electronic) Linking ISSN: 18735061 NLM ISO Abbreviation: Stem Cell Res Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1876-7753
DOI:10.1016/j.scr.2022.102781