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Generation of one control and four iPSCs clones from patients with Emery-Dreifuss muscular dystrophy type 1.
Machowska, Magdalena; Bearzi, Claudia; Piekarowicz, Katarzyna; Laczmanska, Izabela; Rzepecki, Ryszard.
Afiliação
  • Machowska M; Laboratory of Nuclear Proteins, Faculty of Biotechnology, University of Wroclaw, Fryderyka Joliot-Curie 14a, 50-383 Wroclaw, Poland. Electronic address: magdalena.machowska@uwr.edu.pl.
  • Bearzi C; Institute of Genetic and Biomedical Research (IRGB) National Research Council of Italy (CNR), Via Fantoli 16/15, 20138 Milan, Italy; The National Institute of Molecular Genetics (INGM) 'Romeo ed Enrica Invernizzi', Via Francesco Sforza 35, 20122 Milan, Italy.
  • Piekarowicz K; Laboratory of Nuclear Proteins, Faculty of Biotechnology, University of Wroclaw, Fryderyka Joliot-Curie 14a, 50-383 Wroclaw, Poland.
  • Laczmanska I; Department of Genetics, Wroclaw Medical University, Marcinkowskiego 1, 50-368 Wroclaw, Poland.
  • Rzepecki R; Laboratory of Nuclear Proteins, Faculty of Biotechnology, University of Wroclaw, Fryderyka Joliot-Curie 14a, 50-383 Wroclaw, Poland.
Stem Cell Res ; 55: 102487, 2021 08.
Article em En | MEDLINE | ID: mdl-34419748
Emery-Dreifuss muscular dystrophy type 1 (EDMD1) is a rare genetic disease caused by mutations in the EMD gene coding for a nuclear envelope protein emerin. We generated and characterized induced pluripotent stem cells (iPSCs) from two EDMD1 patients bearing a mutation c.del153C and from one healthy donor. That mutation leads to generation of premature STOP codon. Established iPSCs are very valuable tool for disease pathogenesis investigation and for the development of new therapeutic methods after differentiation to cardiac or muscle cells. Obtained iPSCs show the proper morphology, pluripotency markers expression, normal karyotype and potential to differentiate into three germ layers.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article