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Generation and characterisation of four multiple sclerosis iPSC lines from a single family.
Fortune, Alastair J; Taylor, Bruce V; Charlesworth, Jac C; Burdon, Kathryn P; Blackburn, Nicholas B; Fletcher, Jessica L; Mehta, Ashish; Young, Kaylene M.
Affiliation
  • Fortune AJ; Menzies Institute for Medical Research, University of Tasmania, Hobart, Australia.
  • Taylor BV; Menzies Institute for Medical Research, University of Tasmania, Hobart, Australia.
  • Charlesworth JC; Menzies Institute for Medical Research, University of Tasmania, Hobart, Australia.
  • Burdon KP; Menzies Institute for Medical Research, University of Tasmania, Hobart, Australia.
  • Blackburn NB; Menzies Institute for Medical Research, University of Tasmania, Hobart, Australia.
  • Fletcher JL; Menzies Institute for Medical Research, University of Tasmania, Hobart, Australia.
  • Mehta A; Menzies Institute for Medical Research, University of Tasmania, Hobart, Australia.
  • Young KM; Menzies Institute for Medical Research, University of Tasmania, Hobart, Australia. Electronic address: kaylene.young@utas.edu.au.
Stem Cell Res ; 62: 102828, 2022 07.
Article in En | MEDLINE | ID: mdl-35679759
ABSTRACT
Multiple sclerosis (MS) is a complex neuroinflammatory/degenerative disease of the central nervous system (CNS) that results in the formation of demyelinated lesions and axon degeneration. MS aetiology is complex, with genetics estimated to account for ∼48% of MS risk (International Multiple Sclerosis Genetics Consortium, 2019). Despite this, families with a high incidence of MS are rare. We have generated four induced pluripotent stem cell (iPSC) lines from individuals with relapsing-remitting and secondary progressive MS within a single family. The generation of disease-specific iPSC lines from multiple members of a single family will facilitate MS genetic and functional studies.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Induced Pluripotent Stem Cells / Multiple Sclerosis Limits: Humans Language: En Journal: Stem Cell Res Year: 2022 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Induced Pluripotent Stem Cells / Multiple Sclerosis Limits: Humans Language: En Journal: Stem Cell Res Year: 2022 Document type: Article Affiliation country:
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