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Generation of an induced pluripotent stem cell line, CSSi011-A (6534), from an Amyotrophic lateral sclerosis patient with heterozygous L145F mutation in SOD1 gene

  • Angela D'Anzi
  • , Filomena Altieri
  • , Elisa Perciballi
  • , Daniela Ferrari
  • , Laura Bernardini
  • , Marina Goldoni
  • , Letizia Mazzini
  • , Fabiola De Marchi
  • , Alice Di Pierro
  • , Sandra D'Alfonso
  • , Maurizio Gelati
  • , Angelo Luigi Vescovi
  • , Jessica Rosati

Risultato della ricerca: Contributo su rivistaArticolo in rivistapeer review

Abstract

Among the known causative genes of familial ALS, SOD1 mutation is one of the most common. It encodes for the ubiquitous detoxifying copper/zinc binding SOD1 enzyme, whose mutations selectively cause motor neuron death, although the mechanisms are not as yet clear. What is known is that mutant-mediated toxicity is not caused by loss of its detoxifying activity but by a gain-of-function. In order to better understand the pathogenic mechanisms of SOD1 mutation, a human induced pluripotent stem cell (hiPSC) line was generated from the somatic cells of a female patient carrying a missense variation in SOD1 (L145F).

Lingua originaleInglese
Numero di articolo101924
RivistaStem Cell Research
Volume47
DOI
Stato di pubblicazionePubblicato - ago 2020

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