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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

Authors :
D'Anzi, A
Altieri, F
Perciballi, E
Ferrari, D
Bernardini, L
Goldoni, M
Mazzini, L
De Marchi, F
Di Pierro, A
D'Alfonso, S
Gelati, M
Vescovi, A
Rosati, J
D'Anzi A.
Altieri F.
Perciballi E.
Ferrari D.
Bernardini L.
Goldoni M.
Mazzini L.
De Marchi F.
Di Pierro A.
D'Alfonso S.
Gelati M.
Vescovi A. L.
Rosati J.
D'Anzi, A
Altieri, F
Perciballi, E
Ferrari, D
Bernardini, L
Goldoni, M
Mazzini, L
De Marchi, F
Di Pierro, A
D'Alfonso, S
Gelati, M
Vescovi, A
Rosati, J
D'Anzi A.
Altieri F.
Perciballi E.
Ferrari D.
Bernardini L.
Goldoni M.
Mazzini L.
De Marchi F.
Di Pierro A.
D'Alfonso S.
Gelati M.
Vescovi A. L.
Rosati J.
Publication Year :
2020

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).

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1308937630
Document Type :
Electronic Resource