Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Anastasia Rastokina"'
Autor:
Anastasia Rastokina, Jorge Cebrián, Negin Mozafari, Nicholas H Mandel, C I Edvard Smith, Massimo Lopes, Rula Zain, Sergei M Mirkin
Publikováno v:
Nucleic Acids Research.
Friedreich's ataxia (FRDA) is caused by expansions of GAA•TTC repeats in the first intron of the human FXN gene that occur during both intergenerational transmissions and in somatic cells. Here we describe an experimental system to analyze large-sc
Autor:
Anastasia Rastokina, Negin Mozafari, Jorge Cebrián, C.I Edvard Smith, Sergei M. Mirkin, Rula Zain
The human disease Friedreich’s ataxia (FRDA) is caused by expansions of GAA•TTC repeats in the first intron intron of the frataxin (FXN) gene, and both intergenerational and somatic expansions are crucial for disease development. We and others ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c559b8b1237ae17e4ce513f60375edf8
https://doi.org/10.1101/2022.07.04.498742
https://doi.org/10.1101/2022.07.04.498742
Autor:
Anastasia Rastokina, Jorge Cebrián, Nicholas Mandel, Rula Zain, Massimo Lopes, Sergei M. Mirkin
1AbstractHuman disease Friedreich’s ataxia (FRDA) is caused by large-scale expansions of (GAA)n repeats in the first intron of the FXN gene. While repeat expansions during intergenerational transmissions are causative for the disease development, s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78ced3999cfd39ae81d9c647c515e8f4
https://doi.org/10.1101/2022.07.04.498737
https://doi.org/10.1101/2022.07.04.498737