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A new cellular model to follow Friedreich's ataxia development in a time-resolved way

Friedreich's ataxia (FRDA) is a recessive autosomal ataxia caused by reduced levels of frataxin (FXN), an essential mitochondrial protein that is highly conserved from bacteria to primates. The exact role of frataxin and its primary function remain unclear although this information would be ver...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Dis Model Mech
Päätekijät: Vannocci, Tommaso, Faggianelli, Nathalie, Zaccagnino, Silvia, della Rosa, Ilaria, Adinolfi, Salvatore, Pastore, Annalisa
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: The Company of Biologists 2015
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4486863/
https://ncbi.nlm.nih.gov/pubmed/26035392
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.020545
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