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pro vyhledávání: '"CAVALIERE, PAOLA MARIA GIOVANNA"'
A family of rare but all fatal neurodegenerative diseases which affect not only humans but also various animal species is related to the prion protein (PrP). The unique feature of these diseases is that, in addition to sporadic and inherited forms, t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______152::dc5a62ae5f9cda9aee7b4cd0afd08ff8
http://www.fedoa.unina.it/8681/
http://www.fedoa.unina.it/8681/
Akademický článek
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Autor:
Human Rezaei, Concetta Giancola, Vincenzo Granata, Stéphanie Prigent, Paola Cavaliere, Bruno Pagano, Adriana Zagari
Publikováno v:
Nucleic Acids Research
Nucleic Acids Research, Oxford University Press, 2013, 41 (1), pp.327-39. ⟨10.1093/nar/gks970⟩
Nucleic Acids Research 1 (41), 327-39. (2013)
Nucleic Acids Research, Oxford University Press, 2013, 41 (1), pp.327-39. ⟨10.1093/nar/gks970⟩
Nucleic Acids Research 1 (41), 327-39. (2013)
International audience; Prion protein (PrP) is involved in lethal neurodegenerative diseases, and many issues remain unclear about its physio-pathological role. Quadruplex-forming nucleic acids (NAs) have been found to specifically bind to both PrP c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::925746cf7145776b7cf987df2ee6e2cb
http://europepmc.org/articles/PMC3592392
http://europepmc.org/articles/PMC3592392
Autor:
Carla Carluccio, Paola Cavaliere, Francesco Salvatore, Monica Cerreto, Aurora Daniele, Felice Amato, Adriana Zagari
Hyperphenylalaninemias are genetic diseases prevalently caused by mutations in the phenylalanine hydroxylase (PAH) gene. The wild-type PAH enzyme is a homotetramer regulated by its substrate, cofactor and phosphorylation. We reproduced a full-length
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab0e9095e8e197263af169ae13663797
http://hdl.handle.net/11588/404283
http://hdl.handle.net/11588/404283