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pro vyhledávání: '"Laura Giaretta"'
Autor:
Arianna Di Stadio, Valentina Pegoraro, Laura Giaretta, Laura Dipietro, Roberta Marozzo, Corrado Angelini
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-9 (2018)
Abstract Aim To evaluate the feasibility of microRNAs (miR) in clinical use to fill in the gap of current methodology commonly used to test hearing impairment in MELAS patients. Material and method A literature review was performed using the followin
Externí odkaz:
https://doaj.org/article/4f83ae29ee8b41c795a056723030aac4
Publikováno v:
Expert Review of Neurotherapeutics. 18:693-703
Limb-girdle muscular dystrophies (LGMDs) encompass a clinically heterogeneous group of rare, genetic progressive muscle disorders presenting with weakness and atrophy of predominant pelvic and shoulder muscles. The spectrum of disease severity ranges
Autor:
Corrado Angelini, Valentina Pegoraro, Laura Giaretta, Roberta Marozzo, Laura Dipietro, Arianna Di Stadio
Publikováno v:
Orphanet Journal of Rare Diseases
BioMed Central
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-9 (2018)
BioMed Central
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-9 (2018)
Aim To evaluate the feasibility of microRNAs (miR) in clinical use to fill in the gap of current methodology commonly used to test hearing impairment in MELAS patients. Material and method A literature review was performed using the following keyword
Autor:
Leonardo Nogara, Luigi Bubacco, Federico Lanciai, Marcello Carotti, Laura Giaretta, Elisabetta Bergantino, Stefano Fogal
Publikováno v:
Molecular Biotechnology. 57:45-57
Human tyrosinase is the first enzyme of the multistep process of melanogenesis. It catalyzes the hydroxylation of L-tyrosine to L-dihydroxyphenylalanine and the following oxidation of o-diphenol to the corresponding quinone, L-dopaquinone. In spite o