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2. Alkaptonuria is a novel human secondary amyloidogenic disease. Millucci L, Spreafico A, Tinti L, Braconi D, Ghezzi L, Paccagnini E, Bernardini G, Amato L, Laschi M, Selvi E, Galeazzi M, Mannoni A, Benucci M, Lupetti P, Chellini F, Orlandini M, Santucci A. Biochim Biophys Acta; 2012 Nov; 1822(11):1682-91. PubMed ID: 22850426 [Abstract] [Full Text] [Related]
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8. Ochronotic pigmentation is caused by homogentisic acid and is the key event in alkaptonuria leading to the destructive consequences of the disease-A review. Ranganath LR, Norman BP, Gallagher JA. J Inherit Metab Dis; 2019 Sep; 42(5):776-792. PubMed ID: 31282009 [Abstract] [Full Text] [Related]
9. A novel ex vivo organotypic culture model of alkaptonuria-ochronosis. Tinti L, Spreafico A, Chellini F, Galeazzi M, Santucci A. Clin Exp Rheumatol; 2011 Sep; 29(4):693-6. PubMed ID: 21813063 [Abstract] [Full Text] [Related]
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11. Homogentisic acid induces morphological and mechanical aberration of ochronotic cartilage in alkaptonuria. Bernardini G, Leone G, Millucci L, Consumi M, Braconi D, Spiga O, Galderisi S, Marzocchi B, Viti C, Giorgetti G, Lupetti P, Magnani A, Santucci A. J Cell Physiol; 2019 May; 234(5):6696-6708. PubMed ID: 30341892 [Abstract] [Full Text] [Related]
12. Homogentisic acid induces autophagy alterations leading to chondroptosis in human chondrocytes: Implications in Alkaptonuria. Galderisi S, Milella MS, Rossi M, Cicaloni V, Rossi R, Giustarini D, Spiga O, Tinti L, Salvini L, Tinti C, Braconi D, Millucci L, Lupetti P, Prischi F, Bernardini G, Santucci A. Arch Biochem Biophys; 2022 Mar 15; 717():109137. PubMed ID: 35090868 [Abstract] [Full Text] [Related]
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