Alkaptonuria (AKU) is a rare genetic disease associated with the accumulation of homogentisic acid (HGA) and its oxidized/polymerized products in connective tissues up to the deposition of melanin-like pigments (ochronosis). Since little is known on the effects of HGA and its metabolites on articular cells, we carried out a proteomic and redox-proteomic analysis to investigate how HGA and ascorbic acid (ASC) affect the human chondrocytic protein repertoire. We settled up an in vitro model using a human chondrocytic cell line to evaluate the effects of 0.33 mM HGA, alone or combined with ASC. We found that HGA and ASC significantly affect the levels of proteins with specific functions in protein folding, cell organization and, notably, stres...
Alkaptonuria (AKU) is a rare disease correlated with deficiency of the enzyme homogentisate 1,2 diox...
Alkaptonuria (AKU) is an ultra-rare genetic disease resulting from a lack in activity of the enzyme ...
Alkaptonuria (AKU) is an ultra-rare inborn error of metabolism associated with a defective catabolis...
Alkaptonuria (AKU) is a rare genetic disease associated with the accumulation of homogentisic acid (...
Alkaptonuria (AKU) is a rare inborn error of metabolism associated with a deficient activity of homo...
Alkaptonuria (AKU) is a rare genetic disease associated with the accumulation of homogentisic acid (...
Alkaptonuria (AKU) is an ultra-rare genetic disease caused by a deficient activity of the enzyme hom...
Alkaptonuria (AKU) is an ultra-rare disease caused by the deficient activity of homogentisate 1,2-di...
Alkaptonuria (AKU) is a rare metabolic disease due to a deficient activity of the enzyme homogentisa...
Alkaptonuria (AKU) is a rare autosomal recessive disease, associated with deficiency of homogentisat...
Alkaptonuria (AKU) is a disease caused by a deficient homogentisate 1,2-dioxygenase activity leading...
Alkaptonuria (AKU) is a rare disease correlated with deficiency of the enzyme homogentisate 1,2 diox...
Alkaptonuria (AKU) is an ultra-rare genetic disease resulting from a lack in activity of the enzyme ...
Alkaptonuria (AKU) is an ultra-rare inborn error of metabolism associated with a defective catabolis...
Alkaptonuria (AKU) is a rare genetic disease associated with the accumulation of homogentisic acid (...
Alkaptonuria (AKU) is a rare inborn error of metabolism associated with a deficient activity of homo...
Alkaptonuria (AKU) is a rare genetic disease associated with the accumulation of homogentisic acid (...
Alkaptonuria (AKU) is an ultra-rare genetic disease caused by a deficient activity of the enzyme hom...
Alkaptonuria (AKU) is an ultra-rare disease caused by the deficient activity of homogentisate 1,2-di...
Alkaptonuria (AKU) is a rare metabolic disease due to a deficient activity of the enzyme homogentisa...
Alkaptonuria (AKU) is a rare autosomal recessive disease, associated with deficiency of homogentisat...
Alkaptonuria (AKU) is a disease caused by a deficient homogentisate 1,2-dioxygenase activity leading...
Alkaptonuria (AKU) is a rare disease correlated with deficiency of the enzyme homogentisate 1,2 diox...
Alkaptonuria (AKU) is an ultra-rare genetic disease resulting from a lack in activity of the enzyme ...
Alkaptonuria (AKU) is an ultra-rare inborn error of metabolism associated with a defective catabolis...