Alkaptonuria (AKU) results from defective homogentisate1,2-dioxygenase (HGD), causing degenerative arthropathy. The deposition of ochronotic pigment in joints is so far attributed to homogentisic acid produced by the liver, circulating in the blood and accumulating locally. Human normal and AKU osteoarticular cells were tested for HGD gene expression by RT-PCR, mono- and 2D-Western blotting. HGD gene expression was revealed in chondrocytes, synoviocytes, osteoblasts. Furthermore, HGD expression was confirmed by Western blotting, that also revealed the presence of five enzymatic molecular species. Our findings indicate that AKU osteoarticular cells produce the ochronotic pigment in loco and this may strongly contribute to induction of ochron...
SummaryObjectiveAlkaptonuria (AKU) is a rare genetic disease which results in severe early onset ost...
Alkaptonuria (AKU) is caused by homogentisate 1,2-dioxygenase (HGD) deficiency. This study aimed to ...
Alkaptonuria (AKU) is a rare genetic disease associated with the accumulation of homogentisic acid (...
Alkaptonuria (AKU) results from defective homogentisate1,2-dioxygenase (HGD), causing degenerative a...
Alkaptonuria is an ultra-rare autosomal recessive disease developed from the lack of homogentisate 1...
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 disease caused by the deficient activity of homogentisate 1,2-di...
Alkaptonuria (AKU) is a hereditary disorder that results from altered structure and function of homo...
Alkaptonuria (AKU) is a rare metabolic disease due to a deficient activity of the enzyme homogentisa...
Alkaptonuria (AKU) is a rare inborn error of metabolism associated with a deficient activity of homo...
Alkaptonuria (AKU) is an ultra-rare genetic disease caused by a deficient activity of the enzyme hom...
SummaryObjectiveAlkaptonuria (AKU) is a rare genetic disease which results in severe early onset ost...
Alkaptonuria (AKU) is caused by homogentisate 1,2-dioxygenase (HGD) deficiency. This study aimed to ...
Alkaptonuria (AKU) is a rare genetic disease associated with the accumulation of homogentisic acid (...
Alkaptonuria (AKU) results from defective homogentisate1,2-dioxygenase (HGD), causing degenerative a...
Alkaptonuria is an ultra-rare autosomal recessive disease developed from the lack of homogentisate 1...
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 disease caused by the deficient activity of homogentisate 1,2-di...
Alkaptonuria (AKU) is a hereditary disorder that results from altered structure and function of homo...
Alkaptonuria (AKU) is a rare metabolic disease due to a deficient activity of the enzyme homogentisa...
Alkaptonuria (AKU) is a rare inborn error of metabolism associated with a deficient activity of homo...
Alkaptonuria (AKU) is an ultra-rare genetic disease caused by a deficient activity of the enzyme hom...
SummaryObjectiveAlkaptonuria (AKU) is a rare genetic disease which results in severe early onset ost...
Alkaptonuria (AKU) is caused by homogentisate 1,2-dioxygenase (HGD) deficiency. This study aimed to ...
Alkaptonuria (AKU) is a rare genetic disease associated with the accumulation of homogentisic acid (...