Alkaptonuria (AKU) is a rare disease characterized by high levels of homogentisic acid (HGA); patients suffer from tissue ochronosis: dark brown pigmentation, especially of joint cartilage, leading to severe early osteoarthropathy. No molecular mechanism links elevated HGA to ochronosis; the pigment's chemical identity is still not known, nor how it induces joint cartilage degradation. Here we give key insight on HGA-derived pigment composition and collagen disruption in AKU cartilage. Synthetic pigment and pigmented human cartilage tissue both showed hydroquinone-resembling NMR signals. EPR spectroscopy showed that the synthetic pigment contains radicals. Moreover, we observed intrastrand disruption of collagen triple helix in pigmented AK...
Alkaptonuria (AKU) is a rare inborn error of metabolism associated with a deficient activity of homo...
OBJECTIVES: Alkaptonuria (AKU) is a genetic disorder caused by lack of the enzyme responsible for br...
Objectives. Alkaptonuria (AKU) is a genetic disorder caused by lack of the enzyme responsible for br...
Alkaptonuria (AKU) is a rare disease characterized by high levels of homogentisic acid (HGA); patien...
Alkaptonuria (AKU) is a disease caused by a deficient homogentisate 1,2-dioxygenase activity leading...
Alkaptonuria (AKU) is an ultra-rare disease caused by the deficient activity of homogentisate 1,2-di...
SIR, we report a female with known alkaptonuria (AKU) undergoing routine hip replacement surgery due...
Alkaptonuria (AKU) is a rare genetic disease associated with the accumulation of homogentisic acid (...
Background Alkaptonuria (AKU) is an ultra-rare disease associated to the lack of an enzyme involved ...
Alkaptonuria (AKU) is a rare metabolic disease due to a deficient activity of the enzyme homogentisa...
Alkaptonuria is an iconic disease used by Archibald Garrod to demonstrate the theory of “inborn erro...
Alkaptonuria (AKU) is a rare genetic disease associated with the accumulation of homogentisic acid (...
Alkaptonuria (AKU) is a rare disease correlated with deficiency of the enzyme homogentisate 1,2 diox...
Alkaptonuria (AKU) is a rare genetic disease associated with the accumulation of homogentisic acid (...
OBJECTIVE: Alkaptonuria is a genetic disorder of tyrosine metabolism, resulting in elevated circulat...
Alkaptonuria (AKU) is a rare inborn error of metabolism associated with a deficient activity of homo...
OBJECTIVES: Alkaptonuria (AKU) is a genetic disorder caused by lack of the enzyme responsible for br...
Objectives. Alkaptonuria (AKU) is a genetic disorder caused by lack of the enzyme responsible for br...
Alkaptonuria (AKU) is a rare disease characterized by high levels of homogentisic acid (HGA); patien...
Alkaptonuria (AKU) is a disease caused by a deficient homogentisate 1,2-dioxygenase activity leading...
Alkaptonuria (AKU) is an ultra-rare disease caused by the deficient activity of homogentisate 1,2-di...
SIR, we report a female with known alkaptonuria (AKU) undergoing routine hip replacement surgery due...
Alkaptonuria (AKU) is a rare genetic disease associated with the accumulation of homogentisic acid (...
Background Alkaptonuria (AKU) is an ultra-rare disease associated to the lack of an enzyme involved ...
Alkaptonuria (AKU) is a rare metabolic disease due to a deficient activity of the enzyme homogentisa...
Alkaptonuria is an iconic disease used by Archibald Garrod to demonstrate the theory of “inborn erro...
Alkaptonuria (AKU) is a rare genetic disease associated with the accumulation of homogentisic acid (...
Alkaptonuria (AKU) is a rare disease correlated with deficiency of the enzyme homogentisate 1,2 diox...
Alkaptonuria (AKU) is a rare genetic disease associated with the accumulation of homogentisic acid (...
OBJECTIVE: Alkaptonuria is a genetic disorder of tyrosine metabolism, resulting in elevated circulat...
Alkaptonuria (AKU) is a rare inborn error of metabolism associated with a deficient activity of homo...
OBJECTIVES: Alkaptonuria (AKU) is a genetic disorder caused by lack of the enzyme responsible for br...
Objectives. Alkaptonuria (AKU) is a genetic disorder caused by lack of the enzyme responsible for br...