Alkaptonuria
Alkaptonuria is a rare inborn error of metabolism caused by the deficiency of homogentisate
1, 2-dioxygenase activity. The consequent homogentisic acid (HGA) accumulation in body …
1, 2-dioxygenase activity. The consequent homogentisic acid (HGA) accumulation in body …
Alkaptonuria: From Molecular Insights to a Dedicated Digital Platform
Alkaptonuria (AKU) is a genetic disorder that affects connective tissues of several body
compartments causing cartilage degeneration, tendon calcification, heart problems, and an …
compartments causing cartilage degeneration, tendon calcification, heart problems, and an …
Phenolic polymers as model melanins
HA Galeb, J Eichhorn, S Harley… - Macromolecular …, 2023 - Wiley Online Library
Melanins are a class of conjugated biopolymers with varying compositions and functions,
which have a variety of potential medical and technical applications. Here, this work …
which have a variety of potential medical and technical applications. Here, this work …
New aspects characterizing non-obese NAFLD by the analysis of the intestinal flora and metabolites using a mouse model
W Zhang, W Cheng, JH Li, Z Huang, H Lin, W Zhang - Msystems, 2024 - Am Soc Microbiol
Non-alcoholic fatty liver disease (NAFLD) is a major public health problem due to the high
incidence affecting approximately one-third of the world's population. NAFLD is usually …
incidence affecting approximately one-third of the world's population. NAFLD is usually …
Genomic Insights into Moderately Thermophilic Methanotrophs of the Genus Methylocaldum
Considering the increasing interest in understanding the biotic component of methane
removal from our atmosphere, it becomes essential to study the physiological characteristics …
removal from our atmosphere, it becomes essential to study the physiological characteristics …