[HTML][HTML] Xanthine oxidoreductase: One enzyme for multiple physiological tasks
Human xanthine oxidoreductase (XOR) is a multiple-level regulated enzyme, resulting from
a complicated evolutionary process that assigned it many physiological roles. The main …
a complicated evolutionary process that assigned it many physiological roles. The main …
Reactive oxygen-related diseases: therapeutic targets and emerging clinical indications
Significance: Enhanced levels of reactive oxygen species (ROS) have been associated with
different disease states. Most attempts to validate and exploit these associations by chronic …
different disease states. Most attempts to validate and exploit these associations by chronic …
Genetic susceptibility to diabetic kidney disease is linked to promoter variants of XOR
Q Wang, H Qi, Y Wu, L Yu, R Bouchareb, S Li… - Nature …, 2023 - nature.com
The lifetime risk of kidney disease in people with diabetes is 10–30%, implicating genetic
predisposition in the cause of diabetic kidney disease (DKD). Here we identify an …
predisposition in the cause of diabetic kidney disease (DKD). Here we identify an …
A mouse model for inherited renal fibrosis associated with endoplasmic reticulum stress
Renal fibrosis is a common feature of renal failure resulting from multiple etiologies,
including diabetic nephropathy, hypertension and inherited renal disorders. However, the …
including diabetic nephropathy, hypertension and inherited renal disorders. However, the …
Kidney Failure Secondary to Hereditary Xanthinuria due to a Homozygous Deletion of the XDH Gene in the Absence of Overt Kidney Stone Disease
PL Gonçalves, H Diniz, I Tavares, S Dória, J Dong… - Nephron, 2024 - karger.com
Hereditary xanthinuria (HXAN) is a rare metabolic disorder that results from mutations in
either the xanthine dehydrogenase (XDH) or the molybdenum cofactor sulfurase genes …
either the xanthine dehydrogenase (XDH) or the molybdenum cofactor sulfurase genes …
The presence of xanthine dehydrogenase is crucial for the maturation of the rat kidneys
LV Dissanayake, O Kravtsova, M Lowe… - Clinical …, 2024 - portlandpress.com
The development of the kidney involves essential cellular processes, such as cell
proliferation and differentiation, which are led by interactions between multiple signaling …
proliferation and differentiation, which are led by interactions between multiple signaling …
N-ethyl-N-Nitrosourea (ENU) Induced Mutations within the Klotho Gene Lead to Ectopic Calcification and Reduced Lifespan in Mouse Models
Ectopic calcification (EC), which is the pathological deposition of calcium and phosphate in
extra-skeletal tissues, may be associated with hypercalcaemic and hyperphosphataemic …
extra-skeletal tissues, may be associated with hypercalcaemic and hyperphosphataemic …
Mice with an N-Ethyl-N-Nitrosourea (ENU) Induced Tyr209Asn Mutation in Natriuretic Peptide Receptor 3 (NPR3) Provide a Model for Kyphosis Associated with …
Non-syndromic kyphosis is a common disorder that is associated with significant morbidity
and has a strong genetic involvement; however, the causative genes remain to be identified …
and has a strong genetic involvement; however, the causative genes remain to be identified …
Role of oxidative stress in melanoma and steatohepaititis
I Pardo Sánchez - 2023 - portalinvestigacion.um.es
Durante el desarrollo de esta Tesis, utilizamos modelos de pez cebra para estudiar el
impacto de la Dual Oxidasa 1 (Duox1) y la Xantina deshidrogenasa (Xdh), dos de las …
impacto de la Dual Oxidasa 1 (Duox1) y la Xantina deshidrogenasa (Xdh), dos de las …
An N Ethyl N Nitrosourea (ENU) Mutagenized Mouse Model for Autosomal Dominant Nonsyndromic Kyphoscoliosis Due to Vertebral Fusion
Kyphosis and scoliosis are common spinal disorders that occur as part of complex
syndromes or as nonsyndromic, idiopathic diseases. Familial and twin studies implicate …
syndromes or as nonsyndromic, idiopathic diseases. Familial and twin studies implicate …