[HTML][HTML] Xanthine oxidoreductase: One enzyme for multiple physiological tasks

M Bortolotti, L Polito, MG Battelli, A Bolognesi - Redox biology, 2021 - Elsevier
Human xanthine oxidoreductase (XOR) is a multiple-level regulated enzyme, resulting from
a complicated evolutionary process that assigned it many physiological roles. The main …

Reactive oxygen-related diseases: therapeutic targets and emerging clinical indications

AI Casas, VTV Dao, A Daiber, GJ Maghzal… - Antioxidants & redox …, 2015 - liebertpub.com
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 …

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 …

A mouse model for inherited renal fibrosis associated with endoplasmic reticulum stress

SE Piret, E Olinger, AAC Reed… - Disease models & …, 2017 - journals.biologists.com
Renal fibrosis is a common feature of renal failure resulting from multiple etiologies,
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 …

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 …

N-ethyl-N-Nitrosourea (ENU) Induced Mutations within the Klotho Gene Lead to Ectopic Calcification and Reduced Lifespan in Mouse Models

CT Esapa, FM Hannan, VN Babinsky, P Potter… - PLoS …, 2015 - journals.plos.org
Ectopic calcification (EC), which is the pathological deposition of calcium and phosphate in
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 …

CT Esapa, SE Piret, MA Nesbit, NY Loh, G Thomas… - PLoS …, 2016 - journals.plos.org
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 …

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 …

An N Ethyl N Nitrosourea (ENU) Mutagenized Mouse Model for Autosomal Dominant Nonsyndromic Kyphoscoliosis Due to Vertebral Fusion

CT Esapa, SE Piret, MA Nesbit… - Journal of Bone and …, 2018 - academic.oup.com
Kyphosis and scoliosis are common spinal disorders that occur as part of complex
syndromes or as nonsyndromic, idiopathic diseases. Familial and twin studies implicate …