Zobrazeno 1 - 10
of 630
pro vyhledávání: '"SLC2A9"'
Publikováno v:
Frontiers in Nephrology, Vol 4 (2024)
Renal hypouricemia (RHUC) is a rare genetic disorder characterized by impaired uric acid reabsorption which leads to persistently low serum uric acid levels. This condition predisposes individuals to complications such as uric acid kidney stones and
Externí odkaz:
https://doaj.org/article/cdac4ee007414b4492000e46c4b1046c
Publikováno v:
Žurnal Grodnenskogo Gosudarstvennogo Medicinskogo Universiteta, Vol 22, Iss 1, Pp 41-50 (2024)
Цель. Изучить частоту встречаемости генотипов и аллелей полиморфизма rs734553 гена SLC2A9, уровень мочевой кислоты (МК) и метаболитов пуриново
Externí odkaz:
https://doaj.org/article/1684343a59894748b2479ab20ed796af
Publikováno v:
Renal Failure, Vol 46, Iss 2 (2024)
Primary renal hypouricemia (RHUC) is a rare autosomal recessive disorder with a mean duration of end-stage acute kidney injury (EIAKI) of 14 days. The pathogenesis of EIAKI in patients with RHUC remains unclear. Several hypotheses have been proposed,
Externí odkaz:
https://doaj.org/article/8ebb83df43bf404fb44a1e142785f420
Publikováno v:
BMC Nephrology, Vol 24, Iss 1, Pp 1-8 (2023)
Abstract Background Hereditary renal hypouricemia (RHUC) is a heterogenous disorder characterized by defective uric acid (UA) reabsorption resulting in hypouricemia and increased fractional excretion of UA. RHUC is an important cause of exercise-indu
Externí odkaz:
https://doaj.org/article/4fc891fd585a460e962e5a2ac3253498
Publikováno v:
BIO Integration, Vol 5, Iss 1 (2024)
Background: The relationships between uric acid levels, specific single nucleotide polymorphisms (SNPs) in genes linked to uric acid metabolism [xanthine dehydrogenase (XDH) and Solute carrier family 2 member 9 (SLC2A9) genes], and control of HbA1c l
Externí odkaz:
https://doaj.org/article/869db4a0481a4282a2ab2af388d2216e
Publikováno v:
Jichu yixue yu linchuang, Vol 43, Iss 9, Pp 1467-1471 (2023)
ABCG2 and SLC2A9 encode the uric acid transporters ABCG2 and GLUT9. ABCG2 single nucleotide polymorphism (SNP) can reduce the expression and transport function of ABCG2 protein, and then cause intestinal uric acid excretion dysfunction, resulting in
Externí odkaz:
https://doaj.org/article/1b96ec3449b74047aae1facb654835ee
Akademický článek
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Publikováno v:
Vietnam Journal of Science, Technology and Engineering, Vol 64, Iss 1 (2023)
Gout is a common form of inflammatory arthritis that is strongly associated with elevated uric acid concentration in the blood. The development of the disease is not only triggered by environmental factors but also genetic variations. Previous studie
Externí odkaz:
https://doaj.org/article/e5a37d121f754a25a0b22511d8421fa5
Autor:
Yuki Ohashi, Hiroshi Ooyama, Hideki Makinoshima, Tappei Takada, Hirotaka Matsuo, Kimiyoshi Ichida
Publikováno v:
Biomedicines, Vol 12, Iss 2, p 300 (2024)
Gout results from monosodium urate deposition caused by hyperuricemia, but most individuals with hyperuricemia remain asymptomatic. The pathogenesis of gout remains uncertain. To identify potential biomarkers distinguishing gout from asymptomatic hyp
Externí odkaz:
https://doaj.org/article/219815994aeb497cadffb363e407f268
Akademický článek
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