Zobrazeno 1 - 10
of 308
pro vyhledávání: '"water reabsorption"'
Autor:
Ruixia Dong, Junjie Pan, Guangshan Zhao, Qiuyan Zhao, Shiqiong Wang, Ning Li, Lianjun Song, Xianqing Huang, Shuxing Miao, Junhui Ying, Fangying Wu, Dongxu Wang, Kejun Cheng, Daniel Granato, Qiuyan Ban
Publikováno v:
Frontiers in Nutrition, Vol 10 (2023)
IntroductionExcessive calorie intake and physical inactivity have dramatically increased nutrient overload-associated disease, becoming a global public health issue. Chimonanthus salicifolius S. Y. Hu (CHI) is a homology plant of food and medicine in
Externí odkaz:
https://doaj.org/article/23e44fea5e664971a3564841961fa11f
Publikováno v:
Frontiers in Physiology, Vol 13 (2022)
Lepus yarkandensis is a desert-dwelling animal that has various adaptations to cope with drought. The kidney maintains water and acid-base balance mainly through the vasopressin-regulated water reabsorption pathway and proximal tubular bicarbonate re
Externí odkaz:
https://doaj.org/article/5ddda2f204f24aa7aa67ff7355d03a39
Autor:
Qian Li, Bichao Lu, Jia Yang, Chao Li, Yanchun Li, Hui Chen, Naishi Li, Lian Duan, Feng Gu, Jianmin Zhang, Weibo Xia
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
The aquaporin 2 (AQP2) plays a critical role in water reabsorption to maintain water homeostasis. AQP2 mutation leads to nephrogenic diabetes insipidus (NDI), characterized by polyuria, polydipsia, and hypernatremia. We previously reported that a nov
Externí odkaz:
https://doaj.org/article/60be86ea8e6946e2ae09420f718463c7
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Congenital nephrogenic diabetes insipidus (CNDI) is a rare hereditary tubular dysfunction caused mainly by X-linked recessive inheritance of AVPR2 gene mutations. Pathogenic genes are a result of mutations in AVPR2 on chromosome Xq28 and in AQP2 on c
Externí odkaz:
https://doaj.org/article/2957ebc9355843719886ba28b772208a
Akademický článek
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Autor:
Takahiro Masuda, Shigeaki Muto, Keiko Fukuda, Minami Watanabe, Ken Ohara, Hermann Koepsell, Volker Vallon, Daisuke Nagata
Publikováno v:
Physiological Reports, Vol 8, Iss 2, Pp n/a-n/a (2020)
Abstract Most of the filtered glucose is reabsorbed in the early proximal tubule by the sodium‐glucose cotransporter SGLT2. The glycosuric effect of the SGLT2 inhibitor ipragliflozin is linked to a diuretic and natriuretic effect that activates com
Externí odkaz:
https://doaj.org/article/7f897b7c175e45e0a5eefad60dc7a9bc
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
Congenital nephrogenic diabetes insipidus (CNDI) is a rare renal disorder caused by mutations in arginine vasopressin receptor 2 (AVPR2) or aquaporin 2 (AQP2). The clinical signs of CNDI include polyuria, compensatory polydipsia, dehydration, electro
Externí odkaz:
https://doaj.org/article/242d0e168c0a4e14a55299a9a71a31a6
Publikováno v:
Frontiers in Plant Science, Vol 10 (2019)
The improvement of crop productivity under abiotic stress is one of the biggest challenges faced by the agricultural scientific community. Despite extensive research, the research-to-commercial transfer rate of abiotic stress-resistant crops remains
Externí odkaz:
https://doaj.org/article/a45e5b81d3624674b0dd09fbf16c3381
Publikováno v:
Вавиловский журнал генетики и селекции, Vol 20, Iss 2, Pp 234-242 (2016)
In mammals, arginine-vasopressin (AVP) is a major hormone involved in the regulation of renal water reabsorption, acting via an increase in the osmotic permeability of the collecting duct epithelium. The AVP-induced intracellular events include, as a
Externí odkaz:
https://doaj.org/article/f438f21abbed4405991309dc90e45784
Akademický článek
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