Zobrazeno 1 - 10
of 61
pro vyhledávání: '"Renal absorption"'
Autor:
Pickel, Virginia M., Nirenberg, Melissa J., Chan, June, Mosckovitz, Rachel, Udenfriend, Sidney, Tate, Suresh S.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1993 Aug . 90(16), 7779-7783.
Externí odkaz:
https://www.jstor.org/stable/2362804
Publikováno v:
Experimental and Therapeutic Medicine
Sodium glucose cotransporter-2 (SGLT2) is a sodium-dependent glucose transporter responsible for renal absorption of glucose. Dapagliflozin is an SGLT2 inhibitor used in patients with type 1 diabetes to promote urinary glucose excretion, but to date,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::521ca19b160900d4c8fa557eab9069d6
http://europepmc.org/articles/PMC7918543
http://europepmc.org/articles/PMC7918543
Publikováno v:
Global Pediatric Health
Global Pediatric Health, Vol 8 (2021)
Global Pediatric Health, Vol 8 (2021)
Diuretic therapy, commonly used in the newborn intensive care unit, is associated with a variety of electrolyte abnormalities such as hyponatremia, hypokalemia, and hypochloremia. Hypochloremia, often ignored, is associated with significant morbiditi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2b7cc025fb4aa1e78ce1fd3dbb2dc3f
http://europepmc.org/articles/PMC7868482
http://europepmc.org/articles/PMC7868482
Autor:
Fatina I. Fadel, Soal Kamel, Yasim Ramadan, Mostafa Alahmady, Manal F. Elshamaa, Hebatallah Farouk
Publikováno v:
Turk J Urol
Objective Nephrolithiasis results from metabolic and anatomic abnormalities together with genetic factors. Claudin 14 (CLDN14) is a protein that regulates the passage of small solutes through the kidneys. Alkaline phosphatase (ALPL) hydrolyzes the py
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8d930580914fc069f06e0360debd512
https://pubmed.ncbi.nlm.nih.gov/33052825
https://pubmed.ncbi.nlm.nih.gov/33052825
Publikováno v:
Physiological Reports, Vol 8, Iss 4, Pp n/a-n/a (2020)
Physiological Reports
Physiological Reports
STK39 encodes a serine threonine kinase, SPAK, which is part of a multi‐kinase network that determines renal Na+ reabsorption and blood pressure (BP) through regulation of sodium‐chloride co‐transporters in the kidney. Variants within STK39 are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f0c28a0395488371b817c8224508fcf
https://doi.org/10.14814/phy2.14379
https://doi.org/10.14814/phy2.14379
Akademický článek
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Autor:
Michael N. Weedon, Angela C. Shore, Anna Murray, Francesco Casanova, Samuel E. Jones, Andrew R. Wood, Andrew T. Hattersley, Timothy M. Frayling, Robin N Beaumont, Jessica Tyrrell, Yingjie Ji
Publikováno v:
Hum Mol Genet
Human Molecular Genetics
Human Molecular Genetics
Raised albumin–creatinine ratio (ACR) is an indicator of microvascular damage and renal disease. We aimed to identify genetic variants associated with raised ACR and study the implications of carrying multiple ACR-raising alleles with metabolic and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b9ccbaacbd629722f548b84ee95616d
https://pubmed.ncbi.nlm.nih.gov/35246685
https://pubmed.ncbi.nlm.nih.gov/35246685
Autor:
Yixiao Zhang, Qing Chang, Jingqi Fu, Weiwei Kong, Yanqiu Wang, Hua Zhou, Congcong Jiao, Jeffrey B. Kopp, Junjun Luan, Gabor G. Illei, Chengjie Chen, Detian Li, Jingbo Pi
Publikováno v:
Arthritis Research & Therapy
Arthritis Research & Therapy, Vol 21, Iss 1, Pp 1-14 (2019)
Arthritis Research & Therapy, Vol 21, Iss 1, Pp 1-14 (2019)
Background The prevalence of lupus nephritis (LN) remains high despite various emerging monoclonal antibodies against with targeting systemic lupus erythematosus (SLE). Renal fibrosis is the main feature of late stage LN, and novel therapeutic agents
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3e0beefcdf33fe18f5794db9e34c2d6
https://pubmed.ncbi.nlm.nih.gov/31829247
https://pubmed.ncbi.nlm.nih.gov/31829247
Publikováno v:
Kidney International Reports. 5:S224
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a41211d347de1ed845846655bc59be30
https://doi.org/10.1016/j.ekir.2020.02.572
https://doi.org/10.1016/j.ekir.2020.02.572
Autor:
Nayara I. Viana, Fabio Cesar Miranda Torricelli, Fabio C. Vicentini, Eduardo Mazzucchi, Ruan Pimenta, Miguel Srougi, Katia R. M. Leite, Ronaldo Morales Guimarães, Giovanni Scala Marchini, Alexandre Danilovic, Sabrina T. Reis, William C. Nahas
Publikováno v:
Journal of Cellular and Molecular Medicine
The aim of our study was to determine regions of loss of heterozygosity, copy number variation analysis, and single nucleotide polymorphisms (SNPs) in Brazilian patients with cystinuria. A linkage study was performed using DNA samples from six patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6d718cef014cd3943e76dd0bea174de
https://pubmed.ncbi.nlm.nih.gov/30450686
https://pubmed.ncbi.nlm.nih.gov/30450686