These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
129 related articles for article (PubMed ID: 36420936)
1. Variants in AQP11 may result in autosomal recessive bilateral cystic renal dysgenesis. Price ME; Fishler KP; Muff-Luett M; Mauch TJ; Brunelli L; Euteneuer JC Am J Med Genet A; 2023 Feb; 191(2):612-616. PubMed ID: 36420936 [TBL] [Abstract][Full Text] [Related]
2. Temporal deletion of Rützler M; Rojek A; Damgaard MV; Andreasen A; Fenton RA; Nielsen S Am J Physiol Renal Physiol; 2017 Feb; 312(2):F343-F351. PubMed ID: 27582095 [TBL] [Abstract][Full Text] [Related]
3. Disruption of aquaporin-11 produces polycystic kidneys following vacuolization of the proximal tubule. Morishita Y; Matsuzaki T; Hara-chikuma M; Andoo A; Shimono M; Matsuki A; Kobayashi K; Ikeda M; Yamamoto T; Verkman A; Kusano E; Ookawara S; Takata K; Sasaki S; Ishibashi K Mol Cell Biol; 2005 Sep; 25(17):7770-9. PubMed ID: 16107722 [TBL] [Abstract][Full Text] [Related]
4. Aberrant glycosylation and localization of polycystin-1 cause polycystic kidney in an AQP11 knockout model. Inoue Y; Sohara E; Kobayashi K; Chiga M; Rai T; Ishibashi K; Horie S; Su X; Zhou J; Sasaki S; Uchida S J Am Soc Nephrol; 2014 Dec; 25(12):2789-99. PubMed ID: 24854278 [TBL] [Abstract][Full Text] [Related]
5. Aquaporin-11 knockout mice and polycystic kidney disease animals share a common mechanism of cyst formation. Okada S; Misaka T; Tanaka Y; Matsumoto I; Ishibashi K; Sasaki S; Abe K FASEB J; 2008 Oct; 22(10):3672-84. PubMed ID: 18606867 [TBL] [Abstract][Full Text] [Related]
6. The distribution and function of aquaporins in the kidney: resolved and unresolved questions. Matsuzaki T; Yaguchi T; Shimizu K; Kita A; Ishibashi K; Takata K Anat Sci Int; 2017 Mar; 92(2):187-199. PubMed ID: 26798062 [TBL] [Abstract][Full Text] [Related]
7. Enhanced Autophagy in Polycystic Kidneys of AQP11 Null Mice. Tanaka Y; Watari M; Saito T; Morishita Y; Ishibashi K Int J Mol Sci; 2016 Nov; 17(12):. PubMed ID: 27916883 [TBL] [Abstract][Full Text] [Related]
9. [Aberrant glycosylation and localization of polycystin-1 caused polycystic kidney in an AQP11 knockout model]. Inoue Y Nihon Jinzo Gakkai Shi; 2015; 57(8):1316-8. PubMed ID: 26817158 [No Abstract] [Full Text] [Related]
10. Aquaporin-11 (AQP11) Expression in the Mouse Brain. Koike S; Tanaka Y; Matsuzaki T; Morishita Y; Ishibashi K Int J Mol Sci; 2016 Jun; 17(6):. PubMed ID: 27258268 [TBL] [Abstract][Full Text] [Related]
11. Single amino acid substitution in aquaporin 11 causes renal failure. Tchekneva EE; Khuchua Z; Davis LS; Kadkina V; Dunn SR; Bachman S; Ishibashi K; Rinchik EM; Harris RC; Dikov MM; Breyer MD J Am Soc Nephrol; 2008 Oct; 19(10):1955-64. PubMed ID: 18701606 [TBL] [Abstract][Full Text] [Related]
12. New members of mammalian aquaporins: AQP10-AQP12. Ishibashi K Handb Exp Pharmacol; 2009; (190):251-62. PubMed ID: 19096782 [TBL] [Abstract][Full Text] [Related]
13. Aquaporin-11: a channel protein lacking apparent transport function expressed in brain. Gorelick DA; Praetorius J; Tsunenari T; Nielsen S; Agre P BMC Biochem; 2006 May; 7():14. PubMed ID: 16650285 [TBL] [Abstract][Full Text] [Related]
14. Aquaporins in Urinary System. Qiu Z; Jiang T; Li Y; Wang W; Yang B Adv Exp Med Biol; 2023; 1398():155-177. PubMed ID: 36717493 [TBL] [Abstract][Full Text] [Related]
15. Liver-specific Aquaporin 11 knockout mice show rapid vacuolization of the rough endoplasmic reticulum in periportal hepatocytes after amino acid feeding. Rojek A; Füchtbauer EM; Füchtbauer A; Jelen S; Malmendal A; Fenton RA; Nielsen S Am J Physiol Gastrointest Liver Physiol; 2013 Mar; 304(5):G501-15. PubMed ID: 23275615 [TBL] [Abstract][Full Text] [Related]
16. Aquaporins in Renal Diseases. He J; Yang B Int J Mol Sci; 2019 Jan; 20(2):. PubMed ID: 30654539 [TBL] [Abstract][Full Text] [Related]