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.
22. The tuberous sclerosis proteins regulate formation of the primary cilium via a rapamycin-insensitive and polycystin 1-independent pathway. Hartman TR; Liu D; Zilfou JT; Robb V; Morrison T; Watnick T; Henske EP Hum Mol Genet; 2009 Jan; 18(1):151-63. PubMed ID: 18845692 [TBL] [Abstract][Full Text] [Related]
23. Ciliary dysfunction in polycystic kidney disease: an emerging model with polarizing potential. Kolb RJ; Nauli SM Front Biosci; 2008 May; 13():4451-66. PubMed ID: 18508522 [TBL] [Abstract][Full Text] [Related]
24. Polycystins: what polycystic kidney disease tells us about sperm. Kierszenbaum AL Mol Reprod Dev; 2004 Apr; 67(4):385-8. PubMed ID: 14991728 [TBL] [Abstract][Full Text] [Related]
25. [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]
26. Polycystins and mechanosensation in renal and nodal cilia. Nauli SM; Zhou J Bioessays; 2004 Aug; 26(8):844-56. PubMed ID: 15273987 [TBL] [Abstract][Full Text] [Related]
27. Putative roles of cilia in polycystic kidney disease. Winyard P; Jenkins D Biochim Biophys Acta; 2011 Oct; 1812(10):1256-62. PubMed ID: 21586324 [TBL] [Abstract][Full Text] [Related]
28. 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]
29. Polycystins: from mechanosensation to gene regulation. Delmas P Cell; 2004 Jul; 118(2):145-8. PubMed ID: 15260985 [TBL] [Abstract][Full Text] [Related]
30. Regulation of polycystin-1 ciliary trafficking by motifs at its C-terminus and polycystin-2 but not by cleavage at the GPS site. Su X; Wu M; Yao G; El-Jouni W; Luo C; Tabari A; Zhou J J Cell Sci; 2015 Nov; 128(22):4063-73. PubMed ID: 26430213 [TBL] [Abstract][Full Text] [Related]
31. Development of polycystic kidney disease in juvenile cystic kidney mice: insights into pathogenesis, ciliary abnormalities, and common features with human disease. Smith LA; Bukanov NO; Husson H; Russo RJ; Barry TC; Taylor AL; Beier DR; Ibraghimov-Beskrovnaya O J Am Soc Nephrol; 2006 Oct; 17(10):2821-31. PubMed ID: 16928806 [TBL] [Abstract][Full Text] [Related]
32. Polycystin-1, STAT6, and P100 function in a pathway that transduces ciliary mechanosensation and is activated in polycystic kidney disease. Low SH; Vasanth S; Larson CH; Mukherjee S; Sharma N; Kinter MT; Kane ME; Obara T; Weimbs T Dev Cell; 2006 Jan; 10(1):57-69. PubMed ID: 16399078 [TBL] [Abstract][Full Text] [Related]
33. The native TRPP2-dependent channel of murine renal primary cilia. Kleene SJ; Kleene NK Am J Physiol Renal Physiol; 2017 Jan; 312(1):F96-F108. PubMed ID: 27760766 [TBL] [Abstract][Full Text] [Related]
34. Loss of primary cilia results in deregulated and unabated apical calcium entry in ARPKD collecting duct cells. Siroky BJ; Ferguson WB; Fuson AL; Xie Y; Fintha A; Komlosi P; Yoder BK; Schwiebert EM; Guay-Woodford LM; Bell PD Am J Physiol Renal Physiol; 2006 Jun; 290(6):F1320-8. PubMed ID: 16396941 [TBL] [Abstract][Full Text] [Related]
35. Intraflagellar transport is required for the vectorial movement of TRPV channels in the ciliary membrane. Qin H; Burnette DT; Bae YK; Forscher P; Barr MM; Rosenbaum JL Curr Biol; 2005 Sep; 15(18):1695-9. PubMed ID: 16169494 [TBL] [Abstract][Full Text] [Related]
36. Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney disease. Lu H; Galeano MCR; Ott E; Kaeslin G; Kausalya PJ; Kramer C; Ortiz-Brüchle N; Hilger N; Metzis V; Hiersche M; Tay SY; Tunningley R; Vij S; Courtney AD; Whittle B; Wühl E; Vester U; Hartleben B; Neuber S; Frank V; Little MH; Epting D; Papathanasiou P; Perkins AC; Wright GD; Hunziker W; Gee HY; Otto EA; Zerres K; Hildebrandt F; Roy S; Wicking C; Bergmann C Nat Genet; 2017 Jul; 49(7):1025-1034. PubMed ID: 28530676 [TBL] [Abstract][Full Text] [Related]
37. A polycystin-1 multiprotein complex is disrupted in polycystic kidney disease cells. Roitbak T; Ward CJ; Harris PC; Bacallao R; Ness SA; Wandinger-Ness A Mol Biol Cell; 2004 Mar; 15(3):1334-46. PubMed ID: 14718571 [TBL] [Abstract][Full Text] [Related]
38. The KLP-6 kinesin is required for male mating behaviors and polycystin localization in Caenorhabditis elegans. Peden EM; Barr MM Curr Biol; 2005 Mar; 15(5):394-404. PubMed ID: 15753033 [TBL] [Abstract][Full Text] [Related]