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Items: 17

1.

New Insights into the Molecular Mechanisms Targeting Tubular Channels/Transporters in PKD Development.

Wu M, Yu S.

Kidney Dis (Basel). 2016 Oct;2(3):128-135. Epub 2016 Mar 25. Review.

PMID:
27921040
2.

The native TRPP2-dependent channel of murine renal primary cilia.

Kleene SJ, Kleene NK.

Am J Physiol Renal Physiol. 2017 Jan 1;312(1):F96-F108. doi: 10.1152/ajprenal.00272.2016. Epub 2016 Oct 19.

PMID:
27760766
3.

Far Upstream Element-Binding Protein 1 Binds the 3' Untranslated Region of PKD2 and Suppresses Its Translation.

Zheng W, Shen F, Hu R, Roy B, Yang J, Wang Q, Zhang F, King JC, Sergi C, Liu SM, Cordat E, Tang J, Cao Y, Ali D, Chen XZ.

J Am Soc Nephrol. 2016 Sep;27(9):2645-57. doi: 10.1681/ASN.2015070836. Epub 2016 Feb 2.

PMID:
26839368
4.

Molecular genetic analysis of PKHD1 by next-generation sequencing in Czech families with autosomal recessive polycystic kidney disease.

Obeidova L, Seeman T, Elisakova V, Reiterova J, Puchmajerova A, Stekrova J.

BMC Med Genet. 2015 Dec 22;16:116. doi: 10.1186/s12881-015-0261-3.

5.

Autosomal recessive polycystic kidney disease: a hepatorenal fibrocystic disorder with pleiotropic effects.

Hartung EA, Guay-Woodford LM.

Pediatrics. 2014 Sep;134(3):e833-45. doi: 10.1542/peds.2013-3646. Epub 2014 Aug 11. Review.

6.

Loss of polycystin-1 inhibits Bicc1 expression during mouse development.

Lian P, Li A, Li Y, Liu H, Liang D, Hu B, Lin D, Jiang T, Moeckel G, Qin D, Wu G.

PLoS One. 2014 Mar 3;9(3):e88816. doi: 10.1371/journal.pone.0088816. eCollection 2014.

7.

Strategies targeting cAMP signaling in the treatment of polycystic kidney disease.

Torres VE, Harris PC.

J Am Soc Nephrol. 2014 Jan;25(1):18-32. doi: 10.1681/ASN.2013040398. Epub 2013 Dec 12. Review.

8.

TRPV4 dysfunction promotes renal cystogenesis in autosomal recessive polycystic kidney disease.

Zaika O, Mamenko M, Berrout J, Boukelmoune N, O'Neil RG, Pochynyuk O.

J Am Soc Nephrol. 2013 Mar;24(4):604-16. doi: 10.1681/ASN.2012050442. Epub 2013 Feb 14.

9.

Functional polycystin-1 dosage governs autosomal dominant polycystic kidney disease severity.

Hopp K, Ward CJ, Hommerding CJ, Nasr SH, Tuan HF, Gainullin VG, Rossetti S, Torres VE, Harris PC.

J Clin Invest. 2012 Nov;122(11):4257-73. doi: 10.1172/JCI64313. Epub 2012 Oct 15.

10.

Calcium-mediated mechanisms of cystic expansion.

Abdul-Majeed S, Nauli SM.

Biochim Biophys Acta. 2011 Oct;1812(10):1281-90. doi: 10.1016/j.bbadis.2010.09.016. Epub 2010 Oct 12. Review.

11.

Incompletely penetrant PKD1 alleles mimic the renal manifestations of ARPKD.

Vujic M, Heyer CM, Ars E, Hopp K, Markoff A, Orndal C, Rudenhed B, Nasr SH, Torres VE, Torra R, Bogdanova N, Harris PC.

J Am Soc Nephrol. 2010 Jul;21(7):1097-102. doi: 10.1681/ASN.2009101070. Epub 2010 Jun 17.

12.

Polycystic kidney disease protein fibrocystin localizes to the mitotic spindle and regulates spindle bipolarity.

Zhang J, Wu M, Wang S, Shah JV, Wilson PD, Zhou J.

Hum Mol Genet. 2010 Sep 1;19(17):3306-19. doi: 10.1093/hmg/ddq233. Epub 2010 Jun 16.

13.

Activation of Trpv4 reduces the hyperproliferative phenotype of cystic cholangiocytes from an animal model of ARPKD.

Gradilone SA, Masyuk TV, Huang BQ, Banales JM, Lehmann GL, Radtke BN, Stroope A, Masyuk AI, Splinter PL, LaRusso NF.

Gastroenterology. 2010 Jul;139(1):304-14.e2. doi: 10.1053/j.gastro.2010.04.010. Epub 2010 Apr 14.

14.

Molecular diagnostics for autosomal dominant polycystic kidney disease.

Harris PC, Rossetti S.

Nat Rev Nephrol. 2010 Apr;6(4):197-206. doi: 10.1038/nrneph.2010.18. Epub 2010 Feb 23. Review.

15.

Conditional mutation of Pkd2 causes cystogenesis and upregulates beta-catenin.

Kim I, Ding T, Fu Y, Li C, Cui L, Li A, Lian P, Liang D, Wang DW, Guo C, Ma J, Zhao P, Coffey RJ, Zhan Q, Wu G.

J Am Soc Nephrol. 2009 Dec;20(12):2556-69. doi: 10.1681/ASN.2009030271. Epub 2009 Nov 25.

16.

Autosomal dominant polycystic kidney disease: the last 3 years.

Torres VE, Harris PC.

Kidney Int. 2009 Jul;76(2):149-68. doi: 10.1038/ki.2009.128. Epub 2009 May 20. Review.

17.

Primary cilia and signaling pathways in mammalian development, health and disease.

Veland IR, Awan A, Pedersen LB, Yoder BK, Christensen ST.

Nephron Physiol. 2009;111(3):p39-53. doi: 10.1159/000208212. Epub 2009 Mar 10. Review.

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