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Items: 1 to 20 of 61

1.

The stumpy gene is required for mammalian ciliogenesis.

Town T, Breunig JJ, Sarkisian MR, Spilianakis C, Ayoub AE, Liu X, Ferrandino AF, Gallagher AR, Li MO, Rakic P, Flavell RA.

Proc Natl Acad Sci U S A. 2008 Feb 26;105(8):2853-8. doi: 10.1073/pnas.0712385105. Epub 2008 Feb 19.

2.

Kidney-specific inactivation of the KIF3A subunit of kinesin-II inhibits renal ciliogenesis and produces polycystic kidney disease.

Lin F, Hiesberger T, Cordes K, Sinclair AM, Goldstein LS, Somlo S, Igarashi P.

Proc Natl Acad Sci U S A. 2003 Apr 29;100(9):5286-91. Epub 2003 Apr 2.

3.

The zebrafish fleer gene encodes an essential regulator of cilia tubulin polyglutamylation.

Pathak N, Obara T, Mangos S, Liu Y, Drummond IA.

Mol Biol Cell. 2007 Nov;18(11):4353-64. Epub 2007 Aug 29.

4.

Deletion of the Parkin co-regulated gene causes defects in ependymal ciliary motility and hydrocephalus in the quakingviable mutant mouse.

Wilson GR, Wang HX, Egan GF, Robinson PJ, Delatycki MB, O'Bryan MK, Lockhart PJ.

Hum Mol Genet. 2010 Apr 15;19(8):1593-602. doi: 10.1093/hmg/ddq031. Epub 2010 Jan 27.

5.

PKHD1 protein encoded by the gene for autosomal recessive polycystic kidney disease associates with basal bodies and primary cilia in renal epithelial cells.

Zhang MZ, Mai W, Li C, Cho SY, Hao C, Moeckel G, Zhao R, Kim I, Wang J, Xiong H, Wang H, Sato Y, Wu Y, Nakanuma Y, Lilova M, Pei Y, Harris RC, Li S, Coffey RJ, Sun L, Wu D, Chen XZ, Breyer MD, Zhao ZJ, McKanna JA, Wu G.

Proc Natl Acad Sci U S A. 2004 Feb 24;101(8):2311-6.

6.

Lack of cadherins Celsr2 and Celsr3 impairs ependymal ciliogenesis, leading to fatal hydrocephalus.

Tissir F, Qu Y, Montcouquiol M, Zhou L, Komatsu K, Shi D, Fujimori T, Labeau J, Tyteca D, Courtoy P, Poumay Y, Uemura T, Goffinet AM.

Nat Neurosci. 2010 Jun;13(6):700-7. doi: 10.1038/nn.2555. Epub 2010 May 16.

PMID:
20473291
7.

Polycystic kidney disease in the medaka (Oryzias latipes) pc mutant caused by a mutation in the Gli-Similar3 (glis3) gene.

Hashimoto H, Miyamoto R, Watanabe N, Shiba D, Ozato K, Inoue C, Kubo Y, Koga A, Jindo T, Narita T, Naruse K, Ohishi K, Nogata K, Shin-I T, Asakawa S, Shimizu N, Miyamoto T, Mochizuki T, Yokoyama T, Hori H, Takeda H, Kohara Y, Wakamatsu Y.

PLoS One. 2009 Jul 17;4(7):e6299. doi: 10.1371/journal.pone.0006299.

8.

Cystin, a novel cilia-associated protein, is disrupted in the cpk mouse model of polycystic kidney disease.

Hou X, Mrug M, Yoder BK, Lefkowitz EJ, Kremmidiotis G, D'Eustachio P, Beier DR, Guay-Woodford LM.

J Clin Invest. 2002 Feb;109(4):533-40.

9.

A novel mouse model reveals that polycystin-1 deficiency in ependyma and choroid plexus results in dysfunctional cilia and hydrocephalus.

Wodarczyk C, Rowe I, Chiaravalli M, Pema M, Qian F, Boletta A.

PLoS One. 2009 Sep 23;4(9):e7137. doi: 10.1371/journal.pone.0007137.

10.

Understanding pathogenic mechanisms in polycystic kidney disease provides clues for therapy.

Harris PC, Torres VE.

Curr Opin Nephrol Hypertens. 2006 Jul;15(4):456-63. Review.

PMID:
16775462
11.
12.

LRRC50, a conserved ciliary protein implicated in polycystic kidney disease.

van Rooijen E, Giles RH, Voest EE, van Rooijen C, Schulte-Merker S, van Eeden FJ.

J Am Soc Nephrol. 2008 Jun;19(6):1128-38. doi: 10.1681/ASN.2007080917. Epub 2008 Apr 2.

13.

Riding the wave of ependymal cilia: genetic susceptibility to hydrocephalus in primary ciliary dyskinesia.

Lee L.

J Neurosci Res. 2013 Sep;91(9):1117-32. doi: 10.1002/jnr.23238. Epub 2013 May 17. Review.

PMID:
23686703
14.

Ke 6 gene. Sequence and organization and aberrant regulation in murine polycystic kidney disease.

Maxwell MM, Nearing J, Aziz N.

J Biol Chem. 1995 Oct 20;270(42):25213-9.

15.

Heat shock transcription factor 1 is required for maintenance of ciliary beating in mice.

Takaki E, Fujimoto M, Nakahari T, Yonemura S, Miyata Y, Hayashida N, Yamamoto K, Vallee RB, Mikuriya T, Sugahara K, Yamashita H, Inouye S, Nakai A.

J Biol Chem. 2007 Dec 21;282(51):37285-92. Epub 2007 Oct 27.

16.

Dynein axonemal intermediate chain 2 is required for formation of the left-right body axis and kidney in medaka.

Nagao Y, Cheng J, Kamura K, Seki R, Maeda A, Nihei D, Koshida S, Wakamatsu Y, Fujimoto T, Hibi M, Hashimoto H.

Dev Biol. 2010 Nov 1;347(1):53-61. doi: 10.1016/j.ydbio.2010.08.001. Epub 2010 Aug 11.

17.

Mammalian cilia function is independent of the polymeric state of tubulin glycylation.

Dossou SJ, Bré MH, Hallworth R.

Cell Motil Cytoskeleton. 2007 Nov;64(11):847-55.

18.

KIF19A is a microtubule-depolymerizing kinesin for ciliary length control.

Niwa S, Nakajima K, Miki H, Minato Y, Wang D, Hirokawa N.

Dev Cell. 2012 Dec 11;23(6):1167-75. doi: 10.1016/j.devcel.2012.10.016. Epub 2012 Nov 15.

19.

Disruption of the mouse Jhy gene causes abnormal ciliary microtubule patterning and juvenile hydrocephalus.

Appelbe OK, Bollman B, Attarwala A, Triebes LA, Muniz-Talavera H, Curry DJ, Schmidt JV.

Dev Biol. 2013 Oct 1;382(1):172-85. doi: 10.1016/j.ydbio.2013.07.003. Epub 2013 Jul 29.

20.

A genetic screen in zebrafish identifies cilia genes as a principal cause of cystic kidney.

Sun Z, Amsterdam A, Pazour GJ, Cole DG, Miller MS, Hopkins N.

Development. 2004 Aug;131(16):4085-93. Epub 2004 Jul 21.

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