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Items: 1 to 20 of 78

1.

Congenital hydrocephalus in genetically engineered mice.

Vogel P, Read RW, Hansen GM, Payne BJ, Small D, Sands AT, Zambrowicz BP.

Vet Pathol. 2012 Jan;49(1):166-81. doi: 10.1177/0300985811415708. Epub 2011 Jul 11.

PMID:
21746835
2.

Situs inversus in Dpcd/Poll-/-, Nme7-/- , and Pkd1l1-/- mice.

Vogel P, Read R, Hansen GM, Freay LC, Zambrowicz BP, Sands AT.

Vet Pathol. 2010 Jan;47(1):120-31. doi: 10.1177/0300985809353553.

PMID:
20080492
3.

Hydrocephalus, situs inversus, chronic sinusitis, and male infertility in DNA polymerase lambda-deficient mice: possible implication for the pathogenesis of immotile cilia syndrome.

Kobayashi Y, Watanabe M, Okada Y, Sawa H, Takai H, Nakanishi M, Kawase Y, Suzuki H, Nagashima K, Ikeda K, Motoyama N.

Mol Cell Biol. 2002 Apr;22(8):2769-76.

4.

Cilia in the nervous system: linking cilia function and neurodevelopmental disorders.

Lee JE, Gleeson JG.

Curr Opin Neurol. 2011 Apr;24(2):98-105. doi: 10.1097/WCO.0b013e3283444d05. Review.

5.

Characterization of a model of hydrocephalus in transgenic mice.

Cohen AR, Leifer DW, Zechel M, Flaningan DP, Lewin JS, Lust WD.

J Neurosurg. 1999 Dec;91(6):978-88.

PMID:
10584844
6.

Ectopic expression of human BBS4 can rescue Bardet-Biedl syndrome phenotypes in Bbs4 null mice.

Chamling X, Seo S, Bugge K, Searby C, Guo DF, Drack AV, Rahmouni K, Sheffield VC.

PLoS One. 2013;8(3):e59101. doi: 10.1371/journal.pone.0059101. Epub 2013 Mar 15.

7.

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
8.

Strain-dependent brain defects in mouse models of primary ciliary dyskinesia with mutations in Pcdp1 and Spef2.

Finn R, Evans CC, Lee L.

Neuroscience. 2014 Sep 26;277:552-67. doi: 10.1016/j.neuroscience.2014.07.029. Epub 2014 Jul 27.

9.

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.

PMID:
20106870
10.

Ulk4 Is Essential for Ciliogenesis and CSF Flow.

Liu M, Guan Z, Shen Q, Lalor P, Fitzgerald U, O'Brien T, Dockery P, Shen S.

J Neurosci. 2016 Jul 20;36(29):7589-600. doi: 10.1523/JNEUROSCI.0621-16.2016.

11.

[Research advances on associated genes and pathogenesis of hydrocephalus].

Zhou JJ, Ding MP, Liu JR.

Zhejiang Da Xue Xue Bao Yi Xue Ban. 2010 Nov;39(6):644-9. Review. Chinese.

PMID:
21166061
12.

Loss of function of axonemal dynein Mdnah5 causes primary ciliary dyskinesia and hydrocephalus.

Ibañez-Tallon I, Gorokhova S, Heintz N.

Hum Mol Genet. 2002 Mar 15;11(6):715-21.

PMID:
11912187
13.

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.

14.

[Mice SI/Col: a study model in the research of genes involved in situs inversus].

de Meeus A, Alonso S, Demaille J, Bouvagnet P.

Arch Mal Coeur Vaiss. 1993 May;86(5):617-22. French.

PMID:
8257272
15.

Conditional N-WASP knockout in mouse brain implicates actin cytoskeleton regulation in hydrocephalus pathology.

Jain N, Lim LW, Tan WT, George B, Makeyev E, Thanabalu T.

Exp Neurol. 2014 Apr;254:29-40. doi: 10.1016/j.expneurol.2014.01.011. Epub 2014 Jan 23.

PMID:
24462670
16.

A mouse model for Meckel syndrome type 3.

Cook SA, Collin GB, Bronson RT, Naggert JK, Liu DP, Akeson EC, Davisson MT.

J Am Soc Nephrol. 2009 Apr;20(4):753-64. doi: 10.1681/ASN.2008040412. Epub 2009 Feb 11.

17.

Mutations in Hydin impair ciliary motility in mice.

Lechtreck KF, Delmotte P, Robinson ML, Sanderson MJ, Witman GB.

J Cell Biol. 2008 Feb 11;180(3):633-43. doi: 10.1083/jcb.200710162. Epub 2008 Feb 4.

18.

Loss of the serine/threonine kinase fused results in postnatal growth defects and lethality due to progressive hydrocephalus.

Merchant M, Evangelista M, Luoh SM, Frantz GD, Chalasani S, Carano RA, van Hoy M, Ramirez J, Ogasawara AK, McFarland LM, Filvaroff EH, French DM, de Sauvage FJ.

Mol Cell Biol. 2005 Aug;25(16):7054-68.

20.

Cilia-related diseases.

Afzelius BA.

J Pathol. 2004 Nov;204(4):470-7. Review.

PMID:
15495266

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