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Results: 1 to 20 of 110

1.

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.

PMID:
18250199
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Chlamydomonas reinhardtii hydin is a central pair protein required for flagellar motility.

Lechtreck KF, Witman GB.

J Cell Biol. 2007 Feb 12;176(4):473-82.

PMID:
17296796
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Hydin seek: finding a function in ciliary motility.

Smith EF.

J Cell Biol. 2007 Feb 12;176(4):403-4. Review.

PMID:
17296793
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Recessive HYDIN mutations cause primary ciliary dyskinesia without randomization of left-right body asymmetry.

Olbrich H, Schmidts M, Werner C, Onoufriadis A, Loges NT, Raidt J, Banki NF, Shoemark A, Burgoyne T, Al Turki S, Hurles ME; UK10K Consortium, Köhler G, Schroeder J, Nürnberg G, Nürnberg P, Chung EM, Reinhardt R, Marthin JK, Nielsen KG, Mitchison HM, Omran H.

Am J Hum Genet. 2012 Oct 5;91(4):672-84. doi: 10.1016/j.ajhg.2012.08.016. Epub 2012 Sep 27.

PMID:
23022101
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

The hydrocephalus inducing gene product, Hydin, positions axonemal central pair microtubules.

Dawe HR, Shaw MK, Farr H, Gull K.

BMC Biol. 2007 Aug 7;5:33.

PMID:
17683645
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

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
[PubMed - indexed for MEDLINE]
Free Article
7.

Defective motile cilia in Prickle2-deficient mice.

Sowers LP, Yin T, Mahajan VB, Bassuk AG.

J Neurogenet. 2014 Mar-Jun;28(1-2):146-52. doi: 10.3109/01677063.2014.885966. Epub 2014 Apr 7.

PMID:
24708399
[PubMed - indexed for MEDLINE]
8.

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.

PMID:
23906841
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Biosynthesis of Wdr16, a marker protein for kinocilia-bearing cells, starts at the time of kinocilia formation in rat, and wdr16 gene knockdown causes hydrocephalus in zebrafish.

Hirschner W, Pogoda HM, Kramer C, Thiess U, Hamprecht B, Wiesmüller KH, Lautner M, Verleysdonk S.

J Neurochem. 2007 Apr;101(1):274-88.

PMID:
17394468
[PubMed - indexed for MEDLINE]
10.

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.

PMID:
17965413
[PubMed - indexed for MEDLINE]
Free Article
11.

Loss of SPEF2 function in mice results in spermatogenesis defects and primary ciliary dyskinesia.

Sironen A, Kotaja N, Mulhern H, Wyatt TA, Sisson JH, Pavlik JA, Miiluniemi M, Fleming MD, Lee L.

Biol Reprod. 2011 Oct;85(4):690-701. doi: 10.1095/biolreprod.111.091132. Epub 2011 Jun 29.

PMID:
21715716
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Ventricular ependyma of normal and hydrocephalic subjects: a scanning electronmicroscopic study.

Bannister CM, Chapman SA.

Dev Med Child Neurol. 1980 Dec;22(6):725-35.

PMID:
7450299
[PubMed - indexed for MEDLINE]
13.

Congenital hydrocephalus in hy3 mice is caused by a frameshift mutation in Hydin, a large novel gene.

Davy BE, Robinson ML.

Hum Mol Genet. 2003 May 15;12(10):1163-70.

PMID:
12719380
[PubMed - indexed for MEDLINE]
Free Article
14.

Sperm-associated antigen-17 gene is essential for motile cilia function and neonatal survival.

Teves ME, Zhang Z, Costanzo RM, Henderson SC, Corwin FD, Zweit J, Sundaresan G, Subler M, Salloum FN, Rubin BK, Strauss JF 3rd.

Am J Respir Cell Mol Biol. 2013 Jun;48(6):765-72. doi: 10.1165/rcmb.2012-0362OC.

PMID:
23418344
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Abnormal cilia in a male-sterile mutant mouse.

Bryan JH.

Virchows Arch A Pathol Anat Histopathol. 1983;400(1):77-86.

PMID:
6407195
[PubMed - indexed for MEDLINE]
16.

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
[PubMed - indexed for MEDLINE]
17.

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
[PubMed - indexed for MEDLINE]
18.

Dysfunction of axonemal dynein heavy chain Mdnah5 inhibits ependymal flow and reveals a novel mechanism for hydrocephalus formation.

Ibañez-Tallon I, Pagenstecher A, Fliegauf M, Olbrich H, Kispert A, Ketelsen UP, North A, Heintz N, Omran H.

Hum Mol Genet. 2004 Sep 15;13(18):2133-41. Epub 2004 Jul 21.

PMID:
15269178
[PubMed - indexed for MEDLINE]
Free Article
19.

A novel murine allele of Intraflagellar Transport Protein 172 causes a syndrome including VACTERL-like features with hydrocephalus.

Friedland-Little JM, Hoffmann AD, Ocbina PJ, Peterson MA, Bosman JD, Chen Y, Cheng SY, Anderson KV, Moskowitz IP.

Hum Mol Genet. 2011 Oct 1;20(19):3725-37. doi: 10.1093/hmg/ddr241. Epub 2011 Jun 8.

PMID:
21653639
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

The immotile cilia syndrome. Mice versus man.

Bryan JH.

Virchows Arch A Pathol Anat Histopathol. 1983;399(3):265-75.

PMID:
6407183
[PubMed - indexed for MEDLINE]
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