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Items: 1 to 20 of 290

1.

Systematic discovery of novel ciliary genes through functional genomics in the zebrafish.

Choksi SP, Babu D, Lau D, Yu X, Roy S.

Development. 2014 Sep;141(17):3410-9. doi: 10.1242/dev.108209.

2.

A function for the Joubert syndrome protein Arl13b in ciliary membrane extension and ciliary length regulation.

Lu H, Toh MT, Narasimhan V, Thamilselvam SK, Choksi SP, Roy S.

Dev Biol. 2015 Jan 15;397(2):225-36. doi: 10.1016/j.ydbio.2014.11.009. Epub 2014 Nov 20.

3.

Foxj1 transcription factors are master regulators of the motile ciliogenic program.

Yu X, Ng CP, Habacher H, Roy S.

Nat Genet. 2008 Dec;40(12):1445-53. doi: 10.1038/ng.263. Epub 2008 Nov 16.

PMID:
19011630
4.

The coiled-coil domain containing protein CCDC151 is required for the function of IFT-dependent motile cilia in animals.

Jerber J, Baas D, Soulavie F, Chhin B, Cortier E, Vesque C, Thomas J, Durand B.

Hum Mol Genet. 2014 Feb 1;23(3):563-77. doi: 10.1093/hmg/ddt445. Epub 2013 Sep 18.

PMID:
24067530
5.

Evolutionarily ancient association of the FoxJ1 transcription factor with the motile ciliogenic program.

Vij S, Rink JC, Ho HK, Babu D, Eitel M, Narasimhan V, Tiku V, Westbrook J, Schierwater B, Roy S.

PLoS Genet. 2012;8(11):e1003019. doi: 10.1371/journal.pgen.1003019. Epub 2012 Nov 8.

6.

Human retinopathy-associated ciliary protein retinitis pigmentosa GTPase regulator mediates cilia-dependent vertebrate development.

Ghosh AK, Murga-Zamalloa CA, Chan L, Hitchcock PF, Swaroop A, Khanna H.

Hum Mol Genet. 2010 Jan 1;19(1):90-8. doi: 10.1093/hmg/ddp469.

7.

DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia.

Li Y, Yagi H, Onuoha EO, Damerla RR, Francis R, Furutani Y, Tariq M, King SM, Hendricks G, Cui C, Saydmohammed M, Lee DM, Zahid M, Sami I, Leatherbury L, Pazour GJ, Ware SM, Nakanishi T, Goldmuntz E, Tsang M, Lo CW.

PLoS Genet. 2016 Feb 26;12(2):e1005821. doi: 10.1371/journal.pgen.1005821. eCollection 2016 Feb.

8.

Mutations in CCDC11, which encodes a coiled-coil containing ciliary protein, causes situs inversus due to dysmotility of monocilia in the left-right organizer.

Narasimhan V, Hjeij R, Vij S, Loges NT, Wallmeier J, Koerner-Rettberg C, Werner C, Thamilselvam SK, Boey A, Choksi SP, Pennekamp P, Roy S, Omran H.

Hum Mutat. 2015 Mar;36(3):307-18. doi: 10.1002/humu.22738.

PMID:
25504577
9.

RFX3 governs growth and beating efficiency of motile cilia in mouse and controls the expression of genes involved in human ciliopathies.

El Zein L, Ait-Lounis A, Morlé L, Thomas J, Chhin B, Spassky N, Reith W, Durand B.

J Cell Sci. 2009 Sep 1;122(Pt 17):3180-9. doi: 10.1242/jcs.048348. Epub 2009 Aug 11.

10.

Zebrafish assays of ciliopathies.

Zaghloul NA, Katsanis N.

Methods Cell Biol. 2011;105:257-72. doi: 10.1016/B978-0-12-381320-6.00011-4.

11.

Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia.

Austin-Tse C, Halbritter J, Zariwala MA, Gilberti RM, Gee HY, Hellman N, Pathak N, Liu Y, Panizzi JR, Patel-King RS, Tritschler D, Bower R, O'Toole E, Porath JD, Hurd TW, Chaki M, Diaz KA, Kohl S, Lovric S, Hwang DY, Braun DA, Schueler M, Airik R, Otto EA, Leigh MW, Noone PG, Carson JL, Davis SD, Pittman JE, Ferkol TW, Atkinson JJ, Olivier KN, Sagel SD, Dell SD, Rosenfeld M, Milla CE, Loges NT, Omran H, Porter ME, King SM, Knowles MR, Drummond IA, Hildebrandt F.

Am J Hum Genet. 2013 Oct 3;93(4):672-86. doi: 10.1016/j.ajhg.2013.08.015.

12.

Isolation and expression analysis of foxj1 and foxj1.2 in zebrafish embryos.

Aamar E, Dawid IB.

Int J Dev Biol. 2008;52(7):985-91. doi: 10.1387/ijdb.072477ea.

13.

Identification of FOXJ1 effectors during ciliogenesis in the foetal respiratory epithelium and embryonic left-right organiser of the mouse.

Stauber M, Weidemann M, Dittrich-Breiholz O, Lobschat K, Alten L, Mai M, Beckers A, Kracht M, Gossler A.

Dev Biol. 2017 Mar 15;423(2):170-188. doi: 10.1016/j.ydbio.2016.11.019. Epub 2016 Dec 1.

14.

Wdr18 is required for Kupffer's vesicle formation and regulation of body asymmetry in zebrafish.

Gao W, Xu L, Guan R, Liu X, Han Y, Wu Q, Xiao Y, Qi F, Zhu Z, Lin S, Zhang B.

PLoS One. 2011;6(8):e23386. doi: 10.1371/journal.pone.0023386. Epub 2011 Aug 18.

15.

Loss of zinc finger MYND-type containing 10 (zmynd10) affects cilia integrity and axonemal localization of dynein arms, resulting in ciliary dysmotility, polycystic kidney and scoliosis in medaka (Oryzias latipes).

Kobayashi D, Asano-Hoshino A, Nakakura T, Nishimaki T, Ansai S, Kinoshita M, Ogawa M, Hagiwara H, Yokoyama T.

Dev Biol. 2017 Oct 1;430(1):69-79. doi: 10.1016/j.ydbio.2017.08.016. Epub 2017 Aug 16.

PMID:
28823919
16.

Ciliary defects and genetics of primary ciliary dyskinesia.

Escudier E, Duquesnoy P, Papon JF, Amselem S.

Paediatr Respir Rev. 2009 Jun;10(2):51-4. doi: 10.1016/j.prrv.2009.02.001. Epub 2009 Apr 18. Review.

17.

The forkhead protein Foxj1 specifies node-like cilia in Xenopus and zebrafish embryos.

Stubbs JL, Oishi I, Izpisúa Belmonte JC, Kintner C.

Nat Genet. 2008 Dec;40(12):1454-60. doi: 10.1038/ng.267. Epub 2008 Nov 16.

18.

RFX2 is essential in the ciliated organ of asymmetry and an RFX2 transgene identifies a population of ciliated cells sufficient for fluid flow.

Bisgrove BW, Makova S, Yost HJ, Brueckner M.

Dev Biol. 2012 Mar 1;363(1):166-78. doi: 10.1016/j.ydbio.2011.12.030. Epub 2011 Dec 29.

19.

Genetic defects in ciliary structure and function.

Zariwala MA, Knowles MR, Omran H.

Annu Rev Physiol. 2007;69:423-50. Review.

PMID:
17059358
20.

Both foxj1a and foxj1b are implicated in left-right asymmetric development in zebrafish embryos.

Tian T, Zhao L, Zhang M, Zhao X, Meng A.

Biochem Biophys Res Commun. 2009 Mar 13;380(3):537-42. doi: 10.1016/j.bbrc.2009.01.111. Epub 2009 Jan 23.

PMID:
19284996

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