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Similar articles for PubMed (Select 23153492)

1.

Arl13b in primary cilia regulates the migration and placement of interneurons in the developing cerebral cortex.

Higginbotham H, Eom TY, Mariani LE, Bachleda A, Hirt J, Gukassyan V, Cusack CL, Lai C, Caspary T, Anton ES.

Dev Cell. 2012 Nov 13;23(5):925-38. doi: 10.1016/j.devcel.2012.09.019.

2.

Arl13b-regulated cilia activities are essential for polarized radial glial scaffold formation.

Higginbotham H, Guo J, Yokota Y, Umberger NL, Su CY, Li J, Verma N, Hirt J, Ghukasyan V, Caspary T, Anton ES.

Nat Neurosci. 2013 Aug;16(8):1000-7. doi: 10.1038/nn.3451. Epub 2013 Jun 30.

3.

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.

PMID:
25448689
4.

Active transport and diffusion barriers restrict Joubert Syndrome-associated ARL13B/ARL-13 to an Inv-like ciliary membrane subdomain.

Cevik S, Sanders AA, Van Wijk E, Boldt K, Clarke L, van Reeuwijk J, Hori Y, Horn N, Hetterschijt L, Wdowicz A, Mullins A, Kida K, Kaplan OI, van Beersum SE, Man Wu K, Letteboer SJ, Mans DA, Katada T, Kontani K, Ueffing M, Roepman R, Kremer H, Blacque OE.

PLoS Genet. 2013;9(12):e1003977. doi: 10.1371/journal.pgen.1003977. Epub 2013 Dec 5.

5.

Radial glial dependent and independent dynamics of interneuronal migration in the developing cerebral cortex.

Yokota Y, Gashghaei HT, Han C, Watson H, Campbell KJ, Anton ES.

PLoS One. 2007 Aug 29;2(8):e794.

6.

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.

7.

Structural insights into the small G-protein Arl13B and implications for Joubert syndrome.

Miertzschke M, Koerner C, Spoerner M, Wittinghofer A.

Biochem J. 2014 Jan 15;457(2):301-11. doi: 10.1042/BJ20131097.

PMID:
24168557
8.

Cilia: traffic directors along the road of cortical development.

Métin C, Pedraza M.

Neuroscientist. 2014 Oct;20(5):468-82. doi: 10.1177/1073858414543151. Epub 2014 Jul 18. Review.

PMID:
25037053
9.

Cortical interneurons require Jnk1 to enter and navigate the developing cerebral cortex.

Myers AK, Meechan DW, Adney DR, Tucker ES.

J Neurosci. 2014 Jun 4;34(23):7787-801. doi: 10.1523/JNEUROSCI.4695-13.2014.

10.

The Joubert syndrome-associated missense mutation (V443D) in the Abelson-helper integration site 1 (AHI1) protein alters its localization and protein-protein interactions.

Tuz K, Hsiao YC, Juárez O, Shi B, Harmon EY, Phelps IG, Lennartz MR, Glass IA, Doherty D, Ferland RJ.

J Biol Chem. 2013 May 10;288(19):13676-94. doi: 10.1074/jbc.M112.420786. Epub 2013 Mar 26.

11.

Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome.

Cantagrel V, Silhavy JL, Bielas SL, Swistun D, Marsh SE, Bertrand JY, Audollent S, Attié-Bitach T, Holden KR, Dobyns WB, Traver D, Al-Gazali L, Ali BR, Lindner TH, Caspary T, Otto EA, Hildebrandt F, Glass IA, Logan CV, Johnson CA, Bennett C, Brancati F; International Joubert Syndrome Related Disorders Study Group, Valente EM, Woods CG, Gleeson JG.

Am J Hum Genet. 2008 Aug;83(2):170-9. doi: 10.1016/j.ajhg.2008.06.023.

12.

Cilia localization is essential for in vivo functions of the Joubert syndrome protein Arl13b/Scorpion.

Duldulao NA, Lee S, Sun Z.

Development. 2009 Dec;136(23):4033-42. doi: 10.1242/dev.036350.

13.

Netrin-1-alpha3beta1 integrin interactions regulate the migration of interneurons through the cortical marginal zone.

Stanco A, Szekeres C, Patel N, Rao S, Campbell K, Kreidberg JA, Polleux F, Anton ES.

Proc Natl Acad Sci U S A. 2009 May 5;106(18):7595-600. doi: 10.1073/pnas.0811343106. Epub 2009 Apr 21.

14.

Cortical interneurons require p35/Cdk5 for their migration and laminar organization.

Rakić S, Yanagawa Y, Obata K, Faux C, Parnavelas JG, Nikolić M.

Cereb Cortex. 2009 Aug;19(8):1857-69. doi: 10.1093/cercor/bhn213. Epub 2008 Nov 26.

15.

Differential gene expression in migrating cortical interneurons during mouse forebrain development.

Faux C, Rakic S, Andrews W, Yanagawa Y, Obata K, Parnavelas JG.

J Comp Neurol. 2010 Apr 15;518(8):1232-48. doi: 10.1002/cne.22271.

PMID:
20151419
16.

Variable expressivity of ciliopathy neurological phenotypes that encompass Meckel-Gruber syndrome and Joubert syndrome is caused by complex de-regulated ciliogenesis, Shh and Wnt signalling defects.

Abdelhamed ZA, Wheway G, Szymanska K, Natarajan S, Toomes C, Inglehearn C, Johnson CA.

Hum Mol Genet. 2013 Apr 1;22(7):1358-72. doi: 10.1093/hmg/dds546. Epub 2013 Jan 2.

17.

Arl13b regulates ciliogenesis and the dynamic localization of Shh signaling proteins.

Larkins CE, Aviles GD, East MP, Kahn RA, Caspary T.

Mol Biol Cell. 2011 Dec;22(23):4694-703. doi: 10.1091/mbc.E10-12-0994. Epub 2011 Oct 5.

18.

Defective Wnt-dependent cerebellar midline fusion in a mouse model of Joubert syndrome.

Lancaster MA, Gopal DJ, Kim J, Saleem SN, Silhavy JL, Louie CM, Thacker BE, Williams Y, Zaki MS, Gleeson JG.

Nat Med. 2011 Jun;17(6):726-31. doi: 10.1038/nm.2380. Epub 2011 May 29.

19.

Multidirectional and multizonal tangential migration of GABAergic interneurons in the developing cerebral cortex.

Tanaka DH, Maekawa K, Yanagawa Y, Obata K, Murakami F.

Development. 2006 Jun;133(11):2167-76. Epub 2006 May 3.

20.

Directional guidance of interneuron migration to the cerebral cortex relies on subcortical Slit1/2-independent repulsion and cortical attraction.

Marín O, Plump AS, Flames N, Sánchez-Camacho C, Tessier-Lavigne M, Rubenstein JL.

Development. 2003 May;130(9):1889-901.

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