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Items: 1 to 20 of 109


Conserved Genetic Interactions between Ciliopathy Complexes Cooperatively Support Ciliogenesis and Ciliary Signaling.

Yee LE, Garcia-Gonzalo FR, Bowie RV, Li C, Kennedy JK, Ashrafi K, Blacque OE, Leroux MR, Reiter JF.

PLoS Genet. 2015 Nov 5;11(11):e1005627. doi: 10.1371/journal.pgen.1005627. eCollection 2015 Nov.


IFT-Cargo Interactions and Protein Transport in Cilia.

Lechtreck KF.

Trends Biochem Sci. 2015 Dec;40(12):765-78. doi: 10.1016/j.tibs.2015.09.003. Epub 2015 Oct 21. Review.


Formation of the transition zone by Mks5/Rpgrip1L establishes a ciliary zone of exclusion (CIZE) that compartmentalises ciliary signalling proteins and controls PIP2 ciliary abundance.

Jensen VL, Li C, Bowie RV, Clarke L, Mohan S, Blacque OE, Leroux MR.

EMBO J. 2015 Oct 14;34(20):2537-56. doi: 10.15252/embj.201488044. Epub 2015 Sep 21.


Superresolution Pattern Recognition Reveals the Architectural Map of the Ciliary Transition Zone.

Yang TT, Su J, Wang WJ, Craige B, Witman GB, Tsou MF, Liao JC.

Sci Rep. 2015 Sep 14;5:14096. doi: 10.1038/srep14096.


The ciliary transition zone functions in cell adhesion but is dispensable for axoneme assembly in C. elegans.

Schouteden C, Serwas D, Palfy M, Dammermann A.

J Cell Biol. 2015 Jul 6;210(1):35-44. doi: 10.1083/jcb.201501013. Epub 2015 Jun 29.


Using Stem Cells to Model Diseases of the Outer Retina.

Yvon C, Ramsden CM, Lane A, Powner MB, da Cruz L, Coffey PJ, Carr AJ.

Comput Struct Biotechnol J. 2015 May 6;13:382-9. doi: 10.1016/j.csbj.2015.05.001. eCollection 2015. Review.


RPGR: Its role in photoreceptor physiology, human disease, and future therapies.

Megaw RD, Soares DC, Wright AF.

Exp Eye Res. 2015 Sep;138:32-41. doi: 10.1016/j.exer.2015.06.007. Epub 2015 Jun 17.


Reduced tubulin polyglutamylation suppresses flagellar shortness in Chlamydomonas.

Kubo T, Hirono M, Aikawa T, Kamiya R, Witman GB.

Mol Biol Cell. 2015 Aug 1;26(15):2810-22. doi: 10.1091/mbc.E15-03-0182. Epub 2015 Jun 17.


Ablation of retinal ciliopathy protein RPGR results in altered photoreceptor ciliary composition.

Rao KN, Li L, Anand M, Khanna H.

Sci Rep. 2015 Jun 11;5:11137. doi: 10.1038/srep11137.


Stem cells and fluid flow drive cyst formation in an invertebrate excretory organ.

Thi-Kim Vu H, Rink JC, McKinney SA, McClain M, Lakshmanaperumal N, Alexander R, Sánchez Alvarado A.

Elife. 2015 Jun 9;4. doi: 10.7554/eLife.07405.


Assembly of IFT trains at the ciliary base depends on IFT74.

Brown JM, Cochran DA, Craige B, Kubo T, Witman GB.

Curr Biol. 2015 Jun 15;25(12):1583-93. doi: 10.1016/j.cub.2015.04.060. Epub 2015 Jun 4.


TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport.

Schmidts M, Hou Y, Cortés CR, Mans DA, Huber C, Boldt K, Patel M, van Reeuwijk J, Plaza JM, van Beersum SE, Yap ZM, Letteboer SJ, Taylor SP, Herridge W, Johnson CA, Scambler PJ, Ueffing M, Kayserili H, Krakow D, King SM; UK10K, Beales PL, Al-Gazali L, Wicking C, Cormier-Daire V, Roepman R, Mitchison HM, Witman GB.

Nat Commun. 2015 Jun 5;6:7074. doi: 10.1038/ncomms8074.


The essential roles of transition fibers in the context of cilia.

Wei Q, Ling K, Hu J.

Curr Opin Cell Biol. 2015 Aug;35:98-105. doi: 10.1016/ Epub 2015 May 16. Review.


Cilia and Diseases.

Brown JM, Witman GB.

Bioscience. 2014 Dec 1;64(12):1126-1137.


TMEM231, mutated in orofaciodigital and Meckel syndromes, organizes the ciliary transition zone.

Roberson EC, Dowdle WE, Ozanturk A, Garcia-Gonzalo FR, Li C, Halbritter J, Elkhartoufi N, Porath JD, Cope H, Ashley-Koch A, Gregory S, Thomas S, Sayer JA, Saunier S, Otto EA, Katsanis N, Davis EE, Attié-Bitach T, Hildebrandt F, Leroux MR, Reiter JF.

J Cell Biol. 2015 Apr 13;209(1):129-42. doi: 10.1083/jcb.201411087.


CEP290 alleles in mice disrupt tissue-specific cilia biogenesis and recapitulate features of syndromic ciliopathies.

Rachel RA, Yamamoto EA, Dewanjee MK, May-Simera HL, Sergeev YV, Hackett AN, Pohida K, Munasinghe J, Gotoh N, Wickstead B, Fariss RN, Dong L, Li T, Swaroop A.

Hum Mol Genet. 2015 Jul 1;24(13):3775-91. doi: 10.1093/hmg/ddv123. Epub 2015 Apr 9.


Species-dependent splice recognition of a cryptic exon resulting from a recurrent intronic CEP290 mutation that causes congenital blindness.

Garanto A, Duijkers L, Collin RW.

Int J Mol Sci. 2015 Mar 9;16(3):5285-98. doi: 10.3390/ijms16035285.


Tubulin transport by IFT is upregulated during ciliary growth by a cilium-autonomous mechanism.

Craft JM, Harris JA, Hyman S, Kner P, Lechtreck KF.

J Cell Biol. 2015 Jan 19;208(2):223-37. doi: 10.1083/jcb.201409036. Epub 2015 Jan 12.


Proteomic analysis of isolated ciliary transition zones reveals the presence of ESCRT proteins.

Diener DR, Lupetti P, Rosenbaum JL.

Curr Biol. 2015 Feb 2;25(3):379-84. doi: 10.1016/j.cub.2014.11.066. Epub 2015 Jan 8.

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