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Items: 1 to 20 of 46

1.

Mutations in TRAF3IP1/IFT54 reveal a new role for IFT proteins in microtubule stabilization.

Bizet AA, Becker-Heck A, Ryan R, Weber K, Filhol E, Krug P, Halbritter J, Delous M, Lasbennes MC, Linghu B, Oakeley EJ, Zarhrate M, Nitschké P, Garfa-Traore M, Serluca F, Yang F, Bouwmeester T, Pinson L, Cassuto E, Dubot P, Elshakhs NA, Sahel JA, Salomon R, Drummond IA, Gubler MC, Antignac C, Chibout S, Szustakowski JD, Hildebrandt F, Lorentzen E, Sailer AW, Benmerah A, Saint-Mezard P, Saunier S.

Nat Commun. 2015 Oct 21;6:8666. doi: 10.1038/ncomms9666.

2.

The transition zone protein Rpgrip1l regulates proteasomal activity at the primary cilium.

Gerhardt C, Lier JM, Burmühl S, Struchtrup A, Deutschmann K, Vetter M, Leu T, Reeg S, Grune T, Rüther U.

J Cell Biol. 2015 Jul 6;210(1):115-33. doi: 10.1083/jcb.201408060.

3.

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.

4.

Regulation of cilium length and intraflagellar transport by the RCK-kinases ICK and MOK in renal epithelial cells.

Broekhuis JR, Verhey KJ, Jansen G.

PLoS One. 2014 Sep 22;9(9):e108470. doi: 10.1371/journal.pone.0108470. eCollection 2014.

5.

Nedd9 restrains renal cystogenesis in Pkd1-/- mice.

Nikonova AS, Plotnikova OV, Serzhanova V, Efimov A, Bogush I, Cai KQ, Hensley HH, Egleston BL, Klein-Szanto A, Seeger-Nukpezah T, Golemis EA.

Proc Natl Acad Sci U S A. 2014 Sep 2;111(35):12859-64. doi: 10.1073/pnas.1405362111. Epub 2014 Aug 19.

6.

Loss of primary cilia occurs early in breast cancer development.

Menzl I, Lebeau L, Pandey R, Hassounah NB, Li FW, Nagle R, Weihs K, McDermott KM.

Cilia. 2014 Jul 1;3:7. doi: 10.1186/2046-2530-3-7. eCollection 2014.

7.

Mutations of CEP83 cause infantile nephronophthisis and intellectual disability.

Failler M, Gee HY, Krug P, Joo K, Halbritter J, Belkacem L, Filhol E, Porath JD, Braun DA, Schueler M, Frigo A, Alibeu O, Masson C, Brochard K, Hurault de Ligny B, Novo R, Pietrement C, Kayserili H, Salomon R, Gubler MC, Otto EA, Antignac C, Kim J, Benmerah A, Hildebrandt F, Saunier S.

Am J Hum Genet. 2014 Jun 5;94(6):905-14. doi: 10.1016/j.ajhg.2014.05.002. Epub 2014 May 29.

8.

Case study: polycystic livers in a transgenic mouse line.

Lovaglio J, Artwohl JE, Ward CJ, Diekwisch TG, Ito Y, Fortman JD.

Comp Med. 2014 Apr;64(2):115-20.

9.

Reduction of meckelin leads to general loss of cilia, ciliary microtubule misalignment and distorted cell surface organization.

Picariello T, Valentine MS, Yano J, Van Houten J.

Cilia. 2014 Jan 31;3(1):2. doi: 10.1186/2046-2530-3-2.

10.

Mechanism of cystogenesis in nephrotic kidneys: a histopathological study.

Saraga M, Vukojević K, Krželj V, Puretić Z, Bočina I, Durdov MG, Weber S, Dworniczak B, Ljubanović DG, Saraga-Babić M.

BMC Nephrol. 2014 Jan 8;15:3. doi: 10.1186/1471-2369-15-3.

11.

Meckel-Gruber syndrome and the role of primary cilia in kidney, skeleton, and central nervous system development.

Barker AR, Thomas R, Dawe HR.

Organogenesis. 2014 Jan 1;10(1):96-107. doi: 10.4161/org.27375. Epub 2013 Dec 9. Review.

12.

A role for the Golgi matrix protein giantin in ciliogenesis through control of the localization of dynein-2.

Asante D, Maccarthy-Morrogh L, Townley AK, Weiss MA, Katayama K, Palmer KJ, Suzuki H, Westlake CJ, Stephens DJ.

J Cell Sci. 2013 Nov 15;126(Pt 22):5189-97. doi: 10.1242/jcs.131664. Epub 2013 Sep 17.

13.

The importance of a single primary cilium.

Mahjoub MR.

Organogenesis. 2013 Apr-Jun;9(2):61-9. doi: 10.4161/org.25144. Epub 2013 Apr 1. Review.

14.

Meckelin 3 is necessary for photoreceptor outer segment development in rat Meckel syndrome.

Tiwari S, Hudson S, Gattone VH 2nd, Miller C, Chernoff EA, Belecky-Adams TL.

PLoS One. 2013;8(3):e59306. doi: 10.1371/journal.pone.0059306. Epub 2013 Mar 13.

15.

The Meckel syndrome protein meckelin (TMEM67) is a key regulator of cilia function but is not required for tissue planar polarity.

Leightner AC, Hommerding CJ, Peng Y, Salisbury JL, Gainullin VG, Czarnecki PG, Sussman CR, Harris PC.

Hum Mol Genet. 2013 May 15;22(10):2024-40. doi: 10.1093/hmg/ddt054. Epub 2013 Feb 7.

16.

Cilia, Wnt signaling, and the cytoskeleton.

May-Simera HL, Kelley MW.

Cilia. 2012 May 2;1(1):7. doi: 10.1186/2046-2530-1-7.

17.

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.

18.

Regulation of transport in the connecting tubule and cortical collecting duct.

Staruschenko A.

Compr Physiol. 2012 Apr;2(2):1541-84. Review.

19.

Functional polycystin-1 dosage governs autosomal dominant polycystic kidney disease severity.

Hopp K, Ward CJ, Hommerding CJ, Nasr SH, Tuan HF, Gainullin VG, Rossetti S, Torres VE, Harris PC.

J Clin Invest. 2012 Nov;122(11):4257-73. doi: 10.1172/JCI64313. Epub 2012 Oct 15.

20.

A novel mutation causing nephronophthisis in the Lewis polycystic kidney rat localises to a conserved RCC1 domain in Nek8.

McCooke JK, Appels R, Barrero RA, Ding A, Ozimek-Kulik JE, Bellgard MI, Morahan G, Phillips JK.

BMC Genomics. 2012 Aug 16;13:393. doi: 10.1186/1471-2164-13-393.

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