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The vertebrate primary cilium in development, homeostasis, and disease

published in: Cell

date of publication: 2009-04-03

language: English

Cites articles 118

Date

Title

Authors

2008-08

CP110 suppresses primary cilia formation through its interaction with CEP290, a protein deficient in human ciliary disease

Vivek Malhotra, William Y Tsang, Anand Swaroop, Hemant Khanna
2008-04

Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia

Peter Nürnberg, Heike Olbrich, Heymut Omran, Gudrun Nürnberg, Bernhard Schermer, Hanswalter Zentgraf, Thomas Benzing, Jan Senderek, Klaus Zerres, Soeren S Lienkamp, Janbernd Kirschner, Christian Becker
2008-03-23

Elipsa is an early determinant of ciliogenesis that links the IFT particle to membrane-associated small GTPase Rab8

Saikat Mukhopadhyay, Jarema Malicki
2008-03-18

Bardet-Biedl syndrome proteins are required for the localization of G protein-coupled receptors to primary cilia
2008-04-01

THM1 negatively modulates mouse sonic hedgehog signal transduction and affects retrograde intraflagellar transport in cilia
2008-03-09

Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome

Jose Badano, Nicholas Katsanis, Hélène Dollfus
2008-02-24

Hedgehog signaling and primary cilia are required for the formation of adult neural stem cells

Young-Goo Han, Nathalie Spassky, José M García-Verdugo, Andrea Aguilar, Sylvie Schneider-Maunoury, Arturo Álvarez-Buylla
2008-01-14

Intraflagellar transport motors in cilia: moving along the cell's antenna

Jonathan M Scholey
2008-01

Kif3a constrains beta-catenin-dependent Wnt signalling through dual ciliary and non-ciliary mechanisms
2008-01-01

Ciliary proteins link basal body polarization to planar cell polarity regulation

Christine Petit, Chonnettia Jones
2008-12-24

Molecular architecture of the centriole proteome: the conserved WD40 domain protein POC1 is required for centriole duplication and length control
2008-11-16

Foxj1 transcription factors are master regulators of the motile ciliogenic program
2008-11-16

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

Isao Oishi, Juan Carlos Izpisúa Belmonte
2008-05-22

Beta-arrestin-mediated localization of smoothened to the primary cilium

Robert Lefkowitz
2008-03-04

Primary cilia are required for cerebellar development and Shh-dependent expansion of progenitor pool

Andrea Aguilar, Arturo Álvarez-Buylla
2008-03-18

Depletion of apical transport proteins perturbs epithelial cyst formation and ciliogenesis

Kai Simons, Aki Manninen, Sebastian Schuck
2008-01-14

Cilia orientation and the fluid mechanics of development
2007-10-30

Loss of Bardet Biedl syndrome proteins causes defects in peripheral sensory innervation and function

Nicholas Katsanis, Gregory Germino, Michel R Leroux
2007-11

When cilia go bad: cilia defects and ciliopathies
2007-10-22

Cep164, a novel centriole appendage protein required for primary cilium formation

Erich Nigg, York-Dieter Stierhof
2007-09-30

Disruption of the basal body compromises proteasomal function and perturbs intracellular Wnt response

Jantje Gerdes, Jose Badano, Nicholas Katsanis, Shaneka S. Lawson
2007-10-02

The mouse homeobox gene Noto regulates node morphogenesis, notochordal ciliogenesis, and left right patterning

Christoph Viebahn
2007-08-24

Cep97 and CP110 suppress a cilia assembly program

William Y Tsang
2007-07-30

Functional dissection of Rab GTPases involved in primary cilium formation
2007-07-20

Patched1 regulates hedgehog signaling at the primary cilium
2007-06-01

HEF1-dependent Aurora A activation induces disassembly of the primary cilium

Elena Pugacheva, Sandra A Jablonski
2007-06-01

A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis

Maxence V. Nachury, Diane C Slusarski, Val C Sheffield
2007-07

The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome

Friedhelm Hildebrandt, Corinne Antignac, Tania Attié-Bitach, Michel Vekemans, Sophie Saunier, Nathalie Boddaert, Christelle Golzio, Marion Delous, Sylvie Schneider-Maunoury, Christoph Gerhardt, Marie-Claire Gubler, Patrick Niaudet
2007-07

Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome

Ronald Roepman, Uwe Wolfrum, Tina Märker, Han G. Brunner, Nine V. A. M. Knoers, Frans P M Cremers
2007-07-01

Ftm is a novel basal body protein of cilia involved in Shh signalling
2007-08

The proteome of the mouse photoreceptor sensory cilium complex
2007-05-01

The graded response to Sonic Hedgehog depends on cilia architecture

Tamara Caspary, Kathryn V. Anderson

Article - wd:Q29614609

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