PMC Links for Nucleotide (Select 1675069147) - PMC

Select item 55569741.

The CEP19-RABL2 GTPase complex binds IFT-B to initiate intraflagellar transport at the ciliary base

Tomoharu Kanie, Keene Louis Abbott, Nancie Ann Mooney, Edward Douglas Plowey, Janos Demeter, Peter Kent Jackson

Dev Cell. Author manuscript; available in PMC 2018 Jul 10.

Published in final edited form as: Dev Cell. 2017 Jul 10; 42(1): 22–36.e12. Published online 2017 Jun 15. doi: 10.1016/j.devcel.2017.05.016

PMCID:: PMC5556974

Abstract Article PDF–2.2M

Select item 54696082.

RABL2 interacts with the intraflagellar transport-B complex and CEP19 and participates in ciliary assembly

Yuya Nishijima, Yohei Hagiya, Tomohiro Kubo, Ryota Takei, Yohei Katoh, Kazuhisa Nakayama

Mol Biol Cell. 2017 Jun 15; 28(12): 1652–1666. doi: 10.1091/mbc.E17-01-0017

PMCID:: PMC5469608

Abstract Article PDF–3.3M

Select item 54132153.

IFT81 as a Candidate Gene for Nonsyndromic Retinal Degeneration

Rachayata Dharmat, Wei Liu, Zhongqi Ge, Zixi Sun, Lizhu Yang, Yumei Li, Keqing Wang, Kandace Thomas, Ruifang Sui, Rui Chen

Invest Ophthalmol Vis Sci. 2017 May; 58(5): 2483–2490. doi: 10.1167/iovs.16-19133

PMCID:: PMC5413215

Abstract Article PDF–1.0M

Select item 50359304.

Destabilization of the IFT-B cilia core complex due to mutations in IFT81 causes a Spectrum of Short-Rib Polydactyly Syndrome

Ivan Duran, S. Paige Taylor, Wenjuan Zhang, Jorge Martin, Kimberly N. Forlenza, Rhonda P. Spiro, Deborah A. Nickerson, Michael Bamshad, Daniel H. Cohn, Deborah Krakow

Sci Rep. 2016; 6: 34232. Published online 2016 Sep 26. doi: 10.1038/srep34232

PMCID:: PMC5035930

Abstract Article PDF–1.8M

Select item 48691705.

An organelle-specific protein landscape identifies novel diseases and molecular mechanisms

Karsten Boldt, Jeroen van Reeuwijk, Qianhao Lu, Konstantinos Koutroumpas, Thanh-Minh T. Nguyen, Yves Texier, Sylvia E. C. van Beersum, Nicola Horn, Jason R. Willer, Dorus A. Mans, Gerard Dougherty, Ideke J. C. Lamers, Karlien L. M. Coene, Heleen H. Arts, Matthew J. Betts, Tina Beyer, Emine Bolat, Christian Johannes Gloeckner, Khatera Haidari, Lisette Hetterschijt, Daniela Iaconis, Dagan Jenkins, Franziska Klose, Barbara Knapp, Brooke Latour, Stef J. F. Letteboer, Carlo L. Marcelis, Dragana Mitic, Manuela Morleo, Machteld M. Oud, Moniek Riemersma, Susan Rix, Paulien A. Terhal, Grischa Toedt, Teunis J. P. van Dam, Erik de Vrieze, Yasmin Wissinger, Ka Man Wu, Gordana Apic, Philip L. Beales, Oliver E. Blacque, Toby J. Gibson, Martijn A. Huynen, Nicholas Katsanis, Hannie Kremer, Heymut Omran, Erwin van Wijk, Uwe Wolfrum, François Kepes, Erica E. Davis, Brunella Franco, Rachel H. Giles, Marius Ueffing, Robert B. Russell, Ronald Roepman, UK10K Rare Diseases Group

Nat Commun. 2016; 7: 11491. Published online 2016 May 13. doi: 10.1038/ncomms11491

PMCID:: PMC4869170

Abstract Article PDF–2.0M

Select item 46213726.

IFT81, encoding an IFT-B core protein, as a very rare cause of a ciliopathy phenotype

Isabelle Perrault, Jan Halbritter, Jonathan D Porath, Xavier Gérard, Daniela A Braun, Heon Yung Gee, Hanan M Fathy, Sophie Saunier, Valérie Cormier-Daire, Sophie Thomas, Tania Attié-Bitach, Nathalie Boddaert, Michael Taschner, Markus Schueler, Esben Lorentzen, Richard P Lifton, Jennifer A Lawson, Meriem Garfa-Traore, Edgar A Otto, Philippe Bastin, Catherine Caillaud, Josseline Kaplan, Jean-Michel Rozet, Friedhelm Hildebrandt

J Med Genet. 2015 Oct; 52(10): 657–665. Published online 2015 Aug 14. doi: 10.1136/jmedgenet-2014-102838

PMCID:: PMC4621372

Abstract Article PDF–2.8M

Select item 43599027.

Molecular Basis of Tubulin Transport Within the Cilium by IFT74 and IFT81

Sagar Bhogaraju, Lukas Cajanek, Cécile Fort, Thierry Blisnick, Kristina Weber, Michael Taschner, Naoko Mizuno, Stefan Lamla, Philippe Bastin, Erich A. Nigg, Esben Lorentzen

Science. Author manuscript; available in PMC 2015 Mar 15.

Published in final edited form as: Science. 2013 Aug 30; 341(6149): 1009–1012. doi: 10.1126/science.1240985

PMCID:: PMC4359902

Abstract Article PDF–939K

Select item 67875598.

SANS (USH1G) Molecularly Links the Human Usher Syndrome Protein Network to the Intraflagellar Transport Module by Direct Binding to IFT-B Proteins

Nasrin Sorusch, Adem Yildirim, Barbara Knapp, Julia Janson, Wiebke Fleck, Caroline Scharf, Uwe Wolfrum

Front Cell Dev Biol. 2019; 7: 216. Published online 2019 Oct 4. doi: 10.3389/fcell.2019.00216

PMCID:: PMC6787559

Abstract Article PDF–3.9M

PMC

Result Filters

Article attributes

Text availability

Publication date

Custom date range

Research Funder

Additional filters

Display Settings:

Send to:

Links from Nucleotide

Items: 8

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity