The roles of evolutionarily conserved functional modules in cilia-related trafficking

Signals for Sorting of Transmembrane Proteins to Endosomes and Lysosomes

Bonifacino, J. S., & Traub, L. M. (2003) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.72.121801.161800 · Cited by 2,040 · see citing works

Endocytic recycling

Maxfield, F. R., & McGraw, T. E. (2004) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1315 · Cited by 1,716 · see citing works

A Core Complex of BBS Proteins Cooperates with the GTPase Rab8 to Promote Ciliary Membrane Biogenesis

Nachury, M. V., Loktev, A. V., Zhang, Q., Westlake, C. J., Peränen, J., Merdes, A., Slusarski, D. C., Scheller, R. H., Bazan, J. F., Sheffield, V. C., et al. (2007) · Cell · doi:10.1016/j.cell.2007.03.053 · Cited by 1,384 · see citing works

Ciliopathies

Hildebrandt, F., Benzing, T., & Katsanis, N. (2011) · New England Journal of Medicine · doi:10.1056/nejmra1010172 · Cited by 1,331 · see citing works

A motility in the eukaryotic flagellum unrelated to flagellar beating.

Kozminski, K. G., Johnson, K. A., Forscher, P., & Rosenbaum, J. L. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.12.5519 · Cited by 1,007 · see citing works

Ciliogenesis: building the cell's antenna

Ishikawa, H., & Marshall, W. F. (2011) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3085 · Cited by 956 · see citing works

ARF family G proteins and their regulators: roles in membrane transport, development and disease

Donaldson, J. G., & Jackson, C. L. (2011) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3117 · Cited by 914 · see citing works

Comparative Genomics Identifies a Flagellar and Basal Body Proteome that Includes the BBS5 Human Disease Gene

Li, J. B., Gerdes, J. M., Haycraft, C. J., Fan, Y., Teslovich, T. M., May‐Simera, H., Li, H., Blacque, O. E., Li, L., Leitch, C. C., et al. (2004) · Cell · doi:10.1016/s0092-8674(04)00450-7 · Cited by 760 · see citing works

CENTRIOLES AND THE FORMATION OF RUDIMENTARY CILIA BY FIBROBLASTS AND SMOOTH MUSCLE CELLS

Sorokin, S. (1962) · The Journal of Cell Biology · doi:10.1083/jcb.15.2.363 · Cited by 732 · see citing works

Motile Cilia of Human Airway Epithelia Are Chemosensory

Shah, A. S., Ben‐Shahar, Y., Moninger, T. O., Kline, J. N., & Welsh, M. J. (2009) · Science · doi:10.1126/science.1173869 · Cited by 717 · see citing works

Organization of vesicular trafficking in epithelia

Rodriguez-Boulan, E., Kreitzer, G., & Müsch, A. (2005) · Nature reviews. Molecular cell biology · doi:10.1038/nrm1593 · Cited by 644 · see citing works

A transition zone complex regulates mammalian ciliogenesis and ciliary membrane composition

García-Gonzalo, F. R., Corbit, K. C., Sirerol-Piquer, M. S., Ramaswami, G., Otto, E. A., Noriega, T. R., Seol, A. D., Robinson, J. F., Bennett, C., Josifova, D. J., et al. (2011) · Nature Genetics · doi:10.1038/ng.891 · Cited by 627 · see citing works

The Conserved Bardet-Biedl Syndrome Proteins Assemble a Coat that Traffics Membrane Proteins to Cilia

Jin, H., White, S. R., Shida, T., Schulz, S., Aguiar, M., Gygi, S. P., Bazán, J. F., & Nachury, M. V. (2010) · Cell · doi:10.1016/j.cell.2010.05.015 · Cited by 594 · see citing works

A molecular network for de novo generation of the apical surface and lumen

Bryant, D. M., Datta, A., Rodriguez-Fraticelli, A., Peränen, J., Martín‐Belmonte, F., & Mostov, K. E. (2010) · Nature Cell Biology · doi:10.1038/ncb2106 · Cited by 585 · see citing works

Functional genomic screen for modulators of ciliogenesis and cilium length

Kim, J., Lee, J. E., Heynen‐Genel, S., Suyama, E., Ono, K., Lee, K., Ideker, T. E., Aza‐Blanc, P., & Gleeson, J. G. (2010) · Nature · doi:10.1038/nature08895 · Cited by 548 · see citing works

The Structure of the Nuclear Pore Complex

Hoelz, A., Debler, E., & Blobel, G. (2011) · Annual Review of Biochemistry · doi:10.1146/annurev-biochem-060109-151030 · Cited by 525 · see citing works

Chapter Two Intraflagellar Transport (IFT)

Pedersen, L. B., & Rosenbaum, J. L. (2008) · Current Topics in Developmental Biology · doi:10.1016/s0070-2153(08)00802-8 · Cited by 521 · see citing works

Decoding Cilia Function

Avidor‐Reiss, T., Maer, A. M., Koundakjian, E. J., Polyanovsky, A. D., Keil, T. A., Subramaniam, S., & Zuker, C. S. (2004) · Cell · doi:10.1016/s0092-8674(04)00412-x · Cited by 505 · see citing works

The Intraflagellar Transport Protein IFT20 Is Associated with the Golgi Complex and Is Required for Cilia Assembly

Follit, J. A., Tuft, R. A., Fogarty, K. E., & Pazour, G. J. (2006) · Molecular Biology of the Cell · doi:10.1091/mbc.e06-02-0133 · Cited by 499 · see citing works

Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa.

Sung, C.-H., Schneider, B., Agarwal, N. A., Papermaster, D. S., & Nathans, J. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.19.8840 · Cited by 492 · see citing works

Coordination of Rab8 and Rab11 in primary ciliogenesis

Knödler, A., Feng, S., Zhang, J., Zhang, X., Das, A. K., Peränen, J., & Guo, W. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1002401107 · Cited by 485 · see citing works

The Centrosome in Cells and Organisms

Bornens, M. (2012) · Science · doi:10.1126/science.1209037 · Cited by 480 · see citing works

Rhodopsin’s Carboxy-Terminal Cytoplasmic Tail Acts as a Membrane Receptor for Cytoplasmic Dynein by Binding to the Dynein Light Chain Tctex-1

Tai, A. W., Chuang, J.-Z., Bode, C., Uwe Wolfrum, B., & Sung, C.-H. (1999) · Cell · doi:10.1016/s0092-8674(00)80800-4 · Cited by 478 · see citing works

The base of the cilium: roles for transition fibres and the transition zone in ciliary formation, maintenance and compartmentalization

Reiter, J. F., Blacque, O. E., & Leroux, M. R. (2012) · EMBO Reports · doi:10.1038/embor.2012.73 · Cited by 476 · see citing works

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

Berbari, N. F., Lewis, J. S., Bishop, G. A., Askwith, C. C., & Mykytyn, K. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0711027105 · Cited by 474 · see citing works

MKS and NPHP modules cooperate to establish basal body/transition zone membrane associations and ciliary gate function during ciliogenesis

Williams, C. L., Li, C., Kida, K., Inglis, P. N., Mohan, S., Semenec, L., Bialas, N. J., Stupay, R. M., Chen, N., Blacque, O. E., et al. (2011) · The Journal of Cell Biology · doi:10.1083/jcb.201012116 · Cited by 453 · see citing works

Transport-vesicle targeting: tethers before SNAREs

Pfeffer, S. R. (1999) · Nature Cell Biology · doi:10.1038/8967 · Cited by 449 · see citing works

Primary cilia membrane assembly is initiated by Rab11 and transport protein particle II (TRAPPII) complex-dependent trafficking of Rabin8 to the centrosome

Westlake, C. J., Baye, L. M., Nachury, M. V., Wright, K. J., Ervin, K. E., Phu, L., Chalouni, C. M., Beck, J. S., Kirkpatrick, D. S., Slusarski, D. C., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1018823108 · Cited by 436 · see citing works

TULP3 bridges the IFT-A complex and membrane phosphoinositides to promote trafficking of G protein-coupled receptors into primary cilia

Mukhopadhyay, S., Wen, X., Chih, B., Nelson, C. D., Lane, W. S., Scales, S. J., & Jackson, P. K. (2010) · Genes & Development · doi:10.1101/gad.1966210 · Cited by 435 · see citing works

Homozygosity mapping with SNP arrays identifies TRIM32 , an E3 ubiquitin ligase, as a Bardet–Biedl syndrome gene ( BBS11 )

Chiang, A. P.-F., Beck, J. S., Yen, H.-J., Tayeh, M. K., Scheetz, T. E., Swiderski, R. E., Nishimura, D. Y., Braun, T. A., Kim, K. A., Huang, J., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0600158103 · Cited by 433 · see citing works

Centriole distal appendages promote membrane docking, leading to cilia initiationPreprint

Tanos, B. E., Yang, H.-J., Soni, R. K., Wang, W., Macaluso, F., Asara, J. M., & Tsou, M.-F. B. (2013) · Genes & Development · doi:10.1101/gad.207043.112 · Cited by 417 · see citing works

Functional coordination of intraflagellar transport motors

Ou, G., E. Blacque, O., Snow, J. J., Leroux, M. R., & Scholey, J. M. (2005) · Nature · doi:10.1038/nature03818 · Cited by 411 · see citing works

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

Leitch, C. C., Zaghloul, N. A., Davis, E. E., Stoetzel, C., Dı́az-Font, A., Rix, S., Alfadhel, M., Lewis, R. A., Eyaid, W., Banin, E., et al. (2008) · Nature Genetics · doi:10.1038/ng.97 · Cited by 406 · see citing works

Tracing the origins of centrioles, cilia, and flagella

Carvalho-Santos, Z., Azimzadeh, J., Pereira‐Leal, J. B., & Bettencourt‐Dias, M. (2011) · The Journal of Cell Biology · doi:10.1083/jcb.201011152 · Cited by 405 · see citing works

The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression

Kim, J. C., Badano, J. L., Sibold, S., Esmail, M. A., Hill, J. E., Hoskins, B. E., Leitch, C. C., Venner, K., Ansley, S. J., Ross, A. J., et al. (2004) · Nature Genetics · doi:10.1038/ng1352 · Cited by 403 · see citing works

FINE STRUCTURE OF CELL DIVISION IN CHLAMYDOMONAS REINHARDI

Johnson, U. G., & Porter, K. R. (1968) · The Journal of Cell Biology · doi:10.1083/jcb.38.2.403 · Cited by 395 · see citing works

Localization of intraflagellar transport protein IFT52 identifies basal body transitional fibers as the docking site for IFT particles

Deane, J. A., Cole, D. G., Seeley, E. S., Diener, D. R., & Rosenbaum, J. L. (2001) · Current Biology · doi:10.1016/s0960-9822(01)00484-5 · Cited by 391 · see citing works

Receptor-mediated transcytosis of IgA in MDCK cells is via apical recycling endosomes.

Apodaca, G., Katz, L., & Mostov, K. E. (1994) · The Journal of Cell Biology · doi:10.1083/jcb.125.1.67 · Cited by 380 · see citing works

Functional dissection of Rab GTPases involved in primary cilium formation

Yoshimura, S., Egerer, J., Fuchs, E., Haas, A. K., & Barr, F. A. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200703047 · Cited by 375 · see citing works

Mechanistic insights into Bardet-Biedl syndrome, a model ciliopathy

Zaghloul, N. A., & Katsanis, N. (2009) · Journal of Clinical Investigation · doi:10.1172/jci37041 · Cited by 364 · see citing works

Identification of Ciliary Localization Sequences within the Third Intracellular Loop of G Protein-coupled Receptors

Berbari, N. F., Johnson, A. D., Lewis, J. S., Askwith, C. C., & Mykytyn, K. (2008) · Molecular Biology of the Cell · doi:10.1091/mbc.e07-09-0942 · Cited by 352 · see citing works

Making sense of cilia in disease: The human ciliopathies

Baker, K., & Beales, P. L. (2009) · American Journal of Medical Genetics Part C Seminars in Medical Genetics · doi:10.1002/ajmg.c.30231 · Cited by 348 · see citing works

Planar Cell Polarity Acts Through Septins to Control Collective Cell Movement and Ciliogenesis

Kim, S. K., Shindo, A., Park, T. J., Oh, E. C. T., Ghosh, S., Gray, R. S., Lewis, R. A., Johnson, C. A., Attié‐Bitach, T., Katsanis, N., et al. (2010) · Science · doi:10.1126/science.1191184 · Cited by 348 · see citing works

The <i>Chlamydomonas reinhardtii</i> BBSome is an IFT cargo required for export of specific signaling proteins from flagella

Lechtreck, K.-F., Johnson, E. C., Sakai, T., Cochran, D., Ballif, B. A., Rush, J., Pazour, G. J., Ikebe, M., & Witman, G. B. (2009) · Journal of Cell Biology · doi:10.1083/jcb.200909183 · Cited by 347 · see citing works

Loss of C. elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transportPreprint

Blacque, O. E., Reardon, M. J., Li, C., McCarthy, J., Mahjoub, M. R., Ansley, S. J., Badano, J. L., Mah, A. K., Beales, P. L., Davidson, W. S., et al. (2004) · Genes & Development · doi:10.1101/gad.1194004 · Cited by 347 · see citing works

A rhodopsin gene mutation responsible for autosomal dominant retinitis pigmentosa results in a protein that is defective in localization to the photoreceptor outer segment

Ch, S., Makino, C. L., Baylor, D. A., & Nathans, J. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-10-05818.1994 · Cited by 342 · see citing works

Intraflagellar transport (IFT) cargo

Qin, H., Diener, D. R., Geimer, S., Cole, D. G., & Rosenbaum, J. L. (2004) · The Journal of Cell Biology · doi:10.1083/jcb.200308132 · Cited by 342 · see citing works

Mutations in a member of the Ras superfamily of small GTP-binding proteins causes Bardet-Biedl syndrome

Fan, Y., Esmail, M. A., Ansley, S. J., Blacque, O. E., Boroevich, K. A., Ross, A. J., Moore, S., Badano, J. L., May‐Simera, H., Compton, D. S., et al. (2004) · Nature Genetics · doi:10.1038/ng1414 · Cited by 336 · see citing works

BBS6, BBS10, and BBS12 form a complex with CCT/TRiC family chaperonins and mediate BBSome assembly

Seo, S., Baye, L. M., Schulz, N. P., Beck, J. S., Zhang, Q., Slusarski, D. C., & Sheffield, V. C. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0910268107 · Cited by 322 · see citing works

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

Bhogaraju, S., Cajanek, L., Fort, C., Blisnick, T., Weber, K., Taschner, M., Mizuno, N., Lamla, S., Bastin, P., Nigg, E. A., et al. (2013) · Science · doi:10.1126/science.1240985 · Cited by 317 · see citing works

A BBSome Subunit Links Ciliogenesis, Microtubule Stability, and Acetylation

Loktev, A. V., Zhang, Q., Beck, J. S., Searby, C. C., Scheetz, T. E., Bazán, J. F., Slusarski, D. C., Sheffield, V. C., Jackson, P. K., & Nachury, M. V. (2008) · Developmental Cell · doi:10.1016/j.devcel.2008.11.001 · Cited by 311 · see citing works

Intraflagellar transport is required for polarized recycling of the TCR/CD3 complex to the immune synapse

Finetti, F., Paccani, S. R., Riparbelli, M. G., Giacomello, E., Perinetti, G., Pazour, G. J., Rosenbaum, J. L., & Baldari, C. T. (2009) · Nature Cell Biology · doi:10.1038/ncb1977 · Cited by 310 · see citing works

Apical trafficking in epithelial cells: signals, clusters and motors

Weisz, O. A., & Rodriguez-Boulan, E. J. (2009) · Journal of Cell Science · doi:10.1242/jcs.032615 · Cited by 299 · see citing works

Cep164 mediates vesicular docking to the mother centriole during early steps of ciliogenesis

Schmidt, K. N., Kuhns, S., Neuner, A., Hub, B., Zentgraf, H., & Pereira, G. (2012) · The Journal of Cell Biology · doi:10.1083/jcb.201202126 · Cited by 289 · see citing works

Polycystin-2 traffics to cilia independently of polycystin-1 by using an N-terminal RVxP motif

Geng, L., Okuhara, D. Y., Yu, Z., Tian, X., Cai, Y., Shibazaki, S., & Somlo, S. (2006) · Journal of Cell Science · doi:10.1242/jcs.02818 · Cited by 282 · see citing works

Dyneins Across Eukaryotes: A Comparative Genomic Analysis

Wickstead, B., & Gull, K. (2007) · Traffic · doi:10.1111/j.1600-0854.2007.00646.x · Cited by 281 · see citing works

Centriole/basal body morphogenesis and migration during ciliogenesis in animal cells

Dawe, H. R., Farr, H., & Keith Gull, B. (2006) · Journal of Cell Science · doi:10.1242/jcs.03305 · Cited by 276 · see citing works

Primary Cilia and Signaling Pathways in Mammalian Development, Health and Disease

Veland, I. R., Awan, A., Pedersen, L. B., Yoder, B. K., & Christensen, S. T. (2009) · Nephron Physiology · doi:10.1159/000208212 · Cited by 276 · see citing works

Evolution of the eukaryotic membrane-trafficking system: origin, tempo and mode

Dacks, J. B., & Field, M. C. (2007) · Journal of Cell Science · doi:10.1242/jcs.013250 · Cited by 276 · see citing works

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

Scholey, J. M. (2008) · The Journal of Cell Biology · doi:10.1083/jcb.200709133 · Cited by 272 · see citing works

The Spinocerebellar Ataxia-Associated Gene Tau Tubulin Kinase 2 Controls the Initiation of Ciliogenesis

Goetz, S. C., Liem, K. F., & Anderson, K. V. (2012) · Cell · doi:10.1016/j.cell.2012.10.010 · Cited by 267 · see citing works

Ofd1, a Human Disease Gene, Regulates the Length and Distal Structure of Centrioles

Singla, V., Romaguera-Ros, M., García‐Verdugo, J. M., & Reiter, J. F. (2010) · Developmental Cell · doi:10.1016/j.devcel.2009.12.022 · Cited by 266 · see citing works

Lateral transport of Smoothened from the plasma membrane to the membrane of the cilium

Milenkovic, L., Scott, M. P., & Rohatgi, R. (2009) · Journal of Cell Biology · doi:10.1083/jcb.200907126 · Cited by 263 · see citing works

Polarity of flagellar assembly in Chlamydomonas.

Johnson, K. A., & Rosenbaum, J. L. (1992) · The Journal of Cell Biology · doi:10.1083/jcb.119.6.1605 · Cited by 255 · see citing works

Ciliary targeting motif VxPx directs assembly of a trafficking module through Arf4

Mazelova, J., Astuto‐Gribble, L., Inoue, H., Tam, B. M., Schonteich, E., Prekeris, R., Moritz, O. L., Randazzo, P. A., & Deretic, D. (2009) · The EMBO Journal · doi:10.1038/emboj.2008.267 · Cited by 244 · see citing works

Scoring a backstage pass: Mechanisms of ciliogenesis and ciliary access

García-Gonzalo, F. R., & Reiter, J. F. (2012) · The Journal of Cell Biology · doi:10.1083/jcb.201111146 · Cited by 239 · see citing works

An ARL3–UNC119–RP2 GTPase cycle targets myristoylated NPHP3 to the primary ciliumPreprint

Wright, K. J., Baye, L. M., Olivier-Mason, A., Mukhopadhyay, S., Sang, L., Kwong, M., Wang, W., Pretorius, P. R., Sheffield, V. C., Sengupta, P., et al. (2011) · Genes & Development · doi:10.1101/gad.173443.111 · Cited by 229 · see citing works

Remodelling of Cortical Actin Where Lytic Granules Dock at Natural Killer Cell Immune Synapses Revealed by Super-Resolution Microscopy

Brown, A. C. N., Oddos, S., Dobbie, I. M., Alakoskela, J.-M. I., Parton, R. M., Eissmann, P., Neil, M. A. A., Dunsby, C. W., French, P. M. W., Davis, I., et al. (2011) · PLoS Biology · doi:10.1371/journal.pbio.1001152 · Cited by 228 · see citing works

Functional analysis of an individual IFT protein: IFT46 is required for transport of outer dynein arms into flagella

Hou, Y., Qin, H., Follit, J. A., Pazour, G. J., Rosenbaum, J. L., & Witman, G. B. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200608041 · Cited by 226 · see citing works

Evolution of intraflagellar transport from coated vesicles and autogenous origin of the eukaryotic cilium

Jékely, G., & Arendt, D. (2006) · BioEssays · doi:10.1002/bies.20369 · Cited by 221 · see citing works

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

Omori, Y., Zhao, C., Saras, A., Mukhopadhyay, S., Kim, W., Furukawa, T., Sengupta, P., Veraksa, A. N., & Malicki, J. J. (2008) · Nature Cell Biology · doi:10.1038/ncb1706 · Cited by 218 · see citing works

The cell biology of vision

Sung, C.-H., & Chuang, J.-Z. (2010) · The Journal of Cell Biology · doi:10.1083/jcb.201006020 · Cited by 217 · see citing works

Dopamine receptor 1 localizes to neuronal cilia in a dynamic process that requires the Bardet-Biedl syndrome proteins

Domire, J. S., Green, J. A., Lee, K. G., Johnson, A. D., Askwith, C. C., & Mykytyn, K. (2011) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-010-0603-4 · Cited by 217 · see citing works

IFT25 Links the Signal-Dependent Movement of Hedgehog Components to Intraflagellar Transport

Keady, B. T., Samtani, R., Tobita, K., Tsuchya, M., San Agustin, J. T., Follit, J. A., Jonassen, J. A., Subramanian, R., Lo, C. W., & Pazour, G. J. (2012) · Developmental Cell · doi:10.1016/j.devcel.2012.04.009 · Cited by 216 · see citing works

ARF6 controls post-endocytic recycling through its downstream exocyst complex effector

Prigent, M., Dubois, T., Raposo, G., Derrien, V., Tenza, D., Rossé, C., Camonis, J., & Chavrier, P. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200305029 · Cited by 210 · see citing works

A Proteome-wide Screen for Mammalian SxIP Motif-Containing Microtubule Plus-End Tracking Proteins

Jiang, K., Toedt, G., Montenegro Gouveia, S., Davey, N. E., Hua, S., van der Vaart, B., Grigoriev, I., Larsen, J., Pedersen, L. B., Bezstarosti, K., et al. (2012) · Current Biology · doi:10.1016/j.cub.2012.07.047 · Cited by 209 · see citing works

The BBSome controls IFT assembly and turnaround in cilia

Wei, Q., Zhang, Y., Li, Y., Zhang, Q., Ling, K., & Hu, J. (2012) · Nature Cell Biology · doi:10.1038/ncb2560 · Cited by 208 · see citing works

Predation and eukaryote cell origins: A coevolutionary perspective

Cavalier‐Smith, T. (2008) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2008.10.002 · Cited by 206 · see citing works

Intraflagellar Transport Is Required for the Vectorial Movement of TRPV Channels in the Ciliary Membrane

Qin, H., Burnette, D. T., Bae, Y.-K., Forscher, P., Barr, M. M., & Rosenbaum, J. L. (2005) · Current Biology · doi:10.1016/j.cub.2005.08.047 · Cited by 206 · see citing works

A Novel Protein LZTFL1 Regulates Ciliary Trafficking of the BBSome and Smoothened

Seo, S., Zhang, Q., Bugge, K., Breslow, D. K., Searby, C. C., Nachury, M. V., & Sheffield, V. C. (2011) · PLoS Genetics · doi:10.1371/journal.pgen.1002358 · Cited by 205 · see citing works

Electron-tomographic analysis of intraflagellar transport particle trains in situ

Pigino, G., Geimer, S., Lanzavecchia, S., Paccagnini, E., Cantele, F., Diener, D. R., Rosenbaum, J. L., & Lupetti, P. (2009) · The Journal of Cell Biology · doi:10.1083/jcb.200905103 · Cited by 204 · see citing works

Intraflagellar Transport Protein 27 Is a Small G Protein Involved in Cell-Cycle Control

Qin, H., Wang, Z., Diener, D. R., & Rosenbaum, J. L. (2007) · Current Biology · doi:10.1016/j.cub.2006.12.040 · Cited by 201 · see citing works

Chapter 9 The Primary Cilium

Wong, S. Y., & Reiter, J. F. (2008) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(08)00809-0 · Cited by 194 · see citing works

Function and dynamics of PKD2 in Chlamydomonas reinhardtii flagella

Huang, K., Diener, D. R., Mitchell, A. P., Pazour, G. J., Witman, G. B., & Rosenbaum, J. L. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200704069 · Cited by 192 · see citing works

Architecture and function of IFT complex proteins in ciliogenesis

Taschner, M. J., Bhogaraju, S., & Lorentzen, E. (2011) · Differentiation · doi:10.1016/j.diff.2011.11.001 · Cited by 190 · see citing works

Thousands of Rab GTPases for the Cell Biologist

Diekmann, Y., Seixas, E., Gouw, M., Tavares-Cadete, F., Seabra, M. C., & Pereira‐Leal, J. B. (2011) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002217 · Cited by 189 · see citing works

Intraflagellar transport delivers tubulin isotypes to sensory cilium middle and distal segments

Hao, L., Thein, M. C., Brust‐Mascher, I., Civelekoglu‐Scholey, G., Lu, Y., Açar, Ş., Prevo, B., Shaham, S., & Scholey, J. M. (2011) · Nature Cell Biology · doi:10.1038/ncb2268 · Cited by 188 · see citing works

Bardet-Biedl syndrome: an emerging pathomechanism of intracellular transport

Blacque, O. E., & Leroux, M. R. (2006) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-006-6180-x · Cited by 186 · see citing works

The Exocyst Protein Sec10 Is Necessary for Primary Ciliogenesis and Cystogenesis In Vitro

Zuo, X., Guo, W., & Lipschutz, J. H. (2009) · Molecular Biology of the Cell · doi:10.1091/mbc.e08-07-0772 · Cited by 185 · see citing works

Primary cilia and coordination of receptor tyrosine kinase (RTK) signalling

Christensen, S. T., Clement, C. A., Satir, P., & Pedersen, L. B. (2012) · The Journal of Pathology · doi:10.1002/path.3004 · Cited by 181 · see citing works

Ultrastructure of cilia and flagella - back to the future!

Fisch, C., & Dupuis‐Williams, P. (2011) · Biology of the Cell · doi:10.1042/bc20100139 · Cited by 179 · see citing works

The cytoplasmic tail of fibrocystin contains a ciliary targeting sequence

Follit, J. A., Li, L., Vucica, Y., & Pazour, G. J. (2010) · The Journal of Cell Biology · doi:10.1083/jcb.200910096 · Cited by 168 · see citing works

A “Holistic” Kinesin Phylogeny Reveals New Kinesin Families and Predicts Protein Functions

Wickstead, B., & Gull, K. (2006) · Molecular Biology of the Cell · doi:10.1091/mbc.e05-11-1090 · Cited by 168 · see citing works

ODA16 aids axonemal outer row dynein assembly through an interaction with the intraflagellar transport machinery

Ahmed, N. T., Gao, C., Lucker, B. F., Cole, D. G., & Mitchell, D. R. (2008) · The Journal of Cell Biology · doi:10.1083/jcb.200802025 · Cited by 164 · see citing works

The small GTPases ARL-13 and ARL-3 coordinate intraflagellar transport and ciliogenesis

Li, Y., Wei, Q., Zhang, Y., Ling, K., & Hu, J. (2010) · The Journal of Cell Biology · doi:10.1083/jcb.200912001 · Cited by 163 · see citing works

Intraflagellar transport and the generation of dynamic, structurally and functionally diverse cilia

Silverman, M. A., & Leroux, M. R. (2009) · Trends in Cell Biology · doi:10.1016/j.tcb.2009.04.002 · Cited by 161 · see citing works

Intraflagellar Transport Particles Participate Directly in Cilium-Generated Signaling in Chlamydomonas

Wang, Q., Pan, J., & Snell, W. J. (2006) · Cell · doi:10.1016/j.cell.2006.02.044 · Cited by 154 · see citing works

The Cytoplasmic Tail of Rhodopsin Acts as a Novel Apical Sorting Signal in Polarized MDCK Cells

Chuang, J.-Z., & Sung, C.-H. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.142.5.1245 · Cited by 149 · see citing works

The Compartmentalized Bacteria of the Planctomycetes-Verrucomicrobia-Chlamydiae Superphylum Have Membrane Coat-Like Proteins

Santarella‐Mellwig, R., Franke, J. D., Jaedicke, A., Gorjánácz, M., Bauer, U., Budd, A., Mattaj, I. W., & Devos, D. P. (2010) · PLoS Biology · doi:10.1371/journal.pbio.1000281 · Cited by 149 · see citing works

Mouse Rab23 regulates Hedgehog signaling from Smoothened to Gli proteins

Eggenschwiler, J. T., Bulgakov, O. V., Qin, J., Li, T., & Anderson, K. V. (2005) · Developmental Biology · doi:10.1016/j.ydbio.2005.09.022 · Cited by 147 · see citing works

BBS proteins interact genetically with the IFT pathway to influence SHH-related phenotypes

Zhang, Q., Seo, S., Bugge, K., Stone, E. M., & Sheffield, V. C. (2012) · Human Molecular Genetics · doi:10.1093/hmg/dds004 · Cited by 144 · see citing works

Sensory Ciliogenesis inCaenorhabditis elegans: Assignment of IFT Components into Distinct Modules Based on Transport and Phenotypic Profiles

Ou, G., Koga, M., Blacque, O. E., Murayama, T., Ohshima, Y., Schafer, J. C., Li, C., Yoder, B. K., Leroux, M. R., & Scholey, J. M. (2007) · Molecular Biology of the Cell · doi:10.1091/mbc.e06-09-0805 · Cited by 143 · see citing works

Intraflagellar transport molecules in ciliary and nonciliary cells of the retina

Sedmak, T., & Uwe Wolfrum, B. (2010) · The Journal of Cell Biology · doi:10.1083/jcb.200911095 · Cited by 140 · see citing works

Single molecule imaging reveals a major role for diffusion in the exploration of ciliary space by signaling receptors

Ye, F., Breslow, D. K., Koslover, E. F., Spakowitz, A. J., Nelson, W. J., & Nachury, M. V. (2013) · eLife · doi:10.7554/elife.00654 · Cited by 138 · see citing works

THE DEVELOPMENT OF BASAL BODIES AND FLAGELLA IN ALLOMYCES ARBUSCULUS

Renaud, F. L., & Swift, H. (1964) · The Journal of Cell Biology · doi:10.1083/jcb.23.2.339 · Cited by 137 · see citing works

Exome sequencing identifies mutations in LZTFL1, a BBSome and smoothened trafficking regulator, in a family with Bardet–Biedl syndrome with situs inversus and insertional polydactyly

Marion, V., Stutzmann, F., Gérard, M., Melo, C. D., Schaefer, É., Claussmann, A., Hellé, S., Delague, V., Souied, E. H., Barrey, C., et al. (2012) · Journal of Medical Genetics · doi:10.1136/jmedgenet-2012-100737 · Cited by 126 · see citing works

Rab23, a Negative Regulator of Hedgehog Signaling, Localizes to the Plasma Membrane and the Endocytic Pathway

Evans, T. M., Ferguson, C., Wainwright, B. J., Parton, R. G., & Wicking, C. (2003) · Traffic · doi:10.1046/j.1600-0854.2003.00141.x · Cited by 124 · see citing works

The Centrosome Regulates the Rab11- Dependent Recycling Endosome Pathway at Appendages of the Mother Centriole

Hehnly, H., Chen, C.-T., Powers, C. M., Liu, H.-L., & Doxsey, S. (2012) · Current Biology · doi:10.1016/j.cub.2012.08.022 · Cited by 124 · see citing works

First and last ancestors: reconstructing evolution of the endomembrane system with ESCRTs, vesicle coat proteins, and nuclear pore complexes

Field, M. C., & Dacks, J. B. (2009) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2008.12.004 · Cited by 122 · see citing works

IFT20 is required for opsin trafficking and photoreceptor outer segment development

Keady, B. T., Le, Y. Z., & Pazour, G. J. (2011) · Molecular Biology of the Cell · doi:10.1091/mbc.e10-09-0792 · Cited by 122 · see citing works

Cytoplasmic Dynein Regulation by Subunit Heterogeneity and Its Role in Apical Transport

Tai, A. W., Chuang, J.-Z., & Sung, C.-H. (2001) · The Journal of Cell Biology · doi:10.1083/jcb.153.7.1499 · Cited by 121 · see citing works

The Arf GAP ASAP1 provides a platform to regulate Arf4‐ and Rab11–Rab8‐mediated ciliary receptor targeting

Wang, J., Morita, Y., Mazelova, J., & Deretic, D. (2012) · The EMBO Journal · doi:10.1038/emboj.2012.253 · Cited by 121 · see citing works

More than one way to build a flagellum: comparative genomics of parasitic protozoa

Briggs, L. J., Davidge, J., Wickstead, B., et al. (2004) · Current Biology · doi:10.1016/j.cub.2004.07.041 · Cited by 116 · see citing works

Primary ciliogenesis defects are associated with human astrocytoma/glioblastoma cells

Moser, J. J., Fritzler, M. J., & Rattner, J. B. (2009) · BMC Cancer · doi:10.1186/1471-2407-9-448 · Cited by 112 · see citing works

A conserved signal and GTPase complex are required for the ciliary transport of polycystin-1

Ward, H. H., Brown-Glaberman, U., Wang, J., Morita, Y., Alper, S. L., Bedrick, E. J., Gattone, V. H., Deretic, D., & Wandinger‐Ness, A. (2011) · Molecular Biology of the Cell · doi:10.1091/mbc.e11-01-0082 · Cited by 111 · see citing works

Differential role of Rab proteins in ciliary trafficking: Rab23 regulates Smoothened levels

Boehlke, C. S., Bashkurov, M., Buescher, A., Krick, T., John, A.-K., Nitschke, R., Walz, G., & Kuehn, E. W. (2010) · Journal of Cell Science · doi:10.1242/jcs.058883 · Cited by 110 · see citing works

Impaired photoreceptor protein transport and synaptic transmission in a mouse model of Bardet–Biedl syndrome

Abd‐El‐Barr, M. M., Sykoudis, K., Andrabi, S., Eichers, E. R., Pennesi, M. E., Tan, P. L., Wilson, J. H., Katsanis, N., Lupski, J. R., & Wu, S. M.-S. (2007) · Vision Research · doi:10.1016/j.visres.2007.09.016 · Cited by 109 · see citing works

Rab8 GTPase as a regulator of cell shape

Peränen, J. (2011) · Cytoskeleton · doi:10.1002/cm.20529 · Cited by 109 · see citing works

Crystal structure of the intraflagellar transport complex 25/27

Bhogaraju, S., Taschner, M. J., Morawetz, M., Minard‐Basquin, C., & Lorentzen, E. (2011) · The EMBO Journal · doi:10.1038/emboj.2011.110 · Cited by 104 · see citing works

NDR2‐mediated Rabin8 phosphorylation is crucial for ciliogenesis by switching binding specificity from phosphatidylserine to Sec15

Chiba, S., Amagai, Y., Homma, Y., et al. (2013) · The EMBO Journal · doi:10.1038/emboj.2013.32 · Cited by 104 · see citing works

Intraflagellar Transport (IFT) Protein IFT25 Is a Phosphoprotein Component of IFT Complex B and Physically Interacts with IFT27 in Chlamydomonas

Wang, Z., Fan, Z., Williamson, S. M., & Qin, H. (2009) · PLoS ONE · doi:10.1371/journal.pone.0005384 · Cited by 101 · see citing works

Polycystin-2 takes different routes to the somatic and ciliary plasma membrane

Hoffmeister, H., Babinger, K., Gürster, S., Cedzich, A., Meese, C., Schadendorf, K., Osten, L., de Vries, U., Rascle, A., & Witzgall, R. (2011) · The Journal of Cell Biology · doi:10.1083/jcb.201007050 · Cited by 100 · see citing works

Uncoordinated 119 Protein Controls Trafficking of Lck via the Rab11 Endosome and Is Critical for Immunological Synapse Formation

Gorska, M. M., Liang, Q., Karim, Z., & Alam, R. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0900792 · Cited by 98 · see citing works

Inversin, Wnt signaling and primary cilia

Lienkamp, S. S., Ganner, A., & Walz, G. (2011) · Differentiation · doi:10.1016/j.diff.2011.11.012 · Cited by 96 · see citing works

Endocytosis Genes Facilitate Protein and Membrane Transport in C. elegans Sensory Cilia

Kaplan, O. I., Doroquez, D. B., Cevik, S., Bowie, R. V., Clarke, L., Sanders, A. A. W. M., Kida, K., Rappoport, J. Z., Sengupta, P., & Blacque, O. E. (2012) · Current Biology · doi:10.1016/j.cub.2012.01.060 · Cited by 93 · see citing works

Intraflagellar transport: from molecular characterisation to mechanism

Blacque, O. E. (2007) · Frontiers in bioscience · doi:10.2741/2871 · Cited by 92 · see citing works

On a bender—BARs, ESCRTs, COPs, and finally getting your coat

Field, M. C., Šali, A., & Rout, M. P. (2011) · The Journal of Cell Biology · doi:10.1083/jcb.201102042 · Cited by 88 · see citing works

Mutations in SDCCAG8/NPHP10 Cause Bardet-Biedl Syndrome and Are Associated with Penetrant Renal Disease and Absent Polydactyly

Schaefer, É., Zaloszyc, A., Lauer, J., et al. (2010) · Molecular Syndromology · doi:10.1159/000331268 · Cited by 82 · see citing works

Identification and Functional Analysis of the Vision-Specific BBS3 (ARL6) Long Isoform

Pretorius, P. R., Baye, L. M., Nishimura, D. Y., Searby, C. C., Bugge, K., Yang, B., Mullins, R. F., Stone, E. M., Sheffield, V. C., & Slusarski, D. C. (2010) · PLoS Genetics · doi:10.1371/journal.pgen.1000884 · Cited by 80 · see citing works

RAB-Like 2 Has an Essential Role in Male Fertility, Sperm Intra-Flagellar Transport, and Tail Assembly

Lo, J. C. Y., Jamsai, D., O’Connor, A. E., Borg, C. L., Clark, B. J., Whisstock, J. C., Field, M. C., Adams, V., Ishikawa, T., Aitken, R. J., et al. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1002969 · Cited by 79 · see citing works

IFTA-2 is a conserved cilia protein involved in pathways regulating longevity and dauer formation inCaenorhabditis elegans

Schafer, J. C., Winkelbauer, M. E., Williams, C. L., Haycraft, C. J., Desmond, R. A., & Yoder, B. K. (2006) · Journal of Cell Science · doi:10.1242/jcs.03187 · Cited by 76 · see citing works

cAMP and cGMP signaling: sensory systems with prokaryotic roots adopted by eukaryotic cilia

Johnson, J.-L., & Leroux, M. R. (2010) · Trends in Cell Biology · doi:10.1016/j.tcb.2010.05.005 · Cited by 74 · see citing works

Live-Cell Imaging Evidence for the Ciliary Transport of Rod Photoreceptor Opsin by Heterotrimeric Kinesin-2

Trivedi, D., Colin, E., Louie, C. M., & Williams, D. S. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0015-12.2012 · Cited by 70 · see citing works

Structural Studies of Ciliary Components

Mizuno, N., Taschner, M. J., Engel, B. D., & Lorentzen, E. (2012) · Journal of Molecular Biology · doi:10.1016/j.jmb.2012.05.040 · Cited by 69 · see citing works

Rabs and other small GTPases in ciliary transport

Lim, Y. S., Chua, C. E. L., & Tang, B. L. (2011) · Biology of the Cell · doi:10.1042/bc20100150 · Cited by 69 · see citing works

Intraflagellar transport proteins in ciliogenesis of photoreceptor cells

Sedmak, T., & Wolfrum, U. (2011) · Biology of the Cell · doi:10.1042/bc20110034 · Cited by 68 · see citing works

A novel function for the atypical small G protein Rab-like 5 in the assembly of the trypanosome flagellum

Adhiambo, C., Blisnick, T., Toutirais, G., Delannoy, E., & Bastin, P. (2009) · Journal of Cell Science · doi:10.1242/jcs.040444 · Cited by 65 · see citing works

The AP-1 clathrin adaptor facilitates cilium formation and functions with RAB-8 in C. elegans ciliary membrane transport

Kaplan, O. I., Molla‐Herman, A., Cevik, S., et al. (2010) · Journal of Cell Science · doi:10.1242/jcs.073908 · Cited by 59 · see citing works

Small molecule inhibitors of Smoothened ciliary localization and ciliogenesis

Wu, V., Chen, S. C., Arkin, M. R., & Reiter, J. F. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1207170109 · Cited by 56 · see citing works

Arl3 and RP2 mediated assembly and traffic of membrane associated cilia proteins

Schwarz, N., Hardcastle, A. J., & Cheetham, M. E. (2012) · Vision Research · doi:10.1016/j.visres.2012.07.016 · Cited by 54 · see citing works

The Retrograde IFT Machinery of C. elegans Cilia: Two IFT Dynein Complexes?

Hao, L., Efimenko, E., Swoboda, P., & Scholey, J. M. (2011) · PLoS ONE · doi:10.1371/journal.pone.0020995 · Cited by 47 · see citing works

The emerging role of Arf/Arl small GTPases in cilia and ciliopathies

Li, Y., Ling, K., & Hu, J. (2012) · Journal of Cellular Biochemistry · doi:10.1002/jcb.24116 · Cited by 43 · see citing works

The motile cilium in development and disease: emerging new insights

Roy, S. (2009) · BioEssays · doi:10.1002/bies.200900031 · Cited by 43 · see citing works

The X-linked retinitis pigmentosa protein RP2 facilitates G protein traffic

Schwarz, N., Novoselova, T. V., Wait, R., Hardcastle, A. J., & Cheetham, M. E. (2011) · Human Molecular Genetics · doi:10.1093/hmg/ddr520 · Cited by 35 · see citing works

Tubulin and tektin in sea urchin embryonic cilia: pathways of protein incorporation during turnover and regeneration

Stephens, R. E. (1994) · Journal of Cell Science · doi:10.1242/jcs.107.2.683 · Cited by 33 · see citing works

The RJL family of small GTPases is an ancient eukaryotic invention probably functionally associated with the flagellar apparatus

Eliáš, M., & Archibald, J. M. (2009) · Gene · doi:10.1016/j.gene.2009.04.011 · Cited by 28 · see citing works

Mutations in a Guanylate Cyclase GCY-35/GCY-36 Modify Bardet-Biedl Syndrome–Associated Phenotypes in Caenorhabditis elegans

Mok, C. A., Healey, M. P., Shekhar, T., Leroux, M. R., Héon, E., & Zhen, M. (2011) · PLoS Genetics · doi:10.1371/journal.pgen.1002335 · Cited by 19 · see citing works

Rab23 is a flagellar protein in Trypanosoma brucei

Lumb, J. H., & Field, M. C. (2011) · BMC Research Notes · doi:10.1186/1756-0500-4-190 · Cited by 16 · see citing works

The GTPase TcRjl of the human pathogen Trypanosoma cruzi is involved in the cell growth and differentiation

dos Santos, G. R. R. M., Nepomuceno‐Silva, J. L., de Melo, L. D. B., et al. (2012) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2012.01.119 · Cited by 13 · see citing works

Who drives the ciliary highway?

Malicki, J. J. (2012) · BioArchitecture · doi:10.4161/bioa.21101 · Cited by 12 · see citing works

Genes and molecular pathways underpinning ciliopathies

Reiter, J. F., & Leroux, M. R. (2017) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm.2017.60 · Cited by 1,588 · see citing works

Cellular signalling by primary cilia in development, organ function and disease

Anvarian, Z., Mykytyn, K., Mukhopadhyay, S., Pedersen, L. B., & Christensen, S. T. (2019) · Nature Reviews Nephrology · doi:10.1038/s41581-019-0116-9 · Cited by 845 · see citing works

Ins and outs of GPCR signaling in primary cilia

Schou, K. B., Pedersen, L. B., & Christensen, S. T. (2015) · The EMBO Reports · doi:10.15252/embr.201540530 · Cited by 221 · see citing works

How do cilia organize signalling cascades?

Nachury, M. V. (2014) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2013.0465 · Cited by 150 · see citing works

Intraflagellar transport-A complex mediates ciliary entry and retrograde trafficking of ciliary G protein–coupled receptors

Hirano, T., Katoh, Y., & Nakayama, K. (2017) · Molecular Biology of the Cell · doi:10.1091/mbc.e16-11-0813 · Cited by 141 · see citing works

Ciliary ectosomes: transmissions from the cell's antenna

Wood, C. R., & Rosenbaum, J. L. (2015) · Trends in Cell Biology · doi:10.1016/j.tcb.2014.12.008 · Cited by 153 · see citing works

Multiciliated Cells in Animals

Meunier, A., & Azimzadeh, J. (2016) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a028233 · Cited by 117 · see citing works

Propulsive nanomachines: the convergent evolution of archaella, flagella and cilia

Beeby, M., Ferreira, J. L., Tripp, P., Albers, S.-V., & Mitchell, D. R. (2020) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuaa006 · Cited by 110 · see citing works

TGF-β receptor I/II trafficking and signaling at primary cilia are inhibited by ceramide to attenuate cell migration and tumor metastasis

Gencer, S., Oleinik, N., Kim, J., Panneer Selvam, S., De Palma, R., Dany, M., Nganga, R., Thomas, R. J., Senkal, C. E., Howe, P. H., et al. (2017) · Science Signaling · doi:10.1126/scisignal.aam7464 · Cited by 83 · see citing works

Ciliopathy-associated mutations of IFT122 impair ciliary protein trafficking but not ciliogenesis

Takahara, M., Katoh, Y., Nakamura, K., Hirano, T., Sugawa, M., Tsurumi, Y., & Nakayama, K. (2018) · Human Molecular Genetics · doi:10.1093/hmg/ddx421 · Cited by 62 · see citing works

Regulation of ciliary membrane protein trafficking and signalling by kinesin motor proteins

Morthorst, S. K., Christensen, S. T., & Pedersen, L. B. (2018) · The FEBS Journal · doi:10.1111/febs.14583 · Cited by 49 · see citing works

Loss of ift122, a Retrograde Intraflagellar Transport (IFT) Complex Component, Leads to Slow, Progressive Photoreceptor Degeneration Due to Inefficient Opsin Transport

Boubakri, M., Chaya, T., Hirata, H., Kajimura, N., Kuwahara, R., Ueno, A., Malicki, J., Furukawa, T., & Omori, Y. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.738658 · Cited by 39 · see citing works

TGF‐β Suppresses Ift88 Expression in Chondrocytic ATDC5 Cells

Kawasaki, M., Ezura, Y., Hayata, T., Notomi, T., Izu, Y., & Noda, M. (2015) · Journal of Cellular Physiology · doi:10.1002/jcp.25005 · Cited by 26 · see citing works

PACRG, a protein linked to ciliary motility, mediates cellular signaling

Loucks, C. M., Bialas, N. J., Dekkers, M. P. J., Walker, D. S., Grundy, L. J., Li, C., Inglis, P. N., Kida, K., Schafer, W. R., Blacque, O. E., et al. (2016) · Molecular Biology of the Cell · doi:10.1091/mbc.e15-07-0490 · Cited by 23 · see citing works

Role of Intraflagellar Transport and Primary Cilia in Skeletal Development

Serra, R. A. (2008) · The Anatomical Record · doi:10.1002/ar.20634 · Cited by 51 · see citing works

Intraflagellar transport

Rosenbaum, J. L., & Witman, G. B. (2002) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm952 · Cited by 1,423 · see citing works

Ciliary Length Control

Broekhuis, J. R. (2007) · RePub (Erasmus University Rotterdam)

Intraflagellar transport and cilia-dependent diseases

Pazour, G. J., & Rosenbaum, J. L. (2002) · Trends in Cell Biology · doi:10.1016/s0962-8924(02)02410-8 · Cited by 294 · see citing works

Regulation of Cilium Length and Intraflagellar Transport

(2013) · International Review of Cell and Molecular Biology · doi:10.1016/b978-0-12-407697-6.00003-9 · Cited by 63 · see citing works