T. Avidor-reiss, A. Maer, E. Koundakjian, A. Polyanovsky, T. Keil et al., Decoding Cilia Function, Cell, vol.117, issue.4, pp.527-539, 2004.
DOI : 10.1016/S0092-8674(04)00412-X

J. Li, J. Gerdes, C. Haycraft, Y. Fan, T. Teslovich et al., Comparative Genomics Identifies a Flagellar and Basal Body Proteome that Includes the BBS5 Human Disease Gene, Cell, vol.117, issue.4, pp.541-552, 2004.
DOI : 10.1016/S0092-8674(04)00450-7

L. Kohl and P. Bastin, The Flagellum of Trypanosomes, Int Rev Cytol, vol.244, pp.227-285, 2005.
DOI : 10.1016/S0074-7696(05)44006-1
URL : https://hal.archives-ouvertes.fr/hal-00109408

J. Besharse and C. Horst, The photoreceptor connecting cilium: a model for the transition zone Ciliary and Flagellar Membranes, pp.389-417, 1990.

P. Burton, Ultrastructural studies of microtubules and microtubule organizing centers of the vertebrate olfactory neuron, Microscopy Research and Technique, vol.92, issue.2, pp.142-156, 1992.
DOI : 10.1002/jemt.1070230205

D. Wheatley, Landmarks in the first hundred years of primary (9+0) cilium research, Cell Biology International, vol.29, issue.5, pp.333-339, 2005.
DOI : 10.1016/j.cellbi.2005.03.001

B. Afzelius, A human syndrome caused by immotile cilia, Science, vol.193, issue.4250, pp.317-319, 1976.
DOI : 10.1126/science.1084576

G. Pazour, B. Dickert, Y. Vucica, E. Seeley, J. Rosenbaum et al., 737, Are Required for Assembly of Cilia and Flagella, The Journal of Cell Biology, vol.150, issue.3, pp.709-718, 2000.
DOI : 10.1083/jcb.129.1.169

B. Yoder, X. Hou, and L. Guay-woodford, The Polycystic Kidney Disease Proteins, Polycystin-1, Polycystin-2, Polaris, and Cystin, Are Co-Localized in Renal Cilia, Journal of the American Society of Nephrology, vol.13, issue.10, pp.2508-2516, 2002.
DOI : 10.1097/01.ASN.0000029587.47950.25

J. Davenport and B. Yoder, An incredible decade for the primary cilium: a look at a once-forgotten organelle, AJP: Renal Physiology, vol.289, issue.6, pp.1159-1169, 2005.
DOI : 10.1152/ajprenal.00118.2005

D. Huangfu, A. Liu, A. Rakeman, N. Murcia, L. Niswander et al., Hedgehog signalling in the mouse requires intraflagellar transport proteins, Nature, vol.426, issue.6962, pp.83-87, 2003.
DOI : 10.1038/nature02061

L. Vincensini, T. Blisnick, and P. Bastin, 1001 model organisms to study cilia and flagella, Biology of the Cell, vol.69, issue.3, pp.109-130, 2011.
DOI : 10.1042/BC20100104

G. Adams, B. Huang, and D. Luck, Temperature-sensitive, assembly-defective flagella mutants of CHLAMYDOMONAS REINHARDTII, Genetics, vol.100, pp.579-586, 1982.

J. Buisson and P. Bastin, Flagellum Structure and Function in Trypanosomes, Structures and Organelles in Pathogenic Protists, pp.63-86, 2010.
DOI : 10.1007/978-3-642-12863-9_3

S. Absalon, T. Blisnick, M. Bonhivers, L. Kohl, N. Cayet et al., Flagellum elongation is required for correct structure, orientation and function of the flagellar pocket in Trypanosoma brucei, Journal of Cell Science, vol.121, issue.22, pp.3704-3716, 2008.
DOI : 10.1242/jcs.035626
URL : https://hal.archives-ouvertes.fr/hal-00426339

R. Sharma, E. Gluenz, L. Peacock, W. Gibson, K. Gull et al., The heart of darkness: growth and form of Trypanosoma brucei in the tsetse fly, Trends in Parasitology, vol.25, issue.11, pp.517-524, 2009.
DOI : 10.1016/j.pt.2009.08.001

G. Pazour, N. Agrin, J. Leszyk, and G. Witman, Proteomic analysis of a eukaryotic cilium, The Journal of Cell Biology, vol.63, issue.1, pp.103-113, 2005.
DOI : 10.1242/jcs.01297

R. Broadhead, H. Dawe, H. Farr, S. Griffiths, S. Hart et al., Flagellar motility is required for the viability of the bloodstream trypanosome, Nature, vol.323, issue.7081, pp.224-227, 2006.
DOI : 10.1038/nature04541

P. Overath and M. Engstler, Endocytosis, membrane recycling and sorting of GPI-anchored proteins: Trypanosoma brucei as a model system, Molecular Microbiology, vol.113, issue.3, pp.735-744, 2004.
DOI : 10.1111/j.1365-2958.2004.04224.x

P. Bastin, K. Matthews, and K. Gull, The paraflagellar rod of kinetoplastida: Solved and unsolved questions, Parasitology Today, vol.12, issue.8, pp.302-307, 1996.
DOI : 10.1016/0169-4758(96)10031-4

C. Santrich, L. Moore, T. Sherwin, P. Bastin, C. Brokaw et al., A motility function for the paraflagellar rod of Leishmania parasites revealed by PFR-2 gene knockouts, Molecular and Biochemical Parasitology, vol.90, issue.1, pp.95-109, 1997.
DOI : 10.1016/S0166-6851(97)00149-7

P. Bastin, T. Sherwin, and K. Gull, Paraflagellar rod is vital for trypanosome motility, Nature, vol.391, issue.6667, p.548, 1998.
DOI : 10.1038/35300

N. Portman, S. Lacomble, B. Thomas, P. Mckean, and K. Gull, Combining RNA Interference Mutants and Comparative Proteomics to Identify Protein Components and Dependences in a Eukaryotic Flagellum, Journal of Biological Chemistry, vol.284, issue.9, pp.5610-5619, 2009.
DOI : 10.1074/jbc.M808859200

W. Dentler and J. Rosenbaum, Flagellar elongation and shortening in Chlamydomonas. III. structures attached to the tips of flagellar microtubules and their relationship to the directionality of flagellar microtubule assembly, The Journal of Cell Biology, vol.74, issue.3, pp.747-759, 1977.
DOI : 10.1083/jcb.74.3.747

D. Woolley, C. Gadelha, and K. Gull, Evidence for a sliding-resistance at the tip of the trypanosome flagellum, Cell Motility and the Cytoskeleton, vol.83, issue.12, pp.741-746, 2006.
DOI : 10.1002/cm.20159

T. Cavalier-smith, Basal body and flagellar development during the vegetative cell cycle and the sexual cycle of Chlamydomonas reinhardii, J Cell Sci, vol.16, pp.529-556, 1974.

T. Sherwin and K. Gull, The Cell Division Cycle of Trypanosoma brucei brucei: Timing of Event Markers and Cytoskeletal Modulations, Philosophical Transactions of the Royal Society B: Biological Sciences, vol.323, issue.1218, pp.573-588, 1989.
DOI : 10.1098/rstb.1989.0037

R. Woodward and K. Gull, Timing of nuclear and kinetoplast DNA replication and early morphological events in the cell cycle of Trypanosoma brucei, J Cell Sci, vol.95, pp.49-57, 1990.

E. Ogbadoyi and D. Robinson, A High-Order Trans-Membrane Structural Linkage Is Responsible for Mitochondrial Genome Positioning and Segregation by Flagellar Basal Bodies in Trypanosomes, Molecular Biology of the Cell, vol.14, issue.5, pp.1769-1779, 2003.
DOI : 10.1091/mbc.E02-08-0525

F. Moreira-leite, T. Sherwin, L. Kohl, and K. Gull, A Trypanosome Structure Involved in Transmitting Cytoplasmic Information During Cell Division, Science, vol.294, issue.5542, pp.610-612, 2001.
DOI : 10.1126/science.1063775

L. Briggs, P. Mckean, A. Baines, F. Moreira-leite, J. Davidge et al., The flagella connector of Trypanosoma brucei: an unusual mobile transmembrane junction, Journal of Cell Science, vol.117, issue.9, pp.1641-1651, 2004.
DOI : 10.1242/jcs.00995

L. Kohl, D. Robinson, and P. Bastin, Novel roles for the flagellum in cell morphogenesis and cytokinesis of trypanosomes, The EMBO Journal, vol.22, issue.20, pp.5336-5346, 2003.
DOI : 10.1093/emboj/cdg518
URL : https://hal.archives-ouvertes.fr/hal-00108210

K. Johnson and J. Rosenbaum, Polarity of flagellar assembly in Chlamydomonas, The Journal of Cell Biology, vol.119, issue.6, pp.1605-1611, 1992.
DOI : 10.1083/jcb.119.6.1605

W. Marshall and J. Rosenbaum, Intraflagellar transport balances continuous turnover of outer doublet microtubules, The Journal of Cell Biology, vol.10, issue.3, pp.405-414, 2001.
DOI : 10.1083/jcb.113.6.1255

P. Bastin, T. Macrae, S. Francis, K. Matthews, and K. Gull, Flagellar Morphogenesis: Protein Targeting and Assembly in the Paraflagellar Rod of Trypanosomes, Molecular and Cellular Biology, vol.19, issue.12, pp.8191-8200, 1999.
DOI : 10.1128/MCB.19.12.8191

K. Kozminski, K. Johnson, P. Forscher, and J. Rosenbaum, A motility in the eukaryotic flagellum unrelated to flagellar beating., Proceedings of the National Academy of Sciences, vol.90, issue.12, pp.5519-5523, 1993.
DOI : 10.1073/pnas.90.12.5519

D. Ringo, FLAGELLAR MOTION AND FINE STRUCTURE OF THE FLAGELLAR APPARATUS IN CHLAMYDOMONAS, The Journal of Cell Biology, vol.33, issue.3, pp.543-571, 1967.
DOI : 10.1083/jcb.33.3.543

M. Vashishtha, Z. Walther, and J. Hall, The kinesin-homologous protein encoded by the Chlamydomonas FLA10 gene is associated with basal bodies and centrioles, J Cell Sci, vol.109, pp.541-549, 1996.

K. Kozminski, P. Beech, and J. Rosenbaum, The Chlamydomonas kinesin-like protein FLA10 is involved in motility associated with the flagellar membrane, The Journal of Cell Biology, vol.131, issue.6, pp.1517-1527, 1995.
DOI : 10.1083/jcb.131.6.1517

G. Pigino, S. Geimer, S. Lanzavecchia, E. Paccagnini, F. Cantele et al., Electron-tomographic analysis of intraflagellar transport particle trains in situ, The Journal of Cell Biology, vol.254, issue.1, pp.135-148, 2009.
DOI : 10.1006/jsbi.1997.3934

D. Cole, S. Chinn, K. Wedaman, K. Hall, T. Vuong et al., Novel heterotrimeric kinesin-related protein purified from sea urchin eggs, Nature, vol.366, issue.6452, pp.268-270, 1993.
DOI : 10.1038/366268a0

G. Piperno and K. Mead, Transport of a novel complex in the cytoplasmic matrix of Chlamydomonas flagella, Proceedings of the National Academy of Sciences, vol.94, issue.9, pp.4457-4462, 1997.
DOI : 10.1073/pnas.94.9.4457

D. Cole, D. Diener, A. Himelblau, P. Beech, J. Fuster et al., Sensory Neurons, The Journal of Cell Biology, vol.47, issue.4, pp.993-1008, 1998.
DOI : 10.1073/pnas.93.16.8443

T. Van-dam, M. Townsend, M. Turk, A. Schlessinger, A. Sali et al., Evolution of modular intraflagellar transport from a coatomer-like progenitor, Proceedings of the National Academy of Sciences, vol.110, issue.17, pp.6943-6948, 2013.
DOI : 10.1073/pnas.1221011110

L. Briggs, J. Davidge, B. Wickstead, M. Ginger, and K. Gull, More than one way to build a flagellum: comparative genomics of parasitic protozoa, Current Biology, vol.14, issue.15, pp.611-612, 2004.
DOI : 10.1016/j.cub.2004.07.041

N. Ahmed, C. Gao, B. Lucker, D. Cole, and D. Mitchell, ODA16 aids axonemal outer row dynein assembly through an interaction with the intraflagellar transport machinery, The Journal of Cell Biology, vol.109, issue.2, pp.313-322, 2008.
DOI : 10.1146/annurev.physiol.69.040705.141301

S. Absalon, T. Blisnick, L. Kohl, G. Toutirais, G. Dore et al., Intraflagellar Transport and Functional Analysis of Genes Required for Flagellum Formation in Trypanosomes, Molecular Biology of the Cell, vol.19, issue.3, pp.929-944, 2008.
DOI : 10.1091/mbc.E07-08-0749
URL : https://hal.archives-ouvertes.fr/pasteur-00217549

G. Pazour, B. Dickert, and G. Witman, The DHC1b (DHC2) Isoform of Cytoplasmic Dynein Is Required for Flagellar Assembly, The Journal of Cell Biology, vol.107, issue.3, pp.473-481, 1999.
DOI : 10.1083/jcb.137.7.1537

G. Pazour, C. Wilkerson, and G. Witman, A Dynein Light Chain Is Essential for the Retrograde Particle Movement of Intraflagellar Transport (IFT), The Journal of Cell Biology, vol.108, issue.4, 1998.
DOI : 10.1073/pnas.91.6.2100

M. Porter, R. Bower, J. Knott, P. Byrd, and W. Dentler, Cytoplasmic Dynein Heavy Chain 1b Is Required for Flagellar Assembly in Chlamydomonas, Molecular Biology of the Cell, vol.10, issue.3, pp.693-712, 1999.
DOI : 10.1091/mbc.10.3.693

D. Julkowska and P. Bastin, Tools for Analyzing Intraflagellar Transport in Trypanosomes, Methods Cell Biol, vol.93, pp.59-80, 2009.
DOI : 10.1016/S0091-679X(08)93003-X

J. Scholey, Kinesin-2: A Family of Heterotrimeric and Homodimeric Motors with Diverse Intracellular Transport Functions, Annual Review of Cell and Developmental Biology, vol.29, issue.1, pp.443-469, 2013.
DOI : 10.1146/annurev-cellbio-101512-122335

S. Nonaka, Y. Tanaka, Y. Okada, S. Takeda, A. Harada et al., Randomization of Left???Right Asymmetry due to Loss of Nodal Cilia Generating Leftward Flow of Extraembryonic Fluid in Mice Lacking KIF3B Motor Protein, Cell, vol.95, issue.6, pp.829-837, 1998.
DOI : 10.1016/S0092-8674(00)81705-5

J. Brown, C. Hardin, and J. Gaertig, ROTOKINESIS, A NOVEL PHENOMENON OF CELL LOCOMOTION-ASSISTED CYTOKINESIS IN THE CILIATE TETRAHYMENA THERMOPHILA, Cell Biology International, vol.23, issue.12, pp.841-848, 1999.
DOI : 10.1006/cbir.1999.0480

Z. Sun, A. Amsterdam, G. Pazour, D. Cole, M. Miller et al., A genetic screen in zebrafish identifies cilia genes as a principal cause of cystic kidney, Development, vol.131, issue.16, pp.4085-4093, 2004.
DOI : 10.1242/dev.01240

C. Adhiambo, J. Forney, D. Asai, and J. Lebowitz, The two cytoplasmic dynein-2 isoforms in Leishmania mexicana perform separate functions, Molecular and Biochemical Parasitology, vol.143, issue.2, 2005.
DOI : 10.1016/j.molbiopara.2005.04.017

E. Brooks and J. Wallingford, Control of vertebrate intraflagellar transport by the planar cell polarity effector Fuz, The Journal of Cell Biology, vol.198, issue.1, pp.37-45, 2012.
DOI : 10.1007/978-1-60761-376-3_2

L. Pedersen, S. Geimer, and J. Rosenbaum, Dissecting the Molecular Mechanisms of Intraflagellar Transport in Chlamydomonas, Current Biology, vol.16, issue.5, pp.450-459, 2006.
DOI : 10.1016/j.cub.2006.02.020

P. Lefebvre, C. Silflow, E. Wieben, and J. Rosenbaum, Increased levels of mRNAs for tubulin and other flagellar proteins after amputation or shortening of Chlamydomonas Flagella, Cell, vol.20, issue.2, pp.469-477, 1980.
DOI : 10.1016/0092-8674(80)90633-9

J. Davies and A. Grossman, Sequences controlling transcription of the Chlamydomonas reinhardtii beta 2-tubulin gene after deflagellation and during the cell cycle., Molecular and Cellular Biology, vol.14, issue.8, pp.5165-5174, 1994.
DOI : 10.1128/MCB.14.8.5165

C. Wood, Z. Wang, D. Diener, J. Zones, J. Rosenbaum et al., IFT Proteins Accumulate during Cell Division and Localize to the Cleavage Furrow in Chlamydomonas, PLoS ONE, vol.29, issue.2, p.30729, 2012.
DOI : 10.1371/journal.pone.0030729.s008

V. Stolc, M. Samanta, W. Tongprasit, and W. Marshall, Genome-wide transcriptional analysis of flagellar regeneration in Chlamydomonas reinhardtii identifies orthologs of ciliary disease genes, Proceedings of the National Academy of Sciences, vol.102, issue.10, pp.3703-3707, 2005.
DOI : 10.1073/pnas.0408358102

S. Archer, D. Inchaustegui, R. Queiroz, and C. Clayton, The Cell Cycle Regulated Transcriptome of Trypanosoma brucei, PLoS ONE, vol.23, issue.Pt 7, p.18425, 2011.
DOI : 10.1371/journal.pone.0018425.s007

L. Kohl, T. Sherwin, and K. Gull, Assembly of the Paraflagellar Rod and the Flagellum Attachment Zone Complex During the Trypanosoma brucei Cell Cycle, The Journal of Eukaryotic Microbiology, vol.95, issue.2, pp.105-109, 1999.
DOI : 10.1083/jcb.104.3.439

J. Rosenbaum, J. Moulder, and D. Ringo, FLAGELLAR ELONGATION AND SHORTENING IN CHLAMYDOMONAS: The Use of Cycloheximide and Colchicine to Study the Synthesis and Assembly of Flagellar Proteins, The Journal of Cell Biology, vol.41, issue.2, pp.600-619, 1969.
DOI : 10.1083/jcb.41.2.600

B. Engel, W. Ludington, and W. Marshall, Intraflagellar transport particle size scales inversely with flagellar length: revisiting the balance-point length control model, The Journal of Cell Biology, vol.47, issue.1, pp.81-89, 2009.
DOI : 10.1128/EC.3.5.1307-1319.2004

J. Deane, D. Cole, E. Seeley, D. Diener, and J. Rosenbaum, Localization of intraflagellar transport protein IFT52 identifies basal body transitional fibers as the docking site for IFT particles, Current Biology, vol.11, issue.20, pp.1586-1590, 2001.
DOI : 10.1016/S0960-9822(01)00484-5

E. Richey and H. Qin, Dissecting the Sequential Assembly and Localization of Intraflagellar Transport Particle Complex B in Chlamydomonas, PLoS ONE, vol.7, issue.8, p.43118, 2012.
DOI : 10.1371/journal.pone.0043118.g008

R. Behal, M. Miller, H. Qin, B. Lucker, A. Jones et al., Subunit Interactions and Organization of the Chlamydomonas reinhardtii Intraflagellar Transport Complex A Proteins, Journal of Biological Chemistry, vol.287, issue.15, pp.11689-11703, 2012.
DOI : 10.1074/jbc.M111.287102

M. Taschner, S. Bhogaraju, M. Vetter, M. Morawetz, and E. Lorentzen, Biochemical Mapping of Interactions within the Intraflagellar Transport (IFT) B Core Complex, Journal of Biological Chemistry, vol.286, issue.30, pp.26344-26352, 2011.
DOI : 10.1074/jbc.M111.254920

W. Dentler, flagella, The Journal of Cell Biology, vol.89, issue.4, pp.649-659, 2005.
DOI : 10.1083/jcb.126.1.175

J. Buisson, N. Chenouard, T. Lagache, T. Blisnick, J. Olivo-marin et al., Intraflagellar transport proteins cycle between the flagellum and its base, Journal of Cell Science, vol.126, issue.1, pp.327-338, 2013.
DOI : 10.1242/jcs.117069

C. Iomini, V. Babaev-khaimov, M. Sassaroli, and G. Piperno, Flagella Undergo a Transport Cycle Consisting of Four Phases, The Journal of Cell Biology, vol.1, issue.1, pp.13-24, 2001.
DOI : 10.1083/jcb.126.1.175

H. Qin, Z. Wang, D. Diener, and J. Rosenbaum, Intraflagellar Transport Protein 27 Is a Small G Protein Involved in Cell-Cycle Control, Current Biology, vol.17, issue.3, pp.193-202, 2007.
DOI : 10.1016/j.cub.2006.12.040

K. Lechtreck, E. Johnson, T. Sakai, D. Cochran, B. Ballif et al., BBSome is an IFT cargo required for export of specific signaling proteins from flagella, The Journal of Cell Biology, vol.47, issue.7, pp.1117-1132, 2009.
DOI : 10.1172/JCI37041

M. Miller, J. Esparza, A. Lippa, F. Lux, . Iii et al., Mutant Kinesin-2 Motor Subunits Increase Chromosome Loss, Molecular Biology of the Cell, vol.16, issue.8, pp.3810-3820, 2005.
DOI : 10.1091/mbc. E05-05-0404

J. Mueller, C. Perrone, R. Bower, D. Cole, and M. Porter, The FLA3 KAP Subunit Is Required for Localization of Kinesin-2 to the Site of Flagellar Assembly and Processive Anterograde Intraflagellar Transport, Molecular Biology of the Cell, vol.16, issue.3, pp.1341-1354, 2005.
DOI : 10.1091/mbc.E04-10-0931

M. Berriman, E. Ghedin, C. Hertz-fowler, G. Blandin, H. Renauld et al., The Genome of the African Trypanosome Trypanosoma brucei, Science, vol.309, issue.5733, pp.416-422, 2005.
DOI : 10.1126/science.1112642

H. Kee, J. Dishinger, T. Blasius, C. Liu, B. Margolis et al., A size-exclusion permeability barrier and nucleoporins characterize a ciliary pore complex that regulates transport into cilia, Nature Cell Biology, vol.19, issue.4, pp.431-437, 2012.
DOI : 10.1083/jcb.201001057

J. Franklin and E. Ullu, Biochemical analysis of PIFTC3, the Trypanosoma brucei orthologue of nematode DYF-13, reveals interactions with established and putative intraflagellar transport components, Molecular Microbiology, vol.178, pp.173-186, 2010.
DOI : 10.1111/j.1365-2958.2010.07322.x

D. Silva, X. Huang, R. Behal, D. Cole, and H. Qin, The RABL5 homolog IFT22 regulates the cellular pool size and the amount of IFT particles partitioned to the flagellar compartment in Chlamydomonas reinhardtii, Cytoskeleton, vol.192, issue.6, pp.33-48, 2012.
DOI : 10.1002/cm.20546

C. Adhiambo, T. Blisnick, G. Toutirais, E. Delannoy, and P. Bastin, A novel function for the atypical small G protein Rab-like 5 in the assembly of the trypanosome flagellum, Journal of Cell Science, vol.122, issue.6, pp.834-841, 2009.
DOI : 10.1242/jcs.040444

C. Wood, K. Huang, D. Diener, and J. Rosenbaum, The Cilium Secretes Bioactive Ectosomes, Current Biology, vol.23, issue.10, pp.906-911, 2013.
DOI : 10.1016/j.cub.2013.04.019

R. Brown, S. Johnson, and H. Bold, ELECTRON AND PHASE-CONTRAST MICROSCOPY OF SEXUAL REPRODUCTION IN CHLAMYDOMONAS MOEWUSII, Journal of Phycology, vol.8, issue.2, pp.100-120, 1968.
DOI : 10.1002/jcp.1030610308

K. Bergman, U. Goodenough, D. Goodenough, J. Jawitz, and H. Martin, Gametic differentiation in Chlamydomonas reinhardtii. II. Flagellar membranes and the agglutination reaction, The Journal of Cell Biology, vol.67, issue.3, pp.606-622, 1975.
DOI : 10.1083/jcb.67.3.606

W. Dentler, A Role for the Membrane in Regulating Chlamydomonas Flagellar Length, PLoS ONE, vol.47, issue.1, p.53366, 2013.
DOI : 10.1371/journal.pone.0053366.s007

P. Rompolas, L. Pedersen, R. Patel-king, and S. King, Chlamydomonas FAP133 is a dynein intermediate chain associated with the retrograde intraflagellar transport motor, Journal of Cell Science, vol.120, issue.20, pp.3653-3665, 2007.
DOI : 10.1242/jcs.012773

K. Pfister, E. Fisher, I. Gibbons, T. Hays, E. Holzbaur et al., Cytoplasmic dynein nomenclature: Table I., The Journal of Cell Biology, vol.108, issue.3, pp.411-413, 2005.
DOI : 10.1073/pnas.90.17.7928

R. Patel-king, R. Gilberti, E. Hom, and S. King, WD60/FAP163 is a dynein intermediate chain required for retrograde intraflagellar transport in cilia, Molecular Biology of the Cell, vol.24, issue.17, pp.2668-2677, 2013.
DOI : 10.1091/mbc.E13-05-0266

B. Gibbons, D. Asai, W. Tang, T. Hays, and I. Gibbons, Phylogeny and expression of axonemal and cytoplasmic dynein genes in sea urchins., Molecular Biology of the Cell, vol.5, issue.1, pp.57-70, 1994.
DOI : 10.1091/mbc.5.1.57

C. Iomini, L. Li, J. Esparza, and S. Dutcher, Retrograde Intraflagellar Transport Mutants Identify Complex A Proteins With Multiple Genetic Interactions in Chlamydomonas reinhardtii, Genetics, vol.183, issue.3, pp.885-896, 2009.
DOI : 10.1534/genetics.109.101915

G. Piperno, E. Siuda, S. Henderson, M. Segil, H. Vaananen et al., Distinct Mutants of Retrograde Intraflagellar Transport (IFT) Share Similar Morphological and Molecular Defects, The Journal of Cell Biology, vol.47, issue.6, pp.1591-1601, 1998.
DOI : 10.1083/jcb.126.1.175

I. Perrault, S. Saunier, S. Hanein, E. Filhol, A. Bizet et al., Mainzer-Saldino Syndrome Is a Ciliopathy Caused by IFT140 Mutations, The American Journal of Human Genetics, vol.90, issue.5, pp.864-870, 2012.
DOI : 10.1016/j.ajhg.2012.03.006
URL : https://hal.archives-ouvertes.fr/inserm-00752958

E. Davis, Q. Zhang, Q. Liu, B. Diplas, L. Davey et al., TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum, Nature Genetics, vol.36, issue.3, pp.189-196, 2012.
DOI : 10.1073/pnas.0610155104

H. Arts, E. Bongers, D. Mans, S. Van-beersum, M. Oud et al., C14ORF179 encoding IFT43 is mutated in Sensenbrenner syndrome, Journal of Medical Genetics, vol.48, issue.6, pp.390-395, 2011.
DOI : 10.1136/jmg.2011.088864
URL : https://hal.archives-ouvertes.fr/hal-00613258

H. Hoops and G. Witman, Outer doublet heterogeneity reveals structural polarity related to beat direction in Chlamydomonas flagella, The Journal of Cell Biology, vol.97, issue.3, pp.902-908, 1983.
DOI : 10.1083/jcb.97.3.902

W. Marshall, H. Qin, R. Brenni, M. Rosenbaum, and J. , Flagellar Length Control System: Testing a Simple Model Based on Intraflagellar Transport and Turnover, Molecular Biology of the Cell, vol.16, issue.1, pp.270-278, 2005.
DOI : 10.1091/mbc.E04-07-0586

B. Rotureau, I. Subota, and P. Bastin, Molecular bases of cytoskeleton plasticity during the Trypanosoma brucei parasite cycle, Cellular Microbiology, vol.95, issue.5, pp.705-716, 2011.
DOI : 10.1111/j.1462-5822.2010.01566.x
URL : https://hal.archives-ouvertes.fr/pasteur-01371324