L. Kapitein and C. Hoogenraad, Which way to go? Cytoskeletal organization and polarized transport in neurons, Molecular and Cellular Neuroscience, vol.46, issue.1, pp.9-20, 2011.
DOI : 10.1016/j.mcn.2010.08.015

B. Clark, E. Goldberg, and R. B. , Electrogenic Tuning of the Axon Initial Segment, The Neuroscientist, vol.12, issue.6, pp.651-668, 2009.
DOI : 10.1083/jcb.143.5.1295

M. Rasband, The axon initial segment and the maintenance of neuronal polarity, Nature Reviews Neuroscience, vol.64, issue.8, pp.552-562, 2010.
DOI : 10.1113/jphysiol.1973.sp010273

A. Brachet, Ankyrin G restricts ion channel diffusion at the axonal initial segment before the establishment of the diffusion barrier, The Journal of Cell Biology, vol.79, issue.2, pp.383-395, 2010.
DOI : 10.1083/jcb.201003042.dv
URL : https://hal.archives-ouvertes.fr/hal-01701554

A. Bréchet, Protein kinase CK2 contributes to the organization of sodium channels in axonal membranes by regulating their interactions with ankyrin G, The Journal of Cell Biology, vol.267, issue.6, pp.1101-1114, 2008.
DOI : 10.1083/jcb.143.5.1295

J. Garrido, A Targeting Motif Involved in Sodium Channel Clustering at the Axonal Initial Segment, Science, vol.300, issue.5628, pp.2091-2094, 2003.
DOI : 10.1126/science.1085167

M. Kole, Action potential generation requires a high sodium channel density in the axon initial segment, Nature Neuroscience, vol.26, issue.2, pp.178-186, 2008.
DOI : 10.1113/jphysiol.1982.sp014296

B. Winckler, P. Forscher, and I. Mellman, A diffusion barrier maintains distribution of membrane proteins in polarized neurons, Nature, vol.20, issue.6721, pp.698-701, 1999.
DOI : 10.1016/S0896-6273(00)80468-7

C. Nakada, Accumulation of anchored proteins forms membrane diffusion barriers during neuronal polarization, Nature Cell Biology, vol.20, issue.7, pp.626-632, 2003.
DOI : 10.1021/bi00521a027

A. Song, A Selective Filter for Cytoplasmic Transport at the Axon Initial Segment, Cell, vol.136, issue.6, pp.1148-1160, 2009.
DOI : 10.1016/j.cell.2009.01.016

K. Hedstrom, Y. Ogawa, and M. Rasband, AnkyrinG is required for maintenance of the axon initial segment and neuronal polarity, The Journal of Cell Biology, vol.120, issue.4, pp.635-640, 2008.
DOI : 10.1038/ncb1603

J. Sobotzik, AnkyrinG is required to maintain axo-dendritic polarity in vivo, Proceedings of the National Academy of Sciences, vol.37, issue.2, pp.17564-17569, 2009.
DOI : 10.1016/0165-0270(91)90128-M
URL : http://www.pnas.org/content/106/41/17564.full.pdf

A. Akhmanova and M. Steinmetz, Tracking the ends: a dynamic protein network controls the fate of microtubule tips, Nature Reviews Molecular Cell Biology, vol.112, issue.4, pp.309-322, 2008.
DOI : 10.1038/nrm2369

H. Vacher, Cdk-mediated phosphorylation of the Kv??2 auxiliary subunit regulates Kv1 channel axonal targeting, The Journal of Cell Biology, vol.19, issue.5, pp.813-824, 2011.
DOI : 10.1073/pnas.95.4.1846
URL : https://hal.archives-ouvertes.fr/hal-00751800

C. Gu, The Microtubule Plus-End Tracking Protein EB1 Is Required for Kv1 Voltage-Gated K+ Channel Axonal Targeting, Neuron, vol.52, issue.5, pp.803-816, 2006.
DOI : 10.1016/j.neuron.2006.10.022

S. Geraldo, U. Khanzada, M. Parsons, J. Chilton, and P. Gordon-weeks, Targeting of the F-actin-binding protein drebrin by the microtubule plus-tip protein EB3 is required for neuritogenesis, Nature Cell Biology, vol.93, issue.10, pp.1181-1189, 2008.
DOI : 10.1093/jb/117.2.231

J. Jaworski, Dynamic Microtubules Regulate Dendritic Spine Morphology and Synaptic Plasticity, Neuron, vol.61, issue.1, pp.85-100, 2009.
DOI : 10.1016/j.neuron.2008.11.013
URL : https://doi.org/10.1016/j.neuron.2008.11.013

T. Stepanova, Visualization of Microtubule Growth in Cultured Neurons via the Use of EB3-GFP (End-Binding Protein 3-Green Fluorescent Protein), The Journal of Neuroscience, vol.23, issue.7, pp.2655-2664, 2003.
DOI : 10.1523/JNEUROSCI.23-07-02655.2003

T. Boiko, Ankyrin-Dependent and -Independent Mechanisms Orchestrate Axonal Compartmentalization of L1 Family Members Neurofascin and L1/Neuron-Glia Cell Adhesion Molecule, Journal of Neuroscience, vol.27, issue.3, pp.590-603, 2007.
DOI : 10.1523/JNEUROSCI.4302-06.2007

W. Bu and L. Su, Regulation of microtubule assembly by human EB1 family proteins, Oncogene, vol.20, issue.25, pp.3185-3192, 2001.
DOI : 10.1083/jcb.145.5.993

A. Akhmanova and M. Steinmetz, Microtubule +TIPs at a glance, Journal of Cell Science, vol.123, issue.20, pp.3415-3419, 2010.
DOI : 10.1242/jcs.062414
URL : http://jcs.biologists.org/content/joces/123/20/3415.full.pdf

S. Honnappa, An EB1-Binding Motif Acts as a Microtubule Tip Localization Signal, Cell, vol.138, issue.2, pp.366-376, 2009.
DOI : 10.1016/j.cell.2009.04.065
URL : https://doi.org/10.1016/j.cell.2009.04.065

Y. Komarova, EB1 and EB3 Control CLIP Dissociation from the Ends of Growing Microtubules, Molecular Biology of the Cell, vol.16, issue.11, pp.5334-5345, 2005.
DOI : 10.1091/mbc.E05-07-0614

K. Hedstrom, Neurofascin assembles a specialized extracellular matrix at the axon initial segment, The Journal of Cell Biology, vol.19, issue.5, pp.875-886, 2007.
DOI : 10.1083/jcb.143.5.1295

T. Nakata and N. Hirokawa, Microtubules provide directional cues for polarized axonal transport through interaction with kinesin motor head, The Journal of Cell Biology, vol.112, issue.6, pp.1045-1055, 2003.
DOI : 10.1083/jcb.143.4.1077
URL : http://jcb.rupress.org/content/jcb/162/6/1045.full.pdf

Y. Konishi and M. Setou, Tubulin tyrosination navigates the kinesin-1 motor domain to axons, Nature Neuroscience, vol.196, issue.5, pp.559-567, 2009.
DOI : 10.1083/jcb.200512058

M. Stone, M. Nguyen, J. Tao, D. Allender, and M. Rolls, Global Up-Regulation of Microtubule Dynamics and Polarity Reversal during Regeneration of an Axon from a Dendrite, Molecular Biology of the Cell, vol.21, issue.5, pp.767-777, 2010.
DOI : 10.1091/mbc.E09-11-0967

V. Bennett and J. Healy, Membrane Domains Based on Ankyrin and Spectrin Associated with Cell-Cell Interactions, Cold Spring Harbor Perspectives in Biology, vol.1, issue.6, p.3012, 2009.
DOI : 10.1101/cshperspect.a003012
URL : http://cshperspectives.cshlp.org/content/1/6/a003012.full.pdf

R. Karlsson, P. Katsamba, H. Nordin, E. Pol, and D. Myszka, Analyzing a kinetic titration series using affinity biosensors, Analytical Biochemistry, vol.349, issue.1, pp.136-147, 2006.
DOI : 10.1016/j.ab.2005.09.034

Y. Komarova, EB1 and EB3 Control CLIP Dissociation from the Ends of Growing Microtubules, Molecular Biology of the Cell, vol.16, issue.11, pp.5334-5345, 2005.
DOI : 10.1091/mbc.E05-07-0614

K. Hedstrom, Neurofascin assembles a specialized extracellular matrix at the axon initial segment, The Journal of Cell Biology, vol.19, issue.5, pp.875-886, 2007.
DOI : 10.1083/jcb.143.5.1295

X. Zhang and V. Bennett, -specific Domains, The Journal of Cell Biology, vol.16, issue.6, pp.1571-1581, 1998.
DOI : 10.1074/jbc.273.46.30785

P. Mohler, A. Gramolini, and V. Bennett, The Ankyrin-B C-terminal Domain Determines Activity of Ankyrin-B/G Chimeras in Rescue of Abnormal Inositol 1,4,5-Trisphosphate and Ryanodine Receptor Distribution in Ankyrin-B (???/???) Neonatal Cardiomyocytes, Journal of Biological Chemistry, vol.268, issue.12, pp.10599-10607, 2002.
DOI : 10.1083/jcb.200109026

Y. Komarova, Mammalian end binding proteins control persistent microtubule growth, The Journal of Cell Biology, vol.112, issue.Pt 14, pp.691-706, 2009.
DOI : 10.1016/j.neuron.2004.05.011
URL : http://jcb.rupress.org/content/jcb/184/5/691.full.pdf

Y. Mimori-kiyosue, N. Shiina, and S. Tsukita, The dynamic behavior of the APC-binding protein EB1 on the distal ends of microtubules, Current Biology, vol.10, issue.14, pp.865-868, 2000.
DOI : 10.1016/S0960-9822(00)00600-X

K. Kizhatil, Ankyrin-G Is a Molecular Partner of E-cadherin in Epithelial Cells and Early Embryos, Journal of Biological Chemistry, vol.264, issue.36, pp.26552-26561, 2007.
DOI : 10.1074/jbc.273.37.23952

K. Abdi, P. Mohler, J. Davis, and V. Bennett, Isoform Specificity of Ankyrin-B, Journal of Biological Chemistry, vol.236, issue.9, pp.5741-5749, 2006.
DOI : 10.1083/jcb.137.3.703

F. Coquelle, LIS1, CLIP-170's Key to the Dynein/Dynactin Pathway, Molecular and Cellular Biology, vol.22, issue.9, pp.3089-3102, 2002.
DOI : 10.1128/MCB.22.9.3089-3102.2002
URL : http://mcb.asm.org/content/22/9/3089.full.pdf

A. Akhmanova, CLASPs Are CLIP-115 and -170 Associating Proteins Involved in the Regional Regulation of Microtubule Dynamics in Motile Fibroblasts, Cell, vol.104, issue.6, pp.923-935, 2001.
DOI : 10.1016/S0092-8674(01)00288-4

E. Meijering, Design and validation of a tool for neurite tracing and analysis in fluorescence microscopy images, Cytometry, vol.13, issue.2, pp.167-176, 2004.
DOI : 10.1007/978-1-4757-6465-9

S. Preibisch, S. Saalfeld, and P. Tomancak, Globally optimal stitching of tiled 3D microscopic image acquisitions, Bioinformatics, vol.20, issue.11, pp.1463-1465, 2009.
DOI : 10.1007/s11263-006-0002-3