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Referencias:

• Levi-Montalcini, R., The nerve growth factor 35 years later (1987) Science, 237, pp. 1154-1162
• Yuen, E.C., Mobley, W.C., Therapeutic applications of neurotrophic factors in disorders of motor neurons and peripheral nerves (1995) Mol. Med. Today, 1, pp. 278-286
• Campenot, R.B., MacInnis, B.L., Retrograde transport of neurotrophins: fact and function (2004) J. Neurobiol., 58, pp. 217-229
• Di Fiore, P.P., De Camilli, P., Endocytosis and signaling: an inseparable partnership (2001) Cell, 106, pp. 1-4
• Delcroix, J.D., Valletta, J.S., Wu, C.B., Hunt, S.J., Kowal, A.S., Mobley, W.C., NGF signaling in sensory neurons: evidence that early endosomes carry NGF retrograde signals (2003) Neuron, 39, pp. 69-84
• Grimes, M.L., Endocytosis of activated TrkA: evidence that nerve growth factor induces formation of signaling endosomes (1996) J. Neurosci., 16, pp. 7950-7964
• Hendry, I.A., Iversen, L.L., Reduction in concentration of nerve growth factor in mice after sialectomy and castration (1973) Nature, 243, pp. 500-504
• Hendry, I.A., Stockel, K., Thoenen, H., Iversen, L.L., Retrograde axonal transport of nerve growth factor (1974) Brain Res., 68, pp. 103-121
• Vallee, R.B., Shpetner, H.S., Paschal, B.M., The role of dynein in retrograde axonal transport (1989) Trends Neurosci., 12, pp. 66-70
• Tani, T., Miyamoto, Y., Fujimori, K.E., Taguchi, T., Yanagida, T., Sako, Y., Harada, Y., Trafficking of a ligand-receptor complex on the growth cones as an essential step for the uptake of nerve growth factor at the distal end of the axon: a single-molecule analysis (2005) J. Neurosci., 25, pp. 2181-2191
• Vu, T.Q., Maddipati, R., Blute, T.A., Nehilla, B.J., Nusblat, L., Desai, T.A., Peptide-conjugated quantum dots activate neuronal receptors and initiate downstream signaling of neurite growth (2005) Nano Lett., 5, pp. 603-607
• Lidke, D.S., Lidke, K.A., Rieger, B., Jovin, T.M., Arndt-Jovin, D.J., Reaching out for signals: filopodia sense EGF and respond by directed retrograde transport of activated receptors (2005) J. Cell Biol., 170, pp. 619-626
• Lidke, D.S., Nagy, P., Heintzmann, R., Arndt-Jovin, D.J., Post, J.N., Grecco, H.E., Jares-Erijman, E.A., Jovin, T.M., Quantum dot ligands provide new insights into erbB/HER receptor-mediated signal transduction (2004) Nat. Biotechnol., 22, pp. 198-203
• Dahan, M., Levi, S., Luccardini, C., Rostaing, P., Riveau, B., Triller, A., Diffusion dynamics of glycine receptors revealed by single-quantum dot tracking (2003) Science, 302, pp. 442-445
• Smith, A., Gao, X., Nie, S., Quantum-dot nanocrystals for in vivo molecular and cellular imaging (2004) Photochem. Photobiol., 80, pp. 377-385
• Lehmann, M.J., Sherer, N.M., Marks, C.B., Pypaert, M., Mothes, W., Actin- and myosin-driven movement of viruses along filopodia precedes their entry into cells (2005) J. Cell Biol., 170, pp. 317-325
• Gao, X., Yang, L., Petros, J.A., Marshall, F.F., Simons, J.W., Nie, S., In vivo molecular and cellular imaging with quantum dots (2005) Curr. Opin. Biotechnol., 16, pp. 63-72
• Fu, A., Gu, W., Larabell, C., Alivisatos, A.P., Semiconductor nanocrystals for biological imaging (2005) Curr. Opin. Neurobiol., 15, pp. 568-575
• Bronfman, F.C., Tcherpakov, M., Jovin, T.M., Fainzilber, M., Ligand-induced internalization of the p75 neurotrophin receptor: a slow route to the signaling endosome (2003) J. Neurosci., 23, pp. 3209-3220
• Grecco, H.E., Lidke, K.A., Heintzmann, R., Lidke, D.S., Spagnuolo, C., Martinez, O.E., Jares-Erijman, E.A., Jovin, T.M., Ensemble and single particle photophysical properties (two-photon excitation, anisotropy, FRET, lifetime, spectral conversion) of commercial quantum dots in solution and in live cells (2004) Microsc. Res. Tech., 65, pp. 169-179
• Buxser, S., Decker, D., Ruppel, P., Relationship among types of nerve growth factor receptors on PC12 Cells (1990) J. Biol. Chem., 265, pp. 12701-12710
• Bernd, P., Greene, L.A., Association of I125 nerve growth factor with PC12 pheochromocytoma cells: evidence for Internalization via high-affinity receptors only and for long-term regulation by nerve growth factor of both high-affinity and low-affinity receptors (1984) J. Biol. Chem., 259, pp. 5509-5516
• Jullien, J., Guili, V., Reichardt, L.F., Rudkin, B.B., Molecular kinetics of nerve growth factor receptor trafficking and activation (2002) J. Biol. Chem., 277, pp. 38700-38708
• Mahadeo, D., Kaplan, L., Chao, M.V., Hempstead, B.L., High-affinity nerve growth-factor binding displays a faster rate of association than P140(Trk) binding - implications for multisubunit polypeptide receptors (1994) J. Biol. Chem., 269, pp. 6884-6891
• Zapf-Colby, A., Olefsky, J.M., Nerve growth factor processing and trafficking events following TrkA-mediated endocytosis (1998) Endocrinology, 139, pp. 3232-3240
• Ure, D.R., Campenot, R.B., Retrograde transport and steady-state distribution of I125 nerve growth factor in rat sympathetic neurons in compartmented cultures (1997) J. Neurosci., 17, pp. 1282-1290
• Watson, F.L., Heerssen, H.M., Moheban, D.B., Lin, M.Z., Sauvageot, C.M., Bhattacharyya, A., Pomeroy, S.L., Segal, R.A., Rapid nuclear responses to target-derived neurotrophins require retrograde transport of ligand-receptor complex (1999) J. Neurosci., 19, pp. 7889-7900
• Heerssen, H.M., Pazyra, M.F., Segal, R.A., Dynein motors transport activated Trks to promote survival of target-dependent neurons (2004) Nat. Neurosci., 7, pp. 596-604
• Yano, H., Lee, F.S., Kong, H., Chuang, J.-Z., Arevalo, J.C., Perez, P., Sung, C.-H., Chao, M.V., Association of Trk neurotrophin receptors with components of the cytoplasmic dynein motor (2001) J. Neurosci., 21 (RC 125), pp. 1-7
• Nakata, T., Terada, S., Hirokawa, N., Visualization of the dynamics of synaptic vesicle and plasma membrane proteins in living axons (1998) J. Cell Biol., 140, pp. 659-674
• Lalli, G., Schiavo, G., Analysis of retrograde transport in motor neurons reveals common endocytic carriers for tetanus toxin and neurotrophin receptor p75NTR (2002) J. Cell Biol., 156, pp. 233-240
• Wang, Z., Khan, S., Sheetz, M., Single cytoplasmic dynein molecule movements: characterization and comparison with kinesin (1995) Biophys. J., 69, pp. 2011-2023
• Gross, S.P., Welte, M.A., Block, S.M., Wieschaus, E.F., Dynein-mediated cargo transport in vivo: a switch controls travel distance (2000) J. Cell Biol., 148, pp. 945-955
• Hirakawa, E., Higuchi, H., Toyoshima, Y.Y., Processive movement of single 22S dynein molecules occurs only at low ATP concentrations (2000) Proc. Natl. Acad. Sci. USA, 97, pp. 2533-2537
• Jullien, J., Guili, V., Derrington, E.A., Darlix, J.L., Reichardt, L.F., Rudkin, B.B., Trafficking of TrkA-green fluorescent protein chimerae during nerve growth factor-induced differentiation (2003) J. Biol. Chem., 278, pp. 8706-8716
• Mallik, R., Carter, B.C., Lex, S.A., King, S.J., Gross, S.P., Cytoplasmic dynein functions as a gear in response to load (2004) Nature, 427, pp. 649-652
• Hill, D.B., Plaza, M.J., Bonin, K., Holzwarth, G., Fast vesicle transport in PC12 neurites: velocities and forces (2004) Eur. Biophys. J. Biophys. Lett., 33, pp. 623-632
• Block, S.M., Goldstein, L.S.B., Schnapp, B.J., Bead movement by single kinesin molecules studied with optical tweezers (1990) Nature, 348, pp. 348-352
• Weible, M.W., Hendry, I.A., What is the importance of multivesicular bodies in retrograde axonal transport in vivo? (2004) J. Neurobiol., 58, pp. 230-243
• Hirokawa, N., Takemura, R., Molecular motors and mechanisms of directional transport in neurons (2005) Nat. Rev. Neurosci., 6, pp. 201-214
• Kural, C., Kim, H., Syed, S., Goshima, G., Gelfand, V.I., Selvin, P.R., Kinesin and dynein move a peroxisome in vivo: a tug-of-war or coordinated movement? (2005) Science, 308, pp. 1469-1472
• Levi, V., Serpinskaya, A.S., Gratton, E., Gelfand, V., Organelle transport along microtubules in Xenopus melanophores: evidence for cooperation between multiple motors (2006) Biophys. J., 90, pp. 318-327
• Bhattacharyya, A., Watson, F.L., Pomeroy, S.L., Zhang, Y.Z.Z., Stiles, C.D., Segal, R.A., High-resolution imaging demonstrates dynein-based vesicular transport of activated Trk receptors (2002) J. Neurobiol., 51, pp. 302-312
• Rajan, S., Vu, T.Q., Quantum dots monitor TrkA receptor dynamics in the interior of neural PC12 cells (2006) Nano Lett., 6, pp. 2049-2059
• Ross, J.L., Wallace, K., Shuman, H., Goldman, Y.E., Holzbaur, E.L., Processive bidirectional motion of dynein-dynactin complexes in vitro (2006) Nat. Cell Biol., 8, pp. 562-570
• Nan, X., Sims, P.A., Chen, P., Xie, X.S., Observation of individual microtubule motor steps in living cells with endocytosed quantum dots (2005) J. Phys. Chem. B Condens. Matter Mater. Surf. Interfaces Biophys., 109, pp. 24220-24224
• Alivisatos, P., The use of nanocrystals in biological detection (2004) Nat. Biotechnol., 22, pp. 47-52

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