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Pan, B., Fromholt, S. E., Hess, E. J., Crawford, T. O., Griffin, J. W., Sheikh, K. A., and Schnaar, R. L.
(2005). Myelin-associated glycoprotein and complementary axonal ligands, gangliosides, mediate
axon stability in the CNS and PNS: Neuropathology and behavioral deficits in single- and double-
null mice. Exp. Neurol. 195, 208-217.
Patel, H., Cross, H., Proukakis, C., Hershberger, R., Bork, P., Ciccarelli, F. D., Patton, M. A.,
McKusick, V. A., and Crosby, A. H. (2002). SPG20 is mutated in Troyer syndrome, an hereditary
spastic paraplegia. Nat. Genet. 31, 347-348.
Pedrola, L., Espert, A., Valdes-Sanchez, T., Sanchez-Piris, M., Sirkowski, E. E., Scherer, S. S.,
Farinas, I., and Palau, F. (2008). Cell expression of GDAP1 in the nervous system and pathogene-
sis of Charcot-Marie-Tooth type 4A disease. J. Cell. Mol. Med. 12, 679-689.
Perlson, E., Hanz, S., Ben-Yaakov, K., Segal-Ruder, Y., Seger, R., and Fainzilber, M. (2005).
Vimentin-dependent spatial translocation of an activated MAP kinase in injured nerve.
Neuron
45, 715-726.
Pilling, A. D., Horiuchi, D., Lively, C. M., and Saxton, W. M. (2006). Kinesin-1 and Dynein are the
primary motors for fast transport of mitochondria in Drosophila motor axons.
Mol. Biol. Cell 17,
2057-2068.
Puls, I., Jonnakuty, C., LaMonte, B. H., Holzbaur, E. L., Tokito, M., Mann, E., Floeter, M. K.,
Bidus, K., Drayna, D., Oh, S. J., Brown, R. H., Jr., Ludlow, C. L.,
et al
. (2003). Mutant dynactin in
Nat. Genet. 33, 455-456.
Read, D. J., Li, Y., Chao, M. V., Cavanagh, J. B., and Glynn, P. (2009). Neuropathy target esterase is
required for adult vertebrate axon maintenance.
motor neuron disease.
J. Neurosci. 29, 11594-11600.
Reid, E., Kloos, M., Ashley-Koch, A., Hughes, L., Bevan, S., Svenson, I. K., Graham, F. L.,
Gaskell, P. C., Dearlove, A., Pericak-Vance, M. A., Rubinsztein, D. C., and Marchuk, D. A.
(2002). A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10).
Am.
J. Hum. Genet. 71, 1189-1194.
Riano, E., Martignoni, M., Mancuso, G., Cartelli, D., Crippa, F., Toldo, I., Siciliano, G., Di Bella, D.,
Taroni, F., Bassi, M. T., Cappelletti, G., and Rugarli, E. I. (2009). Pleiotropic effects of spastin on
neurite growth depending on expression levels. J. Neurochem. 108, 1277-1288.
Ries, V., Silva, R. M., Oo, T. F., Cheng, H. C., Rzhetskaya, M., Kholodilov, N., Flavell, R. A.,
Kuan, C. Y., Rakic, P., and Burke, R. E. (2008). JNK2 and JNK3 combined are essential for
apoptosis in dopamine neurons of the substantia nigra, but are not required for axon degeneration.
J. Neurochem. 107, 1578-1588.
Rintoul, G. L., Filiano, A. J., Brocard, J. B., Kress, G. J., and Reynolds, I. J. (2003). Glutamate
decreases mitochondrial size and movement in primary forebrain neurons.
J. Neurosci. 23,
7881-7888.
Saigoh, K., Wang, Y. L., Suh, J. G., Yamanishi, T., Sakai, Y., Kiyosawa, H., Harada, T., Ichihara, N.,
Wakana, S., Kikuchi, T., and Wada, K. (1999). Intragenic deletion in the gene encoding
ubiquitin carboxy-terminal hydrolase in gad mice.
Nat. Genet. 23, 47-51.
Salinas, S., Bilsland, L. G., and Schiavo, G. (2008). Molecular landmarks along the axonal route:
Axonal transport in health and disease.
Curr. Opin. Cell Biol. 20, 445-453.
Sasaki, Y., Vohra, B. P., Lund, F. E., and Milbrandt, J. (2009). Nicotinamide mononucleotide
adenylyl transferase-mediated axonal protection requires enzymatic activity but not increased
levels of neuronal nicotinamide adenine dinucleotide.
J. Neurosci. 29, 5525-5535.
Schaefer, M. K., Schmalbruch, H., Buhler, E., Lopez, C., Martin, N., Guenet, J. L., and Haase, G.
(2007). Progressive motor neuronopathy: A critical role of the tubulin chaperone TBCE in axonal
tubulin routing from the Golgi apparatus.
J. Neurosci. 27, 8779-8789.
Schluter, O. M., Schmitz, F., Jahn, R., Rosenmund, C., and Sudhof, T. C. (2004). A complete genetic
analysis of neuronal Rab3 function.
J. Neurosci. 24, 6629-6637.
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