Amyotrophic Lateral Sclerosis Part 5
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Tham khảo tài liệu amyotrophic lateral sclerosis part 5, khoa học tự nhiên, công nghệ sinh học phục vụ nhu cầu học tập, nghiên cứu và làm việc hiệu quả
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Amyotrophic Lateral Sclerosis Part 5142 Amyotrophic Lateral SclerosisCorona, J.C. & Tapia, R. (2007). Ca2+-permeable AMPA receptors and intracellular Ca2+ determine motoneuron vulnerability in rat spinal cord in vivo. Neuropharmacology, 52, 5, (Apr), pp. (1219-1228), 0028-3908 (Print) 0028-3908 (Linking)Corrado, L., Del Bo, R., Castellotti, B., Ratti, A., Cereda, C., Penco, S., Soraru, G., Carlomagno, Y., Ghezzi, S., Pensato, V., Colombrita, C., Gagliardi, S., Cozzi, L., Orsetti, V., Mancuso, M., Siciliano, G., Mazzini, L., Comi, G.P., Gellera, C., Ceroni, M., DAlfonso, S. & Silani, V. (2010). Mutations of FUS gene in sporadic amyotrophic lateral sclerosis. J Med Genet, 47, 3, (Mar), pp. (190-194), 1468-6244 (Electronic) 0022-2593 (Linking)Corrado, L., Gagliardi, S., Carlomagno, Y., Mennini, T., Ticozzi, N., Mazzini, L., Silani, V., Cereda, C. & DAlfonso, S. (2011). VPS54 genetic analysis in ALS Italian cohort. Eur J Neurol, 18, 4, (Apr), pp. (e41-42), 1468-1331 (Electronic) 1351-5101 (Linking)Corrado, L., Ratti, A., Gellera, C., Buratti, E., Castellotti, B., Carlomagno, Y., Ticozzi, N., Mazzini, L., Testa, L., Taroni, F., Baralle, F.E., Silani, V. & DAlfonso, S. (2009). High frequency of TARDBP gene mutations in Italian patients with amyotrophic lateral sclerosis. Hum Mutat, 30, 4, (Apr), pp. (688-694), 1098-1004 (Electronic) 1059-7794 (Linking)Cote, F., Collard, J.F. & Julien, J.P. (1993). Progressive neuronopathy in transgenic mice expressing the human neurofilament heavy gene: a mouse model of amyotrophic lateral sclerosis. Cell, 73, 1, (Apr 9), pp. (35-46), 0092-8674 (Print) 0092-8674 (Linking)Cox, G.A., Mahaffey, C.L. & Frankel, W.N. (1998). Identification of the mouse neuromuscular degeneration gene and mapping of a second site suppressor allele. Neuron, 21, 6, (Dec), pp. (1327-1337), 0896-6273 (Print) 0896-6273 (Linking)Crowther, R.A. & Goedert, M. (2000). Abnormal tau-containing filaments in neurodegenerative diseases. J Struct Biol, 130, 2-3, (Jun), pp. (271-279), 1047-8477 (Print) 1047-8477 (Linking)Dal Canto, M.C. & Gurney, M.E. (1994). Development of central nervous system pathology in a murine transgenic model of human amyotrophic lateral sclerosis. Am J Pathol, 145, 6, (Dec), pp. (1271-1279), 0002-9440 (Print) 0002-9440 (Linking)Delobel, P., Flament, S., Hamdane, M., Delacourte, A., Vilain, J.P. & Buee, L. (2002). Modelling Alzheimer-specific abnormal Tau phosphorylation independently of GSK3beta and PKA kinase activities. FEBS Lett, 516, 1-3, (Apr 10), pp. (151-155), 0014-5793 (Print) 0014-5793 (Linking)Deng, H.X., Hentati, A., Tainer, J.A., Iqbal, Z., Cayabyab, A., Hung, W.Y., Getzoff, E.D., Hu, P., Herzfeldt, B., Roos, R.P. & et al. (1993). Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase. Science, 261, 5124, (Aug 20), pp. (1047-1051), 0036-8075 (Print) 0036-8075 (Linking)Devon, R.S., Orban, P.C., Gerrow, K., Barbieri, M.A., Schwab, C., Cao, L.P., Helm, J.R., Bissada, N., Cruz-Aguado, R., Davidson, T.L., Witmer, J., Metzler, M., Lam, C.K., Tetzlaff, W., Simpson, E.M., McCaffery, J.M., El-Husseini, A.E., Leavitt, B.R. & Hayden, M.R. (2006). Als2-deficient mice exhibit disturbances in endosome trafficking associated with motor behavioral abnormalities. Proc Natl Acad Sci U S A, 103, 25, (Jun 20), pp. (9595-9600), 0027-8424 (Print) 0027-8424 (Linking) 143Advantages and Pitfalls in Experimental Models Of ALSDickson, D.W., Josephs, K.A. & Amador-Ortiz, C. (2007). TDP-43 in differential diagnosis of motor neuron disorders. Acta Neuropathol, 114, 1, (Jul), pp. (71-79), 0001-6322 (Print) 0001-6322 (Linking)Dimos, J.T., Rodolfa, K.T., Niakan, K.K., Weisenthal, L.M., Mitsumoto, H., Chung, W., Croft, G.F., Saphier, G., Leibel, R., Goland, R., Wichterle, H., Henderson, C.E. & Eggan, K. (2008). Induced pluripotent stem cells generated from patients with ALS can be differentiated into motor neurons. Science, 321, 5893, (Aug 29), pp. (1218-1221), 1095-9203 (Electronic) 0036-8075 (Linking)Djabali, K., Zissopoulou, A., de Hoop, M.J., Georgatos, S.D. & Dotti, C.G. (1993). Peripherin expression in hippocampal neurons induced by muscle soluble factor(s). J Cell Biol, 123, 5, (Dec), pp. (1197-1206), 0021-9525 (Print) 0021-9525 (Linking)Du, F., Qian, Z.M., Zhu, L., Wu, X.M., Qian, C., Chan, R. & Ke, Y. (2010). Purity, cell viability, expression of GFAP and bystin in astrocytes cultured by di ...
Nội dung trích xuất từ tài liệu:
Amyotrophic Lateral Sclerosis Part 5142 Amyotrophic Lateral SclerosisCorona, J.C. & Tapia, R. (2007). Ca2+-permeable AMPA receptors and intracellular Ca2+ determine motoneuron vulnerability in rat spinal cord in vivo. Neuropharmacology, 52, 5, (Apr), pp. (1219-1228), 0028-3908 (Print) 0028-3908 (Linking)Corrado, L., Del Bo, R., Castellotti, B., Ratti, A., Cereda, C., Penco, S., Soraru, G., Carlomagno, Y., Ghezzi, S., Pensato, V., Colombrita, C., Gagliardi, S., Cozzi, L., Orsetti, V., Mancuso, M., Siciliano, G., Mazzini, L., Comi, G.P., Gellera, C., Ceroni, M., DAlfonso, S. & Silani, V. (2010). Mutations of FUS gene in sporadic amyotrophic lateral sclerosis. J Med Genet, 47, 3, (Mar), pp. (190-194), 1468-6244 (Electronic) 0022-2593 (Linking)Corrado, L., Gagliardi, S., Carlomagno, Y., Mennini, T., Ticozzi, N., Mazzini, L., Silani, V., Cereda, C. & DAlfonso, S. (2011). VPS54 genetic analysis in ALS Italian cohort. Eur J Neurol, 18, 4, (Apr), pp. (e41-42), 1468-1331 (Electronic) 1351-5101 (Linking)Corrado, L., Ratti, A., Gellera, C., Buratti, E., Castellotti, B., Carlomagno, Y., Ticozzi, N., Mazzini, L., Testa, L., Taroni, F., Baralle, F.E., Silani, V. & DAlfonso, S. (2009). High frequency of TARDBP gene mutations in Italian patients with amyotrophic lateral sclerosis. Hum Mutat, 30, 4, (Apr), pp. (688-694), 1098-1004 (Electronic) 1059-7794 (Linking)Cote, F., Collard, J.F. & Julien, J.P. (1993). Progressive neuronopathy in transgenic mice expressing the human neurofilament heavy gene: a mouse model of amyotrophic lateral sclerosis. Cell, 73, 1, (Apr 9), pp. (35-46), 0092-8674 (Print) 0092-8674 (Linking)Cox, G.A., Mahaffey, C.L. & Frankel, W.N. (1998). Identification of the mouse neuromuscular degeneration gene and mapping of a second site suppressor allele. Neuron, 21, 6, (Dec), pp. (1327-1337), 0896-6273 (Print) 0896-6273 (Linking)Crowther, R.A. & Goedert, M. (2000). Abnormal tau-containing filaments in neurodegenerative diseases. J Struct Biol, 130, 2-3, (Jun), pp. (271-279), 1047-8477 (Print) 1047-8477 (Linking)Dal Canto, M.C. & Gurney, M.E. (1994). Development of central nervous system pathology in a murine transgenic model of human amyotrophic lateral sclerosis. Am J Pathol, 145, 6, (Dec), pp. (1271-1279), 0002-9440 (Print) 0002-9440 (Linking)Delobel, P., Flament, S., Hamdane, M., Delacourte, A., Vilain, J.P. & Buee, L. (2002). Modelling Alzheimer-specific abnormal Tau phosphorylation independently of GSK3beta and PKA kinase activities. FEBS Lett, 516, 1-3, (Apr 10), pp. (151-155), 0014-5793 (Print) 0014-5793 (Linking)Deng, H.X., Hentati, A., Tainer, J.A., Iqbal, Z., Cayabyab, A., Hung, W.Y., Getzoff, E.D., Hu, P., Herzfeldt, B., Roos, R.P. & et al. (1993). Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase. Science, 261, 5124, (Aug 20), pp. (1047-1051), 0036-8075 (Print) 0036-8075 (Linking)Devon, R.S., Orban, P.C., Gerrow, K., Barbieri, M.A., Schwab, C., Cao, L.P., Helm, J.R., Bissada, N., Cruz-Aguado, R., Davidson, T.L., Witmer, J., Metzler, M., Lam, C.K., Tetzlaff, W., Simpson, E.M., McCaffery, J.M., El-Husseini, A.E., Leavitt, B.R. & Hayden, M.R. (2006). Als2-deficient mice exhibit disturbances in endosome trafficking associated with motor behavioral abnormalities. Proc Natl Acad Sci U S A, 103, 25, (Jun 20), pp. (9595-9600), 0027-8424 (Print) 0027-8424 (Linking) 143Advantages and Pitfalls in Experimental Models Of ALSDickson, D.W., Josephs, K.A. & Amador-Ortiz, C. (2007). TDP-43 in differential diagnosis of motor neuron disorders. Acta Neuropathol, 114, 1, (Jul), pp. (71-79), 0001-6322 (Print) 0001-6322 (Linking)Dimos, J.T., Rodolfa, K.T., Niakan, K.K., Weisenthal, L.M., Mitsumoto, H., Chung, W., Croft, G.F., Saphier, G., Leibel, R., Goland, R., Wichterle, H., Henderson, C.E. & Eggan, K. (2008). Induced pluripotent stem cells generated from patients with ALS can be differentiated into motor neurons. Science, 321, 5893, (Aug 29), pp. (1218-1221), 1095-9203 (Electronic) 0036-8075 (Linking)Djabali, K., Zissopoulou, A., de Hoop, M.J., Georgatos, S.D. & Dotti, C.G. (1993). Peripherin expression in hippocampal neurons induced by muscle soluble factor(s). J Cell Biol, 123, 5, (Dec), pp. (1197-1206), 0021-9525 (Print) 0021-9525 (Linking)Du, F., Qian, Z.M., Zhu, L., Wu, X.M., Qian, C., Chan, R. & Ke, Y. (2010). Purity, cell viability, expression of GFAP and bystin in astrocytes cultured by di ...
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