-
1
-
-
67650741437
-
Frontotemporal dementia and motor neurone disease: Overlapping clinic-pathological disorders
-
Lillo, P., and Hodges, J. R. (2009) Frontotemporal dementia and motor neurone disease: overlapping clinic-pathological disorders. J. Clin. Neurosci. 16, 1131-1135
-
(2009)
J. Clin. Neurosci.
, vol.16
, pp. 1131-1135
-
-
Lillo, P.1
Hodges, J.R.2
-
2
-
-
77956850818
-
TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia
-
Mackenzie, I. R., Rademakers, R., and Neumann, M. (2010) TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia. Lancet Neurol. 9, 995-1007
-
(2010)
Lancet Neurol.
, vol.9
, pp. 995-1007
-
-
Mackenzie, I.R.1
Rademakers, R.2
Neumann, M.3
-
3
-
-
78649632679
-
An estimate of amyotrophic lateral sclerosis heritability using twin data
-
Al-Chalabi, A., Fang, F., Hanby, M. F., Leigh, P. N., Shaw, C. E., Ye, W., and Rijsdijk, F. (2010) An estimate of amyotrophic lateral sclerosis heritability using twin data. J. Neurol. Neurosurg. 81, 1324-1326
-
(2010)
J. Neurol. Neurosurg.
, vol.81
, pp. 1324-1326
-
-
Al-Chalabi, A.1
Fang, F.2
Hanby, M.F.3
Leigh, P.N.4
Shaw, C.E.5
Ye, W.6
Rijsdijk, F.7
-
4
-
-
0027164824
-
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
-
Rosen, D. R. (1993) Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Nature 364, 362
-
(1993)
Nature
, vol.364
, pp. 362
-
-
Rosen, D.R.1
-
5
-
-
0034785483
-
A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2
-
Hadano, S., Hand, C. K., Osuga, H., Yanagisawa, Y., Otomo, A., Devon, R. S., Miyamoto, N., Showguchi-Miyata, J., Okada, Y., Singaraja, R., Figlewicz, D. A., Kwiatkowski, T., Hosler, B. A., Sagie, T., Skaug, J., Nasir, J., Brown, R. H., Scherer, S. W., Rouleau, G. A., Hayden, M. R., and Ikeda, J. E. (2001) A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2. Nat. Genet. 29, 166-173
-
(2001)
Nat. Genet.
, vol.29
, pp. 166-173
-
-
Hadano, S.1
Hand, C.K.2
Osuga, H.3
Yanagisawa, Y.4
Otomo, A.5
Devon, R.S.6
Miyamoto, N.7
Showguchi-Miyata, J.8
Okada, Y.9
Singaraja, R.10
Figlewicz, D.A.11
Kwiatkowski, T.12
Hosler, B.A.13
Sagie, T.14
Skaug, J.15
Nasir, J.16
Brown, R.H.17
Scherer, S.W.18
Rouleau, G.A.19
Hayden, M.R.20
Ikeda, J.E.21
more..
-
6
-
-
2442658908
-
DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4)
-
Chen, Y. Z., Bennett, C. L., Huynh, H. M., Blair, I. P., Puls, I., Irobi, J., Dierick, I., Abel, A., Kennerson, M. L., Rabin, B. A., Nicholson, G. A., Auer-Grumbach, M., Wagner, K., De Jonghe, P., Griffin, J. W., Fischbeck, K. H., Timmerman, V., Cornblath, D. R., and Chance, P. F. (2004) DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4). Am. J. Hum. Genet. 74, 1128-1135
-
(2004)
Am. J. Hum. Genet.
, vol.74
, pp. 1128-1135
-
-
Chen, Y.Z.1
Bennett, C.L.2
Huynh, H.M.3
Blair, I.P.4
Puls, I.5
Irobi, J.6
Dierick, I.7
Abel, A.8
Kennerson, M.L.9
Rabin, B.A.10
Nicholson, G.A.11
Auer-Grumbach, M.12
Wagner, K.13
De Jonghe, P.14
Griffin, J.W.15
Fischbeck, K.H.16
Timmerman, V.17
Cornblath, D.R.18
Chance, P.F.19
-
7
-
-
6344257200
-
A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis
-
Nishimura, A. L., Mitne-Neto, M., Silva, H. C., Richieri-Costa, A., Middleton, S., Cascio, D., Kok, F., Oliveira, J. R., Gillingwater, T., Webb, J., Skehel, P., and Zatz, M. (2004) A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis. Am. J. Hum. Genet. 75, 822-831
-
(2004)
Am. J. Hum. Genet.
, vol.75
, pp. 822-831
-
-
Nishimura, A.L.1
Mitne-Neto, M.2
Silva, H.C.3
Richieri-Costa, A.4
Middleton, S.5
Cascio, D.6
Kok, F.7
Oliveira, J.R.8
Gillingwater, T.9
Webb, J.10
Skehel, P.11
Zatz, M.12
-
8
-
-
33749632259
-
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
Neumann, M., Sampathu, D. M., Kwong, L. K., Truax, A. C., Micsenyi, M. C., Chou, T. T., Bruce, J., Schuck, T., Grossman, M., Clark, C. M., McCluskey, L. F., Miller, B. L., Masliah, E., Mackenzie, I. R., Feldman, H., Feiden, W., Kretzschmar, H. A., Trojanowski, J. Q., and Lee, V. M. (2006) Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science 314, 130-133
-
(2006)
Science
, vol.314
, pp. 130-133
-
-
Neumann, M.1
Sampathu, D.M.2
Kwong, L.K.3
Truax, A.C.4
Micsenyi, M.C.5
Chou, T.T.6
Bruce, J.7
Schuck, T.8
Grossman, M.9
Clark, C.M.10
McCluskey, L.F.11
Miller, B.L.12
Masliah, E.13
Mackenzie, I.R.14
Feldman, H.15
Feiden, W.16
Kretzschmar, H.A.17
Trojanowski, J.Q.18
Lee, V.M.19
-
9
-
-
41149180753
-
TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis
-
Sreedharan, J., Blair, I. P., Tripathi, V. B., Hu, X., Vance, C., Rogelj, B., Ackerley, S., Durnall, J. C., Williams, K. L., Buratti, E., Baralle, F., de Belleroche, J., Mitchell, J. D., Leigh, P. N., Al-Chalabi, A., Miller, C. C., Nicholson, G., and Shaw, C. E. (2008) TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis. Science 319, 1668-1672
-
(2008)
Science
, vol.319
, pp. 1668-1672
-
-
Sreedharan, J.1
Blair, I.P.2
Tripathi, V.B.3
Hu, X.4
Vance, C.5
Rogelj, B.6
Ackerley, S.7
Durnall, J.C.8
Williams, K.L.9
Buratti, E.10
Baralle, F.11
De Belleroche, J.12
Mitchell, J.D.13
Leigh, P.N.14
Al-Chalabi, A.15
Miller, C.C.16
Nicholson, G.17
Shaw, C.E.18
-
10
-
-
61349162349
-
Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6
-
Vance, C., Rogelj, B., Hortobagyi, T., De Vos, K. J., Nishimura, A. L., Sreedharan, J., Hu, X., Smith, B., Ruddy, D., Wright, P., Ganesalingam, J., Williams, K. L., Tripathi, V., Al-Saraj, S., Al-Chalabi, A., Leigh, P. N., Blair, I. P., Nicholson, G., de Belleroche, J., Gallo, J. M., Miller, C. C., and Shaw, C. E. (2009) Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6. Science 323, 1208-1211
-
(2009)
Science
, vol.323
, pp. 1208-1211
-
-
Vance, C.1
Rogelj, B.2
Hortobagyi, T.3
De Vos, K.J.4
Nishimura, A.L.5
Sreedharan, J.6
Hu, X.7
Smith, B.8
Ruddy, D.9
Wright, P.10
Ganesalingam, J.11
Williams, K.L.12
Tripathi, V.13
Al-Saraj, S.14
Al-Chalabi, A.15
Leigh, P.N.16
Blair, I.P.17
Nicholson, G.18
De Belleroche, J.19
Gallo, J.M.20
Miller, C.C.21
Shaw, C.E.22
more..
-
11
-
-
61349156118
-
Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis
-
Kwiatkowski, T. J., Jr., Bosco, D. A., Leclerc, A. L., Tamrazian, E., Vanderburg, C. R., Russ, C., Davis, A., Gilchrist, J., Kasarskis, E. J., Munsat, T., Valdmanis, P., Rouleau, G. A., Hosler, B. A., Cortelli, P., de Jong, P. J., Yoshinaga, Y., Haines, J. L., Pericak-Vance, M. A., Yan, J., Ticozzi, N., Siddique, T., McKenna-Yasek, D., Sapp, P. C., Horvitz, H. R., Landers, J. E., and Brown, R. H., Jr. (2009) Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis. Science 323, 1205-1208
-
(2009)
Science
, vol.323
, pp. 1205-1208
-
-
Kwiatkowski, T.J.1
Bosco, D.A.2
Leclerc, A.L.3
Tamrazian, E.4
Vanderburg, C.R.5
Russ, C.6
Davis, A.7
Gilchrist, J.8
Kasarskis, E.J.9
Munsat, T.10
Valdmanis, P.11
Rouleau, G.A.12
Hosler, B.A.13
Cortelli, P.14
De Jong, P.J.15
Yoshinaga, Y.16
Haines, J.L.17
Pericak-Vance, M.A.18
Yan, J.19
Ticozzi, N.20
Siddique, T.21
McKenna-Yasek, D.22
Sapp, P.C.23
Horvitz, H.R.24
Landers, J.E.25
Brown, R.H.26
more..
-
12
-
-
78649941297
-
Exome sequencing reveals VCP mutations as a cause of familial ALS
-
Johnson, J. O., Mandrioli, J., Benatar, M., Abramzon, Y., Van Deerlin, V. M., Trojanowski, J. Q., Gibbs, J. R., Brunetti, M., Gronka, S., Wuu, J., Ding, J. H., McCluskey, L., Martinez-Lage, M., Falcone, D., Hernandez, D. G., Arepalli, S., Chong, S., Schymick, J. C., Rothstein, J., Landi, F., Wang, Y. D., Calvo, A., Mora, G., Sabatelli, M., Monsurro, M. R., Battistini, S., Salvi, F., Spataro, R., Sola, P., Borghero, G., Galassi, G., Scholz, S. W., Taylor, J. P., Restagno, G., Chio, A., Traynor, B. J., and Consortium, I. (2010) Exome sequencing reveals VCP mutations as a cause of familial ALS. Neuron 68, 857-864
-
(2010)
Neuron
, vol.68
, pp. 857-864
-
-
Johnson, J.O.1
Mandrioli, J.2
Benatar, M.3
Abramzon, Y.4
Van Deerlin, V.M.5
Trojanowski, J.Q.6
Gibbs, J.R.7
Brunetti, M.8
Gronka, S.9
Wuu, J.10
Ding, J.H.11
McCluskey, L.12
Martinez-Lage, M.13
Falcone, D.14
Hernandez, D.G.15
Arepalli, S.16
Chong, S.17
Schymick, J.C.18
Rothstein, J.19
Landi, F.20
Wang, Y.D.21
Calvo, A.22
Mora, G.23
Sabatelli, M.24
Monsurro, M.R.25
Battistini, S.26
Salvi, F.27
Spataro, R.28
Sola, P.29
Borghero, G.30
Galassi, G.31
Scholz, S.W.32
Taylor, J.P.33
Restagno, G.34
Chio, A.35
Traynor, B.J.36
more..
-
13
-
-
84865235172
-
Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis
-
Wu, C. H., Fallini, C., Ticozzi, N., Keagle, P. J., Sapp, P. C., Piotrowska, K., Lowe, P., Koppers, M., McKenna-Yasek, D., Baron, D. M., Kost, J. E., Gonzalez-Perez, P., Fox, A. D., Adams, J., Taroni, F., Tiloca, C., Leclerc, A. L., Chafe, S. C., Mangroo, D., Moore, M. J., Zitzewitz, J. A., Xu, Z. S., van den Berg, L. H., Glass, J. D., Siciliano, G., Cirulli, E. T., Goldstein, D. B., Salachas, F., Meininger, V., Rossoll, W., Ratti, A., Gellera, C., Bosco, D. A., Bassell, G. J., Silani, V., Drory, V. E., Brown, R. H., Jr., and Landers, J. E. (2012) Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis. Nature 488, 499-503
-
(2012)
Nature
, vol.488
, pp. 499-503
-
-
Wu, C.H.1
Fallini, C.2
Ticozzi, N.3
Keagle, P.J.4
Sapp, P.C.5
Piotrowska, K.6
Lowe, P.7
Koppers, M.8
McKenna-Yasek, D.9
Baron, D.M.10
Kost, J.E.11
Gonzalez-Perez, P.12
Fox, A.D.13
Adams, J.14
Taroni, F.15
Tiloca, C.16
Leclerc, A.L.17
Chafe, S.C.18
Mangroo, D.19
Moore, M.J.20
Zitzewitz, J.A.21
Xu, Z.S.22
Van Den Berg, L.H.23
Glass, J.D.24
Siciliano, G.25
Cirulli, E.T.26
Goldstein, D.B.27
Salachas, F.28
Meininger, V.29
Rossoll, W.30
Ratti, A.31
Gellera, C.32
Bosco, D.A.33
Bassell, G.J.34
Silani, V.35
Drory, V.E.36
Brown, R.H.37
Landers, J.E.38
more..
-
14
-
-
84875441083
-
The changing scene of amyotrophic lateral sclerosis
-
Robberecht, W., and Philips, T. (2013) The changing scene of amyotrophic lateral sclerosis. Nat. Rev. Neurosci. 14, 248-264
-
(2013)
Nat. Rev. Neurosci.
, vol.14
, pp. 248-264
-
-
Robberecht, W.1
Philips, T.2
-
15
-
-
80054837386
-
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALSFTD
-
Renton, A. E., Majounie, E., Waite, A., Simón-Sánchez, J., Rollinson, S., Gibbs, J. R., Schymick, J. C., Laaksovirta, H., van Swieten, J. C., Myllykangas, L., Kalimo, H., Paetau, A., Abramzon, Y., Remes, A. M., Kaganovich, A., Scholz, S. W., Duckworth, J., Ding, J., Harmer, D. W., Hernandez, D. G., Johnson, J. O., Mok, K., Ryten, M., Trabzuni, D., Guerreiro, R. J., Orrell, R. W., Neal, J., Murray, A., Pearson, J., Jansen, I. E., Sondervan, D., Seelaar, H., Blake, D., Young, K., Halliwell, N., Callister, J. B., Toulson, G., Richardson, A., Gerhard, A., Snowden, J., Mann, D., Neary, D., Nalls, M. A., Peuralinna, T., Jansson, L., Isoviita, V.-M., Kaivorinne, A.-L., Hölttä-Vuori, M., Ikonen, E., Sulkava, R., Benatar, M., Wuu, J., Chio', A., Restagno, G., Borghero, G., Sabatelli, M., Heckerman, D., Rogaeva, E., Zinman, L., Rothstein, J. D., Sendtner, M., Drepper, C., Eichler, E. E., Alkan, C., Abdullaev, Z., Pack, S. D., Dutra, A., Pak, E., Hardy, J., Singleton, A., Williams, N. M., Heutink, P., Pickering-Brown, S., Morris, H. R., Tienari, P. J., and Traynor, B. J. (2011) A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALSFTD. Neuron 72, 257-268
-
(2011)
Neuron
, vol.72
, pp. 257-268
-
-
Renton, A.E.1
Majounie, E.2
Waite, A.3
Simón-Sánchez, J.4
Rollinson, S.5
Gibbs, J.R.6
Schymick, J.C.7
Laaksovirta, H.8
Van Swieten, J.C.9
Myllykangas, L.10
Kalimo, H.11
Paetau, A.12
Abramzon, Y.13
Remes, A.M.14
Kaganovich, A.15
Scholz, S.W.16
Duckworth, J.17
Ding, J.18
Harmer, D.W.19
Hernandez, D.G.20
Johnson, J.O.21
Mok, K.22
Ryten, M.23
Trabzuni, D.24
Guerreiro, R.J.25
Orrell, R.W.26
Neal, J.27
Murray, A.28
Pearson, J.29
Jansen, I.E.30
Sondervan, D.31
Seelaar, H.32
Blake, D.33
Young, K.34
Halliwell, N.35
Callister, J.B.36
Toulson, G.37
Richardson, A.38
Gerhard, A.39
Snowden, J.40
Mann, D.41
Neary, D.42
Nalls, M.A.43
Peuralinna, T.44
Jansson, L.45
Isoviita, V.-M.46
Kaivorinne, A.-L.47
Hölttä-Vuori, M.48
Ikonen, E.49
Sulkava, R.50
Benatar, M.51
Wuu, J.52
Chiò, A.53
Restagno, G.54
Borghero, G.55
Sabatelli, M.56
Heckerman, D.57
Rogaeva, E.58
Zinman, L.59
Rothstein, J.D.60
Sendtner, M.61
Drepper, C.62
Eichler, E.E.63
Alkan, C.64
Abdullaev, Z.65
Pack, S.D.66
Dutra, A.67
Pak, E.68
Hardy, J.69
Singleton, A.70
Williams, N.M.71
Heutink, P.72
Pickering-Brown, S.73
Morris, H.R.74
Tienari, P.J.75
Traynor, B.J.76
more..
-
16
-
-
80054832080
-
Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS
-
DeJesus-Hernandez, M., Mackenzie, I. R., Boeve, B. F., Boxer, A. L., Baker, M., Rutherford, N. J., Nicholson, A. M., Finch, N. A., Flynn, H., Adamson, J., Kouri, N., Wojtas, A., Sengdy, P., Hsiung, G. Y., Karydas, A., Seeley, W. W., Josephs, K. A., Coppola, G., Geschwind, D. H., Wszolek, Z. K., Feldman, H., Knopman, D. S., Petersen, R. C., Miller, B. L., Dickson, D. W., Boylan, K. B., Graff-Radford, N. R., and Rademakers, R. (2011) Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS. Neuron 72, 245-256
-
(2011)
Neuron
, vol.72
, pp. 245-256
-
-
DeJesus-Hernandez, M.1
Mackenzie, I.R.2
Boeve, B.F.3
Boxer, A.L.4
Baker, M.5
Rutherford, N.J.6
Nicholson, A.M.7
Finch, N.A.8
Flynn, H.9
Adamson, J.10
Kouri, N.11
Wojtas, A.12
Sengdy, P.13
Hsiung, G.Y.14
Karydas, A.15
Seeley, W.W.16
Josephs, K.A.17
Coppola, G.18
Geschwind, D.H.19
Wszolek, Z.K.20
Feldman, H.21
Knopman, D.S.22
Petersen, R.C.23
Miller, B.L.24
Dickson, D.W.25
Boylan, K.B.26
Graff-Radford, N.R.27
Rademakers, R.28
more..
-
17
-
-
84930000577
-
C9orf72 FTLD/ALS-associated Gly-Ala dipeptide repeat proteins cause neuronal toxicity and Unc119 sequestration
-
May, S., Hornburg, D., Schludi, M. H., Arzberger, T., Rentzsch, K., Schwenk, B. M., Grasser, F. A., Mori, K., Kremmer, E., Banzhaf-Strathmann, J., Mann, M., Meissner, F., and Edbauer, D. (2014) C9orf72 FTLD/ALS-associated Gly-Ala dipeptide repeat proteins cause neuronal toxicity and Unc119 sequestration. Acta Neuropathol. 128, 485-503
-
(2014)
Acta Neuropathol.
, vol.128
, pp. 485-503
-
-
May, S.1
Hornburg, D.2
Schludi, M.H.3
Arzberger, T.4
Rentzsch, K.5
Schwenk, B.M.6
Grasser, F.A.7
Mori, K.8
Kremmer, E.9
Banzhaf-Strathmann, J.10
Mann, M.11
Meissner, F.12
Edbauer, D.13
-
18
-
-
84865843186
-
The genetics and neuropathology of amyotrophic lateral sclerosis
-
Al-Chalabi, A., Jones, A., Troakes, C., King, A., Al-Sarraj, S., and van den Berg, L. H. (2012) The genetics and neuropathology of amyotrophic lateral sclerosis. Acta Neuropathol, 124, 339-352
-
(2012)
Acta Neuropathol
, vol.124
, pp. 339-352
-
-
Al-Chalabi, A.1
Jones, A.2
Troakes, C.3
King, A.4
Al-Sarraj, S.5
Van Den Berg, L.H.6
-
19
-
-
80755163102
-
Molecular pathways of motor neuron injury in amyotrophic lateral sclerosis
-
Ferraiuolo, L., Kirby, J., Grierson, A. J., Sendtner, M., and Shaw, P. J. (2011) Molecular pathways of motor neuron injury in amyotrophic lateral sclerosis. Nat. Rev. Neurol. 7, 616-630
-
(2011)
Nat. Rev. Neurol.
, vol.7
, pp. 616-630
-
-
Ferraiuolo, L.1
Kirby, J.2
Grierson, A.J.3
Sendtner, M.4
Shaw, P.J.5
-
20
-
-
84862145991
-
Spinal muscular atrophy: The role of SMN in axonal mRNA regulation
-
Fallini, C., Bassell, G. J., and Rossoll, W. (2012) Spinal muscular atrophy: the role of SMN in axonal mRNA regulation. Brain Res. 1462, 81-92
-
(2012)
Brain Res.
, vol.1462
, pp. 81-92
-
-
Fallini, C.1
Bassell, G.J.2
Rossoll, W.3
-
21
-
-
84866745607
-
Cellular and molecular approaches to motor neuron therapy in amyotrophic lateral sclerosis and spinal muscular atrophy
-
O'Connor, D. M., and Boulis, N. M. (2012) Cellular and molecular approaches to motor neuron therapy in amyotrophic lateral sclerosis and spinal muscular atrophy. Neurosci. Lett. 527, 78-84
-
(2012)
Neurosci. Lett.
, vol.527
, pp. 78-84
-
-
O'Connor, D.M.1
Boulis, N.M.2
-
22
-
-
0028284779
-
Motor-neuron degeneration in mice that express a human Cu,Zn superoxide-dismutase mutation
-
Gurney, M. E., Pu, H. F., Chiu, A. Y., Dalcanto, M. C., Polchow, C. Y., Alexander, D. D., Caliendo, J., Hentati, A., Kwon, Y. W., Deng, H. X., Chen, W. J., Zhai, P., Sufit, R. L., and Siddique, T. (1994) Motor-neuron degeneration in mice that express a human Cu,Zn superoxide-dismutase mutation. Science 264, 1772-1775
-
(1994)
Science
, vol.264
, pp. 1772-1775
-
-
Gurney, M.E.1
Pu, H.F.2
Chiu, A.Y.3
Dalcanto, M.C.4
Polchow, C.Y.5
Alexander, D.D.6
Caliendo, J.7
Hentati, A.8
Kwon, Y.W.9
Deng, H.X.10
Chen, W.J.11
Zhai, P.12
Sufit, R.L.13
Siddique, T.14
-
23
-
-
43449099127
-
The amyotrophic lateral sclerosis 8 protein VAPB is cleaved, secreted, and acts as a ligand for Eph receptors
-
Tsuda, H., Han, S. M., Yang, Y. F., Tong, C., Lin, Y. Q., Mohan, K., Haueter, C., Zoghbi, A., Harati, Y., Kwan, J., Miller, M. A., and Bellen, H. J. (2008) The amyotrophic lateral sclerosis 8 protein VAPB is cleaved, secreted, and acts as a ligand for Eph receptors. Cell 133, 963-977
-
(2008)
Cell
, vol.133
, pp. 963-977
-
-
Tsuda, H.1
Han, S.M.2
Yang, Y.F.3
Tong, C.4
Lin, Y.Q.5
Mohan, K.6
Haueter, C.7
Zoghbi, A.8
Harati, Y.9
Kwan, J.10
Miller, M.A.11
Bellen, H.J.12
-
24
-
-
78149429744
-
Progranulin is neurotrophic in vivo and protects against a mutant TDP-43 induced axonopathy
-
Laird, A. S., Van Hoecke, A., De Muynck, L., Timmers, M., Van den Bosch, L., Van Damme, P., and Robberecht, W. (2010) Progranulin is neurotrophic in vivo and protects against a mutant TDP-43 induced axonopathy. PLoS One 5, e13368
-
(2010)
PLoS One
, vol.5
-
-
Laird, A.S.1
Van Hoecke, A.2
De Muynck, L.3
Timmers, M.4
Van Den Bosch, L.5
Van Damme, P.6
Robberecht, W.7
-
25
-
-
75149138783
-
Isolation and enrichment of embryonic mouse motoneurons from the lumbar spinal cord of individual mouse embryos
-
Wiese, S., Herrmann, T., Drepper, C., Jablonka, S., Funk, N., Klausmeyer, A., Rogers, M. L., Rush, R., and Sendtner, M. (2010) Isolation and enrichment of embryonic mouse motoneurons from the lumbar spinal cord of individual mouse embryos. Nat. Protoc. 5, 31-38
-
(2010)
Nat. Protoc.
, vol.5
, pp. 31-38
-
-
Wiese, S.1
Herrmann, T.2
Drepper, C.3
Jablonka, S.4
Funk, N.5
Klausmeyer, A.6
Rogers, M.L.7
Rush, R.8
Sendtner, M.9
-
26
-
-
0026465350
-
Neuroblastoma x spinal cord (NSC) hybrid cell lines resemble developing motor neurons
-
Cashman, N. R., Durham, H. D., Blusztajn, J. K., Oda, K., Tabira, T., Shaw, I. T., Dahrouge, S., and Antel, J. P. (1992) Neuroblastoma x spinal cord (NSC) hybrid cell lines resemble developing motor neurons. Dev. Dyn. 194, 209-221
-
(1992)
Dev. Dyn.
, vol.194
, pp. 209-221
-
-
Cashman, N.R.1
Durham, H.D.2
Blusztajn, J.K.3
Oda, K.4
Tabira, T.5
Shaw, I.T.6
Dahrouge, S.7
Antel, J.P.8
-
27
-
-
38449116842
-
Superoxide dismutase 1 mutants related to amyotrophic lateral sclerosis induce endoplasmic stress in neuro2a cells
-
Oh, Y. K., Shin, K. S., Yuan, J., and Kang, S. J. (2008) Superoxide dismutase 1 mutants related to amyotrophic lateral sclerosis induce endoplasmic stress in neuro2a cells. J. Neurochem. 104, 993-1005
-
(2008)
J. Neurochem.
, vol.104
, pp. 993-1005
-
-
Oh, Y.K.1
Shin, K.S.2
Yuan, J.3
Kang, S.J.4
-
28
-
-
38849199865
-
Characterization and use of the NSC-34 cell line for study of neurotrophin receptor trafficking
-
Matusica, D., Fenech, M. P., Rogers, M. L., and Rush, R. A. (2008) Characterization and use of the NSC-34 cell line for study of neurotrophin receptor trafficking. J. Neurosci. Res. 86, 553-565
-
(2008)
J. Neurosci. Res.
, vol.86
, pp. 553-565
-
-
Matusica, D.1
Fenech, M.P.2
Rogers, M.L.3
Rush, R.A.4
-
29
-
-
0034048839
-
Development and characterisation of a glutamate-sensitive motor neurone cell line
-
Eggett, C. J., Crosier, S., Manning, P., Cookson, M. R., Menzies, F. M., McNeil, C. J., and Shaw, P. J. (2000) Development and characterisation of a glutamate-sensitive motor neurone cell line. J. Neurochem. 74, 1895-1902
-
(2000)
J. Neurochem.
, vol.74
, pp. 1895-1902
-
-
Eggett, C.J.1
Crosier, S.2
Manning, P.3
Cookson, M.R.4
Menzies, F.M.5
McNeil, C.J.6
Shaw, P.J.7
-
30
-
-
63049110388
-
Comparative proteomic phenotyping of cell lines and primary cells to assess preservation of cell type-specific functions
-
Pan, C., Kumar, C., Bohl, S., Klingmueller, U., and Mann, M. (2009) Comparative proteomic phenotyping of cell lines and primary cells to assess preservation of cell type-specific functions. Mol. Cell. Proteomics 8, 443-450
-
(2009)
Mol. Cell. Proteomics
, vol.8
, pp. 443-450
-
-
Pan, C.1
Kumar, C.2
Bohl, S.3
Klingmueller, U.4
Mann, M.5
-
31
-
-
80855128254
-
Deep proteome and transcriptome mapping of a human cancer cell line
-
Nagaraj, N., Wisniewski, J. R., Geiger, T., Cox, J., Kircher, M., Kelso, J., Paabo, S., and Mann, M. (2011) Deep proteome and transcriptome mapping of a human cancer cell line. Mol. Syst. Biol. 7, 548
-
(2011)
Mol. Syst. Biol.
, vol.7
, pp. 548
-
-
Nagaraj, N.1
Wisniewski, J.R.2
Geiger, T.3
Cox, J.4
Kircher, M.5
Kelso, J.6
Paabo, S.7
Mann, M.8
-
32
-
-
80855128111
-
The quantitative proteome of a human cell line
-
Beck, M., Schmidt, A., Malmstroem, J., Claassen, M., Ori, A., Szymborska, A., Herzog, F., Rinner, O., Ellenberg, J., and Aebersold, R. (2011) The quantitative proteome of a human cell line. Mol. Syst. Biol. 7, 549
-
(2011)
Mol. Syst. Biol.
, vol.7
, pp. 549
-
-
Beck, M.1
Schmidt, A.2
Malmstroem, J.3
Claassen, M.4
Ori, A.5
Szymborska, A.6
Herzog, F.7
Rinner, O.8
Ellenberg, J.9
Aebersold, R.10
-
33
-
-
84871297843
-
Next-generation proteomics: Towards an integrative view of proteome dynamics
-
Altelaar, A. F., Munoz, J., and Heck, A. J. (2013) Next-generation proteomics: towards an integrative view of proteome dynamics. Nat. Rev. Genet. 14, 35-48
-
(2013)
Nat. Rev. Genet.
, vol.14
, pp. 35-48
-
-
Altelaar, A.F.1
Munoz, J.2
Heck, A.J.3
-
34
-
-
80052769923
-
Mass spectrometry-based proteomics using Q Exactive, a high-performance benchtop quadrupole Orbitrap mass spectrometer
-
Michalski, A. D. E., Hauschild, J. P., Lange, O., Wieghaus, A., Makarov, A., Nagaraj, N., Cox, J., Mann, M., and Horning, S. (2011) Mass spectrometry-based proteomics using Q Exactive, a high-performance benchtop quadrupole Orbitrap mass spectrometer. Mol. Cell. Proteomics 10, M111 011015
-
(2011)
Mol. Cell. Proteomics
, vol.10
, pp. M111011015
-
-
Michalski, A.D.E.1
Hauschild, J.P.2
Lange, O.3
Wieghaus, A.4
Makarov, A.5
Nagaraj, N.6
Cox, J.7
Mann, M.8
Horning, S.9
-
35
-
-
84865576726
-
Quantitative mass spectrometry in proteomics: Critical review update from 2007 to the present
-
Bantscheff, M., Lemeer, S., Savitski, M. M., and Kuster, B. (2012) Quantitative mass spectrometry in proteomics: critical review update from 2007 to the present. Anal. Bioanal. Chem. 404, 939-965
-
(2012)
Anal. Bioanal. Chem.
, vol.404
, pp. 939-965
-
-
Bantscheff, M.1
Lemeer, S.2
Savitski, M.M.3
Kuster, B.4
-
36
-
-
84855549488
-
System-wide perturbation analysis with nearly complete coverage of the yeast proteome by single-shot ultra HPLC runs on a bench top Orbitrap
-
M111.013722
-
Nagaraj, N., Kulak, N. A., Cox, J., Neuhauser, N., Mayr, K., Hoerning, O., Vorm, O., and Mann, M. (2012) System-wide perturbation analysis with nearly complete coverage of the yeast proteome by single-shot ultra HPLC runs on a bench top Orbitrap. Mol. Cell. Proteomics 11, M111.013722
-
(2012)
Mol. Cell. Proteomics
, vol.11
-
-
Nagaraj, N.1
Kulak, N.A.2
Cox, J.3
Neuhauser, N.4
Mayr, K.5
Hoerning, O.6
Vorm, O.7
Mann, M.8
-
37
-
-
71549117585
-
Combination of FASP and StageTip-based fractionation allows in-depth analysis of the hippocampal membrane proteome
-
Wisniewski, J. R., Zougman, A., and Mann, M. (2009) Combination of FASP and StageTip-based fractionation allows in-depth analysis of the hippocampal membrane proteome. J. Proteome Res. 8, 5674-5678
-
(2009)
J. Proteome Res.
, vol.8
, pp. 5674-5678
-
-
Wisniewski, J.R.1
Zougman, A.2
Mann, M.3
-
38
-
-
34548183872
-
Protocol for micropurification, enrichment, pre-fractionation and storage of peptides for proteomics using StageTips
-
Rappsilber, J., Mann, M., and Ishihama, Y. (2007) Protocol for micropurification, enrichment, pre-fractionation and storage of peptides for proteomics using StageTips. Nat. Protoc. 2, 1896-1906
-
(2007)
Nat. Protoc.
, vol.2
, pp. 1896-1906
-
-
Rappsilber, J.1
Mann, M.2
Ishihama, Y.3
-
39
-
-
34548336772
-
Higher-energy C-trap dissociation for peptide modification analysis
-
Olsen, J. V., Macek, B., Lange, O., Makarov, A., Horning, S., and Mann, M. (2007) Higher-energy C-trap dissociation for peptide modification analysis. Nat. Methods 4, 709-712
-
(2007)
Nat. Methods
, vol.4
, pp. 709-712
-
-
Olsen, J.V.1
Macek, B.2
Lange, O.3
Makarov, A.4
Horning, S.5
Mann, M.6
-
40
-
-
57449099865
-
MaxQuant enables high peptide identification rates, individualized p.P.B.-range mass accuracies and proteome-wide protein quantification
-
Cox, J., and Mann, M. (2008) MaxQuant enables high peptide identification rates, individualized p.p.b.-range mass accuracies and proteome-wide protein quantification. Nat. Biotechnol. 26, 1367-1372
-
(2008)
Nat. Biotechnol.
, vol.26
, pp. 1367-1372
-
-
Cox, J.1
Mann, M.2
-
41
-
-
79953701087
-
Andromeda: A peptide search engine integrated into the MaxQuant environment
-
Cox, J., Neuhauser, N., Michalski, A., Scheltema, R. A., Olsen, J. V., and Mann, M. (2011) Andromeda: a peptide search engine integrated into the MaxQuant environment. J. Proteome Res. 10, 1794-1805
-
(2011)
J. Proteome Res.
, vol.10
, pp. 1794-1805
-
-
Cox, J.1
Neuhauser, N.2
Michalski, A.3
Scheltema, R.A.4
Olsen, J.V.5
Mann, M.6
-
42
-
-
84907197082
-
MaxLFQ allows accurate proteome-wide label-free quantification by delayed normalization and maximal peptide ratio extraction
-
M113.031591
-
Cox, J., Hein, M. Y., Luber, C. A., Paron, I., Nagaraj, N., and Mann, M. (2014) MaxLFQ allows accurate proteome-wide label-free quantification by delayed normalization and maximal peptide ratio extraction. Mol. Cell. Proteomics M113.031591
-
(2014)
Mol. Cell. Proteomics
-
-
Cox, J.1
Hein, M.Y.2
Luber, C.A.3
Paron, I.4
Nagaraj, N.5
Mann, M.6
-
43
-
-
79956322553
-
Global quantification of mammalian gene expression control
-
Schwanhausser, B., Busse, D., Li, N., Dittmar, G., Schuchhardt, J., Wolf, J., Chen, W., and Selbach, M. (2011) Global quantification of mammalian gene expression control. Nature 473, 337-342
-
(2011)
Nature
, vol.473
, pp. 337-342
-
-
Schwanhausser, B.1
Busse, D.2
Li, N.3
Dittmar, G.4
Schuchhardt, J.5
Wolf, J.6
Chen, W.7
Selbach, M.8
-
45
-
-
77952344256
-
Quantitative proteomics combined with BAC TransgeneOmics reveals in vivo protein interactions
-
Hubner, N. C., Bird, A. W., Cox, J., Splettstoesser, B., Bandilla, P., Poser, I., Hyman, A., and Mann, M. (2010) Quantitative proteomics combined with BAC TransgeneOmics reveals in vivo protein interactions. J. Cell Biol. 189, 739-754
-
(2010)
J. Cell Biol.
, vol.189
, pp. 739-754
-
-
Hubner, N.C.1
Bird, A.W.2
Cox, J.3
Splettstoesser, B.4
Bandilla, P.5
Poser, I.6
Hyman, A.7
Mann, M.8
-
46
-
-
0035942271
-
Significance analysis of microarrays applied to the ionizing radiation response
-
Tusher, V. G., Tibshirani, R., and Chu, G. (2001) Significance analysis of microarrays applied to the ionizing radiation response. Proc. Natl. Acad. Sci. U.S.A. 98, 5116-5121
-
(2001)
Proc. Natl. Acad. Sci. U.S.A.
, vol.98
, pp. 5116-5121
-
-
Tusher, V.G.1
Tibshirani, R.2
Chu, G.3
-
47
-
-
0034069495
-
Gene ontology: Tool for the unification of biology. The Gene Ontology Consortium
-
Ashburner, M., Ball, C. A., Blake, J. A., Botstein, D., Butler, H., Cherry, J. M., Davis, A. P., Dolinski, K., Dwight, S. S., Eppig, J. T., Harris, M. A., Hill, D. P., Issel-Tarver, L., Kasarskis, A., Lewis, S., Matese, J. C., Richardson, J. E., Ringwald, M., Rubin, G. M., and Sherlock, G. (2000) Gene ontology: tool for the unification of biology. The Gene Ontology Consortium. Nat. Genet. 25, 25-29
-
(2000)
Nat. Genet.
, vol.25
, pp. 25-29
-
-
Ashburner, M.1
Ball, C.A.2
Blake, J.A.3
Botstein, D.4
Butler, H.5
Cherry, J.M.6
Davis, A.P.7
Dolinski, K.8
Dwight, S.S.9
Eppig, J.T.10
Harris, M.A.11
Hill, D.P.12
Issel-Tarver, L.13
Kasarskis, A.14
Lewis, S.15
Matese, J.C.16
Richardson, J.E.17
Ringwald, M.18
Rubin, G.M.19
Sherlock, G.20
more..
-
48
-
-
84858983547
-
KEGG for integration and interpretation of large-scale molecular data sets
-
Kanehisa, M., Goto, S., Sato, Y., Furumichi, M., and Tanabe, M. (2012) KEGG for integration and interpretation of large-scale molecular data sets. Nucleic Acids Res. 40, D109-D114
-
(2012)
Nucleic Acids Res.
, vol.40
, pp. D109-D114
-
-
Kanehisa, M.1
Goto, S.2
Sato, Y.3
Furumichi, M.4
Tanabe, M.5
-
49
-
-
79960976768
-
UniProt Knowledgebase: A hub of integrated protein data
-
Magrane, M., and Consortium, U. (2011) UniProt Knowledgebase: a hub of integrated protein data. Database 2011, bar009
-
(2011)
Database
, vol.2011
, pp. bar009
-
-
Magrane, M.1
Consortium, U.2
-
50
-
-
84883445886
-
Synergistic binding of transcription factors to cell-specific enhancers programs motor neuron identity
-
Mazzoni, E. O., Mahony, S., Closser, M., Morrison, C. A., Nedelec, S., Williams, D. J., An, D., Gifford, D. K., and Wichterle, H. (2013) Synergistic binding of transcription factors to cell-specific enhancers programs motor neuron identity. Nat. Neurosci. 16, 1219-1227
-
(2013)
Nat. Neurosci.
, vol.16
, pp. 1219-1227
-
-
Mazzoni, E.O.1
Mahony, S.2
Closser, M.3
Morrison, C.A.4
Nedelec, S.5
Williams, D.J.6
An, D.7
Gifford, D.K.8
Wichterle, H.9
-
51
-
-
84857938446
-
Comparative proteomic analysis of eleven common cell lines reveals ubiquitous but varying expression of most proteins
-
M111.014050
-
Geiger, T. W. A., Schaab, C., Cox, J., and Mann, M. (2012) Comparative proteomic analysis of eleven common cell lines reveals ubiquitous but varying expression of most proteins. Mol. Cell. Proteomics 11 M111.014050
-
(2012)
Mol. Cell. Proteomics
, vol.11
-
-
Geiger, T.W.A.1
Schaab, C.2
Cox, J.3
Mann, M.4
-
52
-
-
84872685287
-
Extensive quantitative remodeling of the proteome between normal colon tissue and adenocarcinoma
-
Wisniewski, J. R., Ostasiewicz, P., Dus, K., Zielinska, D. F., Gnad, F., and Mann, M. (2012) Extensive quantitative remodeling of the proteome between normal colon tissue and adenocarcinoma. Mol. Syst. Biol. 8, 611
-
(2012)
Mol. Syst. Biol.
, vol.8
, pp. 611
-
-
Wisniewski, J.R.1
Ostasiewicz, P.2
Dus, K.3
Zielinska, D.F.4
Gnad, F.5
Mann, M.6
-
53
-
-
67650498361
-
Axon guidance proteins: Novel therapeutic targets for ALS?
-
Schmidt, E. R., Pasterkamp, R. J., and van den Berg, L. H. (2009) Axon guidance proteins: novel therapeutic targets for ALS? Prog. Neurobiol. 88, 286-301
-
(2009)
Prog. Neurobiol.
, vol.88
, pp. 286-301
-
-
Schmidt, E.R.1
Pasterkamp, R.J.2
Van Den Berg, L.H.3
-
54
-
-
79951704433
-
Neuroinflammation in amyotrophic lateral sclerosis: Role of glial activation in motor neuron disease
-
Philips, T., and Robberecht, W. (2011) Neuroinflammation in amyotrophic lateral sclerosis: role of glial activation in motor neuron disease. Lancet Neurol. 10, 253-263
-
(2011)
Lancet Neurol.
, vol.10
, pp. 253-263
-
-
Philips, T.1
Robberecht, W.2
-
55
-
-
84857980282
-
Analysis of high accuracy, quantitative proteomics data in the MaxQB database
-
M111.014068
-
Schaab, C., Geiger, T., Stoehr, G., Cox, J., and Mann, M. (2012) Analysis of high accuracy, quantitative proteomics data in the MaxQB database. Mol. Cell. Proteomics 11, M111.014068
-
(2012)
Mol. Cell. Proteomics
, vol.11
-
-
Schaab, C.1
Geiger, T.2
Stoehr, G.3
Cox, J.4
Mann, M.5
-
56
-
-
33751229311
-
The role of excitotoxicity in the pathogenesis of amyotrophic lateral sclerosis
-
Van Den Bosch, L., Van Damme, P., Bogaert, E., and Robberecht, W. (2006) The role of excitotoxicity in the pathogenesis of amyotrophic lateral sclerosis. Biochim. Biophys. Acta 1762, 1068-1082
-
(2006)
Biochim. Biophys. Acta
, vol.1762
, pp. 1068-1082
-
-
Van Den Bosch, L.1
Van Damme, P.2
Bogaert, E.3
Robberecht, W.4
-
57
-
-
0027328895
-
Spinal cord motoneurons express p75NGFR and p145trkB mRNA in amyotrophic lateral sclerosis
-
Seeburger, J. L., Tarras, S., Natter, H., and Springer, J. E. (1993) Spinal cord motoneurons express p75NGFR and p145trkB mRNA in amyotrophic lateral sclerosis. Brain Res. 621, 111-115
-
(1993)
Brain Res.
, vol.621
, pp. 111-115
-
-
Seeburger, J.L.1
Tarras, S.2
Natter, H.3
Springer, J.E.4
-
58
-
-
0030271362
-
Potential roles of gene expression change in adult rat spinal motoneurons following axonal injury: A comparison among c-jun, off- affinity nerve growth factor receptor (LNGFR), and nitric oxide synthase (NOS)
-
Wu, W. (1996) Potential roles of gene expression change in adult rat spinal motoneurons following axonal injury: a comparison among c-jun, off- affinity nerve growth factor receptor (LNGFR), and nitric oxide synthase (NOS). Exp. Neurol. 141, 190-200
-
(1996)
Exp. Neurol.
, vol.141
, pp. 190-200
-
-
Wu, W.1
-
59
-
-
38649087009
-
Nogo receptor antagonizes p75NTR-dependent motor neuron death
-
Dupuis, L., Pehar, M., Cassina, P., Rene, F., Castellanos, R., Rouaux, C., Gandelman, M., Dimou, L., Schwab, M. E., Loeffler, J. P., Barbeito, L., and Gonzalez de Aguilar, J. L. (2008) Nogo receptor antagonizes p75NTR-dependent motor neuron death. Proc. Natl. Acad. Sci. U.S.A. 105, 740-745
-
(2008)
Proc. Natl. Acad. Sci. U.S.A.
, vol.105
, pp. 740-745
-
-
Dupuis, L.1
Pehar, M.2
Cassina, P.3
Rene, F.4
Castellanos, R.5
Rouaux, C.6
Gandelman, M.7
Dimou, L.8
Schwab, M.E.9
Loeffler, J.P.10
Barbeito, L.11
Gonzalez De Aguilar, J.L.12
-
60
-
-
23044488902
-
The yin and yang of neurotrophin action
-
Lu, B., Pang, P. T., and Woo, N. H. (2005) The yin and yang of neurotrophin action. Nat. Rev. Neurosci. 6, 603-614
-
(2005)
Nat. Rev. Neurosci.
, vol.6
, pp. 603-614
-
-
Lu, B.1
Pang, P.T.2
Woo, N.H.3
-
61
-
-
77954653461
-
Neurotoxic effects of TDP-43 overexpression in C. Elegans
-
Ash, P. E., Zhang, Y. J., Roberts, C. M., Saldi, T., Hutter, H., Buratti, E., Petrucelli, L., and Link, C. D. (2010) Neurotoxic effects of TDP-43 overexpression in C. elegans. Hum. Mol. Genet. 19, 3206-3218
-
(2010)
Hum. Mol. Genet.
, vol.19
, pp. 3206-3218
-
-
Ash, P.E.1
Zhang, Y.J.2
Roberts, C.M.3
Saldi, T.4
Hutter, H.5
Buratti, E.6
Petrucelli, L.7
Link, C.D.8
-
62
-
-
77649269011
-
TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration
-
Wils, H., Kleinberger, G., Janssens, J., Pereson, S., Joris, G., Cuijt, I., Smits, V., Ceuterick-de Groote, C., Van Broeckhoven, C., and Kumar-Singh, S. (2010) TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration. Proc. Natl. Acad. Sci. U.S.A. 107, 3858-3863
-
(2010)
Proc. Natl. Acad. Sci. U.S.A.
, vol.107
, pp. 3858-3863
-
-
Wils, H.1
Kleinberger, G.2
Janssens, J.3
Pereson, S.4
Joris, G.5
Cuijt, I.6
Smits, V.7
Ceuterick-de Groote, C.8
Van Broeckhoven, C.9
Kumar-Singh, S.10
-
63
-
-
80054024011
-
Pathogenic protein seeding in Alzheimer disease and other neurodegenerative disorders
-
Jucker, M., and Walker, L. C. (2011) Pathogenic protein seeding in Alzheimer disease and other neurodegenerative disorders. Ann. Neurol. 70, 532-540
-
(2011)
Ann. Neurol.
, vol.70
, pp. 532-540
-
-
Jucker, M.1
Walker, L.C.2
|