-
1
-
-
0037461283
-
Corticospinal tract degeneration in the progressive muscular atrophy variant of ALS
-
Ince, P.G., Evans, J., Knopp, M., Forster, G., Hamdalla, H.H., Wharton, S.B. and Shaw, P.J. (2003) Corticospinal tract degeneration in the progressive muscular atrophy variant of ALS. Neurology, 60, 1252-1258.
-
(2003)
Neurology
, vol.60
, pp. 1252-1258
-
-
Ince, P.G.1
Evans, J.2
Knopp, M.3
Forster, G.4
Hamdalla, H.H.5
Wharton, S.B.6
Shaw, P.J.7
-
2
-
-
0027401203
-
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
-
Rosen, D.R., Siddique, T., Patterson, D., Figlewicz, D.A., Sapp, P., Hentati, A., Donaldson, D., Goto, J., O'Regan, J.P., Deng, H.X. et al. (1993) Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Nature, 362, 59-62.
-
(1993)
Nature
, vol.362
, pp. 59-62
-
-
Rosen, D.R.1
Siddique, T.2
Patterson, D.3
Figlewicz, D.A.4
Sapp, P.5
Hentati, A.6
Donaldson, D.7
Goto, J.8
O'Regan, J.P.9
Deng, H.X.10
-
3
-
-
6344257200
-
A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis
-
Nishimura, A.L., Mitne-Nato, M., Silva, H.C., Richieri-Costa, A., Middleton, S., Cascio, D., Kok, F., Oliveira, J.R., Gillingwater, T., Webb, J. et al. (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-Nato, 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
-
4
-
-
33751250197
-
Genetics of familial and sporadic amyotrophic lateral sclerosis
-
First published February 10 2006 doi:10.1016/j.bbadis.2006.01.004
-
Gros-Louis, F., Gaspar, C. and Rouleau, G.A. (2006) Genetics of familial and sporadic amyotrophic lateral sclerosis. Biochim. Biophys. Acta. First published February 10, 2006. doi:10.1016/j.bbadis.2006.01.004.
-
(2006)
Biochim. Biophys. Acta
-
-
Gros-Louis, F.1
Gaspar, C.2
Rouleau, G.A.3
-
5
-
-
0037426388
-
Are amyotrophic lateral sclerosis patients cognitively normal?
-
Lomen-Hoerth, C., Murphy, J., Langmore, S., Kramer, J.H., Olney, R.K. and Miller, B. (2003) Are amyotrophic lateral sclerosis patients cognitively normal? Neurology, 60, 1094-1097.
-
(2003)
Neurology
, vol.60
, pp. 1094-1097
-
-
Lomen-Hoerth, C.1
Murphy, J.2
Langmore, S.3
Kramer, J.H.4
Olney, R.K.5
Miller, B.6
-
6
-
-
23844511513
-
Prevalence and patterns of cognitive impairment in sporadic ALS
-
Ringholz, G.M., Appel, S.H., Bradshaw, M., Cooke, N.A., Mosnik, D.M. and Schulz, P.E. (2005) Prevalence and patterns of cognitive impairment in sporadic ALS. Neurology, 65, 586-590.
-
(2005)
Neurology
, vol.65
, pp. 586-590
-
-
Ringholz, G.M.1
Appel, S.H.2
Bradshaw, M.3
Cooke, N.A.4
Mosnik, D.M.5
Schulz, P.E.6
-
7
-
-
0026691337
-
Hippocampal and neocortical ubiquitin-immunoreactive inclusions in amyotrophic lateral sclerosis with dementia
-
Wightman, G., Anderson, V.E., Martin, J., Swash, M., Anderton, B.H., Neary, D., Mann, D., Luthert, P. and Leigh, P.N. (1992) Hippocampal and neocortical ubiquitin-immunoreactive inclusions in amyotrophic lateral sclerosis with dementia. Neurosci. Lett., 139, 269-274.
-
(1992)
Neurosci. Lett.
, vol.139
, pp. 269-274
-
-
Wightman, G.1
Anderson, V.E.2
Martin, J.3
Swash, M.4
Anderton, B.H.5
Neary, D.6
Mann, D.7
Luthert, P.8
Leigh, P.N.9
-
8
-
-
3843089299
-
Neuronal ubiquitinated intranuclear inclusions in familial and non-familial frontotemporal dementia of the motor neuron disease type associated with amyotrophic lateral sclerosis
-
Bigio, E.H., Johnson, N.A., Rademaker, A.W., Fung, B.B., Mesulam, M.M., Siddique, N., Dellefave, L., Caliendo, J., Freeman, S. and Siddique, T. (2004) Neuronal ubiquitinated intranuclear inclusions in familial and non-familial frontotemporal dementia of the motor neuron disease type associated with amyotrophic lateral sclerosis. J. Neuropathol. Exp. Neurol., 63, 801-811.
-
(2004)
J. Neuropathol. Exp. Neurol.
, vol.63
, pp. 801-811
-
-
Bigio, E.H.1
Johnson, N.A.2
Rademaker, A.W.3
Fung, B.B.4
Mesulam, M.M.5
Siddique, N.6
Dellefave, L.7
Caliendo, J.8
Freeman, S.9
Siddique, T.10
-
9
-
-
26844447994
-
Frontotemporal dementia
-
Neary, D., Snowden, J. and Mann, D. (2005) Frontotemporal dementia. Lancet Neurol., 4, 771-780.
-
(2005)
Lancet Neurol.
, vol.4
, pp. 771-780
-
-
Neary, D.1
Snowden, J.2
Mann, D.3
-
10
-
-
0032543684
-
Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17
-
Hutton, M., Lendon, C.L., Rizzu, P., Baker, M., Froelich, S., Houlden, H., Pickering-Brown, S., Chakraverty, S., Isaacs, A., Graver, A. et al. (1998) Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17. Nature, 393, 702-705.
-
(1998)
Nature
, vol.393
, pp. 702-705
-
-
Hutton, M.1
Lendon, C.L.2
Rizzu, P.3
Baker, M.4
Froelich, S.5
Houlden, H.6
Pickering-Brown, S.7
Chakraverty, S.8
Isaacs, A.9
Graver, A.10
-
11
-
-
33645059953
-
Frontal temporal dementia: Dissecting the aetiology and pathogenesis
-
Hardy, J., Momeni, P. and Traynor, B.J. (2006) Frontal temporal dementia: Dissecting the aetiology and pathogenesis. Brain, 129, 830-831.
-
(2006)
Brain
, vol.129
, pp. 830-831
-
-
Hardy, J.1
Momeni, P.2
Traynor, B.J.3
-
12
-
-
0033041179
-
Association of an extended haplotype in the tau gene with progressive supranuclear palsy
-
Baker, M., Litvan, I., Houlden, H., Adamson, J., Dickson, D., Perez-Tur, J., Hardy, J., Lynch, T., Bigio, E. and Hutton, M. (1999) Association of an extended haplotype in the tau gene with progressive supranuclear palsy. Hum. Mol. Genet., 8, 711-715.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 711-715
-
-
Baker, M.1
Litvan, I.2
Houlden, H.3
Adamson, J.4
Dickson, D.5
Perez-Tur, J.6
Hardy, J.7
Lynch, T.8
Bigio, E.9
Hutton, M.10
-
13
-
-
0035954364
-
Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype
-
Houlden, H., Baker, M., Morris, H.R., MacDonald, N., Pickering-Brown, S., Adamson; J., Lees, A.J., Rossor, M.N., Quinn, N.P., Kertesz, A. et al. (2001) Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype. Neurology, 56, 1702-1706.
-
(2001)
Neurology
, vol.56
, pp. 1702-1706
-
-
Houlden, H.1
Baker, M.2
Morris, H.R.3
MacDonald, N.4
Pickering-Brown, S.5
Adamson, J.6
Lees, A.J.7
Rossor, M.N.8
Quinn, N.P.9
Kertesz, A.10
-
14
-
-
0034426011
-
Neurofibrillary tangles, amyotrophy and progressive motor disturbance in mice expressing mutant (P301L) tau protein
-
Lewis, J., McGowan, E., Rockwood, J., Melrose, H., Nacharaju, P., Van Slegtenhorst, M., Gwinn-Hardy, K., Paul Murphy, M., Baker, M., Yu, X. et al. (2000) Neurofibrillary tangles, amyotrophy and progressive motor disturbance in mice expressing mutant (P301L) tau protein. Nat. Genet., 25, 402-405.
-
(2000)
Nat. Genet.
, vol.25
, pp. 402-405
-
-
Lewis, J.1
McGowan, E.2
Rockwood, J.3
Melrose, H.4
Nacharaju, P.5
Van Slegtenhorst, M.6
Gwinn-Hardy, K.7
Paul Murphy, M.8
Baker, M.9
Yu, X.10
-
15
-
-
33745654119
-
Tau protein hyperphosphorylation in sporadic ALS with cognitive impairment
-
Strong, M.J., Yang, W., Strong, W.L., Leystra-Lantz, C., Jaffe, H. and Pant, H.C. (2006) Tau protein hyperphosphorylation in sporadic ALS with cognitive impairment. Neurology, 66, 1770-1771.
-
(2006)
Neurology
, vol.66
, pp. 1770-1771
-
-
Strong, M.J.1
Yang, W.2
Strong, W.L.3
Leystra-Lantz, C.4
Jaffe, H.5
Pant, H.C.6
-
16
-
-
0034605478
-
Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22
-
Hosler, B.A., Siddique, T., Sapp, P.C., Sailor, W., Huang, M.C., Hossain, A., Daube, J.R., Nance, M., Fan, C., Kaplan, J. et al. (2000) Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22. JAMA, 284, 1664-1669.
-
(2000)
JAMA
, vol.284
, pp. 1664-1669
-
-
Hosler, B.A.1
Siddique, T.2
Sapp, P.C.3
Sailor, W.4
Huang, M.C.5
Hossain, A.6
Daube, J.R.7
Nance, M.8
Fan, C.9
Kaplan, J.10
-
17
-
-
0041664055
-
Two families with familial amyotrophic lateral sclerosis are linked to a novel locus on chromosome 16q
-
Ruddy, D.M., Parton, M.J., Al-Chalabi, A., Lewis, C.M., Vance, C., Smith, B.N., Leigh, P.N., Powell, J.F., Siddique, T., Meyjes, E.P. et al. (2003) Two families with familial amyotrophic lateral sclerosis are linked to a novel locus on chromosome 16q. Am. J. Hum. Genet., 73, 390-396.
-
(2003)
Am. J. Hum. Genet.
, vol.73
, pp. 390-396
-
-
Ruddy, D.M.1
Parton, M.J.2
Al-Chalabi, A.3
Lewis, C.M.4
Vance, C.5
Smith, B.N.6
Leigh, P.N.7
Powell, J.F.8
Siddique, T.9
Meyjes, E.P.10
-
18
-
-
33645069660
-
Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2-21.3
-
Vance, C., Al-Chalabi, A., Ruddy, D., Smith, B.N., Hu, X., Sreedharan, J., Siddique, T., Schelhaas, H.J., Kusters, B., Troost, D. et al. (2006) Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2-21.3. Brain, 129, 868-876.
-
(2006)
Brain
, vol.129
, pp. 868-876
-
-
Vance, C.1
Al-Chalabi, A.2
Ruddy, D.3
Smith, B.N.4
Hu, X.5
Sreedharan, J.6
Siddique, T.7
Schelhaas, H.J.8
Kusters, B.9
Troost, D.10
-
19
-
-
33645062075
-
A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia
-
Morita, M., Al-Chalabi, A., Andersen, P.M., Hosler, B., Sapp, P., Englund, E., Mitchell, J.E., Habgood, J.J., de Belleroche, J., Xi, J. et al. (2006) A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia. Neurology, 66, 839-844.
-
(2006)
Neurology
, vol.66
, pp. 839-844
-
-
Morita, M.1
Al-Chalabi, A.2
Andersen, P.M.3
Hosler, B.4
Sapp, P.5
Englund, E.6
Mitchell, J.E.7
Habgood, J.J.8
de Belleroche, J.9
Xi, J.10
-
20
-
-
33749009080
-
A major novel locus for ALS/FTD on chromosome 9p21 and its pathological correlates: S61.006
-
Yan, J., Siddique, N., Slifer, S., Bigio, E., Mao, H., Chen, W., Liu, E., Shi, Y., Khan, S., Haines, J. et al. (2006) A major novel locus for ALS/FTD on chromosome 9p21 and its pathological correlates: S61.006. Neurology, 67, 186.
-
(2006)
Neurology
, vol.67
, pp. 186
-
-
Yan, J.1
Siddique, N.2
Slifer, S.3
Bigio, E.4
Mao, H.5
Chen, W.6
Liu, E.7
Shi, Y.8
Khan, S.9
Haines, J.10
-
21
-
-
0029119112
-
Familial non-specific dementia maps to chromosome 3
-
Brown, J., Ashworth, A., Gydesen, S., Sorensen, A., Rossor, M., Hardy, J. and Collinge, J. (1995) Familial non-specific dementia maps to chromosome 3. Hum. Mol. Genet., 4, 1625-1628.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1625-1628
-
-
Brown, J.1
Ashworth, A.2
Gydesen, S.3
Sorensen, A.4
Rossor, M.5
Hardy, J.6
Collinge, J.7
-
22
-
-
0037180476
-
Chromosome 3 linked frontotemporal dementia (FTD-3)
-
Gydesen, S., Brown, J.M., Brun, A., Chakrabarti, L., Gade, A., Johamusen, P., Rossor, M., Thusgaard, T., Grove, A., Yancopoulou, D. et al. (2002) Chromosome 3 linked frontotemporal dementia (FTD-3). Neurology, 59, 1585-1594.
-
(2002)
Neurology
, vol.59
, pp. 1585-1594
-
-
Gydesen, S.1
Brown, J.M.2
Brun, A.3
Chakrabarti, L.4
Gade, A.5
Johamusen, P.6
Rossor, M.7
Thusgaard, T.8
Grove, A.9
Yancopoulou, D.10
-
23
-
-
23044471011
-
Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia
-
Skibinski, G., Parkinson, N.J., Brown, J.M., Chakrabarti, L., Lloyd, S.L., Hummerich, H., Nielsen, J.E., Hodges, J.R., Spillantini, M.G., Thusgaard, T. et al. (2005) Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia. Nat. Genet., 37, 806-808.
-
(2005)
Nat. Genet.
, vol.37
, pp. 806-808
-
-
Skibinski, G.1
Parkinson, N.J.2
Brown, J.M.3
Chakrabarti, L.4
Lloyd, S.L.5
Hummerich, H.6
Nielsen, J.E.7
Hodges, J.R.8
Spillantini, M.G.9
Thusgaard, T.10
-
24
-
-
33646000253
-
CHMP2B mutations are not a common cause of frontotemporal lobar degeneration
-
Cannon, A., Baker, M., Boeve, B., Josephs, K., Knopman, D., Petersen, R., Parisi, J., Dickison, D., Adamson, J., Snowden, J. et al. (2006) CHMP2B mutations are not a common cause of frontotemporal lobar degeneration. Neurosci. Lett., 398, 83-84.
-
(2006)
Neurosci. Lett.
, vol.398
, pp. 83-84
-
-
Cannon, A.1
Baker, M.2
Boeve, B.3
Josephs, K.4
Knopman, D.5
Petersen, R.6
Parisi, J.7
Dickison, D.8
Adamson, J.9
Snowden, J.10
-
25
-
-
33749006845
-
ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B)
-
First published on-line June, 28, 2006. doi:10.1212/01.wnl.0000231510.89311:8b
-
Parkinson, N., Ince, P.G., Smith, M.O., Highley, R., Skibinski, G., Andersen, P.M., Morrison, K.E., Pall, H.S., Hardiman, O., Collinge, J. et al. (2006) ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B). Neurology. First published on-line June, 28, 2006. doi:10.121B/01.wnl.0000231510.89311:8b.
-
(2006)
Neurology
-
-
Parkinson, N.1
Ince, P.G.2
Smith, M.O.3
Highley, R.4
Skibinski, G.5
Andersen, P.M.6
Morrison, K.E.7
Pall, H.S.8
Hardiman, O.9
Collinge, J.10
-
27
-
-
0037734370
-
Mutations in dynein link motor neuron degeneration to defects in retrograde transport
-
Hafezparast, M., Klocke, R., Ruhrberg, C., Marquardt, A., Ahmad-Annuar, A., Bowen, S., Lalli, G., Witherden, A.S., Hummerich, H., Nicholson, S. et al. (2003) Mutations in dynein link motor neuron degeneration to defects in retrograde transport. Science, 300, 808-812.
-
(2003)
Science
, vol.300
, pp. 808-812
-
-
Hafezparast, M.1
Klocke, R.2
Ruhrberg, C.3
Marquardt, A.4
Ahmad-Annuar, A.5
Bowen, S.6
Lalli, G.7
Witherden, A.S.8
Hummerich, H.9
Nicholson, S.10
-
28
-
-
0037198698
-
Disruption of dynein/dynactin inhibits axonal transport in motor neurons causing late-onset progressive degeneration
-
LaMonte, B.H., Wallace, K.E., Holloway, B.A., Shelly, S.S., Ascano, J., Tokito, M., Van Winkle, T., Howland, D.S. and Holzbaur, E.L. (2002) Disruption of dynein/dynactin inhibits axonal transport in motor neurons causing late-onset progressive degeneration. Neuron, 34, 715-727.
-
(2002)
Neuron
, vol.34
, pp. 715-727
-
-
LaMonte, B.H.1
Wallace, K.E.2
Holloway, B.A.3
Shelly, S.S.4
Ascano, J.5
Tokito, M.6
Van Winkle, T.7
Howland, D.S.8
Holzbaur, E.L.9
-
29
-
-
0037382240
-
Mutant dynactin in motor neuron disease
-
Puls, I., Jonnakuty, C., LaMonte, B.H., Holzbaur, E.L., Tokito, M., Mann, E., Floeter, M.K., Bidus, K., Drayna, D., Oh, S.J. et al. (2003) Mutant dynactin in motor neuron disease. Nat. Genet., 33, 455-456.
-
(2003)
Nat. Genet.
, vol.33
, pp. 455-456
-
-
Puls, I.1
Jonnakuty, C.2
LaMonte, B.H.3
Holzbaur, E.L.4
Tokito, M.5
Mann, E.6
Floeter, M.K.7
Bidus, K.8
Drayna, D.9
Oh, S.J.10
-
30
-
-
4143084861
-
Point mutations of the p150 subunit of dynactin (DCTN1) gene in ALS
-
Munch, C., Sedlmeier, R., Meyer, T., Homberg, V., Sperfeld, A.D., Kurt, A., Prudlo, J., Peraus, G., Hanemann, C.O., Stumm, G. et al. (2004) Point mutations of the p150 subunit of dynactin (DCTN1) gene in ALS. Neurology, 63, 724-726.
-
(2004)
Neurology
, vol.63
, pp. 724-726
-
-
Munch, C.1
Sedlmeier, R.2
Meyer, T.3
Homberg, V.4
Sperfeld, A.D.5
Kurt, A.6
Prudlo, J.7
Peraus, G.8
Hanemann, C.O.9
Stumm, G.10
-
31
-
-
27644558934
-
Heterozygous R1101K mutation of the DCTN1 gene in a family with ALS and FTD
-
Munch, C., Rosenbohm, A., Sperfeld, A.D., Uttner, I., Reske, S., Krause, B.J., Sedlmeier, R., Meyer, T., Hanemann, C.O., Stumm, G. et al. (2005) Heterozygous R1101K mutation of the DCTN1 gene in a family with ALS and FTD. Ann. Neurol., 58, 777-780.
-
(2005)
Ann. Neurol.
, vol.58
, pp. 777-780
-
-
Munch, C.1
Rosenbohm, A.2
Sperfeld, A.D.3
Uttner, I.4
Reske, S.5
Krause, B.J.6
Sedlmeier, R.7
Meyer, T.8
Hanemann, C.O.9
Stumm, G.10
-
32
-
-
18244381306
-
Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: Hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia
-
Kovach, M.J., Waggoner, B., Leal, S.M., Gelber, D., Khardori, R., Levenstien, M.A., Shanks, C.A., Gregg, G., Al-Lozi, M.T., Miller, T. et al. (2001) Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: Hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia. Mol. Genet. Metab., 74, 458-475.
-
(2001)
Mol. Genet. Metab.
, vol.74
, pp. 458-475
-
-
Kovach, M.J.1
Waggoner, B.2
Leal, S.M.3
Gelber, D.4
Khardori, R.5
Levenstien, M.A.6
Shanks, C.A.7
Gregg, G.8
Al-Lozi, M.T.9
Miller, T.10
-
33
-
-
1842483843
-
Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein
-
Watts, G.D., Wymer, J., Kovach, M.J., Mehta, S.G., Mumm, S., Darvish, D., Pestronk, A., Whyte, M.P. and Kimonis, V.E. (2004) Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein. Nat. Genet., 36, 377-381.
-
(2004)
Nat. Genet.
, vol.36
, pp. 377-381
-
-
Watts, G.D.1
Wymer, J.2
Kovach, M.J.3
Mehta, S.G.4
Mumm, S.5
Darvish, D.6
Pestronk, A.7
Whyte, M.P.8
Kimonis, V.E.9
-
34
-
-
33745224935
-
p97: The cell's molecular purgatory?
-
Halawani, D. and Latterich, M. (2006) p97: The cell's molecular purgatory? Mol. Cell, 22, 713-717.
-
(2006)
Mol. Cell
, vol.22
, pp. 713-717
-
-
Halawani, D.1
Latterich, M.2
-
35
-
-
20044373638
-
Mutant valosin-containing protein causes a novel type of frontotemporal dementia
-
Schroder, R., Watts, G.D., Mehta, S.G., Evert, B.O., Broich, P., Fliessbach, K., Pauls, K., Hans, V.H., Kimonis, V. and Thal, D.R. (2005) Mutant valosin-containing protein causes a novel type of frontotemporal dementia. Ann. Neurol., 57, 457-461.
-
(2005)
Ann. Neurol.
, vol.57
, pp. 457-461
-
-
Schroder, R.1
Watts, G.D.2
Mehta, S.G.3
Evert, B.O.4
Broich, P.5
Fliessbach, K.6
Pauls, K.7
Hans, V.H.8
Kimonis, V.9
Thal, D.R.10
-
36
-
-
33746693220
-
Novel ubiquitin neuropathology in frontotemporal dementia with valosin-containing protein gene mutations
-
Forman, M.S., Mackenzie, I.R., Cairns, N.J., Swanson, E., Boyer, P.J., Drachman, D.A., Jhaveri, B.S., Karlawish, J.H., Pestronk, A., Smith, T.W. et al. (2006) Novel ubiquitin neuropathology in frontotemporal dementia with valosin-containing protein gene mutations. J. Neuropathol. Exp. Neurol., 65, 571-581.
-
(2006)
J. Neuropathol. Exp. Neurol.
, vol.65
, pp. 571-581
-
-
Forman, M.S.1
Mackenzie, I.R.2
Cairns, N.J.3
Swanson, E.4
Boyer, P.J.5
Drachman, D.A.6
Jhaveri, B.S.7
Karlawish, J.H.8
Pestronk, A.9
Smith, T.W.10
-
37
-
-
31144470450
-
Inclusion body myopathy-associated mutations in p97/VCP impair endoplasmic reticulum-associated degradation
-
Weihl, C.C., Dalal, S., Pestronk, A. and Hanson, P.I. (2006) Inclusion body myopathy-associated mutations in p97/VCP impair endoplasmic reticulum-associated degradation. Hum. Mol. Genet., 15, 189-199.
-
(2006)
Hum. Mol. Genet.
, vol.15
, pp. 189-199
-
-
Weihl, C.C.1
Dalal, S.2
Pestronk, A.3
Hanson, P.I.4
-
38
-
-
33746919083
-
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
-
First published on-line July 16, 2006. doi:10.1038/nature05016
-
Baker, M., Mackenzie, I.R., Pickering-Brown, S.M., Gass, J., Rademakers, R., Lindholm, C., Snowden, J., Adamson, J., Sadovnick, A.D., Rollinson, S. et al. (2006) Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17. Nature. First published on-line July 16, 2006. doi:10.1038/nature05016.
-
(2006)
Nature
-
-
Baker, M.1
Mackenzie, I.R.2
Pickering-Brown, S.M.3
Gass, J.4
Rademakers, R.5
Lindholm, C.6
Snowden, J.7
Adamson, J.8
Sadovnick, A.D.9
Rollinson, S.10
-
39
-
-
33746910649
-
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
-
First published on-line July 16, 2006. doi:10.1038/nature05017
-
Cruts, M., Gijselinck, I., van der Zee, J., Engelborghs, S., Wils, H., Pirici, D., Rademakers, R., Vandenberghe, R., Dermaut, B., Martin, J.J, et al. (2006) Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21. Nature, First published on-line July 16, 2006. doi:10.1038/nature05017.
-
(2006)
Nature
-
-
Cruts, M.1
Gijselinck, I.2
van der Zee, J.3
Engelborghs, S.4
Wils, H.5
Pirici, D.6
Rademakers, R.7
Vandenberghe, R.8
Dermaut, B.9
Martin, J.J.10
-
40
-
-
33645072728
-
A family with tau-negative frontotemporal dementia and neuronal intranuclear inclusions linked to chromosome 17
-
Mackenzie, I.R., Baker, M., West, G., Woulfe, J., Qadi, N., Gass, J., Cannon, A., Adamson, J., Feldman, H., Lindholm, C. et al. (2006) A family with tau-negative frontotemporal dementia and neuronal intranuclear inclusions linked to chromosome 17. Brain, 129, 853-867.
-
(2006)
Brain
, vol.129
, pp. 853-867
-
-
Mackenzie, I.R.1
Baker, M.2
West, G.3
Woulfe, J.4
Qadi, N.5
Gass, J.6
Cannon, A.7
Adamson, J.8
Feldman, H.9
Lindholm, C.10
-
41
-
-
4544367851
-
PC cell-derived growth factor (PCDGF/GP88, progranulin) stimulates migration, invasiveness and VEGF expression in breast cancer cells
-
Tangkeangsirisin, W. and Serrero, G. (2004) PC cell-derived growth factor (PCDGF/GP88, progranulin) stimulates migration, invasiveness and VEGF expression in breast cancer cells. Carcinogenesis, 25, 1587-1592.
-
(2004)
Carcinogenesis
, vol.25
, pp. 1587-1592
-
-
Tangkeangsirisin, W.1
Serrero, G.2
-
42
-
-
0041903805
-
VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death
-
Lambrechts, D., Storkebaum, E., Morimoto, M., Del-Favero, J., Desmet, F., Marklund, S.L., Wyns, S., Thijs, V., Andersson, J., van Marion, I. et al. (2003) VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death. Nat. Genet., 34, 383-394.
-
(2003)
Nat. Genet.
, vol.34
, pp. 383-394
-
-
Lambrechts, D.1
Storkebaum, E.2
Morimoto, M.3
Del-Favero, J.4
Desmet, F.5
Marklund, S.L.6
Wyns, S.7
Thijs, V.8
Andersson, J.9
van Marion, I.10
|