-
1
-
-
0022871177
-
Ballooned neurone in select neurodegenerative diseases contain phosphorylated neurofilament epitopes
-
Dickson, D. W. et al. Ballooned neurone in select neurodegenerative diseases contain phosphorylated neurofilament epitopes. Acta Neuropathol. 71, 216-223 (1986).
-
(1986)
Acta Neuropathol.
, vol.71
, pp. 216-223
-
-
Dickson, D.W.1
-
2
-
-
0022616904
-
Cytoskeletal protein abnormalities in neurodegenerative diseases
-
Goldman, J. E. & Yen, S. H. Cytoskeletal protein abnormalities in neurodegenerative diseases. Ann. Neurol 19, 209-223 (1987).
-
(1987)
Ann. Neurol
, vol.19
, pp. 209-223
-
-
Goldman, J.E.1
Yen, S.H.2
-
3
-
-
0022758234
-
2,5-Hexanedione neuropathy is associated with covalent crosslinking of neurofilament proteins
-
Carden, M. J., Lee, V. M.-Y. & Schlaepfer, W. W. 2,5-Hexanedione neuropathy is associated with covalent crosslinking of neurofilament proteins. Neurochem. Pathol. 5, 25-35 (1986).
-
(1986)
Neurochem. Pathol.
, vol.5
, pp. 25-35
-
-
Carden, M.J.1
Lee, V.M.-Y.2
Schlaepfer, W.W.3
-
4
-
-
0024321887
-
Effect of a single dose of β,β′ -Iminodipropionitrile in vivo on the properties of neurofilaments in vitro: Comparison with the effect of Imminodipropionitrile added directly to neurofilaments in vitro
-
Eyer, J., McLean, W. G. & Leterrier, J. F. Effect of a single dose of β,β′ -Iminodipropionitrile in vivo on the properties of neurofilaments in vitro: comparison with the effect of Imminodipropionitrile added directly to neurofilaments in vitro. J. Neurochem. 52, 1759-1765 (1989).
-
(1989)
J. Neurochem.
, vol.52
, pp. 1759-1765
-
-
Eyer, J.1
McLean, W.G.2
Leterrier, J.F.3
-
5
-
-
0027314026
-
Pathology and biology of the Lewy body
-
Pollanen, M. S., Dickson, D. W. & Bergeron, C. Pathology and biology of the Lewy body. J. Neuropathol. Exp. Neurol. 52, 183-191 (1993).
-
(1993)
J. Neuropathol. Exp. Neurol.
, vol.52
, pp. 183-191
-
-
Pollanen, M.S.1
Dickson, D.W.2
Bergeron, C.3
-
6
-
-
0025807172
-
Epitopes located in spatially separate domains of each neurofilament subunit are present in Parkinson's disease Lewy body
-
Hill, W. D., Lee, V. M.-Y., Hurtig, H., Murray, J. M. & Trojanowski, J. Q. Epitopes located in spatially separate domains of each neurofilament subunit are present in Parkinson's disease Lewy body. J. Comp. Neurol. 109, 150-160 (1991).
-
(1991)
J. Comp. Neurol.
, vol.109
, pp. 150-160
-
-
Hill, W.D.1
Lee, V.M.-Y.2
Hurtig, H.3
Murray, J.M.4
Trojanowski, J.Q.5
-
7
-
-
0004008681
-
-
(eds Spencer, P. & Schaumburg, H. H.) Williams and Wilkins, Baltimore
-
Griffin, J. W. & Price, D. L. in Experimental and Clinical Neurotoxicology (eds Spencer, P. & Schaumburg, H. H.) 161-178 (Williams and Wilkins, Baltimore, 1980).
-
(1980)
Experimental and Clinical Neurotoxicology
, pp. 161-178
-
-
Griffin, J.W.1
Price, D.L.2
-
8
-
-
0014336826
-
Proximal axonal enlargement in motor neuron disease
-
Carpenter, S. Proximal axonal enlargement in motor neuron disease. Neurology 18, 841-851 (1968).
-
(1968)
Neurology
, vol.18
, pp. 841-851
-
-
Carpenter, S.1
-
9
-
-
0028063968
-
Neurofilament function and dysfunction: Involvement in axonal growth and neuronal disease
-
Lee, M. K. & Cleveland, D. W. Neurofilament function and dysfunction: involvement in axonal growth and neuronal disease. Curr. Opin. Cell Biol 6, 34-40 (1994).
-
(1994)
Curr. Opin. Cell Biol
, vol.6
, pp. 34-40
-
-
Lee, M.K.1
Cleveland, D.W.2
-
10
-
-
0027465098
-
Progressive neuronopathy in transgenic mice expressing the human neurofilament heavy gene: A mouse model of amyotrophic lateral sclerosis
-
Coté, F, Collard, J. F. & Julien, J. P. Progressive neuronopathy in transgenic mice expressing the human neurofilament heavy gene: a mouse model of amyotrophic lateral sclerosis. Cell 73, 35-46 (1993).
-
(1993)
Cell
, vol.73
, pp. 35-46
-
-
Coté, F.1
Collard, J.F.2
Julien, J.P.3
-
11
-
-
0028116467
-
A mutant neurofilament subunit causes massive, selective motor neuron death; implications for the pathogenesis of human motor neuron disease
-
Lee, M. K., Marszalek, J. R. & Cleveland, D.W. A mutant neurofilament subunit causes massive, selective motor neuron death; implications for the pathogenesis of human motor neuron disease. Neuron 13, 975-988 (1994).
-
(1994)
Neuron
, vol.13
, pp. 975-988
-
-
Lee, M.K.1
Marszalek, J.R.2
Cleveland, D.W.3
-
12
-
-
0027410516
-
Increased expression of neurofilament subunit NF-L produces morphological alterations that resemble the pathology of human motor neuron disease
-
Xu, Z. H., Cork, L. C., Griffin, J. W. & Cleveland, D. W. Increased expression of neurofilament subunit NF-L produces morphological alterations that resemble the pathology of human motor neuron disease. Cell 73, 23-33 (1993).
-
(1993)
Cell
, vol.73
, pp. 23-33
-
-
Xu, Z.H.1
Cork, L.C.2
Griffin, J.W.3
Cleveland, D.W.4
-
13
-
-
10244256425
-
Mechanisms of selective motor neurons death in transgenic mouse models of motor neuron disease
-
Cleveland, D. W. et al. Mechanisms of selective motor neurons death in transgenic mouse models of motor neuron disease. Neurology 47, 54-61 (1996).
-
(1996)
Neurology
, vol.47
, pp. 54-61
-
-
Cleveland, D.W.1
-
14
-
-
0030598838
-
An essential cytoskeletal linker protein connecting actin microfilaments ot intermediate filaments
-
Yang, Y. et al. An essential cytoskeletal linker protein connecting actin microfilaments ot intermediate filaments. Cell 86, 655-665 (1996).
-
(1996)
Cell
, vol.86
, pp. 655-665
-
-
Yang, Y.1
-
15
-
-
0029035706
-
The mouse dystonia musculorum gene is a neural isoform of bullous pemphigoid antigen 1
-
Brown, A., Bernier, G., Mathieu, M., Rossant, J. & Kothary, R. The mouse dystonia musculorum gene is a neural isoform of bullous pemphigoid antigen 1. Nature Genet. 10, 301-306 (1995).
-
(1995)
Nature Genet.
, vol.10
, pp. 301-306
-
-
Brown, A.1
Bernier, G.2
Mathieu, M.3
Rossant, J.4
Kothary, R.5
-
16
-
-
0027401203
-
Mutations in Cu/Zn Superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
-
Rosen, D. R. et al. Mutations in Cu/Zn Superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Nature 362, 59-62 (1993).
-
(1993)
Nature
, vol.362
, pp. 59-62
-
-
Rosen, D.R.1
-
17
-
-
0029053881
-
An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria
-
Wong, P. C. et al. An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria. Neuron 14, 1105-1116 (1995).
-
(1995)
Neuron
, vol.14
, pp. 1105-1116
-
-
Wong, P.C.1
-
18
-
-
0028261670
-
Neurofilament-deficient axons and perikaryal aggregates in viable transgenic mice expressing a neurofilament-β-galactosidase fusion protein
-
Eyer, J. & Peterson, A. C. Neurofilament-deficient axons and perikaryal aggregates in viable transgenic mice expressing a neurofilament-β-galactosidase fusion protein. Neuron 12, 389-405 (1994).
-
(1994)
Neuron
, vol.12
, pp. 389-405
-
-
Eyer, J.1
Peterson, A.C.2
-
19
-
-
0029557363
-
Accelerated and widespread neuronal loss occurs in motor neuron degeneration (MND) mice expressing a neurofilament-disrupting transgene
-
Plummer, J., Peterson, A. & Messer, A. Accelerated and widespread neuronal loss occurs in motor neuron degeneration (MND) mice expressing a neurofilament-disrupting transgene. Mol. Cell. Neurosci. 6, 532-543 (1995).
-
(1995)
Mol. Cell. Neurosci.
, vol.6
, pp. 532-543
-
-
Plummer, J.1
Peterson, A.2
Messer, A.3
-
20
-
-
0030614372
-
Selective degeneration of Purkinje cells with Lewy body-like inclusions in aged NFHlacZ transgenic mice
-
Tu, P.-H. et al. Selective degeneration of Purkinje cells with Lewy body-like inclusions in aged NFHlacZ transgenic mice. J. Neurosci. 17, 1064-1074 (1997).
-
(1997)
J. Neurosci.
, vol.17
, pp. 1064-1074
-
-
Tu, P.-H.1
-
21
-
-
0029066406
-
Gene targeting of BPAG1: Abnormalities in mechanical strength and cell migration in stratified squamos epithelia and severe neurologic degeneration
-
Guo, L. et al. Gene targeting of BPAG1: abnormalities in mechanical strength and cell migration in stratified squamos epithelia and severe neurologic degeneration. Cell 81, 233-243 (1995).
-
(1995)
Cell
, vol.81
, pp. 233-243
-
-
Guo, L.1
-
22
-
-
0016914818
-
Dystonia musculorum: An inherited disease of the nervous system in the mouse
-
Duchen, L. W. Dystonia musculorum: an inherited disease of the nervous system in the mouse. Adv. Neurol 14, 353-365 (1976).
-
(1976)
Adv. Neurol
, vol.14
, pp. 353-365
-
-
Duchen, L.W.1
-
23
-
-
0023747623
-
A transgene containing lacZ inserted into the dystonia locus is expressed in neural tube
-
Kothary, R. et al. A transgene containing lacZ inserted into the dystonia locus is expressed in neural tube. Nature 335, 435-437 (1988).
-
(1988)
Nature
, vol.335
, pp. 435-437
-
-
Kothary, R.1
-
24
-
-
0026630111
-
An intrinsic neuronal defect operates in dystonia musculorum: A study of dt/dt ↔ +/+ chimeras
-
Campbell, R. M. & Peterson, A. C. An intrinsic neuronal defect operates in dystonia musculorum: a study of dt/dt ↔ +/+ chimeras. Neuron 9, 693-703 (1992).
-
(1992)
Neuron
, vol.9
, pp. 693-703
-
-
Campbell, R.M.1
Peterson, A.C.2
-
25
-
-
0023698294
-
Pathologic changes in the CNS of dystonia musculorum mutant mouse: An animal model for human spinocerebellar ataxia
-
Sotelo, C. & Guenet, J. F. Pathologic changes in the CNS of dystonia musculorum mutant mouse: an animal model for human spinocerebellar ataxia. Neuroscience 27, 403-424 (1988).
-
(1988)
Neuroscience
, vol.27
, pp. 403-424
-
-
Sotelo, C.1
Guenet, J.F.2
-
26
-
-
0028284779
-
Motor neuron degeneration in mice that express a human Cu, Zn Superoxide dismutase mutation
-
Gurney, M. E. et al. Motor neuron degeneration in mice that express a human Cu, Zn Superoxide dismutase mutation. Science 264, 1772-1775 (1994).
-
(1994)
Science
, vol.264
, pp. 1772-1775
-
-
Gurney, M.E.1
-
27
-
-
0027293275
-
ALS, SOD and peroxynitrite
-
Beckman, J. S., Carson, M., Smith, C. D. & Koppenol, W. H. ALS, SOD and peroxynitrite. Nature 364, 584 (1993).
-
(1993)
Nature
, vol.364
, pp. 584
-
-
Beckman, J.S.1
Carson, M.2
Smith, C.D.3
Koppenol, W.H.4
-
28
-
-
0029004898
-
Defective axonal transport in a transgenic mouse model of amyotrophic lateral sclerosis
-
Collard, J.-F., Cote, F. & Julien, J. P. Defective axonal transport in a transgenic mouse model of amyotrophic lateral sclerosis. Nature 375, 61-64 (1995).
-
(1995)
Nature
, vol.375
, pp. 61-64
-
-
Collard, J.-F.1
Cote, F.2
Julien, J.P.3
-
29
-
-
0028001606
-
Variant alleles of the neurofilament heavy gene associated with amyotrophic lateral sclerosis
-
Figlewicz, D. et al. Variant alleles of the neurofilament heavy gene associated with amyotrophic lateral sclerosis. Hum. Mol. Genet. 3, 1757-1761 (1994).
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 1757-1761
-
-
Figlewicz, D.1
-
30
-
-
0029970685
-
Sequence variants in human neurofilament proteins: Absence of linkage ot familial amyotrophic lateral sclerosis
-
Vechio, J., Bruijn, L., Brown, R. & Cleveland, D. Sequence variants in human neurofilament proteins: absence of linkage ot familial amyotrophic lateral sclerosis. Ann. Neurol. 40, 603-610 (1996).
-
(1996)
Ann. Neurol.
, vol.40
, pp. 603-610
-
-
Vechio, J.1
Bruijn, L.2
Brown, R.3
Cleveland, D.4
|