-
1
-
-
0024436464
-
Fine structural study of the spinal cord and spinal ganglia in mice afflicted with a hereditary sensory neuropathy,dystonia musculorum
-
Al-Ali S. Y., Al-Zuhair A. G. H. Fine structural study of the spinal cord and spinal ganglia in mice afflicted with a hereditary sensory neuropathy,dystonia musculorum. J. Submicrosc. Cytol. Pathol. 21:1989;737-748.
-
(1989)
J. Submicrosc. Cytol. Pathol.
, vol.21
, pp. 737-748
-
-
Al-Ali, S.Y.1
Al-Zuhair, A.G.H.2
-
2
-
-
0029558104
-
Dystonin expression in the developing nervous system predominates in the neurons that degenerate indystonia musculorum
-
Bernier G., Brown A., Dalpé G., De Repentigny Y., Mathieu M., Kothary R. Dystonin expression in the developing nervous system predominates in the neurons that degenerate indystonia musculorum. Mol. Cell. Neurosci. 6:1995;509-520.
-
(1995)
Mol. Cell. Neurosci.
, vol.6
, pp. 509-520
-
-
Bernier, G.1
Brown, A.2
Dalpé, G.3
De Repentigny, Y.4
Mathieu, M.5
Kothary, R.6
-
3
-
-
0029035706
-
The mousedystonia musculorum
-
Brown A., Bernier G., Mathieu M., Rossant J., Kothary R. The mousedystonia musculorum. Nature Genet. 10:1995;301-306.
-
(1995)
Nature Genet.
, vol.10
, pp. 301-306
-
-
Brown, A.1
Bernier, G.2
Mathieu, M.3
Rossant, J.4
Kothary, R.5
-
4
-
-
0028465450
-
Human homolog of a mouse sequence from thedystonia musculorum
-
Brown A., Lemieux N., Rossant J., Kothary R. Human homolog of a mouse sequence from thedystonia musculorum. Mamm. Genome. 5:1994;434-437.
-
(1994)
Mamm. Genome
, vol.5
, pp. 434-437
-
-
Brown, A.1
Lemieux, N.2
Rossant, J.3
Kothary, R.4
-
5
-
-
0028960506
-
Amyotrophic lateral sclerosis: Recent insights from genetics and transgenic mice
-
Brown R. H. Jr. Amyotrophic lateral sclerosis: Recent insights from genetics and transgenic mice. Cell. 80:1996;687-692.
-
(1996)
Cell
, vol.80
, pp. 687-692
-
-
Brown R.H., Jr.1
-
6
-
-
0026630111
-
An intrinsic neuronal defect operates indystonia musculorum:dtdt
-
Campbell R. M., Peterson A. C. An intrinsic neuronal defect operates indystonia musculorum:dtdt. Neuron. 9:1992;693-703.
-
(1992)
Neuron
, vol.9
, pp. 693-703
-
-
Campbell, R.M.1
Peterson, A.C.2
-
7
-
-
0023515543
-
Two-stage expression of neurofilament polypeptides during rat neurogenesis with early establishment of adult phosphorylation patterns
-
Carden M. J., Trojanowski J. A., Schlaepfer W. W., Lee V. M.-Y. Two-stage expression of neurofilament polypeptides during rat neurogenesis with early establishment of adult phosphorylation patterns. J. Neurosci. 7:1987;3489-3504.
-
(1987)
J. Neurosci.
, vol.7
, pp. 3489-3504
-
-
Carden, M.J.1
Trojanowski, J.A.2
Schlaepfer, W.W.3
Lee, V.M.-Y.4
-
8
-
-
0023896370
-
Neurofilamentous abnormalities in motor neurons in spontaneously occurring animal disorders
-
Cork L. C., Troncoso J. C., Klavan G. G., Johnson E. S., Sternberger L. A., Sternberger N. H., Price D. L. Neurofilamentous abnormalities in motor neurons in spontaneously occurring animal disorders. J. Neuropathol. Exp. Neurol. 47:1988;420-431.
-
(1988)
J. Neuropathol. Exp. Neurol.
, vol.47
, pp. 420-431
-
-
Cork, L.C.1
Troncoso, J.C.2
Klavan, G.G.3
Johnson, E.S.4
Sternberger, L.A.5
Sternberger, N.H.6
Price, D.L.7
-
9
-
-
0016914818
-
Dystonia musculorum
-
Duchen L. W. Dystonia musculorum. Adv. Neurol. 14:1976;353-365.
-
(1976)
Adv. Neurol.
, vol.14
, pp. 353-365
-
-
Duchen, L.W.1
-
10
-
-
0002858267
-
Dystonia musculorum. A hereditary neuropathy of mice affecting mainly sensory pathways
-
Duchen L. W., Falconer D. S., Strich S. J. Dystonia musculorum. A hereditary neuropathy of mice affecting mainly sensory pathways. J. Physiol. 165:1963;7-9.
-
(1963)
J. Physiol.
, vol.165
, pp. 7-9
-
-
Duchen, L.W.1
Falconer, D.S.2
Strich, S.J.3
-
11
-
-
0001011390
-
Clinical and pathological studies of an hereditary neuropathy in mice (dystonia musculorum
-
Duchen L. W., Strich S. J. Clinical and pathological studies of an hereditary neuropathy in mice (dystonia musculorum. Brain. 87:1964;367-378.
-
(1964)
Brain
, vol.87
, pp. 367-378
-
-
Duchen, L.W.1
Strich, S.J.2
-
12
-
-
0024520321
-
Neuronal degeneration and neurofilament accumulation in trigeminal ganglia of Creutzfeld-Jacob disease
-
Guiroy D. L., Shankar S. K., Gibbs C. J., Messenheimer J. A., Das S., Gajdusek D. C. Neuronal degeneration and neurofilament accumulation in trigeminal ganglia of Creutzfeld-Jacob disease. Ann. Neurol. 25:1989;102.
-
(1989)
Ann. Neurol.
, vol.25
, pp. 102
-
-
Guiroy, D.L.1
Shankar, S.K.2
Gibbs, C.J.3
Messenheimer, J.A.4
Das, S.5
Gajdusek, D.C.6
-
13
-
-
0029066406
-
Gene targeting ofBPAG1:
-
Guo L., Degenstein L., Dowling J., Yu Q.-C., Wollmann R., Perman B., Fuchs E. Gene targeting ofBPAG1: Cell. 81:1995;233-243.
-
(1995)
Cell
, vol.81
, pp. 233-243
-
-
Guo, L.1
Degenstein, L.2
Dowling, J.3
Yu, Q.-C.4
Wollmann, R.5
Perman, B.6
Fuchs, E.7
-
14
-
-
0029164597
-
Is dystonia a sensory disorder?
-
Hallett M. Is dystonia a sensory disorder? Ann. Neurol. 38:1995;139-140.
-
(1995)
Ann. Neurol.
, vol.38
, pp. 139-140
-
-
Hallett, M.1
-
15
-
-
0015440792
-
Ultrastructural studies of an hereditary sensory neuropathy in mice (dystonia musculorum
-
Janota I. Ultrastructural studies of an hereditary sensory neuropathy in mice (dystonia musculorum. Brain. 95:1972;529-536.
-
(1972)
Brain
, vol.95
, pp. 529-536
-
-
Janota, I.1
-
16
-
-
0028351190
-
Targeted disruption of the BDNF gene perturbs brain and sensory neuron development but not motor neuron development
-
Jones K. R., Farinas I., Backus C., Reichardt L. F. Targeted disruption of the BDNF gene perturbs brain and sensory neuron development but not motor neuron development. Cell. 76:1994;989-999.
-
(1994)
Cell
, vol.76
, pp. 989-999
-
-
Jones, K.R.1
Farinas, I.2
Backus, C.3
Reichardt, L.F.4
-
17
-
-
0023747623
-
A transgene containinglacZdystonia
-
Kothary R., Clapoff S., Brown A., Campbell R., Peterson A., Rossant J. A transgene containinglacZdystonia. Nature. 335:1988;435-437.
-
(1988)
Nature
, vol.335
, pp. 435-437
-
-
Kothary, R.1
Clapoff, S.2
Brown, A.3
Campbell, R.4
Peterson, A.5
Rossant, J.6
-
19
-
-
0030051923
-
Requirement for LIM homeobox geneIsl1
-
Pfaff S. L., Mendelsohn M., Stewart C. L., Edlund T., Jessell T. M. Requirement for LIM homeobox geneIsl1. Cell. 84:1996;309-320.
-
(1996)
Cell
, vol.84
, pp. 309-320
-
-
Pfaff, S.L.1
Mendelsohn, M.2
Stewart, C.L.3
Edlund, T.4
Jessell, T.M.5
-
20
-
-
0029014180
-
Expression analysis of the ataxin-1 protein in tissues from normal and spinocerebellar ataxia type I individuals
-
Servadio A., Koshy B., Armstrong D., Antalffy B., Orr H. T., Zoghbi H. Y. Expression analysis of the ataxin-1 protein in tissues from normal and spinocerebellar ataxia type I individuals. Nature Genet. 10:1995;94-98.
-
(1995)
Nature Genet.
, vol.10
, pp. 94-98
-
-
Servadio, A.1
Koshy, B.2
Armstrong, D.3
Antalffy, B.4
Orr, H.T.5
Zoghbi, H.Y.6
-
21
-
-
0023698294
-
Pathologic changes in the CNS ofdystonia musculorum
-
Sotelo C., Guenet J. L. Pathologic changes in the CNS ofdystonia musculorum. Neuroscience. 27:1988;403-424.
-
(1988)
Neuroscience
, vol.27
, pp. 403-424
-
-
Sotelo, C.1
Guenet, J.L.2
-
22
-
-
0030598838
-
An essential cytoskeletal linker protein connecting actin microfilaments to intermediate filaments
-
Yang Y., Dowling J., Yu Q.-C., Kouklis P., Cleveland D. W., Fuchs E. An essential cytoskeletal linker protein connecting actin microfilaments to intermediate filaments. Cell. 86:1996;655-665.
-
(1996)
Cell
, vol.86
, pp. 655-665
-
-
Yang, Y.1
Dowling, J.2
Yu, Q.-C.3
Kouklis, P.4
Cleveland, D.W.5
Fuchs, E.6
|