-
1
-
-
0024228818
-
Epidemiology of focal and generalized dystonia in Rochester. Minnesota
-
Nutt, J.G., Muenter, M.D., Aronson, A., Kurland, L.T. and Melton, L.J. (1988) Epidemiology of focal and generalized dystonia in Rochester. Minnesota. Mov. Disord., 3, 188-194.
-
(1988)
Mov. Disord.
, vol.3
, pp. 188-194
-
-
Nutt, J.G.1
Muenter, M.D.2
Aronson, A.3
Kurland, L.T.4
Melton, L.J.5
-
2
-
-
0028151448
-
Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene
-
Ichinose, H., Ohye, T., Takahashi, E., Seki, N., Hori, T., Segawa, M., Nomura, Y., Endo, K., Tanaka, H., Tsuij, S., Fujita, K. and Nagatsu, T. (1994) Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene. Nature Genet., 8, 236-242.
-
(1994)
Nature Genet.
, vol.8
, pp. 236-242
-
-
Ichinose, H.1
Ohye, T.2
Takahashi, E.3
Seki, N.4
Hori, T.5
Segawa, M.6
Nomura, Y.7
Endo, K.8
Tanaka, H.9
Tsuij, S.10
Fujita, K.11
Nagatsu, T.12
-
3
-
-
0028816765
-
A point mutation in the tyrosine hydroxylase gene associated with Segawa's syndrome
-
Ludecke, B., Dworniczak, B. and Bartholomé, K. (1995) A point mutation in the tyrosine hydroxylase gene associated with Segawa's syndrome. Hum. Genet., 95, 123-125.
-
(1995)
Hum. Genet.
, vol.95
, pp. 123-125
-
-
Ludecke, B.1
Dworniczak, B.2
Bartholomé, K.3
-
4
-
-
16944366666
-
The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein
-
Ozelius, L.J., Hewett, J.W., Page, C.E., Bressman, S.B., Kramer, P.L., Shalish, C., de Leon, D., Brin, M., Raymond, D., Corey, D.P., Fahn, S., Risch, N.J., Buckler, A.J., Gusella, J.F. and Breakefield, X.O. (1997) The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein. Nature Genet., 17, 40-48.
-
(1997)
Nature Genet.
, vol.17
, pp. 40-48
-
-
Ozelius, L.J.1
Hewett, J.W.2
Page, C.E.3
Bressman, S.B.4
Kramer, P.L.5
Shalish, C.6
De Leon, D.7
Brin, M.8
Raymond, D.9
Corey, D.P.10
Fahn, S.11
Risch, N.J.12
Buckler, A.J.13
Gusella, J.F.14
Breakefield, X.O.15
-
5
-
-
7144256520
-
De novo mutations (GAG deletion) in the DYT1 gene in two non-Jewish patients with early-onset dystonia
-
Klein, C., Brin, M.E., de Leon, D., Limborska, S.A., Ivanova-Smolenskaya, I.A., Bressman, S.B., Friedman, A., Markova, E.D., Risch, N.J., Breakefield, X.O. and Ozelius, L.J. (1998) De novo mutations (GAG deletion) in the DYT1 gene in two non-Jewish patients with early-onset dystonia. Hum. Mol. Genet., 7, 1133-1136.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 1133-1136
-
-
Klein, C.1
Brin, M.E.2
De Leon, D.3
Limborska, S.A.4
Ivanova-Smolenskaya, I.A.5
Bressman, S.B.6
Friedman, A.7
Markova, E.D.8
Risch, N.J.9
Breakefield, X.O.10
Ozelius, L.J.11
-
6
-
-
0000892022
-
-
Watts, R.L. and Koller, W.C. (eds), McGraw-Hill, New York, NY
-
Jankovic, J. (1997) In Watts, R.L. and Koller, W.C. (eds), Movement Disorders: Neurologic Principles and Practice. McGraw-Hill, New York, NY, pp. 443-454.
-
(1997)
Movement Disorders: Neurologic Principles and Practice
, pp. 443-454
-
-
Jankovic, J.1
-
8
-
-
0002785854
-
-
North, R.A. (ed.), CRC Press, Boca Raton, FL
-
Goldin, A.L. (1995) In North, R.A. (ed.), Handbook of Receptors and Channels: Ligand-and Voltage-Gated Channels. CRC Press, Boca Raton, FL, pp. 73-113.
-
(1995)
Handbook of Receptors and Channels: Ligand-and Voltage-gated Channels
, pp. 73-113
-
-
Goldin, A.L.1
-
9
-
-
0345034603
-
Evolution and diversity of mammalian sodium channels
-
in press
-
Plummer, N.W. and Meisler, M.H. (1999) Evolution and diversity of mammalian sodium channels. Genomics, 56, in press.
-
(1999)
Genomics
, vol.56
-
-
Plummer, N.W.1
Meisler, M.H.2
-
10
-
-
0029111866
-
Mutation of a new sodium channel gene, Scn8a, in the mouse mutant 'motor endplate disease'
-
Burgess, D.L., Kohrman, D.C., Galt, J., Plummer, N.W., Jones, J.M., Spear, B. and Meisler, M.H. (1995) Mutation of a new sodium channel gene, Scn8a, in the mouse mutant 'motor endplate disease'. Nature Genet., 10, 461-465.
-
(1995)
Nature Genet.
, vol.10
, pp. 461-465
-
-
Burgess, D.L.1
Kohrman, D.C.2
Galt, J.3
Plummer, N.W.4
Jones, J.M.5
Spear, B.6
Meisler, M.H.7
-
11
-
-
0029075539
-
A novel, abundant sodium channel expressed in neurons and glia
-
Schaller, K.L., Krzemien, D.M., Yarowsky, P.J., Krueger, B.K. and Caldwell, J.H. (1995) A novel, abundant sodium channel expressed in neurons and glia. J. Neurosci., 15, 3231-3242.
-
(1995)
J. Neurosci.
, vol.15
, pp. 3231-3242
-
-
Schaller, K.L.1
Krzemien, D.M.2
Yarowsky, P.J.3
Krueger, B.K.4
Caldwell, J.H.5
-
12
-
-
0031127498
-
Sodium channel alpha-subunit mRNAs I, II, III, NaG, Na6 and hNE (PN1): Different expression patterns in developing rat nervous system
-
Fetls, P.A., Yokoyama, S., Dib-Hajj, S., Black, J.A. and Waxman, S.G. (1997) Sodium channel alpha-subunit mRNAs I, II, III, NaG, Na6 and hNE (PN1): different expression patterns in developing rat nervous system. Mol. Brain Res., 45, 71-82.
-
(1997)
Mol. Brain Res.
, vol.45
, pp. 71-82
-
-
Fetls, P.A.1
Yokoyama, S.2
Dib-Hajj, S.3
Black, J.A.4
Waxman, S.G.5
-
13
-
-
0031431679
-
Ion channel mutations in mouse models of inherited neurological disease
-
Meisler, M.H., Sprunger, L.K., Plummer, N.W., Escayg, A. and Jones, J.M. (1997) Ion channel mutations in mouse models of inherited neurological disease. Ann. Med., 29, 569-574.
-
(1997)
Ann. Med.
, vol.29
, pp. 569-574
-
-
Meisler, M.H.1
Sprunger, L.K.2
Plummer, N.W.3
Escayg, A.4
Jones, J.M.5
-
14
-
-
0003307948
-
New mutants report
-
Searle, A.G. (1962) New mutants report. Mouse Newslett., 27, 34-35.
-
(1962)
Mouse Newslett.
, vol.27
, pp. 34-35
-
-
Searle, A.G.1
-
15
-
-
0005555241
-
An hereditary motor endplate disease in the mouse
-
Duchen, L.W., Searle, A.G. and Strich, S.J. (1967) An hereditary motor endplate disease in the mouse. J. Physiol. (Lond.), 189, 4P-6P.
-
(1967)
J. Physiol. (Lond.)
, vol.189
-
-
Duchen, L.W.1
Searle, A.G.2
Strich, S.J.3
-
16
-
-
0029789472
-
A missense mutation in the sodium channel Scn8a is responsible for cerebellar ataxia in the mouse mutant jolting
-
Kohrman, D.C., Smith, M.R., Goldin, A.L., Harris, J. and Meisler, M.H. (1996) A missense mutation in the sodium channel Scn8a is responsible for cerebellar ataxia in the mouse mutant jolting. J. Neurosci., 16, 5993-5999.
-
(1996)
J. Neurosci.
, vol.16
, pp. 5993-5999
-
-
Kohrman, D.C.1
Smith, M.R.2
Goldin, A.L.3
Harris, J.4
Meisler, M.H.5
-
17
-
-
0030015959
-
J alleles of the sodium channel Scn8a - Unusual splicing due to a minor class AT-AC intron
-
J alleles of the sodium channel Scn8a - unusual splicing due to a minor class AT-AC intron. J. Biol. Chem., 271, 17576-17581.
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 17576-17581
-
-
Kohrman, D.C.1
Harris, J.B.2
Meisler, M.H.3
-
18
-
-
0018369346
-
Inherited muscle and nerve diseases in mice: A tabulation with commentary
-
Sidman, R.L., Cowen, J.S. and Eicher, E.M. (1979) Inherited muscle and nerve diseases in mice: a tabulation with commentary. Ann. NY Acad. Sci., 317, 497-505.
-
(1979)
Ann. NY Acad. Sci.
, vol.317
, pp. 497-505
-
-
Sidman, R.L.1
Cowen, J.S.2
Eicher, E.M.3
-
19
-
-
0028978478
-
Interaction between undulated and patch leads to an extreme form of spina bifida in double-mutant mice
-
Helwig, U., Imai, K., Schmahl, W., Thomas, B.E., Varnum, D.S., Nadeau, J. and Balling, R. (1995) Interaction between undulated and Patch leads to an extreme form of spina bifida in double-mutant mice. Nature Genet., 11, 60-63.
-
(1995)
Nature Genet.
, vol.11
, pp. 60-63
-
-
Helwig, U.1
Imai, K.2
Schmahl, W.3
Thomas, B.E.4
Varnum, D.S.5
Nadeau, J.6
Balling, R.7
-
20
-
-
0028244488
-
Multifactorial inheritance of neural tube defects: Localization of the major gene and recognition of modifiers in ct mutant mice
-
Neumann, P.E., Frankel, W.N., Letts, V.A., Coffin, J.M., Copp, A.J. and Bernfield, M. (1994) Multifactorial inheritance of neural tube defects: localization of the major gene and recognition of modifiers in ct mutant mice. Nature Genet., 6, 357-362.
-
(1994)
Nature Genet.
, vol.6
, pp. 357-362
-
-
Neumann, P.E.1
Frankel, W.N.2
Letts, V.A.3
Coffin, J.M.4
Copp, A.J.5
Bernfield, M.6
-
21
-
-
13344282728
-
Modulation of disease severity in cystic fibrosis transmembrane conductance regulator deficient mice by a secondary genetic factor
-
Rozmahel, R., Wilschanski, M., Matin, A., Plyte, S., Oliver, M., Auerbach, W., Moore, A., Forstner, J., Durie, P., Nadeau, J., Bear, C. and Tsui, L.-C. (1996) Modulation of disease severity in cystic fibrosis transmembrane conductance regulator deficient mice by a secondary genetic factor. Nature Genet., 12, 280-287.
-
(1996)
Nature Genet.
, vol.12
, pp. 280-287
-
-
Rozmahel, R.1
Wilschanski, M.2
Matin, A.3
Plyte, S.4
Oliver, M.5
Auerbach, W.6
Moore, A.7
Forstner, J.8
Durie, P.9
Nadeau, J.10
Bear, C.11
Tsui, L.-C.12
-
22
-
-
0031039041
-
Mapping of a major genetic modifier of embryonic lethality in TGFβ1 knockout mice
-
Bonyadi, M., Rusholme, S.A.B., Cousins, F.M., Su, H.C., Biron, C.A., Farrall, M. and Akhurst, R.J. (1997) Mapping of a major genetic modifier of embryonic lethality in TGFβ1 knockout mice. Nature Genet., 15, 207-211.
-
(1997)
Nature Genet.
, vol.15
, pp. 207-211
-
-
Bonyadi, M.1
Rusholme, S.A.B.2
Cousins, F.M.3
Su, H.C.4
Biron, C.A.5
Farrall, M.6
Akhurst, R.J.7
-
23
-
-
0025997867
-
Ras1 and a putative guanine nucleotide exchange factor perform crucial steps in signaling by the sevenless protein tyrosine kinase
-
Simon, M.A., Bowtell, D.D.L., Dodson, G.S., Laverty, T.R. and Rubin, G.M. (1991) Ras1 and a putative guanine nucleotide exchange factor perform crucial steps in signaling by the sevenless protein tyrosine kinase. Cell, 67, 701-716.
-
(1991)
Cell
, vol.67
, pp. 701-716
-
-
Simon, M.A.1
Bowtell, D.D.L.2
Dodson, G.S.3
Laverty, T.R.4
Rubin, G.M.5
-
24
-
-
0027515605
-
Synthetic enhancement in gene interaction: A genetic tool come of age
-
Guarente, L. (1993) Synthetic enhancement in gene interaction: a genetic tool come of age. Trends Genet., 9, 362-366.
-
(1993)
Trends Genet.
, vol.9
, pp. 362-366
-
-
Guarente, L.1
-
25
-
-
0020702117
-
Modification of helper and suppressor/cytotoxic lymphocyte subsets in mice with motor end-plate disease
-
Ezine, S., Papiernik, M., Rieger, F. and Pinçon-Raymond, M. (1983) Modification of helper and suppressor/cytotoxic lymphocyte subsets in mice with motor end-plate disease. Clin. Exp. Immunol., 51, 475-478.
-
(1983)
Clin. Exp. Immunol.
, vol.51
, pp. 475-478
-
-
Ezine, S.1
Papiernik, M.2
Rieger, F.3
Pinçon-Raymond, M.4
-
26
-
-
0028922292
-
Insertional mutation of the motor endplate disease (med) locus on mouse chromosome 15
-
Kohrman, D.C., Plummer, N.W., Schuster, T., Jones, J.M., Jang, W., Burgess, D.L., Galt, J., Spear, B.T. and Meisler, M.H. (1995) Insertional mutation of the motor endplate disease (med) locus on mouse chromosome 15. Genomics, 26, 171-177.
-
(1995)
Genomics
, vol.26
, pp. 171-177
-
-
Kohrman, D.C.1
Plummer, N.W.2
Schuster, T.3
Jones, J.M.4
Jang, W.5
Burgess, D.L.6
Galt, J.7
Spear, B.T.8
Meisler, M.H.9
-
27
-
-
0002131194
-
-
Tsui, J.K.C. and Calne, D.B. (eds), Marcel Dekker, New York, NY
-
Lorden, J.F. (1995) In Tsui, J.K.C. and Calne, D.B. (eds), Handbook of Dystonia. Marcel Dekker, New York, NY, Vol. 39, pp. 5-42.
-
(1995)
Handbook of Dystonia
, vol.39
, pp. 5-42
-
-
Lorden, J.F.1
-
28
-
-
0032040365
-
Pathology of idiopathic dystonia: Findings from genetic animal models
-
Richter, A. and Löscher, W. (1998) Pathology of idiopathic dystonia: findings from genetic animal models. Prog. Neurobiol., 54, 633-677.
-
(1998)
Prog. Neurobiol.
, vol.54
, pp. 633-677
-
-
Richter, A.1
Löscher, W.2
-
29
-
-
0014980365
-
Electrophysiological studies of neuromuscular transmission in hereditary 'motor end-plate disease' of the mouse
-
Duchen, L. W. and Stefani, E. (1971) Electrophysiological studies of neuromuscular transmission in hereditary 'motor end-plate disease' of the mouse. J. Physiol., 212, 535-548.
-
(1971)
J. Physiol.
, vol.212
, pp. 535-548
-
-
Duchen, L.W.1
Stefani, E.2
-
30
-
-
0022981880
-
Neuromuscular transmission in the murine mutants 'motor endplate disease' and 'jolting'
-
Harris, J.B. and Pollard, S.L. (1986) Neuromuscular transmission in the murine mutants 'motor endplate disease' and 'jolting'. J. Neurosci., 76, 239-253.
-
(1986)
J. Neurosci.
, vol.76
, pp. 239-253
-
-
Harris, J.B.1
Pollard, S.L.2
-
31
-
-
0032527590
-
The sodium channel Scn8a is the major contributor to the postnatal developmental increase of sodium current density in spinal motoneurons
-
Garcia, K.D., Sprunger, L.K., Meisler, M.H. and Beam, K.G. (1998) The sodium channel Scn8a is the major contributor to the postnatal developmental increase of sodium current density in spinal motoneurons. J. Neurosci., 18, 5234-5239.
-
(1998)
J. Neurosci.
, vol.18
, pp. 5234-5239
-
-
Garcia, K.D.1
Sprunger, L.K.2
Meisler, M.H.3
Beam, K.G.4
-
32
-
-
0031006852
-
The vibrator mutation causes neurodegeneration via reduced expression of PITP alpha: Positional complementation cloning and extragenic suppression
-
Hamilton, B.A., Smith, D.J., Mueller, K.L., Kerrebrock, A.W., Bronson, R.T., van Berkel, V., Daly, M.J., Kruglyak, L., Reeve, M.P., Nemhauser, J.L., Hawkins, T.L., Rubin, E.M. and Lander, E.S. (1997) The vibrator mutation causes neurodegeneration via reduced expression of PITP alpha: positional complementation cloning and extragenic suppression. Neuron, 18, 711-722.
-
(1997)
Neuron
, vol.18
, pp. 711-722
-
-
Hamilton, B.A.1
Smith, D.J.2
Mueller, K.L.3
Kerrebrock, A.W.4
Bronson, R.T.5
Van Berkel, V.6
Daly, M.J.7
Kruglyak, L.8
Reeve, M.P.9
Nemhauser, J.L.10
Hawkins, T.L.11
Rubin, E.M.12
Lander, E.S.13
-
33
-
-
17644442703
-
Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene
-
Probst, F.J., Fridell, R.A., Raphael, Y., Saunders, T.L., Wang, A., Liang, Y., Morell, R.J., Touchman, J.W., Lyons, R.H., Noben-Trauth, K., Friedman, T.B. and Camper, S.A. (1998) Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene. Science, 280, 1444-1447.
-
(1998)
Science
, vol.280
, pp. 1444-1447
-
-
Probst, F.J.1
Fridell, R.A.2
Raphael, Y.3
Saunders, T.L.4
Wang, A.5
Liang, Y.6
Morell, R.J.7
Touchman, J.W.8
Lyons, R.H.9
Noben-Trauth, K.10
Friedman, T.B.11
Camper, S.A.12
-
34
-
-
0004559935
-
-
Watts, R.L. and Koller, W.C. (eds). McGraw-Hill, New York, NY
-
Bressman, S.B. and Fahn, S. (1997) In Watts, R.L. and Koller, W.C. (eds). Movement Disorders: Neurologic Principles and Practice. McGraw-Hill, New York, NY, pp. 419-428.
-
(1997)
Movement Disorders: Neurologic Principles and Practice
, pp. 419-428
-
-
Bressman, S.B.1
Fahn, S.2
-
35
-
-
0001934473
-
-
Watts, R.L. and Koller, W.C. (eds), McGraw-Hill, New York, NY
-
Tolosa, E.S. and Marti, M.J. (1997) In Watts, R.L. and Koller, W.C. (eds), Movement Disorders: Neurologic Principles and Practice. McGraw-Hill, New York, NY, pp. 429-441.
-
(1997)
Movement Disorders: Neurologic Principles and Practice
, pp. 429-441
-
-
Tolosa, E.S.1
Marti, M.J.2
-
36
-
-
0025280709
-
Dystonia and cerebellar ataxia
-
Lees, A. (1990) Dystonia and cerebellar ataxia. Mov. Disord., 5, 178.
-
(1990)
Mov. Disord.
, vol.5
, pp. 178
-
-
Lees, A.1
-
37
-
-
0024194827
-
Degenerative cerebellar ataxia and focal dystonia
-
Fletcher, N.A., Stell, R., Harding, A.E. and Marsden, C.D. (1988) Degenerative cerebellar ataxia and focal dystonia. Mov. Disord., 3, 336-342.
-
(1988)
Mov. Disord.
, vol.3
, pp. 336-342
-
-
Fletcher, N.A.1
Stell, R.2
Harding, A.E.3
Marsden, C.D.4
-
38
-
-
0031867881
-
The pathophysiology of primary dystonia
-
Berardelli, A., Rothwell, J.C., Hallett, M., Thompson, P.D., Manfredi, M. and Marsden, C.D. (1998) The pathophysiology of primary dystonia. Brain, 121, 1195-1212.
-
(1998)
Brain
, vol.121
, pp. 1195-1212
-
-
Berardelli, A.1
Rothwell, J.C.2
Hallett, M.3
Thompson, P.D.4
Manfredi, M.5
Marsden, C.D.6
-
39
-
-
0030834501
-
Altered subthreshold sodium currents and disrupted firing patterns in Purkinje neurons of Scn8a mutant mice
-
Raman, I.M., Sprunger, L.K., Meisler, M.H. and Bean, B.P. (1997) Altered subthreshold sodium currents and disrupted firing patterns in Purkinje neurons of Scn8a mutant mice. Neuron, 19, 881-891.
-
(1997)
Neuron
, vol.19
, pp. 881-891
-
-
Raman, I.M.1
Sprunger, L.K.2
Meisler, M.H.3
Bean, B.P.4
-
40
-
-
0032402234
-
Exon organization, coding sequence, physical mapping and polymorphic intragenic markers for the human neuronal sodium channel gene SCN8a
-
Plummer, N.W., Galt, J., Jones, J.M., Burgess, D.L., Spninger, L.K., Kohrman, D.C. and Meisler, M.H. (1998) Exon organization, coding sequence, physical mapping and polymorphic intragenic markers for the human neuronal sodium channel gene SCN8A. Genomics, 54, 287-296.
-
(1998)
Genomics
, vol.54
, pp. 287-296
-
-
Plummer, N.W.1
Galt, J.2
Jones, J.M.3
Burgess, D.L.4
Spninger, L.K.5
Kohrman, D.C.6
Meisler, M.H.7
-
41
-
-
0030931136
-
Dominant and digenic mutations in the peripherin/RDS and ROM1 genes in retinitis pigmentosa
-
Dryja, T.P., Hahn, L.B., Kajiwara, K. and Berson, E.L. (1997) Dominant and digenic mutations in the peripherin/RDS and ROM1 genes in retinitis pigmentosa. Invest. Ophthalmol. Visual Sci., 38, 1972-1982.
-
(1997)
Invest. Ophthalmol. Visual Sci.
, vol.38
, pp. 1972-1982
-
-
Dryja, T.P.1
Hahn, L.B.2
Kajiwara, K.3
Berson, E.L.4
-
42
-
-
0030947238
-
Cooperation of Pax2 and Pax5 in midbrain and cerebellum development
-
Urbanek, P., Fetka, I., Meisler, M.H. and Busslinger, M. (1997) Cooperation of Pax2 and Pax5 in midbrain and cerebellum development. Proc. Natl Acad. Sci. USA, 95, 5703-5708.
-
(1997)
Proc. Natl Acad. Sci. USA
, vol.95
, pp. 5703-5708
-
-
Urbanek, P.1
Fetka, I.2
Meisler, M.H.3
Busslinger, M.4
-
43
-
-
0030797904
-
Secretory phospholipase Pla2g2a confers resistance to intestinal tumorigenesis
-
Cormier, R.T., Hong, K.H., Halberg, R.B., Hawkins, T.L., Richardson, P., Mulherkar, R., Dove, W.F. and Lander, E.S. (1997) Secretory phospholipase Pla2g2a confers resistance to intestinal tumorigenesis. Nature Genet., 17, 88-91.
-
(1997)
Nature Genet.
, vol.17
, pp. 88-91
-
-
Cormier, R.T.1
Hong, K.H.2
Halberg, R.B.3
Hawkins, T.L.4
Richardson, P.5
Mulherkar, R.6
Dove, W.F.7
Lander, E.S.8
-
44
-
-
0030777698
-
Mutant mice and neuroscience: Recommendations concerning genetic background
-
Banbury Conference on Genetic Background in Mice (1997) Mutant mice and neuroscience: recommendations concerning genetic background. Neuron, 19, 755-759.
-
(1997)
Neuron
, vol.19
, pp. 755-759
-
-
-
45
-
-
0031469707
-
Ectopically expressed CAG repeats cause intranuclear inclusions and a progressive late onset neurological phenotype in the mouse
-
Ordway, J.M., Tallaksen-Greene, S., Gutekunst, C.A., Bernstein, E.M., Cearley, J.A., Wiener, H.W., Dure, L.S., Lindsey, R., Hersch, S.M., Jope, R.S., Albin, R.L. and Detloff, P.J. (1997) Ectopically expressed CAG repeats cause intranuclear inclusions and a progressive late onset neurological phenotype in the mouse. Cell, 91, 753-763.
-
(1997)
Cell
, vol.91
, pp. 753-763
-
-
Ordway, J.M.1
Tallaksen-Greene, S.2
Gutekunst, C.A.3
Bernstein, E.M.4
Cearley, J.A.5
Wiener, H.W.6
Dure, L.S.7
Lindsey, R.8
Hersch, S.M.9
Jope, R.S.10
Albin, R.L.11
Detloff, P.J.12
-
46
-
-
0029833389
-
Neuron death in the substantia nigra of weaver mouse occurs late in development and is not apoptotic
-
Oo, T.F., Blazeski, R., Harrison, S.M.W., Henchcliffe, C., Mason, C.A., Roffler-Tarlov, S.K. and Burke, R.E. (1996) Neuron death in the substantia nigra of weaver mouse occurs late in development and is not apoptotic. J. Neurosci., 16, 6134-6145.
-
(1996)
J. Neurosci.
, vol.16
, pp. 6134-6145
-
-
Oo, T.F.1
Blazeski, R.2
Harrison, S.M.W.3
Henchcliffe, C.4
Mason, C.A.5
Roffler-Tarlov, S.K.6
Burke, R.E.7
-
47
-
-
0030790634
-
Functional deficits in medial gastrocnemius grafts in rats: Relation to muscle metabolism and beta-Ar regulation
-
Larkin, L.M., Faulkner, J.A., Hinkle, R.T., Hassett, C.A., Supiano, M.A. and Halter, J.B. (1997) Functional deficits in medial gastrocnemius grafts in rats: relation to muscle metabolism and beta-AR regulation. J. Appl. Physiol., 83, 67-73.
-
(1997)
J. Appl. Physiol.
, vol.83
, pp. 67-73
-
-
Larkin, L.M.1
Faulkner, J.A.2
Hinkle, R.T.3
Hassett, C.A.4
Supiano, M.A.5
Halter, J.B.6
|