-
1
-
-
0037201934
-
Current thoughts on the phosphatidylinositol transfer protein family
-
V. Allen-Baume, B. Segui, and S. Cockcroft Current thoughts on the phosphatidylinositol transfer protein family FEBS Lett. 531 2002 74 80
-
(2002)
FEBS Lett.
, vol.531
, pp. 74-80
-
-
Allen-Baume, V.1
Segui, B.2
Cockcroft, S.3
-
2
-
-
0027031341
-
The intracisternal a particle derived solo LTR promoter of the rat oncomodulin gene is not present in the mouse gene
-
D. Banville, M. Rotaru, and Y. Boie The intracisternal A particle derived solo LTR promoter of the rat oncomodulin gene is not present in the mouse gene Genetica 86 1992 85 97
-
(1992)
Genetica
, vol.86
, pp. 85-97
-
-
Banville, D.1
Rotaru, M.2
Boie, Y.3
-
3
-
-
0025437989
-
Quantitative autoradiography reveals selective changes in cerebellar GABA receptors of the rat mutant dystonic
-
M. Beales, J.F. Lorden, E. Walz, and G.A. Oltmans Quantitative autoradiography reveals selective changes in cerebellar GABA receptors of the rat mutant dystonic J. Neurosci. 10 1990 1874 1885
-
(1990)
J. Neurosci.
, vol.10
, pp. 1874-1885
-
-
Beales, M.1
Lorden, J.F.2
Walz, E.3
Oltmans, G.A.4
-
4
-
-
0242361309
-
Mutations in a novel gene encoding a CRAL-TRIO domain cause human Cayman ataxia and ataxia/dystonia in the jittery mouse
-
J.M. Bomar, P.J. Benke, E.L. Slattery, R. Puttagunta, L.P. Taylor, E. Seong, A. Nystuen, W. Chen, R.L. Albin, P.D. Patel, R.A. Kittles, V.C. Sheffield, and M. Burmeister Mutations in a novel gene encoding a CRAL-TRIO domain cause human Cayman ataxia and ataxia/dystonia in the jittery mouse Nat. Genet. 35 2003 264 269
-
(2003)
Nat. Genet.
, vol.35
, pp. 264-269
-
-
Bomar, J.M.1
Benke, P.J.2
Slattery, E.L.3
Puttagunta, R.4
Taylor, L.P.5
Seong, E.6
Nystuen, A.7
Chen, W.8
Albin, R.L.9
Patel, P.D.10
Kittles, R.A.11
Sheffield, V.C.12
Burmeister, M.13
-
5
-
-
0024331630
-
Local cerebral glucose utilization reveals widespread abnormalities in the motor system of the rat mutant dystonic
-
L.L. Brown, and J.F. Lorden Local cerebral glucose utilization reveals widespread abnormalities in the motor system of the rat mutant dystonic J. Neurosci. 9 1989 4033 4041
-
(1989)
J. Neurosci.
, vol.9
, pp. 4033-4041
-
-
Brown, L.L.1
Lorden, J.F.2
-
6
-
-
0031889483
-
Ataxia with isolated vitamin e deficiency: Heterogeneity of mutations and phenotypic variability in a large number of families
-
L. Cavalier, K. Ouahchi, H.J. Kayden, S. Di Donato, L. Reutenauer, J.L. Mandel, and M. Koenig Ataxia with isolated vitamin E deficiency: heterogeneity of mutations and phenotypic variability in a large number of families Am. J. Hum. Genet. 62 1998 301 310
-
(1998)
Am. J. Hum. Genet.
, vol.62
, pp. 301-310
-
-
Cavalier, L.1
Ouahchi, K.2
Kayden, H.J.3
Di Donato, S.4
Reutenauer, L.5
Mandel, J.L.6
Koenig, M.7
-
7
-
-
2942555396
-
Retrotransposon-derived elements in the mammalian genome: A potential source of disease
-
R. Druker, and E. Whitelaw Retrotransposon-derived elements in the mammalian genome: a potential source of disease J. Inherit. Metab. Dis. 27 2004 319 330
-
(2004)
J. Inherit. Metab. Dis.
, vol.27
, pp. 319-330
-
-
Druker, R.1
Whitelaw, E.2
-
8
-
-
7444264729
-
Complex patterns of transcription at the insertion site of a retrotransposon in the mouse
-
R. Druker, T.J. Bruxner, N.J. Lehrbach, and E. Whitelaw Complex patterns of transcription at the insertion site of a retrotransposon in the mouse Nucleic Acids Res. 32 2004 5800 5808
-
(2004)
Nucleic Acids Res.
, vol.32
, pp. 5800-5808
-
-
Druker, R.1
Bruxner, T.J.2
Lehrbach, N.J.3
Whitelaw, E.4
-
9
-
-
0000613043
-
Classification and investigation of dystonia
-
C.D. Marsden S. Fahn Butterworths Press London
-
S. Fahn, C.D. Marsden, and D.B. Calne Classification and investigation of dystonia C.D. Marsden S. Fahn Movement Disorders 2 1987 Butterworths Press London 332 358
-
(1987)
Movement Disorders 2
, pp. 332-358
-
-
Fahn, S.1
Marsden, C.D.2
Calne, D.B.3
-
10
-
-
0036348327
-
Triggers of paroxysmal dyskinesia in the calcium channel mouse mutant tottering
-
B.E. Fureman, H.A. Jinnah, and E.J. Hess Triggers of paroxysmal dyskinesia in the calcium channel mouse mutant tottering Pharmacol. Biochem. Behav. 73 2002 631 637
-
(2002)
Pharmacol. Biochem. Behav.
, vol.73
, pp. 631-637
-
-
Fureman, B.E.1
Jinnah, H.A.2
Hess, E.J.3
-
11
-
-
3042818807
-
Characterization of a mutagenic B1 retrotransposon insertion in the jittery mouse
-
N. Gilbert, J.M. Bomar, M. Burmeister, and J.V. Moran Characterization of a mutagenic B1 retrotransposon insertion in the jittery mouse Hum. Mutat. 24 2004 9 13
-
(2004)
Hum. Mutat.
, vol.24
, pp. 9-13
-
-
Gilbert, N.1
Bomar, J.M.2
Burmeister, M.3
Moran, J.V.4
-
12
-
-
0032783976
-
Metastatic rat carcinoma cells express a new retrotransposon
-
M. Grassi, J.M. Girault, W.P. Wang, J.P. Thiery, and J. Jouanneau Metastatic rat carcinoma cells express a new retrotransposon Gene 233 1999 59 66
-
(1999)
Gene
, vol.233
, pp. 59-66
-
-
Grassi, M.1
Girault, J.M.2
Wang, W.P.3
Thiery, J.P.4
Jouanneau, J.5
-
13
-
-
0031770826
-
Intracisternal A-particle element transposition into the murine beta-glucuronidase gene correlates with loss of enzyme activity: A new model for beta-glucuronidase deficiency in the C3H mouse
-
B. Gwynn, K. Lueders, M.S. Sands, and E.H. Birkenmeier Intracisternal A-particle element transposition into the murine beta-glucuronidase gene correlates with loss of enzyme activity: a new model for beta-glucuronidase deficiency in the C3H mouse Mol. Cell. Biol. 18 1998 6474 6481
-
(1998)
Mol. Cell. Biol.
, vol.18
, pp. 6474-6481
-
-
Gwynn, B.1
Lueders, K.2
Sands, M.S.3
Birkenmeier, E.H.4
-
14
-
-
0031006852
-
The vibrator mutation causes neurodegeneration via reduced expression of PITPa: Positional complementation cloning and extragenic suppression
-
B.A. Hamilton, D.J. Smith, K.L. Mueller, A.W. Kerrebrock, R.T. Bronson, V. van Berkel, M.J. Daly, L. Kruglyak, M.P. Reeve, J.L. Nemhauser, T.L. Hawkins, E.M. Rubin, and E.S. Lander The vibrator mutation causes neurodegeneration via reduced expression of PITPa: positional complementation cloning and extragenic suppression Neuron 18 1997 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
-
15
-
-
0033680967
-
Long-term depression of the cerebellar climbing fiber-Purkinje neuron synapse
-
C. Hansel, and D.J. Linden Long-term depression of the cerebellar climbing fiber-Purkinje neuron synapse Neuron 26 2000 473 482
-
(2000)
Neuron
, vol.26
, pp. 473-482
-
-
Hansel, C.1
Linden, D.J.2
-
16
-
-
0038338498
-
Carbonic anhydrase-related protein is a novel binding protein for inositol 1,4,5-trisphosphate receptor type 1
-
J. Hirota, H. Ando, K. Hamada, and K. Mikoshiba Carbonic anhydrase-related protein is a novel binding protein for inositol 1,4,5-trisphosphate receptor type 1 Biochem. J. 372 2003 435 441
-
(2003)
Biochem. J.
, vol.372
, pp. 435-441
-
-
Hirota, J.1
Ando, H.2
Hamada, K.3
Mikoshiba, K.4
-
17
-
-
27744541539
-
Carbonic anhydrase-related protein VIII deficiency is associated with a distinctive lifelong gait disorder in waddles mice
-
Y. Jiao, J. Yan, Y. Zhao, L.R. Donahue, W.G. Beamer, X. Li, B. Roe, M. LeDoux, and W. Gu Carbonic anhydrase-related protein VIII deficiency is associated with a distinctive lifelong gait disorder in waddles mice Genetics 2005 (Epub ahead of print)
-
(2005)
Genetics
-
-
Jiao, Y.1
Yan, J.2
Zhao, Y.3
Donahue, L.R.4
Beamer, W.G.5
Li, X.6
Roe, B.7
Ledoux, M.8
Gu, W.9
-
18
-
-
84882325932
-
Assessment of movement disorders in rodents
-
M.S. LeDoux Elsevier San Diego
-
H.A. Jinnah, and E.J. Hess Assessment of movement disorders in rodents M.S. LeDoux Animal Models of Movement Disorders 2004 Elsevier San Diego 55 71
-
(2004)
Animal Models of Movement Disorders
, pp. 55-71
-
-
Jinnah, H.A.1
Hess, E.J.2
-
19
-
-
18144430546
-
Rodent models for dystonia research: Characteristics, evaluation, and utility
-
H.A. Jinnah, E.J. Hess, M.S. LeDoux, N. Sharma, M.G. Baxter, and M.R. Delong Rodent models for dystonia research: characteristics, evaluation, and utility Mov. Disord. 20 2005 283 292
-
(2005)
Mov. Disord.
, vol.20
, pp. 283-292
-
-
Jinnah, H.A.1
Hess, E.J.2
Ledoux, M.S.3
Sharma, N.4
Baxter, M.G.5
Delong, M.R.6
-
20
-
-
0033061834
-
Inner ear and kidney anomalies caused by IAP insertion in an intron of the Eya1 gene in a mouse model of BOR syndrome
-
K.R. Johnson, S.A. Cook, L.C. Erway, A.N. Matthews, L.P. Sanford, N.E. Paradies, and R.A. Friedman Inner ear and kidney anomalies caused by IAP insertion in an intron of the Eya1 gene in a mouse model of BOR syndrome Hum. Mol. Genet. 8 1999 645 653
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 645-653
-
-
Johnson, K.R.1
Cook, S.A.2
Erway, L.C.3
Matthews, A.N.4
Sanford, L.P.5
Paradies, N.E.6
Friedman, R.A.7
-
21
-
-
0030217889
-
The neurological mouse mutations jittery and hesitant are allelic and map to the region of mouse chromosome 10 homologous to 19p13.3
-
D. Kapfhamer, H.O. Sweet, D. Sufalko, S. Warren, K.R. Johnson, and M. Burmeister The neurological mouse mutations jittery and hesitant are allelic and map to the region of mouse chromosome 10 homologous to 19p13.3 Genomics 35 1996 533 538
-
(1996)
Genomics
, vol.35
, pp. 533-538
-
-
Kapfhamer, D.1
Sweet, H.O.2
Sufalko, D.3
Warren, S.4
Johnson, K.R.5
Burmeister, M.6
-
22
-
-
0038674744
-
Isoelectric point mobility shift assay for rapid screening of charged and uncharged ligands bound to proteins
-
P. Kempna, R. Cipollone, L. Villacorta, R. Ricciarelli, and J.M. Zingg Isoelectric point mobility shift assay for rapid screening of charged and uncharged ligands bound to proteins IUBMB Life 2 2003 103 107
-
(2003)
IUBMB Life
, vol.2
, pp. 103-107
-
-
Kempna, P.1
Cipollone, R.2
Villacorta, L.3
Ricciarelli, R.4
Zingg, J.M.5
-
23
-
-
0024254164
-
The intracisternal A-particle gene family: Structure and functional aspects
-
E.L. Kuff, and K.K. Lueders The intracisternal A-particle gene family: structure and functional aspects Adv. Cancer Res. 51 1988 183 276
-
(1988)
Adv. Cancer Res.
, vol.51
, pp. 183-276
-
-
Kuff, E.L.1
Lueders, K.K.2
-
24
-
-
84882324034
-
The genetically dystonic rat
-
M.S. LeDoux Elsevier San Diego
-
M.S. LeDoux The genetically dystonic rat M.S. LeDoux Animal Models of Movement Disorders 2004 Elsevier San Diego 241 252
-
(2004)
Animal Models of Movement Disorders
, pp. 241-252
-
-
Ledoux, M.S.1
-
25
-
-
27744528872
-
Animal models and the science of movement disorders
-
M.S. LeDoux Elsevier San Diego
-
M.S. LeDoux Animal models and the science of movement disorders M.S. LeDoux Animal Models of Movement Disorders 2004 Elsevier San Diego 13 31
-
(2004)
Animal Models of Movement Disorders
, pp. 13-31
-
-
Ledoux, M.S.1
-
26
-
-
0037246324
-
Secondary cervical dystonia associated with structural lesions of the central nervous system
-
M.S. LeDoux, and K.A. Brady Secondary cervical dystonia associated with structural lesions of the central nervous system Mov. Disord. 18 2003 60 69
-
(2003)
Mov. Disord.
, vol.18
, pp. 60-69
-
-
Ledoux, M.S.1
Brady, K.A.2
-
27
-
-
0036038893
-
Abnormal spontaneous and harmaline-stimulated Purkinje cell activity in the awake genetically dystonic rat
-
M.S. LeDoux, and J.F. Lorden Abnormal spontaneous and harmaline-stimulated Purkinje cell activity in the awake genetically dystonic rat Exp. Brain Res. 145 2002 457 467
-
(2002)
Exp. Brain Res.
, vol.145
, pp. 457-467
-
-
Ledoux, M.S.1
Lorden, J.F.2
-
28
-
-
0027251669
-
Cerebellectomy eliminates the motor syndrome of the genetically dystonic rat
-
M.S. LeDoux, J.F. Lorden, and J.M. Ervin Cerebellectomy eliminates the motor syndrome of the genetically dystonic rat Exp. Neurol. 120 1993 302 310
-
(1993)
Exp. Neurol.
, vol.120
, pp. 302-310
-
-
Ledoux, M.S.1
Lorden, J.F.2
Ervin, J.M.3
-
29
-
-
0032101623
-
Single-unit activity of cerebellar nuclear cells in the awake genetically dystonic rat
-
M.S. LeDoux, D.C. Hurst, and J.F. Lorden Single-unit activity of cerebellar nuclear cells in the awake genetically dystonic rat Neuroscience 86 1998 533 545
-
(1998)
Neuroscience
, vol.86
, pp. 533-545
-
-
Ledoux, M.S.1
Hurst, D.C.2
Lorden, J.F.3
-
30
-
-
0021222931
-
Characterization of the rat mutant dystonic (dt): A new animal model of dystonia musculorum deformans
-
J.F. Lorden, T.W. McKeon, H.J. Baker, N. Cox, and S.U. Walkley Characterization of the rat mutant dystonic (dt): a new animal model of dystonia musculorum deformans J. Neurosci. 4 1984 1925 1932
-
(1984)
J. Neurosci.
, vol.4
, pp. 1925-1932
-
-
Lorden, J.F.1
McKeon, T.W.2
Baker, H.J.3
Cox, N.4
Walkley, S.U.5
-
31
-
-
0022345297
-
Decreased cerebellar 3′,5′-cyclic guanosine monophosphate levels and insensitivity to harmaline in the genetically dystonic rat (dt)
-
J.F. Lorden, G.A. Oltmans, T.W. McKeon, J. Lutes, and M. Beales Decreased cerebellar 3′,5′-cyclic guanosine monophosphate levels and insensitivity to harmaline in the genetically dystonic rat (dt) J. Neurosci. 5 1985 2618 2625
-
(1985)
J. Neurosci.
, vol.5
, pp. 2618-2625
-
-
Lorden, J.F.1
Oltmans, G.A.2
McKeon, T.W.3
Lutes, J.4
Beales, M.5
-
32
-
-
0021101072
-
Comparison of the sequence organization of related retrovirus-like multigene families in three evolutionarily distant rodent genomes
-
K.K. Lueders, and E.L. Kuff Comparison of the sequence organization of related retrovirus-like multigene families in three evolutionarily distant rodent genomes Nucleic Acids Res. 11 1983 4391 4408
-
(1983)
Nucleic Acids Res.
, vol.11
, pp. 4391-4408
-
-
Lueders, K.K.1
Kuff, E.L.2
-
33
-
-
4644251975
-
Long terminal repeat retrotransposons of Mus musculus
-
E.M. McCarthy, and J.F. McDonald Long terminal repeat retrotransposons of Mus musculus Genome Biol. 5 2004 R14
-
(2004)
Genome Biol.
, vol.5
, pp. 14
-
-
McCarthy, E.M.1
McDonald, J.F.2
-
34
-
-
0022525658
-
Glutamic acid decarboxylase activity in micropunches of the deep cerebellar nuclei of the genetically dystonic (dt) rat
-
G.A. Oltmans, M. Beales, and J.F. Lorden Glutamic acid decarboxylase activity in micropunches of the deep cerebellar nuclei of the genetically dystonic (dt) rat Brain Res. 385 1986 148 151
-
(1986)
Brain Res.
, vol.385
, pp. 148-151
-
-
Oltmans, G.A.1
Beales, M.2
Lorden, J.F.3
-
35
-
-
0038348648
-
Ligand specificity in the CRAL-TRIO protein family
-
C. Panagabko, S. Morley, M. Hernandez, P. Cassolato, H. Gordon, R. Parsons, D. Manor, and J. Atkinson Ligand specificity in the CRAL-TRIO protein family Biochemistry 42 2003 6467 6474
-
(2003)
Biochemistry
, vol.42
, pp. 6467-6474
-
-
Panagabko, C.1
Morley, S.2
Hernandez, M.3
Cassolato, P.4
Gordon, H.5
Parsons, R.6
Manor, D.7
Atkinson, J.8
-
36
-
-
0036460973
-
Dystonia in spinocerebellar ataxia type 6
-
K.D. Sethi, and J. Jankovic Dystonia in spinocerebellar ataxia type 6 Mov. Disord. 17 2002 150 153
-
(2002)
Mov. Disord.
, vol.17
, pp. 150-153
-
-
Sethi, K.D.1
Jankovic, J.2
-
37
-
-
0036320968
-
Glutamate release during LTD at cerebellar climbing fiber-Purkinje cell synapses
-
Y. Shen, C. Hansel, and D.J. Linden Glutamate release during LTD at cerebellar climbing fiber-Purkinje cell synapses Nat. Neurosci. 5 2002 725 726
-
(2002)
Nat. Neurosci.
, vol.5
, pp. 725-726
-
-
Shen, Y.1
Hansel, C.2
Linden, D.J.3
-
38
-
-
0031021124
-
The type 1 inositol 1,4,5-trisphosphate receptor gene is altered in the opisthotonos mouse
-
V.A. Street, M.M. Bosma, V.P. Demas, M.R. Regan, D.D. Lin, L.C. Robinson, W.S. Agnew, and B.L. Tempel The type 1 inositol 1,4,5-trisphosphate receptor gene is altered in the opisthotonos mouse J. Neurosci. 17 1997 635 645
-
(1997)
J. Neurosci.
, vol.17
, pp. 635-645
-
-
Street, V.A.1
Bosma, M.M.2
Demas, V.P.3
Regan, M.R.4
Lin, D.D.5
Robinson, L.C.6
Agnew, W.S.7
Tempel, B.L.8
-
39
-
-
3242809764
-
Negative and positive effects of an IAP-LTR on nearby Pcdaalpha gene expression in the central nervous system and neuroblastoma cell lines
-
H. Sugino, T. Toyama, Y. Taguchi, S. Esumi, M. Miyazaki, and T. Yagi Negative and positive effects of an IAP-LTR on nearby Pcdaalpha gene expression in the central nervous system and neuroblastoma cell lines Gene 337 2004 91 103
-
(2004)
Gene
, vol.337
, pp. 91-103
-
-
Sugino, H.1
Toyama, T.2
Taguchi, Y.3
Esumi, S.4
Miyazaki, M.5
Yagi, T.6
-
40
-
-
0033546752
-
A point mutation in a plasma membrane Ca(2+)-ATPase gene causes deafness in Wriggle Mouse Sagami
-
K. Takahashi, and K. Kitamura A point mutation in a plasma membrane Ca(2+)-ATPase gene causes deafness in Wriggle Mouse Sagami Biochem. Biophys. Res. Commun. 261 1999 773 778
-
(1999)
Biochem. Biophys. Res. Commun.
, vol.261
, pp. 773-778
-
-
Takahashi, K.1
Kitamura, K.2
-
41
-
-
0036842130
-
Synaptic defects in ataxia mice result from a mutation in Usp14, encoding a ubiquitin-specific protease
-
S.M. Wilson, B. Bhattacharyya, R.A. Rachel, V. Coppola, L. Tessarollo, D.B. Householder, C.F. Fletcher, R.J. Miller, N.G. Copel, and N.A. Jenkins Synaptic defects in ataxia mice result from a mutation in Usp14, encoding a ubiquitin-specific protease Nat. Genet. 32 2002 420 425
-
(2002)
Nat. Genet.
, vol.32
, pp. 420-425
-
-
Wilson, S.M.1
Bhattacharyya, B.2
Rachel, R.A.3
Coppola, V.4
Tessarollo, L.5
Householder, D.B.6
Fletcher, C.F.7
Miller, R.J.8
Copel, N.G.9
Jenkins, N.A.10
-
42
-
-
4544320300
-
Dystonia as a presenting sign of spinocerebellar ataxia type 1
-
Y.R. Wu, G.J. Lee-Chen, A.E. Lang, C.M. Chen, H.Y. Lin, and S.T. Chen Dystonia as a presenting sign of spinocerebellar ataxia type 1 Mov. Disord. 19 2004 586 587
-
(2004)
Mov. Disord.
, vol.19
, pp. 586-587
-
-
Wu, Y.R.1
Lee-Chen, G.J.2
Lang, A.E.3
Chen, C.M.4
Lin, H.Y.5
Chen, S.T.6
-
43
-
-
0242391849
-
Cloning, developmental regulation and neural localization of rat ε-sarcoglycan
-
J. Xiao, and M.S. LeDoux Cloning, developmental regulation and neural localization of rat ε-sarcoglycan Mol. Brain Res. 26 2003 132 143
-
(2003)
Mol. Brain Res.
, vol.26
, pp. 132-143
-
-
Xiao, J.1
Ledoux, M.S.2
-
44
-
-
0029133262
-
Germ-line Tsc2 mutation in a dominantly inherited cancer model defines a novel family of rat intracisternal-A particle elements
-
G.H. Xiao, F. Jin, and R.S. Yeung Germ-line Tsc2 mutation in a dominantly inherited cancer model defines a novel family of rat intracisternal-A particle elements Oncogene 11 1995 81 87
-
(1995)
Oncogene
, vol.11
, pp. 81-87
-
-
Xiao, G.H.1
Jin, F.2
Yeung, R.S.3
-
45
-
-
3343026533
-
Developmental expression of rat torsinA transcript and protein
-
J. Xiao, S. Gong, Y. Zhao, and M.S. LeDoux Developmental expression of rat torsinA transcript and protein Dev. Brain Res. 152 2004 47 60
-
(2004)
Dev. Brain Res.
, vol.152
, pp. 47-60
-
-
Xiao, J.1
Gong, S.2
Zhao, Y.3
Ledoux, M.S.4
-
46
-
-
18344378034
-
Molecular cloning and expression of rat torsinA in the normal and genetically dystonic (dt) rat
-
P. Ziefer, J. Leung, T. Razzano, C. Shalish, M.S. LeDoux, J.F. Lorden, L. Ozelius, X.O. Breakefield, D.G. Standaert, and S.J. Augood Molecular cloning and expression of rat torsinA in the normal and genetically dystonic (dt) rat Mol. Brain Res. 10 2002 132 135
-
(2002)
Mol. Brain Res.
, vol.10
, pp. 132-135
-
-
Ziefer, P.1
Leung, J.2
Razzano, T.3
Shalish, C.4
Ledoux, M.S.5
Lorden, J.F.6
Ozelius, L.7
Breakefield, X.O.8
Standaert, D.G.9
Augood, S.J.10
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