-
1
-
-
51449092440
-
Motor and cognitive deficits in the heterozygous leaner mouse, a Cav2.1 voltage-gated Ca2+ channel mutant. Neurobiol
-
Alonso I., Marques J.M., Sousa N., et al. Motor and cognitive deficits in the heterozygous leaner mouse, a Cav2.1 voltage-gated Ca2+ channel mutant. Neurobiol. Aging 2008, 29:1733-1743.
-
(2008)
Aging
, vol.29
, pp. 1733-1743
-
-
Alonso, I.1
Marques, J.M.2
Sousa, N.3
-
2
-
-
21544446985
-
Brain-derived neurotrophic factor is required for the establishment of the proper number of dopaminergic neurons in the substantia nigra pars compacta
-
Baquet Z.C., Bickford P.C., Jones K.R. Brain-derived neurotrophic factor is required for the establishment of the proper number of dopaminergic neurons in the substantia nigra pars compacta. J. Neurosci. 2005, 25:6251-6259.
-
(2005)
J. Neurosci.
, vol.25
, pp. 6251-6259
-
-
Baquet, Z.C.1
Bickford, P.C.2
Jones, K.R.3
-
3
-
-
2442506955
-
Early striatal dendrite deficits followed by neuron loss with advanced age in the absence of anterograde cortical brain-derived neurotrophic factor
-
Baquet Z.C., Gorski J.A., Jones K.R. Early striatal dendrite deficits followed by neuron loss with advanced age in the absence of anterograde cortical brain-derived neurotrophic factor. J. Neurosci. 2004, 24:4250-4258.
-
(2004)
J. Neurosci.
, vol.24
, pp. 4250-4258
-
-
Baquet, Z.C.1
Gorski, J.A.2
Jones, K.R.3
-
4
-
-
34547851814
-
Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes
-
Bi W., Yan J., Shi X., et al. Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes. Hum. Mol. Genet. 2007, 16:1802-1813.
-
(2007)
Hum. Mol. Genet.
, vol.16
, pp. 1802-1813
-
-
Bi, W.1
Yan, J.2
Shi, X.3
-
5
-
-
33747862027
-
Primitive reflex evaluation in the clinical assessment of extrapyramidal syndromes
-
Borroni B., Broli M., Costanzi C., Gipponi S., Gilberti N., Agosti C., Padovani A. Primitive reflex evaluation in the clinical assessment of extrapyramidal syndromes. Eur. J. Neurol. 2006, 13:1026-1028.
-
(2006)
Eur. J. Neurol.
, vol.13
, pp. 1026-1028
-
-
Borroni, B.1
Broli, M.2
Costanzi, C.3
Gipponi, S.4
Gilberti, N.5
Agosti, C.6
Padovani, A.7
-
6
-
-
0017073956
-
The placing reaction in adult neurology
-
Botez M.I. The placing reaction in adult neurology. Can. J. Neurol. Sci. 1976, 3:189-198.
-
(1976)
Can. J. Neurol. Sci.
, vol.3
, pp. 189-198
-
-
Botez, M.I.1
-
7
-
-
77958479351
-
A point mutation in the dynein heavy chain gene leads to striatal atrophy and compromises neurite outgrowth of striatal neurons
-
Braunstein K.E., Eschbach J., Rona-Vörös K., et al. A point mutation in the dynein heavy chain gene leads to striatal atrophy and compromises neurite outgrowth of striatal neurons. Hum. Mol. Genet. 2010, 19:4385-4398.
-
(2010)
Hum. Mol. Genet.
, vol.19
, pp. 4385-4398
-
-
Braunstein, K.E.1
Eschbach, J.2
Rona-Vörös, K.3
-
8
-
-
0025962662
-
Neurological signs in Alzheimer's disease
-
Burns A., Jacoby R., Levy R. Neurological signs in Alzheimer's disease. Age Ageing 1991, 20:45-51.
-
(1991)
Age Ageing
, vol.20
, pp. 45-51
-
-
Burns, A.1
Jacoby, R.2
Levy, R.3
-
9
-
-
0018788266
-
Structural and quantitative studies on the normal C3H and Lurcher mutant mouse
-
Caddy K.W.T., Biscoe T.J. Structural and quantitative studies on the normal C3H and Lurcher mutant mouse. Philos. Trans. Roy. Soc. Lond. Biol. 1979, 287:167-201.
-
(1979)
Philos. Trans. Roy. Soc. Lond. Biol.
, vol.287
, pp. 167-201
-
-
Caddy, K.W.T.1
Biscoe, T.J.2
-
10
-
-
25644444565
-
The histaminergic signaling system exerts a neuroprotective role against neurodegenerative-induced processes in the hamster
-
Canonaco M., Madeo M., Alo R., et al. The histaminergic signaling system exerts a neuroprotective role against neurodegenerative-induced processes in the hamster. J. Pharmacol. Exp. Ther. 2005, 315:188-195.
-
(2005)
J. Pharmacol. Exp. Ther.
, vol.315
, pp. 188-195
-
-
Canonaco, M.1
Madeo, M.2
Alo, R.3
-
11
-
-
41149136769
-
Selective cerebral volume reduction in Rett syndrome: a multiple-approach MR imaging study
-
Carter J.C., Lanham D.C., Pham D., et al. Selective cerebral volume reduction in Rett syndrome: a multiple-approach MR imaging study. Am. J. Neuroradiol. 2008, 29:436-441.
-
(2008)
Am. J. Neuroradiol.
, vol.29
, pp. 436-441
-
-
Carter, J.C.1
Lanham, D.C.2
Pham, D.3
-
12
-
-
0036566229
-
YAC transgenic mice carrying pathological alleles of the MJD1 locus exhibit a mild and slowly progressive cerebellar deficit
-
Cemal C.K., Carroll C.J., Lawrence L., et al. YAC transgenic mice carrying pathological alleles of the MJD1 locus exhibit a mild and slowly progressive cerebellar deficit. Hum. Mol. Genet. 2002, 11:1075-1094.
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 1075-1094
-
-
Cemal, C.K.1
Carroll, C.J.2
Lawrence, L.3
-
13
-
-
45049085458
-
Polyglutamine-expanded ataxin-3 causes cerebellar dysfunction of SCA3 transgenic mice by inducing transriptional dysregulation
-
Chou A.-H., Yeh T.-H., Ouyang P., et al. Polyglutamine-expanded ataxin-3 causes cerebellar dysfunction of SCA3 transgenic mice by inducing transriptional dysregulation. Neurobiol. Dis. 2008, 31:89-101.
-
(2008)
Neurobiol. Dis.
, vol.31
, pp. 89-101
-
-
Chou, A.-H.1
Yeh, T.-H.2
Ouyang, P.3
-
14
-
-
77149137999
-
Polyglutamine-expanded ataxin-7 causes cerebellar dysfunction by inducing transcriptional dysregulation
-
Chou A.-H., Chen C.-Y., Chen S.-Y., et al. Polyglutamine-expanded ataxin-7 causes cerebellar dysfunction by inducing transcriptional dysregulation. Neurochem. Int. 2010, 56:329-339.
-
(2010)
Neurochem. Int.
, vol.56
, pp. 329-339
-
-
Chou, A.-H.1
Chen, C.-Y.2
Chen, S.-Y.3
-
15
-
-
44449132518
-
Dicer loss in striatal neurons produces behavioral and neuroanatomical phenotypes in the absence of neurodegeneration
-
Cuellar T.L., Davis T.H., Nelson P.T., et al. Dicer loss in striatal neurons produces behavioral and neuroanatomical phenotypes in the absence of neurodegeneration. Proc. Natl. Acad. Sci. U. S. A. 2008, 105:5614-5619.
-
(2008)
Proc. Natl. Acad. Sci. U. S. A.
, vol.105
, pp. 5614-5619
-
-
Cuellar, T.L.1
Davis, T.H.2
Nelson, P.T.3
-
16
-
-
77954162482
-
Reversal of neuropathy phenotypes in conditional mouse model of Charcot-Marie-Tooth disease type 2E
-
Dequen F., Filali M., Larivière R.C., et al. Reversal of neuropathy phenotypes in conditional mouse model of Charcot-Marie-Tooth disease type 2E. Hum. Mol. Genet. 2010, 19:2616-2629.
-
(2010)
Hum. Mol. Genet.
, vol.19
, pp. 2616-2629
-
-
Dequen, F.1
Filali, M.2
Larivière, R.C.3
-
17
-
-
0026597658
-
The incidence of the grasp reflex following hemispheric lesion and its relation to frontal damage
-
De Renzi E., Barbieri C. The incidence of the grasp reflex following hemispheric lesion and its relation to frontal damage. Brain 1992, 115:293-313.
-
(1992)
Brain
, vol.115
, pp. 293-313
-
-
De Renzi, E.1
Barbieri, C.2
-
18
-
-
0035108653
-
Rett syndrome: review of biological abnormalities
-
Dunn H.G., MacLeod P.M. Rett syndrome: review of biological abnormalities. Can. J. Neurol. Sci. 2001, 28:16-29.
-
(2001)
Can. J. Neurol. Sci.
, vol.28
, pp. 16-29
-
-
Dunn, H.G.1
MacLeod, P.M.2
-
19
-
-
57649107154
-
Mice with a mutation in the dynein heavy chain 1 gene display sensory neuropathy but lack motor neuron disease
-
Dupuis L., Fergani A., Braunstein K.E., et al. Mice with a mutation in the dynein heavy chain 1 gene display sensory neuropathy but lack motor neuron disease. Exp. Neurol. 2009, 215:146-152.
-
(2009)
Exp. Neurol.
, vol.215
, pp. 146-152
-
-
Dupuis, L.1
Fergani, A.2
Braunstein, K.E.3
-
20
-
-
44649093889
-
Identification of a battery of tests for drug candidate evaluation in the SMNDelta7 neonate model of spinal muscular atrophy
-
El-Khodor B.F., Edgar N., Chen A., et al. Identification of a battery of tests for drug candidate evaluation in the SMNDelta7 neonate model of spinal muscular atrophy. Exp. Neurol. 2008, 212:29-43.
-
(2008)
Exp. Neurol.
, vol.212
, pp. 29-43
-
-
El-Khodor, B.F.1
Edgar, N.2
Chen, A.3
-
21
-
-
0346993599
-
MPTP potentiates 3-nitropropionic acid-induced striatal damage in mice: reference to striatonigral degeneration
-
Fernagut P.O., Diguet E., Bioulac B., et al. MPTP potentiates 3-nitropropionic acid-induced striatal damage in mice: reference to striatonigral degeneration. Exp. Neurol. 2004, 185:47-62.
-
(2004)
Exp. Neurol.
, vol.185
, pp. 47-62
-
-
Fernagut, P.O.1
Diguet, E.2
Bioulac, B.3
-
22
-
-
0027432621
-
The neurologic syndrome of severe Alzheimer's disease: relationship to functional decline
-
Franssen E.H., Kluger A., Torossian C.L., et al. The neurologic syndrome of severe Alzheimer's disease: relationship to functional decline. Arch. Neurol. 1993, 50:1029-1039.
-
(1993)
Arch. Neurol.
, vol.50
, pp. 1029-1039
-
-
Franssen, E.H.1
Kluger, A.2
Torossian, C.L.3
-
23
-
-
77953928277
-
Neural mechanism and clinical significance of the plantar grasp reflex in infants
-
Futagi Y., Suzuki Y. Neural mechanism and clinical significance of the plantar grasp reflex in infants. Pediatr. Neurol. 2010, 43:81-86.
-
(2010)
Pediatr. Neurol.
, vol.43
, pp. 81-86
-
-
Futagi, Y.1
Suzuki, Y.2
-
24
-
-
0037096365
-
Polyglutamine-expanded ataxin-7 promotes non-cell-autonomous Purkinje cell degeneration and displays proteolytic cleavage in ataxic transgenic mice
-
Garden G.A., Libby R.T., Fu Y.H., et al. Polyglutamine-expanded ataxin-7 promotes non-cell-autonomous Purkinje cell degeneration and displays proteolytic cleavage in ataxic transgenic mice. J. Neurosci. 2002, 22:4897-4905.
-
(2002)
J. Neurosci.
, vol.22
, pp. 4897-4905
-
-
Garden, G.A.1
Libby, R.T.2
Fu, Y.H.3
-
25
-
-
0030831353
-
Cerebellar disorganization characteristic of reeler in scrambler mutant mice despite presence of reelin
-
Goldowitz D., Cushing R.C., Laywell E., et al. Cerebellar disorganization characteristic of reeler in scrambler mutant mice despite presence of reelin. J. Neurosci. 1997, 17:8767-8777.
-
(1997)
J. Neurosci.
, vol.17
, pp. 8767-8777
-
-
Goldowitz, D.1
Cushing, R.C.2
Laywell, E.3
-
26
-
-
80055101576
-
A simple composite phenotype scoring system for evaluating mouse models of cerebellar ataxia
-
pii: 1787. doi: 10.3791/1787
-
Guyenet S.J., Furrer S.A., Damian V.M., et al. A simple composite phenotype scoring system for evaluating mouse models of cerebellar ataxia. J. Vis. Exp. 2010, 21(39). pii: 1787. doi: 10.3791/1787.
-
(2010)
J. Vis. Exp.
, vol.21
, Issue.39
-
-
Guyenet, S.J.1
Furrer, S.A.2
Damian, V.M.3
-
27
-
-
0031693525
-
Contribution of the supplementary motor area and anterior cingulate gyrus to pathological grasping phenomena
-
Hashimoto R., Tanaka Y. Contribution of the supplementary motor area and anterior cingulate gyrus to pathological grasping phenomena. Eur. Neurol. 1998, 40:151-158.
-
(1998)
Eur. Neurol.
, vol.40
, pp. 151-158
-
-
Hashimoto, R.1
Tanaka, Y.2
-
28
-
-
0033867386
-
CAG repeat length in RAI1 is associated with age at onset variability in spinocerebellar ataxia type 2 (SCA2)
-
Hayes S., Turecki G., Brisebois K., et al. CAG repeat length in RAI1 is associated with age at onset variability in spinocerebellar ataxia type 2 (SCA2). Hum. Mol. Genet. 2000, 9:1753-1758.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1753-1758
-
-
Hayes, S.1
Turecki, G.2
Brisebois, K.3
-
29
-
-
0028271668
-
Quantitative morphological analysis of the cerebellar nuclei in normal and Lurcher mutant mice. I. Morphol cell number
-
Heckroth J.A. Quantitative morphological analysis of the cerebellar nuclei in normal and Lurcher mutant mice. I. Morphol cell number. J. Comp. Neurol. 1994, 343:173-182.
-
(1994)
J. Comp. Neurol.
, vol.343
, pp. 173-182
-
-
Heckroth, J.A.1
-
30
-
-
34548161707
-
Longitudinal evaluation of the Hdh(CAG)150 knock-in murine model of Huntington's disease
-
Heng M.Y., Tallaksen-Greene S.J., Detloff P.J., et al. Longitudinal evaluation of the Hdh(CAG)150 knock-in murine model of Huntington's disease. J. Neurosci. 2007, 27:8989-8998.
-
(2007)
J. Neurosci.
, vol.27
, pp. 8989-8998
-
-
Heng, M.Y.1
Tallaksen-Greene, S.J.2
Detloff, P.J.3
-
31
-
-
0021001448
-
Role of staggerer gene in determining cell number in cerebellar cortex. I. Granule cell death is an indirect consequence of staggerer gene action, Dev
-
Herrup K. Role of staggerer gene in determining cell number in cerebellar cortex. I. Granule cell death is an indirect consequence of staggerer gene action, Dev. Brain Res. 1983, 11:267-274.
-
(1983)
Brain Res.
, vol.11
, pp. 267-274
-
-
Herrup, K.1
-
32
-
-
0018578749
-
Regional variation and absence of large neurons in the cerebellum of the staggerer mouse
-
Herrup K., Mullen R.J. Regional variation and absence of large neurons in the cerebellum of the staggerer mouse. Brain Res. 1979, 172:1-12.
-
(1979)
Brain Res.
, vol.172
, pp. 1-12
-
-
Herrup, K.1
Mullen, R.J.2
-
33
-
-
0023551058
-
Regional differences in cytoarchitecture of the weaver cerebellum suggest a new model for weaver gene action
-
Herrup K., Trenkner E. Regional differences in cytoarchitecture of the weaver cerebellum suggest a new model for weaver gene action. Neuroscience 1987, 23:871-885.
-
(1987)
Neuroscience
, vol.23
, pp. 871-885
-
-
Herrup, K.1
Trenkner, E.2
-
34
-
-
0015578770
-
Cerebellar alterations in the weaver mouse
-
Hirano A., Dembitzer H.M. Cerebellar alterations in the weaver mouse. J. Cell Biol. 1973, 56:478-486.
-
(1973)
J. Cell Biol.
, vol.56
, pp. 478-486
-
-
Hirano, A.1
Dembitzer, H.M.2
-
35
-
-
0023035434
-
Relationship between primitive reflexes and severity in Parkinson's disease
-
Huber S.J., Paulson G.W. Relationship between primitive reflexes and severity in Parkinson's disease. J. Neurol. Neurosurg. Psychiatry 1986, 49:1298-1300.
-
(1986)
J. Neurol. Neurosurg. Psychiatry
, vol.49
, pp. 1298-1300
-
-
Huber, S.J.1
Paulson, G.W.2
-
36
-
-
34547619240
-
Frontal release signs and cognition in people with schizophrenia, their siblings and healthy controls
-
Hyde T.M., Goldberg T.E., Egan M.F., et al. Frontal release signs and cognition in people with schizophrenia, their siblings and healthy controls. Br. J. Psychiatry 2007, 191:120-125.
-
(2007)
Br. J. Psychiatry
, vol.191
, pp. 120-125
-
-
Hyde, T.M.1
Goldberg, T.E.2
Egan, M.F.3
-
37
-
-
0014424692
-
Comprehensive observational assessment: 1a. A systematic, quantitative procedure for assessing the behavioral and physiologic state of the mouse
-
Irwin S. Comprehensive observational assessment: 1a. A systematic, quantitative procedure for assessing the behavioral and physiologic state of the mouse. Psychopharmacologia 1968, 13:222-257.
-
(1968)
Psychopharmacologia
, vol.13
, pp. 222-257
-
-
Irwin, S.1
-
38
-
-
70349459713
-
Grasping activity in utero: a significant indicator of fetal behavior (the role of the grasping reflex in fetal ethology)
-
Jakobovits A.A. Grasping activity in utero: a significant indicator of fetal behavior (the role of the grasping reflex in fetal ethology). J. Perinat. Med. 2009, 37:571-572.
-
(2009)
J. Perinat. Med.
, vol.37
, pp. 571-572
-
-
Jakobovits, A.A.1
-
39
-
-
0027319398
-
Stereotyped hand clasping: an unusual tardive movement disorder
-
Kaneko K., Yuasa T., Miyatake T., et al. Stereotyped hand clasping: an unusual tardive movement disorder. Mov. Disord. 1993, 8:230-231.
-
(1993)
Mov. Disord.
, vol.8
, pp. 230-231
-
-
Kaneko, K.1
Yuasa, T.2
Miyatake, T.3
-
40
-
-
33646800306
-
Loss of autophagy in the central nervous system causes neurodegeneration in mice
-
Komatsu M., Waguri S., Chiba T., et al. Loss of autophagy in the central nervous system causes neurodegeneration in mice. Nature 2006, 441:880-884.
-
(2006)
Nature
, vol.441
, pp. 880-884
-
-
Komatsu, M.1
Waguri, S.2
Chiba, T.3
-
41
-
-
0030972375
-
The winged helix gene, Mf3, is required for normal development of the diencephalon and midbrain, postnatal growth and the milk-ejection reflex
-
Labosky P.A., Winnier G.E., Jetton T.L., et al. The winged helix gene, Mf3, is required for normal development of the diencephalon and midbrain, postnatal growth and the milk-ejection reflex. Development 1997, 124:1263-1274.
-
(1997)
Development
, vol.124
, pp. 1263-1274
-
-
Labosky, P.A.1
Winnier, G.E.2
Jetton, T.L.3
-
42
-
-
0023138621
-
Motor abnormalities in weaver mutant mice
-
Lalonde R. Motor abnormalities in weaver mutant mice. Exp. Brain Res. 1987, 65:479-481.
-
(1987)
Exp. Brain Res.
, vol.65
, pp. 479-481
-
-
Lalonde, R.1
-
43
-
-
0023580234
-
Motor abnormalities in staggerer mutant mice
-
Lalonde R. Motor abnormalities in staggerer mutant mice. Exp. Brain Res. 1987, 68:417-420.
-
(1987)
Exp. Brain Res.
, vol.68
, pp. 417-420
-
-
Lalonde, R.1
-
44
-
-
4644335036
-
Exploratory activity, anxiety, and motor coordination in bigenic APPswe+PS1/δE9 mice
-
Lalonde R., Kim H.-D., Fukuchi K. Exploratory activity, anxiety, and motor coordination in bigenic APPswe+PS1/δE9 mice. Neurosci. Lett. 2004, 369:156-161.
-
(2004)
Neurosci. Lett.
, vol.369
, pp. 156-161
-
-
Lalonde, R.1
Kim, H.-D.2
Fukuchi, K.3
-
45
-
-
24944436289
-
Primary neurologic screening and motor coordination of Dstdt-J mutant mice (dystonia musculorum) with spinocerebellar atrophy
-
Lalonde R., Marchetti N., Strazielle C. Primary neurologic screening and motor coordination of Dstdt-J mutant mice (dystonia musculorum) with spinocerebellar atrophy. Physiol. Behav. 2005, 86:46-51.
-
(2005)
Physiol. Behav.
, vol.86
, pp. 46-51
-
-
Lalonde, R.1
Marchetti, N.2
Strazielle, C.3
-
46
-
-
0023859072
-
Spontaneous alternation and exploration in staggerer mutant mice
-
Lalonde R., Manseau M., Botez M.I. Spontaneous alternation and exploration in staggerer mutant mice. Behav. Brain Res. 1988, 27:273-276.
-
(1988)
Behav. Brain Res.
, vol.27
, pp. 273-276
-
-
Lalonde, R.1
Manseau, M.2
Botez, M.I.3
-
47
-
-
11144294808
-
Neurobehavioral characterization of APP23 transgenic mice with the SHIRPA primary screen
-
Lalonde R., Dumont M., Staufenbiel M., et al. Neurobehavioral characterization of APP23 transgenic mice with the SHIRPA primary screen. Behav. Brain Res. 2005, 157:91-98.
-
(2005)
Behav. Brain Res.
, vol.157
, pp. 91-98
-
-
Lalonde, R.1
Dumont, M.2
Staufenbiel, M.3
-
48
-
-
0022645156
-
Spontaneous alternation and habituation in Lurcher mutant mice
-
Lalonde R., Lamarre Y., Smith A.M., et al. Spontaneous alternation and habituation in Lurcher mutant mice. Brain Res. 1986, 362:161-164.
-
(1986)
Brain Res.
, vol.362
, pp. 161-164
-
-
Lalonde, R.1
Lamarre, Y.2
Smith, A.M.3
-
49
-
-
0038022595
-
Neurobehavioral testing of transgenic βAPP695SWE (Tg2576) mice with the Swedish mutation
-
Lalonde R., Lewis T.L., Strazielle C., et al. Neurobehavioral testing of transgenic βAPP695SWE (Tg2576) mice with the Swedish mutation. Brain Res. 2003, 977:38-45.
-
(2003)
Brain Res.
, vol.977
, pp. 38-45
-
-
Lalonde, R.1
Lewis, T.L.2
Strazielle, C.3
-
50
-
-
0028891145
-
Huntington's disease gene: regional and cellular expression in brain of normal and affected individuals
-
Landwehrmeyer G.B., McNeill S.M., Dure L.S., et al. Huntington's disease gene: regional and cellular expression in brain of normal and affected individuals. Ann. Neurol. 1995, 37:218-230.
-
(1995)
Ann. Neurol.
, vol.37
, pp. 218-230
-
-
Landwehrmeyer, G.B.1
McNeill, S.M.2
Dure, L.S.3
-
52
-
-
33746096547
-
Paradoxical effects of prenatal acetylcholinesterase blockade on neuro-behavioral development and drug-induced stereotypies in reeler mutant mice
-
Laviola G., Adriani W., Gaudino C., et al. Paradoxical effects of prenatal acetylcholinesterase blockade on neuro-behavioral development and drug-induced stereotypies in reeler mutant mice. Psychopharmacology 2006, 187:331-344.
-
(2006)
Psychopharmacology
, vol.187
, pp. 331-344
-
-
Laviola, G.1
Adriani, W.2
Gaudino, C.3
-
53
-
-
48249090873
-
Transcription factor MEF2C influences neural stem/progenitor cell differentiation and maturation in vivo
-
Li H., Radford J.C., Ragusa M.J., Shea K.L., et al. Transcription factor MEF2C influences neural stem/progenitor cell differentiation and maturation in vivo. Proc. Natl. Acad. Sci. U. S. A. 2008, 105:9397-9402.
-
(2008)
Proc. Natl. Acad. Sci. U. S. A.
, vol.105
, pp. 9397-9402
-
-
Li, H.1
Radford, J.C.2
Ragusa, M.J.3
Shea, K.L.4
-
54
-
-
0027484673
-
Huntington's disease (IT15) is widely expressed in human and rat tissues
-
Li S.H., Schilling G., Young W.S., et al. Huntington's disease (IT15) is widely expressed in human and rat tissues. Neuron 1993, 11:985-993.
-
(1993)
Neuron
, vol.11
, pp. 985-993
-
-
Li, S.H.1
Schilling, G.2
Young, W.S.3
-
55
-
-
0035862896
-
Neurological abnormalities in a knock-in mouse model of Huntington's disease
-
Lin C.H., Tallaksen-Greene S., Chien W.M., et al. Neurological abnormalities in a knock-in mouse model of Huntington's disease. Hum. Mol. Genet. 2001, 10:137-144.
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 137-144
-
-
Lin, C.H.1
Tallaksen-Greene, S.2
Chien, W.M.3
-
56
-
-
0242456044
-
Altered depression-related behaviors and functional changes in the dorsal raphe nucleus of serotonin transporter-deficient mice
-
Lira A., Zhou M., Castanon N., et al. Altered depression-related behaviors and functional changes in the dorsal raphe nucleus of serotonin transporter-deficient mice. Biol. Psychiatry 2003, 54:960-971.
-
(2003)
Biol. Psychiatry
, vol.54
, pp. 960-971
-
-
Lira, A.1
Zhou, M.2
Castanon, N.3
-
57
-
-
26444449018
-
The neuronal ceroid lipofuscinosis Cln8 gene expression is developmentally regulated in mouse brain and up-regulated in the hippocampal kindling model of epilepsy
-
Lonka L., Aalto A., Kopra O., et al. The neuronal ceroid lipofuscinosis Cln8 gene expression is developmentally regulated in mouse brain and up-regulated in the hippocampal kindling model of epilepsy. BMC Neurosci. 2005, 13(6):27.
-
(2005)
BMC Neurosci.
, vol.13
, Issue.6
, pp. 27
-
-
Lonka, L.1
Aalto, A.2
Kopra, O.3
-
58
-
-
0021222931
-
Characterization of the rat mutant dystonic (dt): a new animal model of dystonia musculorum deformans
-
Lorden J.F., McKeon T.W., Baker H.J., et al. Characterization of the rat mutant dystonic (dt): a new animal model of dystonia musculorum deformans. J. Neurosci. 1984, 4:1925-1932.
-
(1984)
J. Neurosci.
, vol.4
, pp. 1925-1932
-
-
Lorden, J.F.1
McKeon, T.W.2
Baker, H.J.3
-
59
-
-
16044373842
-
Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice
-
Mangiarini L., Sathasivam K., Seller M., et al. Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice. Cell 1996, 87:493-506.
-
(1996)
Cell
, vol.87
, pp. 493-506
-
-
Mangiarini, L.1
Sathasivam, K.2
Seller, M.3
-
60
-
-
0036713608
-
A mouse model of spinal and bulbar muscular atrophy
-
McManamny P., Chy H.S., Finkelstein D.I., et al. A mouse model of spinal and bulbar muscular atrophy. Hum. Mol. Genet. 2002, 11:2103-2111.
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 2103-2111
-
-
McManamny, P.1
Chy, H.S.2
Finkelstein, D.I.3
-
61
-
-
0034048845
-
Decrease in striatal enkephalin mRNA in mouse models of Huntington's disease
-
Menalled L., Zanjani H., MacKenzie L., et al. Decrease in striatal enkephalin mRNA in mouse models of Huntington's disease. Exp. Neurol. 2000, 162:328-342.
-
(2000)
Exp. Neurol.
, vol.162
, pp. 328-342
-
-
Menalled, L.1
Zanjani, H.2
MacKenzie, L.3
-
62
-
-
0037107191
-
Early motor dysfunction and striosomal distribution of huntingtin microaggregates in Huntington's disease knock-in mice
-
Menalled L.B., Sison J.D., Wu Y., et al. Early motor dysfunction and striosomal distribution of huntingtin microaggregates in Huntington's disease knock-in mice. J. Neurosci. 2002, 22:8266-8276.
-
(2002)
J. Neurosci.
, vol.22
, pp. 8266-8276
-
-
Menalled, L.B.1
Sison, J.D.2
Wu, Y.3
-
63
-
-
0022976796
-
Autosomal dominance in a late-onset motor neuron disease in the mouse
-
Messer A., Flaherty L. Autosomal dominance in a late-onset motor neuron disease in the mouse. J. Neurogenet. 1986, 3:345-355.
-
(1986)
J. Neurogenet.
, vol.3
, pp. 345-355
-
-
Messer, A.1
Flaherty, L.2
-
64
-
-
10744226948
-
Late onset Tay-Sachs disease in mice with targeted disruption of the Hexa gene: behavioral changes and pathology of the central nervous system
-
Miklyaeva E.I., Dong W., Bureau A., et al. Late onset Tay-Sachs disease in mice with targeted disruption of the Hexa gene: behavioral changes and pathology of the central nervous system. Brain Res. 2004, 1001:37-50.
-
(2004)
Brain Res.
, vol.1001
, pp. 37-50
-
-
Miklyaeva, E.I.1
Dong, W.2
Bureau, A.3
-
65
-
-
33947099370
-
The role of the cerebellum for predictive control of grasping
-
Nowak D.A., Topka H., Timmann D., et al. The role of the cerebellum for predictive control of grasping. Cerebellum 2007, 6:7-17.
-
(2007)
Cerebellum
, vol.6
, pp. 7-17
-
-
Nowak, D.A.1
Topka, H.2
Timmann, D.3
-
66
-
-
0029115971
-
A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation
-
Patil N., Cox D.R., Bhat D., et al. A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation. Nat. Genet. 1995, 11:126-129.
-
(1995)
Nat. Genet.
, vol.11
, pp. 126-129
-
-
Patil, N.1
Cox, D.R.2
Bhat, D.3
-
68
-
-
33750492325
-
Loss of cyclin D1 impairs cerebellar development and suppresses medulloblastoma formation
-
Pogoriler J., Millen K., Utset M., et al. Loss of cyclin D1 impairs cerebellar development and suppresses medulloblastoma formation. Development 2006, 133:3929-3937.
-
(2006)
Development
, vol.133
, pp. 3929-3937
-
-
Pogoriler, J.1
Millen, K.2
Utset, M.3
-
69
-
-
76149121821
-
Global deprivation of brain-derived neurotrophic factor in the CNS reveals an area-specific requirement for dendritic growth
-
Rauskolb S., Zagrebelsky M., Dreznjak A., et al. Global deprivation of brain-derived neurotrophic factor in the CNS reveals an area-specific requirement for dendritic growth. J. Neurosci. 2010, 30:1739-1749.
-
(2010)
J. Neurosci.
, vol.30
, pp. 1739-1749
-
-
Rauskolb, S.1
Zagrebelsky, M.2
Dreznjak, A.3
-
70
-
-
17344367977
-
Behavioural abnormalities and selective neuronal loss in HD transgenic mice expressing mutated full-length HD cDNA
-
Reddy P.H., Williams M., Charles V., et al. Behavioural abnormalities and selective neuronal loss in HD transgenic mice expressing mutated full-length HD cDNA. Nat. Genet. 1998, 20:198-202.
-
(1998)
Nat. Genet.
, vol.20
, pp. 198-202
-
-
Reddy, P.H.1
Williams, M.2
Charles, V.3
-
71
-
-
73449130230
-
Use of the frontal assessment battery in evaluating executive dysfunction in patients with Huntington's disease
-
Rodrigues G.R., Souza C.P., Cetlin R.S., et al. Use of the frontal assessment battery in evaluating executive dysfunction in patients with Huntington's disease. J. Neurol. 2009, 256:1809-1815.
-
(2009)
J. Neurol.
, vol.256
, pp. 1809-1815
-
-
Rodrigues, G.R.1
Souza, C.P.2
Cetlin, R.S.3
-
72
-
-
0022980571
-
Expression of the weaver gene in dopamine-containing neural systems is dose-dependent and affects both striatal and nonstriatal regions
-
Roffler-Tarlov S., Graybiel A.M. Expression of the weaver gene in dopamine-containing neural systems is dose-dependent and affects both striatal and nonstriatal regions. J. Neurosci. 1986, 6:3319-3330.
-
(1986)
J. Neurosci.
, vol.6
, pp. 3319-3330
-
-
Roffler-Tarlov, S.1
Graybiel, A.M.2
-
73
-
-
0029962959
-
Cell death in the midbrain of the murine mutation weaver
-
Roffler-Tarlov S., Martin B., Graybiel A.M., et al. Cell death in the midbrain of the murine mutation weaver. J. Neurosci. 1996, 16:1819-1826.
-
(1996)
J. Neurosci.
, vol.16
, pp. 1819-1826
-
-
Roffler-Tarlov, S.1
Martin, B.2
Graybiel, A.M.3
-
74
-
-
0027317253
-
Rapid neurophysiological effects of corticosterone on medullary neurons: relationship to stress-induced suppression of courtship clasping in an amphibian
-
Rose J.D., Moore F.L., Orchinik M. Rapid neurophysiological effects of corticosterone on medullary neurons: relationship to stress-induced suppression of courtship clasping in an amphibian. Neuroendocrinology 1993, 57:815-824.
-
(1993)
Neuroendocrinology
, vol.57
, pp. 815-824
-
-
Rose, J.D.1
Moore, F.L.2
Orchinik, M.3
-
75
-
-
34247106769
-
Evidence for abnormal early development in a mouse model of Rett syndrome
-
Santos M., Silva-Fernandes A., Oliveira P., et al. Evidence for abnormal early development in a mouse model of Rett syndrome. Genes Brain Behav. 2007, 6:277-286.
-
(2007)
Genes Brain Behav.
, vol.6
, pp. 277-286
-
-
Santos, M.1
Silva-Fernandes, A.2
Oliveira, P.3
-
77
-
-
0029111934
-
Cyclin D1 provides a link between development and oncogenesis in the retina and breast
-
Sicinski P., Donaher J.L., Parker S.B., et al. Cyclin D1 provides a link between development and oncogenesis in the retina and breast. Cell 1995, 82:621-630.
-
(1995)
Cell
, vol.82
, pp. 621-630
-
-
Sicinski, P.1
Donaher, J.L.2
Parker, S.B.3
-
79
-
-
35548937443
-
Expression profiling of Huntington's disease models suggests that brain-derived neurotrophic factor depletion plays a major role in striatal degeneration
-
Strand A.D., Baquet Z.C., Aragaki A.K., et al. Expression profiling of Huntington's disease models suggests that brain-derived neurotrophic factor depletion plays a major role in striatal degeneration. J. Neurosci. 2007, 27:11758-11768.
-
(2007)
J. Neurosci.
, vol.27
, pp. 11758-11768
-
-
Strand, A.D.1
Baquet, Z.C.2
Aragaki, A.K.3
-
80
-
-
0030281598
-
Scrambler, a new neurological mutation of the mouse with abnormalities of neuronal migration
-
Sweet H.O., Bronson R.T., Johnson R., et al. Scrambler, a new neurological mutation of the mouse with abnormalities of neuronal migration. Mamm. Genome 1996, 7:798-802.
-
(1996)
Mamm. Genome
, vol.7
, pp. 798-802
-
-
Sweet, H.O.1
Bronson, R.T.2
Johnson, R.3
-
81
-
-
74449090697
-
Neonatal motor functions in Cacna1α mutant rolling Nagoya mice
-
Takahashi E., Niimi K., Itakura C. Neonatal motor functions in Cacna1α mutant rolling Nagoya mice. Behav. Brain Res. 2010, 207:273-279.
-
(2010)
Behav. Brain Res.
, vol.207
, pp. 273-279
-
-
Takahashi, E.1
Niimi, K.2
Itakura, C.3
-
82
-
-
67649403105
-
Motor coordination impairment in aged heterozygous rolling Nagoya, Cav2.1 mutant mice
-
Takahashi E., Niimi K., Itakura C. Motor coordination impairment in aged heterozygous rolling Nagoya, Cav2.1 mutant mice. Brain Res. 2009, 1279:50-57.
-
(2009)
Brain Res.
, vol.1279
, pp. 50-57
-
-
Takahashi, E.1
Niimi, K.2
Itakura, C.3
-
83
-
-
10344220545
-
Critical roles of the guanylyl cyclase B receptor in endochondral ossification and development of female reproductive organs
-
Tamura N., Doolittle L.K., Hammer R.E., et al. Critical roles of the guanylyl cyclase B receptor in endochondral ossification and development of female reproductive organs. Proc. Natl. Acad. Sci. U. S. A. 2004, 101:17300-17305.
-
(2004)
Proc. Natl. Acad. Sci. U. S. A.
, vol.101
, pp. 17300-17305
-
-
Tamura, N.1
Doolittle, L.K.2
Hammer, R.E.3
-
84
-
-
0023944083
-
Mesencephalic dopamine cell deficit involves areas A8, A9 and A10 in weaver mutant mice
-
Triarhou L.C., Norton J., Ghetti B. Mesencephalic dopamine cell deficit involves areas A8, A9 and A10 in weaver mutant mice. Exp. Brain Res. 1988, 70:256-265.
-
(1988)
Exp. Brain Res.
, vol.70
, pp. 256-265
-
-
Triarhou, L.C.1
Norton, J.2
Ghetti, B.3
-
85
-
-
33745852268
-
Neurological abnormalities in caveolin-1 knockout out mice
-
Trushina E., Du Charme J., Parisi J., et al. Neurological abnormalities in caveolin-1 knockout out mice. Behav. Brain Res. 2006, 172:24-32.
-
(2006)
Behav. Brain Res.
, vol.172
, pp. 24-32
-
-
Trushina, E.1
Du Charme, J.2
Parisi, J.3
-
86
-
-
0028580180
-
Topographic organization of embryonic motor neurons defined by expression of LIM homeobox genes
-
Tsuchida T., Ensini M., Morton S.B., et al. Topographic organization of embryonic motor neurons defined by expression of LIM homeobox genes. Cell 1994, 79:957-970.
-
(1994)
Cell
, vol.79
, pp. 957-970
-
-
Tsuchida, T.1
Ensini, M.2
Morton, S.B.3
-
87
-
-
14344263222
-
Analysis of cholinergic markers, biogenic amines, and amino acids in the CNS of two APP overexpression mouse models
-
Van Dam D., Marescau B., Engelborghs S., et al. Analysis of cholinergic markers, biogenic amines, and amino acids in the CNS of two APP overexpression mouse models. Neurochem. Int. 2005, 46:409-422.
-
(2005)
Neurochem. Int.
, vol.46
, pp. 409-422
-
-
Van Dam, D.1
Marescau, B.2
Engelborghs, S.3
-
88
-
-
0032754386
-
Targeted inactivation of Hoxb8 affects survival of a spinal ganglion and causes aberrant limb reflexes
-
van den Akker E., Reijnen M., Korving J., et al. Targeted inactivation of Hoxb8 affects survival of a spinal ganglion and causes aberrant limb reflexes. Mech. Dev. 1999, 89:103-114.
-
(1999)
Mech. Dev.
, vol.89
, pp. 103-114
-
-
van den Akker, E.1
Reijnen, M.2
Korving, J.3
-
90
-
-
67349103903
-
Cytoplasmic prion protein induces forebrain neurotoxicity
-
Wang X., Bowers S.L., Wang F., et al. Cytoplasmic prion protein induces forebrain neurotoxicity. Biochim. Biophys. Acta 2009, 1792:555-563.
-
(2009)
Biochim. Biophys. Acta
, vol.1792
, pp. 555-563
-
-
Wang, X.1
Bowers, S.L.2
Wang, F.3
-
91
-
-
0037087771
-
Early phenotypes that presage late-onset neurodegenerative disease allow testing of modifiers in Hdh CAG knock-in mice
-
Wheeler V.C., Gutekunst C.A., Vrbanac V., et al. Early phenotypes that presage late-onset neurodegenerative disease allow testing of modifiers in Hdh CAG knock-in mice. Hum. Mol. Genet. 2002, 11:633-640.
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 633-640
-
-
Wheeler, V.C.1
Gutekunst, C.A.2
Vrbanac, V.3
-
92
-
-
0026689958
-
Spontaneous forelimb grasping in free feeding by rats: motor cortex aids limb and digit positioning
-
Whishaw I.Q., Dringenberg H.C., Pellis S.M. Spontaneous forelimb grasping in free feeding by rats: motor cortex aids limb and digit positioning. Behav. Brain Res. 1992, 48:113-125.
-
(1992)
Behav. Brain Res.
, vol.48
, pp. 113-125
-
-
Whishaw, I.Q.1
Dringenberg, H.C.2
Pellis, S.M.3
-
93
-
-
34548553576
-
Age-dependent axonal degeneration in an Alzheimer mouse model
-
Wirths O., Weis J., Kayed R., et al. Age-dependent axonal degeneration in an Alzheimer mouse model. Neurobiol. Aging 2007, 28:1689-1699.
-
(2007)
Neurobiol. Aging
, vol.28
, pp. 1689-1699
-
-
Wirths, O.1
Weis, J.2
Kayed, R.3
-
94
-
-
77951207088
-
Synaptic circuit abnormalities of motor-frontal layer 2/3 pyramidal neurons in a mutant mouse model of Rett syndrome
-
Wood L., Shepherd G.M. Synaptic circuit abnormalities of motor-frontal layer 2/3 pyramidal neurons in a mutant mouse model of Rett syndrome. Neurobiol. Dis. 2010, 38:281-287.
-
(2010)
Neurobiol. Dis.
, vol.38
, pp. 281-287
-
-
Wood, L.1
Shepherd, G.M.2
-
95
-
-
73549111347
-
Subtle neurological signs predict the severity of subacute cognitive and functional impairments after traumatic brain injury
-
Wortzel H.S., Frey K.L., Anderson C.A., et al. Subtle neurological signs predict the severity of subacute cognitive and functional impairments after traumatic brain injury. J. Neuropsychiatry Clin. Neurosci. 2009, 21:463-466.
-
(2009)
J. Neuropsychiatry Clin. Neurosci.
, vol.21
, pp. 463-466
-
-
Wortzel, H.S.1
Frey, K.L.2
Anderson, C.A.3
-
96
-
-
57749193495
-
Loss of Purkinje cells in the PKCγ H101Y transgenic mouse
-
Zhang Y., Snider A., Willard L., et al. Loss of Purkinje cells in the PKCγ H101Y transgenic mouse. Biochem. Biophys. Res. Commun. 2009, 378:524-528.
-
(2009)
Biochem. Biophys. Res. Commun.
, vol.378
, pp. 524-528
-
-
Zhang, Y.1
Snider, A.2
Willard, L.3
-
97
-
-
77952973905
-
MeCP2 is required for normal development of GABAergic circuits in the thalamus
-
Zhang Z.W., Zak J.D., Liu H. MeCP2 is required for normal development of GABAergic circuits in the thalamus. J. Neurophysiol. 2010, 103:2470-2481.
-
(2010)
J. Neurophysiol.
, vol.103
, pp. 2470-2481
-
-
Zhang, Z.W.1
Zak, J.D.2
Liu, H.3
-
98
-
-
0030800468
-
Neurodegeneration in Lurcher mutant mice caused by mutation in delta 2 glutamate receptor gene
-
Zuo J., De Jager P.L., Takahashi K.A., et al. Neurodegeneration in Lurcher mutant mice caused by mutation in delta 2 glutamate receptor gene. Nature 1997, 388:769-773.
-
(1997)
Nature
, vol.388
, pp. 769-773
-
-
Zuo, J.1
De Jager, P.L.2
Takahashi, K.A.3
|