| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Activation of the γ-secretase complex and presence of γ-secretase-activating protein may contribute to Aβ42 production in sporadic inclusion-body myositis muscle fibers
|
Nogalska, Anna
|
|
2012
|
48 |
1 |
p. 141-149
9 p.
|
artikel
|
| 2 |
Alpha-synuclein transgenic mice display age-related slowing of gastrointestinal motility associated with transgene expression in the vagal system
|
Noorian, Ali Reza
|
|
2012
|
48 |
1 |
p. 9-19
11 p.
|
artikel
|
| 3 |
Editorial Board
|
|
|
2012
|
48 |
1 |
p. ii-
1 p.
|
artikel
|
| 4 |
Effects of dopamine and serotonin antagonist injections into the striatopallidal complex of asymptomatic MPTP-treated monkeys
|
Neumane, Sara
|
|
2012
|
48 |
1 |
p. 27-39
13 p.
|
artikel
|
| 5 |
Functional analysis of dopaminergic systems in a DYT1 knock-in mouse model of dystonia
|
Song, Chang-Hyun
|
|
2012
|
48 |
1 |
p. 66-78
13 p.
|
artikel
|
| 6 |
Glut1 deficiency (G1D): Epilepsy and metabolic dysfunction in a mouse model of the most common human phenotype
|
Marin-Valencia, Isaac
|
|
2012
|
48 |
1 |
p. 92-101
10 p.
|
artikel
|
| 7 |
Long non-coding RNA expression profiles predict clinical phenotypes in glioma
|
Zhang, Xiaoqin
|
|
2012
|
48 |
1 |
p. 1-8
8 p.
|
artikel
|
| 8 |
Mitigation of augmented extrasynaptic NMDAR signaling and apoptosis in cortico-striatal co-cultures from Huntington's disease mice
|
Milnerwood, Austen J.
|
|
2012
|
48 |
1 |
p. 40-51
12 p.
|
artikel
|
| 9 |
Motor terminal degeneration unaffected by activity changes in SOD1G93A mice; a possible role for glycolysis
|
Carrasco, Dario I.
|
|
2012
|
48 |
1 |
p. 132-140
9 p.
|
artikel
|
| 10 |
Oxidative burden and mitochondrial dysfunction in a mouse model of Rett syndrome
|
Großer, Emanuel
|
|
2012
|
48 |
1 |
p. 102-114
13 p.
|
artikel
|
| 11 |
Prostaglandin FP receptor inhibitor reduces ischemic brain damage and neurotoxicity
|
Kim, Yun Tai
|
|
2012
|
48 |
1 |
p. 58-65
8 p.
|
artikel
|
| 12 |
Selective knockdown of mutant SOD1 in Schwann cells ameliorates disease in G85R mutant SOD1 transgenic mice
|
Wang, Lijun
|
|
2012
|
48 |
1 |
p. 52-57
6 p.
|
artikel
|
| 13 |
Selective pattern of motor system damage in gamma-synuclein transgenic mice mirrors the respective pathology in amyotrophic lateral sclerosis
|
Peters, Owen M.
|
|
2012
|
48 |
1 |
p. 124-131
8 p.
|
artikel
|
| 14 |
The GABRG2 nonsense mutation, Q40X, associated with Dravet syndrome activated NMD and generated a truncated subunit that was partially rescued by aminoglycoside-induced stop codon read-through
|
Huang, Xuan
|
|
2012
|
48 |
1 |
p. 115-123
9 p.
|
artikel
|
| 15 |
The nigrostriatal system in the presymptomatic and symptomatic stages in the MPTP monkey model: A PET, histological and biochemical study
|
Blesa, J.
|
|
2012
|
48 |
1 |
p. 79-91
13 p.
|
artikel
|
| 16 |
Wide therapeutic time-window of low-frequency stimulation at the subiculum for temporal lobe epilepsy treatment in rats
|
Zhong, Kai
|
|
2012
|
48 |
1 |
p. 20-26
7 p.
|
artikel
|
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