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PubMed 12217951 Identification of a presymptomatic molecular phenotype in Hdh CAG knock-in mice. The hallmark striatal neurodegeneration of Huntington's disease (HD) is first triggered by a dominant property of the e 1.56 KB 2020-01-28 7 0
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PubMed 15743924 Quantitative measurement of changes in amyloid-beta(40) in the rat brain and cerebrospinal fluid following treatment with the gamma-secretase inhibitor LY-411575 [N2-[(2S)-2-(3,5-difluorophenyl)-2-hyd 2.03 KB 2015-11-22 6 0
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PubMed 22171043 Optimizing the decoding of movement goals from local field potentials in macaque cortex. The successful development of motor neuroprosthetic devices hinges on the ability to accurately and reliably de 1.63 KB 2020-01-21 8 0
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PubMed 16260499 Localization of MMR proteins on meiotic chromosomes in mice indicates distinct functions during prophase I. Mammalian MutL homologues function in DNA mismatch repair (MMR) after replication errors and 1.17 KB 2020-01-28 6 0
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PubMed 11161632 Selective blockade of the mGluR1 receptor reduces traumatic neuronal injury in vitro and improvesoOutcome after brain trauma. The effects of selective blockade of group I metabotropic glutamate recept 1.81 KB 2015-11-21 4 0
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PubMed 17054581 Microsatellite instability and novel mismatch repair gene mutations in northern Chinese population with hereditary non-polyposis colorectal cancer. OBJECTIVE: Hereditary non-polyposis colorectal cance 2.79 KB 2015-12-25 8 0
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PubMed 22592643 Apocynum venetum leaf extract attenuates disruption of the blood-brain barrier and upregulation of matrix metalloproteinase-9/-2 in a rat model of cerebral ischemia-reperfusion injury. We investigated 1.55 KB 2016-01-09 8 0
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PubMed 24652679 Changes in matrix metalloprotease activity and progranulin levels may contribute to the pathophysiological function of mutant leucine-rich repeat kinase 2. Increasing evidence suggests that Parkinson' 1.74 KB 2020-01-22 12 0
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PubMed 20382224 LRRK2-mediated neurodegeneration and dysfunction of dopaminergic neurons in a Caenorhabditis elegans model of Parkinson's disease. Mutations in LRRK2 are thus far the most frequent known cause of auto 1.69 KB 2020-01-29 11 0
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PubMed 16029963 Basal ganglia local field potential activity: character and functional significance in the human. Functional neurosurgery in patients with movement disorders has provided a unique opportunity to recor 1.46 KB 2015-12-01 6 0
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