PAPER Esteves AR, Gozes I, Cardoso SM
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PAPER Vogt-Eisele A, Krüger C, Duning K, Weber D, Spoelgen R, Pitzer C, Plaas C, Eisenhardt G, Meyer A, Vogt G, Krieger M, Handwerker E, Wennmann DO, Weide T, Skryabin BV, Klugmann M, Pavenstädt H, Huentelmann MJ, Kremerskothen J, Schneider A
KIBRA (KIdney/BRAin protein) regulates learning and memory and stabilizes Protein kinase Mζ
J Neurochem. 2013 Oct 7; PubMed: 24117625PAPER Yamano K, Youle RJ
PINK1 is degraded through the N-end rule pathway.
Autophagy. 2013 Nov 1;9(11):1758-69. PubMed: 24121706PAPER Osellame LD, Duchen MR
Quality Control Gone Wrong: Mitochondria, Lysosomal Storage Disorders and Neurodegeneration.
Br J Pharmacol. 2013 Oct 10; PubMed: 24116849PAPER Olivieri C, Castioni CA, Livigni S, Bersano E, Cantello R, Della Corte F, Mazzini L
Non-invasive ventilation after surgery in amyotrophic lateral sclerosis.
Acta Neurol Scand. 2013 Oct 1; PubMed: 24117131PAPER Ma X, Turnbull P, Peterson R, Turnbull J
Trophic and proliferative effects of Shh on motor neurons in embryonic spinal cord culture from wildtype and G93A SOD1 mice.
BMC Neurosci. 2013;14:119. PubMed: 24119209PAPER Li J, Li T, Zhang X, Tang Y, Yang J, Le W
Human superoxide dismutase 1 overexpression in motor neurons of Caenorhabditis elegans causes axon guidance defect and neurodegeneration.
Neurobiol Aging. 2013 Oct 11; PubMed: 24126158PAPER Kloster E, Saft C, Akkad DA, Epplen JT, Arning L
Association of age at onset in Huntington disease with functional promoter variations in NPY and NPY2R.
J Mol Med (Berl). 2013 Oct 13; PubMed: 24121255PAPER Rhodes SL, Buchanan DD, Ahmed I, Taylor KD, Loriot MA, Sinsheimer JS, Bronstein JM, Elbaz A, Mellick GD, Rotter JI, Ritz B
Pooled Analysis of Iron-related Genes in Parkinson's Disease: Association with Transferrin.
Neurobiol Dis. 2013 Oct 8;62C:172-178. PubMed: 24121126PAPER Marcon G, Indaco A, Di Fede G, Suardi S, Finato N, Moretti V, Micoli S, Fociani P, Zerbi P, Pincherle A, Redaelli V, Tagliavini F, Giaccone G
Panencephalopathic Creutzfeldt-Jakob disease with distinct pattern of prion protein deposition in a patient with D178N mutation and homozygosity for valine at codon 129 of the prion protein gene.
Brain Pathol. 2013 Oct 10; PubMed: 24118545PAPER Elmallah MI, Borgmeyer U, Betzel C, Redecke L
Impact of methionine oxidation as an initial event on the pathway of human prion protein conversion.
Prion. 2013 Oct 9;7(5) PubMed: 24121542PAPER Haidet-Phillips AM, Gross SK, Williams T, Tuteja A, Sherman A, Ko M, Jeong YH, Wong PC, Maragakis NJ
Altered astrocytic expression of TDP-43 does not influence motor neuron survival.
Exp Neurol. 2013 Dec;250:250-9. PubMed: 24120466PAPER Snow WM, Stoesz BM, Kelly DM, Albensi BC
Roles for NF-κB and Gene Targets of NF-κB in Synaptic Plasticity, Memory, and Navigation.
Mol Neurobiol. 2013 Oct 13; PubMed: 24122352PAPER Gonçalves G, Pereira J
[Freezing and gait disorders in Parkinson's disease].
Rev Med Chil. 2013 Jun;141(6):758-64. PubMed: 24121579PAPER Kouri N, Carlomagno Y, Baker M, Liesinger AM, Caselli RJ, Wszolek ZK, Petrucelli L, Boeve BF, Parisi JE, Josephs KA, Uitti RJ, Ross OA, Graff-Radford NR, DeTure MA, Dickson DW, Rademakers R
Novel mutation in MAPT exon 13 (p.N410H) causes corticobasal degeneration.
Acta Neuropathol. 2014 Feb;127(2):271-82. PubMed: 24121548Current Filters
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