186.262 articles found

A search for prions and analyses of genomic rearrangements in fission yeast cells

Ellis DA.

· 2017-01-01

Endoplasmic reticulum structure and function in LRRK2-mediated Parkinson's disease

Nixon-Abell JJ.

· 2017-01-01

In vitro monoamine oxidase A and B inhibitory activity and molecular docking simulations of fucoxanthin

Jung HA, Roy A, Choi JS.

Fish Sci · 2017-01-01

Dopamine D3 Receptor Modulates l-DOPA-Induced Dyskinesia by Targeting D1 Receptor-Mediated Striatal Signaling.

Solís O, Garcia-Montes JR, González-Granillo A, Xu M, Moratalla R.

Cereb Cortex · 2017-01-01

DOI: 10.1093/cercor/bhv231PMID: 26483399

Frequency-Dependent Corticostriatal Disinhibition Resulting from Chronic Dopamine Depletion: Role of Local Striatal cGMP and GABA-AR Signaling.

Jayasinghe VR, Flores-Barrera E, West AR, Tseng KY.

Cereb Cortex · 2017-01-01

DOI: 10.1093/cercor/bhv241PMID: 26508335

Adenosine A2A Receptors Modulate α-Synuclein Aggregation and Toxicity.

Ferreira DG, Batalha VL, Vicente Miranda H, Coelho JE, Gomes R, Gonçalves FQ, Real JI, Rino J, Albino-Teixeira A, Cunha RA, Outeiro TF, Lopes LV.

Cereb Cortex · 2017-01-01

DOI: 10.1093/cercor/bhv268PMID: 26534909

Familial Mutations and Post-translational Modifications of UCH-L1 in Parkinson's Disease and Neurodegenerative Disorders.

Lee YC, Hsu SD.

Curr Protein Pept Sci · 2017-01-01

DOI: 10.2174/1389203717666160217143721PMID: 26899237

Pathogenic Role of Serine Protease HtrA2/Omi in Neurodegenerative Diseases.

Goo HG, Rhim H, Kang S.

Curr Protein Pept Sci · 2017-01-01

DOI: 10.2174/1389203717666160311115750PMID: 26965693

Involvement of Gaucher Disease Mutations in Parkinson Disease.

Vilageliu L, Grinberg D.

Curr Protein Pept Sci · 2017-01-01

DOI: 10.2174/1389203717666160311115956PMID: 26965692

Retromer's Role in Endosomal Trafficking and Impaired Function in Neurodegenerative Diseases.

Follett J, Bugarcic A, Collins BM, Teasdale RD.

Curr Protein Pept Sci · 2017-01-01

DOI: 10.2174/1389203717666160311121246PMID: 26965691

Structure and Function of Fbxo7/PARK15 in Parkinson's Disease.

Randle SJ, Laman H.

Curr Protein Pept Sci · 2017-01-01

DOI: 10.2174/1389203717666160311121433PMID: 26965690

Hereditary Parkinsonism-Associated Genetic Variations in PARK9 Locus Lead to Functional Impairment of ATPase Type 13A2.

Park JS, Sue CM.

Curr Protein Pept Sci · 2017-01-01

DOI: 10.2174/1389203717666160311121534PMID: 26965689