Detalhe da pesquisa
1.
Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia Defects.
Am J Hum Genet
; 99(3): 770-776, 2016 Sep 01.
Artigo
Inglês
| MEDLINE | ID: mdl-27588451
2.
The Evaluation of BMI1 Posttranslational Modifications During Retinal Degeneration to Understand BMI1 Action on Photoreceptor Death Execution.
Adv Exp Med Biol
; 1074: 359-365, 2018.
Artigo
Inglês
| MEDLINE | ID: mdl-29721964
3.
The novel Parkinson's disease linked mutation G51D attenuates in vitro aggregation and membrane binding of α-synuclein, and enhances its secretion and nuclear localization in cells.
Hum Mol Genet
; 23(17): 4491-509, 2014 Sep 01.
Artigo
Inglês
| MEDLINE | ID: mdl-24728187
4.
The H50Q mutation enhances α-synuclein aggregation, secretion, and toxicity.
J Biol Chem
; 289(32): 21856-76, 2014 Aug 08.
Artigo
Inglês
| MEDLINE | ID: mdl-24936070
5.
α-Synuclein in central nervous system and from erythrocytes, mammalian cells, and Escherichia coli exists predominantly as disordered monomer.
J Biol Chem
; 287(19): 15345-64, 2012 May 04.
Artigo
Inglês
| MEDLINE | ID: mdl-22315227
6.
Phosphorylation of synucleins by members of the Polo-like kinase family.
J Biol Chem
; 285(4): 2807-22, 2010 Jan 22.
Artigo
Inglês
| MEDLINE | ID: mdl-19889641