Detalhe da pesquisa
1.
MFN2 mutations in Charcot-Marie-Tooth disease alter mitochondria-associated ER membrane function but do not impair bioenergetics.
Hum Mol Genet
; 28(11): 1782-1800, 2019 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30649465
2.
GTP binding regulates cellular localization of Parkinson's disease-associated LRRK2.
Hum Mol Genet
; 26(14): 2747-2767, 2017 07 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28453723
3.
Metallo-responsive self-assembly of lipophilic guanines in hydrocarbon solvents: a systematic SAXS structural characterization.
Nanoscale
; 12(2): 1022-1031, 2020 Jan 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31845695
4.
Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation.
Mol Neurodegener
; 13(1): 3, 2018 01 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-29357897
5.
LRRK2 phosphorylates pre-synaptic N-ethylmaleimide sensitive fusion (NSF) protein enhancing its ATPase activity and SNARE complex disassembling rate.
Mol Neurodegener
; 11: 1, 2016 Jan 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-26758690