Detalhe da pesquisa
1.
Mutations causing Lopes-Maciel-Rodan syndrome are huntingtin hypomorphs.
Hum Mol Genet
; 30(3-4): 135-148, 2021 04 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-33432339
2.
Novel allele-specific quantification methods reveal no effects of adult onset CAG repeats on HTT mRNA and protein levels.
Hum Mol Genet
; 26(7): 1258-1267, 2017 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28165127
3.
The Polyglutamine Expansion at the N-Terminal of Huntingtin Protein Modulates the Dynamic Configuration and Phosphorylation of the C-Terminal HEAT Domain.
Structure
; 28(9): 1035-1050.e8, 2020 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32668197
4.
Novel DNA Aptamers that Bind to Mutant Huntingtin and Modify Its Activity.
Mol Ther Nucleic Acids
; 11: 416-428, 2018 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29858077
5.
Huntingtin's spherical solenoid structure enables polyglutamine tract-dependent modulation of its structure and function.
Elife
; 5: e11184, 2016 Mar 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-27003594
6.
Intracellular cleavage of amyloid ß by a viral protease NIa prevents amyloid ß-mediated cytotoxicity.
PLoS One
; 9(6): e98650, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24915567
7.
Interaction of crk with Myosin-1c participates in fibronectin-induced cell spreading.
Int J Biol Sci
; 9(8): 778-91, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23983611
8.
SPIN90 knockdown attenuates the formation and movement of endosomal vesicles in the early stages of epidermal growth factor receptor endocytosis.
PLoS One
; 8(12): e82610, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24340049