Detalhe da pesquisa
1.
TDP-43 condensation properties specify its RNA-binding and regulatory repertoire.
Cell
; 184(18): 4680-4696.e22, 2021 09 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34380047
2.
A Liquid to Solid Phase Transition Underlying Pathological Huntingtin Exon1 Aggregation.
Mol Cell
; 70(4): 588-601.e6, 2018 05 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-29754822
3.
Sam68 sequestration and partial loss of function are associated with splicing alterations in FXTAS patients.
EMBO J
; 29(7): 1248-61, 2010 Apr 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-20186122
4.
Reversal of RNA toxicity in myotonic dystrophy via a decoy RNA-binding protein with high affinity for expanded CUG repeats.
Nat Biomed Eng
; 6(2): 207-220, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35145256
5.
Cells of Matter-In Vitro Models for Myotonic Dystrophy.
Front Neurol
; 9: 361, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29875732
6.
Immortalized human myotonic dystrophy muscle cell lines to assess therapeutic compounds.
Dis Model Mech
; 10(4): 487-497, 2017 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28188264
7.
Dystrophin restoration therapy improves both the reduced excitability and the force drop induced by lengthening contractions in dystrophic mdx skeletal muscle.
Skelet Muscle
; 6: 23, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27441081
8.
Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy.
Nat Commun
; 7: 11067, 2016 Apr 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-27063795
9.
Abnormal splicing switch of DMD's penultimate exon compromises muscle fibre maintenance in myotonic dystrophy.
Nat Commun
; 6: 7205, 2015 May 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-26018658
10.
Misregulation of miR-1 processing is associated with heart defects in myotonic dystrophy.
Nat Struct Mol Biol
; 18(7): 840-5, 2011 Jun 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-21685920