Detalhe da pesquisa
1.
Retention of stress susceptibility in the mdx mouse model of Duchenne muscular dystrophy after PGC-1α overexpression or ablation of IDO1 or CD38.
Hum Mol Genet
; 33(7): 594-611, 2024 Mar 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-38181046
2.
Dystrophin missense mutations alter focal adhesion tension and mechanotransduction.
Proc Natl Acad Sci U S A
; 119(25): e2205536119, 2022 06 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-35700360
3.
Phosphorylation alters the mechanical stiffness of a model fragment of the dystrophin homologue utrophin.
J Biol Chem
; 299(2): 102847, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36587764
4.
Enhancing interaction of actin and actin-binding domain 1 of dystrophin with modulators: Toward improved gene therapy for Duchenne muscular dystrophy.
J Biol Chem
; 298(12): 102675, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36372234
5.
Some dystrophy phenotypes of dystrophin-deficient mdx mice are exacerbated by mild, repetitive daily stress.
FASEB J
; 35(4): e21489, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33734502
6.
Dystrophinopathy-associated dysfunction of Krebs cycle metabolism.
Hum Mol Genet
; 28(6): 942-951, 2019 03 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30476171
7.
Persistent upregulation of the ß-tubulin tubb6, linked to muscle regeneration, is a source of microtubule disorganization in dystrophic muscle.
Hum Mol Genet
; 28(7): 1117-1135, 2019 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30535187
8.
Essential nucleotide- and protein-dependent functions of Actb/ß-actin.
Proc Natl Acad Sci U S A
; 115(31): 7973-7978, 2018 07 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-30012594
9.
Variable rescue of microtubule and physiological phenotypes in mdx muscle expressing different miniaturized dystrophins.
Hum Mol Genet
; 27(12): 2090-2100, 2018 06 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29618008
10.
Mouse models of two missense mutations in actin-binding domain 1 of dystrophin associated with Duchenne or Becker muscular dystrophy.
Hum Mol Genet
; 27(3): 451-462, 2018 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29194514
11.
Independent variability of microtubule perturbations associated with dystrophinopathy.
Hum Mol Genet
; 25(22): 4951-4961, 2016 11 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28171583
12.
Neopterin/7,8-dihydroneopterin is elevated in Duchenne muscular dystrophy patients and protects mdx skeletal muscle function.
Exp Physiol
; 103(7): 995-1009, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29791760
13.
Multi-isotope imaging mass spectrometry reveals slow protein turnover in hair-cell stereocilia.
Nature
; 481(7382): 520-4, 2012 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22246323
14.
Disease-proportional proteasomal degradation of missense dystrophins.
Proc Natl Acad Sci U S A
; 112(40): 12414-9, 2015 Oct 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-26392559
15.
Microtubule binding distinguishes dystrophin from utrophin.
Proc Natl Acad Sci U S A
; 111(15): 5723-8, 2014 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24706788
16.
Corrigendum: Persistent upregulation of the ß-tubulin tubb6, linked to muscle regeneration, is a source of microtubule disorganization in dystrophic muscle.
Hum Mol Genet
; 28(11): 1930, 2019 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30753428
17.
Creatine kinase B is necessary to limit myoblast fusion during myogenesis.
Am J Physiol Cell Physiol
; 308(11): C919-31, 2015 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25810257
18.
Variable rescue of microtubule and physiological phenotypes in mdx muscle expressing different miniaturized dystrophins.
Hum Mol Genet
; 27(15): 2773, 2018 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29901725
19.
ß-Actin and fascin-2 cooperate to maintain stereocilia length.
J Neurosci
; 33(19): 8114-21, 2013 May 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-23658152
20.
Two operational modes of atomic force microscopy reveal similar mechanical properties for homologous regions of dystrophin and utrophin.
bioRxiv
; 2024 May 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-38826288