Detalhe da pesquisa
1.
A Muscle-Specific Enhancer RNA Mediates Cohesin Recruitment and Regulates Transcription In trans.
Mol Cell
; 71(1): 129-141.e8, 2018 07 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29979962
2.
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
3.
ß-Actin shows limited mobility and is required only for supraphysiological insulin-stimulated glucose transport in young adult soleus muscle.
Am J Physiol Endocrinol Metab
; 315(1): E110-E125, 2018 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29533739
4.
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
5.
Clearing skeletal muscle with CLARITY for light microscopy imaging.
Cell Biol Int
; 40(4): 478-83, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26732743
6.
Autophagy and mitochondria in Pompe disease: nothing is so new as what has long been forgotten.
Am J Med Genet C Semin Med Genet
; 160C(1): 13-21, 2012 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22253254
7.
Suppression of autophagy in skeletal muscle uncovers the accumulation of ubiquitinated proteins and their potential role in muscle damage in Pompe disease.
Hum Mol Genet
; 17(24): 3897-908, 2008 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-18782848
8.
Differences in the predominance of lysosomal and autophagic pathologies between infants and adults with Pompe disease: implications for therapy.
Mol Genet Metab
; 101(4): 324-31, 2010 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-20801068
9.
Enzyme Replacement Therapy Can Reverse Pathogenic Cascade in Pompe Disease.
Mol Ther Methods Clin Dev
; 18: 199-214, 2020 Sep 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32671132
10.
Misplaced Golgi Elements Produce Randomly Oriented Microtubules and Aberrant Cortical Arrays of Microtubules in Dystrophic Skeletal Muscle Fibers.
Front Cell Dev Biol
; 7: 176, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31620435
11.
Improved efficacy of a next-generation ERT in murine Pompe disease.
JCI Insight
; 4(5)2019 03 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30843882
12.
A new directionality tool for assessing microtubule pattern alterations.
Cytoskeleton (Hoboken)
; 71(4): 230-40, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24497496
13.
The value of muscle biopsies in Pompe disease: identifying lipofuscin inclusions in juvenile- and adult-onset patients.
Acta Neuropathol Commun
; 2: 2, 2014 Jan 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-24383498
14.
Molecular editing of cellular responses by the high-affinity receptor for IgE.
Science
; 343(6174): 1021-5, 2014 Feb 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-24505132
15.
Quantitative evaluation of skeletal muscle defects in second harmonic generation images.
J Biomed Opt
; 18(2): 26005, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23377006
16.
Microtubules that form the stationary lattice of muscle fibers are dynamic and nucleated at Golgi elements.
J Cell Biol
; 203(2): 205-13, 2013 Oct 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-24145165
17.
Differences in neuromuscular junctions of laryngeal and limb muscles in rats.
Laryngoscope
; 122(5): 1093-8, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22374515
18.
Who needs microtubules? Myogenic reorganization of MTOC, Golgi complex and ER exit sites persists despite lack of normal microtubule tracks.
PLoS One
; 6(12): e29057, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-22216166
19.
Fiber type conversion by PGC-1α activates lysosomal and autophagosomal biogenesis in both unaffected and Pompe skeletal muscle.
PLoS One
; 5(12): e15239, 2010 Dec 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-21179212
20.
Suppression of autophagy permits successful enzyme replacement therapy in a lysosomal storage disorder--murine Pompe disease.
Autophagy
; 6(8): 1078-89, 2010 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-20861693