Detalhe da pesquisa
1.
The collagen ColQ binds to LRP4 and regulates the activation of the Muscle-Specific Kinase-LRP4 receptor complex by agrin at the neuromuscular junction.
J Biol Chem;
299(8): 104962, 2023 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37356721
2.
Desmin prevents muscle wasting, exaggerated weakness and fragility, and fatigue in dystrophic mdx mouse.
J Physiol;
598(17): 3667-3689, 2020 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32515007
3.
Wnt proteins contribute to neuromuscular junction formation through distinct signaling pathways.
Development;
144(9): 1712-1724, 2017 05 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28348167
4.
Lamin-Related Congenital Muscular Dystrophy Alters Mechanical Signaling and Skeletal Muscle Growth.
Int J Mol Sci;
22(1)2020 Dec 30.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33396724
5.
Gonad-related factors promote muscle performance gain during postnatal development in male and female mice.
Am J Physiol Endocrinol Metab;
313(1): E12-E25, 2017 07 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28351832
6.
MuSK frizzled-like domain is critical for mammalian neuromuscular junction formation and maintenance.
J Neurosci;
35(12): 4926-41, 2015 Mar 25.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25810523
7.
New mutation in the ß1 propeller domain of LRP4 responsible for congenital myasthenic syndrome associated with Cenani-Lenz syndrome.
Sci Rep;
13(1): 14054, 2023 08 28.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37640745
8.
The cell polarity protein Vangl2 in the muscle shapes the neuromuscular synapse by binding to and regulating the tyrosine kinase MuSK.
Sci Signal;
15(734): eabg4982, 2022 05 17.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35580169
9.
New recessive mutations in SYT2 causing severe presynaptic congenital myasthenic syndromes.
Neurol Genet;
6(6): e534, 2020 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33659639
10.
Mutations in GFPT1-related congenital myasthenic syndromes are associated with synaptic morphological defects and underlie a tubular aggregate myopathy with synaptopathy.
J Neurol;
264(8): 1791-1803, 2017 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28712002
11.
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