Detalhe da pesquisa
1.
The expanding field of IgG4-mediated neurological autoimmune disorders.
Eur J Neurol
; 22(8): 1151-61, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26032110
2.
Pathogenic immune mechanisms at the neuromuscular synapse: the role of specific antibody-binding epitopes in myasthenia gravis.
J Intern Med
; 275(1): 12-26, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24215230
3.
Abnormal myotonic dystrophy protein kinase levels produce only mild myopathy in mice.
Nat Genet
; 13(3): 316-24, 1996 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-8673131
4.
Synaptic assembly of the brain in the absence of neurotransmitter secretion.
Science
; 287(5454): 864-9, 2000 Feb 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-10657302
5.
Neuromuscular synaptic function in mice lacking major subsets of gangliosides.
Neuroscience
; 156(4): 885-97, 2008 Oct 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-18801416
6.
Natural disease history of the dy2J mouse model of laminin α2 (merosin)-deficient congenital muscular dystrophy.
PLoS One
; 13(5): e0197388, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29763467
7.
Monoclonal antibodies raised against Guillain-Barré syndrome-associated Campylobacter jejuni lipopolysaccharides react with neuronal gangliosides and paralyze muscle-nerve preparations.
J Clin Invest
; 104(6): 697-708, 1999 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-10491405
8.
Characterization of acetylcholine release and the compensatory contribution of non-Ca(v)2.1 channels at motor nerve terminals of leaner Ca(v)2.1-mutant mice.
Neuroscience
; 144(4): 1278-87, 2007 Feb 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-17161543
9.
Natural disease history of mouse models for limb girdle muscular dystrophy types 2D and 2F.
PLoS One
; 12(8): e0182704, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28797108
10.
alpha-Neurexins are required for efficient transmitter release and synaptic homeostasis at the mouse neuromuscular junction.
Neuroscience
; 138(2): 433-46, 2006.
Artigo
em Inglês
| MEDLINE | ID: mdl-16406382
11.
Gene dosage-dependent transmitter release changes at neuromuscular synapses of CACNA1A R192Q knockin mice are non-progressive and do not lead to morphological changes or muscle weakness.
Neuroscience
; 135(1): 81-95, 2005.
Artigo
em Inglês
| MEDLINE | ID: mdl-16111830
12.
Development of the mouse neuromuscular junction in the absence of regulated secretion.
Neuroscience
; 120(3): 733-44, 2003.
Artigo
em Inglês
| MEDLINE | ID: mdl-12895513
13.
Mutant P/Q-type calcium channel electrophysiology and migraine.
Curr Opin Investig Drugs
; 2(9): 1250-60, 2001 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-11717812
14.
A non-immunogenic myasthenia gravis model and its application in a study of transsynaptic regulation at the neuromuscular junction.
Eur J Pharmacol
; 196(1): 93-101, 1991 Apr 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-1874282
15.
Role of Munc18-1 in synaptic plasticity at the myasthenic neuromuscular junction.
Ann N Y Acad Sci
; 998: 404-6, 2003 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-14592907
16.
Transmitter release deficits at the neuromuscular synapse of mice with mutations in the Cav2.1 (alpha1A) subunit of the P/Q-type Ca2+ channel.
Ann N Y Acad Sci
; 998: 29-32, 2003 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-14592860
17.
Roles of complex gangliosides at the neuromuscular junction.
Ann N Y Acad Sci
; 998: 401-3, 2003 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-14592906
18.
Involvement of protein kinases in the upregulation of acetylcholine release at endplates of alpha-bungarotoxin-treated rats.
J Physiol
; 493 ( Pt 1): 175-86, 1996 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-8735703
19.
Kinetics of the membrane current mediated by serotonin 5-HT3 receptors in cultured mouse neuroblastoma cells.
J Physiol
; 411: 257-69, 1989 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-2482354
20.
Adaptation of quantal content to decreased postsynaptic sensitivity at single endplates in alpha-bungarotoxin-treated rats.
J Physiol
; 458: 487-99, 1992 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-1302275