Detalhe da pesquisa
1.
Deficiency of hyccin, a newly identified membrane protein, causes hypomyelination and congenital cataract.
Nat Genet
; 38(10): 1111-3, 2006 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-16951682
2.
CD39 is highly involved in mediating the suppression activity of tumor-infiltrating CD8+ T regulatory lymphocytes.
Cancer Immunol Immunother
; 62(5): 851-62, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23359087
3.
Abscisic acid ameliorates the systemic sclerosis fibroblast phenotype in vitro.
Biochem Biophys Res Commun
; 422(1): 70-4, 2012 May 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-22560900
4.
Alteration of Th17 and Treg cell subpopulations co-exist in patients affected with systemic sclerosis.
Clin Immunol
; 139(3): 249-57, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21419712
5.
Caveolin-3 T78M and T78K missense mutations lead to different phenotypes in vivo and in vitro.
Lab Invest
; 88(3): 275-83, 2008 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-18253147
6.
Mitochondrial DNA deletion in a child with mitochondrial encephalomyopathy, growth hormone deficiency, and hypoparathyroidism.
J Child Neurol
; 21(11): 983-5, 2006 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-17092469
7.
GDAP1 mutation in autosomal recessive Charcot-Marie-Tooth with pyramidal features.
J Neurol
; 253(9): 1234-5, 2006 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-16607474
8.
Aquaporin-4 expression is severely reduced in human sarcoglycanopathies and dysferlinopathies.
Cell Cycle
; 7(14): 2199-207, 2008 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-18641458
9.
Pharmacological rescue of the dystrophin-glycoprotein complex in Duchenne and Becker skeletal muscle explants by proteasome inhibitor treatment.
Am J Physiol Cell Physiol
; 290(2): C577-82, 2006 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-16192300