Detalhe da pesquisa
1.
Matriglycan maintains t-tubule structural integrity in cardiac muscle.
Proc Natl Acad Sci U S A
; 121(22): e2402890121, 2024 May 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-38771868
2.
A unique variant of lymphocytic choriomeningitis virus that induces pheromone binding protein MUP: Critical role for CTL.
Proc Natl Acad Sci U S A
; 116(36): 18001-18008, 2019 09 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31427525
3.
Protective role for the N-terminal domain of α-dystroglycan in Influenza A virus proliferation.
Proc Natl Acad Sci U S A
; 116(23): 11396-11401, 2019 06 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31097590
4.
HNK-1 sulfotransferase modulates α-dystroglycan glycosylation by 3-O-sulfation of glucuronic acid on matriglycan.
Glycobiology
; 30(10): 817-829, 2020 09 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-32149355
5.
Biallelic Mutations in TMTC3, Encoding a Transmembrane and TPR-Containing Protein, Lead to Cobblestone Lissencephaly.
Am J Hum Genet
; 99(5): 1181-1189, 2016 Nov 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-27773428
6.
The dystroglycan receptor maintains glioma stem cells in the vascular niche.
Acta Neuropathol
; 138(6): 1033-1052, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31463571
7.
Clinical utility of RNA sequencing to resolve unusual GNE myopathy with a novel promoter deletion.
Muscle Nerve
; 60(1): 98-103, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30990900
8.
LARGE glycans on dystroglycan function as a tunable matrix scaffold to prevent dystrophy.
Nature
; 503(7474): 136-40, 2013 Nov 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-24132234
9.
Role of dystroglycan in limiting contraction-induced injury to the sarcomeric cytoskeleton of mature skeletal muscle.
Proc Natl Acad Sci U S A
; 113(39): 10992-7, 2016 09 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-27625424
10.
Dystroglycan Maintains Inner Limiting Membrane Integrity to Coordinate Retinal Development.
J Neurosci
; 37(35): 8559-8574, 2017 08 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-28760865
11.
Collagen VI deficiency reduces muscle pathology, but does not improve muscle function, in the γ-sarcoglycan-null mouse.
Hum Mol Genet
; 25(7): 1357-69, 2016 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26908621
12.
Structural basis of laminin binding to the LARGE glycans on dystroglycan.
Nat Chem Biol
; 12(10): 810-4, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27526028
13.
Molecular Signatures of Membrane Protein Complexes Underlying Muscular Dystrophy.
Mol Cell Proteomics
; 15(6): 2169-85, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27099343
14.
Neuronal Dystroglycan Is Necessary for Formation and Maintenance of Functional CCK-Positive Basket Cell Terminals on Pyramidal Cells.
J Neurosci
; 36(40): 10296-10313, 2016 10 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27707967
15.
Cav3.2 T-type calcium channel is required for the NFAT-dependent Sox9 expression in tracheal cartilage.
Proc Natl Acad Sci U S A
; 111(19): E1990-8, 2014 May 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-24778262
16.
LARGE2-dependent glycosylation confers laminin-binding ability on proteoglycans.
Glycobiology
; 26(12): 1284-1296, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27496765
17.
Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycan.
Am J Hum Genet
; 92(3): 354-65, 2013 Mar 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-23453667
18.
Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of α-dystroglycan.
Am J Hum Genet
; 93(1): 29-41, 2013 Jul 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-23768512
19.
GMPPB-Associated Dystroglycanopathy: Emerging Common Variants with Phenotype Correlation.
Hum Mutat
; 36(12): 1159-63, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26310427
20.
Endogenous glucuronyltransferase activity of LARGE or LARGE2 required for functional modification of α-dystroglycan in cells and tissues.
J Biol Chem
; 289(41): 28138-48, 2014 Oct 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-25138275