Comparative proteomic profiling of dystroglycan-associated proteins in wild type, mdx, and Galgt2 transgenic mouse skeletal muscle.
about
The biochemical and mass spectrometric profiling of the dystrophin complexome from skeletal muscleIsobaric Tagging-Based Quantification for Proteomic Analysis: A Comparative Study of Spared and Affected Muscles from mdx Mice at the Early Phase of DystrophyIdentification of new dystroglycan complexes in skeletal muscleSimultaneous Pathoproteomic Evaluation of the Dystrophin-Glycoprotein Complex and Secondary Changes in the mdx-4cv Mouse Model of Duchenne Muscular DystrophyCharacterization of a Dmd (EGFP) reporter mouse as a tool to investigate dystrophin expression.Molecular Signatures of Membrane Protein Complexes Underlying Muscular Dystrophy.Concurrent Label-Free Mass Spectrometric Analysis of Dystrophin Isoform Dp427 and the Myofibrosis Marker Collagen in Crude Extracts from mdx-4cv Skeletal Muscles.Circulating Biomarkers for Duchenne Muscular Dystrophy.Vascular delivery of rAAVrh74.MCK.GALGT2 to the gastrocnemius muscle of the rhesus macaque stimulates the expression of dystrophin and laminin α2 surrogates.Proteomic identification of biomarkers of skeletal muscle disorders.Chaperoning heat shock proteins: proteomic analysis and relevance for normal and dystrophin-deficient muscle.What do mouse models of muscular dystrophy tell us about the DAPC and its components?Induction of T-Cell Infiltration and Programmed Death Ligand 2 Expression by Adeno-Associated Virus in Rhesus Macaque Skeletal Muscle and Modulation by Prednisone.B4GALNT2 (GALGT2) Gene Therapy Reduces Skeletal Muscle Pathology in the FKRP P448L Mouse Model of Limb Girdle Muscular Dystrophy 2I.Mass spectrometric identification of dystrophin, the protein product of the Duchenne muscular dystrophy gene, in distinct muscle surface membranes.Cellular events during scar-free skin regeneration in the spiny mouse, Acomys.The molecular cross talk of the dystrophin-glycoprotein complex.Proteomic profiling of the dystrophin complex and membrane fraction from dystrophic mdx muscle reveals decreases in the cytolinker desmoglein and increases in the extracellular matrix stabilizers biglycan and fibronectin.Spatial distribution and molecular dynamics of dystrophin glycoprotein components at the neuromuscular junction in vivo.
P2860
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P2860
Comparative proteomic profiling of dystroglycan-associated proteins in wild type, mdx, and Galgt2 transgenic mouse skeletal muscle.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Comparative proteomic profilin ...... nsgenic mouse skeletal muscle.
@ast
Comparative proteomic profilin ...... nsgenic mouse skeletal muscle.
@en
type
label
Comparative proteomic profilin ...... nsgenic mouse skeletal muscle.
@ast
Comparative proteomic profilin ...... nsgenic mouse skeletal muscle.
@en
prefLabel
Comparative proteomic profilin ...... nsgenic mouse skeletal muscle.
@ast
Comparative proteomic profilin ...... nsgenic mouse skeletal muscle.
@en
P2093
P2860
P356
P1476
Comparative proteomic profilin ...... nsgenic mouse skeletal muscle.
@en
P2093
Eric Johnson
Federica Montanaro
Jung Hae Yoon
Laura T Martin
Paul T Martin
P2860
P304
P356
10.1021/PR300328R
P577
2012-07-30T00:00:00Z