| scholarly article | Q13442814 |
| P2093 | author name string | Rui Xu | |
| Eric Johnson | |||
| Jung Hae Yoon | |||
| Paul T Martin | |||
| Laura T Martin | |||
| Federica Montanaro | |||
| P2860 | cites work | The interaction of dystrophin with beta-dystroglycan is regulated by tyrosine phosphorylation | Q24291543 |
| Spire-type actin nucleators cooperate with Formin-2 to drive asymmetric oocyte division | Q24304847 | ||
| Introduction of Sd(a) carbohydrate antigen in gastrointestinal cancer cells eliminates selectin ligands and inhibits metastasis | Q24307895 | ||
| Adhesion-dependent tyrosine phosphorylation of (beta)-dystroglycan regulates its interaction with utrophin | Q28142159 | ||
| An autosomal transcript in skeletal muscle with homology to dystrophin | Q28251871 | ||
| Rapsyn may function as a link between the acetylcholine receptor and the agrin-binding dystrophin-associated glycoprotein complex | Q28293857 | ||
| beta 2-Syntrophin: localization at the neuromuscular junction in skeletal muscle | Q28582697 | ||
| Differential Association of Syntrophin Pairs with the Dystrophin Complex | Q28584710 | ||
| Target-decoy search strategy for increased confidence in large-scale protein identifications by mass spectrometry | Q29547311 | ||
| Membrane organization of the dystrophin-glycoprotein complex | Q29615149 | ||
| Evaluation of multidimensional chromatography coupled with tandem mass spectrometry (LC/LC-MS/MS) for large-scale protein analysis: the yeast proteome | Q29615379 | ||
| Dystrophin: the protein product of the Duchenne muscular dystrophy locus | Q29618077 | ||
| Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals | Q30050310 | ||
| Loss of IL-15 receptor α alters the endurance, fatigability, and metabolic characteristics of mouse fast skeletal muscles. | Q30503154 | ||
| Epitopes in the interacting regions of beta-dystroglycan (PPxY motif) and dystrophin (WW domain). | Q30993582 | ||
| Reduced expression of regucalcin in young and aged mdx diaphragm indicates abnormal cytosolic calcium handling in dystrophin-deficient muscle. | Q33234154 | ||
| Proteome analysis of the dystrophin-deficient MDX diaphragm reveals a drastic increase in the heat shock protein cvHSP. | Q33249876 | ||
| Proteomic Profiling of the Dystrophin-Deficient MDX Heart Reveals Drastically Altered Levels of Key Metabolic and Contractile Proteins. | Q33871052 | ||
| Overexpression of the cytotoxic T cell GalNAc transferase in skeletal muscle inhibits muscular dystrophy in mdx mice | Q34025748 | ||
| O-mannosyl phosphorylation of alpha-dystroglycan is required for laminin binding. | Q34090655 | ||
| Function and genetics of dystrophin and dystrophin-related proteins in muscle | Q34120764 | ||
| A Human-Specific Deletion in Mouse Cmah Increases Disease Severity in the mdx Model of Duchenne Muscular Dystrophy | Q34175938 | ||
| Murine muscular dystrophy caused by a mutation in the laminin alpha 2 (Lama2) gene | Q34319775 | ||
| Comparative evaluation of mass spectrometry platforms used in large-scale proteomics investigations | Q34445192 | ||
| Proteomic analysis of striated muscle | Q34642389 | ||
| Interleukin-15, IL-15 Receptor-Alpha, and Obesity: Concordance of Laboratory Animal and Human Genetic Studies | Q34974732 | ||
| Dystroglycan glycosylation and its role in matrix binding in skeletal muscle | Q35123507 | ||
| Defective muscle basement membrane and lack of M-laminin in the dystrophic dy/dy mouse | Q35493060 | ||
| Postnatal overexpression of the CT GalNAc transferase inhibits muscular dystrophy in mdx mice without altering muscle growth or neuromuscular development: evidence for a utrophin-independent mechanism | Q35867446 | ||
| Overexpression of the cytotoxic T cell (CT) carbohydrate inhibits muscular dystrophy in the dyW mouse model of congenital muscular dystrophy 1A. | Q35928246 | ||
| A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin. | Q36232550 | ||
| Differential membrane localization and intermolecular associations of alpha-dystrobrevin isoforms in skeletal muscle | Q36290588 | ||
| Utrophin upregulation in Duchenne muscular dystrophy | Q36455607 | ||
| The congenital muscular dystrophies: recent advances and molecular insights | Q36681282 | ||
| Overexpression of Galgt2 in skeletal muscle prevents injury resulting from eccentric contractions in both mdx and wild-type mice | Q37139061 | ||
| Overexpression of Galgt2 reduces dystrophic pathology in the skeletal muscles of alpha sarcoglycan-deficient mice | Q37257159 | ||
| Strategies for shotgun identification of integral membrane proteins by tandem mass spectrometry | Q37264063 | ||
| Power and limitations of electrophoretic separations in proteomics strategies. | Q37346251 | ||
| The synaptic CT carbohydrate modulates binding and expression of extracellular matrix proteins in skeletal muscle: Partial dependence on utrophin | Q37361308 | ||
| The Pax3-Cre transgene exhibits a rostrocaudal gradient of expression in the skeletal muscle lineage | Q37382349 | ||
| Diagnosis and new treatments in muscular dystrophies | Q37521427 | ||
| Structures of sialylated O-linked oligosaccharides of bovine peripheral nerve alpha-dystroglycan. The role of a novel O-mannosyl-type oligosaccharide in the binding of alpha-dystroglycan with laminin | Q38349218 | ||
| Mass spectrometric identification of dystrophin isoform Dp427 by on-membrane digestion of sarcolemma from skeletal muscle | Q39869003 | ||
| Proteome profile of the MCF7 cancer cell line: a mass spectrometric evaluation | Q40229711 | ||
| Definition of pre- and postsynaptic forms of the CT carbohydrate antigen at the neuromuscular junction: ubiquitous expression of the CT antigens and the CT GalNAc transferase in mouse tissues | Q40676930 | ||
| Distinct structures and functions of related pre- and postsynaptic carbohydrates at the mammalian neuromuscular junction | Q41644137 | ||
| Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies | Q42524150 | ||
| New anti-huntingtin monoclonal antibodies: implications for huntingtin conformation and its binding proteins | Q42664318 | ||
| Subproteomics analysis of Ca+-binding proteins demonstrates decreased calsequestrin expression in dystrophic mouse skeletal muscle | Q45063439 | ||
| Overexpression of the CT GalNAc transferase in skeletal muscle alters myofiber growth, neuromuscular structure, and laminin expression. | Q45973809 | ||
| Comparative proteomic analysis of the insulin-induced L6 myotube secretome | Q47200207 | ||
| Limb–girdle muscular dystrophies | Q57390105 | ||
| Dystrophin-related protein is localized to neuromuscular junctions of adult skeletal muscle | Q68255626 | ||
| The molecular basis of muscular dystrophy in the mdx mouse: a point mutation | Q69514522 | ||
| WW and EF hand domains of dystrophin-family proteins mediate dystroglycan binding | Q73419259 | ||
| Evidence for in situ and in vitro association between beta-dystroglycan and the subsynaptic 43K rapsyn protein. Consequence for acetylcholine receptor clustering at the synapse | Q74473419 | ||
| Dystrophin and utrophin bind actin through distinct modes of contact | Q82553551 | ||
| Proteomic profiling of naturally protected extraocular muscles from the dystrophin-deficient mdx mouse | Q84229096 | ||
| P433 | issue | 9 | |
| P304 | page(s) | 4413-4424 | |
| P577 | publication date | 2012-07-30 | |
| P1433 | published in | Journal of Proteome Research | Q3186939 |
| P1476 | title | Comparative proteomic profiling of dystroglycan-associated proteins in wild type, mdx, and Galgt2 transgenic mouse skeletal muscle | |
| P478 | volume | 11 |
| Q39453819 | B4GALNT2 (GALGT2) Gene Therapy Reduces Skeletal Muscle Pathology in the FKRP P448L Mouse Model of Limb Girdle Muscular Dystrophy 2I. |
| Q46633826 | Cellular events during scar-free skin regeneration in the spiny mouse, Acomys |
| Q38217473 | Chaperoning heat shock proteins: proteomic analysis and relevance for normal and dystrophin-deficient muscle. |
| Q37064342 | Characterization of a Dmd (EGFP) reporter mouse as a tool to investigate dystrophin expression |
| Q37610530 | Circulating Biomarkers for Duchenne Muscular Dystrophy. |
| Q92609797 | Comparative Proteomic Analysis in Scar-Free Skin Regeneration in Acomys cahirinus and Scarring Mus musculus |
| Q37566483 | Concurrent Label-Free Mass Spectrometric Analysis of Dystrophin Isoform Dp427 and the Myofibrosis Marker Collagen in Crude Extracts from mdx-4cv Skeletal Muscles |
| Q64120063 | Dynamic Dystroglycan Complexes Mediate Cell Entry of Lassa Virus |
| Q28535211 | Identification of new dystroglycan complexes in skeletal muscle |
| Q38874623 | Induction of T-Cell Infiltration and Programmed Death Ligand 2 Expression by Adeno-Associated Virus in Rhesus Macaque Skeletal Muscle and Modulation by Prednisone |
| Q28534074 | Isobaric Tagging-Based Quantification for Proteomic Analysis: A Comparative Study of Spared and Affected Muscles from mdx Mice at the Early Phase of Dystrophy |
| Q41350434 | Mass spectrometric identification of dystrophin, the protein product of the Duchenne muscular dystrophy gene, in distinct muscle surface membranes. |
| Q37372312 | Molecular Signatures of Membrane Protein Complexes Underlying Muscular Dystrophy. |
| Q38079622 | Proteomic identification of biomarkers of skeletal muscle disorders. |
| Q47959546 | 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. |
| Q35837856 | Simultaneous Pathoproteomic Evaluation of the Dystrophin-Glycoprotein Complex and Secondary Changes in the mdx-4cv Mouse Model of Duchenne Muscular Dystrophy |
| Q91622135 | Soluble Heparin Binding Epidermal Growth Factor-Like Growth Factor Is a Regulator of GALGT2 Expression and GALGT2-Dependent Muscle and Neuromuscular Phenotypes |
| Q48340109 | Spatial distribution and molecular dynamics of dystrophin glycoprotein components at the neuromuscular junction in vivo. |
| Q26770343 | The biochemical and mass spectrometric profiling of the dystrophin complexome from skeletal muscle |
| Q47606106 | The molecular cross talk of the dystrophin-glycoprotein complex. |
| Q37696027 | Vascular delivery of rAAVrh74.MCK.GALGT2 to the gastrocnemius muscle of the rhesus macaque stimulates the expression of dystrophin and laminin α2 surrogates. |
| Q38255744 | What do mouse models of muscular dystrophy tell us about the DAPC and its components? |
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