| scholarly article | Q13442814 |
| P50 | author | Kay Ohlendieck | Q59822544 |
| P2093 | author name string | Dieter Swandulla | |
| Margit Zweyer | |||
| Rustam R Mundegar | |||
| Sandra Murphy | |||
| P2860 | cites work | Myoferlin, a candidate gene and potential modifier of muscular dystrophy | Q22010963 |
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| In-gel digestion for mass spectrometric characterization of proteins and proteomes | Q29547583 | ||
| Divide and conquer: cleavable cross-linkers to study protein conformation and protein-protein interactions | Q30313829 | ||
| Advances in protein complex analysis by chemical cross-linking coupled with mass spectrometry (CXMS) and bioinformatics. | Q30375097 | ||
| Up-regulation of 2-oxoglutarate dehydrogenase as a stress response | Q34032854 | ||
| Calpain 3 is important for muscle regeneration: evidence from patients with limb girdle muscular dystrophies. | Q34207404 | ||
| The biology of desmin filaments: how do mutations affect their structure, assembly, and organisation? | Q34357969 | ||
| Defects in mitochondrial ATP synthesis in dystrophin-deficient mdx skeletal muscles may be caused by complex I insufficiency. | Q34776381 | ||
| Simultaneous Pathoproteomic Evaluation of the Dystrophin-Glycoprotein Complex and Secondary Changes in the mdx-4cv Mouse Model of Duchenne Muscular Dystrophy | Q35837856 | ||
| Multi-level omics analysis in a murine model of dystrophin loss and therapeutic restoration. | Q36252005 | ||
| Absence of Dystrophin Disrupts Skeletal Muscle Signaling: Roles of Ca2+, Reactive Oxygen Species, and Nitric Oxide in the Development of Muscular Dystrophy. | Q36422465 | ||
| Identification of disease specific pathways using in vivo SILAC proteomics in dystrophin deficient mdx mouse. | Q36832437 | ||
| Wasting mechanisms in muscular dystrophy. | Q37138490 | ||
| Molecular Signatures of Membrane Protein Complexes Underlying Muscular Dystrophy. | Q37372312 | ||
| Dysferlin and myoferlin regulate transverse tubule formation and glycerol sensitivity. | Q37415471 | ||
| Caveolins in the development and diseases of musculoskeletal system. | Q37432918 | ||
| Concurrent Label-Free Mass Spectrometric Analysis of Dystrophin Isoform Dp427 and the Myofibrosis Marker Collagen in Crude Extracts from mdx-4cv Skeletal Muscles | Q37566483 | ||
| Dystrophin complex functions as a scaffold for signalling proteins. | Q38135952 | ||
| Catch me if you can: challenges and applications of cross-linking approaches | Q38216441 | ||
| The Pathogenesis and Therapy of Muscular Dystrophies | Q38517557 | ||
| Mitochondrial specialization revealed by single muscle fiber proteomics: focus on the Krebs cycle | Q38640634 | ||
| Crosslinking and Mass Spectrometry: An Integrated Technology to Understand the Structure and Function of Molecular Machines | Q38665348 | ||
| Gel-based chemical cross-linking analysis of 20S proteasome subunit-subunit interactions in breast cancer | Q38755336 | ||
| Chemical Crosslinking: Role in Protein and Peptide Science | Q38907979 | ||
| Label-free mass spectrometric analysis of the mdx-4cv diaphragm identifies the matricellular protein periostin as a potential factor involved in dystrophinopathy-related fibrosis | Q39033229 | ||
| The STRING database in 2017: quality-controlled protein-protein association networks, made broadly accessible | Q39125771 | ||
| Disturbance of mitochondrial functions provoked by the major long-chain 3-hydroxylated fatty acids accumulating in MTP and LCHAD deficiencies in skeletal muscle | Q39637434 | ||
| The role of the dystrophin-glycoprotein complex in the molecular pathogenesis of muscular dystrophies. | Q40754314 | ||
| Towards an understanding of the dystrophin-glycoprotein complex: linkage between the extracellular matrix and the membrane cytoskeleton in muscle fibers. | Q40958054 | ||
| Mass spectrometric identification of dystrophin, the protein product of the Duchenne muscular dystrophy gene, in distinct muscle surface membranes. | Q41350434 | ||
| Drastic reduction of sarcalumenin in Dp427 (dystrophin of 427 kDa)-deficient fibres indicates that abnormal calcium handling plays a key role in muscular dystrophy. | Q41823396 | ||
| A comparative cross-linking strategy to probe conformational changes in protein complexes | Q42155930 | ||
| Cross-linking analysis of the ryanodine receptor and alpha1-dihydropyridine receptor in rabbit skeletal muscle triads. | Q42238130 | ||
| Alisporivir rescues defective mitochondrial respiration in Duchenne muscular dystrophy. | Q42514938 | ||
| Duchenne muscular dystrophy: deficiency of dystrophin at the muscle cell surface | Q44350613 | ||
| The molecular cross talk of the dystrophin-glycoprotein complex. | Q47606106 | ||
| Proteome analysis in dystrophic mdx mouse muscle reveals a drastic alteration of key metabolic and contractile proteins after chronic exercise and the potential modulation by anti-oxidant compounds | Q47718580 | ||
| Comparative proteomic analysis of the contractile-protein-depleted fraction from normal versus dystrophic skeletal muscle. | Q47757661 | ||
| 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. | Q47959546 | ||
| Revisiting the dystrophin-ATP connection: How half a century of research still implicates mitochondrial dysfunction in Duchenne Muscular Dystrophy aetiology | Q47966217 | ||
| Oligomerization of beta-dystroglycan in rabbit diaphragm and brain as revealed by chemical crosslinking | Q48472059 | ||
| In vivo administration of extracellular cGMP normalizes TNF-α and membrane expression of AMPA receptors in hippocampus and spatial reference memory but not IL-1β, NMDA receptors in membrane and working memory in hyperammonemic rats | Q48729930 | ||
| Low intensity training decreases markers of oxidative stress in skeletal muscle of mdx mice. | Q50691969 | ||
| Chemical cross-linking for protein-protein interaction studies. | Q51800934 | ||
| Comparative Label-Free Mass Spectrometric Analysis of Mildly versus Severely Affected mdx Mouse Skeletal Muscles Identifies Annexin, Lamin, and Vimentin as Universal Dystrophic Markers. | Q53457776 | ||
| Duchenne muscular dystrophy: deficiency of dystrophin-associated proteins in the sarcolemma | Q70651010 | ||
| Silver staining of 2D electrophoresis gels | Q84291707 | ||
| Caveolin-1, caveolin-3 and VEGF expression in the masticatory muscles of mdx mice | Q84535349 | ||
| P577 | publication date | 2018-04-20 | |
| P1433 | published in | Electrophoresis | Q3050608 |
| P1476 | title | Comparative gel-based proteomic analysis of chemically crosslinked complexes in dystrophic skeletal muscle |
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