| human | Q5 |
| P227 | GND ID | 1143137280 |
| P496 | ORCID iD | 0000-0002-6266-4510 |
| P1153 | Scopus author ID | 7005597581 |
| P214 | VIAF ID | 229151302948848661055 |
| P108 | employer | Maynooth University | Q2601879 |
| P106 | occupation | researcher | Q1650915 |
| Q28576113 | Aging skeletal muscle shows a drastic increase in the small heat shock proteins alphaB-crystallin/HspB5 and cvHsp/HspB7 |
| Q31027747 | Alcoholic muscle disease and biomembrane perturbations (review). |
| Q50798593 | Analysis of excitation-contraction-coupling components in chronically stimulated canine skeletal muscle. |
| Q68424359 | Analysis of microsomal membrane proteins |
| Q33565229 | Application of fluorescence two-dimensional difference in-gel electrophoresis as a proteomic biomarker discovery tool in muscular dystrophy research |
| Q24795418 | Brain dystrophin-glycoprotein complex: persistent expression of beta-dystroglycan, impaired oligomerization of Dp71 and up-regulation of utrophins in animal models of muscular dystrophy |
| Q28581416 | Ca2+-regulatory muscle proteins in the alcohol-fed rat |
| Q77313388 | Calsequestrin blot overlay of two-dimensional electrophoretically separated microsomal proteins from skeletal muscle |
| Q78010433 | Calsequestrin expression and calcium binding is increased in streptozotocin-induced diabetic rat skeletal muscle though not in cardiac muscle |
| Q38217473 | Chaperoning heat shock proteins: proteomic analysis and relevance for normal and dystrophin-deficient muscle. |
| Q71537185 | Characterisation of the dystrophin-related protein utrophin in highly purified skeletal muscle sarcolemma vesicles |
| Q73549302 | Chemical cross-linking analysis of Ca(2+-)ATPase from rabbit skeletal muscle |
| Q46289186 | Comparative 3-Sample DIGE Analysis of Skeletal Muscles |
| Q47668027 | Comparative DIGE Proteomics. |
| Q53457776 | Comparative Label-Free Mass Spectrometric Analysis of Mildly versus Severely Affected mdx Mouse Skeletal Muscles Identifies Annexin, Lamin, and Vimentin as Universal Dystrophic Markers. |
| Q37566405 | Comparative Skeletal Muscle Proteomics Using Two-Dimensional Gel Electrophoresis. |
| Q73512517 | Comparative analysis of Dp427-deficient mdx tissues shows that the milder dystrophic phenotype of extraocular and toe muscle fibres is associated with a persistent expression of beta-dystroglycan |
| Q73822181 | Comparative analysis of the isoform expression pattern of Ca(2+)-regulatory membrane proteins in fast-twitch, slow-twitch, cardiac, neonatal and chronic low-frequency stimulated muscle fibers |
| Q52313732 | Comparative gel-based proteomic analysis of chemically crosslinked complexes in dystrophic skeletal muscle. |
| Q38218528 | Comparative profiling of the sperm proteome |
| Q47757661 | Comparative proteomic analysis of the contractile-protein-depleted fraction from normal versus dystrophic skeletal muscle. |
| Q37196136 | Comparative proteomic profiling of soleus, extensor digitorum longus, flexor digitorum brevis and interosseus muscles from the mdx mouse model of Duchenne muscular dystrophy |
| Q51475165 | Complex formation of skeletal muscle Ca2+-regulatory membrane proteins by halothane. |
| Q37566483 | Concurrent Label-Free Mass Spectrometric Analysis of Dystrophin Isoform Dp427 and the Myofibrosis Marker Collagen in Crude Extracts from mdx-4cv Skeletal Muscles |
| Q42238130 | Cross-linking analysis of the ryanodine receptor and alpha1-dihydropyridine receptor in rabbit skeletal muscle triads. |
| Q47667887 | DIGE Analysis of Immunodepleted Plasma |
| Q33531048 | DIGE analysis of rat skeletal muscle proteins using nonionic detergent phase extraction of young adult versus aged gastrocnemius tissue. |
| Q59136856 | Dataset on the comparative proteomic profiling of mouse saliva and serum from wild type versus the dystrophic mouse model of dystrophinopathy |
| Q47680227 | Decreased expression of brain beta-dystroglycan in Duchenne muscular dystrophy but not in the mdx animal model. |
| Q59089242 | Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle |
| Q49089952 | Developmental expression of the sea urchin egg receptor for sperm. |
| Q46684929 | Differential expression of the fast skeletal muscle proteome following chronic low-frequency stimulation. |
| Q53969078 | Distal mdx muscle groups exhibiting up-regulation of utrophin and rescue of dystrophin-associated glycoproteins exemplify a protected phenotype in muscular dystrophy. |
| Q24791187 | Diversity of the Brain Dystrophin-Glycoprotein Complex. |
| Q84252149 | Drastic increase of myosin light chain MLC-2 in senescent skeletal muscle indicates fast-to-slow fibre transition in sarcopenia of old age |
| Q64892627 | Drastic reduction in the luminal Ca2+ -binding proteins calsequestrin and sarcalumenin in dystrophin-deficient cardiac muscle. |
| Q41823396 | Drastic reduction of sarcalumenin in Dp427 (dystrophin of 427 kDa)-deficient fibres indicates that abnormal calcium handling plays a key role in muscular dystrophy. |
| Q70177916 | Dystrophin constitutes 5% of membrane cytoskeleton in skeletal muscle |
| Q42052137 | Dystrophin-associated proteins are greatly reduced in skeletal muscle from mdx mice |
| Q68255626 | Dystrophin-related protein is localized to neuromuscular junctions of adult skeletal muscle |
| Q51401380 | Effect of halothane on the oligomerization of the sarcoplasmic reticulum Ca(2+)-ATPase. |
| Q73167268 | Effects of chronic low-frequency stimulation on Ca2+-regulatory membrane proteins in rabbit fast muscle |
| Q70145723 | Enrichment and biochemical characterization of boundary membrane contact sites from rat-liver mitochondria |
| Q46831974 | Expression of the skeletal muscle dystrophin-dystroglycan complex and syntrophin-nitric oxide synthase complex is severely affected in the type 2 diabetic Goto-Kakizaki rat. |
| Q43481247 | Gel electrophoresis-based proteomics of senescent tissues. |
| Q90645664 | Identification of marker proteins of muscular dystrophy in the urine proteome from the mdx-4cv model of dystrophinopathy |
| Q84239609 | Identification of secondary effects of hyperexcitability by proteomic profiling of myotonic mouse muscle |
| Q28579904 | Inactivation of sarcoplasmic reticulum Ca(2+)-atpase in low-frequency stimulated rat muscle |
| Q44263808 | Increased expression of the nicotinic acetylcholine receptor in stimulated muscle. |
| Q44576008 | Increased sensitivity of the ryanodine receptor to halothane-induced oligomerization in malignant hyperthermia-susceptible human skeletal muscle. |
| Q33827791 | Intricate effects of primary motor neuronopathy on contractile proteins and metabolic muscle enzymes as revealed by label-free mass spectrometry. |
| Q39033229 | Label-free mass spectrometric analysis of the mdx-4cv diaphragm identifies the matricellular protein periostin as a potential factor involved in dystrophinopathy-related fibrosis |
| Q36310649 | Label-free mass spectrometric analysis reveals complex changes in the brain proteome from the mdx-4cv mouse model of Duchenne muscular dystrophy |
| Q33349318 | Lectin-based proteomic profiling of aged skeletal muscle: decreased pyruvate kinase isozyme M1 exhibits drastically increased levels of N-glycosylation |
| Q39284545 | Mass Spectrometry-Based Identification of Muscle-Associated and Muscle-Derived Proteomic Biomarkers of Dystrophinopathies |
| Q84966846 | Mass spectrometric characterization of the sarcoplasmic reticulum from rabbit skeletal muscle by on-membrane digestion |
| Q41350434 | Mass spectrometric identification of dystrophin, the protein product of the Duchenne muscular dystrophy gene, in distinct muscle surface membranes. |
| Q36613540 | Mass spectrometry-based proteomic analysis of middle-aged vs. aged vastus lateralis reveals increased levels of carbonic anhydrase isoform 3 in senescent human skeletal muscle. |
| Q43566367 | Native skeletal muscle dihydropyridine receptor exists as a supramolecular triad complex. |
| Q33703934 | New pathobiochemical insights into dystrophinopathy from the proteomics of senescent mdx mouse muscle |
| Q53216634 | Novel proteomic biomarkers for skeletal muscle diseases. |
| Q74031732 | Oligomeric status of the dihydropyridine receptor in aged skeletal muscle |
| Q79902215 | Oligomerisation of sarcoplasmic reticulum Ca2+-ATPase monomers from skeletal muscle |
| Q73941112 | Oligomerization is an intrinsic property of calsequestrin in normal and transformed skeletal muscle |
| Q71771775 | Oligomerization of sarcoplasmic reticulum Ca2+-ATPase from rabbit skeletal muscle |
| Q78056206 | Oligomerization of the sarcoplasmic reticulum Ca2+-ATPase SERCA2 in cardiac muscle |
| Q46873515 | Opposite pathobiochemical fate of pyruvate kinase and adenylate kinase in aged rat skeletal muscle as revealed by proteomic DIGE analysis |
| Q35864829 | Pathobiochemical changes in diabetic skeletal muscle as revealed by mass-spectrometry-based proteomics |
| Q38563300 | Pathoproteomic profiling of the skeletal muscle matrisome in dystrophinopathy associated myofibrosis |
| Q34376937 | Pathoproteomics of testicular tissue deficient in the GARP component VPS54: the wobbler mouse model of globozoospermia |
| Q47667906 | Protein Digestion for DIGE Analysis |
| Q33249876 | Proteome analysis of the dystrophin-deficient MDX diaphragm reveals a drastic increase in the heat shock protein cvHSP. |
| Q39938132 | Proteomic DIGE analysis of the mitochondria-enriched fraction from aged rat skeletal muscle |
| Q35633497 | Proteomic Profiling of Fast-To-Slow Muscle Transitions during Aging |
| Q34706579 | Proteomic Profiling of Mitochondrial Enzymes during Skeletal Muscle Aging |
| Q47607013 | Proteomic Profiling of the Dystrophin-Deficient Brain. |
| Q33871052 | Proteomic Profiling of the Dystrophin-Deficient MDX Heart Reveals Drastically Altered Levels of Key Metabolic and Contractile Proteins. |
| Q82750943 | Proteomic analysis of dystrophic muscle |
| Q38897234 | Proteomic analysis of dystrophin deficiency and associated changes in the aged mdx-4cv heart model of dystrophinopathy-related cardiomyopathy. |
| Q83482006 | Proteomic analysis of muscle affected by motor neuron degeneration: the wobbler mouse model of amyotrophic lateral sclerosis |
| Q50164389 | Proteomic analysis of the sarcolemma-enriched fraction from dystrophic mdx-4cv skeletal muscle |
| Q38079622 | Proteomic identification of biomarkers of skeletal muscle disorders. |
| Q64974023 | Proteomic identification of elevated saliva kallikrein levels in the mdx-4cv mouse model of Duchenne muscular dystrophy. |
| Q37817162 | Proteomic profiling of animal models mimicking skeletal muscle disorders |
| Q33398588 | Proteomic profiling of antisense-induced exon skipping reveals reversal of pathobiochemical abnormalities in dystrophic mdx diaphragm. |
| Q39487740 | Proteomic profiling of bovine M. longissimus lumborum from Crossbred Aberdeen Angus and Belgian Blue sired steers varying in genetic merit for carcass weight |
| Q44232941 | Proteomic profiling of cardiomyopathic tissue from the aged mdx model of Duchenne muscular dystrophy reveals a drastic decrease in laminin, nidogen and annexin |
| Q80817301 | Proteomic profiling of chronic low-frequency stimulated fast muscle |
| Q47333352 | Proteomic profiling of large myofibrillar proteins from dried and long-term stored polyacrylamide gels |
| Q58596612 | Proteomic profiling of liver tissue from the - mouse model of Duchenne muscular dystrophy |
| Q33675040 | Proteomic profiling of mdx-4cv serum reveals highly elevated levels of the inflammation-induced plasma marker haptoglobin in muscular dystrophy |
| Q51664676 | Proteomic profiling of muscle fibre type shifting in neuromuscular diseases. |
| Q84229096 | Proteomic profiling of naturally protected extraocular muscles from the dystrophin-deficient mdx mouse |
| Q38115329 | Proteomic profiling of the contractile apparatus from skeletal muscle. |
| 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. |
| Q27006945 | Proteomic profiling of the dystrophin-deficient mdx phenocopy of dystrophinopathy-associated cardiomyopathy |
| Q92475555 | Proteomic profiling of the mouse diaphragm and refined mass spectrometric analysis of the dystrophic phenotype |
| Q52714051 | Proteomic serum biomarkers for neuromuscular diseases. |
| Q37380758 | Proteomics of skeletal muscle aging |
| Q37727204 | Proteomics of skeletal muscle differentiation, neuromuscular disorders and fiber aging. |
| Q38150887 | Proteomics of the dystrophin-glycoprotein complex and dystrophinopathy. |
| Q73274893 | Rabbit brain and muscle isoforms containing the carboxy-terminal domain of 427 kDa skeletal muscle dystrophin exhibit similar biochemical properties |
| Q33234154 | Reduced expression of regucalcin in young and aged mdx diaphragm indicates abnormal cytosolic calcium handling in dystrophin-deficient muscle. |
| Q46398311 | Reduced expression of sarcalumenin and related Ca2+ -regulatory proteins in aged rat skeletal muscle |
| Q40605462 | Role of the sea urchin egg receptor for sperm in gamete interactions. |
| Q77343188 | Self-aggregation of triadin in the sarcoplasmic reticulum of rabbit skeletal muscle |
| Q35837856 | Simultaneous Pathoproteomic Evaluation of the Dystrophin-Glycoprotein Complex and Secondary Changes in the mdx-4cv Mouse Model of Duchenne Muscular Dystrophy |
| Q83789303 | Skeletal muscle tissue from the Goto-Kakizaki rat model of type-2 diabetes exhibits increased levels of the small heat shock protein Hsp27 |
| Q36383120 | Subproteomic analysis of basic proteins in aged skeletal muscle following offgel pre-fractionation |
| Q55044854 | Subproteomic profiling of sarcolemma from dystrophic mdx-4cv skeletal muscle. |
| Q44135969 | Supramolecular calsequestrin complex. |
| Q78109547 | The 90-kDa junctional sarcoplasmic reticulum protein forms an integral part of a supramolecular triad complex in skeletal muscle |
| Q26770343 | The biochemical and mass spectrometric profiling of the dystrophin complexome from skeletal muscle |
| Q35211052 | The importance of alcohol-induced muscle disease. |
| Q40754314 | The role of the dystrophin-glycoprotein complex in the molecular pathogenesis of muscular dystrophies. |
| Q40577015 | Use of continuous-elution gel electrophoresis as a preparative tool for blot overlay analysis. |
| Q52925630 | [Molecular pathogenesis of Duchenne muscular dystrophy-related fibrosis]. |
| Q73080448 | [Molecular pathogenesis of muscular diseases] |
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