Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Histopathology of Duchenne muscular dystrophy in correlation with changes in proteomic biomarkers.

1 Feb 2022

Abstract excerpt

Duchenne muscular dystrophy is an inherited disorder of early childhood that affects multiple systems in the body. Besides late-onset cardio-respiratory syndrome and various body-wide pathophysiological changes, X-linked muscular dystrophy is primarily classified as a disorder of the skeletal musculature. This is reflected by severe histopathological alterations in voluntary contractile tissues, including...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adipose Tissue and Metabolism
Share to Muscle metabolism and nutrition
Share to Muscle Physiology and Disorders

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 34873679
DOI: 10.14670/hh-18-403

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Histopathology of Duchenne muscular dystrophy in correlation with changes in proteomic biomarkers.PMID 34873679Read ↗

Emerging proteomic biomarkers of X-linked muscular dystrophySemantic proximity Read ↗

Proteomic profiling of the dystrophin-deficient mdx phenocopy of dystrophinopathy-associated cardiomyopathy.Semantic proximity Read ↗

Pathoproteomic profiling of the skeletal muscle matrisome in dystrophinopathy associated myofibrosisSemantic proximity Read ↗

Mass spectrometry‐based protein analysis to unravel the tissue pathophysiology in Duchenne muscular dystrophySemantic proximity Read ↗

Proteomic profiling of fatty acid binding proteins in muscular dystrophySemantic proximity Read ↗

Duchenne muscular dystrophy: pathogenesis and promising therapies.Semantic proximity Read ↗

Proteomic profiling of cardiomyopathic tissue from the aged mdx model of Duchenne muscular dystrophy reveals a drastic decrease in laminin, nidogen and annexinSemantic proximity Read ↗

Molecular pathology of myofibrillar myopathies.Semantic proximity Read ↗

Label‐free mass spectrometric analysis of the mdx‐4cv diaphragm identifies the matricellular protein periostin as a potential factor involved in dystrophinopathy‐related fibrosisSemantic proximity Read ↗

Muscular dystrophies: histology, immunohistochemistry, molecular genetics and management.Semantic proximity Read ↗

Cellular pathogenesis of Duchenne muscular dystrophy: progressive myofibre degeneration, chronic inflammation, reactive myofibrosis and satellite cell dysfunctionSemantic proximity Read ↗

Mutation-independent Proteomic Signatures of Pathological Progression in Murine Models of Duchenne Muscular Dystrophy.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.