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

Learning, memory and blood–brain barrier pathology in Duchenne muscular dystrophy mice lacking Dp427, or Dp427 and Dp140

1 Jun 2024

Abstract excerpt

Abstract Duchenne muscular dystrophy is a severe neuromuscular disorder that is caused by mutations in the DMD gene, resulting in a disruption of dystrophin production. Next to dystrophin expression in the muscle, different isoforms of the protein are also expressed in the brain and lack of these isoforms leads to cognitive and behavioral deficits in patients. It remains unclear how the loss of the shorter...

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 Physiology and Disorders

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 38837620
DOI: 10.1111/gbb.12895

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

Learning, memory and blood–brain barrier pathology in Duchenne muscular dystrophy mice lacking Dp427, or Dp427 and Dp140PMID 38837620Read ↗

Impact of distinct dystrophin gene mutations on behavioral phenotypes of Duchenne muscular dystrophy.Semantic proximity Read ↗

Assessment of Behavioral Characteristics With Procedures of Minimal Human Interference in the mdx Mouse Model for Duchenne Muscular DystrophySemantic proximity Read ↗

Cognitive flexibility deficits in a mouse model for the absence of full‐length dystrophinSemantic proximity Read ↗

Emotional behavior and brain anatomy of the mdx52 mouse model of Duchenne muscular dystrophySemantic proximity Read ↗

Brain dystrophinopathies and cognitive impairment: Pathogenesis, diagnosis, and therapies.Semantic proximity Read ↗

Validation of DE50-MD dogs as a model for the brain phenotype of Duchenne muscular dystrophy.Semantic proximity Read ↗

Muscleblind1, but not Dmpk or Six5, contributes to a complex phenotype of muscular and motivational deficits in mouse models of myotonic dystrophy.Semantic proximity Read ↗

Cognitive and Neurobehavioral Profile in Boys With Duchenne Muscular Dystrophy.Semantic proximity Read ↗

Progression of multiple behavioral deficits with various ages of onset in a murine model of Hurler syndrome.Semantic proximity Read ↗

Changes in object recognition and anxiety-like behaviour in mice expressing a Cx47 mutation that causes Pelizaeus-Merzbacher-like disease.Semantic proximity Read ↗

Detection of dystrophin in the postsynaptic density of rat brain and deficiency in a mouse model of Duchenne muscular dystrophy.Semantic proximity Read ↗

The expression of the distal dystrophin isoforms Dp140 and Dp71 in the human epileptic hippocampus in relation to cognitive functioningSemantic proximity Read ↗

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