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

FGF8 rescues motor deficits in zebrafish model of limb-girdle muscular dystrophy R18.

Biochemical and biophysical research communications - 16 Apr 2023

Ulhaq Zulvikar Syambani, Ogino Yukiko, Tse William Ka Fai

Abstract excerpt

Variants in the gene encoding trafficking protein particle complex 11 (TRAPPC11) cause limb-girdle muscular dystrophy R18 (LGMD R18). Although recently several genes related to myopathies have been identified, correlations between genetic causes and signaling events that lead from mutation to the disease phenotype are still mostly unclear. Here, we utilized zebrafish to model LGMD R18 by specifically inactivating...

Read the complete abstract on PubMed

Topics

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

Share to Muscle, Skeletal
Share to Muscular Diseases
Share to Muscular Dystrophies, Limb-Girdle

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Mutation

Share to Zebrafish

Source

Identifiers

PMID: 36827861
DOI: 10.1016/j.bbrc.2023.02.046

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

FGF8 rescues motor deficits in zebrafish model of limb-girdle muscular dystrophy R18.PMID 36827861Read ↗

Muscular dystrophy modeling in zebrafish.Semantic proximity Read ↗

A Titin Knock-in model for Hereditary Myopathy with Early Respiratory FailureSemantic proximity Read ↗

Rewiring Fibroblast–Muscle Axis Drives Progressive Pathology in Bethlem MyopathySemantic proximity Read ↗

Zebrafish models flex their muscles to shed light on muscular dystrophiesSemantic proximity Read ↗

In vivo characterization of human myofibrillar myopathy genes in zebrafish.Semantic proximity Read ↗

Dystrophin-deficient zebrafish feature aspects of the Duchenne muscular dystrophy pathology.Semantic proximity Read ↗

An <i>in vivo</i> approach to characterize novel variants associated with musculoskeletal disordersSemantic proximity Read ↗

Zebrafish mbnl mutants model physical and molecular phenotypes of myotonic dystrophy.Semantic proximity Read ↗

A pathogenic mechanism associated with myopathies and structural birth defects involves TPM2-directed myogenesisSemantic proximity Read ↗

Inhibition of autophagy rescues muscle atrophy in a LGMDD2 Drosophila model.Semantic proximity Read ↗

Zebrafish <i>mbnl</i> mutants model physical and molecular phenotypes of myotonic dystrophySemantic proximity Read ↗

Lipin 1 deficiency causes adult-onset myasthenia with motor neuron dysfunction in humans and neuromuscular junction defects in zebrafish.Semantic proximity Read ↗

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