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

Structural study of skeletal muscle fibres in healthy and pseudomyotonia affected cattle.

Annals of anatomy = Anatomischer Anzeiger : official organ of the Anatomische Gesellschaft - 1 Sept 2016

Mascarello Francesco, Sacchetto Roberta

Abstract excerpt

Cattle congenital pseudomyotonia (PMT), recognized as naturally occurring animal model of human Brody disease, is an inherited recessive autosomal muscular disorder due to missense mutations in ATP2A1 gene, encoding sarco(endo)plasmic reticulum Ca(2+)-ATPase protein, isoform 1 (SERCA1). PMT has been described in the Chianina and Romagnola italian cattle breeds and as a single case in Dutch improved Red and White...

Read the complete abstract on PubMed

Topics

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

Share to Cattle
Share to Cattle Diseases
Share to Disease Models, Animal

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

Share to Muscle Fibers, Skeletal

Share to Mutation

Share to Sarcoplasmic Reticulum

Share to Sarcoplasmic Reticulum Calcium-Transporting ATPases

Source

Identifiers

PMID: 27210062
DOI: 10.1016/j.aanat.2016.05.002

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

Structural study of skeletal muscle fibres in healthy and pseudomyotonia affected cattle.PMID 27210062Read ↗

Differential Analysis of Gly211Val and Gly286Val Mutations Affecting Sarco(endo)plasmic Reticulum Ca2+-ATPase (SERCA1) in Congenital Pseudomyotonia Romagnola Cattle.Semantic proximity Read ↗

Inhibition of ubiquitin proteasome system rescues the defective sarco(endo)plasmic reticulum Ca2+-ATPase (SERCA1) protein causing Chianina cattle pseudomyotonia.Semantic proximity Read ↗

Pseudomyotonia in Romagnola cattle caused by novel ATP2A1 mutations.Semantic proximity Read ↗

Pseudomyotonia, a muscle function disorder associated with an inherited ATP2A1 (SERCA1) defect in a Dutch Improved Red and White cross-breed calf.Semantic proximity Read ↗

The Accordion Zebrafish tq206 Mutant in the Assessment of a Novel Pharmaceutical Approach to Brody Myopathy.Semantic proximity Read ↗

Brody disease: insights into biochemical features of SERCA1 and identification of a novel mutation.Semantic proximity Read ↗

Frequency of bovine congenital pseudomyotonia carriers in selected Italian Chianina sires.Semantic proximity Read ↗

Mutations in the gene-encoding SERCA1, the fast-twitch skeletal muscle sarcoplasmic reticulum Ca2+ ATPase, are associated with Brody disease.Semantic proximity Read ↗

The mutation of Pro789 to Leu reduces the activity of the fast-twitch skeletal muscle sarco(endo)plasmic reticulum Ca2+ ATPase (SERCA1) and is associated with Brody disease.Semantic proximity Read ↗

Atypical nuclear abnormalities in a patient with Brody disease.Semantic proximity Read ↗

SERCA1 protein expression in muscle of patients with Brody disease and Brody syndrome and in cultured human muscle fibers.Semantic proximity Read ↗

Calpain 3 deficiency affects SERCA expression and function in the skeletal muscle.Semantic proximity Read ↗

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