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

Satellite cell loss and impaired muscle regeneration in selenoprotein N deficiency.

Human molecular genetics - 15 Feb 2011

Castets Perrine, Bertrand Anne T, Beuvin Maud, Ferry Arnaud, Le Grand Fabien, Castets Marie, Chazot Guillaume, Rederstorff Mathieu, Krol Alain, Lescure Alain, Romero Norma B, Guicheney Pascale, Allamand Valérie

Abstract excerpt

Selenoprotein N (SelN) deficiency causes a group of inherited neuromuscular disorders termed SEPN1-related myopathies (SEPN1-RM). Although the function of SelN remains unknown, recent data demonstrated that it is dispensable for mouse embryogenesis and suggested its involvement in the regulation of ryanodine receptors and/or cellular redox homeostasis. Here, we investigate the role of SelN in satellite cell (SC)...

Read the complete abstract on PubMed

Topics

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

Share to Cell Proliferation
Share to Cell Survival

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mice, Knockout

Share to Muscle, Skeletal

Share to Muscular Diseases

Share to Regeneration

Share to Satellite Cells, Skeletal Muscle

Share to Selenoproteins

Source

Identifiers

PMID: 21131290
DOI: 10.1093/hmg/ddq515

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Satellite cell loss and impaired muscle regeneration in selenoprotein N deficiency.PMID 21131290Read ↗

Oxidative stress in SEPN1-related myopathy: from pathophysiology to treatment.Semantic proximity Read ↗

Increased muscle stress-sensitivity induced by selenoprotein N inactivation in mouse: a mammalian model for SEPN1-related myopathy.Semantic proximity Read ↗

Selenoprotein function and muscle disease.Semantic proximity Read ↗

Selenoprotein N deficiency in mice is associated with abnormal lung development.Semantic proximity Read ↗

Selenoprotein N and SEPN1-Related Myopathies: Mechanisms, Models, and Therapeutic Perspectives.Semantic proximity Read ↗

Zebrafish and cellular models of SELENON-Congenital myopathy exhibit novel embryonic and metabolic phenotypes.Semantic proximity Read ↗

Depletion of skeletal muscle satellite cells attenuates pathology in muscular dystrophySemantic proximity Read ↗

Stem cells for skeletal muscle repairSemantic proximity Read ↗

Satellite cell depletion in early adulthood attenuates muscular dystrophy pathogenesisSemantic proximity Read ↗

Single Cell Deconstruction of Muscle Stem Cell Heterogeneity During Aging Reveals Sensitivity to the Neuromuscular JunctionSemantic proximity Read ↗

SMN depletion impairs skeletal muscle formation and maturation in a mouse model of SMASemantic proximity Read ↗

Intact satellite cells lead to remarkable protection against Smn gene defect in differentiated skeletal muscle.Semantic proximity Read ↗

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