1. Novel Biomarkers for Limb Girdle Muscular Dystrophy (LGMD)
    Sara Aguti et al, 2024, Cells CrossRef
  2. Genetic diversity and runs of homozygosity analysis of Hetian sheep populations revealed by Illumina Ovine SNP50K BeadChip
    Zhipeng Han et al, 2023, Frontiers in Ecology and Evolution CrossRef
  3. Clinical features, imaging findings and molecular data of limb-girdle muscular dystrophies in a cohort of Chinese patients
    Feng Lin et al, 2023, Orphanet Journal of Rare Diseases CrossRef
  4. Protein Quality Control at the Sarcomere: Titin Protection and Turnover and Implications for Disease Development
    Sebastian Kötter et al, 2022, Frontiers in Physiology CrossRef
  5. Transcriptome-Based Identification of the Muscle Tissue-Specific Expression Gene CKM and Its Regulation of Proliferation, Apoptosis and Differentiation in Chicken Primary Myoblasts
    Bingjie Chen et al, 2023, Animals CrossRef
  6. Missense mutation of c.635 T > C in CAPN3 impairs muscle injury repair in a Limb‐Girdel Muscular Dystropy Model
    Hou‐Shi Ma et al, 2023, Clinical Genetics CrossRef
  7. The Effects of Antioxidants and Pulsed Magnetic Fields on Slow and Fast Skeletal Muscle Atrophy Induced by Streptozotocin: A Preclinical Study
    Bora Tastekin et al, 2023, Journal of Diabetes Research CrossRef
  8. Transcriptome sequencing analysis of the role of miR-499-5p and SOX6 in chicken skeletal myofiber specification
    Yi-Fan Liu et al, 2022, Frontiers in Genetics CrossRef
  9. Novel mutations in the SGCA gene in unrelated Vietnamese patients with limb-girdle muscular dystrophies disease
    Nam Chung Tran et al, 2023, Frontiers in Genetics CrossRef
  10. Identification and functional characterization of a novel heterozygous splice‑site mutation in the calpain 3 gene causes rare autosomal dominant limb‑girdle muscular dystrophy
    Bin Mao et al, 2024, Experimental and Therapeutic Medicine CrossRef
  11. Family and literature analysis demonstrates phenotypic effect of two variants in the calpain-3 gene
    Maike Tomforde et al, 2023, neurogenetics CrossRef
  12. Molecular and genetic features of calpainopathy
    L. A. Mkrtchyan et al, 2022, Genes & Cells CrossRef
  13. Muscle eosinophilia is a hallmark of chronic disease in facioscapulohumeral muscular dystrophy
    Andreia M Nunes et al, 2024, Human Molecular Genetics CrossRef
  14. Lunar gravity prevents skeletal muscle atrophy but not myofiber type shift in mice
    Takuto Hayashi et al, 2023, Communications Biology CrossRef
  15. Anabolic steroids induced changes at the level of protein expression: Effects of prolonged administration of testosterone and nandrolone to pigs
    Jan Gebauer et al, 2024, Environmental Toxicology and Pharmacology CrossRef