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Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with cores.

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Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye?

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Selective muscle involvement on magnetic resonance imaging in autosomal dominant Emery-Dreifuss muscular dystrophy.

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Neonatal arthrogryposis and absent limb muscles: a muscle developmental gene defect?

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Postcranial osteology of Boverisuchus vorax from the middle Eocene of Wyoming, USA: Implications for terrestrial adaptation in eusuchian crocodyliforms.

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F/HN-pseudotyped lentiviral vector efficiently transduces non-human primate airways with no evidence of relevant toxicity.

Molecular therapy. Advances·2026

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Recent Advances in Mechanobiology-Mediated In Situ Tissue Engineering.

International journal of biomaterials·2026

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Trophoblast cells rewire the epigenetic landscape of vascular smooth muscle cells to modulate plasticity: a regulatory axis disrupted in intrauterine growth restriction.

Cell communication and signaling : CCS·2026

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Reproductive sciences (Thousand Oaks, Calif.)·2026

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Quantitative morphological studies on transplanted muscle in the hamster

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Mutations in MYH7 cause Multi-minicore Disease (MmD) with variable cardiac involvement.

Remission of clinical signs in early duchenne muscular dystrophy on intermittent low-dosage prednisolone therapy.

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Quantitative morphological studies on transplanted muscle in the hamster

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