Fiber-type nomenclature of human skeletal muscle for histochemical purposes

Chaperone-mediated autophagy components are upregulated in sporadic inclusion-body myositis muscle fibres.

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Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementia.

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Myostatin and its precursor protein are increased in the skeletal muscle of patients with Type-II muscle fibre atrophy.

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Increased expression of Noga-A in ALS muscle biopsies is not unique for this disease.

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Parkin and its association with alpha-synuclein and AbetaPP in inclusion-body myositis and AbetaPP-overexpressing cultured human muscle fibers.

Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology·2006

Mutant ubiquitin UBB+1 is accumulated in sporadic inclusion-body myositis muscle fibers.

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Early Rhythm Control vs Usual Care After Acute Ischemic Stroke in Patients With Atrial Fibrillation.

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Normalization Strategies for miRNA RT-qPCR in Blood-Derived Samples in Obesity Research: Current Practices and Methodological Considerations.

International journal of molecular sciences·2026

Urinary Metabolomics in Bladder Cancer: A Scoping Review of Current Evidence and Translation Implications.

International journal of molecular sciences·2026

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Fiber-type nomenclature of human skeletal muscle for histochemical purposes

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Chaperone-mediated autophagy components are upregulated in sporadic inclusion-body myositis muscle fibres.

Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementia.

Myostatin and its precursor protein are increased in the skeletal muscle of patients with Type-II muscle fibre atrophy.

Increased expression of Noga-A in ALS muscle biopsies is not unique for this disease.

Parkin and its association with alpha-synuclein and AbetaPP in inclusion-body myositis and AbetaPP-overexpressing cultured human muscle fibers.

Mutant ubiquitin UBB+1 is accumulated in sporadic inclusion-body myositis muscle fibers.

Differences in Epilepsy Etiology, Type, Syndrome, and Severity Between Māori and Non-Māori-Non-Pasifika Children With Epilepsy in New Zealand.

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Fiber-type nomenclature of human skeletal muscle for histochemical purposes

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