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Cyclosporin A corrects mitochondrial dysfunction and muscle apoptosis in patients with collagen VI myopathies
29/29 checkable references clean · checked 2026-07-23
Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.
The 29 checked references that resolve
resolves10.1093/hmg/7.13.2135
Collagen VI deficiency induces early onset myopathy in the mouse: an animal model for Bethlem myopathy
resolves10.1038/ng1270
Mitochondrial dysfunction and apoptosis in myopathic mice with collagen VI deficiency
resolves10.1016/0003-9861(72)90261-5
Calcium and pyridine nucleotide interaction in mitochondrial membranes
resolves10.1074/jbc.M006825200
Opening of the Mitochondrial Permeability Transition Pore Causes Depletion of Mitochondrial and Cytosolic NAD+and Is a Causative Event in the Death of Myocytes in Postischemic Reperfusion of the Heart
resolves10.1074/jbc.M010603200
Arachidonic Acid Causes Cell Death through the Mitochondrial Permeability Transition
resolves10.1016/S0166-2236(99)01534-9
Mitochondrial membrane potential and neuronal glutamate excitotoxicity: mortality and millivolts
resolves10.1016/S0092-8674(00)80301-3
Mitochondria Are Excitable Organelles Capable of Generating and Conveying Electrical and Calcium Signals
resolves10.1016/S0006-3495(98)77920-2
Imaging the Permeability Pore Transition in Single Mitochondria
resolves10.1016/S0006-3495(99)77239-5
Transient and Long-Lasting Openings of the Mitochondrial Permeability Transition Pore Can Be Monitored Directly in Intact Cells by Changes in Mitochondrial Calcein Fluorescence
resolves10.1042/bj3430311
Fluctuations in mitochondrial membrane potential caused by repetitive gating of the permeability transition pore
resolves10.1074/jbc.M405297200
Desensitization of the Permeability Transition Pore by Cyclosporin A Prevents Activation of the Mitochondrial Apoptotic Pathway and Liver Damage by Tumor Necrosis Factor-α
resolves10.1073/pnas.0610270104
Mitochondrial dysfunction in the pathogenesis of Ullrich congenital muscular dystrophy and prospective therapy with cyclosporins
resolves10.1007/BF02864097
Kongenitale, atonisch-sklerotische Muskeldystrophie, ein weiterer Typus der heredodegenerativen Erkrankungen des neuromuskulären Systems
resolves10.1073/pnas.121027598
Ullrich scleroatonic muscular dystrophy is caused by recessive mutations in collagen type VI
resolves10.1086/377107
New Molecular Mechanism for Ullrich Congenital Muscular Dystrophy: A Heterozygous In-Frame Deletion in the COL6A1 Gene Causes a Severe Phenotype
resolves10.1093/hmg/ddi025
Dominant collagen VI mutations are a common cause of Ullrich congenital muscular dystrophy
resolves10.1086/340608
Mutations in COL6A3 Cause Severe and Mild Phenotypes of Ullrich Congenital Muscular Dystrophy
resolves10.1002/mus.10100
Novel COL6A1 splicing mutation in a family affected by mild Bethlem myopathy
resolves10.1016/S0167-4889(98)00088-3
Quantitative assay by flow cytometry of the mitochondrial membrane potential in intact cells
resolves10.1074/jbc.271.4.2185
Interactions of Cyclophilin with the Mitochondrial Inner Membrane and Regulation of the Permeability Transition Pore, a Cyclosporin A-sensitive Channel
resolves10.1023/B:JOBB.0000041776.31885.45
The Nonimmunosuppressive Cyclosporin Analogs NIM811 and UNIL025 Display Nanomolar Potencies on Permeability Transition in Brain-Derived Mitochondria
resolves10.1016/S0140-6736(76)92781-1
MITOCHONDRIAL CALCIUM OVERLOAD: A GENERAL MECHANISM FOR CELL-NECROSIS IN MUSCLE DISEASES
resolves10.1146/annurev.genet.39.110304.095751
A Mitochondrial Paradigm of Metabolic and Degenerative Diseases, Aging, and Cancer: A Dawn for Evolutionary Medicine
resolves10.1016/S0960-8966(02)00139-6
Bethlem myopathy (BETHLEM) and Ullrich scleroatonic muscular dystrophy: 100th ENMC International Workshop, 23–24 November 2001, Naarden, The Netherlands
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