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 40 checked references that resolve
resolves10.1093/brain/awp236Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population
resolves10.1016/j.yexcr.2008.08.006An enhancer required for transcription of the Col6a1 gene in muscle connective tissue is induced by signals released from muscle cells
resolves10.1097/nen.0b013e3181634ef7Muscle Interstitial Fibroblasts Are the Main Source of Collagen VI Synthesis in Skeletal Muscle: Implications for Congenital Muscular Dystrophy Types Ullrich and Bethlem
resolves10.1073/pnas.121027598Ullrich scleroatonic muscular dystrophy is caused by recessive mutations in collagen type VI
resolves10.1002/ana.1120Frameshift mutation in the collagen VI gene causes Ullrich's disease
resolves10.1086/340608Mutations in COL6A3 Cause Severe and Mild Phenotypes of Ullrich Congenital Muscular Dystrophy
resolves10.1093/hmg/7.13.2135Collagen VI deficiency induces early onset myopathy in the mouse: an animal model for Bethlem myopathy
resolves10.1073/pnas.0610270104Mitochondrial dysfunction in the pathogenesis of Ullrich congenital muscular dystrophy and prospective therapy with cyclosporins
resolves10.1038/ng1270Mitochondrial dysfunction and apoptosis in myopathic mice with collagen VI deficiency
resolves10.1038/nm.2247Autophagy is defective in collagen VI muscular dystrophies, and its reactivation rescues myofiber degeneration
resolves10.1073/pnas.0800962105Cyclosporin A corrects mitochondrial dysfunction and muscle apoptosis in patients with collagen VI myopathies
resolves10.1155/2011/139194Cyclosporine A in Ullrich Congenital Muscular Dystrophy: Long-Term Results
resolves10.1007/s00441-007-0509-0Human bone-marrow-derived mesenchymal stem cells: biological characteristics and potential role in therapy of degenerative diseases
resolves10.1634/stemcells.2005-0342Comparative Analysis of Mesenchymal Stem Cells from Bone Marrow, Umbilical Cord Blood, or Adipose Tissue
resolves10.1074/jbc.M109.093666Recessive COL6A2 C-globular Missense Mutations in Ullrich Congenital Muscular Dystrophy
resolves10.1080/14653240600855905Minimal criteria for defining multipotent mesenchymal stromal cells. The International Society for Cellular Therapy position statement
resolves10.3109/14653249.2010.518609Gene expression signatures of mouse bone marrow-derived mesenchymal stem cells in the cutaneous environment and therapeutic implications for blistering skin disorder
resolves10.1083/jcb.200212064Skeletal muscle repair by adult human mesenchymal stem cells from synovial membrane
resolves10.1634/stemcells.2008-0043<i>SJL</i> Dystrophic Mice Express a Significant Amount of Human Muscle Proteins Following Systemic Delivery of Human Adipose-Derived Stromal Cells Without Immunosuppression
resolves10.1007/s12015-011-9304-0Local Injections of Adipose-Derived Mesenchymal Stem Cells Modulate Inflammation and Increase Angiogenesis Ameliorating the Dystrophic Phenotype in Dystrophin-Deficient Skeletal Muscle
resolves10.1172/JCI10376Myogenic stem cells for the therapy of primary myopathies: wishful thinking or therapeutic perspective?
resolves10.1073/pnas.94.22.12053Severe reduction in leukocyte adhesion and monocyte extravasation in mice deficient in CC chemokine receptor 2
resolves10.1016/S0014-2999(01)01235-3Redundant function of macrophage inflammatory protein-2 and KC in tumor necrosis factor-α-induced extravasation of neutrophils in vivo
resolves10.1242/jcs.066241Chemokine expression and control of muscle cell migration during myogenesis
The 1 reference without a DOI — listed, not checked
no DOI — not checkedUrciuolo A, Quarta M, Morbidoni V, Gattazzo F, Molon S, Grumati P, Montemurro F, Tedesco FS, Blaauw B, Cossu G, Vozzi G, Rando TA, Bonaldo P: Collagen VI regulates satellite cell self-renewal and muscle regeneration. Nat Commun. 1964, 2013: 4-
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