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Human adipose-derived stem cell transplantation as a potential therapy for collagen VI-related congenital muscular dystrophy

https://doi.org/10.1186/scrt411
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40/40 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.

1 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.

The 40 checked references that resolve
resolves10.1038/nrneurol.2011.81
The collagen VI-related myopathies: muscle meets its matrix
resolves10.1016/j.spen.2011.10.010
Congenital Muscular Dystrophies: A Brief Review
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Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population
resolves10.1212/01.wnl.0000271387.10404.4e
Primary collagen VI deficiency is the second most common congenital muscular dystrophy in Japan
resolves10.1212/01.wnl.0000284605.27654.5a
Diagnosis and etiology of congenital muscular dystrophy
resolves10.1136/jmg.2002.002311
Collagen VI related muscle disorders
resolves10.1016/j.yexcr.2008.08.006
An enhancer required for transcription of the Col6a1 gene in muscle connective tissue is induced by signals released from muscle cells
resolves10.1097/nen.0b013e3181634ef7
Muscle Interstitial Fibroblasts Are the Main Source of Collagen VI Synthesis in Skeletal Muscle: Implications for Congenital Muscular Dystrophy Types Ullrich and Bethlem
resolves10.1111/j.1749-6632.1990.tb17917.x
The Structure of Type VI Collagen<sup>a</sup>
resolves10.1073/pnas.121027598
Ullrich scleroatonic muscular dystrophy is caused by recessive mutations in collagen type VI
resolves10.1002/ana.1120
Frameshift mutation in the collagen VI gene causes Ullrich's disease
resolves10.1086/340608
Mutations in COL6A3 Cause Severe and Mild Phenotypes of Ullrich Congenital Muscular Dystrophy
resolves10.1093/hmg/7.13.2135
Collagen VI deficiency induces early onset myopathy in the mouse: an animal model for Bethlem myopathy
resolves10.1073/pnas.0610270104
Mitochondrial dysfunction in the pathogenesis of Ullrich congenital muscular dystrophy and prospective therapy with cyclosporins
resolves10.1038/ng1270
Mitochondrial dysfunction and apoptosis in myopathic mice with collagen VI deficiency
resolves10.1038/nm.2247
Autophagy is defective in collagen VI muscular dystrophies, and its reactivation rescues myofiber degeneration
resolves10.1073/pnas.0800962105
Cyclosporin A corrects mitochondrial dysfunction and muscle apoptosis in patients with collagen VI myopathies
resolves10.1155/2011/139194
Cyclosporine A in Ullrich Congenital Muscular Dystrophy: Long-Term Results
resolves10.2165/11534300-000000000-00000
Stem Cell Therapies to Treat Muscular Dystrophy
resolves10.1007/s00441-007-0509-0
Human bone-marrow-derived mesenchymal stem cells: biological characteristics and potential role in therapy of degenerative diseases
resolves10.1089/hum.2010.173
The Regulation of Differentiation in Mesenchymal Stem Cells
resolves10.1016/j.tibtech.2006.01.010
Fat tissue: an underappreciated source of stem cells for biotechnology
resolves10.1634/stemcells.2005-0342
Comparative Analysis of Mesenchymal Stem Cells from Bone Marrow, Umbilical Cord Blood, or Adipose Tissue
resolves10.1097/01.TP.0000045055.63901.A9
Suppression of allogeneic T-cell proliferation by human marrow stromal cells: implications in transplantation
resolves10.1111/j.1432-1033.1994.tb18727.x
Recombinant expression and structural and binding properties of α1(VI) and α2(VI) chains of human collagen type VI
resolves10.1074/jbc.M109.093666
Recessive COL6A2 C-globular Missense Mutations in Ullrich Congenital Muscular Dystrophy
resolves10.1002/j.1460-2075.1992.tb05527.x
Structure of recombinant N‐terminal globule of type VI collagen alpha 3 chain and its binding to heparin and hyaluronan.
resolves10.1080/14653240600855905
Minimal criteria for defining multipotent mesenchymal stromal cells. The International Society for Cellular Therapy position statement
resolves10.3109/14653249.2010.518609
Gene expression signatures of mouse bone marrow-derived mesenchymal stem cells in the cutaneous environment and therapeutic implications for blistering skin disorder
resolves10.1002/jcp.21895
Cell based therapy for duchenne muscular dystrophy
resolves10.1083/jcb.200212064
Skeletal muscle repair by adult human mesenchymal stem cells from synovial membrane
resolves10.1016/j.nmd.2009.11.007
The contribution of human synovial stem cells to skeletal muscle regeneration
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/s12015-011-9304-0
Local Injections of Adipose-Derived Mesenchymal Stem Cells Modulate Inflammation and Increase Angiogenesis Ameliorating the Dystrophic Phenotype in Dystrophin-Deficient Skeletal Muscle
resolves10.1016/j.cellimm.2009.10.006
Mesenchymal stem cells as anti-inflammatories: Implications for treatment of Duchenne muscular dystrophy
resolves10.1172/JCI10376
Myogenic stem cells for the therapy of primary myopathies: wishful thinking or therapeutic perspective?
resolves10.1073/pnas.94.22.12053
Severe reduction in leukocyte adhesion and monocyte extravasation in mice deficient in CC chemokine receptor 2
resolves10.1016/S0014-2999(01)01235-3
Redundant function of macrophage inflammatory protein-2 and KC in tumor necrosis factor-α-induced extravasation of neutrophils in vivo
resolves10.1242/jcs.066241
Chemokine 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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