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35 in total

1. Extrasynaptic location of laminin beta 2 chain in developing and adult human skeletal muscle.

Authors: U M Wewer; L E Thornell; F Loechel; X Zhang; M E Durkin; S Amano; R E Burgeson; E Engvall; R Albrechtsen; I Virtanen
Journal: Am J Pathol Date: 1997-08 Impact factor: 4.307

2. Alternative splicing of agrin regulates its binding to heparin alpha-dystroglycan, and the cell surface.

Authors: J J O'Toole; K A Deyst; M A Bowe; M A Nastuk; B A McKechnie; J R Fallon
Journal: Proc Natl Acad Sci U S A Date: 1996-07-09 Impact factor: 11.205

3. Substitution of a conserved cysteine-996 in a cysteine-rich motif of the laminin alpha2-chain in congenital muscular dystrophy with partial deficiency of the protein.

Authors: M Nissinen; A Helbling-Leclerc; X Zhang; T Evangelista; H Topaloglu; C Cruaud; J Weissenbach; M Fardeau; F M Tomé; K Schwartz; K Tryggvason; P Guicheney
Journal: Am J Hum Genet Date: 1996-06 Impact factor: 11.025

10. Nanotopography-responsive myotube alignment and orientation as a sensitive phenotypic biomarker for Duchenne Muscular Dystrophy.

Authors: Bin Xu; Alessandro Magli; Yoska Anugrah; Steven J Koester; Rita C R Perlingeiro; Wei Shen
Journal: Biomaterials Date: 2018-08-21 Impact factor: 12.479

Muscular dystrophies: diseases of the dystrophin-glycoprotein complex.

1. Extrasynaptic location of laminin beta 2 chain in developing and adult human skeletal muscle.

2. Alternative splicing of agrin regulates its binding to heparin alpha-dystroglycan, and the cell surface.

3. Substitution of a conserved cysteine-996 in a cysteine-rich motif of the laminin alpha2-chain in congenital muscular dystrophy with partial deficiency of the protein.

4. Early detection of cardiomyopathy in Duchenne muscular dystrophy, is there a role for MRI?

5. Purification of native p94, a muscle-specific calpain, and characterization of its autolysis.

Review 6. The membrane-cytoskeleton interface: the role of dystrophin and utrophin.

Review 7. Effects of aging, exercise, and disease on force transfer in skeletal muscle.

8. Utrophin is lacking at the neuromuscular junctions in the extraocular muscles of normal cat: artefact or true?

9. Syntrophin-dependent expression and localization of Aquaporin-4 water channel protein.

10. Nanotopography-responsive myotube alignment and orientation as a sensitive phenotypic biomarker for Duchenne Muscular Dystrophy.