Pages that link to "Q28505521"

The following pages link to A mouse model for dominant collagen VI disorders: heterozygous deletion of Col6a3 Exon 16 (Q28505521):

Displaying 16 items.

• Collagen, type VI, alpha 5 (Q21496286) ‎ (← links)
• Collagen, type VI, alpha 6 (Q21496287) ‎ (← links)
• Periostin, osteoblast specific factor (Q21989384) ‎ (← links)
• A TALEN-Exon Skipping Design for a Bethlem Myopathy Model in Zebrafish (Q27301818) ‎ (← links)
• A collagen VI-dependent pathogenic mechanism for Hirschsprung's disease (Q27330447) ‎ (← links)
• Defective collagen VI α6 chain expression in the skeletal muscle of patients with collagen VI-related myopathies (Q35046733) ‎ (← links)
• Collagen VI deficiency reduces muscle pathology, but does not improve muscle function, in the γ-sarcoglycan-null mouse (Q36676817) ‎ (← links)
• 212th ENMC International Workshop: Animal models of congenital muscular dystrophies, Naarden, The Netherlands, 29-31 May 2015. (Q37555754) ‎ (← links)
• Non-myogenic Contribution to Muscle Development and Homeostasis: The Role of Connective Tissues (Q37716791) ‎ (← links)
• Tendon Extracellular Matrix Alterations in Ullrich Congenital Muscular Dystrophy (Q39634474) ‎ (← links)
• Comparison of sitting and supine forced vital capacity in collagen VI-related dystrophy and laminin α2-related dystrophy. (Q40381994) ‎ (← links)
• Collagen VI in healthy and diseased nervous system. (Q55472526) ‎ (← links)
• Molecular characterization of physis tissue by RNA sequencing (Q57168455) ‎ (← links)
• Overexpression of miR-29 Leads to Myopathy that Resemble Pathology of Ullrich Congenital Muscular Dystrophy. (Q64974654) ‎ (← links)
• Tendon Extracellular Matrix Remodeling and Defective Cell Polarization in the Presence of Collagen VI Mutations (Q89696735) ‎ (← links)
• Basement membrane collagens and disease mechanisms (Q92459933) ‎ (← links)