Pages that link to "Q55671360"

The following pages link to Autosomal recessive myosclerosis myopathy is a collagen VI disorder (Q55671360):

Displaying 14 items.

• Dermal ultrastructure in collagen VI myopathy (Q45734482) (← links)
• H-1Collagen VI myopathies: pathogenicmechanisms and novel therapeutic perspectives. (Q46025895) (← links)
• Genetic ablation of cyclophilin D rescues mitochondrial defects and prevents muscle apoptosis in collagen VI myopathic mice (Q46085120) (← links)
• NIM811, a cyclophilin inhibitor without immunosuppressive activity, is beneficial in collagen VI congenital muscular dystrophy models. (Q47073612) (← links)
• Identification of COL6A2 mutations in progressive myoclonus epilepsy syndrome (Q48302894) (← links)
• Bethlem Myopathy Phenotypes and Follow Up: Description of 8 Patients at the Mildest End of the Spectrum (Q50223887) (← links)
• Contraction intensity and feeding affect collagen and myofibrillar protein synthesis rates differently in human skeletal muscle. (Q51412357) (← links)
• Genome-wide association study of motor coordination problems in ADHD identifies genes for brain and muscle function. (Q51873167) (← links)
• Body composition, muscle strength, and physical function of patients with Bethlem myopathy and Ullrich congenital muscular dystrophy. (Q54690359) (← links)
• From Structure to Phenotype: Impact of Collagen Alterations on Human Health. (Q55096200) (← links)
• Collagen VI in healthy and diseased nervous system. (Q55472526) (← links)
• myosclerosis (Q55782133) (← links)
• Expression of the collagen VI α5 and α6 chains in normal human skin and in skin of patients with collagen VI-related myopathies (Q56987133) (← links)
• Extracellular Collagen VI Has Prosurvival and Autophagy Instructive Properties in Mouse Fibroblasts (Q58769569) (← links)