Pages that link to "Q35248262"

The following pages link to Muscle proteomics reveals novel insights into the pathophysiological mechanisms of collagen VI myopathies (Q35248262):

Displaying 19 items.

• The Human Skeletal Muscle Proteome Project: a reappraisal of the current literature (Q28068399) (← links)
• Endoplasmic reticulum stress in chondrodysplasias caused by mutations in collagen types II and X (Q28073452) (← links)
• Specific protein changes contribute to the differential muscle mass loss during ageing. (Q35876811) (← links)
• Novel pathogenic variants and genes for myopathies identified by whole exome sequencing (Q35907744) (← links)
• New therapeutic targets in rare genetic skeletal diseases (Q36275329) (← links)
• A Nonsense Variant in COL6A1 in Landseer Dogs with Muscular Dystrophy (Q36383108) (← links)
• Deep RNA profiling identified CLOCK and molecular clock genes as pathophysiological signatures in collagen VI myopathy (Q36856928) (← links)
• Prediction of key genes and miRNAs responsible for loss of muscle force in patients during an acute exacerbation of chronic obstructive pulmonary disease (Q37341435) (← links)
• Costamere proteins and their involvement in myopathic processes. (Q38531654) (← links)
• Understanding the molecular consequences of inherited muscular dystrophies: advancements through proteomic experimentation. (Q38850056) (← links)
• TCA cycle rewiring fosters metabolic adaptation to oxygen restriction in skeletal muscle from rodents and humans (Q41549048) (← links)
• Comparative 3-Sample DIGE Analysis of Skeletal Muscles (Q46289186) (← links)
• ER stress in skeletal muscle remodeling and myopathies (Q47295145) (← links)
• Collagen VI Null Mice as a Model for Early Onset Muscle Decline in Aging. (Q47428333) (← links)
• Contribution of Extracellular Matrix and Signal Mechanotransduction to Epithelial Cell Damage in Inflammatory Bowel Disease Patients: A Proteomic Study (Q47658893) (← links)
• Mapping the human skeletal muscle proteome: progress and potential (Q47986644) (← links)
• Transcriptome analysis of skin fibroblasts with dominant negative COL3A1 mutations provides molecular insights into the etiopathology of vascular Ehlers-Danlos syndrome. (Q48217824) (← links)
• Proteomic profiling of muscle fibre type shifting in neuromuscular diseases. (Q51664676) (← links)
• Comparative proteomic analyses of Duchenne muscular dystrophy and Becker muscular dystrophy muscles: changes contributing to preserve muscle function in Becker muscular dystrophy patients (Q92996733) (← links)