Pages that link to "Q34338854"
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The following pages link to Mitochondrial dysfunction and defective autophagy in the pathogenesis of collagen VI muscular dystrophies. (Q34338854):
Displaying 22 items.
- A TALEN-Exon Skipping Design for a Bethlem Myopathy Model in Zebrafish (Q27301818) (← links)
- Primary Mitochondrial Disease and Secondary Mitochondrial Dysfunction: Importance of Distinction for Diagnosis and Treatment (Q28078384) (← links)
- Increased mitophagy in the skeletal muscle of spinal and bulbar muscular atrophy patients (Q33614611) (← links)
- Src-dependent impairment of autophagy by oxidative stress in a mouse model of Duchenne muscular dystrophy (Q33913903) (← links)
- Nutritional status evaluation in patients affected by bethlem myopathy and ullrich congenital muscular dystrophy. (Q34529706) (← links)
- Defects in calcium homeostasis and mitochondria can be reversed in Pompe disease (Q35853122) (← links)
- Editorial: Pathophysiological Mechanisms of Sarcopenia in Aging and in Muscular Dystrophy: A Translational Approach. (Q35947839) (← links)
- Identification of 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase as a novel autophagy regulator by high content shRNA screening. (Q36069096) (← links)
- The Mitochondrial Permeability Transition Pore: Channel Formation by F-ATP Synthase, Integration in Signal Transduction, and Role in Pathophysiology. (Q36146320) (← links)
- Ultrastructural changes in muscle cells of patients with collagen VI-related myopathies (Q37613885) (← links)
- The mitochondrial permeability transition pore and its adaptive responses in tumor cells (Q38278265) (← links)
- Muscle biopsies from human muscle diseases with myopathic pathology reveal common alterations in mitochondrial function (Q39888514) (← links)
- Two novel COLVI long chains in zebrafish that are essential for muscle development. (Q40547943) (← links)
- Gapmer Antisense Oligonucleotides Suppress the Mutant Allele of COL6A3 and Restore Functional Protein in Ullrich Muscular Dystrophy (Q41191227) (← links)
- Editorial: Mitochondria in Skeletal Muscle Health, Aging and Diseases (Q42386975) (← links)
- Clinical and symptomatological reflections: the fascial system (Q42913372) (← links)
- Regulation of calcium release from the endoplasmic reticulum by the serine hydrolase ABHD2. (Q45062800) (← links)
- Modulation of Protein Quality Control and Proteasome to Autophagy Switch in Immortalized Myoblasts from Duchenne Muscular Dystrophy Patients. (Q47216956) (← links)
- Protective role of Parkin in skeletal muscle contractile and mitochondrial function. (Q52570888) (← links)
- Increase in HDAC9 suppresses myoblast differentiation via epigenetic regulation of autophagy in hypoxia (Q92002408) (← links)
- Loss of function of Colgalt1 disrupts collagen post-translational modification and causes musculoskeletal defects (Q92124230) (← links)
- Substrate-dependent and cyclophilin D-independent regulation of mitochondrial flashes in skeletal and cardiac muscle (Q92367764) (← links)