Pages that link to "Q62108894"

The following pages link to Patients with a Non-dysferlin Miyoshi Myopathy have a Novel Membrane Repair Defect (Q62108894):

Displaying 25 items.

• Membrane damage-induced vesicle-vesicle fusion of dysferlin-containing vesicles in muscle cells requires microtubules and kinesin. (Q28301480) (← links)
• Recombinant MG53 protein modulates therapeutic cell membrane repair in treatment of muscular dystrophy (Q30545559) (← links)
• S100A11 is required for efficient plasma membrane repair and survival of invasive cancer cells (Q30578437) (← links)
• Dysferlin regulates cell membrane repair by facilitating injury-triggered acid sphingomyelinase secretion. (Q30582564) (← links)
• Recessive mutations in the putative calcium-activated chloride channel Anoctamin 5 cause proximal LGMD2L and distal MMD3 muscular dystrophies (Q33645910) (← links)
• Expression levels of sarcolemmal membrane repair proteins following prolonged exercise training in mice (Q33878140) (← links)
• A new distal myopathy with mutation in anoctamin 5. (Q34390012) (← links)
• Cell wounding activates phospholipase D in primary mouse keratinocytes (Q34536468) (← links)
• VBP15, a novel anti-inflammatory and membrane-stabilizer, improves muscular dystrophy without side effects (Q34981147) (← links)
• Mechanism of Ca²⁺-triggered ESCRT assembly and regulation of cell membrane repair (Q35099073) (← links)
• S100 and annexin proteins identify cell membrane damage as the Achilles heel of metastatic cancer cells (Q35141257) (← links)
• Plasma Membrane Repair: A Central Process for Maintaining Cellular Homeostasis (Q36240722) (← links)
• Frequency and characterisation of anoctamin 5 mutations in a cohort of Italian limb-girdle muscular dystrophy patients (Q36406750) (← links)
• Repair of injured plasma membrane by rapid Ca2+-dependent endocytosis (Q36491740) (← links)
• A novel missense mutation in ANO5/TMEM16E is causative for gnathodiaphyseal dyplasia in a large Italian pedigree. (Q36856456) (← links)
• Dysferlin deficiency shows compensatory induction of Rab27A/Slp2a that may contribute to inflammatory onset. (Q36943096) (← links)
• Myoferlin is critical for endocytosis in endothelial cells (Q37338906) (← links)
• Dysferlin and myoferlin regulate transverse tubule formation and glycerol sensitivity. (Q37415471) (← links)
• Ahnak1 modulates L-type Ca(2+) channel inactivation of rodent cardiomyocytes. (Q42980151) (← links)
• Anoctamins/TMEM16 Proteins: Chloride Channels Flirting with Lipids and Extracellular Vesicles (Q50057538) (← links)
• Myopathy caused by anoctamin 5 mutations and necrotizing vasculitis (Q57389951) (← links)
• AMPK Complex Activation Promotes Sarcolemmal Repair in Dysferlinopathy (Q89842749) (← links)
• Enhancing membrane repair increases regeneration in a sciatic injury model (Q91762736) (← links)
• Anoctamin 5/TMEM16E facilitates muscle precursor cell fusion (Q91783058) (← links)
• Dysregulated calcium homeostasis prevents plasma membrane repair in Anoctamin 5/TMEM16E-deficient patient muscle cells (Q92156885) (← links)