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Reported molecular endpoints include VEGFR2 expression and internalisation, FAK and paxillin phosphorylation, growth hormone receptor expression in tendon fibroblasts, and Egr-1 pathway activity
And without needing the painful intramuscular injections
Solvent selection and all handling are determined by the receiving laboratory under its own protocols
Local nerve endings surrounding the painful tendon become desensitised by these pulses, resulting in further pain reduction
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