A biallelic mutation (E366G) in SNIP1 , located near the FHA domain, has been associated with a complex neurodevelopmental disorder in 35 individuals from the Amish community 47,48 , although the underlying mechanistic defect caused by the mutation is unknown
progressive cardiomyopathy, elevated creatine kinase, and skeletal myopathy in childhood
As early as 2004, Loren Pickart published an article in a Russian journal (translated to English here) on Improving Hair Growth with Skin Remodeling Copper Peptides, in which he advocated the usage of skin-remodeling copper peptides (SRCPs), a type of GHK-Cu, for their anti-inflammatory and skin repair (wound-healing) properties as well as their ability to increase the size of hair follicles
And its a mechanism not only supported by multiple animal studies, while happening to be consistent with what Ive observed personally
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