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Abels, Improved distribution analysis of cobalamins and cobalamin analogues in human plasma in which the use of thiol-blocking agents is a prerequisite, Clinica Chimica Acta, Volume 131, Issue 3, 15 July 1983, Pages 211-224, ISSN 0009-8981 Thakkar, K., & Billa, G

The significant up-regulation of Egr1 and Vegfr2 suggests that BPC 157 has vascularising properties, a mechanism that may underlie its ability to regulate ischaemic/recongestive injury

Autosomal-recessive iron deficiency anemia, dystonia and hypermanganesemia caused by new variant mutation of the manganese transporter gene SLC39A14

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[3] Research published by the NIH: National Library of Medicine indicates that people with MTHFR mutations may require higher folate intake to maintain optimal homocysteine levels and overall methylation processes.[4] A study in JAMA Psychiatry suggested an association of individuals with MTHFR function and reports of mood