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Decreased GSH content in the apical fluid in cystic fibrosis could be the result of abnormal GSH transport associated with a defective cystic fibrosis transmembrane conductance regulator as mentioned previously (126)
If were not seeing the results were hoping for, we have to think about what else might be effective for that patient, Dr
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Oral administration: BPC-157 exhibits unique gastric stability among peptides, making oral administration possible for this specific component
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