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Biochemical basis of prolidase deficiency. Polypeptide and RNA phenotypes and the relation to clinical phenotypes.

Cultured skin fibroblasts or lymphoblastoid cells from eight patients with clinical symptoms of prolidase deficiency were analyzed in terms of enzyme activity, presence of material crossreacting with specific antibodies, biosynthesis of the polypeptide, and mRNA corresponding to the enzyme. There ar...

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Publicado no:J Clin Invest
Principais autores: Endo, F, Tanoue, A, Kitano, A, Arata, J, Danks, D M, Lapière, C M, Sei, Y, Wadman, S K, Matsuda, I
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Clinical Investigation 1990
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC296401/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1688567/
https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI114407
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