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ATP-based therapy prevents vascular calcification and extends longevity in a mouse model of Hutchinson–Gilford progeria syndrome

Pyrophosphate deficiency may explain the excessive vascular calcification found in children with Hutchinson–Gilford progeria syndrome (HGPS) and in a mouse model of this disease. The present study found that hydrolysis products of ATP resulted in a <9% yield of pyrophosphate in wild-type blood an...

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Publicat a:Proc Natl Acad Sci U S A
Autor principal: Villa-Bellosta, Ricardo
Format: Artigo
Idioma:Inglês
Publicat: National Academy of Sciences 2019
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6876227/
https://ncbi.nlm.nih.gov/pubmed/31690656
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1910972116
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