Metabolomics‐based identification of metabolic alterations in PARK2

OBJECTIVE: Parkin is the causative gene for autosomal recessive familial Parkinson's disease (PD), although it remains unclear how parkin dysfunction is involved with the general condition. Recently, serum and/or plasma metabolomics revealed alterations in metabolic pathways that might reflect...

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Shranjeno v:
Bibliografske podrobnosti
izdano v:Ann Clin Transl Neurol
Main Authors: Okuzumi, Ayami, Hatano, Taku, Ueno, Shin‐Ichi, Ogawa, Takashi, Saiki, Shinji, Mori, Akio, Koinuma, Takahiro, Oji, Yutaka, Ishikawa, Kei‐Ichi, Fujimaki, Motoki, Sato, Shigeto, Ramamoorthy, Sivapriya, Mohney, Robert P., Hattori, Nobutaka
Format: Artigo
Jezik:Inglês
Izdano: John Wiley and Sons Inc. 2019
Teme:
Research Articles
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC6414487/
https://ncbi.nlm.nih.gov/pubmed/30911576
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/acn3.724
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