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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6414487/
https://www.ncbi.nlm.nih.gov/pubmed/30911576
http://dx.doi.org/10.1002/acn3.724

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6414487/
https://www.ncbi.nlm.nih.gov/pubmed/30911576
http://dx.doi.org/10.1002/acn3.724

Ejemplares similares