X Ma, X Li, W Wang, M Zhang, B Yang… - Frontiers in aging …, 2022 - frontiersin.org
Phosphatidylserine (PS) is an anionic phospholipid in the eukaryotic membrane and is abundant in the brain. Accumulated studies have revealed that PS is involved in the multiple …
A Nishi, S Numata, A Tajima, M Kinoshita… - Schizophrenia …, 2014 - academic.oup.com
Previous studies suggest that elevated blood homocysteine levels and the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism are risk factors for …
Schizophrenia and depression are two common and debilitating psychiatric conditions. Up to 61% of schizophrenic patients have comorbid clinical depression, often undiagnosed …
M Hussain, I Khan, MN Chaudhary, K Ali… - Chemistry and Physics …, 2024 - Elsevier
Phosphatidylserine (PtdS) is classified as a glycerophospholipid and a primary anionic phospholipid and is particularly abundant in the inner leaflet of the plasma membrane in …
D Wang, JX Zhai, DW Liu - Psychiatry research, 2016 - Elsevier
To clarify the relationship between serum folate and schizophrenia (SZ) risk, the meta- analysis was conducted. PubMed, Embase, and Web of Science were searched without …
LR Solomon - European journal of clinical nutrition, 2015 - nature.com
Results: When no oxidant risks were present, older subjects (⩾ 70 years) had higher metabolite values than younger individuals (< 70 years). MMA values were even higher in …
The value of HDL genetics : Current Opinion in Lipidology The value of HDL genetics : Current Opinion in Lipidology Log in or Register Subscribe to journalSubscribe Get new issue alertsGet …
A Coşar, OM İpçioğlu, Ö Özcan… - Turkish Journal of …, 2014 - journals.tubitak.gov.tr
The term'one-carbon metabolism'is commonly used to describe 3 separate metabolic processes: folate metabolism, the homocysteine remethylation cycle, and the …
L Miao, RX Yin, F Huang, WX Chen, XL Cao, JZ Wu - Oncotarget, 2017 - ncbi.nlm.nih.gov
Aim This study aimed to detect the association of the mevalonate kinase (MVK) and methylmalonic aciduria (cobalamin deficiency) cblB type (MMAB) gene variants, their …