Results 111 to 120 of about 1,678 (140)

Changes in the brain [NAD⁺]/[NADH] and [NADPH]/[NADP⁺] with aging and anti-aging dietary restriction. [PDF]

Front Aging Neurosci
Jamerson LE, Bradshaw TD, Bradshaw PC.
europepmc   +1 more source

Purinosomes spatially co-localize with mitochondrial transporters. [PDF]

J Biol Chem
Sha Z, Benkovic SJ.
europepmc   +1 more source

Clinical characteristics and genetic causes of unexplained pediatric liver disease. [PDF]

World J Hepatol
Chen Y, Wang ZY, Chen BQ, Qi YJ, Liu HY, Shi WX, Guo L, Liu Z, Sun LF.   +8 more
europepmc   +1 more source

Prevalence of common autosomal recessive and X-linked conditions in pregnant women in Vietnam: a cross-sectional study. [PDF]

Sci Rep
Nguyen TT, To HTT, Le ANT, Pham AQ, Nguyen ND, Ha HH, Vu HT, Hoang TT, Tran MC.   +8 more
europepmc   +1 more source

Glycolytic reprogramming in endometriosis: molecular mechanisms, immune modulation, and non-hormonal therapeutic opportunities. [PDF]

BMC Womens Health
Guo L, Liu L, Geng Y, Zhang B, Zhao S.
europepmc   +1 more source

The Emerging Role of N-Acetylaspartate in Cancer. [PDF]

Int J Mol Sci
Wu Y, Luo W, Yao L, Huang W, Liu S.
europepmc   +1 more source

Citrin deficiency-The East-side story. [PDF]

J Inherit Metab Dis
Häberle J.
europepmc   +1 more source

Transient Unexplained Severe Acute Hyperbilirubinaemia and Cholestasis in a Patient With Hereditary Spherocytosis. [PDF]

Case Reports Hepatol
Richardson J, Johnston M, Sefcick A, Oien K.   +3 more
europepmc   +1 more source

Identification of technically challenging variants: Whole-genome sequencing improves diagnostic yield in patients with high clinical suspicion of rare diseases. [PDF]

HGG Adv
Ng HY, Ma W, Lam WJ, Lau CS, Luk HM, Au LWC, Cheng SSW, Chong JSC, Ho S, Ma BM, Pang SYY, Hong Kong Genome Project, Chu ATW, Chung BHY.   +13 more
europepmc   +1 more source