Oxygen consumption and biosynthetic function in perfused liver from rats at different stages of development. [PDF]
IOSSA, SUSANNA +3 more
core +1 more source
A Human Model of Oligodendrocyte Development Shows MCL‐1 Influences Oligodendrocyte Morphogenesis
A unified model of oligodendrocyte differentiation from human embryonic stem cells revealed that MCL‐1 is critical for regulating the expression of oligodendrocyte‐related genes and the morphogenesis of myelinating oligodendrocytes. ABSTRACT Oligodendrocytes are the myelinating cells of the central nervous system.
Melanie Gil +2 more
wiley +1 more source
Effect of oral l-carnitine on hepatic function in pediatric patients under repair of congenital cardiac defect. [PDF]
Memari B, Fani K, Dabbagh A, Parast ARV.
europepmc +1 more source
Sertraline‐Associated Riboflavin‐Responsive Lipid Storage Myopathy: Report of Two Case
Sertraline exposure can lead to an acquired riboflavin‐responsive multiple acyl‐CoA dehydrogenase deficiency (MADD). In patients with this acquired form of MADD, riboflavin supplementation can even lead to full clinical recovery and marked serological recovery before discontinuation of sertraline.
Aziz Shaibani, Alexis Taylor
wiley +1 more source
Massive Valproic Acid Overdose With Confirmed Pharmacobezoar Formation and Neuromuscular Toxicity: A Case Report and Literature Review. [PDF]
Alrazooqi MK +3 more
europepmc +1 more source
Carnitine supplementation induces long‐chain acylcarnitine production—Studies in the VLCAD‐deficient mouse [PDF]
Michaela Liebig +8 more
openalex +1 more source
ABSTRACT Aim Acyl‐CoA binding protein plays a vital role in lipid metabolism by mediating the intracellular flux and utilization of long‐chain acyl‐CoAs. We generated an adipocyte‐wide ACBP knockout mouse and a brown adipose tissue‐specific ACBP knockout mouse to investigate ACBP function in adipose tissue.
M. F. Nørremark +13 more
wiley +1 more source
Effects of Insect Cuticular Compounds on Appressorium Formation and Metabolic Activity in <i>Beauveria bassiana</i>. [PDF]
Chen J +6 more
europepmc +1 more source
Abstract Maternally inherited diabetes and deafness (MIDD) is a mitochondrial disorder usually caused by the variant m.3243A>G in the MT‐TL1 gene. We have proposed that diabetes in MIDD arises from a combination of insulin resistance and impaired β‐cell function that is more likely to occur in the presence of high skeletal muscle heteroplasmy and ...
Ahsen Chaudhry +2 more
wiley +1 more source

