Results 261 to 270 of about 99,240 (382)
Proteome Analysis of Corynebacterium diphtheriae–Macrophage Interaction
ABSTRACT Contact of Corynebacterium diphtheriae with macrophages induces adaptations on both bacterial and cellular sides. The study presented here was aiming to shed light on the simultaneous intracellular adaptation of the bacteria and changes in the proteome of the phagocytes in response to the internalization of C. diphtheriae.
Luca Musella+6 more
wiley +1 more source
Homocysteine induced N<sup>6</sup>-methyldeoxyadenosine modification perturbation elicits mitochondria dysfunction contributes to the impairment of learning and memory ability caused by early life stress in rats. [PDF]
Zhang L+9 more
europepmc +1 more source
Quantitative Determination of Coenzyme A by Sorbyl Coenzyme A Formation
Salih J. Wakil, George Hübscher
openaire +2 more sources
ABSTRACT Bacterial ferredoxins are small iron–sulfur binding proteins that function as soluble electron shuttles between redox enzymes in the cell. Their simple 2×(β–α–β) fold, central metabolic function, and ubiquity across all kingdoms of life have led to the proposal that ferredoxins were likely among the earliest proteins.
Jan A. Siess, Vikas Nanda
wiley +1 more source
The Biosynthesis of β-Hydroxy-β-methylglutaryl Coenzyme A in Yeast
Peter R. Stewart, Harry Rudney
openalex +1 more source
The SIRT1 N‐Terminal Domain as a Common Binding Interface for PPARγ Anchoring
ABSTRACT Insulin resistance, a global health threat linked to type 2 diabetes and obesity, can be addressed by modulating the activity of the Sirtuin 1 (SIRT1), a deacetylase that enhances insulin sensitivity by deacetylating the Peroxisome Proliferator‐Activated Receptor Gamma (PPARγ) at lysine 268 and 293. Understanding the binding interfaces between
Caique Camargo Malospirito+7 more
wiley +1 more source
Succinyl Coenzyme A Synthetase from Escherichia coli
John A. Grunau+3 more
openalex +1 more source
ABSTRACT Transport and Golgi Organization 2 Homolog (TANGO2) protein deficiency disorder (TDD) is a rare autosomal recessive disorder characterized by multi‐systemic abnormalities and significant phenotypic variability including neurodevelopmental delay, seizures, intermittent ataxia, hypothyroidism, rhabdomyolysis, life‐threatening metabolic ...
Anne Cooper+6 more
wiley +1 more source
The effects of mitochondrial damage and energy metabolism disorders on the progression of noise-induced deafness and its treatment. [PDF]
Xu L, Jiang H.
europepmc +1 more source