Results 81 to 90 of about 2,082 (136)

Cuproptosis-related genes associated with mitochondrial dysfunction in Parkinson's disease. [PDF]

PLoS One
Liu T, Li J, Zhang J, Wei J.
europepmc   +1 more source

Comparative analysis of mitochondrion-related organelles in anaerobic amoebozoans. [PDF]

Microb Genom, 2023
Záhonová K, Füssy Z, Stairs CW, Leger MM, Tachezy J, Čepička I, Roger AJ, Hampl V.   +7 more
europepmc   +1 more source

A missense mutation in PDHB gene: identification of the patient with pyruvate dehydrogenase deficiency and demonstration of pathogenicity in vitro. [PDF]

Ital J Pediatr
Li Y, Cheng L, Li X, Liu J, Yi L, Bo T.
europepmc   +1 more source

Integrated amplification of NADPH-regenerating modules enhances cytidine biosynthesis in <i>Escherichia coli</i>. [PDF]

Synth Syst Biotechnol
Liu L, Zhang X, Zhu T, Ye T, Li Z, Ding W, Liu H, Fang H.   +7 more
europepmc   +1 more source

Insights into Active Site Cysteine Residues in <i>Mycobacterium tuberculosis</i> Enzymes: Potential Targets for Anti-Tuberculosis Intervention. [PDF]

Int J Mol Sci
Faponle AS, Gauld JW, de Visser SP.
europepmc   +1 more source

Biosynthesis of Glycine from One-Carbon Resources Using an Engineered Escherichia coli Whole-Cell Catalyst. [PDF]

Microorganisms
Fu M, Shi H, Bai X, Gao Q, Liu F, Li D, Kan Y, Xue C, Yao L, Tang C.   +9 more
europepmc   +1 more source

Indazole to 2-Cyanoindole Scaffold Progression for Mycobacterial Lipoamide Dehydrogenase Inhibitors Achieves Extended Target Residence Time and Improved Antibacterial Activity. [PDF]

Angew Chem Int Ed Engl
Sun S, Ginn J, Kochanczyk T, Arango N, Jiang X, Huggins DJ, Bean J, Michino M, Baxt L, Liverton N, Meinke PT, Bryk R.   +11 more
europepmc   +1 more source

Succinylation - encoded metabolic codes: cracking the molecular logic of cellular adaptation. [PDF]

Int J Surg
Cong Y, Zhang X, Wang Z, Cui Z, Li C, Han Y, Deng W, Zhou X, Wu H, Sun J, Fan H, Wu G.   +11 more
europepmc   +1 more source

Cuproptosis-related gene DLD expression correlates with the prognosis and tumor immune microenvironment in clear cell renal cell carcinoma. [PDF]

Discov Oncol
Qian C, He H, You G.
europepmc   +1 more source

Case Report: Biallelic variants in <i>MRPS36</i>, encoding a component of the 2-oxoglutarate dehydrogenase complex, cause leigh syndrome. [PDF]

Front Pediatr
Jiang H, Xu C, Liu Z, Duan R, Yao X, Fu X, Xu J, Kang X, Yu T, Wang Y, Fang F.   +10 more
europepmc   +1 more source