Results 101 to 110 of about 33,309 (204)
HADHA K406 lactylation fuels fatty acid β‐oxidation and HMGCR‐dependent cholesterol biosynthesis, fostering immunosuppressive MDSCs and exhausted CD8+ T cells in gastric cancer. Loss of this modification blocks cholesterol production, remodels the tumor microenvironment, and tumor growth is suppressed via combined inhibition of HMGCR and LDHA ...
Maoxiao Feng +10 more
wiley +1 more source
Nicotinamide adenine dinucleotide (NADH) is a cofactor that serves to shuttle electrons during metabolic processes such as glycolysis, the tricarboxylic acid cycle, and oxidative phosphorylation (OXPHOS).
Kathryn M. Priest +5 more
doaj +1 more source
Redox systems including extracellular cysteine/cystine (Cys/CySS), intracellular glutathione/oxidized glutathione (GSH/GSSG) and nicotinamide adenine dinucleotide reduced/oxidized forms (NADH/NAD+) are critical for maintaining redox homeostasis. Aging as
Yue Dong +3 more
doaj +1 more source
During NETosis, neutrophils shift metabolically toward enhanced OXPHOS and partially reduced glycolysis. This shift is driven by PDHA1 hyperactivity‐dependent selective metabolic reprogramming. The neutrophil‐targeted nanoparticle 3‑FP‑BSA NPs effectively inhibit NETosis and attenuate ALI.
Yu‐Biao Liu +14 more
wiley +1 more source
Reversible enzyme-catalysed NAD(+)/NADH electrochemistry [PDF]
Formate dehydrogenase (FdsDABG) from Cupriavidus necator is a Mo-containing enzyme capable of catalysing both formate oxidation to CO(2) and the reverse CO(2) reduction to formate by utilising NAD(+) or NADH, respectively. This enzyme is part of the NADH
Bernhardt, Paul V +6 more
core +1 more source
This review presents a pathology‐driven framework unifying nanomedicine across TBI, SCI, and PNI. Epidemiological evidence and comparative single‐cell transcriptomic reanalysis define shared pathological modules, injury‐specific effectors, and therapeutic bottlenecks. Six functional paradigms connect nanomaterial structure and biological fate to injury‐
Mouyuan Sun +12 more
wiley +1 more source
Recent Progress in Research of NADH Oxidase
nAdH氧化酶是一类催化nAdH氧化为nAd+并消耗氧气的氧化还原酶,因其能够再生nAd+而成为人工调控微生物代谢流向的重要调控酶.文中综述了nAdH氧化酶的分类、理化性质、反应机制,并分析nAdH氧化酶清除细胞内氧毒性、介入细胞代谢过程,以及调节细胞生理和代谢等重要的生理功能.NADH oxidase is a kind of oxidoreductase which catalyzes the oxidation conversion from NADH to NAD+ along with the
方柏山, 卿三红
core
Intracellular FAD, NAD and NADH rise following irradiation.
Cells were irradiated with 10 Gy or left untreated and incubated for 24 h before harvest and FAD or NAD/NADH assay. A) range of FAD concentrations per 1 million DC2.4. cells (n = 3), B) Mean NADH concentration per 1million cells (n = 2±s.d.), C) mean NAD
Keisuke S. Iwamoto (331733) +2 more
core +1 more source
A compact Phe‐Cys‐Pro‐Phe (FCPF) tag and an environment‐sensitive SBD‐Cl‐derived probe form a sequence‐selective fluorogenic pair for wash‐free live‐cell protein imaging. This minimally perturbing chemistry allows flexible insertion at termini or loops, produces strong fluorescence upon local microenvironment confinement, supports FRET‐assisted ...
Xiao Wang +11 more
wiley +1 more source
Tools for controlled selenol delivery are crucial for exploring Se‐related biology and medicine, but compound platforms for triggerable release of CH3SeH remain lacking. Herein, we report the first general triggered platform (TD‐MSe) for efficient cyclization release of CH3SeH in live cells.
Wenfang Liang +7 more
wiley +1 more source

