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Jyotsna Suresh Ranbhise,Manish Kumar Singh,Songhyun Ju et al. Jyotsna Suresh Ranbhise et al.
These defenses maintain redox homeostasis and sustain oncogenic signaling, notably through the oxidative inactivation of tumor-suppressor phosphatases, such as PTEN, which drives the PI3K/AKT/mTOR pathway.
Tianyi Luo,Xiaohu Dai,Yuting Zhang et al. Tianyi Luo et al.
Antibiotic resistance genes (ARGs) and antibiotic resistant bacteria (ARB) are emerging environmental contaminants that threaten public health, highlighting the urgent need for effective control strategies. Ferrate (Fe(VI)), a strong and ec...
Taylor C Outlaw,Amy T R Robison,Natalie B Schulte et al. Taylor C Outlaw et al.
Although the anaerobic binding of Cu+ or Ag+ moderately diminishes catalytic turnover, these ions sensitize the protein to rapid and complete oxidative inactivation in the presence of oxygen. Oxidative modification of the active site cysteine, including glutathionylation, is reversible.
Pouya Sobhifar,David R Brown Pouya Sobhifar
Loss-of-function of DJ-1 was reported to cause familial PD, and oxidative inactivation of DJ-1 has been observed in sporadic cases, suggesting that both genetic and post-translational events converge on common disease pathways.
Syed Musheer Mohammed Aalam,Megan L Ritting,Hari Ps et al. Syed Musheer Mohammed Aalam et al.
In mammary gland, phosphorylation of the antioxidant enzyme PRDX1 is selectively detected in LPs, consistent with a floodgate model of redox signaling in which transient oxidative inactivation of peroxiredoxins (PRDXs) facilitates RTK signaling under elevated intracellular reactive oxygen species conditions
Arkajit Guha,Ruma Banerjee Arkajit Guha
The enzyme is susceptible to oxidative inactivation and is repaired by methionine synthase reductase (MTRR) in the presence of NADPH and S-adenosylmethionine (AdoMet).
Raunak Raunak,Roopshali Rakshit,Aayush Bahl et al. Raunak Raunak et al.
The recombinant protein exhibited distinctive kinetic properties, characterized by higher substrate affinity yet increased susceptibility to oxidative inactivation compared to its M. tuberculosis counterpart.
Jonas Thomsen,Signe Lett,Helle J Martens et al. Jonas Thomsen et al.
With an iron content of 2 g/kg dry peat, oxidative inactivation of enzymes is an important factor to take into account....A high inactivation constant of 125.91 x10-3 h-1 was found for the used saccharification conditions, but the addition of catalase alleviated the oxidative inactivation and increased the glucose yield with 60% in peat pretreated at 180 °C.
Frances Jourd&#x;heuil,Clinton Mathai,Le Gia Cat Pham et al. Frances Jourd&#x;heuil et al.
In addition, the ectopic expression of cytoglobin in cultured cells limited the inhibitory effect of H2O2 on glycolysis and reversed the oxidative inactivation of the glycolytic enzyme GAPDH. Cytoglobin facilitated the reduction of the thiol-based H2O2 sensor Hyper7 after H2O2 challenge.
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