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CYBB Gene - maayanlab.cloud
CYBB deficiency is one of five described biochemical defects associated with chronic granulomatous disease (CGD). In this disorder, there is decreased activity of phagocyte …
Therefore, our results identify a Zeb1-microRNA-96/182-Cybb pathway that controls cross-presentation in cDC1 and uncover an essential role of Zeb1 in cDC1 homeostasis. Dendritic …
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慢性肉芽肿病 - 百度百科
性联 隐性遗传 的慢性肉芽肿病的各亚型均是由于编码细胞色素b的qp91-phox亚单位基因突变引起，该基因被命名为 CYBB (MIM306400)，含有13个 外显子，位于X染色体xp21.1，约占30kb …
2023年11月3日 · facilitated its survival by inducing CYBB-mediated macrophage ferroptosis leading to its alternative activation and might reveal the potential for a new therapeutic strategy …
A C126R de novo Mutation in CYBB Leads to X-linked Chronic ...
2018年9月11日 · Genetic analysis revealed a de novo mutation in exon 5 of the CYBB gene: a single-nucleotide substitution, c.376T > C, leading to a C126R change. Keywords: chronic …
NADPH Oxidase Subunit CYBB Confers Chemotherapy and …
Herein, we demonstrated that a subunit of NADPH oxidase, CYBB, orchestrated mesenchymal shift and promoted TMZ resistance by modulating the anti-ferroptosis circuitry Nrf2/SOD2 axis. …
CYBB Polyclonal Antibody-Elabscience伊莱瑞特【官网】
Cytochrome b (-245) is composed of cytochrome b alpha (CYBA) and beta (CYBB) chain.It has been proposed as a primary component of the microbicidal oxidase system of …
Scavenging of superoxide by a membrane bound superoxide …
Here we show that CybB from E. coli functions as a superoxide:ubiquinone oxidoreductase, performing a previously undescribed enzymatic reaction in which superoxide is directly …
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