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期刊名:Cell death & disease

缩写:CELL DEATH DIS

ISSN:2041-4889

e-ISSN:2041-4889

IF/分区:9.6/Q1

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Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Tianxu Guo,Han Liu,Junjun Ma et al. Tianxu Guo et al.
The Six1 (SIX homeobox 1) gene is pivotal in renal and pulmonary development and differentiation. Its dysregulation is implicated in oncogenesis and tumor progression via enhancing cell proliferation and delaying senescence. However, whethe...
Qian-Hui Gu,Xiao-Ren Zhu,Jian-Zhuo Jiang et al. Qian-Hui Gu et al.
Identifying novel therapeutic targets for pancreatic cancer (PC) is crucial for improving patient outcomes. This study identified the functions, expression, and associated mechanisms of adhesion G protein-coupled receptor G6 (ADGRG6/ GPR126...
Xuefei Shi,Qiuhui Li,Fengqi Nie et al. Xuefei Shi et al.
Lung adenocarcinoma is one of the most common forms of lung cancer with a low five-year survival rate. The roles of the novel proteins and peptides encoded by circular RNAs (circRNAs) in cancer are emerging. However, the functions and under...
Feiyang Cai,Fan Huang,Christophe Goncalves et al. Feiyang Cai et al.
BRAF V600 inhibitors are clinically approved for the treatment of BRAFV600-mutant melanoma in combination with a MEK inhibitor, but are ineffective in other melanoma subtypes. Moreover, pan-RAF inhibitors, such as belvarafenib, when combine...
Xin-Ren Yu,Yu-Bing Wang,Zhi-Yi Tu et al. Xin-Ren Yu et al.
The special AT-rich sequence-binding protein 2 (SATB2) is associated with human cognitive ability. Mutations in the SATB2 gene lead to SATB2-associated syndrome (SAS), characterized by severe intellectual disability. SATB2 is mainly express...
Xianwen Wang,Qihang Huang,Zhihong Zuo et al. Xianwen Wang et al.
Sepsis disproportionately affects older adults and children, two immunologically vulnerable extremes of age. Yet sepsis is superimposed on distinct baselines-immunosenescence in the elderly and immune immaturity in neonates and young childr...
Qian Zhou,Guangsen Xu,Zhuoran Li et al. Qian Zhou et al.
BCR-ABL1, derived from structural chromosome rearrangements, is the driver mutation in chronic myeloid leukemia (CML). Targeting BCR-ABL1 for degradation is an ideal therapeutic strategy for CML, however, the regulatory mechanisms controlli...
Maciej Wakula,Milena Jablonowska,Mateusz Chmielarczyk et al. Maciej Wakula et al.
Molecular mechanisms underlying congenital neutropenia in patients with HAX1 deficiency are not clear at the moment. HAX1 deficiency was shown to result in the arrest of neutrophil differentiation. Our studies of the effect of HAX1 deficien...