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期刊名:Oncogenesis

缩写:ONCOGENESIS

ISSN:2157-9024

e-ISSN:2157-9024

IF/分区:6.4/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
Inés Romero-Pérez,Elena Díaz-Rodríguez,Laura Sánchez-Díaz et al. Inés Romero-Pérez et al.
Neratinib is a tyrosine kinase inhibitor that is used for the therapy of patients with HER2+ breast tumors. However, despite its clinical benefit, resistance to the drug may arise. Here we have created cellular models of neratinib resistanc...
Weidong Peng,Haojie Zhang,Mingwei Yin et al. Weidong Peng et al.
Bladder cancer is characterized by aberrant activation of the phosphatidylinositol-3-OH kinase (PI3K) signaling, underscoring the significance of directing therapeutic efforts toward the PI3K pathway as a promising strategy. In this study, ...
Merel Elise van Luyk,Ana Krotenberg Garcia,Maria Lamprou et al. Merel Elise van Luyk et al.
Adult tissues set the scene for a continuous battle between cells, where a comparison of cellular fitness results in the elimination of weaker "loser" cells. This phenomenon, named cell competition, is beneficial for tissue integrity and ho...
Shuang Li,Lina Yang,Xiaoyan Ding et al. Shuang Li et al.
The regulatory significance of ubiquitin-specific peptidase 32 (USP32) in tumor is significant, nevertheless, the biological roles and regulatory mechanisms of USP32 in non-small cell lung cancer (NSCLC) remain unclear. According to our res...
Toshinori Ando,Kento Okamoto,Yume Ueda et al. Toshinori Ando et al.
The Hippo pathway and its downstream effectors, Yes-associated protein/transcriptional coactivator with PDZ-binding motif (YAP/TAZ), are essential for cell growth and organ development. Emerging evidence revealed that the Hippo pathway and ...
Anne M van Harten,Ronak Shah,D Vicky de Boer et al. Anne M van Harten et al.
Fanconi anemia (FA) is a rare hereditary disease resulting from an inactivating mutation in the FA/BRCA pathway, critical for the effective repair of DNA interstrand crosslinks (ICLs). The disease is characterized by congenital abnormalitie...
Giovana Carrasco,Ifigeneia Stavrou,Mairi Treanor-Taylor et al. Giovana Carrasco et al.
Kindler syndrome (KS) is a rare genodermatosis resulting from loss-of-function mutations in FERMT1, the gene that encodes Kindlin-1. KS patients have a high propensity to develop aggressive and metastatic cutaneous squamous cell carcinoma (...
Jiazhong Guo,Yunpeng Zhao,Huacong Sui et al. Jiazhong Guo et al.
Lacking effective therapeutic targets heavily restricts the improvement of clinical prognosis for patients diagnosed with esophageal squamous cell carcinoma (ESCC). Ubiquitin Specific Peptidase 21 (USP21) is dysregulated in plenty of human ...
Abhibhav Sharma,Julia Debik,Bjørn Naume et al. Abhibhav Sharma et al.
Breast cancer (BC) is a leading cause of cancer-related death worldwide. The diverse nature and heterogeneous biology of BC pose challenges for survival prediction, as patients with similar diagnoses often respond differently to treatment. ...
Meng Gao,Hang Dong,Siyi Jiang et al. Meng Gao et al.
The hypercoagulable state is a hallmark for patients with multiple myeloma (MM) and is associated with disease progression. Activated platelets secrete exosomes and promote solid tumor growth. However, the role of platelet-derived exosomes ...