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期刊名:Mutation research-fundamental and molecular mechanisms of mutagenesis

缩写:MUTAT RES-FUND MOL M

ISSN:0027-5107

e-ISSN:1873-135X

IF/分区:2.4/Q3

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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
Sai Priyankha,Dhanraj Ganapathy,Smitha Nair et al. Sai Priyankha et al.
Oral melanoma is a rare and aggressive subtype of melanoma that presents significant challenges in terms of delayed diagnosis and treatment. One promising clinical outcome is the detection of KIT gene mutations, which play a key role in tum...
Yuanqiang Zhang,Chunping Yang,Haowen Deng et al. Yuanqiang Zhang et al.
Background: Lung squamous cell carcinoma (LUSC) represents a distinct subtype of lung cancer, diverging significantly from lung adenocarcinoma. It demonstrates the ability to evade the immune system before the tumor has e...
Jixiang Lei,Xianyun Tang,Yuanchao Lin et al. Jixiang Lei et al.
Background: Curcumin exhibits significant antitumor activity, inhibiting proliferation, angiogenesis, invasion, and metastasis, highlighting its potential for cancer treatment. However, its mechanisms in Laryngeal and Pha...
Vinícius Bernardo de Oliveira,João Marcos Oliveira-Silva,Giovanna De Souza Maciel et al. Vinícius Bernardo de Oliveira et al.
Chromosomal instability (CIN) is a pervasive feature of cancer and a major driver of tumor heterogeneity, evolution, and therapeutic resistance. Arising predominantly from defects in chromosome segregation, DNA repair, and mitotic fidelity,...
Xinghui Li,Yannan Jiang,Yanxia Ding et al. Xinghui Li et al.
Background: Melanoma exhibits high malignancy with limited treatment options, while the newly defined type of programmed cell death, ferroptosis, presents a promising therapeutic avenue for melanoma. Notch2 has been impli...
Zeynep Özdemir-Pehlivan,Afife Büke,Ezgi Çevik-Demir et al. Zeynep Özdemir-Pehlivan et al.
Defects in homologous recombination repair genes contribute to hereditary cancer susceptibility beyond BRCA1 and BRCA2, yet clinical interpretation of intermediate-penetrance genes remains challenging. We retrospectively evaluated unrelated...
Amna Saeed,Riffat Iqbal,Mohammad Rahim et al. Amna Saeed et al.
TP53 mutation is one of the most frequently altered genetic variants leading to hepatocellular carcinoma (HCC). Single nucleotide polymorphisms (SNPs) in this gene play a crucial role in predicting the risk of HCC development. This study ai...
Muhammed Deniz Oksal,Turker Kilic,Timucin Avsar Muhammed Deniz Oksal
Glial tumors are the most common malignant brain tumors, and IDH1 serves as an important diagnostic and prognostic molecular marker in gliomas. The mutation status of IDH1 influences prognosis, patient survival, and treatment response in gl...
Sabnam Nasrin Choudhury,Tarikul Huda Mazumder,Sahidul Saikia et al. Sabnam Nasrin Choudhury et al.
Esophageal cancer (ESCA) ranks among the most lethal malignancies worldwide, with late-stage diagnosis, poor prognosis, and limited treatment options contributing to its high mortality. MicroRNAs (miRNAs), short non-coding RNAs with gene-si...
Yunhai Wei,Huancen Guo,Wenjing Hu et al. Yunhai Wei et al.
Background: Gastric cancer (GC) is a highly prevalent gastrointestinal malignancy with poor prognosis worldwide, and its initiation and progression are closely associated with tumor immune escape. Polygonum cuspidatum, a ...