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期刊名:Genetics research

缩写:GENET RES

ISSN:0016-6723

e-ISSN:1469-5073

IF/分区:1.4/Q4

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共收录本刊相关文章索引448
Beina Liu,Rong Wang,Ying He Beina Liu
Purpose: The transcriptional regulatory factors binding to the polymorphic site C-1888T in the promoter region of the palate, lung, and nasal epithelium clone (PLUNC) gene were identified to investigate whether the C-1888T polymorphic site ...
Kun Chen,Lei Pu,Yuzuo Hui Kun Chen
Backgrounds: Glioma stands as one of the most formidable brain tumor types, with patient outcomes remaining bleak even in the face of advancements in treatment modalities. FBXW4, a constituent of the F-box and WD repeat d...
Dongqian Li,Qian Bao,Shiqi Ren et al. Dongqian Li et al.
Background: Hepatocellular carcinoma (HCC), ranking as the second-leading cause of global mortality among malignancies, poses a substantial burden on public health worldwide. Anoikis, a type of programmed cell death, serv...
Junxiao Yu,Bowen Zhao,You Yu Junxiao Yu
Background: Clear cell renal cell carcinoma (ccRCC) is a renal cortical malignancy with a complex pathogenesis. Identifying ideal biomarkers to establish more accurate promising prognostic models is crucial for the surviv...
Jiayan Zhang,Qinghan Jiao,Zhigang Chen Jiayan Zhang
Backgroundsand Aims. Colorectal cancer (CRC) represents a major global health challenge, necessitating comprehensive investigations into its underlying molecular mechanisms to enhance diagnostic and therapeutic strategies. This study focuse...
Yinghong Wu,Wenjie Hu,Zhihong Jia et al. Yinghong Wu et al.
Esophageal cancer is a major global health challenge with a poor prognosis. Recent studies underscore the extracellular matrix (ECM) role in cancer progression, but the full impact of ECM-related genes on patient outcomes remains unclear. O...
Yao Zhou,Xingju Zheng,Zhucheng Sun et al. Yao Zhou et al.
Bladder cancer has recently seen an alarming increase in global diagnoses, ascending as a predominant cause of cancer-related mortalities. Given this pressing scenario, there is a burgeoning need to identify effective biomarkers for both th...
Natalia Nunes,Beatriz Carvalho Nunes,Malú Zamariolli et al. Natalia Nunes et al.
22q11.2 deletion syndrome (22q11.2DS) is a microdeletion syndrome with a broad and heterogeneous phenotype, even though most of the deletions present similar sizes, involving ∼3 Mb of DNA. In a relatively large population of a Brazilian 22...
Maria Tizu,Bogdan Calenic,Mihai Hârza et al. Maria Tizu et al.
Materials and methods: This study included 66 patients with CLL, diagnosed between 2020 and 2022, and 100 healthy controls. HLA class I and class II genes (HLA-A/B/C, HLA-DQA1/DQB1/DPA1/DPB1, and HLA-DRB1/3/4/5) were inve...
Fee Faysal Ahmed,Farah Sumaiya Dola,Md Shohel Ul Islam et al. Fee Faysal Ahmed et al.
Lectin receptor-like kinases (LecRLKs) are a significant subgroup of the receptor-like kinases (RLKs) protein family. They play crucial roles in plant growth, development, immune responses, signal transduction, and stress tolerance. However...