Associated Papers
Genetic analysis and prenatal diagnosis of short-rib thoracic dysplasia 3 with or without polydactyly caused by compound heterozygous variants of DYNC2H1 gene in four Chinese families.
Fang Y et al.
Frontiers in Genetics, 2023
37007936 (PubMed )
Supplement: Table3.XLSX › Sheet1
eIF3a R803K mutation mediates chemotherapy resistance by inducing cellular senescence in small cell lung cancer.
Chen YX et al.
Pharmacological Research, 2021
Using plasma cell-free DNA to monitor the chemoradiotherapy course of cervical cancer.
Tian J et al.
International Journal of Cancer, 2019
Breast Cancer Risk-Associated SNPs in the mTOR Promoter Form De Novo KLF5- and ZEB1-Binding Sites that Influence the Cellular Response to Paclitaxel.
Chen Q et al.
Molecular Cancer Research : Mcr, 2019
The eIF3a Arg803Lys genetic polymorphism is associated with susceptibility to and chemoradiotherapy efficacy in cervical carcinoma.
Xu JZ et al.
The Kaohsiung Journal of Medical Sciences, 2017
Association between eIF3α polymorphism and severe toxicity caused by platinum-based chemotherapy in non-small cell lung cancer patients.
Xu X et al.
British Journal of Clinical Pharmacology, 2013
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