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Frontiers of Medicine
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Identification of novel mutations in and in a family with craniofacial microsomia: evidence of digenic inheritance
family craniofacial microsomia,Identification novel mutations
Frontiers of Medicine
2023.17(5) 1006-1009
Treatment of advanced non-small cell lung cancer with driver mutations: current applications and future directions
non-small cell lung cancer, driver mutations, treatment strategy, resistant mechanism, immune-checkpoint inhibitors
Frontiers of Medicine
2023.17(1) 18-42
Distinct gene expression pattern of mutations coordinated by target repression and promoter hypermethylation in acute myeloid leukemia
RUNX1
, gene mutation, acute myeloid leukemia, transcriptional repression, DNA methylation
Frontiers of Medicine
2022.16(4) 627-636
Genomic Mutations within the Host Microbiome: Adaptive Evolution or Purifying Selection
Review
Jiachao Zhang Rob Knight
Gut microbiota,Genomic mutations,Adaptive evolution,Purifying selection,Single-nucleotide variants
Engineering
2023.20(1) 96-102
Emerging molecular subtypes and therapeutic targets in B-cell precursor acute lymphoblastic leukemia
Jianfeng Li Yuting Dai Liang Wu Ming Zhang Wen Ouyang Jinyan Huang Saijuan Chen
BCP-ALL,subtypes,translocation,aneuploidy,sequence mutations,
Frontiers of Medicine
2021.15(3) 347-371
Research progress on human infection with avian influenza H7N9
Xiaoxin Wu Lanlan Xiao Lanjuan Li
H7N9,pandemic,epidemiology,mutations,vaccine,influenza,
Frontiers of Medicine
2020.14(1) 8-20
Characteristics of compensatory mutations in the
Shengfen Wang Yang Zhou Bing Zhao Xichao Ou Hui Xia Yang Zheng Yuanyuan Song Qian Cheng Xinyang Wang Yanlin Zhao
tuberculosis,drug resistance,compensatory mutations,transmission,
Frontiers of Medicine
2020.14(1) 51-59
Clinical characterization and diagnosis of cystic fibrosis through exome sequencing in Chinese infants with Bartter-syndrome-like hypokalemia alkalosis
Liru Qiu Fengjie Yang Yonghua He Huiqing Yuan Jianhua Zhou
cystic fibrosis,pseudo-Bartter syndrome,hypokalemic alkalosis,
CFTR
gene,mutations,infants,diagnosis,
Frontiers of Medicine
2018.12(5) 550-558
Association of miRNA-122-binding site polymorphism at the interleukin-1 α gene and its interaction with hepatitis B virus mutations with hepatocellular carcinoma risk
Du Yan Han Xue Pu Rui Xie Jiaxin Zhang Yuwei Cao Guangwen
hepatocellular carcinoma (HCC),interaction,miRNA-122-binding site,IL-1A,rs3783553,hepatitis B virus (HBV) mutations
Frontiers of Medicine
2014.8(2) 217-226
Genetic evidence in planar cell polarity signaling pathway in human neural tube defects
Chunquan Cai Ouyan Shi
planar cell polarity,neural tube defects,rare mutations,
Frontiers of Medicine
2014.8(1) 68-78
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