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基因与疾病(英文)
基因与疾病(英文)
基因与疾病(英文)/Journal Genes & DiseasesCSCD
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    Rare dentin defects:Understanding the pathophysiological mechanisms of COLXVA1 mutations

    Isaac Maximiliano BuguenoTristan ReyAlexandra Jimenez-ArmijoMarzena Kawczynski...
    1-5页

    Proteomic analysis of urinary exosomes reveals ferroptosis-associated proteins are involved in diabetic nephropathy

    Kaida MuYanping YangXiaofei AnJie Zhu...
    6-8页

    MACF1 deficiency suppresses tooth mineralization through IGF1 mediated crosstalk between odontoblasts and ameloblasts

    Wuxia QiuXiao LinShaoqing YangZhihao Chen...
    9-12页

    Acyl-CoA thioesterase 7 is oncogenic in breast cancer by promoting oxidative phosphorylation via PGC1α

    Xiangyu SunQiang ZhangMozhi WangLitong Yao...
    13-16页

    Clinical and genetic heterogeneity of adult polyglucosan body disease caused by GBE1 biallelic mutations in China

    Yikun ChenYan ShiYuan GaoYan Hu...
    17-20页

    A novel copper metabolism-related signature model for predicting the prognosis,target drugs,and immunotherapy in stomach adenocarcinoma

    Kai ZhuangSiqi TangHaixin FengJinying Zhang...
    21-24页

    SPNS1 ablation drives skeletal muscle atrophy by disrupting mitophagy,mitochondrial function,and apoptosis in mice

    Xianzhong ZhangFengmin ZhangHaofan WuZhen Yu...
    25-28页

    A new autophagy-related nomogram and mechanism in multiple myeloma

    Hanying HuangYang LiZiang ZhuYang Liu...
    29-32页

    Neurokinin-2 receptor antagonist SR48968 induced necroptosis of myeloid leukemia cells by calcium overload-driven reactive oxygen species accumulation

    Zhibin YanXiangyu HongQihao LinLeijie Wang...
    33-35页

    MAL2 DNA methylation serves as a biomarker for the diagnosis and prognosis of glioma

    Hao LuoXing XiaoWeiliang HouJing Cai...
    36-39页