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成果统计

合作作者[TOP 5]

  • Zhang, Sulin

    合作成果数：5

  • 樊子生

    合作成果数：4

  • Cui, Rongrong

    合作成果数：3

  • 蒋华良

    合作成果数：2

  • 周敬怡

    合作成果数：2

访问统计


  总访问量
 199
  访问来源
    内部： 2
    外部： 197
    国内： 177
    国外： 22

  年访问量
 47
  访问来源
    内部： 0
    外部： 47
    国内： 40
    国外： 7

  月访问量
 3
  访问来源
    内部： 0
    外部： 3
    国内： 2
    国外： 1

访问量

访问量

1. Sequence-based drug design as a concept in computational drug desi.. [591]
2. 143D, a novel selective KRASG12C inhibitor exhibits potent antitum.. [351]
3. Design, Synthesis, and Biological Evaluation of Potent and Selecti.. [347]
4. Targeting STING oligomerization with licochalcone D ameliorates ST.. [301]
5. Recent advances in targeted degradation in the RAS pathway [60]
6. Discovery of 3‑(Fluoro-imidazolyl)pyridazine Derivatives as Poten.. [24]

下载量

1. Sequence-based drug design as a concept in computational drug desi.. [216]
2. Design, Synthesis, and Biological Evaluation of Potent and Selecti.. [15]
3. Targeting STING oligomerization with licochalcone D ameliorates ST.. [5]
4. Discovery of 3‑(Fluoro-imidazolyl)pyridazine Derivatives as Poten.. [5]
5. 143D, a novel selective KRASG12C inhibitor exhibits potent antitum.. [4]
6. Recent advances in targeted degradation in the RAS pathway [3]