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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
 197
  访问来源
    内部： 2
    外部： 195
    国内： 176
    国外： 21

  年访问量
 45
  访问来源
    内部： 0
    外部： 45
    国内： 39
    国外： 6

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

访问量

访问量

1. Sequence-based drug design as a concept in computational drug desi.. [587]
2. 143D, a novel selective KRASG12C inhibitor exhibits potent antitum.. [347]
3. Design, Synthesis, and Biological Evaluation of Potent and Selecti.. [340]
4. Targeting STING oligomerization with licochalcone D ameliorates ST.. [294]
5. Recent advances in targeted degradation in the RAS pathway [57]
6. Discovery of 3‑(Fluoro-imidazolyl)pyridazine Derivatives as Poten.. [21]

下载量

1. Sequence-based drug design as a concept in computational drug desi.. [213]
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]