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Article title matches

  1. Category:L858r (36 bytes)
    1: List of pages with the keyword L858r

Page text matches

  1. 2j6m (6,222 bytes)
    26: ... that gefitinib binds 20-fold more tightly to the L858R mutant than to the wild-type enzyme.
  2. 8f1w (6,171 bytes)
    16: ..., but have lower K(m, ATP) values compared to the L858R variant, which contributes to their lack of sensi...
  3. 8f1x (6,203 bytes)
    16: ..., but have lower K(m, ATP) values compared to the L858R variant, which contributes to their lack of sensi...
  4. 8f1y (6,212 bytes)
    16: ..., but have lower K(m, ATP) values compared to the L858R variant, which contributes to their lack of sensi...
  5. 8f1z (6,229 bytes)
    16: ..., but have lower K(m, ATP) values compared to the L858R variant, which contributes to their lack of sensi...
  6. 2itu (6,171 bytes)
    2: ==Crystal structure of EGFR kinase domain L858R mutation in complex with AFN941==
    26: ... that gefitinib binds 20-fold more tightly to the L858R mutant than to the wild-type enzyme.
  7. 2itq (6,172 bytes)
    26: ... that gefitinib binds 20-fold more tightly to the L858R mutant than to the wild-type enzyme.
  8. 2itt (6,238 bytes)
    2: ==Crystal structure of EGFR kinase domain L858R mutation in complex with AEE788==
    26: ... that gefitinib binds 20-fold more tightly to the L858R mutant than to the wild-type enzyme.
  9. 2itp (6,238 bytes)
    26: ... that gefitinib binds 20-fold more tightly to the L858R mutant than to the wild-type enzyme.
  10. 2itn (6,234 bytes)
    26: ... that gefitinib binds 20-fold more tightly to the L858R mutant than to the wild-type enzyme.
  11. 2itx (6,166 bytes)
    26: ... that gefitinib binds 20-fold more tightly to the L858R mutant than to the wild-type enzyme.
  12. 2itv (6,181 bytes)
    2: ==Crystal structure of EGFR kinase domain L858R mutation in complex with AMP-PNP==
    26: ... that gefitinib binds 20-fold more tightly to the L858R mutant than to the wild-type enzyme.
  13. 2itz (4,868 bytes)
    2: ==Crystal structure of EGFR kinase domain L858R mutation in complex with Iressa==
  14. 2itw (6,157 bytes)
    26: ... that gefitinib binds 20-fold more tightly to the L858R mutant than to the wild-type enzyme.
  15. 3w2p (5,750 bytes)
    2: ==EGFR Kinase domain T790M/L858R mutant with compound 2==
    16: ...ned crystal structures of the wild-type and T790M/L858R double mutant EGFR kinases with reversible and ir...
    18: ...very of Pyrrolo[3,2-d]pyrimidine-Based EGFR T790M/L858R Mutant Inhibitors.,Sogabe S, Kawakita Y, Igaki S,...
  16. 3w2q (5,806 bytes)
    2: ==EGFR kinase domain T790M/L858R mutant with HKI-272==
    16: ...ned crystal structures of the wild-type and T790M/L858R double mutant EGFR kinases with reversible and ir...
    18: ...very of Pyrrolo[3,2-d]pyrimidine-Based EGFR T790M/L858R Mutant Inhibitors.,Sogabe S, Kawakita Y, Igaki S,...
  17. 3w2r (5,795 bytes)
    2: ==EGFR Kinase domain T790M/L858R mutant with compound 4==
    16: ...ned crystal structures of the wild-type and T790M/L858R double mutant EGFR kinases with reversible and ir...
    18: ...very of Pyrrolo[3,2-d]pyrimidine-Based EGFR T790M/L858R Mutant Inhibitors.,Sogabe S, Kawakita Y, Igaki S,...
  18. 4i1z (3,920 bytes)
    2: ... gefitinib/erlotinib resistant EGFR kinase domain L858R+T790M==
  19. 4i20 (3,896 bytes)
    2: ...ure of monomeric (V948R) primary oncogenic mutant L858R EGFR kinase domain==
  20. 4i21 (3,890 bytes)
    2: ==Crystal structure of L858R + T790M EGFR kinase domain in complex with MIG6 p...

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