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Article title matches
- Category:L858r (36 bytes)
1: List of pages with the keyword L858r
Page text matches
- 2j6m (6,222 bytes)
26: ... that gefitinib binds 20-fold more tightly to the L858R mutant than to the wild-type enzyme. - 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. - 2itq (6,172 bytes)
26: ... that gefitinib binds 20-fold more tightly to the L858R mutant than to the wild-type enzyme. - 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. - 2itp (6,238 bytes)
26: ... that gefitinib binds 20-fold more tightly to the L858R mutant than to the wild-type enzyme. - 2itn (6,234 bytes)
26: ... that gefitinib binds 20-fold more tightly to the L858R mutant than to the wild-type enzyme. - 2itx (6,166 bytes)
26: ... that gefitinib binds 20-fold more tightly to the L858R mutant than to the wild-type enzyme. - 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. - 2itz (4,868 bytes)
2: ==Crystal structure of EGFR kinase domain L858R mutation in complex with Iressa== - 2itw (6,157 bytes)
26: ... that gefitinib binds 20-fold more tightly to the L858R mutant than to the wild-type enzyme. - 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,... - 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,... - 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,... - 4i1z (3,920 bytes)
2: ... gefitinib/erlotinib resistant EGFR kinase domain L858R+T790M== - 4i20 (3,896 bytes)
2: ...ure of monomeric (V948R) primary oncogenic mutant L858R EGFR kinase domain== - 4i21 (3,890 bytes)
2: ==Crystal structure of L858R + T790M EGFR kinase domain in complex with MIG6 p... - 4i22 (4,168 bytes)
2: ...948R)gefitinib/erlotinib resistant double mutant (L858R+T790M) EGFR kinase domain co-crystallized with ge... - 3w2o (5,748 bytes)
2: ==EGFR Kinase domain T790M/L858R Mutant with TAK-285==
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,... - 3w2s (5,771 bytes)
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,... - 2jit (6,804 bytes)
25: ...ation increases the ATP affinity of the oncogenic L858R mutant by more than an order of magnitude. The in...
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