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Expert Opinion on Investigational Drugs
|
November 7, 2012
Therapeutic targeting of c-KIT in cancer
Leonie K Ashman, Renate Griffith
Molecules (Basel, Switzerland)
|
February 25, 2023
Computational Evaluation of N-Based Transannular Interactions in Some Model Fused Medium-Sized Heterocyclic Systems and Implications for Drug Design
Renate Griffith, John B Bremner
Drug Discovery Today. Technologies
|
September 21, 2013
Combination of ligand- and structure-based methods in virtual screening
Malgorzata N Drwal, Renate Griffith
Journal of Molecular Graphics & Modelling
|
November 21, 2007
Pharmacophore design and database searching for selective monoamine neurotransmitter transporter ligands
Iain J A Macdougall, Renate Griffith
BMC Bioinformatics
|
December 19, 2014
Combining spatial and chemical information for clustering pharmacophores
Lingxiao Zhou, Renate Griffith, Bruno Gaeta
Journal of Molecular Graphics & Modelling
|
January 13, 2006
Selective pharmacophore design for alpha1-adrenoceptor subtypes
Iain J A MacDougall, Renate Griffith
Iranian Journal of Basic Medical Sciences
|
February 19, 2015
Differences in growth promotion, drug response and intracellular protein trafficking of FLT3 mutants
Baratali Mashkani, Renate Griffith, Leonie Ashman
Bioorganic & Medicinal Chemistry
|
February 17, 2010
Colony stimulating factor-1 receptor as a target for small molecule inhibitors
Baratali Mashkani, Renate Griffith, Leonie K Ashman
Journal of Molecular Graphics & Modelling
|
September 15, 2004
Molecular basis of the constitutive activity and STI571 resistance of Asp816Val mutant KIT receptor tyrosine kinase
Rowan Foster, Renate Griffith, Petranel Ferrao, et al.
Journal of Molecular Graphics & Modelling
|
August 19, 2017
Template selection and refinement considerations for modelling aminergic GPCR-ligand complexes
Kaniz F Urmi, Angela M Finch, Renate Griffith
Page
of 7
Search research articles
Search
Showing results (1-10 of 65) with videos related to
Sort By:
Page
of 7
Expert Opinion on Investigational Drugs
|
November 7, 2012
Therapeutic targeting of c-KIT in cancer
Leonie K Ashman, Renate Griffith
Molecules (Basel, Switzerland)
|
February 25, 2023
Computational Evaluation of N-Based Transannular Interactions in Some Model Fused Medium-Sized Heterocyclic Systems and Implications for Drug Design
Renate Griffith, John B Bremner
Drug Discovery Today. Technologies
|
September 21, 2013
Combination of ligand- and structure-based methods in virtual screening
Malgorzata N Drwal, Renate Griffith
Journal of Molecular Graphics & Modelling
|
November 21, 2007
Pharmacophore design and database searching for selective monoamine neurotransmitter transporter ligands
Iain J A Macdougall, Renate Griffith
BMC Bioinformatics
|
December 19, 2014
Combining spatial and chemical information for clustering pharmacophores
Lingxiao Zhou, Renate Griffith, Bruno Gaeta
Journal of Molecular Graphics & Modelling
|
January 13, 2006
Selective pharmacophore design for alpha1-adrenoceptor subtypes
Iain J A MacDougall, Renate Griffith
Iranian Journal of Basic Medical Sciences
|
February 19, 2015
Differences in growth promotion, drug response and intracellular protein trafficking of FLT3 mutants
Baratali Mashkani, Renate Griffith, Leonie Ashman
Bioorganic & Medicinal Chemistry
|
February 17, 2010
Colony stimulating factor-1 receptor as a target for small molecule inhibitors
Baratali Mashkani, Renate Griffith, Leonie K Ashman
Journal of Molecular Graphics & Modelling
|
September 15, 2004
Molecular basis of the constitutive activity and STI571 resistance of Asp816Val mutant KIT receptor tyrosine kinase
Rowan Foster, Renate Griffith, Petranel Ferrao, et al.
Journal of Molecular Graphics & Modelling
|
August 19, 2017
Template selection and refinement considerations for modelling aminergic GPCR-ligand complexes
Kaniz F Urmi, Angela M Finch, Renate Griffith
Page
of 7