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D Mol

Showing results (31-40 of 47) with videos related to

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Journal of Atrial Fibrillation|May 30, 2019
Additional Diagnostic value of Mini Electrodes in an 8-mm Tip in Cavotricuspid Isthmus AblationD Mol, W R Berger, M Khan, et al.
Cell|September 8, 1995
Crystal structure of human uracil-DNA glycosylase in complex with a protein inhibitor: protein mimicry of DNAC D Mol, A S Arvai, R J Sanderson, et al.
The EMBO Journal|November 14, 1997
The crystal structure of the human DNA repair endonuclease HAP1 suggests the recognition of extra-helical deoxyribose at DNA abasic sitesM A Gorman, S Morera, D G Rothwell, et al.
Bioorganic & Medicinal Chemistry Letters|July 13, 2010
Structure-based design and synthesis of pyrrole derivatives as MEK inhibitorsMichael B Wallace, Mark E Adams, Toufike Kanouni, et al.
Public Health|June 1, 2005
A widening health gap in general practice? Socio-economic differences in morbidity between 1975 and 2000 in The NetherlandsG D Mol, E H van de Lisdonk, J P J M Smits, et al.
Journal of Bacteriology|July 3, 2003
Crystal structures of active fully assembled substrate- and product-bound complexes of UDP-N-acetylmuramic acid:L-alanine ligase (MurC) from Haemophilus influenzaeClifford D Mol, Alexei Brooun, Douglas R Dougan, et al.
The Journal of Biological Chemistry|June 26, 2003
Structure of a c-kit product complex reveals the basis for kinase transactivationClifford D Mol, Kheng B Lim, Vandana Sridhar, et al.
The Journal of Biological Chemistry|May 5, 2004
Structural basis for the autoinhibition and STI-571 inhibition of c-Kit tyrosine kinaseClifford D Mol, Douglas R Dougan, Thomas R Schneider, et al.
Bioorganic & Medicinal Chemistry|February 10, 2009
Design, synthesis and structure-activity relationships of 1,3,4-oxadiazole derivatives as novel inhibitors of glycogen synthase kinase-3betaMorihisa Saitoh, Jun Kunitomo, Eiji Kimura, et al.
Bioorganic & Medicinal Chemistry|August 10, 2013
Design, stereoselective synthesis, and biological evaluation of novel tri-cyclic compounds as inhibitor of apoptosis proteins (IAP) antagonistsMoriteru Asano, Kentaro Hashimoto, Bunnai Saito, et al.
Pageof 5

Showing results (31-40 of 47) with videos related to

Sort By:
Pageof 5
Journal of Atrial Fibrillation|May 30, 2019
Additional Diagnostic value of Mini Electrodes in an 8-mm Tip in Cavotricuspid Isthmus AblationD Mol, W R Berger, M Khan, et al.
Cell|September 8, 1995
Crystal structure of human uracil-DNA glycosylase in complex with a protein inhibitor: protein mimicry of DNAC D Mol, A S Arvai, R J Sanderson, et al.
The EMBO Journal|November 14, 1997
The crystal structure of the human DNA repair endonuclease HAP1 suggests the recognition of extra-helical deoxyribose at DNA abasic sitesM A Gorman, S Morera, D G Rothwell, et al.
Bioorganic & Medicinal Chemistry Letters|July 13, 2010
Structure-based design and synthesis of pyrrole derivatives as MEK inhibitorsMichael B Wallace, Mark E Adams, Toufike Kanouni, et al.
Public Health|June 1, 2005
A widening health gap in general practice? Socio-economic differences in morbidity between 1975 and 2000 in The NetherlandsG D Mol, E H van de Lisdonk, J P J M Smits, et al.
Journal of Bacteriology|July 3, 2003
Crystal structures of active fully assembled substrate- and product-bound complexes of UDP-N-acetylmuramic acid:L-alanine ligase (MurC) from Haemophilus influenzaeClifford D Mol, Alexei Brooun, Douglas R Dougan, et al.
The Journal of Biological Chemistry|June 26, 2003
Structure of a c-kit product complex reveals the basis for kinase transactivationClifford D Mol, Kheng B Lim, Vandana Sridhar, et al.
The Journal of Biological Chemistry|May 5, 2004
Structural basis for the autoinhibition and STI-571 inhibition of c-Kit tyrosine kinaseClifford D Mol, Douglas R Dougan, Thomas R Schneider, et al.
Bioorganic & Medicinal Chemistry|February 10, 2009
Design, synthesis and structure-activity relationships of 1,3,4-oxadiazole derivatives as novel inhibitors of glycogen synthase kinase-3betaMorihisa Saitoh, Jun Kunitomo, Eiji Kimura, et al.
Bioorganic & Medicinal Chemistry|August 10, 2013
Design, stereoselective synthesis, and biological evaluation of novel tri-cyclic compounds as inhibitor of apoptosis proteins (IAP) antagonistsMoriteru Asano, Kentaro Hashimoto, Bunnai Saito, et al.
Pageof 5