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Renate Griffith

Showing results (31-40 of 65) with videos related to

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Molecular & Cellular Proteomics : MCP|June 1, 2010
Glycosylation and sialylation of macrophage-derived human apolipoprotein E analyzed by SDS-PAGE and mass spectrometry: evidence for a novel site of glycosylation on Ser290Youra Lee, Maaike Kockx, Mark J Raftery, et al.
Protein Expression and Purification|December 19, 2012
Expression of biologically active human colony stimulating factor-1 in Pichia pastorisBaratali Mashkani, Adam F Odell, Ellen M Byrnes, et al.
Plos One|May 17, 2011
A novel structural framework for α(1A/D)-adrenoceptor selective antagonists identified using subtype selective pharmacophoresEmily S Stoddart, Sevvandi Senadheera, Iain J A MacDougall, et al.
The Journal of Organic Chemistry|April 19, 2007
Probing molecular shape. 1. Conformational studies of 5-hydroxyhexahydropyrimidine and related compoundsJulie M Locke, Robyn L Crumbie, Renate Griffith, et al.
Plos One|December 10, 2014
Novel DNA topoisomerase IIα inhibitors from combined ligand- and structure-based virtual screeningMalgorzata N Drwal, Jessica Marinello, Stefano G Manzo, et al.
Bioorganic & Medicinal Chemistry|November 25, 2011
Novel indoleamine 2,3-dioxygenase-1 inhibitors from a multistep in silico screenJason R Smith, Krystal J Evans, Adam Wright, et al.
Journal of Neurochemistry|September 30, 2010
Conformational changes in extracellular loop 2 associated with signal transduction in the glycine receptorJennie M E Cederholm, Nathan L Absalom, Silas Sugiharto, et al.
Bioorganic & Medicinal Chemistry|February 15, 2014
Synthesis and biological evaluation of 2,5-di(7-indolyl)-1,3,4-oxadiazoles, and 2- and 7-indolyl 2-(1,3,4-thiadiazolyl)ketones as antimicrobialsHakan Kandemir, Cong Ma, Samuel K Kutty, et al.
Rejuvenation Research|May 27, 2011
The advanced glycation end product-lowering agent ALT-711 is a low-affinity inhibitor of thiamine diphosphokinaseMartina Krautwald, Dale Leech, Stacey Horne, et al.
Biochemical Pharmacology|March 26, 2013
α₁-Adrenoceptor and serotonin 5-HT(1A) receptor affinity of homobivalent 4-aminoquinoline compounds: an investigation of the effect of linker lengthJunli Chen, Ahsan K Murad, Laurence P G Wakelin, et al.
Pageof 7

Showing results (31-40 of 65) with videos related to

Sort By:
Pageof 7
Molecular & Cellular Proteomics : MCP|June 1, 2010
Glycosylation and sialylation of macrophage-derived human apolipoprotein E analyzed by SDS-PAGE and mass spectrometry: evidence for a novel site of glycosylation on Ser290Youra Lee, Maaike Kockx, Mark J Raftery, et al.
Protein Expression and Purification|December 19, 2012
Expression of biologically active human colony stimulating factor-1 in Pichia pastorisBaratali Mashkani, Adam F Odell, Ellen M Byrnes, et al.
Plos One|May 17, 2011
A novel structural framework for α(1A/D)-adrenoceptor selective antagonists identified using subtype selective pharmacophoresEmily S Stoddart, Sevvandi Senadheera, Iain J A MacDougall, et al.
The Journal of Organic Chemistry|April 19, 2007
Probing molecular shape. 1. Conformational studies of 5-hydroxyhexahydropyrimidine and related compoundsJulie M Locke, Robyn L Crumbie, Renate Griffith, et al.
Plos One|December 10, 2014
Novel DNA topoisomerase IIα inhibitors from combined ligand- and structure-based virtual screeningMalgorzata N Drwal, Jessica Marinello, Stefano G Manzo, et al.
Bioorganic & Medicinal Chemistry|November 25, 2011
Novel indoleamine 2,3-dioxygenase-1 inhibitors from a multistep in silico screenJason R Smith, Krystal J Evans, Adam Wright, et al.
Journal of Neurochemistry|September 30, 2010
Conformational changes in extracellular loop 2 associated with signal transduction in the glycine receptorJennie M E Cederholm, Nathan L Absalom, Silas Sugiharto, et al.
Bioorganic & Medicinal Chemistry|February 15, 2014
Synthesis and biological evaluation of 2,5-di(7-indolyl)-1,3,4-oxadiazoles, and 2- and 7-indolyl 2-(1,3,4-thiadiazolyl)ketones as antimicrobialsHakan Kandemir, Cong Ma, Samuel K Kutty, et al.
Rejuvenation Research|May 27, 2011
The advanced glycation end product-lowering agent ALT-711 is a low-affinity inhibitor of thiamine diphosphokinaseMartina Krautwald, Dale Leech, Stacey Horne, et al.
Biochemical Pharmacology|March 26, 2013
α₁-Adrenoceptor and serotonin 5-HT(1A) receptor affinity of homobivalent 4-aminoquinoline compounds: an investigation of the effect of linker lengthJunli Chen, Ahsan K Murad, Laurence P G Wakelin, et al.
Pageof 7