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Acta Crystallographica. Section D, Biological Crystallography
|
February 10, 2015
Structures of lactate dehydrogenase A (LDHA) in apo, ternary and inhibitor-bound forms
Subramaniapillai Kolappan, David L Shen, Renee Mosi, et al.
Journal of Bacteriology
|
January 1, 1991
Telomeric and dispersed repeat sequences in Candida yeasts and their use in strain identification
C Sadhu, M J McEachern, E P Rustchenko-Bulgac, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 5, 2007
Telomerase core components protect Candida telomeres from aberrant overhang accumulation
Min Hsu, Michael J McEachern, Alain T Dandjinou, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 27, 2004
A genome-wide screen for Saccharomyces cerevisiae deletion mutants that affect telomere length
Syed H Askree, Tal Yehuda, Sarit Smolikov, et al.
Psychopharmacology Bulletin
|
January 1, 1988
Self-report vs. instrumental measure in the assessment of the subjective effects of d-amphetamine
J McEachern, L Friedman, M Bird, et al.
Chemical Science
|
July 13, 2018
Analysis of transition state mimicry by tight binding aminothiazoline inhibitors provides insight into catalysis by human <i>O</i>-GlcNAcase
N Cekic, J E Heinonen, K A Stubbs, et al.
Nature Chemical Biology
|
July 1, 2008
A potent mechanism-inspired O-GlcNAcase inhibitor that blocks phosphorylation of tau in vivo
Scott A Yuzwa, Matthew S Macauley, Julia E Heinonen, et al.
Molecular Neurodegeneration
|
October 27, 2014
Pharmacological inhibition of O-GlcNAcase (OGA) prevents cognitive decline and amyloid plaque formation in bigenic tau/APP mutant mice
Scott A Yuzwa, Xiaoyang Shan, Bryan A Jones, et al.
Journal of Medicinal Chemistry
|
March 20, 2010
Discovery of novel small molecule orally bioavailable C-X-C chemokine receptor 4 antagonists that are potent inhibitors of T-tropic (X4) HIV-1 replication
Renato T Skerlj, Gary J Bridger, Al Kaller, et al.
Journal of Medicinal Chemistry
|
September 6, 2019
Discovery of MK-8719, a Potent O-GlcNAcase Inhibitor as a Potential Treatment for Tauopathies
Harold G Selnick, J Fred Hess, Cuyue Tang, et al.
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of 7
Search research articles
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Showing results (51-60 of 62) with videos related to
Sort By:
Page
of 7
Acta Crystallographica. Section D, Biological Crystallography
|
February 10, 2015
Structures of lactate dehydrogenase A (LDHA) in apo, ternary and inhibitor-bound forms
Subramaniapillai Kolappan, David L Shen, Renee Mosi, et al.
Journal of Bacteriology
|
January 1, 1991
Telomeric and dispersed repeat sequences in Candida yeasts and their use in strain identification
C Sadhu, M J McEachern, E P Rustchenko-Bulgac, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 5, 2007
Telomerase core components protect Candida telomeres from aberrant overhang accumulation
Min Hsu, Michael J McEachern, Alain T Dandjinou, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 27, 2004
A genome-wide screen for Saccharomyces cerevisiae deletion mutants that affect telomere length
Syed H Askree, Tal Yehuda, Sarit Smolikov, et al.
Psychopharmacology Bulletin
|
January 1, 1988
Self-report vs. instrumental measure in the assessment of the subjective effects of d-amphetamine
J McEachern, L Friedman, M Bird, et al.
Chemical Science
|
July 13, 2018
Analysis of transition state mimicry by tight binding aminothiazoline inhibitors provides insight into catalysis by human <i>O</i>-GlcNAcase
N Cekic, J E Heinonen, K A Stubbs, et al.
Nature Chemical Biology
|
July 1, 2008
A potent mechanism-inspired O-GlcNAcase inhibitor that blocks phosphorylation of tau in vivo
Scott A Yuzwa, Matthew S Macauley, Julia E Heinonen, et al.
Molecular Neurodegeneration
|
October 27, 2014
Pharmacological inhibition of O-GlcNAcase (OGA) prevents cognitive decline and amyloid plaque formation in bigenic tau/APP mutant mice
Scott A Yuzwa, Xiaoyang Shan, Bryan A Jones, et al.
Journal of Medicinal Chemistry
|
March 20, 2010
Discovery of novel small molecule orally bioavailable C-X-C chemokine receptor 4 antagonists that are potent inhibitors of T-tropic (X4) HIV-1 replication
Renato T Skerlj, Gary J Bridger, Al Kaller, et al.
Journal of Medicinal Chemistry
|
September 6, 2019
Discovery of MK-8719, a Potent O-GlcNAcase Inhibitor as a Potential Treatment for Tauopathies
Harold G Selnick, J Fred Hess, Cuyue Tang, et al.
Page
of 7