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C Maillard

Showing results (101-110 of 109) with videos related to

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Oncogene|March 9, 2010
Higher sensitivity of Adamts12-deficient mice to tumor growth and angiogenesisM El Hour, A Moncada-Pazos, S Blacher, et al.
Journal of Medicinal Chemistry|July 31, 1998
Design, synthesis, and pharmacological evaluation of conformationally constrained analogues of N,N'-diaryl- and N-aryl-N-aralkylguanidines as potent inhibitors of neuronal Na+ channelsM C Maillard, M E Perlman, O Amitay, et al.
Bioorganic & Medicinal Chemistry Letters|November 23, 2018
Development and characterization of a CNS-penetrant benzhydryl hydroxamic acid class IIa histone deacetylase inhibitorChristopher A Luckhurst, Omar Aziz, Vahri Beaumont, et al.
Bioorganic & Medicinal Chemistry|September 10, 2011
Exploiting differences in caspase-2 and -3 S₂ subsites for selectivity: structure-based design, solid-phase synthesis and in vitro activity of novel substrate-based caspase-2 inhibitorsMichel C Maillard, Frederick A Brookfield, Stephen M Courtney, et al.
Journal of Medicinal Chemistry|February 16, 2007
Design, synthesis, and crystal structure of hydroxyethyl secondary amine-based peptidomimetic inhibitors of human beta-secretaseMichel C Maillard, Roy K Hom, Timothy E Benson, et al.
Journal of Medicinal Chemistry|July 11, 2022
Identification of a Potent, Selective, and Brain-Penetrant Rho Kinase Inhibitor and its Activity in a Mouse Model of Huntington's DiseaseTammy Ladduwahetty, Matthew R Lee, Michel C Maillard, et al.
Archives of Gynecology and Obstetrics|October 4, 2016
N Erb, P Dürig, U Dietz, et al.
ACS Medicinal Chemistry Letters|March 19, 2021
Evaluation of 5-(Trifluoromethyl)-1,2,4-oxadiazole-Based Class IIa HDAC Inhibitors for Huntington's DiseaseAndrew J Stott, Michel C Maillard, Vahri Beaumont, et al.
Archives of Gynecology and Obstetrics|October 4, 2016
E Wight, C Küng, P Moreau, et al.
Pageof 11

Showing results (101-110 of 109) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 109 results.
Oncogene|March 9, 2010
Higher sensitivity of Adamts12-deficient mice to tumor growth and angiogenesisM El Hour, A Moncada-Pazos, S Blacher, et al.
Journal of Medicinal Chemistry|July 31, 1998
Design, synthesis, and pharmacological evaluation of conformationally constrained analogues of N,N'-diaryl- and N-aryl-N-aralkylguanidines as potent inhibitors of neuronal Na+ channelsM C Maillard, M E Perlman, O Amitay, et al.
Bioorganic & Medicinal Chemistry Letters|November 23, 2018
Development and characterization of a CNS-penetrant benzhydryl hydroxamic acid class IIa histone deacetylase inhibitorChristopher A Luckhurst, Omar Aziz, Vahri Beaumont, et al.
Bioorganic & Medicinal Chemistry|September 10, 2011
Exploiting differences in caspase-2 and -3 S₂ subsites for selectivity: structure-based design, solid-phase synthesis and in vitro activity of novel substrate-based caspase-2 inhibitorsMichel C Maillard, Frederick A Brookfield, Stephen M Courtney, et al.
Journal of Medicinal Chemistry|February 16, 2007
Design, synthesis, and crystal structure of hydroxyethyl secondary amine-based peptidomimetic inhibitors of human beta-secretaseMichel C Maillard, Roy K Hom, Timothy E Benson, et al.
Journal of Medicinal Chemistry|July 11, 2022
Identification of a Potent, Selective, and Brain-Penetrant Rho Kinase Inhibitor and its Activity in a Mouse Model of Huntington's DiseaseTammy Ladduwahetty, Matthew R Lee, Michel C Maillard, et al.
Archives of Gynecology and Obstetrics|October 4, 2016
N Erb, P Dürig, U Dietz, et al.
ACS Medicinal Chemistry Letters|March 19, 2021
Evaluation of 5-(Trifluoromethyl)-1,2,4-oxadiazole-Based Class IIa HDAC Inhibitors for Huntington's DiseaseAndrew J Stott, Michel C Maillard, Vahri Beaumont, et al.
Archives of Gynecology and Obstetrics|October 4, 2016
E Wight, C Küng, P Moreau, et al.
Pageof 11