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C Marsh

Showing results (551-560 of 654) with videos related to

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Haematologica|June 13, 2012
Allogeneic stem cell transplantation in paroxysmal nocturnal hemoglobinuriaRégis Peffault de Latour, Hubert Schrezenmeier, Andrea Bacigalupo, et al.
Bioorganic & Medicinal Chemistry Letters|February 15, 2011
Chroman and tetrahydroquinoline ureas as potent TRPV1 antagonistsRobert G Schmidt, Erol K Bayburt, Steven P Latshaw, et al.
Bone Marrow Transplantation|April 28, 2015
Efficacy and safety of CDX-301, recombinant human Flt3L, at expanding dendritic cells and hematopoietic stem cells in healthy human volunteersN Anandasabapathy, G Breton, A Hurley, et al.
International Journal of Circumpolar Health|September 23, 2022
Implementation and evaluation of a two-eyed seeing approach using traditional healing and seeking safety in an indigenous residential treatment program in Northern OntarioT N Marsh, C Eshakakogan, J K Eibl, et al.
Bioorganic & Medicinal Chemistry Letters|October 6, 2005
Synthesis and activity of N-acyl azacyclic urea HIV-1 protease inhibitors with high potency against multiple drug resistant viral strainsChen Zhao, Hing L Sham, Minghua Sun, et al.
Journal of Medicinal Chemistry|October 16, 2010
Diaryldiamines with dual inhibition of the histamine H(3) receptor and the norepinephrine transporter and the efficacy of 4-(3-(methylamino)-1-phenylpropyl)-6-(2-(pyrrolidin-1-yl)ethoxy)naphthalen-1-ol in painRobert J Altenbach, Lawrence A Black, Marina I Strakhova, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|September 9, 2000
Vaccine-induced antibodies inhibit CETP activity in vivo and reduce aortic lesions in a rabbit model of atherosclerosisC W Rittershaus, D P Miller, L J Thomas, et al.
Journal of Medicinal Chemistry|August 8, 2008
The alkaloid conessine and analogues as potent histamine H3 receptor antagonistsChen Zhao, Minghua Sun, Youssef L Bennani, et al.
Journal of Medicinal Chemistry|August 25, 2001
Discovery of potent antagonists of leukocyte function-associated antigen-1/intercellular adhesion molecule-1 interaction. 3. Amide (C-ring) structure-activity relationship and improvement of overall properties of arylthio cinnamidesZ Pei, Z Xin, G Liu, et al.
Bioorganic & Medicinal Chemistry|March 1, 2006
Synthesis, antiviral activity, and pharmacokinetic evaluation of P3 pyridylmethyl analogs of oximinoarylsulfonyl HIV-1 protease inhibitorsJohn T Randolph, Peggy P Huang, William J Flosi, et al.
Pageof 66

Showing results (551-560 of 654) with videos related to

Sort By:
Pageof 66
Haematologica|June 13, 2012
Allogeneic stem cell transplantation in paroxysmal nocturnal hemoglobinuriaRégis Peffault de Latour, Hubert Schrezenmeier, Andrea Bacigalupo, et al.
Bioorganic & Medicinal Chemistry Letters|February 15, 2011
Chroman and tetrahydroquinoline ureas as potent TRPV1 antagonistsRobert G Schmidt, Erol K Bayburt, Steven P Latshaw, et al.
Bone Marrow Transplantation|April 28, 2015
Efficacy and safety of CDX-301, recombinant human Flt3L, at expanding dendritic cells and hematopoietic stem cells in healthy human volunteersN Anandasabapathy, G Breton, A Hurley, et al.
International Journal of Circumpolar Health|September 23, 2022
Implementation and evaluation of a two-eyed seeing approach using traditional healing and seeking safety in an indigenous residential treatment program in Northern OntarioT N Marsh, C Eshakakogan, J K Eibl, et al.
Bioorganic & Medicinal Chemistry Letters|October 6, 2005
Synthesis and activity of N-acyl azacyclic urea HIV-1 protease inhibitors with high potency against multiple drug resistant viral strainsChen Zhao, Hing L Sham, Minghua Sun, et al.
Journal of Medicinal Chemistry|October 16, 2010
Diaryldiamines with dual inhibition of the histamine H(3) receptor and the norepinephrine transporter and the efficacy of 4-(3-(methylamino)-1-phenylpropyl)-6-(2-(pyrrolidin-1-yl)ethoxy)naphthalen-1-ol in painRobert J Altenbach, Lawrence A Black, Marina I Strakhova, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|September 9, 2000
Vaccine-induced antibodies inhibit CETP activity in vivo and reduce aortic lesions in a rabbit model of atherosclerosisC W Rittershaus, D P Miller, L J Thomas, et al.
Journal of Medicinal Chemistry|August 8, 2008
The alkaloid conessine and analogues as potent histamine H3 receptor antagonistsChen Zhao, Minghua Sun, Youssef L Bennani, et al.
Journal of Medicinal Chemistry|August 25, 2001
Discovery of potent antagonists of leukocyte function-associated antigen-1/intercellular adhesion molecule-1 interaction. 3. Amide (C-ring) structure-activity relationship and improvement of overall properties of arylthio cinnamidesZ Pei, Z Xin, G Liu, et al.
Bioorganic & Medicinal Chemistry|March 1, 2006
Synthesis, antiviral activity, and pharmacokinetic evaluation of P3 pyridylmethyl analogs of oximinoarylsulfonyl HIV-1 protease inhibitorsJohn T Randolph, Peggy P Huang, William J Flosi, et al.
Pageof 66