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Satoshi Ichikawa

Showing results (31-40 of 277) with videos related to

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Internal Medicine (Tokyo, Japan)|December 4, 2024
Renal Diffuse Large B-cell Lymphoma with Bladder TamponadeSatoshi Ichikawa, Hikaru Kumagai, Tomonori Ishii
Annals of Hematology|August 11, 2019
Successful cord blood transplantation for a paroxysmal nocturnal hemoglobinuria complicated with Budd-Chiari syndrome and myelodysplastic syndromeTaro Takahashi, Satoshi Ichikawa, Hideo Harigae
Bioorganic & Medicinal Chemistry Letters|May 13, 2018
Insight into the recognition mechanism of DNA cytosine-5 methyltransferases (DNMTs) by incorporation of acyclic 5-fluorocytosine (<sup>F</sup>C) nucleosides into DNAShohei Utsumi, Kousuke Sato, Satoshi Ichikawa
The Journal of Organic Chemistry|October 17, 2013
Synthesis of C-glycosyl pyrrolo[3,4-c]carbazole-1,3(2H,6H)-diones as a scaffold for check point kinase 1 inhibitorsSatoshi Ichikawa, Nana Tatebayashi, Akira Matsuda
Nucleic Acids Symposium Series (2004)|September 15, 2009
Rational design and synthesis of ansa-adenosines as potential antitumor agentsKazuhiro Muranaka, Satoshi Ichikawa, Akira Matsuda
Organic Letters|July 9, 2011
Synthesis of L-epi-capreomycidine derivatives via C-H aminationTetsuya Tanino, Satoshi Ichikawa, Akira Matsuda
Bioorganic & Medicinal Chemistry Letters|August 2, 2015
Structure-activity relationship study of syringolin A as a potential anticancer agentTakuya Chiba, Akira Matsuda, Satoshi Ichikawa
Chemical Communications (Cambridge, England)|July 18, 2002
Synthesis of a novel mesoporous tin phosphate, SnPO4Nawal Kishor Mal, Satoshi Ichikawa, Masahiro Fujiwara
Chemical Communications (Cambridge, England)|June 27, 2022
Total synthesis of pseudouridimycin and its epimer <i>via</i> Ugi-type multicomponent reactionRyotaro Okawa, Courtney C Aldrich, Satoshi Ichikawa
The Journal of Organic Chemistry|October 26, 2002
A highly stereoselective samarium diiodide-promoted aldol reaction with 1'-phenylseleno-2'-keto nucleosides. Synthesis of 1'alpha-branched uridine derivativesTetsuya Kodama, Satoshi Shuto, Satoshi Ichikawa, et al.
Pageof 28

Showing results (31-40 of 277) with videos related to

Sort By:
Pageof 28
Internal Medicine (Tokyo, Japan)|December 4, 2024
Renal Diffuse Large B-cell Lymphoma with Bladder TamponadeSatoshi Ichikawa, Hikaru Kumagai, Tomonori Ishii
Annals of Hematology|August 11, 2019
Successful cord blood transplantation for a paroxysmal nocturnal hemoglobinuria complicated with Budd-Chiari syndrome and myelodysplastic syndromeTaro Takahashi, Satoshi Ichikawa, Hideo Harigae
Bioorganic & Medicinal Chemistry Letters|May 13, 2018
Insight into the recognition mechanism of DNA cytosine-5 methyltransferases (DNMTs) by incorporation of acyclic 5-fluorocytosine (<sup>F</sup>C) nucleosides into DNAShohei Utsumi, Kousuke Sato, Satoshi Ichikawa
The Journal of Organic Chemistry|October 17, 2013
Synthesis of C-glycosyl pyrrolo[3,4-c]carbazole-1,3(2H,6H)-diones as a scaffold for check point kinase 1 inhibitorsSatoshi Ichikawa, Nana Tatebayashi, Akira Matsuda
Nucleic Acids Symposium Series (2004)|September 15, 2009
Rational design and synthesis of ansa-adenosines as potential antitumor agentsKazuhiro Muranaka, Satoshi Ichikawa, Akira Matsuda
Organic Letters|July 9, 2011
Synthesis of L-epi-capreomycidine derivatives via C-H aminationTetsuya Tanino, Satoshi Ichikawa, Akira Matsuda
Bioorganic & Medicinal Chemistry Letters|August 2, 2015
Structure-activity relationship study of syringolin A as a potential anticancer agentTakuya Chiba, Akira Matsuda, Satoshi Ichikawa
Chemical Communications (Cambridge, England)|July 18, 2002
Synthesis of a novel mesoporous tin phosphate, SnPO4Nawal Kishor Mal, Satoshi Ichikawa, Masahiro Fujiwara
Chemical Communications (Cambridge, England)|June 27, 2022
Total synthesis of pseudouridimycin and its epimer <i>via</i> Ugi-type multicomponent reactionRyotaro Okawa, Courtney C Aldrich, Satoshi Ichikawa
The Journal of Organic Chemistry|October 26, 2002
A highly stereoselective samarium diiodide-promoted aldol reaction with 1'-phenylseleno-2'-keto nucleosides. Synthesis of 1'alpha-branched uridine derivativesTetsuya Kodama, Satoshi Shuto, Satoshi Ichikawa, et al.
Pageof 28