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Visit USCOThe Design and Synthesis of Novel Proteasome Inhibitors: Studies on the Synthesis of Nagelamide M and Analogs, the Synthesis of Rapamycin Based Proteasome Inhibitors, and the Synthesis of TCH Based Molecular Probes for Binding Site Determination
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Copyright Title
The Design and Synthesis of Novel Proteasome Inhibitors: Studies on the Synthesis of Nagelamide M and Analogs, the Synthesis of Rapamycin Based Proteasome Inhibitors, and the Synthesis of TCH Based Molecular Probes for Binding Site Determination
Status
Published
on 16 May 2017
Year of Creation
2017
Copyright Claimant
Matthew Basil Giletto
Registration Number
TX0008463287
on 16 May 2017Copyright Summary
The U.S. Copyright record (Registration Number: TX0008463287) dated 16 May 2017, pertains to an electronic file (eService) titled "The Design and Synthesis of Novel Proteasome Inhibitors: Studies on the Synthesis of Nagelamide M and Analogs, the Synthesis of Rapamycin Based Proteasome Inhibitors, and the Synthesis of TCH Based Molecular Probes for Binding Site Determination" created in 2017. The copyright holder is Matthew Basil Giletto, known for their creative contributions in text registration. For any inquiries concerning this copyrighted material, kindly reach out to Matthew Basil Giletto.
Application Details
Registration Number
TX0008463287
Registration Date
5/16/2017
Year of Creation
2017
Agency Marc Code
DLC-CO
Record Status
New
Physical Description
Electronic file (eService)
First Publication Nation
United States
Notes
Rights Note: Diana G Zajic, ProQuest-CSA, LLC, 789 E. Eisenhower Parkway, Ann Arbor, MI, 48108-3218, United States, (800) 521-0600 xext77020, disspub@proquest.com
Statements
Application Title Statement: The Design and Synthesis of Novel Proteasome Inhibitors: Studies on the Synthesis of Nagelamide M and Analogs, the Synthesis of Rapamycin Based Proteasome Inhibitors, and the Synthesis of TCH Based Molecular Probes for Binding Site Determination
Author Statement: Matthew Basil Giletto Citizenship: United States Authorship: text
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