Year |
Citation |
Score |
2023 |
Nadendla K, Chintala S, Kover K, Friedman SH. In vivo variable and multi-day response from an insulin-releasing photoactivated depot. Bioorganic & Medicinal Chemistry Letters. 92: 129388. PMID 37369330 DOI: 10.1016/j.bmcl.2023.129388 |
0.744 |
|
2019 |
Friedman SH. Replacing Pumps with Light Controlled Insulin Delivery. Current Diabetes Reports. 19: 122. PMID 31696345 DOI: 10.1007/S11892-019-1233-3 |
0.415 |
|
2019 |
Sarode BR, Kover K, Friedman SH. Visible-Light-Activated High-Density Materials for Controlled in Vivo Insulin Release. Molecular Pharmaceutics. PMID 31647241 DOI: 10.1021/Acs.Molpharmaceut.9B00806 |
0.506 |
|
2019 |
Nadendla K, Sarode B, Friedman SH. Chemical modification of proteins with photocleavable groups. Methods in Enzymology. 624: 113-128. PMID 31370926 DOI: 10.1016/Bs.Mie.2019.04.008 |
0.711 |
|
2019 |
Nadendla K, Sarode BR, Friedman SH. Hydrophobic Tags for Highly Efficient Light Activated Protein Release. Molecular Pharmaceutics. PMID 31117739 DOI: 10.1021/Acs.Molpharmaceut.9B00140 |
0.746 |
|
2018 |
Jain N, Friedman SH. Multiple weak intercalation as a strategy for the inhibition of polymerases. Bioorganic & Medicinal Chemistry Letters. PMID 30579791 DOI: 10.1016/J.Bmcl.2018.12.027 |
0.313 |
|
2018 |
Jain N, Friedman SH. A Tetra-Orthogonal Strategy for the Efficient Synthesis of Scaffolds Based on Cyclic Peptides. International Journal of Peptide Research and Therapeutics. 24: 535-542. PMID 30416404 DOI: 10.1007/S10989-017-9642-0 |
0.324 |
|
2018 |
Jain PK, Friedman SH. The ULTIMATE Reagent: A Universal Photo-Cleavable & Clickable Reagent for the Regiospecific and Reversible End Labeling of Any Nucleic Acid. Chembiochem : a European Journal of Chemical Biology. PMID 29516677 DOI: 10.1002/Cbic.201800028 |
0.525 |
|
2018 |
Jain PK, Friedman SH. Front Cover: The ULTIMATE Reagent: A Universal Photocleavable and Clickable Reagent for the Regiospecific and Reversible End Labeling of Any Nucleic Acid (ChemBioChem 12/2018) Chembiochem. 19: 1196-1196. DOI: 10.1002/Cbic.201800282 |
0.461 |
|
2017 |
Nadendla K, Friedman SH. Light Control of Protein Solubility Through Isoelectric Point Modulation. Journal of the American Chemical Society. 139: 17861-17869. PMID 29192764 DOI: 10.1021/Jacs.7B08465 |
0.747 |
|
2016 |
Sarode BR, Kover K, Tong PY, Zhang C, Friedman SH. Light Control of Insulin Release and Blood Glucose Using an Injectable Photoactivated Depot. Molecular Pharmaceutics. PMID 27653828 DOI: 10.1021/Acs.Molpharmaceut.6B00633 |
0.465 |
|
2016 |
Sarode BR, Jain PK, Friedman SH. Macromol. Biosci. 8/2016. Macromolecular Bioscience. 16: 1250. PMID 27491330 DOI: 10.1002/Mabi.201670032 |
0.581 |
|
2016 |
Sarode BR, Jain PK, Friedman SH. Polymerizing Insulin with Photocleavable Linkers to Make Light-Sensitive Macropolymer Depot Materials. Macromolecular Bioscience. PMID 27171861 DOI: 10.1002/Mabi.201500471 |
0.623 |
|
2014 |
Kala A, Jain PK, Friedman SH. Patterning of cells through patterning of biology. Molecular Biosystems. 10: 1689-92. PMID 24531692 DOI: 10.1039/C3Mb70587K |
0.505 |
|
2014 |
Kala A, Jain PK, Karunakaran D, Shah S, Friedman SH. The synthesis of tetra-modified RNA for the multidimensional control of gene expression via light-activated RNA interference. Nature Protocols. 9: 11-20. PMID 24309973 DOI: 10.1038/Nprot.2013.165 |
0.636 |
|
2013 |
Jain PK, Karunakaran D, Friedman SH. Construction of a photoactivated insulin depot. Angewandte Chemie (International Ed. in English). 52: 1404-9. PMID 23208858 DOI: 10.1002/Anie.201207264 |
0.604 |
|
2012 |
Jain N, Francis S, Friedman SH. Inhibition of therapeutically important polymerases with high affinity bis-intercalators. Bioorganic & Medicinal Chemistry Letters. 22: 4844-8. PMID 22695131 DOI: 10.1016/J.Bmcl.2012.05.041 |
0.303 |
|
2011 |
Kala A, Friedman SH. Enhanced light-activated RNA interference using phosphorothioate-based dsRNA precursors of siRNA. Pharmaceutical Research. 28: 3050-7. PMID 21739319 DOI: 10.1007/S11095-011-0529-Z |
0.392 |
|
2011 |
Jain PK, Shah S, Friedman SH. Patterning of gene expression using new photolabile groups applied to light activated RNAi. Journal of the American Chemical Society. 133: 440-6. PMID 21162570 DOI: 10.1021/Ja107226E |
0.632 |
|
2009 |
Shah S, Jain PK, Kala A, Karunakaran D, Friedman SH. Light-activated RNA interference using double-stranded siRNA precursors modified using a remarkable regiospecificity of diazo-based photolabile groups. Nucleic Acids Research. 37: 4508-17. PMID 19477960 DOI: 10.1093/Nar/Gkp415 |
0.641 |
|
2008 |
Shah S, Friedman SH. An ESI-MS method for characterization of native and modified oligonucleotides used for RNA interference and other biological applications. Nature Protocols. 3: 351-6. PMID 18323805 DOI: 10.1038/Nprot.2007.535 |
0.504 |
|
2007 |
Shah S, Friedman SH. Tolerance of RNA interference toward modifications of the 5' antisense phosphate of small interfering RNA. Oligonucleotides. 17: 35-43. PMID 17461761 DOI: 10.1089/Oli.2006.0067 |
0.54 |
|
2007 |
Rangarajan S, Friedman SH. Design, synthesis, and evaluation of phenanthridine derivatives targeting the telomerase RNA/DNA heteroduplex. Bioorganic & Medicinal Chemistry Letters. 17: 2267-73. PMID 17317174 DOI: 10.1016/J.Bmcl.2007.01.070 |
0.33 |
|
2005 |
Shah S, Rangarajan S, Friedman SH. Light-activated RNA interference. Angewandte Chemie (International Ed. in English). 44: 1328-32. PMID 15643658 DOI: 10.1002/Anie.200461458 |
0.507 |
|
2001 |
West C, Francis R, Friedman SH. Small molecule/nucleic acid affinity chromatography: application for the identification of telomerase inhibitors which target its key RNA/DNA heteroduplex. Bioorganic & Medicinal Chemistry Letters. 11: 2727-30. PMID 11591511 DOI: 10.1016/S0960-894X(01)00553-4 |
0.317 |
|
2001 |
Francis R, West C, Friedman SH. Targeting telomerase via its key RNA/DNA heteroduplex. Bioorganic Chemistry. 29: 107-17. PMID 11300699 DOI: 10.1006/Bioo.2000.1196 |
0.308 |
|
1998 |
Friedman SH, Ganapathi PS, Rubin Y, Kenyon GL. Optimizing the binding of fullerene inhibitors of the HIV-1 protease through predicted increases in hydrophobic desolvation. Journal of Medicinal Chemistry. 41: 2424-9. PMID 9632374 DOI: 10.1021/Jm970689R |
0.469 |
|
1997 |
Friedman SH, Kenyon GL. A computational strategy for the design of regiospecific syntheses of fullerene derivatives Journal of the American Chemical Society. 119: 447-448. DOI: 10.1021/Ja963041X |
0.424 |
|
1995 |
Ganapathi PS, Friedman SH, Kenyon GL, Rubin Y. Sequential "double-Michael" additions of dienolates with C60: Rapid access to sterically congested buckminsterfullerene derivatives with defined stereochemistry The Journal of Organic Chemistry. 60: 2954-2955. DOI: 10.1021/Jo00115A002 |
0.458 |
|
1993 |
Sijbesma R, Srdanov G, Wudl F, Castoro JA, Wilkins C, Friedman SH, DeCamp DL, Kenyon GL. Synthesis of a fullerene derivative for the inhibition of HIV enzymes Journal of the American Chemical Society. 115: 6510-6512. DOI: 10.1021/Ja00068A006 |
0.501 |
|
1993 |
Friedman SH, Decamp DL, Sijbesma RP, Srdanov G, Wudl F, Kenyon GL. Inhibition of the HIV-1 protease by fullerene derivatives: Model building studies and experimental verification Journal of the American Chemical Society. 115: 6506-6509. DOI: 10.1021/Ja00068A005 |
0.499 |
|
1993 |
Sijbesma R, Srdanov G, Wudl F, Castoro JA, Wilkins C, Friedman SH, Decamp DL, Kenyon GL. Synthesis of a fullerene derivative for the Inhibition of HIV enzymes Journal of the American Chemical Society. 115: 6510-6512. |
0.438 |
|
Show low-probability matches. |