| Year |
Citation |
Score |
| 2024 |
Liubomirski Y, Tiram G, Scomparin A, Gnaim S, Das S, Gholap S, Ge L, Yeini E, Shelef O, Zauberman A, Berger N, Kalimi D, Toister-Achituv M, Schröter C, Dickgiesser S, ... ... Shabat D, et al. Potent antitumor activity of anti-HER2 antibody-topoisomerase I inhibitor conjugate based on self-immolative dendritic dimeric-linker. Journal of Controlled Release : Official Journal of the Controlled Release Society. PMID 38228272 DOI: 10.1016/j.jconrel.2024.01.025 |
0.766 |
|
| 2022 |
Gnaim S, Gholap SP, Ge L, Das S, Gutkin S, Green O, Shelef O, Hananya N, Baran PS, Shabat D. Modular Access to Diverse Chemiluminescent Dioxetane-Luminophores Through Convergent Synthesis. Angewandte Chemie (International Ed. in English). PMID 35258138 DOI: 10.1002/anie.202202187 |
0.743 |
|
| 2021 |
Gholap SP, Yao C, Green O, Babjak M, Jakubec P, Malatinský T, Ihssen J, Wick L, Spitz U, Shabat D. Chemiluminescence Detection of Hydrogen Sulfide Release by β-Lactamase-Catalyzed β-Lactam Biodegradation: Unprecedented Pathway for Monitoring β-Lactam Antibiotic Bacterial Resistance. Bioconjugate Chemistry. PMID 33896185 DOI: 10.1021/acs.bioconjchem.1c00149 |
0.742 |
|
| 2020 |
Shabat D, Das S, Ihssen J, Wick L, Spitz U. Chemiluminescence Carbapenem-based Molecular Probe for Detection of Carbapenemase Activity in Live Bacteria. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31957167 DOI: 10.1002/Chem.202000217 |
0.683 |
|
| 2019 |
Gnaim S, Shabat D. Activity-Based Optical Sensing Enabled by Self-Immolative Scaffolds: Monitoring of Release Events by Fluorescence or Chemiluminescence Output. Accounts of Chemical Research. PMID 31483607 DOI: 10.1021/Acs.Accounts.9B00338 |
0.327 |
|
| 2019 |
Hananya N, Shabat D. Recent Advances and Challenges in Luminescent Imaging: Bright Outlook for Chemiluminescence of Dioxetanes in Water. Acs Central Science. 5: 949-959. PMID 31263754 DOI: 10.1021/Acscentsci.9B00372 |
0.314 |
|
| 2019 |
Hananya N, Reid JP, Green O, Sigman MS, Shabat D. Rapid chemiexcitation of phenoxy-dioxetane luminophores yields ultrasensitive chemiluminescence assays. Chemical Science. 10: 1380-1385. PMID 30809354 DOI: 10.1039/C8Sc04280B |
0.322 |
|
| 2019 |
Gnaim S, Shabat D. Chemiluminescence molecular probe with a linear chain reaction amplification mechanism. Organic & Biomolecular Chemistry. PMID 30676601 DOI: 10.1039/C8Ob03042A |
0.328 |
|
| 2018 |
Sun X, Shabat D, Phillips ST, Anslyn EV. Self-Propagating Amplification Reactions for Molecular Detection and Signal Amplification: Advantages, Pitfalls, and Challenges. Journal of Physical Organic Chemistry. 31. PMID 30386006 DOI: 10.1002/Poc.3827 |
0.327 |
|
| 2018 |
Shabat D, Gnaim S, Scomparin A, Das S, Satchi-Fainaro R. Real-Time Monitoring of Prodrug Activation by Direct-Mode of Chemiluminescence. Angewandte Chemie (International Ed. in English). PMID 29786931 DOI: 10.1002/Anie.201804816 |
0.686 |
|
| 2018 |
Bruemmer KJ, Green O, Su TA, Shabat D, Chang CJ. Chemiluminescent Probes for Activity-Based Sensing of Formaldehyde Released from Folate Degradation in Living Mice. Angewandte Chemie (International Ed. in English). PMID 29635731 DOI: 10.1002/Anie.201802143 |
0.325 |
|
| 2018 |
Eilon-Shaffer T, Roth-Konforti M, Eldar-Boock A, Satchi-Fainaro R, Shabat D. ortho-Chlorination of phenoxy 1,2-dioxetane yields superior chemiluminescent probes for in vitro and in vivo imaging. Organic & Biomolecular Chemistry. PMID 29451576 DOI: 10.1039/C8Ob00087E |
0.336 |
|
| 2018 |
Gnaim S, Green O, Shabat D. The emergence of aqueous chemiluminescence: new promising class of phenoxy 1,2-dioxetane luminophores. Chemical Communications (Cambridge, England). PMID 29423487 DOI: 10.1039/C8Cc00428E |
0.313 |
|
| 2017 |
Shabat D, Hananya N. A Glowing Trajectory between Bio- and Chemi-Luminescence: From Luciferin-based Probes to Triggerable Dioxetanes. Angewandte Chemie (International Ed. in English). PMID 28967167 DOI: 10.1002/Anie.201706969 |
0.303 |
|
| 2017 |
Green O, Gnaim S, Blau R, Eldar-Boock A, Satchi-Fainaro R, Shabat D. Near-Infrared Dioxetane Luminophores with Direct Chemiluminescence Emission Mode. Journal of the American Chemical Society. PMID 28853880 DOI: 10.1021/Jacs.7B08446 |
0.326 |
|
| 2017 |
Green O, Eilon T, Hananya N, Gutkin S, Bauer CR, Shabat D. Opening a Gateway for Chemiluminescence Cell Imaging: Distinctive Methodology for Design of Bright Chemiluminescent Dioxetane Probes. Acs Central Science. 3: 349-358. PMID 28470053 DOI: 10.1021/Acscentsci.7B00058 |
0.344 |
|
| 2016 |
Hananya N, Eldar Boock A, Bauer CR, Satchi-Fainaro R, Shabat D. Remarkable Enhancement of Chemiluminescent Signal by Dioxetane-Fluorophore Conjugates: Turn-ON Chemiluminescence Probes with Color Modulation for Sensing and Imaging. Journal of the American Chemical Society. PMID 27652602 DOI: 10.1021/Jacs.6B09173 |
0.318 |
|
| 2016 |
Gnaim S, Scomparin A, Li X, Baran PS, Rader C, Satchi-Fainaro R, Shabat D. Tagging the Untaggable: A Difluoroalkyl-Sulfinate Ketone-Based Reagent for Direct C-H Functionalization of Bioactive Heteroarenes. Bioconjugate Chemistry. PMID 27494153 DOI: 10.1021/Acs.Bioconjchem.6B00382 |
0.557 |
|
| 2016 |
Herbst E, Shabat D. FRET-based cyanine probes for monitoring ligation reactions and their applications to mechanistic studies and catalyst screening. Organic & Biomolecular Chemistry. 14: 3715-28. PMID 26909686 DOI: 10.1039/C5Ob02127H |
0.354 |
|
| 2015 |
Redy-Keisar O, Ferber S, Satchi-Fainaro R, Shabat D. NIR Fluorogenic Dye as a Modular Platform for Prodrug Assembly: Real-Time in vivo Monitoring of Drug Release. Chemmedchem. 10: 999-1007. PMID 25847527 DOI: 10.1002/Cmdc.201500060 |
0.351 |
|
| 2014 |
Gnaim S, Shabat D. Quinone-methide species, a gateway to functional molecular systems: from self-immolative dendrimers to long-wavelength fluorescent dyes. Accounts of Chemical Research. 47: 2970-84. PMID 25181456 DOI: 10.1021/Ar500179Y |
0.362 |
|
| 2014 |
Rader C, Segal DJ, Shabat D. Carlos F. Barbas III (1964-2014): Visionary at the interface of chemistry and biology. Acs Chemical Biology. 9: 1645-6. PMID 25123302 DOI: 10.1021/Cb5005993 |
0.568 |
|
| 2014 |
Kisin-Finfer E, Ferber S, Blau R, Satchi-Fainaro R, Shabat D. Synthesis and evaluation of new NIR-fluorescent probes for cathepsin B: ICT versus FRET as a turn-ON mode-of-action. Bioorganic & Medicinal Chemistry Letters. 24: 2453-8. PMID 24767838 DOI: 10.1016/J.Bmcl.2014.04.022 |
0.32 |
|
| 2014 |
Ferber S, Baabur-Cohen H, Blau R, Epshtein Y, Kisin-Finfer E, Redy O, Shabat D, Satchi-Fainaro R. Polymeric nanotheranostics for real-time non-invasive optical imaging of breast cancer progression and drug release. Cancer Letters. 352: 81-9. PMID 24614283 DOI: 10.1016/J.Canlet.2014.02.022 |
0.326 |
|
| 2014 |
Redy-Keisar O, Kisin-Finfer E, Ferber S, Satchi-Fainaro R, Shabat D. Synthesis and use of QCy7-derived modular probes for the detection and imaging of biologically relevant analytes. Nature Protocols. 9: 27-36. PMID 24309975 DOI: 10.1038/Nprot.2013.166 |
0.328 |
|
| 2013 |
Sella E, Shabat D. Hydroquinone-quinone oxidation by molecular oxygen: a simple tool for signal amplification through auto-generation of hydrogen peroxide. Organic & Biomolecular Chemistry. 11: 5074-8. PMID 23824077 DOI: 10.1039/C3Ob40962G |
0.321 |
|
| 2013 |
Kisin-Finfer E, Shabat D. New repertoire of 'donor-two-acceptor' NIR fluorogenic dyes. Bioorganic & Medicinal Chemistry. 21: 3602-8. PMID 23541837 DOI: 10.1016/J.Bmc.2013.02.049 |
0.302 |
|
| 2012 |
Karton-Lifshin N, Albertazzi L, Bendikov M, Baran PS, Shabat D. "Donor-two-acceptor" dye design: a distinct gateway to NIR fluorescence. Journal of the American Chemical Society. 134: 20412-20. PMID 23194283 DOI: 10.1021/Ja308124Q |
0.314 |
|
| 2012 |
Redy O, Shabat D. Modular theranostic prodrug based on a FRET-activated self-immolative linker. Journal of Controlled Release : Official Journal of the Controlled Release Society. 164: 276-82. PMID 22580227 DOI: 10.1016/J.Jconrel.2012.05.009 |
0.351 |
|
| 2012 |
Redy O, Kisin-Finfer E, Sella E, Shabat D. A simple FRET-based modular design for diagnostic probes. Organic & Biomolecular Chemistry. 10: 710-5. PMID 22159494 DOI: 10.1039/C1Ob06667F |
0.335 |
|
| 2011 |
Perry-Feigenbaum R, Sella E, Shabat D. Autoinductive exponential signal amplification: a diagnostic probe for direct detection of fluoride. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 12123-8. PMID 21905139 DOI: 10.1002/Chem.201101796 |
0.327 |
|
| 2011 |
Karton-Lifshin N, Segal E, Omer L, Portnoy M, Satchi-Fainaro R, Shabat D. A unique paradigm for a Turn-ON near-infrared cyanine-based probe: noninvasive intravital optical imaging of hydrogen peroxide. Journal of the American Chemical Society. 133: 10960-5. PMID 21631116 DOI: 10.1021/Ja203145V |
0.345 |
|
| 2010 |
Sella E, Weinstain R, Erez R, Burns NZ, Baran PS, Shabat D. Sulfhydryl-based dendritic chain reaction. Chemical Communications (Cambridge, England). 46: 6575-7. PMID 20714571 DOI: 10.1039/C0Cc02195D |
0.305 |
|
| 2010 |
Avital-Shmilovici M, Shabat D. Dendritic chain reaction: responsive release of hydrogen peroxide upon generation and enzymatic oxidation of methanol. Bioorganic & Medicinal Chemistry. 18: 3643-7. PMID 20231097 DOI: 10.1016/J.Bmc.2010.02.038 |
0.318 |
|
| 2010 |
Sella E, Lubelski A, Klafter J, Shabat D. Two-component dendritic chain reactions: experiment and theory. Journal of the American Chemical Society. 132: 3945-52. PMID 20192194 DOI: 10.1021/Ja910839N |
0.311 |
|
| 2010 |
Avital-Shmilovici M, Shabat D. Self-immolative dendrimers: A distinctive approach to molecular amplification Soft Matter. 6: 1073-1080. DOI: 10.1039/B922341J |
0.337 |
|
| 2010 |
Keinan E, Shabat D, Carmeli S. The 75th annual meeting of the Israel Chemical Society, Tel Aviv, David intercontinental hotel, january 25-26, 2010 Israel Journal of Chemistry. 50: 255-261. DOI: 10.1002/Ijch.201000050 |
0.454 |
|
| 2009 |
Perry-Feigenbaum R, Baran PS, Shabat D. The pyridinone-methide elimination. Organic & Biomolecular Chemistry. 7: 4825-8. PMID 19907770 DOI: 10.1039/B915265B |
0.325 |
|
| 2009 |
Weinstain R, Baran PS, Shabat D. Activity-linked labeling of enzymes by self-immolative polymers. Bioconjugate Chemistry. 20: 1783-91. PMID 19689155 DOI: 10.1021/Bc9002037 |
0.301 |
|
| 2009 |
Sella E, Shabat D. Dendritic chain reaction. Journal of the American Chemical Society. 131: 9934-6. PMID 19569684 DOI: 10.1021/Ja903032T |
0.3 |
|
| 2009 |
Stern L, Perry R, Ofek P, Many A, Shabat D, Satchi-Fainaro R. A novel antitumor prodrug platform designed to be cleaved by the endoprotease legumain. Bioconjugate Chemistry. 20: 500-10. PMID 19196156 DOI: 10.1021/Bc800448U |
0.305 |
|
| 2008 |
Erez R, Ebner S, Attali B, Shabat D. Chemotherapeutic bone-targeted bisphosphonate prodrugs with hydrolytic mode of activation. Bioorganic & Medicinal Chemistry Letters. 18: 816-20. PMID 18061452 DOI: 10.1016/J.Bmcl.2007.11.029 |
0.305 |
|
| 2007 |
Danieli E, Shabat D. Molecular probe for enzymatic activity with dual output. Bioorganic & Medicinal Chemistry. 15: 7318-24. PMID 17869526 DOI: 10.1016/J.Bmc.2007.08.046 |
0.326 |
|
| 2007 |
Shamis M, Shabat D. Single-triggered AB6 self-immolative dendritic amplifiers. Chemistry (Weinheim An Der Bergstrasse, Germany). 13: 4523-8. PMID 17477455 DOI: 10.1002/Chem.200700142 |
0.335 |
|
| 2007 |
Sagi A, Segal E, Satchi-Fainaro R, Shabat D. Remarkable drug-release enhancement with an elimination-based AB3 self-immolative dendritic amplifier. Bioorganic & Medicinal Chemistry. 15: 3720-7. PMID 17416532 DOI: 10.1016/J.Bmc.2007.03.054 |
0.357 |
|
| 2007 |
Shamis M, Barbas CF, Shabat D. A new visual screening assay for catalytic antibodies with retro-aldol retro-Michael activity. Bioorganic & Medicinal Chemistry Letters. 17: 1172-5. PMID 17234408 DOI: 10.1016/J.Bmcl.2006.12.057 |
0.362 |
|
| 2007 |
Amir RJ, Danieli E, Shabat D. Receiver-amplifier, self-immolative dendritic device. Chemistry (Weinheim An Der Bergstrasse, Germany). 13: 812-21. PMID 17075925 DOI: 10.1002/Chem.200601263 |
0.304 |
|
| 2006 |
Gopin A, Ebner S, Attali B, Shabat D. Enzymatic activation of second-generation dendritic prodrugs: Conjugation of self-immolative dendrimers with poly(ethylene glycol) via click chemistry. Bioconjugate Chemistry. 17: 1432-40. PMID 17105221 DOI: 10.1021/Bc060180N |
0.341 |
|
| 2006 |
Sagi A, Rishpon J, Shabat D. Amperometric assay for aldolase activity: antibody-catalyzed ferrocenylamine formation. Analytical Chemistry. 78: 1459-61. PMID 16503594 DOI: 10.1021/Ac0517141 |
0.389 |
|
| 2006 |
Weinstein R, Lerner RA, Barbas CF, Shabat D. Antibody-Catalyzed Asymmetric Intramolecular Michael Reaction Synfacts. 2006: 71-71. DOI: 10.1055/S-2005-921711 |
0.38 |
|
| 2006 |
Shabat D. Self-immolative dendrimers as novel drug delivery platforms Journal of Polymer Science, Part a: Polymer Chemistry. 44: 1569-1578. DOI: 10.1002/Pola.21258 |
0.335 |
|
| 2005 |
Weinstain R, Lerner RA, Barbas CF, Shabat D. Antibody-catalyzed asymmetric intramolecular Michael addition of aldehydes and ketones to yield the disfavored cis-product. Journal of the American Chemical Society. 127: 13104-5. PMID 16173712 DOI: 10.1021/Ja0536825 |
0.548 |
|
| 2005 |
Amir RJ, Popkov M, Lerner RA, Barbas CF, Shabat D. Prodrug activation gated by a molecular "OR" logic trigger. Angewandte Chemie (International Ed. in English). 44: 4378-81. PMID 15942963 DOI: 10.1002/Anie.200500842 |
0.453 |
|
| 2005 |
Haba K, Popkov M, Shamis M, Lerner RA, Barbas CF, Shabat D. Single-triggered trimeric prodrugs. Angewandte Chemie (International Ed. in English). 44: 716-20. PMID 15657968 DOI: 10.1002/Anie.200461657 |
0.447 |
|
| 2004 |
Shabat D, Amir RJ, Gopin A, Pessah N, Shamis M. Chemical adaptor systems. Chemistry (Weinheim An Der Bergstrasse, Germany). 10: 2626-34. PMID 15195294 DOI: 10.1002/Chem.200305715 |
0.357 |
|
| 2004 |
Pessah N, Reznik M, Shamis M, Yantiri F, Xin H, Bowdish K, Shomron N, Ast G, Shabat D. Bioactivation of carbamate-based 20(S)-camptothecin prodrugs. Bioorganic & Medicinal Chemistry. 12: 1859-66. PMID 15051055 DOI: 10.1016/J.Bmc.2004.01.039 |
0.394 |
|
| 2004 |
Gopin A, Rader C, Shabat D. New chemical adaptor unit designed to release a drug from a tumor targeting device by enzymatic triggering. Bioorganic & Medicinal Chemistry. 12: 1853-8. PMID 15051054 DOI: 10.1016/J.Bmc.2004.01.041 |
0.523 |
|
| 2004 |
Shamis M, Lode HN, Shabat D. Bioactivation of self-immolative dendritic prodrugs by catalytic antibody 38C2. Journal of the American Chemical Society. 126: 1726-31. PMID 14871103 DOI: 10.1021/Ja039052P |
0.385 |
|
| 2003 |
Rader C, Turner JM, Heine A, Shabat D, Sinha SC, Wilson IA, Lerner RA, Barbas CF. A humanized aldolase antibody for selective chemotherapy and adaptor immunotherapy. Journal of Molecular Biology. 332: 889-99. PMID 12972259 DOI: 10.1016/S0022-2836(03)00992-6 |
0.646 |
|
| 2003 |
Jikai J, Shamis M, Huebener N, Schroeder U, Wrasidlo W, Wenkel J, Lange B, Gaedicke G, Shabat D, Lode HN. Neuroblastoma directed therapy by a rational prodrug design of etoposide as a substrate for tyrosine hydroxylase. Cancer Letters. 197: 219-24. PMID 12880985 DOI: 10.1016/S0304-3835(03)00104-6 |
0.315 |
|
| 2003 |
Gopin A, Pessah N, Shamis M, Rader C, Shabat D. A chemical adaptor system designed to link a tumor-targeting device with a prodrug and an enzymatic trigger. Angewandte Chemie (International Ed. in English). 42: 327-32. PMID 12548691 DOI: 10.1002/Anie.200390108 |
0.482 |
|
| 2002 |
Satchi-Fainaro R, Wrasidlo W, Lode HN, Shabat D. Synthesis and characterization of a catalytic antibody-HPMA copolymer-Conjugate as a tool for tumor selective prodrug activation. Bioorganic & Medicinal Chemistry. 10: 3023-9. PMID 12110325 DOI: 10.1016/S0968-0896(02)00156-6 |
0.403 |
|
| 2001 |
Shabat D, Lode HN, Pertl U, Reisfeld RA, Rader C, Lerner RA, Barbas CF. In vivo activity in a catalytic antibody-prodrug system: Antibody catalyzed etoposide prodrug activation for selective chemotherapy. Proceedings of the National Academy of Sciences of the United States of America. 98: 7528-33. PMID 11404472 DOI: 10.1073/Pnas.131187998 |
0.659 |
|
| 1999 |
Shabat D, Rader C, List B, Lerner RA, Barbas CF. Multiple event activation of a generic prodrug trigger by antibody catalysis. Proceedings of the National Academy of Sciences of the United States of America. 96: 6925-30. PMID 10359815 DOI: 10.1073/Pnas.96.12.6925 |
0.698 |
|
| 1999 |
List B, Shabat D, Zhong G, Turner JM, Li A, Bui T, Anderson J, Lerner RA, Barbas CF. A catalytic enantioselective route to hydroxy-substituted quaternary carbon centers: Resolution of tertiary aldols with a catalytic antibody Journal of the American Chemical Society. 121: 7283-7291. DOI: 10.1021/Ja991507G |
0.687 |
|
| 1999 |
Shulman A, Keinan E, Shabat D, Barbas CF. Teaching Catalytic Antibodies to Undergraduate Students: An Organic Chemistry Lab Experiment Journal of Chemical Education. 76: 977-982. DOI: 10.1021/Ed076P977 |
0.586 |
|
| 1999 |
Shabat D, List B, Lerner RA, Barbas CF. A short enantioselective synthesis of 1-deoxy-L-xylulose by antibody catalysis Tetrahedron Letters. 40: 1437-1440. DOI: 10.1016/S0040-4039(98)02699-9 |
0.587 |
|
| 1998 |
Zhong G, Shabat D, List B, Anderson J, Sinha SC, Lerner RA, Barbas Iii CF. Catalytic Enantioselective Retro-Aldol Reactions: Kinetic Resolution of β-Hydroxyketones with Aldolase Antibodies. Angewandte Chemie (International Ed. in English). 37: 2481-2484. PMID 29711357 DOI: 10.1002/(Sici)1521-3773(19981002)37:18<2481::Aid-Anie2481>3.0.Co;2-T |
0.684 |
|
| 1998 |
Shabat D, Shulman H, Itzhaky H, Raymond JL, Keinan E. Enantioselectivity vs. kinetic resolution in antibody catalysis: Formation of the (S) product despite preferential binding of the (R) intermediate Chemical Communications. 1759-1760. DOI: 10.1039/A802374C |
0.537 |
|
| 1998 |
Hoffmann T, Zhong G, List B, Shabat D, Anderson J, Gramatikova S, Lerner RA, Barbas CF. Aldolase antibodies of remarkable scope Journal of the American Chemical Society. 120: 2768-2779. DOI: 10.1021/Ja973676B |
0.68 |
|
| 1998 |
Zhong G, Shabat D, List B, Anderson J, Sinha SC, Lerner RA, Barbas CF. Catalytic enantioselective retro-aldol reactions: Kinetic resolution of β-hydroxyketones with aldolase antibodies Angewandte Chemie - International Edition. 37: 2481-2484. DOI: 10.1002/(SICI)1521-3773(19981002)37:18<2481::AID-ANIE2481>3.0.CO;2-T |
0.607 |
|
| 1998 |
List B, Shabat D, Barbas CF, Lerner RA. Enantioselective total synthesis of some brevicomins using aldolase antibody 38C2 Chemistry - a European Journal. 4: 881-885. DOI: 10.1002/(Sici)1521-3765(19980515)4:5<881::Aid-Chem881>3.0.Co;2-# |
0.605 |
|
| 1998 |
Zhong G, Shabat D, List B, Anderson J, Sinha SC, Lerner RA, Barbas CF. Katalytische enantioselektive Retro-Aldolreaktion: kinetische Racematspaltung von β-Hydroxyketonen durch Aldolase-Antikörper Angewandte Chemie. 110: 2609-2612. DOI: 10.1002/(Sici)1521-3757(19980918)110:18<2609::Aid-Ange2609>3.0.Co;2-E |
0.618 |
|
| 1997 |
Shabat D, Grynszpan F, Saphier S, Turniansky A, Avnir D, Keinan E. An Efficient Sol - Gel Reactor for Antibody-Catalyzed Transformations Chemistry of Materials. 9: 2258-2260. DOI: 10.1021/Cm970193Y |
0.737 |
|
| 1996 |
Ghosh P, Shabat D, Kumar S, Sinha SC, Grynszpan F, Li J, Noodleman L, Keinan E. Using antibodies to perturb the coordination sphere of a transition metal complex. Nature. 382: 339-41. PMID 8684461 DOI: 10.1038/382339A0 |
0.697 |
|
| 1996 |
Shabat D, Sinha SC, Reymond JL, Keinan E. Catalytic antibodies as probes of evolution: Modeling of a primordial glycosidase Angewandte Chemie - International Edition in English. 35: 2628-2630. DOI: 10.1002/Anie.199626281 |
0.584 |
|
| 1996 |
Shabat D, Sinha SC, Reymond J, Keinan E. Katalytische Antikörper als Sonden für die Evolution von Enzymen: Modellierung einer frühen Glycosidase Angewandte Chemie. 108: 2800-2802. DOI: 10.1002/Ange.19961082212 |
0.458 |
|
| 1995 |
Shabat D, Itzhaky H, Reymond JL, Keinan E. Antibody catalysis of a reaction otherwise strongly disfavoured in water. Nature. 374: 143-6. PMID 7877686 DOI: 10.1038/374143A0 |
0.588 |
|
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