Search Results - "Solomon, Ohad"

Using a Single Peptide to Electrochemically Sense Multiple Kinases by Solomon, Ohad, Alshanski, Israel, Shitrit, Ariel, Chen, Yu-Ju, Friedler, Assaf, Yitzchaik, Shlomo

“…Kinases are responsible for regulating cellular and physiological processes, and abnormal kinase activity is associated with various diseases. Therefore,…”
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Electrochemical biosensors based on peptide-kinase interactions at the kinase docking site by Joshi, Pralhad Namdev, Mervinetsky, Evgeniy, Solomon, Ohad, Chen, Yu-Ju, Yitzchaik, Shlomo, Friedler, Assaf

“…Kinases are important cancer biomarkers and are conventionally detected based on their catalytic activity. Kinases regulate cellular activities by…”
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Front Cover: Kinase Sensing Based on Protein Interactions at the Catalytic Site (Chem. Eur. J. 17/2022) by Solomon, Ohad, Sapir, Hannah, Mervinetsky, Evgeniy, Chen, Yu‐Ju, Friedler, Assaf, Yitzchaik, Shlomo

“…An electrochemical biosensor has been developed that is based on the interaction between the catalytic site of the kinase and the phosphorylation site of its…”
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Kinase Sensing Based on Protein Interactions at the Catalytic Site by Solomon, Ohad, Sapir, Hannah, Mervinetsky, Evgeniy, Chen, Yu‐Ju, Friedler, Assaf, Yitzchaik, Shlomo

“…The role kinases play in regulating cellular processes makes them potential biomarkers for detecting the onset and prognosis of various diseases, including…”
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Kinase Sensing Based on Protein Interactions at the Catalytic Site by Solomon, Ohad, Sapir, Hannah, Mervinetsky, Evgeniy, Chen, Yu‐Ju, Friedler, Assaf, Yitzchaik, Shlomo

“…Invited for the cover of this issue is Assaf Friedler, Shlomo Yitzchaik and co‐workers at the Hebrew University of Jerusalem and the Academia Sinica. The image…”
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Peptide‐Based Inhibitors that Target the Docking Site of ERK2 by Solomon, Ohad, Shpilt, Zohar, Sapir, Hannah, Marom, Shir, Bibas, Shai, Chen, Yu‐Ju, Tshuva, Edit Y., Yitzchaik, Shlomo, Friedler, Assaf

“…Abnormal kinase activity is highly associated with disease, especially cancer. Thus, kinases are important targets for developing anti‐cancer drugs. The common…”
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