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Nucleic Acids Research|November 28, 2012
Unusual sequence effects on nucleotide excision repair of arylamine lesions: DNA bending/distortion as a primary recognition factorVipin Jain, Benjamin Hilton, Bin Lin, et al.
Bioorganic & Medicinal Chemistry|June 30, 2016
Parametrization of halogen bonds in the CHARMM general force field: Improved treatment of ligand-protein interactionsIgnacio Soteras Gutiérrez, Fang-Yu Lin, Kenno Vanommeslaeghe, et al.
Biophysical Journal|March 26, 2025
Mapping the distribution and affinities of ligand interaction sites on human serum albuminAsuka A Orr, Agbo-Oma Uwakweh, Xun Li, et al.
ACS Biomaterials Science & Engineering|January 15, 2021
Cholic Acid-Derived Amphiphile which Combats Gram-Positive Bacteria-Mediated Infections via Disintegration of Lipid ClustersSandeep Kumar, Jyoti Thakur, Kavita Yadav, et al.
Chemmedchem|June 26, 2020
Rationally Designed Polypharmacology: α-Helix Mimetics as Dual Inhibitors of the Oncoproteins Mcl-1 and HDM2Ivie L Conlon, Brandon Drennen, Maryanna E Lanning, et al.
Molecular Pharmaceutics|March 3, 2025
Investigating the Interaction between Excipients and Monoclonal Antibodies PGT121 and N49P9.6-FR-LS: A Comprehensive AnalysisXun Li, Asuka A Orr, Mohammad M Sajadi, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|September 21, 2022
Carbodicarbenes and Striking Redox Transitions of their Conjugate Acids: Influence of NHC versus CAAC as Donor SubstituentsRamapada Dolai, Rahul Kumar, Benedict J Elvers, et al.
The Journal of Organic Chemistry|March 1, 2017
Iodobenzene-Catalyzed Synthesis of Phenanthridinones via Oxidative C-H AmidationDongdong Liang, Wenbo Yu, Nam Nguyen, et al.
ACS Chemical Neuroscience|May 30, 2013
Synthesis, modeling, and pharmacological evaluation of UMB 425, a mixed μ agonist/δ antagonist opioid analgesic with reduced tolerance liabilitiesJason R Healy, Padmavani Bezawada, Jihyun Shim, et al.
Biochemistry|August 17, 2011
Importance of domain closure for the autoactivation of ERK2Daniel Barr, Taiji Oashi, Kimberly Burkhard, et al.
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