388 results on '"Iorga, Bogdan I."'
Search Results
52. The Neurotoxic Effect of 13,19-Didesmethyl and 13-Desmethyl Spirolide C Phycotoxins Is Mainly Mediated by Nicotinic Rather Than Muscarinic Acetylcholine Receptors
53. Cyclic Imine Toxins: Chemistry, Origin, Metabolism, Pharmacology, Toxicology, and Detection
54. Optimization of the rapid carbapenem inactivation method for use with AmpC hyperproducers
55. Detection and characterization of VIM-52, a new variant of VIM-1 from clinical isolate
56. Evaluation of docking performance in a blinded virtual screening of fragment-like trypsin inhibitors
57. Prediction of hydration free energies for aliphatic and aromatic chloro derivatives using molecular dynamics simulations with the OPLS-AA force field
58. Biochemical characterization of OXA-244, an emerging OXA-48 variant with reduced β-lactam hydrolytic activity
59. Base‐Mediated Generation of Ketenimines from Ynamides: [3+2] Annulation with Azaallyl Anions
60. Pyridinium Derivatives Of 3-Aminobenzenesulfonamide Are Nanomolar-Potent Inhibitors Of Tumor-Expressed Carbonic Anhydrase Isozymes Ca Ix And Ca Xii
61. From Synthetic Simplified Marine Metabolite Analogues to New Selective Allosteric Inhibitor of Aurora B Kinase
62. Disorder is a critical component of lipoprotein sorting in Gram-negative bacteria
63. Bivalent sequential binding of docetaxel to methyl-β-cyclodextrin
64. Base-Mediated Generation of Ketenimines from Ynamides: [3+2] Annulation with Azaallyl Anions.
65. Pyridinium derivatives of 3-aminobenzenesulfonamide are nanomolar-potent inhibitors of tumor-expressed carbonic anhydrase isozymes CA IX and CA XII
66. Defining the function of OmpA in the Rcs stress response
67. Author response: Defining the function of OmpA in the Rcs stress response
68. How the assembly and protection of the bacterial cell envelope depend on cysteine residues
69. Defining the function of OmpA in the Rcs stress response
70. NMR Characterization of the Influence of Zinc(II) Ions on the Structural and Dynamic Behavior of the New Delhi Metallo-β-Lactamase-1 and on the Binding with Flavonols as Inhibitors
71. Role of Arginine 214 in the Substrate Specificity of OXA-48
72. Substrate Specificity of OXA-48 after β5−β6 Loop Replacement
73. Mutational analysis of the Qi-site proton pathway in yeast cytochrome bc1 complex
74. Azetidinimines as a Novel Series of Non-Covalent Broad-Spectrum Inhibitors of β-Lactamases with Submicromolar Activities Against Carbapenemases of Classes A, B and D
75. LMB-1 producing Citrobacter freundii from Argentina, a novel player in the field of MBLs
76. Prediction of octanol-water partition coefficients for the SAMPL6-$$\log P$$ molecules using molecular dynamics simulations with OPLS-AA, AMBER and CHARMM force fields
77. Biochemical and Structural Characterization of OXA-405, an OXA-48 Variant with Extended-Spectrum β-Lactamase Activity
78. Mitochondrial complex III Qi -site inhibitor resistance mutations found in laboratory selected mutants and field isolates
79. The antimalarial compound ELQ-400 is an unusual inhibitor of the \textitbc _\textrm1 complex, targeting both \textitQ _\textrmo and \textitQ _\textrmi sites
80. Unravelling ceftazidime/avibactam resistance of KPC-28, a KPC-2 variant lacking carbapenemase activity
81. Genetic, Biochemical, and Structural Characterization of CMY-136 β-Lactamase, a Peculiar CMY-2 Variant
82. Deleting a Chromatin Remodeling Gene Increases the Diversity of Secondary Metabolites Produced by Colletotrichum higginsianum
83. Mitochondrial complex III Qi-site inhibitor resistance mutations found in laboratory selected mutants and field isolates
84. mTOR Inhibition via Displacement of Phosphatidic Acid Induces Enhanced Cytotoxicity Specifically in Cancer Cells
85. Blinded evaluation of cathepsin S inhibitors from the D3RGC3 dataset using molecular docking and free energy calculations
86. Genetic and Biochemical Characterization of OXA-519, a Novel OXA-48-Like β-Lactamase
87. The cyclic imine Prorocentrolide-A obtained from cultured Japanese Prorocentrum lima dinoflagellates target muscle- and neuronal-type nicotinic acetylcholine receptors
88. The antimalarial compound ELQ ‐400 is an unusual inhibitor of the bc 1 complex, targeting both Q o and Q i sites
89. (+)- and (−)-Ecarlottones, Uncommon Chalconoids from Fissistigma latifolium with Pro-Apoptotic Activity
90. Stereoselective Synthesis of 1,2‐trans‐Diamines Using the Three‐Component Borono‐Mannich Condensation – Reaction Scope and Mechanistic Insights
91. Characterization of BRP MBL , the Bleomycin Resistance Protein Associated with the Carbapenemase NDM
92. Ligandbook: an online repository for small and drug-like molecule force field parameters
93. Beta-lactamase database (BLDB) – structure and function
94. The unexpected increase of clotrimazole apparent solubility using randomly methylated β-cyclodextrin
95. Mitochondrial complex III Qi‐site inhibitor resistance mutations found in laboratory selected mutants and field isolates.
96. Pro-apoptotic meiogynin A derivatives that target Bcl-xL and Mcl-1
97. (+)- and (−)-Ecarlottones, Uncommon Chalconoids from Fissistigma latifoliumwith Pro-Apoptotic Activity
98. Cyclic imine neurotoxins acting on muscarinic and nicotinic acetylcholine receptors
99. Euphorbia dendroides Latex as a Source of Jatrophane Esters: Isolation, Structural Analysis, Conformational Study, and Anti-CHIKV Activity
100. Selectivity of Spiroimine Phycotoxins Toward Nicotinic Acetylcholine Receptors
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