about
Epicocconone-Hemicyanine Hybrids: Near Infrared Fluorophores for Protein Staining and Cell Imaging.Rapid isolation of novel FK506 binding proteins from multiple organisms using gDNA and cDNA T7 phage display.Design and synthesis of epicocconone analogues with improved fluorescence properties.Enantiodivergence in the Biosynthesis of Bromotyrosine Alkaloids from Sponges?Recombinant prespore-specific antigen from Dictyostelium discoideum is a beta-sheet glycoprotein with a spacer peptide modified by O-linked N-acetylglucosamine.Probing site specificity of DNA binding metallointercalators by NMR spectroscopy and molecular modeling.Antimicrobial mode of action of secretions from the metapleural gland of Myrmecia gulosa (Australian bull ant).Identifying the cellular targets of natural products using T7 phage display.9-Hydroxyfurodysinin-O-ethyl lactone: a new sesquiterpene isolated from the tropical marine sponge Dysidea arenaria.A one-pot synthesis and biological activity of ageladine A and analogues.Rapid identification of a protein binding partner for the marine natural product kahalalide F by using reverse chemical proteomics.Daptomycin, a last-resort antibiotic, binds ribosomal protein S19 in humans.Insights into Enzyme Catalysis and Thyroid Hormone Regulation of Cerebral Ketimine Reductase/μ-Crystallin Under Physiological Conditions.Crellasterones A and B: A-Norsterol Derivatives from the New Caledonian Sponge Crella incrustans.New antimicrobial bromotyrosine analogues from the sponge Pseudoceratina purpurea and its predator Tylodina corticalisReal-time fluorescence monitoring of tryptic digestion in proteomics.Mass spectral compatibility of four proteomics stains.Fluorometric assay for the determination of glutathione reductase activity.Synthesis of Substituted Oxo-Azepines by Regio- and Diastereoselective Hydroxylation.Chemical proteomics, an integrated research engine for exploring drug-target-phenotype interactions.Excited state dynamics of brightly fluorescent second generation epicocconone analogues.The role of different structural motifs in the ultrafast dynamics of second generation protein stains.Tracking of fast moving neuronal vesicles with ageladine A.Expanding antibiotic chemical space around the nidulin pharmacophore.Ketimine reductase/CRYM catalyzes reductive alkylamination of α-keto acids, confirming its function as an imine reductase.Characterisation of a novel UV filter in the lens of the thirteen-lined ground squirrel (Ictidomys tridecemlineatus)Chemical Ecology of the NudibranchsHalopicolinic acids, novel products arising through the degradation of chloro- and bromo-biphenyl by Sphingomonas paucimobilis BPSI-3Rapid screening of the antimicrobial activity of extracts and natural productsMultiple O-glycoforms on the spore coat protein SP96 in Dictyostelium discoideum. Fuc(alpha1-3)GlcNAc-alpha-1-P-Ser is the major modification5-Chloropicolinic acid is produced by specific degradation of 4-chlorobenzoic acid by Sphingomonas paucimobilis BPSI-3Banksialactones and Banksiamarins: Isochromanones and Isocoumarins from an Australian Fungus,Aspergillus banksianusNovel secoiridoids with antioxidant activity from Australian olive mill wasteConcise total synthesis of the marine natural product ageladine AMass spectrometric compatibility of Deep Purple and SYPRO Ruby total protein stains for high-throughput proteomics using large-format two-dimensional gel electrophoresisMechanism of reversible fluorescent staining of protein with epicoccononeUltrafast dynamics of epicocconone, a second generation fluorescent protein stainSynthesis of new BINAP-based aminophosphines and their ³¹P-NMR spectroscopyQuantitation of the anticancer drug abiraterone and its metabolite Δ(4)-abiraterone in human plasma using high-resolution mass spectrometryTalauxins: Hybrid Phenalenone Dimers from Talaromyces stipitatus
P50
Q31143047-2E2FF017-0329-4308-AABD-A6D5BE782EBFQ33501416-6969ACCC-F4D5-4C79-8401-5EA037862E06Q34441226-7F995FCF-2982-4507-AA95-B8E8DFE36476Q36248564-5E9CCC28-A083-4753-A722-2BC1F328221AQ36805030-7723193D-8FCA-441D-B1E2-C443385EBC34Q38302184-754139F7-B576-4D6B-BBD7-BC305E8B7A85Q38573362-B900023B-9DA1-4B49-BA7E-DAABAC9F4CC8Q38768896-9B9A815B-ACF6-4854-A1F4-7FB67760627CQ39355987-58A43312-11BD-4474-89EA-A1D7E284774AQ39574796-DA9E2A12-74A8-4B99-982E-E8779EDA000FQ40019976-472C7BAB-107F-47D5-9352-B078FDA2416FQ40982610-3448990B-48E5-4B9A-85E1-52F54E5F81C0Q40990256-9D136D7D-6981-4811-877A-7E49245FF86DQ41045928-5FA88513-E7C1-41BA-82B1-9C221272D516Q42675481-D19E5AE1-1E5D-4304-8C1F-24010DCB6288Q46872322-12984E50-7C73-4B23-9CB1-BE5B0E45D1CEQ46955492-16AF514B-5E6C-420D-A6E8-1F2F0941B36EQ46959640-9F59CF08-DB7F-409A-93F1-000E5E1F8D45Q48094838-1F1D8C15-1A1A-4D15-B286-40B6F614EB93Q50017799-489537F2-A9C8-44D2-B639-466840FF421CQ50279442-01C3D9AE-AD1E-4EDD-91D8-0BB420D1CA98Q50470050-BB61E92F-8856-4B98-8B87-36BDB63716BBQ50693723-13136A08-FE00-47D2-A31D-61C6D8AEE4E9Q53696911-B1BE9CCD-9D8F-4E5E-B91B-175167CE91F7Q55059197-A78D4186-6DC2-477B-A0A7-4F407A1B62FBQ60640997-CB0BB99F-EC2E-4129-914F-9CD6A0A59D3EQ61534234-66DBD2F4-E2DF-43C9-A1E7-15798B6444E2Q70987453-988D8595-A0C3-4FBF-AD26-5B1EA1D15B60Q71991615-625DAE37-3824-4B77-A3E5-6524F3D3222DQ73680655-E8629BC0-AF1C-4B33-A223-33638134741AQ74088764-FC6AF88F-82AF-4191-9EEB-EBD3B1BABDDDQ78311331-539648FB-FDA4-49B3-9E3B-A7B41CA2E5E3Q79992806-5796C481-B2CC-4CDC-A6F9-95552CA86C3BQ80157539-7E92A305-7498-4E6C-8AB7-CC91E20EFD3EQ80754720-0B1FEA3B-6DD6-4E5D-AB30-B9BEFACD6D6CQ81808694-35A2E63B-B909-4608-BBED-3E30A239FD05Q84727421-C6345533-BD29-4308-BC92-3F90CADBAE02Q86254554-64E51081-E49A-4844-AB92-70CE21C5487AQ88040092-E20838E5-2F7F-47C5-AE88-4BDEEB5DAC63Q89971761-2A701631-684D-46E1-A7FB-703FC3B53B29
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Peter Karuso
@ast
Peter Karuso
@en
Peter Karuso
@es
Peter Karuso
@nl
Peter Karuso
@sl
type
label
Peter Karuso
@ast
Peter Karuso
@en
Peter Karuso
@es
Peter Karuso
@nl
Peter Karuso
@sl
prefLabel
Peter Karuso
@ast
Peter Karuso
@en
Peter Karuso
@es
Peter Karuso
@nl
Peter Karuso
@sl
P1053
D-6442-2013
P106
P1153
6603734227
P21
P31
P3829
P496
0000-0002-0217-6021