Works matching Emil Erlenmeyer
Results: 97
Emil Erlenmeyer's Lehrbuch der organischen Chemie. 8. Lieferung. Redigiert von Dr. Otto Hecht, Professor am Realgymnasium in Würzburg. Leipzig und Heidelberg, C. F. Winter'sche Verlagshandlung. 1889.
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- Archiv der Pharmazie, 1889, v. 227, n. 13, p. 623, doi. 10.1002/ardp.18892271311
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- Article
Lehrbuch der organischen Chemie von Emil Erlenmeyer. Siebente Lieferung. Redigiert von dr. Otto Hecht, Professor am Realgymnasium zu Würzburg. Leipzig und Heidelberg. C. F. Winter'sche Verlags-handlung. 1887.
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- Archiv der Pharmazie, 1888, v. 226, n. 3, p. 135, doi. 10.1002/ardp.18882260306
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Lehrbuch der organischen Chemie von Emil Erlenmeyer. Fünfte Lieferung. Redigirt von Dr. Otto Hecht, Professor am Realgymnasium zu Würzburg. Leipzig und Heidelberg. C. F. Winter'sche Verlagshandlung. 1885.
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- Archiv der Pharmazie, 1885, v. 223, n. 11, p. 455, doi. 10.1002/ardp.18852231111
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Lehrbuch der organischen Chemie von Dr. Emil Erlenmeyer, o. Professor der Chemie an der technischen Hochschule München. Dritte Lieferung. Leipzig und Heidelberg. C. F. Winter'sche Buchhandlung. 1882.
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- Archiv der Pharmazie, 1882, v. 220, n. 6, p. 478, doi. 10.1002/ardp.18822200609
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Zum Gedenken: Richard August Carl Emil Erlenmeyer.
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- Chemkon - Chemie Konkret, 2009, v. 16, n. 2, p. 105, doi. 10.1002/ckon.200990011
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Das Portrait: Emil Erlenmeyer 1825-1909.
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- Chemie in unserer Zeit, 1972, v. 6, n. 2, p. 53, doi. 10.1002/ciuz.19720060204
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Justus von Liebig and August Wilhelm Hofmann in ihren Briefen (Book Review).
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- 1989
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- Book Review
Site‐Selective Protein Conjugation by a Multicomponent Ugi Reaction.
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- Chemistry - A European Journal, 2024, v. 30, n. 14, p. 1, doi. 10.1002/chem.202303242
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Cover Feature: Optimization of the Lead Compound NVP‐BHG712 as a Colorectal Cancer Inhibitor (Chem. Eur. J. 23/2023).
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- Chemistry - A European Journal, 2023, v. 29, n. 23, p. 1, doi. 10.1002/chem.202300918
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Optimization of the Lead Compound NVP‐BHG712 as a Colorectal Cancer Inhibitor.
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- Chemistry - A European Journal, 2023, v. 29, n. 23, p. 1, doi. 10.1002/chem.202203967
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N‐Heterocyclic Carbenes: Molecular Porters of Surface Mounted Ru‐Porphyrins.
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- Angewandte Chemie, 2022, v. 134, n. 49, p. 1, doi. 10.1002/ange.202211877
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Direkte Affinitätsreinigung lang wirksamer PASylierter Proteine mit therapeutischem Anwendungspotential unter Nutzung von L‐Prolinamid zur milden Elution.
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- Angewandte Chemie, 2022, v. 134, n. 25, p. 1, doi. 10.1002/ange.202200079
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Das humane Wirtsabwehrpeptid Cathelicidin LL-37 ist ein nanomolarer Inhibitor der amyloiden Selbstassoziation von Inselamyloid-Polypeptid (IAPP).
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- Angewandte Chemie, 2020, v. 132, n. 31, p. 12937, doi. 10.1002/ange.202000148
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Structural Insight into IAPP‐Derived Amyloid Inhibitors and Their Mechanism of Action.
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- Angewandte Chemie, 2020, v. 132, n. 14, p. 5820, doi. 10.1002/ange.201914559
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Peptid‐basierte molekulare Strategien zum Einsatz bei Proteinfehlfaltung, Proteinaggregation und Zelldegeneration.
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- Angewandte Chemie, 2020, v. 132, n. 9, p. 3396, doi. 10.1002/ange.201906908
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Frontispiz: Snapshots of Dynamic Adaptation: Two‐Dimensional Molecular Architectonics with Linear Bis‐Hydroxamic Acid Modules.
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- Angewandte Chemie, 2019, v. 131, n. 52, p. N.PAG, doi. 10.1002/ange.201985262
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Snapshots of Dynamic Adaptation: Two‐Dimensional Molecular Architectonics with Linear Bis‐Hydroxamic Acid Modules.
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- Angewandte Chemie, 2019, v. 131, n. 52, p. 19124, doi. 10.1002/ange.201912247
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METHimpute: imputation-guided construction of complete methylomes from WGBS data.
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- BMC Genomics, 2018, v. 19, n. 1, p. 1, doi. 10.1186/s12864-018-4641-x
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A MIF-Derived Cyclopeptide that Inhibits MIF Binding and Atherogenic Signaling via the Chemokine Receptor CXCR2.
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- ChemBioChem, 2021, v. 22, n. 6, p. 1012, doi. 10.1002/cbic.202000574
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Engineering a Highly Active Sucrose Isomerase for Enhanced Product Specificity by Using a "Battleship" Strategy.
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- ChemBioChem, 2020, v. 21, n. 15, p. 2161, doi. 10.1002/cbic.202000007
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Scavenging Bacterial Siderophores with Engineered Lipocalin Proteins as an Alternative Antimicrobial Strategy.
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- ChemBioChem, 2020, v. 21, n. 5, p. 601, doi. 10.1002/cbic.201900564
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A Tetrahedral Boronic Acid Diester Formed by an Unnatural Amino Acid in the Ligand Pocket of an Engineered Lipocalin.
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- ChemBioChem, 2020, v. 21, n. 4, p. 469, doi. 10.1002/cbic.201900405
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Acyldepsipeptide Probes Facilitate Specific Detection of Caseinolytic Protease P Independent of Its Oligomeric and Activity State.
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- ChemBioChem, 2020, v. 21, n. 1/2, p. 235, doi. 10.1002/cbic.201900477
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AlphaBeta: computational inference of epimutation rates and spectra from high-throughput DNA methylation data in plants.
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- Genome Biology, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s13059-020-02161-6
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Cross-Amyloid Interaction of Aβ and IAPP at Lipid Membranes.
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- Angewandte Chemie International Edition, 2012, v. 51, n. 3, p. 679, doi. 10.1002/anie.201105877
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Terminating the Amyloid Zipper by Design.
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- Angewandte Chemie International Edition, 2011, v. 50, n. 48, p. 11293, doi. 10.1002/anie.201105706
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Identification of Hot Regions of the Aβ-IAPP Interaction Interface as High-Affinity Binding Sites in both Cross- and Self-Association.
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- Angewandte Chemie International Edition, 2010, v. 49, n. 17, p. 3081, doi. 10.1002/anie.200904902
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Mitotic arrest and slippage induced by pharmacological inhibition of Polo-like kinase 1.
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- Molecular Oncology, 2015, v. 9, n. 1, p. 140, doi. 10.1016/j.molonc.2014.07.020
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Quantitative chemical proteomics reveals a Plk1 inhibitor-compromised cell death pathway in human cells.
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- Cell Research, 2014, v. 24, n. 9, p. 1141, doi. 10.1038/cr.2014.86
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Expression and Purification of EPHA2 Tyrosine Kinase Domain for Crystallographic and NMR Studies.
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- ChemBioChem, 2016, v. 17, n. 23, p. 2257, doi. 10.1002/cbic.201600483
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Phosphoramidates as Novel Activity-Based Probes for Serine Proteases.
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- ChemBioChem, 2014, v. 15, n. 8, p. 1106, doi. 10.1002/cbic.201400013
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Derivatization of Antibody Fab Fragments: A Designer Enzyme for Native Protein Modification.
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- ChemBioChem, 2014, v. 15, n. 8, p. 1096, doi. 10.1002/cbic.201400059
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Shedding Light on Alzheimer's β-Amyloid Aggregation with Chemical Tools.
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- ChemBioChem, 2012, v. 13, n. 1, p. 27, doi. 10.1002/cbic.201100631
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Cover Picture: Dissecting the Role of Single Regions of an IAPP Mimic and IAPP in Inhibition of Aβ40 Amyloid Formation and Cytotoxicity (ChemBioChem 9/2011).
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- ChemBioChem, 2011, v. 12, n. 9, p. 1285, doi. 10.1002/cbic.201190036
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Dissecting the Role of Single Regions of an IAPP Mimic and IAPP in Inhibition of Aβ40 Amyloid Formation and Cytotoxicity.
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- ChemBioChem, 2011, v. 12, n. 9, p. 1313, doi. 10.1002/cbic.201100192
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Identification of CYP106A2 as a Regioselective Allylic Bacterial Diterpene Hydroxylase.
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- ChemBioChem, 2011, v. 12, n. 4, p. 576, doi. 10.1002/cbic.201000404
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Mass-spectrometry-based draft of the human proteome.
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- Nature, 2014, v. 509, n. 7502, p. 1, doi. 10.1038/nature13319
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3-hydroxyisobutyrate dehydrogenase-I from Pseudomonas denitrificans ATCC 13867 degrades 3-hydroxypropionic acid.
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- Biotechnology & Bioprocess Engineering, 2014, v. 19, n. 1, p. 1, doi. 10.1007/s12257-013-0487-x
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Translatomics combined with transcriptomics and proteomics reveals novel functional, recently evolved orphan genes in Escherichia coli O157:H7 (EHEC).
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- BMC Genomics, 2016, v. 17, p. 1, doi. 10.1186/s12864-016-2456-1
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Distinct conformational and energetic features define the specific recognition of (di)aromatic peptide motifs by PEX14.
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- Biological Chemistry, 2023, v. 404, n. 2/3, p. 179, doi. 10.1515/hsz-2022-0177
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Structural basis of Alzheimer β-amyloid peptide recognition by engineered lipocalin proteins with aggregation-blocking activity.
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- Biological Chemistry, 2022, v. 403, n. 5/6, p. 557, doi. 10.1515/hsz-2021-0375
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The extracellular region of bovine milk butyrophilin exhibits closer structural similarity to human myelin oligodendrocyte glycoprotein than to immunological BTN family receptors.
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- Biological Chemistry, 2021, v. 402, n. 10, p. 1187, doi. 10.1515/hsz-2021-0122
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Quantitative proteome profiling of human myoma and myometrium tissue reveals kinase expression signatures with potential for therapeutic intervention.
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- Proteomics, 2015, v. 15, n. 2/3, p. 356, doi. 10.1002/pmic.201400213
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Post-VX exposure treatment of rats with engineered phosphotriesterases.
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- Archives of Toxicology, 2022, v. 96, n. 2, p. 571, doi. 10.1007/s00204-021-03199-6
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Drastic alterations in the loop structure around colchicine upon complex formation with an engineered lipocalin indicate a conformational selection mechanism.
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- Acta Crystallographica: Section F, Structural Biology Communications, 2023, v. 79, n. 9, p. 231, doi. 10.1107/S2053230X23006817
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Studying epigenetic complexes and their inhibitors with the proteomics toolbox.
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- Clinical Epigenetics, 2016, v. 8, p. 1, doi. 10.1186/s13148-016-0244-z
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Predicting the bioactive conformations of macrocycles: a molecular dynamics-based docking procedure with DynaDock.
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- Journal of Molecular Modeling, 2019, v. 25, n. 7, p. N.PAG, doi. 10.1007/s00894-019-4077-5
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Environmental polarity induces conformational transitions in a helical peptide sequence from bacteriophage T4 lysozyme and its tandem duplicate: a molecular dynamics simulation study.
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- Journal of Molecular Modeling, 2015, v. 21, n. 4, p. 1, doi. 10.1007/s00894-015-2621-5
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N‐Heterocyclic Carbenes: Molecular Porters of Surface Mounted Ru‐Porphyrins.
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- Angewandte Chemie International Edition, 2022, v. 61, n. 49, p. 1, doi. 10.1002/anie.202211877
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Direct Affinity Purification of Long‐Acting PASylated Proteins with Therapeutic Potential Using L‐Prolinamide for Mild Elution.
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- Angewandte Chemie International Edition, 2022, v. 61, n. 25, p. 1, doi. 10.1002/anie.202200079
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