Herbert Waldmann
Waldmann, Herbert.
Waldmann, H. (Herbert)
Waldmann, Herbert, 1957-
Waldmann, H.
VIAF ID: 41995511 (Personal)
Permalink: http://viaf.org/viaf/41995511
Preferred Forms
- 100 0 _ ‡a Herbert Waldmann
- 200 _ | ‡a Waldmann ‡b Herbert
- 100 1 _ ‡a Waldmann, H.
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- 100 1 _ ‡a Waldmann, H. ‡q (Herbert)
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- 100 1 _ ‡a Waldmann, H. ‡q (Herbert)
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- 100 1 _ ‡a Waldmann, Herbert
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- 100 1 _ ‡a Waldmann, Herbert
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- 100 1 _ ‡a Waldmann, Herbert ‡d 1957-
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4xx's: Alternate Name Forms (22)
5xx's: Related Names (7)
- 510 2 _ ‡a Diplomarbeit
- 551 _ _ ‡a Dortmund ‡4 ortw ‡4 https://d-nb.info/standards/elementset/gnd#placeOfActivity
- 510 2 _ ‡a John Wiley & Sons
- 510 2 _ ‡a Max-Planck-Institut für Molekulare Physiologie ‡4 affi ‡4 https://d-nb.info/standards/elementset/gnd#affiliation ‡e Affiliation
- 510 2 _ ‡a Max-Planck-Institut für Molekulare Physiologie
- 510 2 _ ‡a Technische Universität Dortmund ‡b Chemische Biologie ‡4 affi ‡4 https://d-nb.info/standards/elementset/gnd#affiliation ‡e Affiliation
- 510 2 _ ‡a Technische Universität Dortmund
Works
Title | Sources |
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Bioorganic chemistry of biological signal transduction | |
Concepts and Case Studies in Chemical Biology | |
Deep painting: cheminformatics approaches to connect the biological profiles of compounds with their structural information | |
Enantioselective Formal C(sp3 )−H Bond Activation in the Synthesis of Bioactive Spiropyrazolone Derivatives | |
Enantioselective Synthesis of Five-Membered-Ring Atropisomers with a Chiral Rh(III) Complex | |
Enantioselective Synthesis of the C10–C20Fragment of Fusicoccin A | |
Enantioselective Synthesis of the Spiro-Tropanyl Oxindole Scaffold Through Bimetallic Relay Catalysis | |
Enantiospecific synthesis of the (9S,18R)-diastereomer of the leukocyte adhesion inhibitor cyclamenol A. | |
Endothelial survival factors and spatial completion, but not pericyte coverage of retinal capillaries determine vessel plasticity | |
Enhancement of the enantioselectivity of penicillin G acylase from E. coli by “substrate tuning” | |
Enzymatic Synthesis of a Characteristic Phosphorylated and Glycosylated Peptide Fragment of the Large Subunit of Mammalian RNA Polymerase II | |
Enzymatic Synthesis of Peptides andRas Lipopeptides Employing Choline Ester as a Solubilizing, Protecting, and Activating Group | |
Enzymatically cleavable linker groups in polymer-supported synthesis | |
Enzyme catalysis in organic synthesis : a comprehensive handbook | |
Enzymic Protecting Group Techniques | |
Epiblastin A Induces Reprogramming of Epiblast Stem Cells Into Embryonic Stem Cells by Inhibition of Casein Kinase 1 | |
Erratum: A crowdsourcing evaluation of the NIH chemical probes | |
Erratum: Corrigendum: Interactive exploration of chemical space with Scaffold Hunter | |
Evolution im Reagenzglas: ein Beitrag zur weißen Biotechnologie : Beiträge der akademischen Festveranstaltung zur Verleihung des Ernst Hellmut Vits-Preises an Prof. Dr. Manfred T. Reetz am 28. November 2006 im Schloss zu Münster | |
Exploiting the Substrate Tolerance of Farnesyltransferase for Site-Selective Protein Derivatization | |
Exploring and exploiting biologically relevant chemical space | |
Exploring Natural Product Fragments for Drug and Probe Discovery | |
Farnesylation of Ras is important for the interaction with phosphoinositide 3-kinase gamma | |
Flexibility of ras lipid modifications studied by 2H solid-state NMR and molecular dynamics simulations | |
Flexible and general synthesis of functionalized phosphoisoprenoids for the study of prenylation in vivo and in vitro | |
Flexible total synthesis of biphenomycin B. | |
Fluorogenic probes for live-cell imaging of the cytoskeleton | |
From protein domains to drug candidates-natural products as guiding principles in the design and synthesis of compound libraries | |
Gamma-pyrone natural products--a privileged compound class provided by nature | |
General Enantioselective C−H Activation with Efficiently Tunable Cyclopentadienyl Ligands | |
Generation of live-cell microarrays by means of DNA-Directed immobilization of specific cell-surface ligands | |
Gibbs energy determinants of lipoprotein insertion into lipid membranes: the case study of Ras proteins. | |
Gold(I)-Catalyzed Synthesis of Benzoxocines by an 8-endo-dig Cyclization | |
Gold(III)-Mediated Aldol Condensations Provide Efficient Access to Nitrogen Heterocycles | |
Guided by evolution: from biology oriented synthesis to pseudo natural products | |
Highly Enantioselective Catalytic [6+3] Cycloadditions of Azomethine Ylides | |
Highly Enantioselective Catalytic Synthesis of Neurite Growth-Promoting Secoyohimbanes | |
Highly Enantioselective Catalytic Vinylogous Propargylation of Coumarins Yields a Class of Autophagy Inhibitors | |
Highly Enantioselective Intramolecular 1,3-Dipolar Cycloaddition: A Route to Piperidino-Pyrrolizidines | |
Highly enantioselective synthesis and cellular evaluation of spirooxindoles inspired by natural products | |
Identification and specificity profiling of protein prenyltransferase inhibitors using new fluorescent phosphoisoprenoids | |
Identification of a small molecule inhibitor that stalls splicing at an early step of spliceosome activation. | |
Identification of Acyl Protein Thioesterases 1 and 2 as the Cellular Targets of the Ras-Signaling Modulators Palmostatin B and M | |
Identification of cytotoxic, glutathione-reactive moieties inducing accumulation of reactive oxygen species via glutathione depletion | |
Identification of hPin1 inhibitors that induce apoptosis in a mammalian Ras transformed cell line. | |
Identification of mono- and bisubstrate inhibitors of protein farnesyltransferase and inducers of apoptosis from a pepticinnamin E library | |
Identification of novel PDEδ interacting proteins | |
Identification of potent Ras signaling inhibitors by pathway-selective phenotype-based screening | |
Identification of pyrazolopyridazinones as PDEδ inhibitors | |
Identification of Quinolinols as Activators of TEAD-Dependent Transcription | |
Identification of siRNA delivery enhancers by a chemical library screen | |
Image-Based Morphological Profiling Identifies a Lysosomotropic, Iron-Sequestering Autophagy Inhibitor | |
Impairment of prostate cancer cell growth by a selective and reversible lysine-specific demethylase 1 inhibitor | |
Indoloquinolizidine Derivatives as Novel and Potent Apoptosis Inducers and Cell-Cycle Blockers | |
Influence of serine O-glycosylation or O-phosphorylation close to the vJun nuclear localisation sequence on nuclear import | |
Influence of the lipid anchor motif of N-ras on the interaction with lipid membranes: a surface plasmon resonance study | |
Inhibiting the palmitoylation/depalmitoylation cycle selectively reduces the growth of hematopoietic cells expressing oncogenic Nras | |
Inhibition of angiogenesis-relevant receptor tyrosine kinases by sulindac analogues | |
Inhibition of Rab Prenylation | |
Inhibitors of protein tyrosine phosphatases: next-generation drugs? | |
Kemikaru baioroji : Seiko jirei kara manabu kenkyu senryaku. | |
n94113551 | |
Natural product-derived modulators of cell cycle progression and viral entry by enantioselective oxa Diels-Alder reactions on the solid phase | |
Organic synthesis highlights, c1991-c1995: | |
Small molecule - protein interactions | |
Solid and solution phase combinatorial chemistry | |
Synthese von Naturstoff-basierten Substanzbibliotheken | |
Systems chemical biology : methods and protocols | |
Visualizing association of lipidated signaling proteins in heterogeneous membranes--partitioning into subdomains, lipid sorting, interfacial adsorption, and protein association | |
کشف مهار کننده های مسیرهای سیگنالینگ Wnt و جوجه تیغی از طریق سنتز enantioselective کاتالیزوری یک مجموعه ترکیبی با الهام از iridoid. | |
মুখবন্ধ | |
ケミカルバイオロジー : 成功事例から学ぶ研究戦略 |