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Durch Polymerase-Kettenreaktion erzeugte DNA-Peptid-Netzwerke als künstliche extrazelluläre Matrix.
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- Angewandte Chemie, 2016, v. 128, n. 34, p. 10291, doi. 10.1002/ange.201604687
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- Article
Oxime bond-linked daunorubicin-GnRH-III bioconjugates exert antitumor activity in castration-resistant prostate cancer cells via the type I GnRH receptor.
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- International Journal of Oncology, 2015, v. 46, n. 1, p. 243, doi. 10.3892/ijo.2014.2730
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- Article
Epitope structure and binding affinity of single chain llama anti-β-amyloid antibodies revealed by proteolytic excision affinity-mass spectrometry.
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- Journal of Molecular Recognition, 2013, v. 26, n. 1, p. 1, doi. 10.1002/jmr.2210
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Designer Extracellular Matrix Based on DNA-Peptide Networks Generated by Polymerase Chain Reaction.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 34, p. 10136, doi. 10.1002/anie.201604687
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- Article
Improved in vivo antitumor effect of a daunorubicin - GnRH-III bioconjugate modified by apoptosis inducing agent butyric acid on colorectal carcinoma bearing mice.
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- Investigational New Drugs, 2016, v. 34, n. 4, p. 416, doi. 10.1007/s10637-016-0354-7
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Protein Expression Profile of HT-29 Human Colon Cancer Cells after Treatment with a Cytotoxic Daunorubicin-GnRH-III Derivative Bioconjugate.
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- PLoS ONE, 2014, v. 9, n. 4, p. 1, doi. 10.1371/journal.pone.0094041
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- Article
Increased Levels of Antigen-Bound β-Amyloid Autoantibodies in Serum and Cerebrospinal Fluid of Alzheimer’s Disease Patients.
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- PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0068996
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Antigen-Bound and Free β-Amyloid Autoantibodies in Serum of Healthy Adults.
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- PLoS ONE, 2012, v. 7, n. 9, p. 1, doi. 10.1371/journal.pone.0044516
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- Article
In vitro degradation and antitumor activity of oxime bond-linked daunorubicin-GnRH-III bioconjugates and DNA-binding properties of daunorubicin-amino acid metabolites.
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- Amino Acids, 2011, v. 41, n. 2, p. 469, doi. 10.1007/s00726-010-0766-1
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- Article
Molecular characterization of the β‐amyloid(4‐10) epitope of plaque specific Aβ antibodies by affinity‐mass spectrometry using alanine site mutation.
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- Journal of Peptide Science, 2018, v. 24, n. 1, p. 1, doi. 10.1002/psc.3047
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- Article
Interaction structure of the complex between neuroprotective factor humanin and Alzheimer's β-amyloid peptide revealed by affinity mass spectrometry and molecular modeling.
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- Journal of Peptide Science, 2012, v. 18, n. 6, p. 373, doi. 10.1002/psc.2404
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Efficient synthesis of an (aminooxy) acetylated-somatostatin derivative using (aminooxy)acetic acid as a 'carbonyl capture' reagent.
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- Journal of Peptide Science, 2011, v. 17, n. 1, p. 39, doi. 10.1002/psc.1294
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Mass spectrometric identification of the trypsin cleavage pathway in lysyl-proline containing oligotuftsin peptides.
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- Journal of Peptide Science, 2007, v. 13, n. 4, p. 227, doi. 10.1002/psc.836
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Synthesis and structural characterization of bioactive peptide conjugates using thioether linkage approaches.
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- Journal of Peptide Science, 2004, v. 10, n. 12, p. 701, doi. 10.1002/psc.583
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- Article
Time- and pH-Dependent Copper Binding to Aβ(1-16) Peptide: An Electrospray Ionization-Mass Spectrometric Approach.
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- International Journal of Peptide Research & Therapeutics, 2015, v. 21, n. 1, p. 125, doi. 10.1007/s10989-014-9437-5
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Design, structural, and immuno-analytical properties of antigenic bioconjugates comprising a β-amyloid-plaque specific epitope.
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- Biopolymers, 2008, v. 90, n. 2, p. 94, doi. 10.1002/bip.20916
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Polypeptide conjugates comprising a β-amyloid plaque-specific epitope as new vaccine structures against Alzheimer's disease.
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- Biopolymers, 2004, v. 76, n. 6, p. 503, doi. 10.1002/bip.20160
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Modification of daunorubicin-GnRH-III bioconjugates with oligoethylene glycol derivatives to improve solubility and bioavailability for targeted cancer chemotherapy.
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- Biopolymers, 2015, v. 104, n. 3, p. 167, doi. 10.1002/bip.22629
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Design, synthesis, in vitro stability and cytostatic effect of multifunctional anticancer drug-bioconjugates containing GnRH-III as a targeting moiety.
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- Biopolymers, 2012, v. 98, n. 1, p. 1, doi. 10.1002/bip.21640
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- Article