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Showing 49 to 56 of 56 entries
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The D-amino acid peptide D3 reduces amyloid fibril boosted HIV-1 infectivity.

AIDS research and therapy

Widera M, Klein AN, Cinar Y, Funke SA, Willbold D, Schaal H.
PMID: 24422713
AIDS Res Ther. 2014 Jan 14;11(1):1. doi: 10.1186/1742-6405-11-1.

BACKGROUND: Amyloid fibrils such as Semen-Derived Enhancer of Viral Infection (SEVI) or amyloid-β-peptide (Aβ) enhance HIV-1 attachment and entry. Inhibitors destroying or converting those fibrils into non-amyloidogenic aggregates effectively reduce viral infectivity. Thus, they seem to be suitable as...

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Widera M, Klein AN, Cinar Y, et al. The D-amino acid peptide D3 reduces amyloid fibril boosted HIV-1 infectivity. AIDS Res Ther. 2014;11(1):1doi: 10.1186/1742-6405-11-1.
Widera, M., Klein, A. N., Cinar, Y., Funke, S. A., Willbold, D., & Schaal, H. (2014). The D-amino acid peptide D3 reduces amyloid fibril boosted HIV-1 infectivity. AIDS research and therapy, 11(1), 1. https://doi.org/10.1186/1742-6405-11-1
Widera, Marek, et al. "The D-amino acid peptide D3 reduces amyloid fibril boosted HIV-1 infectivity." AIDS research and therapy vol. 11,1 (2014): 1. doi: https://doi.org/10.1186/1742-6405-11-1
Widera M, Klein AN, Cinar Y, Funke SA, Willbold D, Schaal H. The D-amino acid peptide D3 reduces amyloid fibril boosted HIV-1 infectivity. AIDS Res Ther. 2014 Jan 14;11(1):1. doi: 10.1186/1742-6405-11-1. PMID: 24422713; PMCID: PMC3899924.
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The tungsten isotopic composition of the Earth's mantle before the terminal bombardment.

Nature

Willbold M, Elliott T, Moorbath S.
PMID: 21901010
Nature. 2011 Sep 07;477(7363):195-8. doi: 10.1038/nature10399.

Many precious, 'iron-loving' metals, such as gold, are surprisingly abundant in the accessible parts of the Earth, given the efficiency with which core formation should have removed them to the planet's deep interior. One explanation of their over-abundance is...

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Willbold M, Elliott T, Moorbath S. The tungsten isotopic composition of the Earth's mantle before the terminal bombardment. Nature. 2011;477(7363):195-8doi: 10.1038/nature10399.
Willbold, M., Elliott, T., & Moorbath, S. (2011). The tungsten isotopic composition of the Earth's mantle before the terminal bombardment. Nature, 477(7363), 195-8. https://doi.org/10.1038/nature10399
Willbold, Matthias, et al. "The tungsten isotopic composition of the Earth's mantle before the terminal bombardment." Nature vol. 477,7363 (2011): 195-8. doi: https://doi.org/10.1038/nature10399
Willbold M, Elliott T, Moorbath S. The tungsten isotopic composition of the Earth's mantle before the terminal bombardment. Nature. 2011 Sep 07;477(7363):195-8. doi: 10.1038/nature10399. PMID: 21901010.
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A comparative pharmaco-metabolomic study of glutaminase inhibitors in glioma stem-like cells confirms biological effectiveness but reveals differences in target-specificity.

Cell death discovery

Koch K, Hartmann R, Tsiampali J, Uhlmann C, Nickel AC, He X, Kamp MA, Sabel M, Barker RA, Steiger HJ, Hänggi D, Willbold D, Maciaczyk J, Kahlert UD.
PMID: 32337072
Cell Death Discov. 2020 Apr 16;6:20. doi: 10.1038/s41420-020-0258-3. eCollection 2020.

Cancer cells upregulate anabolic processes to maintain high rates of cellular turnover. Limiting the supply of macromolecular precursors by targeting enzymes involved in biosynthesis is a promising strategy in cancer therapy. Several tumors excessively metabolize glutamine to generate precursors...

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Koch K, Hartmann R, Tsiampali J, et al. A comparative pharmaco-metabolomic study of glutaminase inhibitors in glioma stem-like cells confirms biological effectiveness but reveals differences in target-specificity. Cell Death Discov. 2020;6:20doi: 10.1038/s41420-020-0258-3.
Koch, K., Hartmann, R., Tsiampali, J., Uhlmann, C., Nickel, A. C., He, X., Kamp, M. A., Sabel, M., Barker, R. A., Steiger, H. J., Hänggi, D., Willbold, D., Maciaczyk, J., & Kahlert, U. D. (2020). A comparative pharmaco-metabolomic study of glutaminase inhibitors in glioma stem-like cells confirms biological effectiveness but reveals differences in target-specificity. Cell death discovery, 620. https://doi.org/10.1038/s41420-020-0258-3
Koch, Katharina, et al. "A comparative pharmaco-metabolomic study of glutaminase inhibitors in glioma stem-like cells confirms biological effectiveness but reveals differences in target-specificity." Cell death discovery vol. 6 (2020): 20. doi: https://doi.org/10.1038/s41420-020-0258-3
Koch K, Hartmann R, Tsiampali J, Uhlmann C, Nickel AC, He X, Kamp MA, Sabel M, Barker RA, Steiger HJ, Hänggi D, Willbold D, Maciaczyk J, Kahlert UD. A comparative pharmaco-metabolomic study of glutaminase inhibitors in glioma stem-like cells confirms biological effectiveness but reveals differences in target-specificity. Cell Death Discov. 2020 Apr 16;6:20. doi: 10.1038/s41420-020-0258-3. eCollection 2020. PMID: 32337072; PMCID: PMC7162917.
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High-affinity binding and catalytic activity of His/Tyr-based sequences: Extending heme-regulatory motifs beyond CP.

Biochimica et biophysica acta. General subjects

Syllwasschy BF, Beck MS, Družeta I, Hopp MT, Ramoji A, Neugebauer U, Nozinovic S, Menche D, Willbold D, Ohlenschläger O, Kühl T, Imhof D.
PMID: 32234408
Biochim Biophys Acta Gen Subj. 2020 Jul;1864(7):129603. doi: 10.1016/j.bbagen.2020.129603. Epub 2020 Mar 29.

BACKGROUND & MOTIVATION: Peptides and proteins can interact with heme through His, Tyr, or Cys in heme-regulatory motifs (HRMs). The Cys-Pro dipeptide is a well investigated HRM, but for His and Tyr such a distinct motif is currently unknown....

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Syllwasschy BF, Beck MS, Družeta I, et al. High-affinity binding and catalytic activity of His/Tyr-based sequences: Extending heme-regulatory motifs beyond CP. Biochim Biophys Acta Gen Subj. 2020;1864(7):129603doi: 10.1016/j.bbagen.2020.129603.
Syllwasschy, B. F., Beck, M. S., Družeta, I., Hopp, M. T., Ramoji, A., Neugebauer, U., Nozinovic, S., Menche, D., Willbold, D., Ohlenschläger, O., Kühl, T., & Imhof, D. (2020). High-affinity binding and catalytic activity of His/Tyr-based sequences: Extending heme-regulatory motifs beyond CP. Biochimica et biophysica acta. General subjects, 1864(7), 129603. https://doi.org/10.1016/j.bbagen.2020.129603
Syllwasschy, Benjamin Franz, et al. "High-affinity binding and catalytic activity of His/Tyr-based sequences: Extending heme-regulatory motifs beyond CP." Biochimica et biophysica acta. General subjects vol. 1864,7 (2020): 129603. doi: https://doi.org/10.1016/j.bbagen.2020.129603
Syllwasschy BF, Beck MS, Družeta I, Hopp MT, Ramoji A, Neugebauer U, Nozinovic S, Menche D, Willbold D, Ohlenschläger O, Kühl T, Imhof D. High-affinity binding and catalytic activity of His/Tyr-based sequences: Extending heme-regulatory motifs beyond CP. Biochim Biophys Acta Gen Subj. 2020 Jul;1864(7):129603. doi: 10.1016/j.bbagen.2020.129603. Epub 2020 Mar 29. PMID: 32234408.
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All.

Journal of medicinal chemistry

Bocharov EV, Gremer L, Urban AS, Okhrimenko IS, Volynsky PE, Nadezhdin KD, Bocharova OV, Kornilov DA, Zagryadskaya YA, Kamynina AV, Kuzmichev PK, Kutzsche J, Bolakhrif N, Müller-Schiffmann A, Dencher NA, Arseniev AS, Efremov RG, Gordeliy VI, Willbold D.
PMID: 34739758
J Med Chem. 2021 Nov 25;64(22):16464-16479. doi: 10.1021/acs.jmedchem.1c00632. Epub 2021 Nov 05.

Alzheimer's disease (AD) is a severe neurodegenerative pathology with no effective treatment known. Toxic amyloid-β peptide (Aβ) oligomers play a crucial role in AD pathogenesis. All

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Bocharov EV, Gremer L, Urban AS, et al. All. J Med Chem. 2021;64(22):16464-16479doi: 10.1021/acs.jmedchem.1c00632.
Bocharov, E. V., Gremer, L., Urban, A. S., Okhrimenko, I. S., Volynsky, P. E., Nadezhdin, K. D., Bocharova, O. V., Kornilov, D. A., Zagryadskaya, Y. A., Kamynina, A. V., Kuzmichev, P. K., Kutzsche, J., Bolakhrif, N., Müller-Schiffmann, A., Dencher, N. A., Arseniev, A. S., Efremov, R. G., Gordeliy, V. I., & Willbold, D. (2021). All. Journal of medicinal chemistry, 64(22), 16464-16479. https://doi.org/10.1021/acs.jmedchem.1c00632
Bocharov, Eduard V, et al. "All." Journal of medicinal chemistry vol. 64,22 (2021): 16464-16479. doi: https://doi.org/10.1021/acs.jmedchem.1c00632
Bocharov EV, Gremer L, Urban AS, Okhrimenko IS, Volynsky PE, Nadezhdin KD, Bocharova OV, Kornilov DA, Zagryadskaya YA, Kamynina AV, Kuzmichev PK, Kutzsche J, Bolakhrif N, Müller-Schiffmann A, Dencher NA, Arseniev AS, Efremov RG, Gordeliy VI, Willbold D. All. J Med Chem. 2021 Nov 25;64(22):16464-16479. doi: 10.1021/acs.jmedchem.1c00632. Epub 2021 Nov 05. PMID: 34739758.
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Sex-Related Motor Deficits in the Tau-P301L Mouse Model.

Biomedicines

Camargo LC, Honold D, Bauer R, Shah NJ, Langen KJ, Willbold D, Kutzsche J, Willuweit A, Schemmert S.
PMID: 34572348
Biomedicines. 2021 Sep 04;9(9). doi: 10.3390/biomedicines9091160.

The contribution of mouse models for basic and translational research at different levels is important to understand neurodegenerative diseases, including tauopathies, by studying the alterations in the corresponding mouse models in detail. Moreover, several studies demonstrated that pathological as...

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Camargo LC, Honold D, Bauer R, et al. Sex-Related Motor Deficits in the Tau-P301L Mouse Model. Biomedicines. 2021;9(9)doi: 10.3390/biomedicines9091160.
Camargo, L. C., Honold, D., Bauer, R., Shah, N. J., Langen, K. J., Willbold, D., Kutzsche, J., Willuweit, A., & Schemmert, S. (2021). Sex-Related Motor Deficits in the Tau-P301L Mouse Model. Biomedicines, 9(9), . https://doi.org/10.3390/biomedicines9091160
Camargo, Luana Cristina, et al. "Sex-Related Motor Deficits in the Tau-P301L Mouse Model." Biomedicines vol. 9,9 (2021). doi: https://doi.org/10.3390/biomedicines9091160
Camargo LC, Honold D, Bauer R, Shah NJ, Langen KJ, Willbold D, Kutzsche J, Willuweit A, Schemmert S. Sex-Related Motor Deficits in the Tau-P301L Mouse Model. Biomedicines. 2021 Sep 04;9(9). doi: 10.3390/biomedicines9091160. PMID: 34572348; PMCID: PMC8471835.
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Electromechanical Assessment of Human Knee Articular Cartilage with Compression-Induced Streaming Potentials.

Cartilage

Becher C, Ricklefs M, Willbold E, Hurschler C, Abedian R.
PMID: 26958318
Cartilage. 2016 Jan;7(1):62-9. doi: 10.1177/1947603515599191.

PURPOSE: To assess the electromechanical properties of human knee articular cartilage with compression-induced streaming potentials for reliability among users and correlation with macroscopic and histological evaluation tools and sulfated glycosaminoglycan (sGAG) content.METHODS: Streaming potentials are induced in cartilage in...

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Becher C, Ricklefs M, Willbold E, et al. Electromechanical Assessment of Human Knee Articular Cartilage with Compression-Induced Streaming Potentials. Cartilage. 2016;7(1):62-9doi: 10.1177/1947603515599191.
Becher, C., Ricklefs, M., Willbold, E., Hurschler, C., & Abedian, R. (2016). Electromechanical Assessment of Human Knee Articular Cartilage with Compression-Induced Streaming Potentials. Cartilage, 7(1), 62-9. https://doi.org/10.1177/1947603515599191
Becher, Christoph, et al. "Electromechanical Assessment of Human Knee Articular Cartilage with Compression-Induced Streaming Potentials." Cartilage vol. 7,1 (2016): 62-9. doi: https://doi.org/10.1177/1947603515599191
Becher C, Ricklefs M, Willbold E, Hurschler C, Abedian R. Electromechanical Assessment of Human Knee Articular Cartilage with Compression-Induced Streaming Potentials. Cartilage. 2016 Jan;7(1):62-9. doi: 10.1177/1947603515599191. PMID: 26958318; PMCID: PMC4749748.
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Phytase blends for enhanced phosphorous mobilization of deoiled seeds.

Enzyme and microbial technology

Infanzón B, Herrmann KR, Hofmann I, Willbold S, Ruff AJ, Schwaneberg U.
PMID: 34847439
Enzyme Microb Technol. 2021 Nov 23;153:109953. doi: 10.1016/j.enzmictec.2021.109953. Epub 2021 Nov 23.

Phytases are hydrolytic enzymes capable of a stepwise phosphate release from phytate which is the main phosphorous storage in seeds, cereals and legumes. Limitations such as low enzyme activity or incomplete phytate hydrolysis to inositol are a great challenge...

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Infanzón B, Herrmann KR, Hofmann I, et al. Phytase blends for enhanced phosphorous mobilization of deoiled seeds. Enzyme Microb Technol. 2021;153:109953doi: 10.1016/j.enzmictec.2021.109953.
Infanzón, B., Herrmann, K. R., Hofmann, I., Willbold, S., Ruff, A. J., & Schwaneberg, U. (2021). Phytase blends for enhanced phosphorous mobilization of deoiled seeds. Enzyme and microbial technology, 153109953. https://doi.org/10.1016/j.enzmictec.2021.109953
Infanzón, Belén, et al. "Phytase blends for enhanced phosphorous mobilization of deoiled seeds." Enzyme and microbial technology vol. 153 (2021): 109953. doi: https://doi.org/10.1016/j.enzmictec.2021.109953
Infanzón B, Herrmann KR, Hofmann I, Willbold S, Ruff AJ, Schwaneberg U. Phytase blends for enhanced phosphorous mobilization of deoiled seeds. Enzyme Microb Technol. 2021 Nov 23;153:109953. doi: 10.1016/j.enzmictec.2021.109953. Epub 2021 Nov 23. PMID: 34847439.
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Showing 49 to 56 of 56 entries