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Corrigendum: Identification of Multiple Druggable Secondary Sites by Fragment Screening against DC-SIGN.

Angewandte Chemie (International ed. in English)

Aretz J, Baukmann H, Shanina E, Hanske J, Wawrzinek R, Zapol'skii VA, Seeberger PH, Kaufmann DE, Rademacher C.
PMID: 28961388
Angew Chem Int Ed Engl. 2017 Oct 02;56(41):12398. doi: 10.1002/anie.201708597.

No abstract available.

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Aretz J, Baukmann H, Shanina E, et al. Corrigendum: Identification of Multiple Druggable Secondary Sites by Fragment Screening against DC-SIGN. Angew Chem Int Ed Engl. 2017;56(41):12398doi: 10.1002/anie.201708597.
Aretz, J., Baukmann, H., Shanina, E., Hanske, J., Wawrzinek, R., Zapol'skii, V. A., Seeberger, P. H., Kaufmann, D. E., & Rademacher, C. (2017). Corrigendum: Identification of Multiple Druggable Secondary Sites by Fragment Screening against DC-SIGN. Angewandte Chemie (International ed. in English), 56(41), 12398. https://doi.org/10.1002/anie.201708597
Aretz, Jonas, et al. "Corrigendum: Identification of Multiple Druggable Secondary Sites by Fragment Screening against DC-SIGN." Angewandte Chemie (International ed. in English) vol. 56,41 (2017): 12398. doi: https://doi.org/10.1002/anie.201708597
Aretz J, Baukmann H, Shanina E, Hanske J, Wawrzinek R, Zapol'skii VA, Seeberger PH, Kaufmann DE, Rademacher C. Corrigendum: Identification of Multiple Druggable Secondary Sites by Fragment Screening against DC-SIGN. Angew Chem Int Ed Engl. 2017 Oct 02;56(41):12398. doi: 10.1002/anie.201708597. PMID: 28961388.
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Identifying erlotinib-sensitive non-small cell lung carcinoma tumors in mice using [(11)C]erlotinib PET.

EJNMMI research

Abourbeh G, Itamar B, Salnikov O, Beltsov S, Mishani E.
PMID: 25853010
EJNMMI Res. 2015 Feb 12;5:4. doi: 10.1186/s13550-014-0080-0. eCollection 2015.

BACKGROUND: Non-small cell lung carcinoma (NSCLC) represents approximately 80% of lung cancer cases, and over 60% of these tumors express the epidermal growth factor receptor (EGFR). Activating mutations in the tyrosine kinase (TK) domain of the EGFR are detected...

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Abourbeh G, Itamar B, Salnikov O, et al. Identifying erlotinib-sensitive non-small cell lung carcinoma tumors in mice using [(11)C]erlotinib PET. EJNMMI Res. 2015;5:4doi: 10.1186/s13550-014-0080-0.
Abourbeh, G., Itamar, B., Salnikov, O., Beltsov, S., & Mishani, E. (2015). Identifying erlotinib-sensitive non-small cell lung carcinoma tumors in mice using [(11)C]erlotinib PET. EJNMMI research, 54. https://doi.org/10.1186/s13550-014-0080-0
Abourbeh, Galith, et al. "Identifying erlotinib-sensitive non-small cell lung carcinoma tumors in mice using [(11)C]erlotinib PET." EJNMMI research vol. 5 (2015): 4. doi: https://doi.org/10.1186/s13550-014-0080-0
Abourbeh G, Itamar B, Salnikov O, Beltsov S, Mishani E. Identifying erlotinib-sensitive non-small cell lung carcinoma tumors in mice using [(11)C]erlotinib PET. EJNMMI Res. 2015 Feb 12;5:4. doi: 10.1186/s13550-014-0080-0. eCollection 2015. PMID: 25853010; PMCID: PMC4385014.
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Stereoselective Synthesis of Fluorinated Galactopyranosides as Potential Molecular Probes for Galactophilic Proteins: Assessment of Monofluorogalactoside-LecA Interactions.

Chemistry (Weinheim an der Bergstrasse, Germany)

Denavit V, Lainé D, Bouzriba C, Shanina E, Gillon É, Fortin S, Rademacher C, Imberty A, Giguère D.
PMID: 30690814
Chemistry. 2019 Mar 21;25(17):4478-4490. doi: 10.1002/chem.201806197. Epub 2019 Feb 27.

The replacement of hydroxyl groups by fluorine atoms on hexopyranoside scaffolds may allow access to invaluable tools for studying various biochemical processes. As part of ongoing activities toward the preparation of fluorinated carbohydrates, a systematic investigation involving the synthesis...

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Denavit V, Lainé D, Bouzriba C, et al. Stereoselective Synthesis of Fluorinated Galactopyranosides as Potential Molecular Probes for Galactophilic Proteins: Assessment of Monofluorogalactoside-LecA Interactions. Chemistry. 2019;25(17):4478-4490doi: 10.1002/chem.201806197.
Denavit, V., Lainé, D., Bouzriba, C., Shanina, E., Gillon, �. �., Fortin, S., Rademacher, C., Imberty, A., & Giguère, D. (2019). Stereoselective Synthesis of Fluorinated Galactopyranosides as Potential Molecular Probes for Galactophilic Proteins: Assessment of Monofluorogalactoside-LecA Interactions. Chemistry (Weinheim an der Bergstrasse, Germany), 25(17), 4478-4490. https://doi.org/10.1002/chem.201806197
Denavit, Vincent, et al. "Stereoselective Synthesis of Fluorinated Galactopyranosides as Potential Molecular Probes for Galactophilic Proteins: Assessment of Monofluorogalactoside-LecA Interactions." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 25,17 (2019): 4478-4490. doi: https://doi.org/10.1002/chem.201806197
Denavit V, Lainé D, Bouzriba C, Shanina E, Gillon É, Fortin S, Rademacher C, Imberty A, Giguère D. Stereoselective Synthesis of Fluorinated Galactopyranosides as Potential Molecular Probes for Galactophilic Proteins: Assessment of Monofluorogalactoside-LecA Interactions. Chemistry. 2019 Mar 21;25(17):4478-4490. doi: 10.1002/chem.201806197. Epub 2019 Feb 27. PMID: 30690814.
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Protein-observed 19F NMR of LecA from Pseudomonas aeruginosa.

Glycobiology

Shanina E, Siebs E, Zhang H, Varón Silva D, Joachim I, Titz A, Rademacher C.
PMID: 32573695
Glycobiology. 2021 Feb 09;31(2):159-165. doi: 10.1093/glycob/cwaa057.

The carbohydrate-binding protein LecA (PA-IL) from Pseudomonas aeruginosa plays an important role in the formation of biofilms in chronic infections. Development of inhibitors to disrupt LecA-mediated biofilms is desired but it is limited to carbohydrate-based ligands. Moreover, discovery of...

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Shanina E, Siebs E, Zhang H, et al. Protein-observed 19F NMR of LecA from Pseudomonas aeruginosa. Glycobiology. 2021;31(2):159-165doi: 10.1093/glycob/cwaa057.
Shanina, E., Siebs, E., Zhang, H., Varón Silva, D., Joachim, I., Titz, A., & Rademacher, C. (2021). Protein-observed 19F NMR of LecA from Pseudomonas aeruginosa. Glycobiology, 31(2), 159-165. https://doi.org/10.1093/glycob/cwaa057
Shanina, Elena, et al. "Protein-observed 19F NMR of LecA from Pseudomonas aeruginosa." Glycobiology vol. 31,2 (2021): 159-165. doi: https://doi.org/10.1093/glycob/cwaa057
Shanina E, Siebs E, Zhang H, Varón Silva D, Joachim I, Titz A, Rademacher C. Protein-observed 19F NMR of LecA from Pseudomonas aeruginosa. Glycobiology. 2021 Feb 09;31(2):159-165. doi: 10.1093/glycob/cwaa057. PMID: 32573695; PMCID: PMC7874386.
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Development and preclinical evaluation of novel fluorinated ammonium salts for PET myocardial perfusion imaging.

Scientific reports

Shamni O, Grievink H, Kolevzon N, Krajewski S, Steczek L, Meltzer E, Yitshak S, Mishani E, Abourbeh G.
PMID: 34608204
Sci Rep. 2021 Oct 04;11(1):19693. doi: 10.1038/s41598-021-99212-0.

We previously presented the radiolabeled ammonium salt [

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Shamni O, Grievink H, Kolevzon N, et al. Development and preclinical evaluation of novel fluorinated ammonium salts for PET myocardial perfusion imaging. Sci Rep. 2021;11(1):19693doi: 10.1038/s41598-021-99212-0.
Shamni, O., Grievink, H., Kolevzon, N., Krajewski, S., Steczek, L., Meltzer, E., Yitshak, S., Mishani, E., & Abourbeh, G. (2021). Development and preclinical evaluation of novel fluorinated ammonium salts for PET myocardial perfusion imaging. Scientific reports, 11(1), 19693. https://doi.org/10.1038/s41598-021-99212-0
Shamni, Ofer, et al. "Development and preclinical evaluation of novel fluorinated ammonium salts for PET myocardial perfusion imaging." Scientific reports vol. 11,1 (2021): 19693. doi: https://doi.org/10.1038/s41598-021-99212-0
Shamni O, Grievink H, Kolevzon N, Krajewski S, Steczek L, Meltzer E, Yitshak S, Mishani E, Abourbeh G. Development and preclinical evaluation of novel fluorinated ammonium salts for PET myocardial perfusion imaging. Sci Rep. 2021 Oct 04;11(1):19693. doi: 10.1038/s41598-021-99212-0. PMID: 34608204; PMCID: PMC8490395.
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Targeting the Central Pocket of the Pseudomonas aeruginosa Lectin LecA.

Chembiochem : a European journal of chemical biology

Siebs E, Shanina E, Kuhaudomlarp S, da Silva Figueiredo Celestino Gomes P, Fortin C, Seeberger PH, Rognan D, Rademacher C, Imberty A, Titz A.
PMID: 34788491
Chembiochem. 2021 Nov 17; doi: 10.1002/cbic.202100563. Epub 2021 Nov 17.

Pseudomonas aeruginosa is an opportunistic ESKAPE pathogen that produces two lectins, LecA and LecB, as part of its large arsenal of virulence factors. Both carbohydrate-binding proteins are central to the initial and later persistent infection processes, i. e. bacterial...

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Siebs E, Shanina E, Kuhaudomlarp S, et al. Targeting the Central Pocket of the Pseudomonas aeruginosa Lectin LecA. Chembiochem. 2021;doi: 10.1002/cbic.202100563.
Siebs, E., Shanina, E., Kuhaudomlarp, S., da Silva Figueiredo Celestino Gomes, P., Fortin, C., Seeberger, P. H., Rognan, D., Rademacher, C., Imberty, A., & Titz, A. (2021). Targeting the Central Pocket of the Pseudomonas aeruginosa Lectin LecA. Chembiochem : a European journal of chemical biology, . https://doi.org/10.1002/cbic.202100563
Siebs, Eike, et al. "Targeting the Central Pocket of the Pseudomonas aeruginosa Lectin LecA." Chembiochem : a European journal of chemical biology vol. (2021). doi: https://doi.org/10.1002/cbic.202100563
Siebs E, Shanina E, Kuhaudomlarp S, da Silva Figueiredo Celestino Gomes P, Fortin C, Seeberger PH, Rognan D, Rademacher C, Imberty A, Titz A. Targeting the Central Pocket of the Pseudomonas aeruginosa Lectin LecA. Chembiochem. 2021 Nov 17; doi: 10.1002/cbic.202100563. Epub 2021 Nov 17. PMID: 34788491.
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The pH of Smokeless Tobacco Determines Nicotine Buccal Absorption: Results of a Randomized Crossover Trial.

Clinical pharmacology and therapeutics

Wilhelm J, Mishina E, Viray L, Paredes A, Pickworth WB.
PMID: 34826137
Clin Pharmacol Ther. 2021 Nov 26; doi: 10.1002/cpt.2493. Epub 2021 Nov 26.

Nicotine absorption rate influences tobacco products' addictiveness. For smokeless tobacco, nicotine buccal absorption is associated with its free-base form; the pH of smokeless tobacco defines the proportion of free-base (i.e., unprotonated) vs. protonated nicotine. This was the first study...

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Wilhelm J, Mishina E, Viray L, et al. The pH of Smokeless Tobacco Determines Nicotine Buccal Absorption: Results of a Randomized Crossover Trial. Clin Pharmacol Ther. 2021;doi: 10.1002/cpt.2493.
Wilhelm, J., Mishina, E., Viray, L., Paredes, A., & Pickworth, W. B. (2021). The pH of Smokeless Tobacco Determines Nicotine Buccal Absorption: Results of a Randomized Crossover Trial. Clinical pharmacology and therapeutics, . https://doi.org/10.1002/cpt.2493
Wilhelm, Jess, et al. "The pH of Smokeless Tobacco Determines Nicotine Buccal Absorption: Results of a Randomized Crossover Trial." Clinical pharmacology and therapeutics vol. (2021). doi: https://doi.org/10.1002/cpt.2493
Wilhelm J, Mishina E, Viray L, Paredes A, Pickworth WB. The pH of Smokeless Tobacco Determines Nicotine Buccal Absorption: Results of a Randomized Crossover Trial. Clin Pharmacol Ther. 2021 Nov 26; doi: 10.1002/cpt.2493. Epub 2021 Nov 26. PMID: 34826137.
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Modification of the Ceramic Implant Surfaces from Zirconia by the Magnetron Sputtering of Different Calcium Phosphate Targets: A Comparative Study.

Materials (Basel, Switzerland)

Kozelskaya AI, Bolbasov EN, Golovkin AS, Mishanin AI, Viknianshchuk AN, Shesterikov EV, Ashrafov А, Novikov VA, Fedotkin AY, Khlusov IA, Tverdokhlebov SI.
PMID: 30314394
Materials (Basel). 2018 Oct 11;11(10). doi: 10.3390/ma11101949.

In this study, thin calcium phosphate (Ca-P) coatings were deposited on zirconia substrates by radiofrequency (RF) magnetron sputtering using different calcium phosphate targets (calcium phosphate tribasic (CPT), hydroxyapatite (HA), calcium phosphate monobasic, calcium phosphate dibasic dehydrate (DCPD) and calcium...

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Kozelskaya AI, Bolbasov EN, Golovkin AS, et al. Modification of the Ceramic Implant Surfaces from Zirconia by the Magnetron Sputtering of Different Calcium Phosphate Targets: A Comparative Study. Materials (Basel). 2018;11(10)doi: 10.3390/ma11101949.
Kozelskaya, A. I., Bolbasov, E. N., Golovkin, A. S., Mishanin, A. I., Viknianshchuk, A. N., Shesterikov, E. V., Ashrafov, �. �., Novikov, V. A., Fedotkin, A. Y., Khlusov, I. A., & Tverdokhlebov, S. I. (2018). Modification of the Ceramic Implant Surfaces from Zirconia by the Magnetron Sputtering of Different Calcium Phosphate Targets: A Comparative Study. Materials (Basel, Switzerland), 11(10), . https://doi.org/10.3390/ma11101949
Kozelskaya, Anna I, et al. "Modification of the Ceramic Implant Surfaces from Zirconia by the Magnetron Sputtering of Different Calcium Phosphate Targets: A Comparative Study." Materials (Basel, Switzerland) vol. 11,10 (2018). doi: https://doi.org/10.3390/ma11101949
Kozelskaya AI, Bolbasov EN, Golovkin AS, Mishanin AI, Viknianshchuk AN, Shesterikov EV, Ashrafov А, Novikov VA, Fedotkin AY, Khlusov IA, Tverdokhlebov SI. Modification of the Ceramic Implant Surfaces from Zirconia by the Magnetron Sputtering of Different Calcium Phosphate Targets: A Comparative Study. Materials (Basel). 2018 Oct 11;11(10). doi: 10.3390/ma11101949. PMID: 30314394; PMCID: PMC6213365.
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Time- and Ventricular-Specific Expression Profiles of Genes Encoding Z-Disk Proteins in Pressure Overload Model of Left Ventricular Hypertrophy.

Frontiers in genetics

Knyazeva A, Krutikov A, Golovkin A, Mishanin A, Pavlov G, Smolina N, Hushkina A, Sejersen T, Sjoberg G, Galagudza M, Kostareva A.
PMID: 30666270
Front Genet. 2019 Jan 07;9:684. doi: 10.3389/fgene.2018.00684. eCollection 2018.

Mechanotransduction is an essential mechanism of transforming external mechanical stimulus to biochemical response. In cardiomyocytes mechanotransduction plays an important role in contraction, stretch sensing and homeostasis regulation. One of the major mechanosensitive area in cardiomyocytes, the Z-disk, consists of...

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Knyazeva A, Krutikov A, Golovkin A, et al. Time- and Ventricular-Specific Expression Profiles of Genes Encoding Z-Disk Proteins in Pressure Overload Model of Left Ventricular Hypertrophy. Front Genet. 2019;9:684doi: 10.3389/fgene.2018.00684.
Knyazeva, A., Krutikov, A., Golovkin, A., Mishanin, A., Pavlov, G., Smolina, N., Hushkina, A., Sejersen, T., Sjoberg, G., Galagudza, M., & Kostareva, A. (2018). Time- and Ventricular-Specific Expression Profiles of Genes Encoding Z-Disk Proteins in Pressure Overload Model of Left Ventricular Hypertrophy. Frontiers in genetics, 9684. https://doi.org/10.3389/fgene.2018.00684
Knyazeva, Anastasia, et al. "Time- and Ventricular-Specific Expression Profiles of Genes Encoding Z-Disk Proteins in Pressure Overload Model of Left Ventricular Hypertrophy." Frontiers in genetics vol. 9 (2018): 684. doi: https://doi.org/10.3389/fgene.2018.00684
Knyazeva A, Krutikov A, Golovkin A, Mishanin A, Pavlov G, Smolina N, Hushkina A, Sejersen T, Sjoberg G, Galagudza M, Kostareva A. Time- and Ventricular-Specific Expression Profiles of Genes Encoding Z-Disk Proteins in Pressure Overload Model of Left Ventricular Hypertrophy. Front Genet. 2019 Jan 07;9:684. doi: 10.3389/fgene.2018.00684. eCollection 2018. PMID: 30666270; PMCID: PMC6330284.
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Graphical displays for effective reporting of evidence quality tables in research syntheses.

Reproductive health

Mignini L, Champaneria R, Mishanina E, Khan KS.
PMID: 26957125
Reprod Health. 2016 Mar 09;13:21. doi: 10.1186/s12978-016-0130-3.

BACKGROUND: When generating guidelines, quality of the evidence is tabulated to capture its several domains, often using the GRADE (Grading of Recommendations Assessment, Development and Evaluation) approach. We developed a graphic display to capture deficiencies, outliers and similarities across...

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Mignini L, Champaneria R, Mishanina E, et al. Graphical displays for effective reporting of evidence quality tables in research syntheses. Reprod Health. 2016;13:21doi: 10.1186/s12978-016-0130-3.
Mignini, L., Champaneria, R., Mishanina, E., Khan, K. S. (2016). Graphical displays for effective reporting of evidence quality tables in research syntheses. Reproductive health, 1321. https://doi.org/10.1186/s12978-016-0130-3
Mignini, Luciano, et al. "Graphical displays for effective reporting of evidence quality tables in research syntheses." Reproductive health vol. 13 (2016): 21. doi: https://doi.org/10.1186/s12978-016-0130-3
Mignini L, Champaneria R, Mishanina E, Khan KS. Graphical displays for effective reporting of evidence quality tables in research syntheses. Reprod Health. 2016 Mar 09;13:21. doi: 10.1186/s12978-016-0130-3. PMID: 26957125; PMCID: PMC4784278.
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Neuromyelitis optica phenotype associated with therapy-responsive acute peripheral neuropathy.

Neurology(R) neuroimmunology & neuroinflammation

Feyissa AM, Shanina E, Shah R, Smith RG.
PMID: 25798448
Neurol Neuroimmunol Neuroinflamm. 2015 Mar 12;2(3):e83. doi: 10.1212/NXI.0000000000000083. eCollection 2015 Jun.

No abstract available.

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Feyissa AM, Shanina E, Shah R, et al. Neuromyelitis optica phenotype associated with therapy-responsive acute peripheral neuropathy. Neurol Neuroimmunol Neuroinflamm. 2015;2(3):e83doi: 10.1212/NXI.0000000000000083.
Feyissa, A. M., Shanina, E., Shah, R., & Smith, R. G. (2015). Neuromyelitis optica phenotype associated with therapy-responsive acute peripheral neuropathy. Neurology(R) neuroimmunology & neuroinflammation, 2(3), e83. https://doi.org/10.1212/NXI.0000000000000083
Feyissa, Anteneh M, et al. "Neuromyelitis optica phenotype associated with therapy-responsive acute peripheral neuropathy." Neurology(R) neuroimmunology & neuroinflammation vol. 2,3 (2015): e83. doi: https://doi.org/10.1212/NXI.0000000000000083
Feyissa AM, Shanina E, Shah R, Smith RG. Neuromyelitis optica phenotype associated with therapy-responsive acute peripheral neuropathy. Neurol Neuroimmunol Neuroinflamm. 2015 Mar 12;2(3):e83. doi: 10.1212/NXI.0000000000000083. eCollection 2015 Jun. PMID: 25798448; PMCID: PMC4360793.
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Druggable Allosteric Sites in β-Propeller Lectins.

Angewandte Chemie (International ed. in English)

Shanina E, Kuhaudomlarp S, Lal K, Seeberger PH, Imberty A, Rademacher C.
PMID: 34713573
Angew Chem Int Ed Engl. 2022 Jan 03;61(1):e202109339. doi: 10.1002/anie.202109339. Epub 2021 Nov 23.

Carbohydrate-binding proteins (lectins) are auspicious targets in drug discovery to combat antimicrobial resistance; however, their non-carbohydrate drug-like inhibitors are still unavailable. Here, we present a druggable pocket in a β-propeller lectin BambL from Burkholderia ambifaria as a potential target...

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Shanina E, Kuhaudomlarp S, Lal K, et al. Druggable Allosteric Sites in β-Propeller Lectins. Angew Chem Int Ed Engl. 2021;61(1):e202109339doi: 10.1002/anie.202109339.
Shanina, E., Kuhaudomlarp, S., Lal, K., Seeberger, P. H., Imberty, A., & Rademacher, C. (2022). Druggable Allosteric Sites in β-Propeller Lectins. Angewandte Chemie (International ed. in English), 61(1), e202109339. https://doi.org/10.1002/anie.202109339
Shanina, Elena, et al. "Druggable Allosteric Sites in β-Propeller Lectins." Angewandte Chemie (International ed. in English) vol. 61,1 (2022): e202109339. doi: https://doi.org/10.1002/anie.202109339
Shanina E, Kuhaudomlarp S, Lal K, Seeberger PH, Imberty A, Rademacher C. Druggable Allosteric Sites in β-Propeller Lectins. Angew Chem Int Ed Engl. 2022 Jan 03;61(1):e202109339. doi: 10.1002/anie.202109339. Epub 2021 Nov 23. PMID: 34713573.
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