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[Pharmaceutical education and continuing education in the People's Republic of Hungary. A report of a study trip].

Die Pharmazie

Rettinghaus R.
PMID: 935243
Pharmazie. 1976 Apr;31(4):91-5.

No abstract available.

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Rettinghaus R. Die Aus- und Weiterbildung pharmazeutischer Berufe in der Ungarischen Volksrepublik. Bericht einer Studienreise [Pharmaceutical education and continuing education in the People's Republic of Hungary. A report of a study trip]. Pharmazie. 1976;31(4):91-5
Rettinghaus, R. (1976). Die Aus- und Weiterbildung pharmazeutischer Berufe in der Ungarischen Volksrepublik. Bericht einer Studienreise [Pharmaceutical education and continuing education in the People's Republic of Hungary. A report of a study trip]. Die Pharmazie, 31(4), 91-5.
Rettinghaus, R. "Die Aus- und Weiterbildung pharmazeutischer Berufe in der Ungarischen Volksrepublik. Bericht einer Studienreise" [Pharmaceutical education and continuing education in the People's Republic of Hungary. A report of a study trip]. Die Pharmazie vol. 31,4 (1976): 91-5.
Rettinghaus R. Die Aus- und Weiterbildung pharmazeutischer Berufe in der Ungarischen Volksrepublik. Bericht einer Studienreise [Pharmaceutical education and continuing education in the People's Republic of Hungary. A report of a study trip]. Pharmazie. 1976 Apr;31(4):91-5. German. PMID: 935243.
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COOH-terminated SAMs on gold fabricated from an azobenzene derivative with a 1,2-dithiolane headgroup.

Applied surface science

Siemeling U, Rittinghaus S, Weidner T, Brison J, Castner DG.
PMID: 24482551
Appl Surf Sci. 2010 Jan 01;256(6):1832-1836. doi: 10.1016/j.apsusc.2009.10.015.

Well-defined and homogeneous, contamination-free self-assembled monolayers (SAMs) were fabricated by the chemisorption of lip-NH-

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Siemeling U, Rittinghaus S, Weidner T, et al. COOH-terminated SAMs on gold fabricated from an azobenzene derivative with a 1,2-dithiolane headgroup. Appl Surf Sci. 2010;256(6):1832-1836doi: 10.1016/j.apsusc.2009.10.015.
Siemeling, U., Rittinghaus, S., Weidner, T., Brison, J., & Castner, D. G. (2010). COOH-terminated SAMs on gold fabricated from an azobenzene derivative with a 1,2-dithiolane headgroup. Applied surface science, 256(6), 1832-1836. https://doi.org/10.1016/j.apsusc.2009.10.015
Siemeling, Ulrich, et al. "COOH-terminated SAMs on gold fabricated from an azobenzene derivative with a 1,2-dithiolane headgroup." Applied surface science vol. 256,6 (2010): 1832-1836. doi: https://doi.org/10.1016/j.apsusc.2009.10.015
Siemeling U, Rittinghaus S, Weidner T, Brison J, Castner DG. COOH-terminated SAMs on gold fabricated from an azobenzene derivative with a 1,2-dithiolane headgroup. Appl Surf Sci. 2010 Jan 01;256(6):1832-1836. doi: 10.1016/j.apsusc.2009.10.015. PMID: 24482551; PMCID: PMC3904768.
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Entwicklung von schichtweise ausgerichteten Faserverbundstrukturen.

Biomedizinische Technik. Biomedical engineering

Rittinghaus T, Zernetsch H, Glasmacher B.
PMID: 24042673
Biomed Tech (Berl). 2013 Aug;58. doi: 10.1515/bmt-2013-4071. Epub 2013 Sep 07.

No abstract available.

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Rittinghaus T, Zernetsch H, Glasmacher B. Entwicklung von schichtweise ausgerichteten Faserverbundstrukturen. Biomed Tech (Berl). 2013;58doi: 10.1515/bmt-2013-4071.
Rittinghaus, T., Zernetsch, H., & Glasmacher, B. (2013). Entwicklung von schichtweise ausgerichteten Faserverbundstrukturen. Biomedizinische Technik. Biomedical engineering, 58. https://doi.org/10.1515/bmt-2013-4071
Rittinghaus, Tim, et al. "Entwicklung von schichtweise ausgerichteten Faserverbundstrukturen." Biomedizinische Technik. Biomedical engineering vol. 58 (2013). doi: https://doi.org/10.1515/bmt-2013-4071
Rittinghaus T, Zernetsch H, Glasmacher B. Entwicklung von schichtweise ausgerichteten Faserverbundstrukturen. Biomed Tech (Berl). 2013 Aug;58. doi: 10.1515/bmt-2013-4071. Epub 2013 Sep 07. PMID: 24042673.
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Silencing of the ER and Integrative Stress Responses in the Liver of Mice with Error-Prone Translation.

Cells

Moore J, Osinnii I, Grimm A, Oettinghaus B, Eckert A, Frank S, Böttger EC.
PMID: 34831079
Cells. 2021 Oct 23;10(11). doi: 10.3390/cells10112856.

Translational errors frequently arise during protein synthesis, producing misfolded and dysfunctional proteins. Chronic stress resulting from translation errors may be particularly relevant in tissues that must synthesize and secrete large amounts of secretory proteins. Here, we studied the proteostasis...

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Moore J, Osinnii I, Grimm A, et al. Silencing of the ER and Integrative Stress Responses in the Liver of Mice with Error-Prone Translation. Cells. 2021;10(11)doi: 10.3390/cells10112856.
Moore, J., Osinnii, I., Grimm, A., Oettinghaus, B., Eckert, A., Frank, S., & Böttger, E. C. (2021). Silencing of the ER and Integrative Stress Responses in the Liver of Mice with Error-Prone Translation. Cells, 10(11), . https://doi.org/10.3390/cells10112856
Moore, James, et al. "Silencing of the ER and Integrative Stress Responses in the Liver of Mice with Error-Prone Translation." Cells vol. 10,11 (2021). doi: https://doi.org/10.3390/cells10112856
Moore J, Osinnii I, Grimm A, Oettinghaus B, Eckert A, Frank S, Böttger EC. Silencing of the ER and Integrative Stress Responses in the Liver of Mice with Error-Prone Translation. Cells. 2021 Oct 23;10(11). doi: 10.3390/cells10112856. PMID: 34831079; PMCID: PMC8616113.
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DomainSenticNet: An Ontology and a Methodology Enabling Domain-Aware Sentic Computing.

Cognitive computation

Distante D, Faralli S, Rittinghaus S, Rosso P, Samsami N.
PMID: 33558822
Cognit Comput. 2021 Feb 04;1-16. doi: 10.1007/s12559-021-09825-w. Epub 2021 Feb 04.

In recent years, SenticNet and OntoSenticNet have represented important developments in the novel interdisciplinary field of research known as sentic computing, enabling the development of a variety of Sentic applications. In this paper, we propose an extension of the...

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Distante D, Faralli S, Rittinghaus S, et al. DomainSenticNet: An Ontology and a Methodology Enabling Domain-Aware Sentic Computing. Cognit Comput. 2021;1-16doi: 10.1007/s12559-021-09825-w.
Distante, D., Faralli, S., Rittinghaus, S., Rosso, P., & Samsami, N. (2021). DomainSenticNet: An Ontology and a Methodology Enabling Domain-Aware Sentic Computing. Cognitive computation, 1-16. https://doi.org/10.1007/s12559-021-09825-w
Distante, Damiano, et al. "DomainSenticNet: An Ontology and a Methodology Enabling Domain-Aware Sentic Computing." Cognitive computation vol. (2021): 1-16. doi: https://doi.org/10.1007/s12559-021-09825-w
Distante D, Faralli S, Rittinghaus S, Rosso P, Samsami N. DomainSenticNet: An Ontology and a Methodology Enabling Domain-Aware Sentic Computing. Cognit Comput. 2021 Feb 04;1-16. doi: 10.1007/s12559-021-09825-w. Epub 2021 Feb 04. PMID: 33558822; PMCID: PMC7859726.
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New Kids in Lactide Polymerization: Highly Active and Robust Iron Guanidine Complexes as Superior Catalysts.

ChemSusChem

Rittinghaus RD, Schäfer PM, Albrecht P, Conrads C, Hoffmann A, Ksiazkiewicz AN, Bienemann O, Pich A, Herres-Pawlis S.
PMID: 30811863
ChemSusChem. 2019 May 21;12(10):2161-2165. doi: 10.1002/cssc.201900481. Epub 2019 Mar 19.

Polylactide is a biodegradable versatile material based on annually renewable resources and thus CO

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Rittinghaus RD, Schäfer PM, Albrecht P, et al. New Kids in Lactide Polymerization: Highly Active and Robust Iron Guanidine Complexes as Superior Catalysts. ChemSusChem. 2019;12(10):2161-2165doi: 10.1002/cssc.201900481.
Rittinghaus, R. D., Schäfer, P. M., Albrecht, P., Conrads, C., Hoffmann, A., Ksiazkiewicz, A. N., Bienemann, O., Pich, A., & Herres-Pawlis, S. (2019). New Kids in Lactide Polymerization: Highly Active and Robust Iron Guanidine Complexes as Superior Catalysts. ChemSusChem, 12(10), 2161-2165. https://doi.org/10.1002/cssc.201900481
Rittinghaus, Ruth D, et al. "New Kids in Lactide Polymerization: Highly Active and Robust Iron Guanidine Complexes as Superior Catalysts." ChemSusChem vol. 12,10 (2019): 2161-2165. doi: https://doi.org/10.1002/cssc.201900481
Rittinghaus RD, Schäfer PM, Albrecht P, Conrads C, Hoffmann A, Ksiazkiewicz AN, Bienemann O, Pich A, Herres-Pawlis S. New Kids in Lactide Polymerization: Highly Active and Robust Iron Guanidine Complexes as Superior Catalysts. ChemSusChem. 2019 May 21;12(10):2161-2165. doi: 10.1002/cssc.201900481. Epub 2019 Mar 19. PMID: 30811863.
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Master of Chaos and Order: Opposite Microstructures of PCL-coPGA-co-PLA Accessible by a Single Catalyst.

Angewandte Chemie (International ed. in English)

Herres-Pawlis S, Rittinghaus RD, Zenner J, Pich A, Kol M.
PMID: 34984790
Angew Chem Int Ed Engl. 2022 Jan 04; doi: 10.1002/anie.202112853. Epub 2022 Jan 04.

One catalyst, two reaction set-ups, three monomers and unlimited macromolecular microstructural designs: The iron guanidine complex [FeCl 2 (TMG5NMe 2 asme)] ( 1 ) polymerizes lactide faster than the industrially used Sn(Oct) 2 and shows high activity towards glycolide...

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Herres-Pawlis S, Rittinghaus RD, Zenner J, et al. Master of Chaos and Order: Opposite Microstructures of PCL-coPGA-co-PLA Accessible by a Single Catalyst. Angew Chem Int Ed Engl. 2022;doi: 10.1002/anie.202112853.
Herres-Pawlis, S., Rittinghaus, R. D., Zenner, J., Pich, A., & Kol, M. (2022). Master of Chaos and Order: Opposite Microstructures of PCL-coPGA-co-PLA Accessible by a Single Catalyst. Angewandte Chemie (International ed. in English), . https://doi.org/10.1002/anie.202112853
Herres-Pawlis, Sonja, et al. "Master of Chaos and Order: Opposite Microstructures of PCL-coPGA-co-PLA Accessible by a Single Catalyst." Angewandte Chemie (International ed. in English) vol. (2022). doi: https://doi.org/10.1002/anie.202112853
Herres-Pawlis S, Rittinghaus RD, Zenner J, Pich A, Kol M. Master of Chaos and Order: Opposite Microstructures of PCL-coPGA-co-PLA Accessible by a Single Catalyst. Angew Chem Int Ed Engl. 2022 Jan 04; doi: 10.1002/anie.202112853. Epub 2022 Jan 04. PMID: 34984790.
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Active in Sleep: Iron Guanidine Catalyst Performs ROP on Dormant Side of ATRP.

Angewandte Chemie (International ed. in English)

Rittinghaus RD, Karabulut A, Hoffmann A, Herres-Pawlis S.
PMID: 34270162
Angew Chem Int Ed Engl. 2021 Sep 27;60(40):21795-21800. doi: 10.1002/anie.202109053. Epub 2021 Aug 11.

Copolymers are the answer to property limitations of homopolymers. In order to use the full variety of monomers available, catalysts active in more than one polymerization mechanism are currently investigated. Iron guanidine catalysts have shown to be extraordinarily active...

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Rittinghaus RD, Karabulut A, Hoffmann A, et al. Active in Sleep: Iron Guanidine Catalyst Performs ROP on Dormant Side of ATRP. Angew Chem Int Ed Engl. 2021;60(40):21795-21800doi: 10.1002/anie.202109053.
Rittinghaus, R. D., Karabulut, A., Hoffmann, A., & Herres-Pawlis, S. (2021). Active in Sleep: Iron Guanidine Catalyst Performs ROP on Dormant Side of ATRP. Angewandte Chemie (International ed. in English), 60(40), 21795-21800. https://doi.org/10.1002/anie.202109053
Rittinghaus, Ruth D, et al. "Active in Sleep: Iron Guanidine Catalyst Performs ROP on Dormant Side of ATRP." Angewandte Chemie (International ed. in English) vol. 60,40 (2021): 21795-21800. doi: https://doi.org/10.1002/anie.202109053
Rittinghaus RD, Karabulut A, Hoffmann A, Herres-Pawlis S. Active in Sleep: Iron Guanidine Catalyst Performs ROP on Dormant Side of ATRP. Angew Chem Int Ed Engl. 2021 Sep 27;60(40):21795-21800. doi: 10.1002/anie.202109053. Epub 2021 Aug 11. PMID: 34270162; PMCID: PMC8518923.
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Corrigendum: Highly Active N,O Zinc Guanidine Catalysts for the Ring-Opening Polymerization of Lactide.

ChemSusChem

Schäfer PM, Fuchs M, Ohligschläger A, Rittinghaus R, McKeown P, Akin E, Schmidt M, Hoffmann A, Liauw MA, Jones MD, Herres-Pawlis S.
PMID: 29218842
ChemSusChem. 2017 Dec 08;10(23):4799. doi: 10.1002/cssc.201702066. Epub 2017 Nov 14.

No abstract available.

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Schäfer PM, Fuchs M, Ohligschläger A, et al. Corrigendum: Highly Active N,O Zinc Guanidine Catalysts for the Ring-Opening Polymerization of Lactide. ChemSusChem. 2017;10(23):4799doi: 10.1002/cssc.201702066.
Schäfer, P. M., Fuchs, M., Ohligschläger, A., Rittinghaus, R., McKeown, P., Akin, E., Schmidt, M., Hoffmann, A., Liauw, M. A., Jones, M. D., & Herres-Pawlis, S. (2017). Corrigendum: Highly Active N,O Zinc Guanidine Catalysts for the Ring-Opening Polymerization of Lactide. ChemSusChem, 10(23), 4799. https://doi.org/10.1002/cssc.201702066
Schäfer, Pascal M, et al. "Corrigendum: Highly Active N,O Zinc Guanidine Catalysts for the Ring-Opening Polymerization of Lactide." ChemSusChem vol. 10,23 (2017): 4799. doi: https://doi.org/10.1002/cssc.201702066
Schäfer PM, Fuchs M, Ohligschläger A, Rittinghaus R, McKeown P, Akin E, Schmidt M, Hoffmann A, Liauw MA, Jones MD, Herres-Pawlis S. Corrigendum: Highly Active N,O Zinc Guanidine Catalysts for the Ring-Opening Polymerization of Lactide. ChemSusChem. 2017 Dec 08;10(23):4799. doi: 10.1002/cssc.201702066. Epub 2017 Nov 14. PMID: 29218842.
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Solving Biocompatibility Layer by Layer: Designing Scaffolds for Tissues.

Biomedizinische Technik. Biomedical engineering

Zernetsch H, Repanas A, Gryshkov A, Al Halabi F, Rittinghaus T, Wienecke S, Müller M, Glasmacher B.
PMID: 24042739
Biomed Tech (Berl). 2013 Aug;58. doi: 10.1515/bmt-2013-4065. Epub 2013 Sep 07.

No abstract available.

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Zernetsch H, Repanas A, Gryshkov A, et al. Solving Biocompatibility Layer by Layer: Designing Scaffolds for Tissues. Biomed Tech (Berl). 2013;58doi: 10.1515/bmt-2013-4065.
Zernetsch, H., Repanas, A., Gryshkov, A., Al Halabi, F., Rittinghaus, T., Wienecke, S., Müller, M., & Glasmacher, B. (2013). Solving Biocompatibility Layer by Layer: Designing Scaffolds for Tissues. Biomedizinische Technik. Biomedical engineering, 58. https://doi.org/10.1515/bmt-2013-4065
Zernetsch, H, et al. "Solving Biocompatibility Layer by Layer: Designing Scaffolds for Tissues." Biomedizinische Technik. Biomedical engineering vol. 58 (2013). doi: https://doi.org/10.1515/bmt-2013-4065
Zernetsch H, Repanas A, Gryshkov A, Al Halabi F, Rittinghaus T, Wienecke S, Müller M, Glasmacher B. Solving Biocompatibility Layer by Layer: Designing Scaffolds for Tissues. Biomed Tech (Berl). 2013 Aug;58. doi: 10.1515/bmt-2013-4065. Epub 2013 Sep 07. PMID: 24042739.
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Unsymmetrical N-heterocyclic carbenes with a 1,1'-ferrocenediyl backbone.

Dalton transactions (Cambridge, England : 2003)

Rittinghaus S, Färber C, Bruhn C, Siemeling U.
PMID: 24424525
Dalton Trans. 2014 Mar 07;43(9):3508-20. doi: 10.1039/c3dt52669k.

This paper focuses on ferrocene-based expanded-ring N-heterocyclic carbenes (NHCs) of the type [Fe(C5H4-NR-C-NR'-C5H4)] (), which contain two different N-substituents. Three combinations were addressed, with R = neopentyl (Np) in each case and R' being either 2-adamantyl (Ad), phenyl (Ph)...

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Rittinghaus S, Färber C, Bruhn C, et al. Unsymmetrical N-heterocyclic carbenes with a 1,1'-ferrocenediyl backbone. Dalton Trans. 2014;43(9):3508-20doi: 10.1039/c3dt52669k.
Rittinghaus, S., Färber, C., Bruhn, C., & Siemeling, U. (2014). Unsymmetrical N-heterocyclic carbenes with a 1,1'-ferrocenediyl backbone. Dalton transactions (Cambridge, England : 2003), 43(9), 3508-20. https://doi.org/10.1039/c3dt52669k
Rittinghaus, Stefan, et al. "Unsymmetrical N-heterocyclic carbenes with a 1,1'-ferrocenediyl backbone." Dalton transactions (Cambridge, England : 2003) vol. 43,9 (2014): 3508-20. doi: https://doi.org/10.1039/c3dt52669k
Rittinghaus S, Färber C, Bruhn C, Siemeling U. Unsymmetrical N-heterocyclic carbenes with a 1,1'-ferrocenediyl backbone. Dalton Trans. 2014 Mar 07;43(9):3508-20. doi: 10.1039/c3dt52669k. PMID: 24424525.
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Tuning a robust system: N,O zinc guanidine catalysts for the ROP of lactide.

Dalton transactions (Cambridge, England : 2003)

Schäfer PM, McKeown P, Fuchs M, Rittinghaus RD, Hermann A, Henkel J, Seidel S, Roitzheim C, Ksiazkiewicz AN, Hoffmann A, Pich A, Jones MD, Herres-Pawlis S.
PMID: 30758389
Dalton Trans. 2019 May 07;48(18):6071-6082. doi: 10.1039/c8dt04938f.

Non-toxic, highly active and robust complexes are the holy grail as ideal green catalysts for the polymerisation of biorenewable and biodegradable polylactide. Four new zinc guanidine complexes [ZnCl2(TMG4NMe2asme)], [ZnCl2(TMG5Clasme)], [ZnCl2(TMG5Measme)] and [ZnCl2(TMG5NMe2asme)] with different electron-donating and electron-withdrawing groups on...

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Schäfer PM, McKeown P, Fuchs M, et al. Tuning a robust system: N,O zinc guanidine catalysts for the ROP of lactide. Dalton Trans. 2019;48(18):6071-6082doi: 10.1039/c8dt04938f.
Schäfer, P. M., McKeown, P., Fuchs, M., Rittinghaus, R. D., Hermann, A., Henkel, J., Seidel, S., Roitzheim, C., Ksiazkiewicz, A. N., Hoffmann, A., Pich, A., Jones, M. D., & Herres-Pawlis, S. (2019). Tuning a robust system: N,O zinc guanidine catalysts for the ROP of lactide. Dalton transactions (Cambridge, England : 2003), 48(18), 6071-6082. https://doi.org/10.1039/c8dt04938f
Schäfer, Pascal M, et al. "Tuning a robust system: N,O zinc guanidine catalysts for the ROP of lactide." Dalton transactions (Cambridge, England : 2003) vol. 48,18 (2019): 6071-6082. doi: https://doi.org/10.1039/c8dt04938f
Schäfer PM, McKeown P, Fuchs M, Rittinghaus RD, Hermann A, Henkel J, Seidel S, Roitzheim C, Ksiazkiewicz AN, Hoffmann A, Pich A, Jones MD, Herres-Pawlis S. Tuning a robust system: N,O zinc guanidine catalysts for the ROP of lactide. Dalton Trans. 2019 May 07;48(18):6071-6082. doi: 10.1039/c8dt04938f. PMID: 30758389.
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