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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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[Why study pharmacy?].

Medizinische Monatsschrift fur Pharmazeuten

Heinzl S.
PMID: 1762599
Med Monatsschr Pharm. 1991 Nov;14(11):321.

No abstract available.

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Heinzl S. Warum Pharmazie studieren? [Why study pharmacy?]. Med Monatsschr Pharm. 1991;14(11):321
Heinzl, S. (1991). Warum Pharmazie studieren? [Why study pharmacy?]. Medizinische Monatsschrift fur Pharmazeuten, 14(11), 321.
Heinzl, S. "Warum Pharmazie studieren?" [Why study pharmacy?]. Medizinische Monatsschrift fur Pharmazeuten vol. 14,11 (1991): 321.
Heinzl S. Warum Pharmazie studieren? [Why study pharmacy?]. Med Monatsschr Pharm. 1991 Nov;14(11):321. German. PMID: 1762599.
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[Dispersion systems in pharmacy].

Medizinische Monatsschrift

List PH.
PMID: 5884687
Med Monatsschr. 1965 Dec;19(12):534-7.

No abstract available.

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List PH. Disperse Systeme in der Pharmazie. [Dispersion systems in pharmacy]. Med Monatsschr. 1965;19(12):534-7
List, P. H. (1965). Disperse Systeme in der Pharmazie. [Dispersion systems in pharmacy]. Medizinische Monatsschrift, 19(12), 534-7.
List, P H. "Disperse Systeme in der Pharmazie." [Dispersion systems in pharmacy]. Medizinische Monatsschrift vol. 19,12 (1965): 534-7.
List PH. Disperse Systeme in der Pharmazie. [Dispersion systems in pharmacy]. Med Monatsschr. 1965 Dec;19(12):534-7. German. PMID: 5884687.
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[Preparation of biological research material for HPLC analysis].

Die Pharmazie

Wolff M, Polleit I.
PMID: 3045845
Pharmazie. 1988 Apr;43(4):281-4.

No abstract available.

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Wolff M, Polleit I. Vorbereitung von biologischem Untersuchungsmaterial für die HPLC-Analytik. [Preparation of biological research material for HPLC analysis]. Pharmazie. 1988;43(4):281-4
Wolff, M., & Polleit, I. (1988). Vorbereitung von biologischem Untersuchungsmaterial für die HPLC-Analytik. [Preparation of biological research material for HPLC analysis]. Die Pharmazie, 43(4), 281-4.
Wolff, M, and Polleit, I. "Vorbereitung von biologischem Untersuchungsmaterial für die HPLC-Analytik." [Preparation of biological research material for HPLC analysis]. Die Pharmazie vol. 43,4 (1988): 281-4.
Wolff M, Polleit I. Vorbereitung von biologischem Untersuchungsmaterial für die HPLC-Analytik. [Preparation of biological research material for HPLC analysis]. Pharmazie. 1988 Apr;43(4):281-4. German. PMID: 3045845.
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[Studies on the evaporation of thermolabile drugs].

Archiv der Pharmazie und Berichte der Deutschen Pharmazeutischen Gesellschaft

Müller F, Herrmann G.
PMID: 5276819
Arch Pharm Ber Dtsch Pharm Ges. 1971 Jan;304(1):10-5.

No abstract available.

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Müller F, Herrmann G. Untersuchungen über das Eindampfen thermolabiler Stoffe. [Studies on the evaporation of thermolabile drugs]. Arch Pharm Ber Dtsch Pharm Ges. 1971;304(1):10-5
Müller, F., & Herrmann, G. (1971). Untersuchungen über das Eindampfen thermolabiler Stoffe. [Studies on the evaporation of thermolabile drugs]. Archiv der Pharmazie und Berichte der Deutschen Pharmazeutischen Gesellschaft, 304(1), 10-5.
Müller, F, and Herrmann, G. "Untersuchungen über das Eindampfen thermolabiler Stoffe." [Studies on the evaporation of thermolabile drugs]. Archiv der Pharmazie und Berichte der Deutschen Pharmazeutischen Gesellschaft vol. 304,1 (1971): 10-5.
Müller F, Herrmann G. Untersuchungen über das Eindampfen thermolabiler Stoffe. [Studies on the evaporation of thermolabile drugs]. Arch Pharm Ber Dtsch Pharm Ges. 1971 Jan;304(1):10-5. German. PMID: 5276819.
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[Substitution effects in phenothiazine radicals. 3. Cation radicals from phenothiazine derivatives with electron donor substituents].

Archiv der Pharmazie und Berichte der Deutschen Pharmazeutischen Gesellschaft

Fenner H.
PMID: 5276827
Arch Pharm Ber Dtsch Pharm Ges. 1971 Jan;304(1):47-51. doi: 10.1002/ardp.19713040110.

No abstract available.

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Fenner H. Substituenteneffekte bei Phenothiazin-Radikalen. 3. Radikalkationen aus Phenothiazin-Derivaten mit Elektronen-Donator-Substituenten. [Substitution effects in phenothiazine radicals. 3. Cation radicals from phenothiazine derivatives with electron donor substituents]. Arch Pharm Ber Dtsch Pharm Ges. 1971;304(1):47-51doi: 10.1002/ardp.19713040110.
Fenner, H. (1971). Substituenteneffekte bei Phenothiazin-Radikalen. 3. Radikalkationen aus Phenothiazin-Derivaten mit Elektronen-Donator-Substituenten. [Substitution effects in phenothiazine radicals. 3. Cation radicals from phenothiazine derivatives with electron donor substituents]. Archiv der Pharmazie und Berichte der Deutschen Pharmazeutischen Gesellschaft, 304(1), 47-51. https://doi.org/10.1002/ardp.19713040110
Fenner, H. "Substituenteneffekte bei Phenothiazin-Radikalen. 3. Radikalkationen aus Phenothiazin-Derivaten mit Elektronen-Donator-Substituenten." [Substitution effects in phenothiazine radicals. 3. Cation radicals from phenothiazine derivatives with electron donor substituents]. Archiv der Pharmazie und Berichte der Deutschen Pharmazeutischen Gesellschaft vol. 304,1 (1971): 47-51. doi: https://doi.org/10.1002/ardp.19713040110
Fenner H. Substituenteneffekte bei Phenothiazin-Radikalen. 3. Radikalkationen aus Phenothiazin-Derivaten mit Elektronen-Donator-Substituenten. [Substitution effects in phenothiazine radicals. 3. Cation radicals from phenothiazine derivatives with electron donor substituents]. Arch Pharm Ber Dtsch Pharm Ges. 1971 Jan;304(1):47-51. doi: 10.1002/ardp.19713040110. German. PMID: 5276827.
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[Dihydroisoquinoline rearrangement. 14. Influence of some substituents on nitrogen].

Archiv der Pharmazie und Berichte der Deutschen Pharmazeutischen Gesellschaft

Knabe J, Powilleit H.
PMID: 5276828
Arch Pharm Ber Dtsch Pharm Ges. 1971 Jan;304(1):52-7. doi: 10.1002/ardp.19713040111.

No abstract available.

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Knabe J, Powilleit H. Dihydroisochinolin-Umlagerung. 14. Uber den Eifluss einiger Substituenten am Stickstoff. [Dihydroisoquinoline rearrangement. 14. Influence of some substituents on nitrogen]. Arch Pharm Ber Dtsch Pharm Ges. 1971;304(1):52-7doi: 10.1002/ardp.19713040111.
Knabe, J., & Powilleit, H. (1971). Dihydroisochinolin-Umlagerung. 14. Uber den Eifluss einiger Substituenten am Stickstoff. [Dihydroisoquinoline rearrangement. 14. Influence of some substituents on nitrogen]. Archiv der Pharmazie und Berichte der Deutschen Pharmazeutischen Gesellschaft, 304(1), 52-7. https://doi.org/10.1002/ardp.19713040111
Knabe, J, and Powilleit, H. "Dihydroisochinolin-Umlagerung. 14. Uber den Eifluss einiger Substituenten am Stickstoff." [Dihydroisoquinoline rearrangement. 14. Influence of some substituents on nitrogen]. Archiv der Pharmazie und Berichte der Deutschen Pharmazeutischen Gesellschaft vol. 304,1 (1971): 52-7. doi: https://doi.org/10.1002/ardp.19713040111
Knabe J, Powilleit H. Dihydroisochinolin-Umlagerung. 14. Uber den Eifluss einiger Substituenten am Stickstoff. [Dihydroisoquinoline rearrangement. 14. Influence of some substituents on nitrogen]. Arch Pharm Ber Dtsch Pharm Ges. 1971 Jan;304(1):52-7. doi: 10.1002/ardp.19713040111. PMID: 5276828.
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Semiconductor photocatalysis--mechanistic and synthetic aspects.

Angewandte Chemie (International ed. in English)

Kisch H.
PMID: 23212748
Angew Chem Int Ed Engl. 2013 Jan 14;52(3):812-47. doi: 10.1002/anie.201201200. Epub 2012 Dec 04.

Preceding work on photoelectrochemistry at semiconductor single-crystal electrodes has formed the basis for the tremendous growth in the three last decades in the field of photocatalysis at semiconductor powders. The reason for this is the unique ability of inorganic...

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Kisch H. Semiconductor photocatalysis--mechanistic and synthetic aspects. Angew Chem Int Ed Engl. 2012;52(3):812-47doi: 10.1002/anie.201201200.
Kisch, H. (2013). Semiconductor photocatalysis--mechanistic and synthetic aspects. Angewandte Chemie (International ed. in English), 52(3), 812-47. https://doi.org/10.1002/anie.201201200
Kisch, Horst. "Semiconductor photocatalysis--mechanistic and synthetic aspects." Angewandte Chemie (International ed. in English) vol. 52,3 (2013): 812-47. doi: https://doi.org/10.1002/anie.201201200
Kisch H. Semiconductor photocatalysis--mechanistic and synthetic aspects. Angew Chem Int Ed Engl. 2013 Jan 14;52(3):812-47. doi: 10.1002/anie.201201200. Epub 2012 Dec 04. PMID: 23212748.
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Octopamine Underlies the Counter-Regulatory Response to a Glucose Deficit in Honeybees (.

Frontiers in systems neuroscience

Buckemüller C, Siehler O, Göbel J, Zeumer R, Ölschläger A, Eisenhardt D.
PMID: 28912693
Front Syst Neurosci. 2017 Aug 30;11:63. doi: 10.3389/fnsys.2017.00063. eCollection 2017.

An animal's internal state is a critical parameter required for adaptation to a given environment. An important aspect of an animal's internal state is the energy state that is adjusted to the needs of an animal by energy homeostasis....

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Buckemüller C, Siehler O, Göbel J, et al. Octopamine Underlies the Counter-Regulatory Response to a Glucose Deficit in Honeybees (. Front Syst Neurosci. 2017;11:63doi: 10.3389/fnsys.2017.00063.
Buckemüller, C., Siehler, O., Göbel, J., Zeumer, R., Ölschläger, A., & Eisenhardt, D. (2017). Octopamine Underlies the Counter-Regulatory Response to a Glucose Deficit in Honeybees (. Frontiers in systems neuroscience, 1163. https://doi.org/10.3389/fnsys.2017.00063
Buckemüller, Christina, et al. "Octopamine Underlies the Counter-Regulatory Response to a Glucose Deficit in Honeybees (." Frontiers in systems neuroscience vol. 11 (2017): 63. doi: https://doi.org/10.3389/fnsys.2017.00063
Buckemüller C, Siehler O, Göbel J, Zeumer R, Ölschläger A, Eisenhardt D. Octopamine Underlies the Counter-Regulatory Response to a Glucose Deficit in Honeybees (. Front Syst Neurosci. 2017 Aug 30;11:63. doi: 10.3389/fnsys.2017.00063. eCollection 2017. PMID: 28912693; PMCID: PMC5582081.
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Cell Fixation by Light-Triggered Release of Glutaraldehyde.

Angewandte Chemie (International ed. in English)

Schelkle KM, Schmid C, Yserentant K, Bender M, Wacker I, Petzoldt M, Hamburger M, Herten DP, Wombacher R, Schröder RR, Bunz UH.
PMID: 28328078
Angew Chem Int Ed Engl. 2017 Apr 18;56(17):4724-4728. doi: 10.1002/anie.201612112. Epub 2017 Mar 22.

Chemical fixation of living cells for microscopy is commonly achieved by crosslinking of intracellular proteins with dialdehydes prior to examination. We herein report a photocleavable protecting group for glutaraldehyde that results in a light-triggered and membrane-permeable fixative, which is...

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Schelkle KM, Schmid C, Yserentant K, et al. Cell Fixation by Light-Triggered Release of Glutaraldehyde. Angew Chem Int Ed Engl. 2017;56(17):4724-4728doi: 10.1002/anie.201612112.
Schelkle, K. M., Schmid, C., Yserentant, K., Bender, M., Wacker, I., Petzoldt, M., Hamburger, M., Herten, D. P., Wombacher, R., Schröder, R. R., & Bunz, U. H. (2017). Cell Fixation by Light-Triggered Release of Glutaraldehyde. Angewandte Chemie (International ed. in English), 56(17), 4724-4728. https://doi.org/10.1002/anie.201612112
Schelkle, Korwin M, et al. "Cell Fixation by Light-Triggered Release of Glutaraldehyde." Angewandte Chemie (International ed. in English) vol. 56,17 (2017): 4724-4728. doi: https://doi.org/10.1002/anie.201612112
Schelkle KM, Schmid C, Yserentant K, Bender M, Wacker I, Petzoldt M, Hamburger M, Herten DP, Wombacher R, Schröder RR, Bunz UH. Cell Fixation by Light-Triggered Release of Glutaraldehyde. Angew Chem Int Ed Engl. 2017 Apr 18;56(17):4724-4728. doi: 10.1002/anie.201612112. Epub 2017 Mar 22. PMID: 28328078.
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Switchable Charge Injection Barrier in an Organic Supramolecular Semiconductor.

ACS applied materials & interfaces

Gorbunov AV, Haedler AT, Putzeys T, Zha RH, Schmidt HW, Kivala M, Urbanavičiu̅tė I, Wübbenhorst M, Meijer EW, Kemerink M.
PMID: 27246280
ACS Appl Mater Interfaces. 2016 Jun 22;8(24):15535-42. doi: 10.1021/acsami.6b02988. Epub 2016 Jun 08.

We disclose a supramolecular material that combines semiconducting and dipolar functionalities. The material consists of a discotic semiconducting carbonyl-bridged triarylamine core, which is surrounded by three dipolar amide groups. In thin films, the material self-organizes in a hexagonal columnar...

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Gorbunov AV, Haedler AT, Putzeys T, et al. Switchable Charge Injection Barrier in an Organic Supramolecular Semiconductor. ACS Appl Mater Interfaces. 2016;8(24):15535-42doi: 10.1021/acsami.6b02988.
Gorbunov, A. V., Haedler, A. T., Putzeys, T., Zha, R. H., Schmidt, H. W., Kivala, M., Urbanavičiu̅tė, I., Wübbenhorst, M., Meijer, E. W., & Kemerink, M. (2016). Switchable Charge Injection Barrier in an Organic Supramolecular Semiconductor. ACS applied materials & interfaces, 8(24), 15535-42. https://doi.org/10.1021/acsami.6b02988
Gorbunov, Andrey V, et al. "Switchable Charge Injection Barrier in an Organic Supramolecular Semiconductor." ACS applied materials & interfaces vol. 8,24 (2016): 15535-42. doi: https://doi.org/10.1021/acsami.6b02988
Gorbunov AV, Haedler AT, Putzeys T, Zha RH, Schmidt HW, Kivala M, Urbanavičiu̅tė I, Wübbenhorst M, Meijer EW, Kemerink M. Switchable Charge Injection Barrier in an Organic Supramolecular Semiconductor. ACS Appl Mater Interfaces. 2016 Jun 22;8(24):15535-42. doi: 10.1021/acsami.6b02988. Epub 2016 Jun 08. PMID: 27246280.
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Fixation and release of intact E₄ tetrahedra (E=P, As).

Angewandte Chemie (International ed. in English)

Spitzer F, Sierka M, Latronico M, Mastrorilli P, Virovets AV, Scheer M.
PMID: 25677593
Angew Chem Int Ed Engl. 2015 Mar 27;54(14):4392-6. doi: 10.1002/anie.201411451. Epub 2015 Feb 10.

By the reaction of [NacnacCuCH3CN] with white phosphorus (P4) and yellow arsenic (As4), the stabilization and enclosure of the intact E4 tetrahedra are realized and the disubstituted complexes [(NacnacCu)2(μ,η(2:2)-E4)] (1 a: E=P, 1 b: E=As) are formed. The mono-substituted...

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Spitzer F, Sierka M, Latronico M, et al. Fixation and release of intact E₄ tetrahedra (E=P, As). Angew Chem Int Ed Engl. 2015;54(14):4392-6doi: 10.1002/anie.201411451.
Spitzer, F., Sierka, M., Latronico, M., Mastrorilli, P., Virovets, A. V., & Scheer, M. (2015). Fixation and release of intact E₄ tetrahedra (E=P, As). Angewandte Chemie (International ed. in English), 54(14), 4392-6. https://doi.org/10.1002/anie.201411451
Spitzer, Fabian, et al. "Fixation and release of intact E₄ tetrahedra (E=P, As)." Angewandte Chemie (International ed. in English) vol. 54,14 (2015): 4392-6. doi: https://doi.org/10.1002/anie.201411451
Spitzer F, Sierka M, Latronico M, Mastrorilli P, Virovets AV, Scheer M. Fixation and release of intact E₄ tetrahedra (E=P, As). Angew Chem Int Ed Engl. 2015 Mar 27;54(14):4392-6. doi: 10.1002/anie.201411451. Epub 2015 Feb 10. PMID: 25677593.
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Showing 1 to 12 of 920 entries