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Supramolecular frameworks based on [60]fullerene hexakisadducts.

Beilstein journal of organic chemistry

Kraft A, Stangl J, Krause AM, Müller-Buschbaum K, Beuerle F.
PMID: 28179942
Beilstein J Org Chem. 2017 Jan 02;13:1-9. doi: 10.3762/bjoc.13.1. eCollection 2017.

[60]Fullerene hexakisadducts possessing 12 carboxylic acid side chains form crystalline hydrogen-bonding frameworks in the solid state. Depending on the length of the linker between the reactive sites and the malonate units, the distance of the [60]fullerene nodes and thereby...

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Kraft A, Stangl J, Krause AM, et al. Supramolecular frameworks based on [60]fullerene hexakisadducts. Beilstein J Org Chem. 2017;13:1-9doi: 10.3762/bjoc.13.1.
Kraft, A., Stangl, J., Krause, A. M., Müller-Buschbaum, K., & Beuerle, F. (2017). Supramolecular frameworks based on [60]fullerene hexakisadducts. Beilstein journal of organic chemistry, 131-9. https://doi.org/10.3762/bjoc.13.1
Kraft, Andreas, et al. "Supramolecular frameworks based on [60]fullerene hexakisadducts." Beilstein journal of organic chemistry vol. 13 (2017): 1-9. doi: https://doi.org/10.3762/bjoc.13.1
Kraft A, Stangl J, Krause AM, Müller-Buschbaum K, Beuerle F. Supramolecular frameworks based on [60]fullerene hexakisadducts. Beilstein J Org Chem. 2017 Jan 02;13:1-9. doi: 10.3762/bjoc.13.1. eCollection 2017. PMID: 28179942; PMCID: PMC5238557.
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Critical Assessment of Small Molecule Identification 2016: automated methods.

Journal of cheminformatics

Schymanski EL, Ruttkies C, Krauss M, Brouard C, Kind T, Dührkop K, Allen F, Vaniya A, Verdegem D, Böcker S, Rousu J, Shen H, Tsugawa H, Sajed T, Fiehn O, Ghesquière B, Neumann S.
PMID: 29086042
J Cheminform. 2017 Mar 27;9(1):22. doi: 10.1186/s13321-017-0207-1.

BACKGROUND: The fourth round of the Critical Assessment of Small Molecule Identification (CASMI) Contest ( www.casmi-contest.org ) was held in 2016, with two new categories for automated methods. This article covers the 208 challenges in Categories 2 and 3,...

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Schymanski EL, Ruttkies C, Krauss M, et al. Critical Assessment of Small Molecule Identification 2016: automated methods. J Cheminform. 2017;9(1):22doi: 10.1186/s13321-017-0207-1.
Schymanski, E. L., Ruttkies, C., Krauss, M., Brouard, C., Kind, T., Dührkop, K., Allen, F., Vaniya, A., Verdegem, D., Böcker, S., Rousu, J., Shen, H., Tsugawa, H., Sajed, T., Fiehn, O., Ghesquière, B., & Neumann, S. (2017). Critical Assessment of Small Molecule Identification 2016: automated methods. Journal of cheminformatics, 9(1), 22. https://doi.org/10.1186/s13321-017-0207-1
Schymanski, Emma L, et al. "Critical Assessment of Small Molecule Identification 2016: automated methods." Journal of cheminformatics vol. 9,1 (2017): 22. doi: https://doi.org/10.1186/s13321-017-0207-1
Schymanski EL, Ruttkies C, Krauss M, Brouard C, Kind T, Dührkop K, Allen F, Vaniya A, Verdegem D, Böcker S, Rousu J, Shen H, Tsugawa H, Sajed T, Fiehn O, Ghesquière B, Neumann S. Critical Assessment of Small Molecule Identification 2016: automated methods. J Cheminform. 2017 Mar 27;9(1):22. doi: 10.1186/s13321-017-0207-1. PMID: 29086042; PMCID: PMC5368104.
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Ligand Surface Chemistry Dictates Light Emission from Nanocrystals.

The journal of physical chemistry letters

Krause MM, Jethi L, Mack TG, Kambhampati P.
PMID: 26538044
J Phys Chem Lett. 2015 Nov 05;6(21):4292-6. doi: 10.1021/acs.jpclett.5b02015. Epub 2015 Oct 14.

There are several contradictory accounts of the changes to the emissive behavior of semiconductor nanocrystal upon a ligand exchange from trioctylphosphine/cadmium-phosphonates passivation to N-butylamine. This communication explains the contradictory accounts of this reaction using new insights into ligand chemistry....

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Krause MM, Jethi L, Mack TG, et al. Ligand Surface Chemistry Dictates Light Emission from Nanocrystals. J Phys Chem Lett. 2015;6(21):4292-6doi: 10.1021/acs.jpclett.5b02015.
Krause, M. M., Jethi, L., Mack, T. G., & Kambhampati, P. (2015). Ligand Surface Chemistry Dictates Light Emission from Nanocrystals. The journal of physical chemistry letters, 6(21), 4292-6. https://doi.org/10.1021/acs.jpclett.5b02015
Krause, Michael M, et al. "Ligand Surface Chemistry Dictates Light Emission from Nanocrystals." The journal of physical chemistry letters vol. 6,21 (2015): 4292-6. doi: https://doi.org/10.1021/acs.jpclett.5b02015
Krause MM, Jethi L, Mack TG, Kambhampati P. Ligand Surface Chemistry Dictates Light Emission from Nanocrystals. J Phys Chem Lett. 2015 Nov 05;6(21):4292-6. doi: 10.1021/acs.jpclett.5b02015. Epub 2015 Oct 14. PMID: 26538044.
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Optimization of LC-Orbitrap-HRMS acquisition and MZmine 2 data processing for nontarget screening of environmental samples using design of experiments.

Analytical and bioanalytical chemistry

Hu M, Krauss M, Brack W, Schulze T.
PMID: 27714402
Anal Bioanal Chem. 2016 Nov;408(28):7905-7915. doi: 10.1007/s00216-016-9919-8. Epub 2016 Oct 07.

Liquid chromatography-high resolution mass spectrometry (LC-HRMS) is a well-established technique for nontarget screening of contaminants in complex environmental samples. Automatic peak detection is essential, but its performance has only rarely been assessed and optimized so far. With the aim...

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Hu M, Krauss M, Brack W, et al. Optimization of LC-Orbitrap-HRMS acquisition and MZmine 2 data processing for nontarget screening of environmental samples using design of experiments. Anal Bioanal Chem. 2016;408(28):7905-7915doi: 10.1007/s00216-016-9919-8.
Hu, M., Krauss, M., Brack, W., & Schulze, T. (2016). Optimization of LC-Orbitrap-HRMS acquisition and MZmine 2 data processing for nontarget screening of environmental samples using design of experiments. Analytical and bioanalytical chemistry, 408(28), 7905-7915. https://doi.org/10.1007/s00216-016-9919-8
Hu, Meng, et al. "Optimization of LC-Orbitrap-HRMS acquisition and MZmine 2 data processing for nontarget screening of environmental samples using design of experiments." Analytical and bioanalytical chemistry vol. 408,28 (2016): 7905-7915. doi: https://doi.org/10.1007/s00216-016-9919-8
Hu M, Krauss M, Brack W, Schulze T. Optimization of LC-Orbitrap-HRMS acquisition and MZmine 2 data processing for nontarget screening of environmental samples using design of experiments. Anal Bioanal Chem. 2016 Nov;408(28):7905-7915. doi: 10.1007/s00216-016-9919-8. Epub 2016 Oct 07. PMID: 27714402.
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Selective Epitaxy of InP on Si and Rectification in Graphene/InP/Si Hybrid Structure.

ACS applied materials & interfaces

Niu G, Capellini G, Hatami F, Di Bartolomeo A, Niermann T, Hussein EH, Schubert MA, Krause HM, Zaumseil P, Skibitzki O, Lupina G, Masselink WT, Lehmann M, Xie YH, Schroeder T.
PMID: 27642767
ACS Appl Mater Interfaces. 2016 Oct 12;8(40):26948-26955. doi: 10.1021/acsami.6b09592. Epub 2016 Sep 28.

The epitaxial integration of highly heterogeneous material systems with silicon (Si) is a central topic in (opto-)electronics owing to device applications. InP could open new avenues for the realization of novel devices such as high-mobility transistors in next-generation CMOS...

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Niu G, Capellini G, Hatami F, et al. Selective Epitaxy of InP on Si and Rectification in Graphene/InP/Si Hybrid Structure. ACS Appl Mater Interfaces. 2016;8(40):26948-26955doi: 10.1021/acsami.6b09592.
Niu, G., Capellini, G., Hatami, F., Di Bartolomeo, A., Niermann, T., Hussein, E. H., Schubert, M. A., Krause, H. M., Zaumseil, P., Skibitzki, O., Lupina, G., Masselink, W. T., Lehmann, M., Xie, Y. H., & Schroeder, T. (2016). Selective Epitaxy of InP on Si and Rectification in Graphene/InP/Si Hybrid Structure. ACS applied materials & interfaces, 8(40), 26948-26955. https://doi.org/10.1021/acsami.6b09592
Niu, Gang, et al. "Selective Epitaxy of InP on Si and Rectification in Graphene/InP/Si Hybrid Structure." ACS applied materials & interfaces vol. 8,40 (2016): 26948-26955. doi: https://doi.org/10.1021/acsami.6b09592
Niu G, Capellini G, Hatami F, Di Bartolomeo A, Niermann T, Hussein EH, Schubert MA, Krause HM, Zaumseil P, Skibitzki O, Lupina G, Masselink WT, Lehmann M, Xie YH, Schroeder T. Selective Epitaxy of InP on Si and Rectification in Graphene/InP/Si Hybrid Structure. ACS Appl Mater Interfaces. 2016 Oct 12;8(40):26948-26955. doi: 10.1021/acsami.6b09592. Epub 2016 Sep 28. PMID: 27642767.
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Using Bayesian-PBPK modeling for assessment of inter-individual variability and subgroup stratification.

In silico pharmacology

Krauss M, Burghaus R, Lippert J, Niemi M, Neuvonen P, Schuppert A, Willmann S, Kuepfer L, Görlitz L.
PMID: 25505651
In Silico Pharmacol. 2013 Apr 11;1:6. doi: 10.1186/2193-9616-1-6. eCollection 2013.

PURPOSE: Inter-individual variability in clinical endpoints and occurrence of potentially severe adverse effects represent an enormous challenge in drug development at all phases of (pre-)clinical research. To ensure patient safety it is important to identify adverse events or critical...

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Krauss M, Burghaus R, Lippert J, et al. Using Bayesian-PBPK modeling for assessment of inter-individual variability and subgroup stratification. In Silico Pharmacol. 2013;1:6doi: 10.1186/2193-9616-1-6.
Krauss, M., Burghaus, R., Lippert, J., Niemi, M., Neuvonen, P., Schuppert, A., Willmann, S., Kuepfer, L., & Görlitz, L. (2013). Using Bayesian-PBPK modeling for assessment of inter-individual variability and subgroup stratification. In silico pharmacology, 16. https://doi.org/10.1186/2193-9616-1-6
Krauss, Markus, et al. "Using Bayesian-PBPK modeling for assessment of inter-individual variability and subgroup stratification." In silico pharmacology vol. 1 (2013): 6. doi: https://doi.org/10.1186/2193-9616-1-6
Krauss M, Burghaus R, Lippert J, Niemi M, Neuvonen P, Schuppert A, Willmann S, Kuepfer L, Görlitz L. Using Bayesian-PBPK modeling for assessment of inter-individual variability and subgroup stratification. In Silico Pharmacol. 2013 Apr 11;1:6. doi: 10.1186/2193-9616-1-6. eCollection 2013. PMID: 25505651; PMCID: PMC4230716.
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Polycyclic aromatic hydrocarbons and polychlorinated biphenyls in forest soils: depth distribution as indicator of different fate.

Environmental pollution (Barking, Essex : 1987)

Krauss M, Wilcke W, Zech W.
PMID: 15092858
Environ Pollut. 2000 Oct;110(1):79-88. doi: 10.1016/s0269-7491(99)00280-8.

We determined 20 polycyclic aromatic hydrocarbons (PAHs) and 12 polychlorinated biphenyls (PCBs) in Oi, Oe, and Oa horizons and at 0-5 and 15-20 cm mineral soil depth of 16 Norway spruce (Picea abies) stands in north Bavaria. The sum...

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Krauss M, Wilcke W, Zech W. Polycyclic aromatic hydrocarbons and polychlorinated biphenyls in forest soils: depth distribution as indicator of different fate. Environ Pollut. 2000;110(1):79-88doi: 10.1016/s0269-7491(99)00280-8.
Krauss, M., Wilcke, W., & Zech, W. (2000). Polycyclic aromatic hydrocarbons and polychlorinated biphenyls in forest soils: depth distribution as indicator of different fate. Environmental pollution (Barking, Essex : 1987), 110(1), 79-88. https://doi.org/10.1016/s0269-7491(99)00280-8
Krauss, M, et al. "Polycyclic aromatic hydrocarbons and polychlorinated biphenyls in forest soils: depth distribution as indicator of different fate." Environmental pollution (Barking, Essex : 1987) vol. 110,1 (2000): 79-88. doi: https://doi.org/10.1016/s0269-7491(99)00280-8
Krauss M, Wilcke W, Zech W. Polycyclic aromatic hydrocarbons and polychlorinated biphenyls in forest soils: depth distribution as indicator of different fate. Environ Pollut. 2000 Oct;110(1):79-88. doi: 10.1016/s0269-7491(99)00280-8. PMID: 15092858.
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Relationship Between beta-Lactamase Activity and Resistance of Enterobacter to Cephalothin.

Infection and immunity

Farrar WE, Krause JM.
PMID: 16557885
Infect Immun. 1970 Nov;2(5):610-6. doi: 10.1128/iai.2.5.610-616.1970.

The relationship between cephalosporin beta-lactamase activity and resistance to cephalothin was investigated in strains of Enterobacter cloacae and E. aerogenes. beta-Lactamase activity was detected in all strains, but a quantitative correlation between amount of beta-lactamase activity and level of...

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Farrar WE, Krause JM. Relationship Between beta-Lactamase Activity and Resistance of Enterobacter to Cephalothin. Infect Immun. 1970;2(5):610-6doi: 10.1128/iai.2.5.610-616.1970.
Farrar, W. E., & Krause, J. M. (1970). Relationship Between beta-Lactamase Activity and Resistance of Enterobacter to Cephalothin. Infection and immunity, 2(5), 610-6. https://doi.org/10.1128/iai.2.5.610-616.1970
Farrar, W E, and Krause, J M. "Relationship Between beta-Lactamase Activity and Resistance of Enterobacter to Cephalothin." Infection and immunity vol. 2,5 (1970): 610-6. doi: https://doi.org/10.1128/iai.2.5.610-616.1970
Farrar WE, Krause JM. Relationship Between beta-Lactamase Activity and Resistance of Enterobacter to Cephalothin. Infect Immun. 1970 Nov;2(5):610-6. doi: 10.1128/iai.2.5.610-616.1970. PMID: 16557885; PMCID: PMC416058.
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Responses of Heterotrophic Cultures of Chlorella vulgaris Beyerinck to Darkness and Light. II. Action Spectrum for and Mechanism of the Light Requirement for Heterotrophic Growth.

Plant physiology

Karlander EP, Krauss RW.
PMID: 16656234
Plant Physiol. 1966 Jan;41(1):7-14. doi: 10.1104/pp.41.1.7.

Chlorella vulgaris Beyerinck (Emerson's strain), fails to grow in the dark even when sugars are provided. This phenomenon was clearly demonstrated in the alga, C. vulgaris, for which the growth rate in darkness on a glucose medium remained constant...

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Karlander EP, Krauss RW. Responses of Heterotrophic Cultures of Chlorella vulgaris Beyerinck to Darkness and Light. II. Action Spectrum for and Mechanism of the Light Requirement for Heterotrophic Growth. Plant Physiol. 1966;41(1):7-14doi: 10.1104/pp.41.1.7.
Karlander, E. P., & Krauss, R. W. (1966). Responses of Heterotrophic Cultures of Chlorella vulgaris Beyerinck to Darkness and Light. II. Action Spectrum for and Mechanism of the Light Requirement for Heterotrophic Growth. Plant physiology, 41(1), 7-14. https://doi.org/10.1104/pp.41.1.7
Karlander, E P, and Krauss, R W. "Responses of Heterotrophic Cultures of Chlorella vulgaris Beyerinck to Darkness and Light. II. Action Spectrum for and Mechanism of the Light Requirement for Heterotrophic Growth." Plant physiology vol. 41,1 (1966): 7-14. doi: https://doi.org/10.1104/pp.41.1.7
Karlander EP, Krauss RW. Responses of Heterotrophic Cultures of Chlorella vulgaris Beyerinck to Darkness and Light. II. Action Spectrum for and Mechanism of the Light Requirement for Heterotrophic Growth. Plant Physiol. 1966 Jan;41(1):7-14. doi: 10.1104/pp.41.1.7. PMID: 16656234; PMCID: PMC1086289.
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Cross-reactions of streptococcal group-specific substances in antipneumococcal serums.

Science (New York, N.Y.)

Heidelberger M, Krause RM, Elliott SD.
PMID: 17779536
Science. 1966 Apr 29;152(3722):675. doi: 10.1126/science.152.3722.675.

No abstract available.

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Heidelberger M, Krause RM, Elliott SD. Cross-reactions of streptococcal group-specific substances in antipneumococcal serums. Science. 1966;152(3722):675doi: 10.1126/science.152.3722.675.
Heidelberger, M., Krause, R. M., & Elliott, S. D. (1966). Cross-reactions of streptococcal group-specific substances in antipneumococcal serums. Science (New York, N.Y.), 152(3722), 675. https://doi.org/10.1126/science.152.3722.675
Heidelberger, M, et al. "Cross-reactions of streptococcal group-specific substances in antipneumococcal serums." Science (New York, N.Y.) vol. 152,3722 (1966): 675. doi: https://doi.org/10.1126/science.152.3722.675
Heidelberger M, Krause RM, Elliott SD. Cross-reactions of streptococcal group-specific substances in antipneumococcal serums. Science. 1966 Apr 29;152(3722):675. doi: 10.1126/science.152.3722.675. PMID: 17779536.
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Differential Absorption of Metal Chelate Components by Plant Roots.

Plant physiology

Tiffin LO, Brown JC, Krauss RW.
PMID: 16655357
Plant Physiol. 1960 May;35(3):362-7. doi: 10.1104/pp.35.3.362.

No abstract available.

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Tiffin LO, Brown JC, Krauss RW. Differential Absorption of Metal Chelate Components by Plant Roots. Plant Physiol. 1960;35(3):362-7doi: 10.1104/pp.35.3.362.
Tiffin, L. O., Brown, J. C., & Krauss, R. W. (1960). Differential Absorption of Metal Chelate Components by Plant Roots. Plant physiology, 35(3), 362-7. https://doi.org/10.1104/pp.35.3.362
Tiffin, L O, et al. "Differential Absorption of Metal Chelate Components by Plant Roots." Plant physiology vol. 35,3 (1960): 362-7. doi: https://doi.org/10.1104/pp.35.3.362
Tiffin LO, Brown JC, Krauss RW. Differential Absorption of Metal Chelate Components by Plant Roots. Plant Physiol. 1960 May;35(3):362-7. doi: 10.1104/pp.35.3.362. PMID: 16655357; PMCID: PMC405972.
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Surface temperature-field imaging with laser-induced thermographic phosphorescence.

Applied optics

Edge AC, Laufer G, Krauss RH.
PMID: 18337924
Appl Opt. 2000 Feb 01;39(4):546-53. doi: 10.1364/ao.39.000546.

A technique to remotely image temperature distributions of heated metallic surfaces is extended to higher temperatures. It uses a Dy(+3):YAG thermographic phosphor (TP) bonded to the surface and excited by radiation at 355 nm. Digital images of the emission...

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Edge AC, Laufer G, Krauss RH. Surface temperature-field imaging with laser-induced thermographic phosphorescence. Appl Opt. 2000;39(4):546-53doi: 10.1364/ao.39.000546.
Edge, A. C., Laufer, G., & Krauss, R. H. (2000). Surface temperature-field imaging with laser-induced thermographic phosphorescence. Applied optics, 39(4), 546-53. https://doi.org/10.1364/ao.39.000546
Edge, A C, et al. "Surface temperature-field imaging with laser-induced thermographic phosphorescence." Applied optics vol. 39,4 (2000): 546-53. doi: https://doi.org/10.1364/ao.39.000546
Edge AC, Laufer G, Krauss RH. Surface temperature-field imaging with laser-induced thermographic phosphorescence. Appl Opt. 2000 Feb 01;39(4):546-53. doi: 10.1364/ao.39.000546. PMID: 18337924.
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