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Showing 1 to 12 of 164 entries
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Patient-reported symptoms at hospital discharge independently can predict death and hospitalization burden in advanced heart failure.

The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation

Alpert CM, Hummel EK, Koelling TM, Palardy M, Hummel SL.
PMID: 29129370
J Heart Lung Transplant. 2017 Oct 23; doi: 10.1016/j.healun.2017.10.013. Epub 2017 Oct 23.

No abstract available.

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Alpert CM, Hummel EK, Koelling TM, et al. Patient-reported symptoms at hospital discharge independently can predict death and hospitalization burden in advanced heart failure. J Heart Lung Transplant. 2017;doi: 10.1016/j.healun.2017.10.013.
Alpert, C. M., Hummel, E. K., Koelling, T. M., Palardy, M., & Hummel, S. L. (2017). Patient-reported symptoms at hospital discharge independently can predict death and hospitalization burden in advanced heart failure. The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation, . https://doi.org/10.1016/j.healun.2017.10.013
Alpert, Craig M, et al. "Patient-reported symptoms at hospital discharge independently can predict death and hospitalization burden in advanced heart failure." The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation vol. (2017). doi: https://doi.org/10.1016/j.healun.2017.10.013
Alpert CM, Hummel EK, Koelling TM, Palardy M, Hummel SL. Patient-reported symptoms at hospital discharge independently can predict death and hospitalization burden in advanced heart failure. J Heart Lung Transplant. 2017 Oct 23; doi: 10.1016/j.healun.2017.10.013. Epub 2017 Oct 23. PMID: 29129370.
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Estimating maximum horizontal area of pheromone plumes.

Journal of chemical ecology

Stanley BH, Hummel HE, Ruesink WG.
PMID: 24310335
J Chem Ecol. 1985 Aug;11(8):1129-46. doi: 10.1007/BF01020680.

Graphs and simple Gaussian plume equations are presented for estimating the maximum horizontal area within a pheromone plume. In its simplest form the area,A R , for a given scaling factor,R = Q/(Ku), isA R = AI R (β),...

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Stanley BH, Hummel HE, Ruesink WG. Estimating maximum horizontal area of pheromone plumes. J Chem Ecol. 1985;11(8):1129-46doi: 10.1007/BF01020680.
Stanley, B. H., Hummel, H. E., & Ruesink, W. G. (1985). Estimating maximum horizontal area of pheromone plumes. Journal of chemical ecology, 11(8), 1129-46. https://doi.org/10.1007/BF01020680
Stanley, B H, et al. "Estimating maximum horizontal area of pheromone plumes." Journal of chemical ecology vol. 11,8 (1985): 1129-46. doi: https://doi.org/10.1007/BF01020680
Stanley BH, Hummel HE, Ruesink WG. Estimating maximum horizontal area of pheromone plumes. J Chem Ecol. 1985 Aug;11(8):1129-46. doi: 10.1007/BF01020680. PMID: 24310335.
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Developing a prototype system for integrating pharmacogenomics findings into clinical practice.

Journal of personalized medicine

Overby CL, Tarczy-Hornoch P, Kalet IJ, Thummel KE, Smith JW, Del Fiol G, Fenstermacher D, Devine EB.
PMID: 23741623
J Pers Med. 2012 Nov 20;2(4):241-56. doi: 10.3390/jpm2040241.

Findings from pharmacogenomics (PGx) studies have the potential to be applied to individualize drug therapy to improve efficacy and reduce adverse drug events. Researchers have identified factors influencing uptake of genomics in medicine, but little is known about the...

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Overby CL, Tarczy-Hornoch P, Kalet IJ, et al. Developing a prototype system for integrating pharmacogenomics findings into clinical practice. J Pers Med. 2012;2(4):241-56doi: 10.3390/jpm2040241.
Overby, C. L., Tarczy-Hornoch, P., Kalet, I. J., Thummel, K. E., Smith, J. W., Del Fiol, G., Fenstermacher, D., & Devine, E. B. (2012). Developing a prototype system for integrating pharmacogenomics findings into clinical practice. Journal of personalized medicine, 2(4), 241-56. https://doi.org/10.3390/jpm2040241
Overby, Casey Lynnette, et al. "Developing a prototype system for integrating pharmacogenomics findings into clinical practice." Journal of personalized medicine vol. 2,4 (2012): 241-56. doi: https://doi.org/10.3390/jpm2040241
Overby CL, Tarczy-Hornoch P, Kalet IJ, Thummel KE, Smith JW, Del Fiol G, Fenstermacher D, Devine EB. Developing a prototype system for integrating pharmacogenomics findings into clinical practice. J Pers Med. 2012 Nov 20;2(4):241-56. doi: 10.3390/jpm2040241. PMID: 23741623; PMCID: PMC3670105.
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Diastereoselective Formation and Photophysical Behavior of a Chiral Copper(I) Phenanthroline Complex.

Inorganic chemistry

Riesgo EC, Credi A, De Cola L, Thummel RP.
PMID: 11670368
Inorg Chem. 1998 May 04;37(9):2145-2149. doi: 10.1021/ic971267a.

The Friedländer condensation of (1R,5S)-(+)- and (1S,5R)-(-)-nopinone with 8-aminoquinoline-7-carbaldehyde leads to the corresponding enantiomerically pure (2,3-b)-pineno-1,10-phenanthrolines. Coordination of these ligands with Cu(I) affords non-interconvertable chiral complexes which show equal and opposite Cotton effects in their CD spectra as well...

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Riesgo EC, Credi A, De Cola L, et al. Diastereoselective Formation and Photophysical Behavior of a Chiral Copper(I) Phenanthroline Complex. Inorg Chem. 1998;37(9):2145-2149doi: 10.1021/ic971267a.
Riesgo, E. C., Credi, A., De Cola, L., & Thummel, R. P. (1998). Diastereoselective Formation and Photophysical Behavior of a Chiral Copper(I) Phenanthroline Complex. Inorganic chemistry, 37(9), 2145-2149. https://doi.org/10.1021/ic971267a
Riesgo, Elvira C., et al. "Diastereoselective Formation and Photophysical Behavior of a Chiral Copper(I) Phenanthroline Complex." Inorganic chemistry vol. 37,9 (1998): 2145-2149. doi: https://doi.org/10.1021/ic971267a
Riesgo EC, Credi A, De Cola L, Thummel RP. Diastereoselective Formation and Photophysical Behavior of a Chiral Copper(I) Phenanthroline Complex. Inorg Chem. 1998 May 04;37(9):2145-2149. doi: 10.1021/ic971267a. PMID: 11670368.
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Ruthenium(II) Complexes of 2-Aryl-1,10-phenanthrolines: Synthesis, Structure, and Photophysical Properties.

Inorganic chemistry

Wu F, Riesgo E, Pavalova A, Kipp RA, Schmehl RH, Thummel RP.
PMID: 11671292
Inorg Chem. 1999 Nov 29;38(24):5620-5628. doi: 10.1021/ic990706y.

The synthesis, characterization, and photochemical investigation of a series of Ru(II) complexes having 2-phenyl- and 2,9-diphenyl substituted phenanthroline ligands are reported. Structural characterization of some of the complexes revealed that the phenyl substituents of the phenanthroline ligand are oriented...

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Wu F, Riesgo E, Pavalova A, et al. Ruthenium(II) Complexes of 2-Aryl-1,10-phenanthrolines: Synthesis, Structure, and Photophysical Properties. Inorg Chem. 1999;38(24):5620-5628doi: 10.1021/ic990706y.
Wu, F., Riesgo, E., Pavalova, A., Kipp, R. A., Schmehl, R. H., & Thummel, R. P. (1999). Ruthenium(II) Complexes of 2-Aryl-1,10-phenanthrolines: Synthesis, Structure, and Photophysical Properties. Inorganic chemistry, 38(24), 5620-5628. https://doi.org/10.1021/ic990706y
Wu, Feiyue, et al. "Ruthenium(II) Complexes of 2-Aryl-1,10-phenanthrolines: Synthesis, Structure, and Photophysical Properties." Inorganic chemistry vol. 38,24 (1999): 5620-5628. doi: https://doi.org/10.1021/ic990706y
Wu F, Riesgo E, Pavalova A, Kipp RA, Schmehl RH, Thummel RP. Ruthenium(II) Complexes of 2-Aryl-1,10-phenanthrolines: Synthesis, Structure, and Photophysical Properties. Inorg Chem. 1999 Nov 29;38(24):5620-5628. doi: 10.1021/ic990706y. PMID: 11671292.
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Enzyme-catalyzed processes of first-pass hepatic and intestinal drug extraction.

Advanced drug delivery reviews

Shen DD, Kunze KL, Thummel KE.
PMID: 10837554
Adv Drug Deliv Rev. 1997 Sep 15;27(2):99-127. doi: 10.1016/s0169-409x(97)00039-2.

Oral bioavailability of pharmacologically effective drugs is often limited by first-pass biotransformation. In humans, both hepatic and intestinal enzymes can catalyze the metabolism of a drug as it transits between the gastrointestinal lumen and systemic blood for the first...

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Shen DD, Kunze KL, Thummel KE. Enzyme-catalyzed processes of first-pass hepatic and intestinal drug extraction. Adv Drug Deliv Rev. 1997;27(2):99-127doi: 10.1016/s0169-409x(97)00039-2.
Shen, D. D., Kunze, K. L., & Thummel, K. E. (1997). Enzyme-catalyzed processes of first-pass hepatic and intestinal drug extraction. Advanced drug delivery reviews, 27(2), 99-127. https://doi.org/10.1016/s0169-409x(97)00039-2
Shen, et al. "Enzyme-catalyzed processes of first-pass hepatic and intestinal drug extraction." Advanced drug delivery reviews vol. 27,2 (1997): 99-127. doi: https://doi.org/10.1016/s0169-409x(97)00039-2
Shen DD, Kunze KL, Thummel KE. Enzyme-catalyzed processes of first-pass hepatic and intestinal drug extraction. Adv Drug Deliv Rev. 1997 Sep 15;27(2):99-127. doi: 10.1016/s0169-409x(97)00039-2. PMID: 10837554.
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Friedländer approach for the incorporation of 6-bromoquinoline into novel chelating ligands.

Organic letters

Hu YZ, Zhang G, Thummel RP.
PMID: 12816421
Org Lett. 2003 Jun 26;5(13):2251-3. doi: 10.1021/ol034559q.

Nitration of 3-bromobenzaldehyde followed by sodium dithionite reduction provides 5-bromo-2-aminobenzaldehyde, which undergoes the Friedländer condensation with a variety of enolizable ketones to afford bidentate and tridentate 6-bromoquinoline derivatives. These species may be dimerized with Ni(0) to form biquinolines or...

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Hu YZ, Zhang G, Thummel RP. Friedländer approach for the incorporation of 6-bromoquinoline into novel chelating ligands. Org Lett. 2003;5(13):2251-3doi: 10.1021/ol034559q.
Hu, Y. Z., Zhang, G., & Thummel, R. P. (2003). Friedländer approach for the incorporation of 6-bromoquinoline into novel chelating ligands. Organic letters, 5(13), 2251-3. https://doi.org/10.1021/ol034559q
Hu, Yi-Zhen, et al. "Friedländer approach for the incorporation of 6-bromoquinoline into novel chelating ligands." Organic letters vol. 5,13 (2003): 2251-3. doi: https://doi.org/10.1021/ol034559q
Hu YZ, Zhang G, Thummel RP. Friedländer approach for the incorporation of 6-bromoquinoline into novel chelating ligands. Org Lett. 2003 Jun 26;5(13):2251-3. doi: 10.1021/ol034559q. PMID: 12816421.
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Young Produced from Ovaries Subjected to Endocrine Imbalance.

Proceedings of the National Academy of Sciences of the United States of America

Little CC, Hummel KP, Eddy M, Rupple B.
PMID: 16578398
Proc Natl Acad Sci U S A. 1951 Oct;37(10):666-9. doi: 10.1073/pnas.37.10.666.

No abstract available.

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Little CC, Hummel KP, Eddy M, et al. Young Produced from Ovaries Subjected to Endocrine Imbalance. Proc Natl Acad Sci U S A. 1951;37(10):666-9doi: 10.1073/pnas.37.10.666.
Little, C. C., Hummel, K. P., Eddy, M., & Rupple, B. (1951). Young Produced from Ovaries Subjected to Endocrine Imbalance. Proceedings of the National Academy of Sciences of the United States of America, 37(10), 666-9. https://doi.org/10.1073/pnas.37.10.666
Little, C C, et al. "Young Produced from Ovaries Subjected to Endocrine Imbalance." Proceedings of the National Academy of Sciences of the United States of America vol. 37,10 (1951): 666-9. doi: https://doi.org/10.1073/pnas.37.10.666
Little CC, Hummel KP, Eddy M, Rupple B. Young Produced from Ovaries Subjected to Endocrine Imbalance. Proc Natl Acad Sci U S A. 1951 Oct;37(10):666-9. doi: 10.1073/pnas.37.10.666. PMID: 16578398; PMCID: PMC1063442.
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Preparation and study of a family of dinuclear Ru(II) complexes that catalyze the decomposition of water.

Inorganic chemistry

Deng Z, Tseng HW, Zong R, Wang D, Thummel R.
PMID: 18330974
Inorg Chem. 2008 Mar 17;47(6):1835-48. doi: 10.1021/ic7010875.

An approach is developed for the four-electron oxidation of water to provide dioxygen that involves the juxtaposition of two Ru(II) centers such that a metal-bound water molecule might interact with one or both of the metals. The key element...

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Deng Z, Tseng HW, Zong R, et al. Preparation and study of a family of dinuclear Ru(II) complexes that catalyze the decomposition of water. Inorg Chem. 2008;47(6):1835-48doi: 10.1021/ic7010875.
Deng, Z., Tseng, H. W., Zong, R., Wang, D., & Thummel, R. (2008). Preparation and study of a family of dinuclear Ru(II) complexes that catalyze the decomposition of water. Inorganic chemistry, 47(6), 1835-48. https://doi.org/10.1021/ic7010875
Deng, Zeping, et al. "Preparation and study of a family of dinuclear Ru(II) complexes that catalyze the decomposition of water." Inorganic chemistry vol. 47,6 (2008): 1835-48. doi: https://doi.org/10.1021/ic7010875
Deng Z, Tseng HW, Zong R, Wang D, Thummel R. Preparation and study of a family of dinuclear Ru(II) complexes that catalyze the decomposition of water. Inorg Chem. 2008 Mar 17;47(6):1835-48. doi: 10.1021/ic7010875. PMID: 18330974.
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2,9-Di-(2'-pyridyl)-1,10-phenanthroline: a tetradentate ligand for Ru(II).

Journal of the American Chemical Society

Zong R, Thummel RP.
PMID: 15339138
J Am Chem Soc. 2004 Sep 08;126(35):10800-1. doi: 10.1021/ja047410y.

The tetradentate ligand 2,9-di-(2'-pyridyl)-1,10-phenanthroline is synthesized in 62% yield by the Stille coupling of 2,9-dichloro-1,10-phenanthroline and 2-(tri-n-butylstannyl)pyridine. Treatment of this ligand with RuCl3.3H2O and a 4-substituted pyridine results in the formation of a complex in which the tetradentate ligand...

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Zong R, Thummel RP. 2,9-Di-(2'-pyridyl)-1,10-phenanthroline: a tetradentate ligand for Ru(II). J Am Chem Soc. 2004;126(35):10800-1doi: 10.1021/ja047410y.
Zong, R., & Thummel, R. P. (2004). 2,9-Di-(2'-pyridyl)-1,10-phenanthroline: a tetradentate ligand for Ru(II). Journal of the American Chemical Society, 126(35), 10800-1. https://doi.org/10.1021/ja047410y
Zong, Ruifa, and Thummel, Randolph P. "2,9-Di-(2'-pyridyl)-1,10-phenanthroline: a tetradentate ligand for Ru(II)." Journal of the American Chemical Society vol. 126,35 (2004): 10800-1. doi: https://doi.org/10.1021/ja047410y
Zong R, Thummel RP. 2,9-Di-(2'-pyridyl)-1,10-phenanthroline: a tetradentate ligand for Ru(II). J Am Chem Soc. 2004 Sep 08;126(35):10800-1. doi: 10.1021/ja047410y. PMID: 15339138.
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Proton transfer with a twist? Femtosecond dynamics of 7-(2-pyridyl)indole in condensed phase and in supersonic jets.

Angewandte Chemie (International ed. in English)

Nosenko Y, Wiosna-Sałyga G, Kunitski M, Petkova I, Singh A, Buma WJ, Thummel RP, Brutschy B, Waluk J.
PMID: 18604789
Angew Chem Int Ed Engl. 2008;47(32):6037-40. doi: 10.1002/anie.200801350.

No abstract available.

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Nosenko Y, Wiosna-Sałyga G, Kunitski M, et al. Proton transfer with a twist? Femtosecond dynamics of 7-(2-pyridyl)indole in condensed phase and in supersonic jets. Angew Chem Int Ed Engl. 2008;47(32):6037-40doi: 10.1002/anie.200801350.
Nosenko, Y., Wiosna-Sałyga, G., Kunitski, M., Petkova, I., Singh, A., Buma, W. J., Thummel, R. P., Brutschy, B., & Waluk, J. (2008). Proton transfer with a twist? Femtosecond dynamics of 7-(2-pyridyl)indole in condensed phase and in supersonic jets. Angewandte Chemie (International ed. in English), 47(32), 6037-40. https://doi.org/10.1002/anie.200801350
Nosenko, Y, et al. "Proton transfer with a twist? Femtosecond dynamics of 7-(2-pyridyl)indole in condensed phase and in supersonic jets." Angewandte Chemie (International ed. in English) vol. 47,32 (2008): 6037-40. doi: https://doi.org/10.1002/anie.200801350
Nosenko Y, Wiosna-Sałyga G, Kunitski M, Petkova I, Singh A, Buma WJ, Thummel RP, Brutschy B, Waluk J. Proton transfer with a twist? Femtosecond dynamics of 7-(2-pyridyl)indole in condensed phase and in supersonic jets. Angew Chem Int Ed Engl. 2008;47(32):6037-40. doi: 10.1002/anie.200801350. PMID: 18604789.
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Evidence That Ceriporiopsis subvermispora Degrades Nonphenolic Lignin Structures by a One-Electron-Oxidation Mechanism.

Applied and environmental microbiology

Srebotnik E, Jensen KA, Kawai S, Hammel KE.
PMID: 16535732
Appl Environ Microbiol. 1997 Nov;63(11):4435-40. doi: 10.1128/aem.63.11.4435-4440.1997.

The white-rot fungus Ceriporiopsis subvermispora is able to degrade nonphenolic lignin structures but appears to lack lignin peroxidase (LiP), which is generally thought to be responsible for these reactions. It is well established that LiP-producing fungi such as Phanerochaete...

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Srebotnik E, Jensen KA, Kawai S, et al. Evidence That Ceriporiopsis subvermispora Degrades Nonphenolic Lignin Structures by a One-Electron-Oxidation Mechanism. Appl Environ Microbiol. 1997;63(11):4435-40doi: 10.1128/aem.63.11.4435-4440.1997.
Srebotnik, E., Jensen, K. A., Kawai, S., & Hammel, K. E. (1997). Evidence That Ceriporiopsis subvermispora Degrades Nonphenolic Lignin Structures by a One-Electron-Oxidation Mechanism. Applied and environmental microbiology, 63(11), 4435-40. https://doi.org/10.1128/aem.63.11.4435-4440.1997
Srebotnik, E, et al. "Evidence That Ceriporiopsis subvermispora Degrades Nonphenolic Lignin Structures by a One-Electron-Oxidation Mechanism." Applied and environmental microbiology vol. 63,11 (1997): 4435-40. doi: https://doi.org/10.1128/aem.63.11.4435-4440.1997
Srebotnik E, Jensen KA, Kawai S, Hammel KE. Evidence That Ceriporiopsis subvermispora Degrades Nonphenolic Lignin Structures by a One-Electron-Oxidation Mechanism. Appl Environ Microbiol. 1997 Nov;63(11):4435-40. doi: 10.1128/aem.63.11.4435-4440.1997. PMID: 16535732; PMCID: PMC1389288.
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Showing 1 to 12 of 164 entries