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Cultural competence in interdisciplinary collaborations: A method for respecting diversity in research partnerships

Cultural Transformation in the Geoscience Community AND Program Evaluation

Reich SM, Reich JA.
GSID: io005PtXrSAJ
SM Reich, JA Reich - American journal of community psychology, 2006 - Springer

There is growing recognition of the need by funding agencies, universities, and research units for interdisciplinary research to tackle complex societal problems that cannot be adequately addressed by single disciplines alone. Interdisciplinary collaboration capitalizes on a diversity of perspectives...

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Reich, S. M., & Reich, J. A. (2006). Cultural competence in interdisciplinary collaborations: A method for respecting diversity in research partnerships. American journal of community psychology, 38(1), 51-62.
Reich, Stephanie M., and Jennifer A. Reich. "Cultural competence in interdisciplinary collaborations: A method for respecting diversity in research partnerships." American journal of community psychology 38.1 (2006): 51-62.
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Size-extensivity-corrected multireference configuration interaction schemes to accurately predict bond dissociation energies of oxygenated hydrocarbons.

The Journal of chemical physics

Oyeyemi VB, Krisiloff DB, Keith JA, Libisch F, Pavone M, Carter EA.
PMID: 25669533
J Chem Phys. 2014 Jan 28;140(4):044317. doi: 10.1063/1.4862159.

Oxygenated hydrocarbons play important roles in combustion science as renewable fuels and additives, but many details about their combustion chemistry remain poorly understood. Although many methods exist for computing accurate electronic energies of molecules at equilibrium geometries, a consistent...

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Oyeyemi VB, Krisiloff DB, Keith JA, et al. Size-extensivity-corrected multireference configuration interaction schemes to accurately predict bond dissociation energies of oxygenated hydrocarbons. J Chem Phys. 2014;140(4):044317doi: 10.1063/1.4862159.
Oyeyemi, V. B., Krisiloff, D. B., Keith, J. A., Libisch, F., Pavone, M., & Carter, E. A. (2014). Size-extensivity-corrected multireference configuration interaction schemes to accurately predict bond dissociation energies of oxygenated hydrocarbons. The Journal of chemical physics, 140(4), 044317. https://doi.org/10.1063/1.4862159
Oyeyemi, Victor B, et al. "Size-extensivity-corrected multireference configuration interaction schemes to accurately predict bond dissociation energies of oxygenated hydrocarbons." The Journal of chemical physics vol. 140,4 (2014): 044317. doi: https://doi.org/10.1063/1.4862159
Oyeyemi VB, Krisiloff DB, Keith JA, Libisch F, Pavone M, Carter EA. Size-extensivity-corrected multireference configuration interaction schemes to accurately predict bond dissociation energies of oxygenated hydrocarbons. J Chem Phys. 2014 Jan 28;140(4):044317. doi: 10.1063/1.4862159. PMID: 25669533.
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Quantum Chemical Benchmarking, Validation, and Prediction of Acidity Constants for Substituted Pyridinium Ions and Pyridinyl Radicals.

Journal of chemical theory and computation

Keith JA, Carter EA.
PMID: 26605730
J Chem Theory Comput. 2012 Sep 11;8(9):3187-206. doi: 10.1021/ct300295g. Epub 2012 Aug 23.

Sensibly modeling (photo)electrocatalytic reactions involving proton and electron transfer with computational quantum chemistry requires accurate descriptions of protonated, deprotonated, and radical species in solution. Procedures to do this are generally nontrivial, especially in cases that involve radical anions that...

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Keith JA, Carter EA. Quantum Chemical Benchmarking, Validation, and Prediction of Acidity Constants for Substituted Pyridinium Ions and Pyridinyl Radicals. J Chem Theory Comput. 2012;8(9):3187-206doi: 10.1021/ct300295g.
Keith, J. A., & Carter, E. A. (2012). Quantum Chemical Benchmarking, Validation, and Prediction of Acidity Constants for Substituted Pyridinium Ions and Pyridinyl Radicals. Journal of chemical theory and computation, 8(9), 3187-206. https://doi.org/10.1021/ct300295g
Keith, John A, and Carter, Emily A. "Quantum Chemical Benchmarking, Validation, and Prediction of Acidity Constants for Substituted Pyridinium Ions and Pyridinyl Radicals." Journal of chemical theory and computation vol. 8,9 (2012): 3187-206. doi: https://doi.org/10.1021/ct300295g
Keith JA, Carter EA. Quantum Chemical Benchmarking, Validation, and Prediction of Acidity Constants for Substituted Pyridinium Ions and Pyridinyl Radicals. J Chem Theory Comput. 2012 Sep 11;8(9):3187-206. doi: 10.1021/ct300295g. Epub 2012 Aug 23. PMID: 26605730.
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The leech condo: an innovative approach to containing leeches on a congested flap.

Eplasty

Viviano SL, Hahn E, Lee ES, Keith JD.
PMID: 25987944
Eplasty. 2015 Apr 08;15:ic21. eCollection 2015.

No abstract available.

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Viviano SL, Hahn E, Lee ES, et al. The leech condo: an innovative approach to containing leeches on a congested flap. Eplasty. 2015;15:ic21
Viviano, S. L., Hahn, E., Lee, E. S., & Keith, J. D. (2015). The leech condo: an innovative approach to containing leeches on a congested flap. Eplasty, 15ic21.
Viviano, Stephen L, et al. "The leech condo: an innovative approach to containing leeches on a congested flap." Eplasty vol. 15 (2015): ic21.
Viviano SL, Hahn E, Lee ES, Keith JD. The leech condo: an innovative approach to containing leeches on a congested flap. Eplasty. 2015 Apr 08;15:ic21. eCollection 2015. PMID: 25987944; PMCID: PMC4396404.
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Correction to Impact of Coordination Geometry, Bite Angle, and Trans Influence on Metal-Ligand Covalency in Phenyl-Substituted Phosphine Complexes of Ni and Pd.

Inorganic chemistry

Donahue CM, McCollom SP, Forrest CM, Blake AV, Bellott BJ, Keith JM, Daly SR.
PMID: 26280192
Inorg Chem. 2015 Sep 08;54(17):8857. doi: 10.1021/acs.inorgchem.5b01794. Epub 2015 Aug 17.

No abstract available.

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Donahue CM, McCollom SP, Forrest CM, et al. Correction to Impact of Coordination Geometry, Bite Angle, and Trans Influence on Metal-Ligand Covalency in Phenyl-Substituted Phosphine Complexes of Ni and Pd. Inorg Chem. 2015;54(17):8857doi: 10.1021/acs.inorgchem.5b01794.
Donahue, C. M., McCollom, S. P., Forrest, C. M., Blake, A. V., Bellott, B. J., Keith, J. M., & Daly, S. R. (2015). Correction to Impact of Coordination Geometry, Bite Angle, and Trans Influence on Metal-Ligand Covalency in Phenyl-Substituted Phosphine Complexes of Ni and Pd. Inorganic chemistry, 54(17), 8857. https://doi.org/10.1021/acs.inorgchem.5b01794
Donahue, Courtney M, et al. "Correction to Impact of Coordination Geometry, Bite Angle, and Trans Influence on Metal-Ligand Covalency in Phenyl-Substituted Phosphine Complexes of Ni and Pd." Inorganic chemistry vol. 54,17 (2015): 8857. doi: https://doi.org/10.1021/acs.inorgchem.5b01794
Donahue CM, McCollom SP, Forrest CM, Blake AV, Bellott BJ, Keith JM, Daly SR. Correction to Impact of Coordination Geometry, Bite Angle, and Trans Influence on Metal-Ligand Covalency in Phenyl-Substituted Phosphine Complexes of Ni and Pd. Inorg Chem. 2015 Sep 08;54(17):8857. doi: 10.1021/acs.inorgchem.5b01794. Epub 2015 Aug 17. PMID: 26280192.
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Characteristics of Successful and Probationary Football Officials.

The Physician and sportsmedicine

Spurqeon JH, Blair SV, Keith JA, McGinn CJ.
PMID: 27437749
Phys Sportsmed. 1978 Sep;6(9):106-12. doi: 10.1080/00913847.1978.11710761.

These researchers suggest that safe, enjoyable football games are more likely to occur with successful officials who are more physically fit, less fat, and psychologically different than probationary officials.

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Spurqeon JH, Blair SV, Keith JA, et al. Characteristics of Successful and Probationary Football Officials. Phys Sportsmed. 1978;6(9):106-12doi: 10.1080/00913847.1978.11710761.
Spurqeon, J. H., Blair, S. V., Keith, J. A., & McGinn, C. J. (1978). Characteristics of Successful and Probationary Football Officials. The Physician and sportsmedicine, 6(9), 106-12. https://doi.org/10.1080/00913847.1978.11710761
Spurqeon, J H, et al. "Characteristics of Successful and Probationary Football Officials." The Physician and sportsmedicine vol. 6,9 (1978): 106-12. doi: https://doi.org/10.1080/00913847.1978.11710761
Spurqeon JH, Blair SV, Keith JA, McGinn CJ. Characteristics of Successful and Probationary Football Officials. Phys Sportsmed. 1978 Sep;6(9):106-12. doi: 10.1080/00913847.1978.11710761. PMID: 27437749.
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Erratum to: Sequence Segmentation with changeptGUI.

Methods in molecular biology (Clifton, N.J.)

Tasker E, Keith JM.
PMID: 28220404
Methods Mol Biol. 2017;1525:E1. doi: 10.1007/978-1-4939-6622-6_19.

No abstract available.

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Tasker E, Keith JM. Erratum to: Sequence Segmentation with changeptGUI. Methods Mol Biol. 2017;1525:E1doi: 10.1007/978-1-4939-6622-6_19.
Tasker, E., & Keith, J. M. (2017). Erratum to: Sequence Segmentation with changeptGUI. Methods in molecular biology (Clifton, N.J.), 1525E1. https://doi.org/10.1007/978-1-4939-6622-6_19
Tasker, Edward, and Keith, Jonathan M. "Erratum to: Sequence Segmentation with changeptGUI." Methods in molecular biology (Clifton, N.J.) vol. 1525 (2017): E1. doi: https://doi.org/10.1007/978-1-4939-6622-6_19
Tasker E, Keith JM. Erratum to: Sequence Segmentation with changeptGUI. Methods Mol Biol. 2017;1525:E1. doi: 10.1007/978-1-4939-6622-6_19. PMID: 28220404.
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Preclinical Characterization of the FAAH Inhibitor JNJ-42165279.

ACS medicinal chemistry letters

Keith JM, Jones WM, Tichenor M, Liu J, Seierstad M, Palmer JA, Webb M, Karbarz M, Scott BP, Wilson SJ, Luo L, Wennerholm ML, Chang L, Rizzolio M, Rynberg R, Chaplan SR, Breitenbucher JG.
PMID: 26713105
ACS Med Chem Lett. 2015 Nov 02;6(12):1204-8. doi: 10.1021/acsmedchemlett.5b00353. eCollection 2015 Dec 10.

The pre-clinical characterization of the aryl piperazinyl urea inhibitor of fatty acid amide hydrolase (FAAH) JNJ-42165279 is described. JNJ-42165279 covalently inactivates the FAAH enzyme, but is highly selective with regard to other enzymes, ion channels, transporters, and receptors. JNJ-42165279...

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Keith JM, Jones WM, Tichenor M, et al. Preclinical Characterization of the FAAH Inhibitor JNJ-42165279. ACS Med Chem Lett. 2015;6(12):1204-8doi: 10.1021/acsmedchemlett.5b00353.
Keith, J. M., Jones, W. M., Tichenor, M., Liu, J., Seierstad, M., Palmer, J. A., Webb, M., Karbarz, M., Scott, B. P., Wilson, S. J., Luo, L., Wennerholm, M. L., Chang, L., Rizzolio, M., Rynberg, R., Chaplan, S. R., & Breitenbucher, J. G. (2015). Preclinical Characterization of the FAAH Inhibitor JNJ-42165279. ACS medicinal chemistry letters, 6(12), 1204-8. https://doi.org/10.1021/acsmedchemlett.5b00353
Keith, John M, et al. "Preclinical Characterization of the FAAH Inhibitor JNJ-42165279." ACS medicinal chemistry letters vol. 6,12 (2015): 1204-8. doi: https://doi.org/10.1021/acsmedchemlett.5b00353
Keith JM, Jones WM, Tichenor M, Liu J, Seierstad M, Palmer JA, Webb M, Karbarz M, Scott BP, Wilson SJ, Luo L, Wennerholm ML, Chang L, Rizzolio M, Rynberg R, Chaplan SR, Breitenbucher JG. Preclinical Characterization of the FAAH Inhibitor JNJ-42165279. ACS Med Chem Lett. 2015 Nov 02;6(12):1204-8. doi: 10.1021/acsmedchemlett.5b00353. eCollection 2015 Dec 10. PMID: 26713105; PMCID: PMC4677372.
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Aims, applications and achievements. An introductory essay.

FEBS letters

Reich JG.
PMID: 11946357
FEBS Lett. 1969 Mar;2:S3-S8. doi: 10.1016/0014-5793(69)80069-4.

No abstract available.

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Reich JG. Aims, applications and achievements. An introductory essay. FEBS Lett. 1969;2:S3-S8doi: 10.1016/0014-5793(69)80069-4.
Reich, J. G. (1969). Aims, applications and achievements. An introductory essay. FEBS letters, 2S3-S8. https://doi.org/10.1016/0014-5793(69)80069-4
Reich, J G.. "Aims, applications and achievements. An introductory essay." FEBS letters vol. 2 (1969): S3-S8. doi: https://doi.org/10.1016/0014-5793(69)80069-4
Reich JG. Aims, applications and achievements. An introductory essay. FEBS Lett. 1969 Mar;2:S3-S8. doi: 10.1016/0014-5793(69)80069-4. PMID: 11946357.
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A Stereospecific, Intermolecular Biaryl-Coupling Approach to Korupensamine A En Route to the Michellamines.

Angewandte Chemie (International ed. in English)

Lipshutz BH, Keith JM.
PMID: 10602232
Angew Chem Int Ed Engl. 1999 Dec 03;38(23):3530-3533.

By what means and how well can axial chirality be controlled in an intermolecular Suzuki biaryl cross-coupling reaction? The directionality of reductive elimination [Eq. (1)] is completely controlled by using a strategically positioned internal ligand L to afford a...

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Lipshutz BH, Keith JM. A Stereospecific, Intermolecular Biaryl-Coupling Approach to Korupensamine A En Route to the Michellamines. Angew Chem Int Ed Engl. 1999;38(23):3530-3533
Lipshutz, B. H., & Keith, J. M. (1999). A Stereospecific, Intermolecular Biaryl-Coupling Approach to Korupensamine A En Route to the Michellamines. Angewandte Chemie (International ed. in English), 38(23), 3530-3533.
Lipshutz, and Keith. "A Stereospecific, Intermolecular Biaryl-Coupling Approach to Korupensamine A En Route to the Michellamines." Angewandte Chemie (International ed. in English) vol. 38,23 (1999): 3530-3533.
Lipshutz BH, Keith JM. A Stereospecific, Intermolecular Biaryl-Coupling Approach to Korupensamine A En Route to the Michellamines. Angew Chem Int Ed Engl. 1999 Dec 03;38(23):3530-3533. PMID: 10602232.
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Parameter estimation and enzyme kinetic models.

FEBS letters

Reich JG.
PMID: 11947682
FEBS Lett. 1970 Aug 31;9(5):245-251. doi: 10.1016/0014-5793(70)80367-2.

No abstract available.

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Reich JG. Parameter estimation and enzyme kinetic models. FEBS Lett. 1970;9(5):245-251doi: 10.1016/0014-5793(70)80367-2.
Reich, J. G. (1970). Parameter estimation and enzyme kinetic models. FEBS letters, 9(5), 245-251. https://doi.org/10.1016/0014-5793(70)80367-2
Reich, J G.. "Parameter estimation and enzyme kinetic models." FEBS letters vol. 9,5 (1970): 245-251. doi: https://doi.org/10.1016/0014-5793(70)80367-2
Reich JG. Parameter estimation and enzyme kinetic models. FEBS Lett. 1970 Aug 31;9(5):245-251. doi: 10.1016/0014-5793(70)80367-2. PMID: 11947682.
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Ischemic stroke and n-3 fatty acids.

Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association

Seidelin KN, Jensen B, Haugaard SB, Reith J, Olsen TS.
PMID: 17895042
J Stroke Cerebrovasc Dis. 1997 Oct-Nov;6(6):405-9. doi: 10.1016/s1052-3057(97)80042-0.

The content of fatty acids in subcutaneous adipose tissue was measured to determine whether differences of fatty acids correlate with presence or absence of cerebral infarction in individual patients. Adipose tissue microbiopsies was sampled from 10 patients with computed...

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Seidelin KN, Jensen B, Haugaard SB, et al. Ischemic stroke and n-3 fatty acids. J Stroke Cerebrovasc Dis. 1997;6(6):405-9doi: 10.1016/s1052-3057(97)80042-0.
Seidelin, K. N., Jensen, B., Haugaard, S. B., Reith, J., & Olsen, T. S. (1997). Ischemic stroke and n-3 fatty acids. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association, 6(6), 405-9. https://doi.org/10.1016/s1052-3057(97)80042-0
Seidelin, K N, et al. "Ischemic stroke and n-3 fatty acids." Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association vol. 6,6 (1997): 405-9. doi: https://doi.org/10.1016/s1052-3057(97)80042-0
Seidelin KN, Jensen B, Haugaard SB, Reith J, Olsen TS. Ischemic stroke and n-3 fatty acids. J Stroke Cerebrovasc Dis. 1997 Oct-Nov;6(6):405-9. doi: 10.1016/s1052-3057(97)80042-0. PMID: 17895042.
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Showing 1 to 12 of 193 entries