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[Health pedagogy].

Ugeskrift for laeger

Jørgensen K, Schnack K.
PMID: 483402
Ugeskr Laeger. 1979 Aug 13;141(33):2275-6.

No abstract available.

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Jørgensen K, Schnack K. Sundhedspaedagogik. [Health pedagogy]. Ugeskr Laeger. 1979;141(33):2275-6
Jørgensen, K., & Schnack, K. (1979). Sundhedspaedagogik. [Health pedagogy]. Ugeskrift for laeger, 141(33), 2275-6.
Jørgensen, K, and Schnack, K. "Sundhedspaedagogik." [Health pedagogy]. Ugeskrift for laeger vol. 141,33 (1979): 2275-6.
Jørgensen K, Schnack K. Sundhedspaedagogik. [Health pedagogy]. Ugeskr Laeger. 1979 Aug 13;141(33):2275-6. Danish. PMID: 483402.
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Asymmetric formation of bridged benzoxazocines through an organocatalytic multicomponent dienamine-mediated one-pot cascade.

Organic letters

Ransborg LK, Overgaard M, Hejmanowska J, Barfüsser S, Jørgensen KA, Albrecht Ł.
PMID: 25084456
Org Lett. 2014 Aug 15;16(16):4182-5. doi: 10.1021/ol501882x. Epub 2014 Aug 01.

An organocatalytic one-pot cascade leading to the stereoselective formation of novel bridged benzoxazocines is presented. The developed methodology is based on the first example of a γ-selective-Mannich-initiated cascade reaction and allows for direct annulation of the bridged benzoxazocines by...

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Ransborg LK, Overgaard M, Hejmanowska J, et al. Asymmetric formation of bridged benzoxazocines through an organocatalytic multicomponent dienamine-mediated one-pot cascade. Org Lett. 2014;16(16):4182-5doi: 10.1021/ol501882x.
Ransborg, L. K., Overgaard, M., Hejmanowska, J., Barfüsser, S., Jørgensen, K. A., & Albrecht, �. �. (2014). Asymmetric formation of bridged benzoxazocines through an organocatalytic multicomponent dienamine-mediated one-pot cascade. Organic letters, 16(16), 4182-5. https://doi.org/10.1021/ol501882x
Ransborg, Lars Krogager, et al. "Asymmetric formation of bridged benzoxazocines through an organocatalytic multicomponent dienamine-mediated one-pot cascade." Organic letters vol. 16,16 (2014): 4182-5. doi: https://doi.org/10.1021/ol501882x
Ransborg LK, Overgaard M, Hejmanowska J, Barfüsser S, Jørgensen KA, Albrecht Ł. Asymmetric formation of bridged benzoxazocines through an organocatalytic multicomponent dienamine-mediated one-pot cascade. Org Lett. 2014 Aug 15;16(16):4182-5. doi: 10.1021/ol501882x. Epub 2014 Aug 01. PMID: 25084456.
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Objectively measured physical activity level and sedentary behavior in Norwegian children during a week in preschool.

Preventive medicine reports

Andersen E, Borch-Jenssen J, Øvreås S, Ellingsen H, Jørgensen KA, Moser T.
PMID: 28660120
Prev Med Rep. 2017 Jun 09;7:130-135. doi: 10.1016/j.pmedr.2017.06.003. eCollection 2017 Sep.

Although many studies have reported on physical activity (PA) levels using accelerometers, a thorough description of the PA pattern in preschool children during their stay in the preschool, is lacking in the current literature. Furthermore, there remains a lack...

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Andersen E, Borch-Jenssen J, Øvreås S, et al. Objectively measured physical activity level and sedentary behavior in Norwegian children during a week in preschool. Prev Med Rep. 2017;7:130-135doi: 10.1016/j.pmedr.2017.06.003.
Andersen, E., Borch-Jenssen, J., Øvreås, S., Ellingsen, H., Jørgensen, K. A., & Moser, T. (2017). Objectively measured physical activity level and sedentary behavior in Norwegian children during a week in preschool. Preventive medicine reports, 7130-135. https://doi.org/10.1016/j.pmedr.2017.06.003
Andersen, Eivind, et al. "Objectively measured physical activity level and sedentary behavior in Norwegian children during a week in preschool." Preventive medicine reports vol. 7 (2017): 130-135. doi: https://doi.org/10.1016/j.pmedr.2017.06.003
Andersen E, Borch-Jenssen J, Øvreås S, Ellingsen H, Jørgensen KA, Moser T. Objectively measured physical activity level and sedentary behavior in Norwegian children during a week in preschool. Prev Med Rep. 2017 Jun 09;7:130-135. doi: 10.1016/j.pmedr.2017.06.003. eCollection 2017 Sep. PMID: 28660120; PMCID: PMC5479964.
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Model selection for Gaussian kernel PCA denoising.

IEEE transactions on neural networks and learning systems

Jørgensen KW, Hansen LK.
PMID: 24808465
IEEE Trans Neural Netw Learn Syst. 2012 Jan;23(1):163-8. doi: 10.1109/TNNLS.2011.2178325.

We propose kernel parallel analysis (kPA) for automatic kernel scale and model order selection in Gaussian kernel principal component analysis (KPCA). Parallel analysis is based on a permutation test for covariance and has previously been applied for model order...

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Jørgensen KW, Hansen LK. Model selection for Gaussian kernel PCA denoising. IEEE Trans Neural Netw Learn Syst. 2012;23(1):163-8doi: 10.1109/TNNLS.2011.2178325.
Jørgensen, K. W., & Hansen, L. K. (2012). Model selection for Gaussian kernel PCA denoising. IEEE transactions on neural networks and learning systems, 23(1), 163-8. https://doi.org/10.1109/TNNLS.2011.2178325
Jørgensen, Kasper Winther, and Hansen, Lars Kai. "Model selection for Gaussian kernel PCA denoising." IEEE transactions on neural networks and learning systems vol. 23,1 (2012): 163-8. doi: https://doi.org/10.1109/TNNLS.2011.2178325
Jørgensen KW, Hansen LK. Model selection for Gaussian kernel PCA denoising. IEEE Trans Neural Netw Learn Syst. 2012 Jan;23(1):163-8. doi: 10.1109/TNNLS.2011.2178325. PMID: 24808465.
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Enantioselective Formal [4+2] Cycloadditions to 3-Nitroindoles by Trienamine Catalysis: Synthesis of Chiral Dihydrocarbazoles.

Angewandte Chemie (International ed. in English)

Li Y, Tur F, Nielsen RP, Jiang H, Jensen F, Jørgensen KA.
PMID: 26636665
Angew Chem Int Ed Engl. 2016 Jan 18;55(3):1020-4. doi: 10.1002/anie.201509693. Epub 2015 Dec 04.

The first enantioselective formal [4+2] cycloadditions of 3-nitroindoles are presented. By using 3-nitroindoles in combination with an organocatalyst, chiral dihydrocarbazole scaffolds are formed in moderate to good yields (up to 87%) and enantioselectivities (up to 97% ee). The reaction...

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Li Y, Tur F, Nielsen RP, et al. Enantioselective Formal [4+2] Cycloadditions to 3-Nitroindoles by Trienamine Catalysis: Synthesis of Chiral Dihydrocarbazoles. Angew Chem Int Ed Engl. 2015;55(3):1020-4doi: 10.1002/anie.201509693.
Li, Y., Tur, F., Nielsen, R. P., Jiang, H., Jensen, F., & Jørgensen, K. A. (2016). Enantioselective Formal [4+2] Cycloadditions to 3-Nitroindoles by Trienamine Catalysis: Synthesis of Chiral Dihydrocarbazoles. Angewandte Chemie (International ed. in English), 55(3), 1020-4. https://doi.org/10.1002/anie.201509693
Li, Yang, et al. "Enantioselective Formal [4+2] Cycloadditions to 3-Nitroindoles by Trienamine Catalysis: Synthesis of Chiral Dihydrocarbazoles." Angewandte Chemie (International ed. in English) vol. 55,3 (2016): 1020-4. doi: https://doi.org/10.1002/anie.201509693
Li Y, Tur F, Nielsen RP, Jiang H, Jensen F, Jørgensen KA. Enantioselective Formal [4+2] Cycloadditions to 3-Nitroindoles by Trienamine Catalysis: Synthesis of Chiral Dihydrocarbazoles. Angew Chem Int Ed Engl. 2016 Jan 18;55(3):1020-4. doi: 10.1002/anie.201509693. Epub 2015 Dec 04. PMID: 26636665.
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Mechanistic Insights into the Mode of Action of Bifunctional Pyrrolidine-Squaramide-Derived Organocatalysts.

Chemistry (Weinheim an der Bergstrasse, Germany)

Roca-López D, Uria U, Reyes E, Carrillo L, Jørgensen KA, Vicario JL, Merino P.
PMID: 26612630
Chemistry. 2016 Jan 18;22(3):884-9. doi: 10.1002/chem.201504705. Epub 2015 Dec 11.

The catalytic modes of action of three squaramide-derived bifunctional organocatalysts have been investigated using DFT methods. The [5+2] cycloaddition between oxidopyrylium ylides and enals was used as the model reaction. Two primary modes were possible for the different catalysts...

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Roca-López D, Uria U, Reyes E, et al. Mechanistic Insights into the Mode of Action of Bifunctional Pyrrolidine-Squaramide-Derived Organocatalysts. Chemistry. 2015;22(3):884-9doi: 10.1002/chem.201504705.
Roca-López, D., Uria, U., Reyes, E., Carrillo, L., Jørgensen, K. A., Vicario, J. L., & Merino, P. (2016). Mechanistic Insights into the Mode of Action of Bifunctional Pyrrolidine-Squaramide-Derived Organocatalysts. Chemistry (Weinheim an der Bergstrasse, Germany), 22(3), 884-9. https://doi.org/10.1002/chem.201504705
Roca-López, David, et al. "Mechanistic Insights into the Mode of Action of Bifunctional Pyrrolidine-Squaramide-Derived Organocatalysts." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 22,3 (2016): 884-9. doi: https://doi.org/10.1002/chem.201504705
Roca-López D, Uria U, Reyes E, Carrillo L, Jørgensen KA, Vicario JL, Merino P. Mechanistic Insights into the Mode of Action of Bifunctional Pyrrolidine-Squaramide-Derived Organocatalysts. Chemistry. 2016 Jan 18;22(3):884-9. doi: 10.1002/chem.201504705. Epub 2015 Dec 11. PMID: 26612630.
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Evaluation of Muscle microRNA Expression in Relation to Human Peripheral Insulin Sensitivity: A Cross-Sectional Study in Metabolically Distinct Subject Groups.

Frontiers in physiology

Dahlmans D, Houzelle A, Jörgensen JA, Phielix E, Lindeboom L, Hesselink MKC, Schrauwen P, Hoeks J.
PMID: 28983252
Front Physiol. 2017 Sep 21;8:711. doi: 10.3389/fphys.2017.00711. eCollection 2017.

In recent years, several microRNAs (miRNAs)-post-transcriptional regulators of gene expression-have been linked to the regulation of peripheral insulin sensitivity. Many of these studies, however, have been conducted in cell or animal models and the few human studies available lack...

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Dahlmans D, Houzelle A, Jörgensen JA, et al. Evaluation of Muscle microRNA Expression in Relation to Human Peripheral Insulin Sensitivity: A Cross-Sectional Study in Metabolically Distinct Subject Groups. Front Physiol. 2017;8:711doi: 10.3389/fphys.2017.00711.
Dahlmans, D., Houzelle, A., Jörgensen, J. A., Phielix, E., Lindeboom, L., Hesselink, M. K. C., Schrauwen, P., & Hoeks, J. (2017). Evaluation of Muscle microRNA Expression in Relation to Human Peripheral Insulin Sensitivity: A Cross-Sectional Study in Metabolically Distinct Subject Groups. Frontiers in physiology, 8711. https://doi.org/10.3389/fphys.2017.00711
Dahlmans, Dennis, et al. "Evaluation of Muscle microRNA Expression in Relation to Human Peripheral Insulin Sensitivity: A Cross-Sectional Study in Metabolically Distinct Subject Groups." Frontiers in physiology vol. 8 (2017): 711. doi: https://doi.org/10.3389/fphys.2017.00711
Dahlmans D, Houzelle A, Jörgensen JA, Phielix E, Lindeboom L, Hesselink MKC, Schrauwen P, Hoeks J. Evaluation of Muscle microRNA Expression in Relation to Human Peripheral Insulin Sensitivity: A Cross-Sectional Study in Metabolically Distinct Subject Groups. Front Physiol. 2017 Sep 21;8:711. doi: 10.3389/fphys.2017.00711. eCollection 2017. PMID: 28983252; PMCID: PMC5613141.
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Organocatalytic stereoselective [8+2] and [6+4] cycloadditions.

Nature chemistry

Mose R, Preegel G, Larsen J, Jakobsen S, Iversen EH, Jørgensen KA.
PMID: 28430196
Nat Chem. 2017 May;9(5):487-492. doi: 10.1038/nchem.2682. Epub 2016 Dec 19.

Cycloadditions that involve more than six π electrons are termed higher-order cycloadditions and are an excellent tool for solving complex synthetic challenges, as they provide direct access to polycyclic scaffolds that contain medium-sized rings. They have interesting synthetic potential...

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Mose R, Preegel G, Larsen J, et al. Organocatalytic stereoselective [8+2] and [6+4] cycloadditions. Nat Chem. 2016;9(5):487-492doi: 10.1038/nchem.2682.
Mose, R., Preegel, G., Larsen, J., Jakobsen, S., Iversen, E. H., & Jørgensen, K. A. (2017). Organocatalytic stereoselective [8+2] and [6+4] cycloadditions. Nature chemistry, 9(5), 487-492. https://doi.org/10.1038/nchem.2682
Mose, Rasmus, et al. "Organocatalytic stereoselective [8+2] and [6+4] cycloadditions." Nature chemistry vol. 9,5 (2017): 487-492. doi: https://doi.org/10.1038/nchem.2682
Mose R, Preegel G, Larsen J, Jakobsen S, Iversen EH, Jørgensen KA. Organocatalytic stereoselective [8+2] and [6+4] cycloadditions. Nat Chem. 2017 May;9(5):487-492. doi: 10.1038/nchem.2682. Epub 2016 Dec 19. PMID: 28430196.
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The stereoselective formation of highly substituted CF3-dihydropyrans as versatile building blocks.

Chemical communications (Cambridge, England)

Donslund BS, Monleón A, Larsen J, Ibsen L, Jørgensen KA.
PMID: 26225818
Chem Commun (Camb). 2015 Sep 14;51(71):13666-9. doi: 10.1039/c5cc04874e.

The highly enantioselective dienamine-mediated formation of 5-bromo-6-(trifluoromethyl)-3,4-dihydro-2H-pyrans from α,β-unsaturated aldehydes and α-bromo-(trifluoromethyl)-enones employing a C2-symmetric aminocatalyst is described. The products are demonstrated to be applicable in coupling reactions directly onto the ring, thereby granting access to a broad scope...

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Donslund BS, Monleón A, Larsen J, et al. The stereoselective formation of highly substituted CF3-dihydropyrans as versatile building blocks. Chem Commun (Camb). 2015;51(71):13666-9doi: 10.1039/c5cc04874e.
Donslund, B. S., Monleón, A., Larsen, J., Ibsen, L., & Jørgensen, K. A. (2015). The stereoselective formation of highly substituted CF3-dihydropyrans as versatile building blocks. Chemical communications (Cambridge, England), 51(71), 13666-9. https://doi.org/10.1039/c5cc04874e
Donslund, Bjarke S, et al. "The stereoselective formation of highly substituted CF3-dihydropyrans as versatile building blocks." Chemical communications (Cambridge, England) vol. 51,71 (2015): 13666-9. doi: https://doi.org/10.1039/c5cc04874e
Donslund BS, Monleón A, Larsen J, Ibsen L, Jørgensen KA. The stereoselective formation of highly substituted CF3-dihydropyrans as versatile building blocks. Chem Commun (Camb). 2015 Sep 14;51(71):13666-9. doi: 10.1039/c5cc04874e. PMID: 26225818.
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Asymmetric Brønsted Base Catalyzed and Directed [3+2] Cycloaddition of 2-Acyl Cycloheptatrienes with Azomethine Ylides.

Chemistry (Weinheim an der Bergstrasse, Germany)

Lauridsen VH, Ibsen L, Blom J, Jørgensen KA.
PMID: 26807826
Chemistry. 2016 Mar 01;22(10):3259-3263. doi: 10.1002/chem.201600255. Epub 2016 Feb 02.

Conjugated cyclic trienes have the potential for different types of cycloaddition reactions. In the present work, we will, in a novel asymmetric cycloaddition reaction, demonstrate that the organocatalytic reaction of 2-acyl cycloheptatrienes with azomethine ylides proceeds as a [3+2]...

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Lauridsen VH, Ibsen L, Blom J, et al. Asymmetric Brønsted Base Catalyzed and Directed [3+2] Cycloaddition of 2-Acyl Cycloheptatrienes with Azomethine Ylides. Chemistry. 2016;22(10):3259-3263doi: 10.1002/chem.201600255.
Lauridsen, V. H., Ibsen, L., Blom, J., & Jørgensen, K. A. (2016). Asymmetric Brønsted Base Catalyzed and Directed [3+2] Cycloaddition of 2-Acyl Cycloheptatrienes with Azomethine Ylides. Chemistry (Weinheim an der Bergstrasse, Germany), 22(10), 3259-3263. https://doi.org/10.1002/chem.201600255
Lauridsen, Vibeke H, et al. "Asymmetric Brønsted Base Catalyzed and Directed [3+2] Cycloaddition of 2-Acyl Cycloheptatrienes with Azomethine Ylides." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 22,10 (2016): 3259-3263. doi: https://doi.org/10.1002/chem.201600255
Lauridsen VH, Ibsen L, Blom J, Jørgensen KA. Asymmetric Brønsted Base Catalyzed and Directed [3+2] Cycloaddition of 2-Acyl Cycloheptatrienes with Azomethine Ylides. Chemistry. 2016 Mar 01;22(10):3259-3263. doi: 10.1002/chem.201600255. Epub 2016 Feb 02. PMID: 26807826.
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Formal Asymmetric α-Alkenylation of Aldehydes and the Synthetic Application toward Forming α-exo-Methylene-γ-butyrolactones and Skipped Dienes.

Organic letters

Li Y, Ibsen L, Jørgensen KA.
PMID: 28230372
Org Lett. 2017 Mar 03;19(5):1200-1203. doi: 10.1021/acs.orglett.7b00254. Epub 2017 Feb 23.

A formal asymmetric α-alkenylation of aldehydes is reported based on the organocatalytic reaction of aldehydes with nitroacrylates. The reaction proceeds in a one-pot manner forming the products with up to 77% yield and up to >99% ee. This strategy...

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Li Y, Ibsen L, Jørgensen KA. Formal Asymmetric α-Alkenylation of Aldehydes and the Synthetic Application toward Forming α-exo-Methylene-γ-butyrolactones and Skipped Dienes. Org Lett. 2017;19(5):1200-1203doi: 10.1021/acs.orglett.7b00254.
Li, Y., Ibsen, L., & Jørgensen, K. A. (2017). Formal Asymmetric α-Alkenylation of Aldehydes and the Synthetic Application toward Forming α-exo-Methylene-γ-butyrolactones and Skipped Dienes. Organic letters, 19(5), 1200-1203. https://doi.org/10.1021/acs.orglett.7b00254
Li, Yang, et al. "Formal Asymmetric α-Alkenylation of Aldehydes and the Synthetic Application toward Forming α-exo-Methylene-γ-butyrolactones and Skipped Dienes." Organic letters vol. 19,5 (2017): 1200-1203. doi: https://doi.org/10.1021/acs.orglett.7b00254
Li Y, Ibsen L, Jørgensen KA. Formal Asymmetric α-Alkenylation of Aldehydes and the Synthetic Application toward Forming α-exo-Methylene-γ-butyrolactones and Skipped Dienes. Org Lett. 2017 Mar 03;19(5):1200-1203. doi: 10.1021/acs.orglett.7b00254. Epub 2017 Feb 23. PMID: 28230372.
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Phytochrome control of RNA levels in developing pea and mung-bean leaves.

Planta

Thompson WF, Everett M, Polans NO, Jorgensen RA, Palmer JD.
PMID: 24264922
Planta. 1983 Aug;158(6):487-500. doi: 10.1007/BF00397240.

We have examined phytochrome effects on the abundance of transcripts from several nuclear and chloroplast genes in buds of dark-grown pea seedlings and primary leaves of dark-grown mung-bean seedlings. Probes for nuclear-coded RNAs were selected from a library of...

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Thompson WF, Everett M, Polans NO, et al. Phytochrome control of RNA levels in developing pea and mung-bean leaves. Planta. 1983;158(6):487-500doi: 10.1007/BF00397240.
Thompson, W. F., Everett, M., Polans, N. O., Jorgensen, R. A., & Palmer, J. D. (1983). Phytochrome control of RNA levels in developing pea and mung-bean leaves. Planta, 158(6), 487-500. https://doi.org/10.1007/BF00397240
Thompson, W F, et al. "Phytochrome control of RNA levels in developing pea and mung-bean leaves." Planta vol. 158,6 (1983): 487-500. doi: https://doi.org/10.1007/BF00397240
Thompson WF, Everett M, Polans NO, Jorgensen RA, Palmer JD. Phytochrome control of RNA levels in developing pea and mung-bean leaves. Planta. 1983 Aug;158(6):487-500. doi: 10.1007/BF00397240. PMID: 24264922.
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Showing 1 to 12 of 360 entries