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Mobile apps for reflection in learning: A design research in K‐12 education

k-12

Leinonen T, Keune A, Veermans M.
GSID: -myJah4Mc38J
T Leinonen, A Keune, M Veermans… - British Journal of …, 2016 - Wiley Online Library

… In this study, we focus on mobile applications that were specifically designed for use in K-12 school and classroom learning. The motivation behind the research is the increasing interest to use mobile devices in classrooms and the apps'...

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Leinonen, T., Keune, A., Veermans, M., & Toikkanen, T. (2016). Mobile apps for reflection in learning: A design research in K‐12 education. British Journal of Educational Technology, 47(1), 184-202.
Leinonen, Teemu, et al. "Mobile apps for reflection in learning: A design research in K‐12 education." British Journal of Educational Technology 47.1 (2016): 184-202.
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Draft Genome Sequences of Eight Obligate Methane Oxidizers Occupying Distinct Niches Based on Their Nitrogen Metabolism.

Genome announcements

Heylen K, De Vos P, Vekeman B.
PMID: 27491982
Genome Announc. 2016 Aug 04;4(4). doi: 10.1128/genomeA.00421-16.

The genome sequences of Methylomonas methanica (NCIMB 11130(T), R-45363, and R-45371), Methylomonas koyamae (R-45378, R-45383, and R-49807), Methylomonas lenta (R-45370), and Methylosinus sp. (R-45379) were obtained. These aerobic methanotrophs were isolated from terrestrial ecosystems, and their distinct phenotypes related...

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Heylen K, De Vos P, Vekeman B. Draft Genome Sequences of Eight Obligate Methane Oxidizers Occupying Distinct Niches Based on Their Nitrogen Metabolism. Genome Announc. 2016;4(4)doi: 10.1128/genomeA.00421-16.
Heylen, K., De Vos, P., & Vekeman, B. (2016). Draft Genome Sequences of Eight Obligate Methane Oxidizers Occupying Distinct Niches Based on Their Nitrogen Metabolism. Genome announcements, 4(4), . https://doi.org/10.1128/genomeA.00421-16
Heylen, Kim, et al. "Draft Genome Sequences of Eight Obligate Methane Oxidizers Occupying Distinct Niches Based on Their Nitrogen Metabolism." Genome announcements vol. 4,4 (2016). doi: https://doi.org/10.1128/genomeA.00421-16
Heylen K, De Vos P, Vekeman B. Draft Genome Sequences of Eight Obligate Methane Oxidizers Occupying Distinct Niches Based on Their Nitrogen Metabolism. Genome Announc. 2016 Aug 04;4(4). doi: 10.1128/genomeA.00421-16. PMID: 27491982; PMCID: PMC4974303.
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Controlling for genetic identity of varieties, pollen contamination and stigma receptivity is essential to characterize the self-incompatibility system of .

Evolutionary applications

Saumitou-Laprade P, Vernet P, Vekemans X, Castric V, Barcaccia G, Khadari B, Baldoni L.
PMID: 29151877
Evol Appl. 2017 Jun 29;10(9):860-866. doi: 10.1111/eva.12498. eCollection 2017 Oct.

Bervillé et al. express concern about the existence of the diallelic self-incompatibility (DSI) system in

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Saumitou-Laprade P, Vernet P, Vekemans X, et al. Controlling for genetic identity of varieties, pollen contamination and stigma receptivity is essential to characterize the self-incompatibility system of . Evol Appl. 2017;10(9):860-866doi: 10.1111/eva.12498.
Saumitou-Laprade, P., Vernet, P., Vekemans, X., Castric, V., Barcaccia, G., Khadari, B., & Baldoni, L. (2017). Controlling for genetic identity of varieties, pollen contamination and stigma receptivity is essential to characterize the self-incompatibility system of . Evolutionary applications, 10(9), 860-866. https://doi.org/10.1111/eva.12498
Saumitou-Laprade, Pierre, et al. "Controlling for genetic identity of varieties, pollen contamination and stigma receptivity is essential to characterize the self-incompatibility system of ." Evolutionary applications vol. 10,9 (2017): 860-866. doi: https://doi.org/10.1111/eva.12498
Saumitou-Laprade P, Vernet P, Vekemans X, Castric V, Barcaccia G, Khadari B, Baldoni L. Controlling for genetic identity of varieties, pollen contamination and stigma receptivity is essential to characterize the self-incompatibility system of . Evol Appl. 2017 Jun 29;10(9):860-866. doi: 10.1111/eva.12498. eCollection 2017 Oct. PMID: 29151877; PMCID: PMC5680419.
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Elucidation of the genetic architecture of self-incompatibility in olive: Evolutionary consequences and perspectives for orchard management.

Evolutionary applications

Saumitou-Laprade P, Vernet P, Vekemans X, Billiard S, Gallina S, Essalouh L, Mhaïs A, Moukhli A, El Bakkali A, Barcaccia G, Alagna F, Mariotti R, Cultrera NGM, Pandolfi S, Rossi M, Khadari B, Baldoni L.
PMID: 29151878
Evol Appl. 2017 May 20;10(9):867-880. doi: 10.1111/eva.12457. eCollection 2017 Oct.

The olive (

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Saumitou-Laprade P, Vernet P, Vekemans X, et al. Elucidation of the genetic architecture of self-incompatibility in olive: Evolutionary consequences and perspectives for orchard management. Evol Appl. 2017;10(9):867-880doi: 10.1111/eva.12457.
Saumitou-Laprade, P., Vernet, P., Vekemans, X., Billiard, S., Gallina, S., Essalouh, L., Mhaïs, A., Moukhli, A., El Bakkali, A., Barcaccia, G., Alagna, F., Mariotti, R., Cultrera, N. G. M., Pandolfi, S., Rossi, M., Khadari, B., & Baldoni, L. (2017). Elucidation of the genetic architecture of self-incompatibility in olive: Evolutionary consequences and perspectives for orchard management. Evolutionary applications, 10(9), 867-880. https://doi.org/10.1111/eva.12457
Saumitou-Laprade, Pierre, et al. "Elucidation of the genetic architecture of self-incompatibility in olive: Evolutionary consequences and perspectives for orchard management." Evolutionary applications vol. 10,9 (2017): 867-880. doi: https://doi.org/10.1111/eva.12457
Saumitou-Laprade P, Vernet P, Vekemans X, Billiard S, Gallina S, Essalouh L, Mhaïs A, Moukhli A, El Bakkali A, Barcaccia G, Alagna F, Mariotti R, Cultrera NGM, Pandolfi S, Rossi M, Khadari B, Baldoni L. Elucidation of the genetic architecture of self-incompatibility in olive: Evolutionary consequences and perspectives for orchard management. Evol Appl. 2017 May 20;10(9):867-880. doi: 10.1111/eva.12457. eCollection 2017 Oct. PMID: 29151878; PMCID: PMC5680433.
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Cosmology: A giant in the young Universe.

Nature

Venemans B.
PMID: 25719662
Nature. 2015 Feb 26;518(7540):490-1. doi: 10.1038/518490b.

No abstract available.

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Venemans B. Cosmology: A giant in the young Universe. Nature. 2015;518(7540):490-1doi: 10.1038/518490b.
Venemans, B. (2015). Cosmology: A giant in the young Universe. Nature, 518(7540), 490-1. https://doi.org/10.1038/518490b
Venemans, Bram. "Cosmology: A giant in the young Universe." Nature vol. 518,7540 (2015): 490-1. doi: https://doi.org/10.1038/518490b
Venemans B. Cosmology: A giant in the young Universe. Nature. 2015 Feb 26;518(7540):490-1. doi: 10.1038/518490b. PMID: 25719662.
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Hydrogen-Bonded Complexes of Diaminopyridines and Diaminotriazines: Opposite Effect of Acylation on Complex Stabilities.

The Journal of organic chemistry

Beijer FH, Sijbesma RP, Vekemans JA, Meijer EW, Kooijman H, Spek AL.
PMID: 11667479
J Org Chem. 1996 Sep 06;61(18):6371-6380. doi: 10.1021/jo960612v.

The association behavior of several 2,4-diamino-s-triazines, 2,6-diaminopyridines, and their acylated derivatives with uracil derivatives was studied. In solution (1)H-NMR and IR spectroscopy were used, and in the solid state as (co)crystals X-ray diffraction was used. Acylation of 2,6-diaminopyridine leads...

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Beijer FH, Sijbesma RP, Vekemans JA, et al. Hydrogen-Bonded Complexes of Diaminopyridines and Diaminotriazines: Opposite Effect of Acylation on Complex Stabilities. J Org Chem. 1996;61(18):6371-6380doi: 10.1021/jo960612v.
Beijer, F. H., Sijbesma, R. P., Vekemans, J. A., Meijer, E. W., Kooijman, H., & Spek, A. L. (1996). Hydrogen-Bonded Complexes of Diaminopyridines and Diaminotriazines: Opposite Effect of Acylation on Complex Stabilities. The Journal of organic chemistry, 61(18), 6371-6380. https://doi.org/10.1021/jo960612v
Beijer, Felix H., et al. "Hydrogen-Bonded Complexes of Diaminopyridines and Diaminotriazines: Opposite Effect of Acylation on Complex Stabilities." The Journal of organic chemistry vol. 61,18 (1996): 6371-6380. doi: https://doi.org/10.1021/jo960612v
Beijer FH, Sijbesma RP, Vekemans JA, Meijer EW, Kooijman H, Spek AL. Hydrogen-Bonded Complexes of Diaminopyridines and Diaminotriazines: Opposite Effect of Acylation on Complex Stabilities. J Org Chem. 1996 Sep 06;61(18):6371-6380. doi: 10.1021/jo960612v. PMID: 11667479.
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Ladderlike oligomers; intramolecular hydrogen bonding, push-pull character, and electron affinity.

Chemistry (Weinheim an der Bergstrasse, Germany)

Pieterse K, Vekemans JA, Kooijman H, Spek AL, Meijer EW.
PMID: 11192093
Chemistry. 2000 Dec 15;6(24):4597-603. doi: 10.1002/1521-3765(20001215)6:24<4597::aid-chem4597>3.0.co;2-4.

Symmetrical 2,5-bis(2-aminophenyl)pyrazines have been synthesized by application of the Stille coupling strategy. These cotrimers feature three important properties, namely strong intramolecular hydrogen bonding, push-pull character, and high electron affinity. The presence of intramolecular hydrogen bonds has been confirmed by...

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Pieterse K, Vekemans JA, Kooijman H, et al. Ladderlike oligomers; intramolecular hydrogen bonding, push-pull character, and electron affinity. Chemistry. 2000;6(24):4597-603doi: 10.1002/1521-3765(20001215)6:24<4597::aid-chem4597>3.0.co;2-4.
Pieterse, K., Vekemans, J. A., Kooijman, H., Spek, A. L., & Meijer, E. W. (2000). Ladderlike oligomers; intramolecular hydrogen bonding, push-pull character, and electron affinity. Chemistry (Weinheim an der Bergstrasse, Germany), 6(24), 4597-603. https://doi.org/10.1002/1521-3765(20001215)6:24<4597::aid-chem4597>3.0.co;2-4
Pieterse, K, et al. "Ladderlike oligomers; intramolecular hydrogen bonding, push-pull character, and electron affinity." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 6,24 (2000): 4597-603. doi: https://doi.org/10.1002/1521-3765(20001215)6:24<4597::aid-chem4597>3.0.co;2-4
Pieterse K, Vekemans JA, Kooijman H, Spek AL, Meijer EW. Ladderlike oligomers; intramolecular hydrogen bonding, push-pull character, and electron affinity. Chemistry. 2000 Dec 15;6(24):4597-603. doi: 10.1002/1521-3765(20001215)6:24<4597::aid-chem4597>3.0.co;2-4. PMID: 11192093.
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Patterns of allozymic variation within calluna vulgaris populations at seed bank and adult stages .

Heredity

Mahy G, Vekemans X, Jacquemart AL.
PMID: 10383662
Heredity (Edinb). 1999 Apr;82:432-40. doi: 10.1038/sj.hdy.6884990.

We investigated the spatial genetic structure within and between two plots of Calluna vulgaris and the extent to which the soil seed bank differed genetically from adults at seven allozyme loci. Averaged over the two plots, the seed bank...

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Mahy G, Vekemans X, Jacquemart AL. Patterns of allozymic variation within calluna vulgaris populations at seed bank and adult stages . Heredity (Edinb). 1999;82:432-40doi: 10.1038/sj.hdy.6884990.
Mahy, G., Vekemans, X., & Jacquemart, A. L. (1999). Patterns of allozymic variation within calluna vulgaris populations at seed bank and adult stages . Heredity, 82432-40. https://doi.org/10.1038/sj.hdy.6884990
Mahy, et al. "Patterns of allozymic variation within calluna vulgaris populations at seed bank and adult stages ." Heredity vol. 82 (1999): 432-40. doi: https://doi.org/10.1038/sj.hdy.6884990
Mahy G, Vekemans X, Jacquemart AL. Patterns of allozymic variation within calluna vulgaris populations at seed bank and adult stages . Heredity (Edinb). 1999 Apr;82:432-40. doi: 10.1038/sj.hdy.6884990. PMID: 10383662.
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Potential source of human exposure to Mycobacterium bovis in Burkina Faso, in the context of the HIV epidemic.

Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases

Vekemans M, Cartoux M, Diagbouga S, Dembélé M, Koné B, Delafosse A, Dera A, Perre P.
PMID: 11851692
Clin Microbiol Infect. 1999 Oct;5(10):617-21. doi: 10.1111/j.1469-0691.1999.tb00418.x.

OBJECTIVE: To identify potential sources of human Mycobacterium bovis infection in Bobo-Dioulasso, Burkina Faso.METHODS: A tuberculin survey among 174 cattle was performed. Mycobacteriologic identification in 64 samples of pooled milk, and in 199 tissue samples collected from the slaughterhouse...

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Vekemans M, Cartoux M, Diagbouga S, et al. Potential source of human exposure to Mycobacterium bovis in Burkina Faso, in the context of the HIV epidemic. Clin Microbiol Infect. 1999;5(10):617-21doi: 10.1111/j.1469-0691.1999.tb00418.x.
Vekemans, M., Cartoux, M., Diagbouga, S., Dembélé, M., Koné, B., Delafosse, A., Dera, A., & Perre, P. (1999). Potential source of human exposure to Mycobacterium bovis in Burkina Faso, in the context of the HIV epidemic. Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases, 5(10), 617-21. https://doi.org/10.1111/j.1469-0691.1999.tb00418.x
Vekemans, M, et al. "Potential source of human exposure to Mycobacterium bovis in Burkina Faso, in the context of the HIV epidemic." Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases vol. 5,10 (1999): 617-21. doi: https://doi.org/10.1111/j.1469-0691.1999.tb00418.x
Vekemans M, Cartoux M, Diagbouga S, Dembélé M, Koné B, Delafosse A, Dera A, Perre P. Potential source of human exposure to Mycobacterium bovis in Burkina Faso, in the context of the HIV epidemic. Clin Microbiol Infect. 1999 Oct;5(10):617-21. doi: 10.1111/j.1469-0691.1999.tb00418.x. PMID: 11851692.
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Cytotoxic reactions of CC531s towards liver sinusoidal endothelial cells: a microscopical study.

Comparative hepatology

Vekemans K, Timmers M, Vermijlen D, Zanger RD, Wisse E, Braet F.
PMID: 14960201
Comp Hepatol. 2004 Jan 14;3:S49. doi: 10.1186/1476-5926-2-S1-S49.

No abstract available.

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Vekemans K, Timmers M, Vermijlen D, et al. Cytotoxic reactions of CC531s towards liver sinusoidal endothelial cells: a microscopical study. Comp Hepatol. 2004;3:S49doi: 10.1186/1476-5926-2-S1-S49.
Vekemans, K., Timmers, M., Vermijlen, D., Zanger, R. D., Wisse, E., & Braet, F. (2004). Cytotoxic reactions of CC531s towards liver sinusoidal endothelial cells: a microscopical study. Comparative hepatology, 3S49. https://doi.org/10.1186/1476-5926-2-S1-S49
Vekemans, Katrien, et al. "Cytotoxic reactions of CC531s towards liver sinusoidal endothelial cells: a microscopical study." Comparative hepatology vol. 3 (2004): S49. doi: https://doi.org/10.1186/1476-5926-2-S1-S49
Vekemans K, Timmers M, Vermijlen D, Zanger RD, Wisse E, Braet F. Cytotoxic reactions of CC531s towards liver sinusoidal endothelial cells: a microscopical study. Comp Hepatol. 2004 Jan 14;3:S49. doi: 10.1186/1476-5926-2-S1-S49. PMID: 14960201; PMCID: PMC2410264.
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Chiral polymers by iterative tandem catalysis.

Chemical communications (Cambridge, England)

van Buijtenen J, van As BA, Meuldijk J, Palmans AR, Vekemans JA, Hulshof LA, Meijer EW.
PMID: 17028732
Chem Commun (Camb). 2006 Aug 14;(30):3169-71. doi: 10.1039/b606241e. Epub 2006 Jun 21.

Racemic omega-substituted caprolactones can be completely converted into chiral polyesters of remarkable MW and high ee by combining lipase-catalyzed ring-opening polymerization with Ru-catalyzed racemization.

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van Buijtenen J, van As BA, Meuldijk J, et al. Chiral polymers by iterative tandem catalysis. Chem Commun (Camb). 2006;(30):3169-71doi: 10.1039/b606241e.
van Buijtenen, J., van As, B. A., Meuldijk, J., Palmans, A. R., Vekemans, J. A., Hulshof, L. A., & Meijer, E. W. (2006). Chiral polymers by iterative tandem catalysis. Chemical communications (Cambridge, England), (30), 3169-71. https://doi.org/10.1039/b606241e
van Buijtenen, Jeroen, et al. "Chiral polymers by iterative tandem catalysis." Chemical communications (Cambridge, England) vol. ,30 (2006): 3169-71. doi: https://doi.org/10.1039/b606241e
van Buijtenen J, van As BA, Meuldijk J, Palmans AR, Vekemans JA, Hulshof LA, Meijer EW. Chiral polymers by iterative tandem catalysis. Chem Commun (Camb). 2006 Aug 14;(30):3169-71. doi: 10.1039/b606241e. Epub 2006 Jun 21. PMID: 17028732.
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Synthesis of 3,6-diaminophthalimides for ureidophthalimide-based foldamers.

Organic letters

Sinkeldam RW, van Houtem MH, Koeckelberghs G, Vekemans JA, Meijer EW.
PMID: 16435840
Org Lett. 2006 Feb 02;8(3):383-5. doi: 10.1021/ol0524757.

[reaction: see text]. Herein, we report an improved methodology for the synthesis of a variety of 3,6-diaminophthalimides in high yields. This enables decoration of the periphery of foldamers with a wide range of functionalities.

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Sinkeldam RW, van Houtem MH, Koeckelberghs G, et al. Synthesis of 3,6-diaminophthalimides for ureidophthalimide-based foldamers. Org Lett. 2006;8(3):383-5doi: 10.1021/ol0524757.
Sinkeldam, R. W., van Houtem, M. H., Koeckelberghs, G., Vekemans, J. A., & Meijer, E. W. (2006). Synthesis of 3,6-diaminophthalimides for ureidophthalimide-based foldamers. Organic letters, 8(3), 383-5. https://doi.org/10.1021/ol0524757
Sinkeldam, Renatus W, et al. "Synthesis of 3,6-diaminophthalimides for ureidophthalimide-based foldamers." Organic letters vol. 8,3 (2006): 383-5. doi: https://doi.org/10.1021/ol0524757
Sinkeldam RW, van Houtem MH, Koeckelberghs G, Vekemans JA, Meijer EW. Synthesis of 3,6-diaminophthalimides for ureidophthalimide-based foldamers. Org Lett. 2006 Feb 02;8(3):383-5. doi: 10.1021/ol0524757. PMID: 16435840.
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