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Overeating to impress: conspicuous food consumption among males (811.15)

STEM and males

Wansink B.
GSID: MiwWO5y3jSMJ
K Kniffin, B Wansink - The FASEB Journal, 2014 - Wiley Online Library

To what extent is overeating among men an artifact of women's mate preferences or intrasexual competition? While previous research concerning sexual selection pressures upon eating behaviors has focused on disordered consumption among women, we present three studies that consider...

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Kniffin, K., & Wansink, B. (2014). Overeating to impress: conspicuous food consumption among males (811.15). The FASEB Journal, 28, 811-15.
Kniffin, Kevin, and Brian Wansink. "Overeating to impress: conspicuous food consumption among males (811.15)." The FASEB Journal 28 (2014): 811-15.
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Monitoring the inputs required to extend and sustain hygiene promotion: findings from the GLAAS 2013/2014 survey.

Tropical medicine & international health : TM & IH

Moreland LD, Gore FM, Andre N, Cairncross S, Ensink JH.
PMID: 27169937
Trop Med Int Health. 2016 Aug;21(8):1029-1039. doi: 10.1111/tmi.12723. Epub 2016 May 31.

OBJECTIVES: There are significant gaps in information about the inputs required to effectively extend and sustain hygiene promotion activities to improve people's health outcomes through water, sanitation and hygiene (WASH) interventions. We sought to analyse current country and global...

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Moreland LD, Gore FM, Andre N, et al. Monitoring the inputs required to extend and sustain hygiene promotion: findings from the GLAAS 2013/2014 survey. Trop Med Int Health. 2016;21(8):1029-1039doi: 10.1111/tmi.12723.
Moreland, L. D., Gore, F. M., Andre, N., Cairncross, S., & Ensink, J. H. (2016). Monitoring the inputs required to extend and sustain hygiene promotion: findings from the GLAAS 2013/2014 survey. Tropical medicine & international health : TM & IH, 21(8), 1029-1039. https://doi.org/10.1111/tmi.12723
Moreland, Leslie D, et al. "Monitoring the inputs required to extend and sustain hygiene promotion: findings from the GLAAS 2013/2014 survey." Tropical medicine & international health : TM & IH vol. 21,8 (2016): 1029-1039. doi: https://doi.org/10.1111/tmi.12723
Moreland LD, Gore FM, Andre N, Cairncross S, Ensink JH. Monitoring the inputs required to extend and sustain hygiene promotion: findings from the GLAAS 2013/2014 survey. Trop Med Int Health. 2016 Aug;21(8):1029-1039. doi: 10.1111/tmi.12723. Epub 2016 May 31. PMID: 27169937.
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[Masters in Nursing. Professional practice at an academic level].

TVZ : het vakblad voor de verpleging

Mensink F, Sinoo M, van Linge R.
PMID: 8397844
TVZ. 1993 Jun 24;(12):404-7.

No abstract available.

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Mensink F, Sinoo M, van Linge R. Masters in de verpleging. Professionele beroepsuitoefening op academisch niveau. [Masters in Nursing. Professional practice at an academic level]. TVZ. 1993;(12):404-7
Mensink, F., Sinoo, M., & van Linge, R. (1993). Masters in de verpleging. Professionele beroepsuitoefening op academisch niveau. [Masters in Nursing. Professional practice at an academic level]. TVZ : het vakblad voor de verpleging, (12), 404-7.
Mensink, F, et al. "Masters in de verpleging. Professionele beroepsuitoefening op academisch niveau." [Masters in Nursing. Professional practice at an academic level]. TVZ : het vakblad voor de verpleging vol. ,12 (1993): 404-7.
Mensink F, Sinoo M, van Linge R. Masters in de verpleging. Professionele beroepsuitoefening op academisch niveau. [Masters in Nursing. Professional practice at an academic level]. TVZ. 1993 Jun 24;(12):404-7. Dutch. PMID: 8397844.
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1D-3,4-Di-O-(diphenylmethylphosphonio)-1,2,5, 6-tetra-O-methyl-chiro-inositol diiodide.

Acta crystallographica. Section C, Crystal structure communications

Gainsford GJ, Lensink C, Hart JB, Falshaw A.
PMID: 11077312
Acta Crystallogr C. 2000 Nov;56:1396-8. doi: 10.1107/s0108270100011574.

The title compound, 3,4,5,6-tetramethoxycyclohexane-1, 2-diyldioxybis(methyldiphenylphosphonium) diiodide, C(36)H(44)O(6)P(2)(2+).2I(-), was prepared from a New Zealand natural product, D-chiro-inositol, in order to develop new catalytic metal complexes. The inositol ring retains its usual chair conformation with only minor perturbations caused by the...

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Gainsford GJ, Lensink C, Hart JB, et al. 1D-3,4-Di-O-(diphenylmethylphosphonio)-1,2,5, 6-tetra-O-methyl-chiro-inositol diiodide. Acta Crystallogr C. 2000;56:1396-8doi: 10.1107/s0108270100011574.
Gainsford, G. J., Lensink, C., Hart, J. B., & Falshaw, A. (2000). 1D-3,4-Di-O-(diphenylmethylphosphonio)-1,2,5, 6-tetra-O-methyl-chiro-inositol diiodide. Acta crystallographica. Section C, Crystal structure communications, 561396-8. https://doi.org/10.1107/s0108270100011574
Gainsford, G J, et al. "1D-3,4-Di-O-(diphenylmethylphosphonio)-1,2,5, 6-tetra-O-methyl-chiro-inositol diiodide." Acta crystallographica. Section C, Crystal structure communications vol. 56 (2000): 1396-8. doi: https://doi.org/10.1107/s0108270100011574
Gainsford GJ, Lensink C, Hart JB, Falshaw A. 1D-3,4-Di-O-(diphenylmethylphosphonio)-1,2,5, 6-tetra-O-methyl-chiro-inositol diiodide. Acta Crystallogr C. 2000 Nov;56:1396-8. doi: 10.1107/s0108270100011574. PMID: 11077312.
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Lifestyle intervention, glucose tolerance, and risk of developing type 2 diabetes mellitus.

Metabolic syndrome and related disorders

Mensink M.
PMID: 18370707
Metab Syndr Relat Disord. 2005;3(1):26-34. doi: 10.1089/met.2005.3.26.

Diabetes mellitus is rapidly becoming one of the main health issues in the 21st century. Environmental factors such as lifestyle habits (i.e., physical inactivity and dietary intake) and obesity may act as initiating factors or progression factors for type...

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Mensink M. Lifestyle intervention, glucose tolerance, and risk of developing type 2 diabetes mellitus. Metab Syndr Relat Disord. 2005;3(1):26-34doi: 10.1089/met.2005.3.26.
Mensink, M. (2005). Lifestyle intervention, glucose tolerance, and risk of developing type 2 diabetes mellitus. Metabolic syndrome and related disorders, 3(1), 26-34. https://doi.org/10.1089/met.2005.3.26
Mensink, Marco. "Lifestyle intervention, glucose tolerance, and risk of developing type 2 diabetes mellitus." Metabolic syndrome and related disorders vol. 3,1 (2005): 26-34. doi: https://doi.org/10.1089/met.2005.3.26
Mensink M. Lifestyle intervention, glucose tolerance, and risk of developing type 2 diabetes mellitus. Metab Syndr Relat Disord. 2005;3(1):26-34. doi: 10.1089/met.2005.3.26. PMID: 18370707.
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Organocatalytic one-pot asymmetric synthesis of functionalized tricyclic carbon frameworks from a triple-cascade/Diels-Alder sequence.

Angewandte Chemie (International ed. in English)

Enders D, Hüttl MR, Runsink J, Raabe G, Wendt B.
PMID: 17154207
Angew Chem Int Ed Engl. 2007;46(3):467-9. doi: 10.1002/anie.200603434.

No abstract available.

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Enders D, Hüttl MR, Runsink J, et al. Organocatalytic one-pot asymmetric synthesis of functionalized tricyclic carbon frameworks from a triple-cascade/Diels-Alder sequence. Angew Chem Int Ed Engl. 2007;46(3):467-9doi: 10.1002/anie.200603434.
Enders, D., Hüttl, M. R., Runsink, J., Raabe, G., & Wendt, B. (2007). Organocatalytic one-pot asymmetric synthesis of functionalized tricyclic carbon frameworks from a triple-cascade/Diels-Alder sequence. Angewandte Chemie (International ed. in English), 46(3), 467-9. https://doi.org/10.1002/anie.200603434
Enders, Dieter, et al. "Organocatalytic one-pot asymmetric synthesis of functionalized tricyclic carbon frameworks from a triple-cascade/Diels-Alder sequence." Angewandte Chemie (International ed. in English) vol. 46,3 (2007): 467-9. doi: https://doi.org/10.1002/anie.200603434
Enders D, Hüttl MR, Runsink J, Raabe G, Wendt B. Organocatalytic one-pot asymmetric synthesis of functionalized tricyclic carbon frameworks from a triple-cascade/Diels-Alder sequence. Angew Chem Int Ed Engl. 2007;46(3):467-9. doi: 10.1002/anie.200603434. PMID: 17154207.
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Lifting a wet glass from a table: a microscopic picture.

Langmuir : the ACS journal of surfaces and colloids

van der Spoel D, Wensink EJ, Hoffmann AC.
PMID: 16768492
Langmuir. 2006 Jun 20;22(13):5666-72. doi: 10.1021/la053284f.

Why is it so hard to lift a wet glass from a table? Is it easier when there is whiskey between the glass and the table? Macroscopically, the picture is quite simple: two surfaces have to be disrupted that...

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van der Spoel D, Wensink EJ, Hoffmann AC. Lifting a wet glass from a table: a microscopic picture. Langmuir. 2006;22(13):5666-72doi: 10.1021/la053284f.
van der Spoel, D., Wensink, E. J., & Hoffmann, A. C. (2006). Lifting a wet glass from a table: a microscopic picture. Langmuir : the ACS journal of surfaces and colloids, 22(13), 5666-72. https://doi.org/10.1021/la053284f
van der Spoel, David, et al. "Lifting a wet glass from a table: a microscopic picture." Langmuir : the ACS journal of surfaces and colloids vol. 22,13 (2006): 5666-72. doi: https://doi.org/10.1021/la053284f
van der Spoel D, Wensink EJ, Hoffmann AC. Lifting a wet glass from a table: a microscopic picture. Langmuir. 2006 Jun 20;22(13):5666-72. doi: 10.1021/la053284f. PMID: 16768492.
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Pre-slaughter conditions, animal stress and welfare: current status and possible future research.

Animal : an international journal of animal bioscience

Terlouw EM, Arnould C, Auperin B, Berri C, Le Bihan-Duval E, Deiss V, Lefèvre F, Lensink BJ, Mounier L.
PMID: 22443909
Animal. 2008 Oct;2(10):1501-17. doi: 10.1017/S1751731108002723.

The present paper describes the main procedures used to slaughter fowl, pigs, calves and adult cattle, sheep, and farmed fish, starting on the farm and ending with the death of the animal at the abattoir. It reviews the currently...

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Terlouw EM, Arnould C, Auperin B, et al. Pre-slaughter conditions, animal stress and welfare: current status and possible future research. Animal. 2008;2(10):1501-17doi: 10.1017/S1751731108002723.
Terlouw, E. M., Arnould, C., Auperin, B., Berri, C., Le Bihan-Duval, E., Deiss, V., Lefèvre, F., Lensink, B. J., & Mounier, L. (2008). Pre-slaughter conditions, animal stress and welfare: current status and possible future research. Animal : an international journal of animal bioscience, 2(10), 1501-17. https://doi.org/10.1017/S1751731108002723
Terlouw, E M C, et al. "Pre-slaughter conditions, animal stress and welfare: current status and possible future research." Animal : an international journal of animal bioscience vol. 2,10 (2008): 1501-17. doi: https://doi.org/10.1017/S1751731108002723
Terlouw EM, Arnould C, Auperin B, Berri C, Le Bihan-Duval E, Deiss V, Lefèvre F, Lensink BJ, Mounier L. Pre-slaughter conditions, animal stress and welfare: current status and possible future research. Animal. 2008 Oct;2(10):1501-17. doi: 10.1017/S1751731108002723. PMID: 22443909.
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Ruthenium and osmium complexes of hemilabile chiral monophosphinite ligands derived from 1D-pinitol or 1D-chiro-inositol as catalysts for asymmetric hydrogenation reactions.

Dalton transactions (Cambridge, England : 2003)

Slade AT, Lensink C, Falshaw A, Clark GR, Wright LJ.
PMID: 25315464
Dalton Trans. 2014 Dec 07;43(45):17163-71. doi: 10.1039/c4dt02558j.

The monophosphinite ligands, 1D-1,2;5,6-di-O-cyclopentylidene-3-O-methyl-4-O-diphenylphosphino-chiro-inositol (D-P1), 1D-1,2;5,6-di-O-isopropylidene-3-O-methyl-4-O-diphenylphosphino-chiro-inositol (D-P2), 1D-1,2;5,6-di-O-cyclohexylidene-3-O-methyl-4-O-diphenylphosphino-chiro-inositol (D-P3), and 1D-1,2;5,6-di-O-cyclopentylidene-3-O-ethyl-4-O-diphenylphosphino-chiro-inositol (D-P4), can be conveniently prepared from the chiral natural products 1D-pinitol or 1D-chiro-inositol. On treatment of toluene solutions of RuCl2(PPh3)3 with two mole equivalents of the ligands D-PY...

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Slade AT, Lensink C, Falshaw A, et al. Ruthenium and osmium complexes of hemilabile chiral monophosphinite ligands derived from 1D-pinitol or 1D-chiro-inositol as catalysts for asymmetric hydrogenation reactions. Dalton Trans. 2014;43(45):17163-71doi: 10.1039/c4dt02558j.
Slade, A. T., Lensink, C., Falshaw, A., Clark, G. R., & Wright, L. J. (2014). Ruthenium and osmium complexes of hemilabile chiral monophosphinite ligands derived from 1D-pinitol or 1D-chiro-inositol as catalysts for asymmetric hydrogenation reactions. Dalton transactions (Cambridge, England : 2003), 43(45), 17163-71. https://doi.org/10.1039/c4dt02558j
Slade, Angela T, et al. "Ruthenium and osmium complexes of hemilabile chiral monophosphinite ligands derived from 1D-pinitol or 1D-chiro-inositol as catalysts for asymmetric hydrogenation reactions." Dalton transactions (Cambridge, England : 2003) vol. 43,45 (2014): 17163-71. doi: https://doi.org/10.1039/c4dt02558j
Slade AT, Lensink C, Falshaw A, Clark GR, Wright LJ. Ruthenium and osmium complexes of hemilabile chiral monophosphinite ligands derived from 1D-pinitol or 1D-chiro-inositol as catalysts for asymmetric hydrogenation reactions. Dalton Trans. 2014 Dec 07;43(45):17163-71. doi: 10.1039/c4dt02558j. PMID: 25315464.
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Molecular Diagnosis of Acute Myeloid Leukemia with Maturation, FAB-Type M2.

Methods in molecular medicine

Mensink EJ, van de Locht LT.
PMID: 21380695
Methods Mol Med. 1996;6:37-45. doi: 10.1385/0-89603-341-4:37.

Nonrandom chromosome abnormalities frequently are seen in particular subtypes of human leukemia and lymphoma. These abnormalities are considered to be involved in the neoplastic transformation and in tumor progression. The translocation (8;21) (q22;q22) is consistently associated with acute myeloid...

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Mensink EJ, van de Locht LT. Molecular Diagnosis of Acute Myeloid Leukemia with Maturation, FAB-Type M2. Methods Mol Med. 1996;6:37-45doi: 10.1385/0-89603-341-4:37.
Mensink, E. J., & van de Locht, L. T. (1996). Molecular Diagnosis of Acute Myeloid Leukemia with Maturation, FAB-Type M2. Methods in molecular medicine, 637-45. https://doi.org/10.1385/0-89603-341-4:37
Mensink, E J, and van de Locht, L T. "Molecular Diagnosis of Acute Myeloid Leukemia with Maturation, FAB-Type M2." Methods in molecular medicine vol. 6 (1996): 37-45. doi: https://doi.org/10.1385/0-89603-341-4:37
Mensink EJ, van de Locht LT. Molecular Diagnosis of Acute Myeloid Leukemia with Maturation, FAB-Type M2. Methods Mol Med. 1996;6:37-45. doi: 10.1385/0-89603-341-4:37. PMID: 21380695.
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A Three-Dimensional Model of Women's Empowerment: Implications in the Field of Microfinance and Future Directions.

Frontiers in psychology

Huis MA, Hansen N, Otten S, Lensink R.
PMID: 29033873
Front Psychol. 2017 Sep 28;8:1678. doi: 10.3389/fpsyg.2017.01678. eCollection 2017.

Women's empowerment is an important goal in achieving sustainable development worldwide. Offering access to microfinance services to women is one way to increase women's empowerment. However, empirical evidence provides mixed results with respect to its effectiveness. We reviewed previous...

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Huis MA, Hansen N, Otten S, et al. A Three-Dimensional Model of Women's Empowerment: Implications in the Field of Microfinance and Future Directions. Front Psychol. 2017;8:1678doi: 10.3389/fpsyg.2017.01678.
Huis, M. A., Hansen, N., Otten, S., & Lensink, R. (2017). A Three-Dimensional Model of Women's Empowerment: Implications in the Field of Microfinance and Future Directions. Frontiers in psychology, 81678. https://doi.org/10.3389/fpsyg.2017.01678
Huis, Marloes A, et al. "A Three-Dimensional Model of Women's Empowerment: Implications in the Field of Microfinance and Future Directions." Frontiers in psychology vol. 8 (2017): 1678. doi: https://doi.org/10.3389/fpsyg.2017.01678
Huis MA, Hansen N, Otten S, Lensink R. A Three-Dimensional Model of Women's Empowerment: Implications in the Field of Microfinance and Future Directions. Front Psychol. 2017 Sep 28;8:1678. doi: 10.3389/fpsyg.2017.01678. eCollection 2017. PMID: 29033873; PMCID: PMC5625566.
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Diastereoselective Synthesis of Highly Substituted Five-Membered-Ring Oxygen Heterocycles by Zirconocene-Mediated C-C Coupling Reactions.

Angewandte Chemie (International ed. in English)

Enders D, Kroll M, Raabe G, Runsink J.
PMID: 29711525
Angew Chem Int Ed Engl. 1998 Jul 03;37(12):1673-1675. doi: 10.1002/(SICI)1521-3773(19980703)37:12<1673::AID-ANIE1673>3.0.CO;2-A.

As homoenolate equivalents, zirconocene-1-aza-1,3-diene complexes were used for the first time in stereoselective synthesis. By insertion of an unsymmetrical ketone in the Zr-C σ bond, sterically demanding trisubstituted dihydro- and tetrahydrofuran derivatives were prepared in good overall yields and...

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Enders D, Kroll M, Raabe G, et al. Diastereoselective Synthesis of Highly Substituted Five-Membered-Ring Oxygen Heterocycles by Zirconocene-Mediated C-C Coupling Reactions. Angew Chem Int Ed Engl. 1998;37(12):1673-1675doi: 10.1002/(SICI)1521-3773(19980703)37:12<1673::AID-ANIE1673>3.0.CO;2-A.
Enders, D., Kroll, M., Raabe, G., & Runsink, J. (1998). Diastereoselective Synthesis of Highly Substituted Five-Membered-Ring Oxygen Heterocycles by Zirconocene-Mediated C-C Coupling Reactions. Angewandte Chemie (International ed. in English), 37(12), 1673-1675. https://doi.org/10.1002/(SICI)1521-3773(19980703)37:12<1673::AID-ANIE1673>3.0.CO;2-A
Enders, Dieter, et al. "Diastereoselective Synthesis of Highly Substituted Five-Membered-Ring Oxygen Heterocycles by Zirconocene-Mediated C-C Coupling Reactions." Angewandte Chemie (International ed. in English) vol. 37,12 (1998): 1673-1675. doi: https://doi.org/10.1002/(SICI)1521-3773(19980703)37:12<1673::AID-ANIE1673>3.0.CO;2-A
Enders D, Kroll M, Raabe G, Runsink J. Diastereoselective Synthesis of Highly Substituted Five-Membered-Ring Oxygen Heterocycles by Zirconocene-Mediated C-C Coupling Reactions. Angew Chem Int Ed Engl. 1998 Jul 03;37(12):1673-1675. doi: 10.1002/(SICI)1521-3773(19980703)37:12<1673::AID-ANIE1673>3.0.CO;2-A. PMID: 29711525.
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