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Developing after-school programs for youth in high risk environments

after school programs, family programs

Witt P.
GSID: 2YDy1cw_GisJ
P Witt, D Baker - Journal of Physical Education, Recreation & …, 1997 - Taylor & Francis

… after school or attend structured, supervised after-school programs. Self-care children tend to be more involved with peers, have more contact with deviant peers, and boys have poorer parent-adolescent relations (Galambos & Maggs, 1991). Steinberg (1986) found that children...

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Witt, P., & Baker, D. (1997). Developing after-school programs for youth in high risk environments. Journal of Physical Education, Recreation & Dance, 68(9), 18-20.
Witt, Peter, and Dwayne Baker. "Developing after-school programs for youth in high risk environments." Journal of Physical Education, Recreation & Dance 68.9 (1997): 18-20.
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The Availability and Utility of Services to Address Risk Factors for Recidivism among Justice-Involved Veterans.

Criminal justice policy review

Blonigen DM, Rodriguez AL, Manfredi L, Britt J, Nevedal A, Finlay AK, Rosenthal J, Smelson D, Timko C.
PMID: 26924887
Crim Justice Policy Rev. 2017 Oct;28(8):790-813. doi: 10.1177/0887403416628601. Epub 2016 Feb 10.

The availability and utility of services to address recidivism risk factors among justice-involved veterans is unknown. We explored these issues through qualitative interviews with 63 Specialists from the Department of Veterans Affairs' (VA) Veterans Justice Programs. To guide the...

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Blonigen DM, Rodriguez AL, Manfredi L, et al. The Availability and Utility of Services to Address Risk Factors for Recidivism among Justice-Involved Veterans. Crim Justice Policy Rev. 2016;28(8):790-813doi: 10.1177/0887403416628601.
Blonigen, D. M., Rodriguez, A. L., Manfredi, L., Britt, J., Nevedal, A., Finlay, A. K., Rosenthal, J., Smelson, D., & Timko, C. (2017). The Availability and Utility of Services to Address Risk Factors for Recidivism among Justice-Involved Veterans. Criminal justice policy review, 28(8), 790-813. https://doi.org/10.1177/0887403416628601
Blonigen, Daniel M, et al. "The Availability and Utility of Services to Address Risk Factors for Recidivism among Justice-Involved Veterans." Criminal justice policy review vol. 28,8 (2017): 790-813. doi: https://doi.org/10.1177/0887403416628601
Blonigen DM, Rodriguez AL, Manfredi L, Britt J, Nevedal A, Finlay AK, Rosenthal J, Smelson D, Timko C. The Availability and Utility of Services to Address Risk Factors for Recidivism among Justice-Involved Veterans. Crim Justice Policy Rev. 2017 Oct;28(8):790-813. doi: 10.1177/0887403416628601. Epub 2016 Feb 10. PMID: 26924887; PMCID: PMC4765911.
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Tailoring Pore Size and Chemical Interior of near 1 nm Sized Pores in a Nanoporous Polymer Based on a Discotic Liquid Crystal.

Macromolecules

Bhattacharjee S, Lugger JAM, Sijbesma RP.
PMID: 28416888
Macromolecules. 2017 Apr 11;50(7):2777-2783. doi: 10.1021/acs.macromol.7b00013. Epub 2017 Mar 23.

A triazine based disc shaped molecule with two hydrolyzable units, imine and ester groups, was polymerized via acyclic diene metathesis in the columnar hexagonal (Col

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Bhattacharjee S, Lugger JAM, Sijbesma RP. Tailoring Pore Size and Chemical Interior of near 1 nm Sized Pores in a Nanoporous Polymer Based on a Discotic Liquid Crystal. Macromolecules. 2017;50(7):2777-2783doi: 10.1021/acs.macromol.7b00013.
Bhattacharjee, S., Lugger, J. A. M., & Sijbesma, R. P. (2017). Tailoring Pore Size and Chemical Interior of near 1 nm Sized Pores in a Nanoporous Polymer Based on a Discotic Liquid Crystal. Macromolecules, 50(7), 2777-2783. https://doi.org/10.1021/acs.macromol.7b00013
Bhattacharjee, Subham, et al. "Tailoring Pore Size and Chemical Interior of near 1 nm Sized Pores in a Nanoporous Polymer Based on a Discotic Liquid Crystal." Macromolecules vol. 50,7 (2017): 2777-2783. doi: https://doi.org/10.1021/acs.macromol.7b00013
Bhattacharjee S, Lugger JAM, Sijbesma RP. Tailoring Pore Size and Chemical Interior of near 1 nm Sized Pores in a Nanoporous Polymer Based on a Discotic Liquid Crystal. Macromolecules. 2017 Apr 11;50(7):2777-2783. doi: 10.1021/acs.macromol.7b00013. Epub 2017 Mar 23. PMID: 28416888; PMCID: PMC5391558.
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Osteogenic stem cell selection for repair and regeneration.

Bone reports

Tillotson M, Logan N, Brett P.
PMID: 28326344
Bone Rep. 2016 Jan 28;5:22-32. doi: 10.1016/j.bonr.2016.01.003. eCollection 2016 Dec.

The first osteogenic cells to attach to a titanium (Ti) implant after placement are the multipotent stromal cells (MSCs) that circulate in the bloodstream and are recruited to the site of tissue damage. The reservoirs of these cells are...

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Tillotson M, Logan N, Brett P. Osteogenic stem cell selection for repair and regeneration. Bone Rep. 2016;5:22-32doi: 10.1016/j.bonr.2016.01.003.
Tillotson, M., Logan, N., & Brett, P. (2016). Osteogenic stem cell selection for repair and regeneration. Bone reports, 522-32. https://doi.org/10.1016/j.bonr.2016.01.003
Tillotson, Marcus, et al. "Osteogenic stem cell selection for repair and regeneration." Bone reports vol. 5 (2016): 22-32. doi: https://doi.org/10.1016/j.bonr.2016.01.003
Tillotson M, Logan N, Brett P. Osteogenic stem cell selection for repair and regeneration. Bone Rep. 2016 Jan 28;5:22-32. doi: 10.1016/j.bonr.2016.01.003. eCollection 2016 Dec. PMID: 28326344; PMCID: PMC4926815.
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Chronic Obstructive Pulmonary Disease-Derived Circulating Cells Release IL-18 and IL-33 under Ultrafine Particulate Matter Exposure in a Caspase-1/8-Independent Manner.

Frontiers in immunology

De Falco G, Colarusso C, Terlizzi M, Popolo A, Pecoraro M, Commodo M, Minutolo P, Sirignano M, D'Anna A, Aquino RP, Pinto A, Molino A, Sorrentino R.
PMID: 29123531
Front Immunol. 2017 Oct 26;8:1415. doi: 10.3389/fimmu.2017.01415. eCollection 2017.

Chronic obstructive pulmonary disease (COPD) is considered the fourth-leading causes of death worldwide; COPD is caused by inhalation of noxious indoor and outdoor particles, especially cigarette smoke that represents the first risk factor for this respiratory disorder. To mimic...

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De Falco G, Colarusso C, Terlizzi M, et al. Chronic Obstructive Pulmonary Disease-Derived Circulating Cells Release IL-18 and IL-33 under Ultrafine Particulate Matter Exposure in a Caspase-1/8-Independent Manner. Front Immunol. 2017;8:1415doi: 10.3389/fimmu.2017.01415.
De Falco, G., Colarusso, C., Terlizzi, M., Popolo, A., Pecoraro, M., Commodo, M., Minutolo, P., Sirignano, M., D'Anna, A., Aquino, R. P., Pinto, A., Molino, A., & Sorrentino, R. (2017). Chronic Obstructive Pulmonary Disease-Derived Circulating Cells Release IL-18 and IL-33 under Ultrafine Particulate Matter Exposure in a Caspase-1/8-Independent Manner. Frontiers in immunology, 81415. https://doi.org/10.3389/fimmu.2017.01415
De Falco, Gianluigi, et al. "Chronic Obstructive Pulmonary Disease-Derived Circulating Cells Release IL-18 and IL-33 under Ultrafine Particulate Matter Exposure in a Caspase-1/8-Independent Manner." Frontiers in immunology vol. 8 (2017): 1415. doi: https://doi.org/10.3389/fimmu.2017.01415
De Falco G, Colarusso C, Terlizzi M, Popolo A, Pecoraro M, Commodo M, Minutolo P, Sirignano M, D'Anna A, Aquino RP, Pinto A, Molino A, Sorrentino R. Chronic Obstructive Pulmonary Disease-Derived Circulating Cells Release IL-18 and IL-33 under Ultrafine Particulate Matter Exposure in a Caspase-1/8-Independent Manner. Front Immunol. 2017 Oct 26;8:1415. doi: 10.3389/fimmu.2017.01415. eCollection 2017. PMID: 29123531; PMCID: PMC5662642.
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Hydroxylation of the surface of PbS nanocrystals passivated with oleic acid.

Science (New York, N.Y.)

Zherebetskyy D, Scheele M, Zhang Y, Bronstein N, Thompson C, Britt D, Salmeron M, Alivisatos P, Wang LW.
PMID: 24876347
Science. 2014 Jun 20;344(6190):1380-4. doi: 10.1126/science.1252727. Epub 2014 May 29.

Controlling the structure of colloidal nanocrystals (NCs) is key to the generation of their complex functionality. This requires an understanding of the NC surface at the atomic level. The structure of colloidal PbS NCs passivated with oleic acid has...

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Zherebetskyy D, Scheele M, Zhang Y, et al. Hydroxylation of the surface of PbS nanocrystals passivated with oleic acid. Science. 2014;344(6190):1380-4doi: 10.1126/science.1252727.
Zherebetskyy, D., Scheele, M., Zhang, Y., Bronstein, N., Thompson, C., Britt, D., Salmeron, M., Alivisatos, P., & Wang, L. W. (2014). Hydroxylation of the surface of PbS nanocrystals passivated with oleic acid. Science (New York, N.Y.), 344(6190), 1380-4. https://doi.org/10.1126/science.1252727
Zherebetskyy, Danylo, et al. "Hydroxylation of the surface of PbS nanocrystals passivated with oleic acid." Science (New York, N.Y.) vol. 344,6190 (2014): 1380-4. doi: https://doi.org/10.1126/science.1252727
Zherebetskyy D, Scheele M, Zhang Y, Bronstein N, Thompson C, Britt D, Salmeron M, Alivisatos P, Wang LW. Hydroxylation of the surface of PbS nanocrystals passivated with oleic acid. Science. 2014 Jun 20;344(6190):1380-4. doi: 10.1126/science.1252727. Epub 2014 May 29. PMID: 24876347.
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Natural polysaccharides platforms for oral controlled release of ketoprofen lysine salt.

Drug development and industrial pharmacy

Cerciello A, Auriemma G, Del Gaudio P, Cantarini M, Aquino RP.
PMID: 27237337
Drug Dev Ind Pharm. 2016 Dec;42(12):2063-2069. doi: 10.1080/03639045.2016.1195401. Epub 2016 Jun 14.

CONTEXT: Ketoprofen lysinate (KL) is one of the most widely used non-steroidal anti-inflammatory drugs in the symptomatic treatment of some chronic inflammatory diseases. Compared to ketoprofen, KL shows better pharmacokinetics and tolerability. However, due to its short half-life of...

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Cerciello A, Auriemma G, Del Gaudio P, et al. Natural polysaccharides platforms for oral controlled release of ketoprofen lysine salt. Drug Dev Ind Pharm. 2016;42(12):2063-2069doi: 10.1080/03639045.2016.1195401.
Cerciello, A., Auriemma, G., Del Gaudio, P., Cantarini, M., & Aquino, R. P. (2016). Natural polysaccharides platforms for oral controlled release of ketoprofen lysine salt. Drug development and industrial pharmacy, 42(12), 2063-2069. https://doi.org/10.1080/03639045.2016.1195401
Cerciello, Andrea, et al. "Natural polysaccharides platforms for oral controlled release of ketoprofen lysine salt." Drug development and industrial pharmacy vol. 42,12 (2016): 2063-2069. doi: https://doi.org/10.1080/03639045.2016.1195401
Cerciello A, Auriemma G, Del Gaudio P, Cantarini M, Aquino RP. Natural polysaccharides platforms for oral controlled release of ketoprofen lysine salt. Drug Dev Ind Pharm. 2016 Dec;42(12):2063-2069. doi: 10.1080/03639045.2016.1195401. Epub 2016 Jun 14. PMID: 27237337.
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Beyond Dispersity: Deterministic Control of Polymer Molecular Weight Distribution.

Journal of the American Chemical Society

Gentekos DT, Dupuis LN, Fors BP.
PMID: 26824147
J Am Chem Soc. 2016 Feb 17;138(6):1848-51. doi: 10.1021/jacs.5b13565. Epub 2016 Feb 02.

The breadth of the molecular weight distributions (MWD) of polymers influences their physical properties; however, no synthetic methods allow precise control of the exact shape and composition of a distribution. We report a modular strategy that enables deterministic control...

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Gentekos DT, Dupuis LN, Fors BP. Beyond Dispersity: Deterministic Control of Polymer Molecular Weight Distribution. J Am Chem Soc. 2016;138(6):1848-51doi: 10.1021/jacs.5b13565.
Gentekos, D. T., Dupuis, L. N., & Fors, B. P. (2016). Beyond Dispersity: Deterministic Control of Polymer Molecular Weight Distribution. Journal of the American Chemical Society, 138(6), 1848-51. https://doi.org/10.1021/jacs.5b13565
Gentekos, Dillon T, et al. "Beyond Dispersity: Deterministic Control of Polymer Molecular Weight Distribution." Journal of the American Chemical Society vol. 138,6 (2016): 1848-51. doi: https://doi.org/10.1021/jacs.5b13565
Gentekos DT, Dupuis LN, Fors BP. Beyond Dispersity: Deterministic Control of Polymer Molecular Weight Distribution. J Am Chem Soc. 2016 Feb 17;138(6):1848-51. doi: 10.1021/jacs.5b13565. Epub 2016 Feb 02. PMID: 26824147.
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Topochemical polymerization in self-assembled rodlike micelles of bisurea bolaamphiphiles.

Soft matter

Pal A, Voudouris P, Koenigs MM, Besenius P, Wyss HM, Degirmenci V, Sijbesma RP.
PMID: 24983103
Soft Matter. 2014 Feb 21;10(7):952-6. doi: 10.1039/c3sm52605d.

Rod-like micelles, formed from bolaamphiphiles with oligo(ethylene oxide) hydrophilic outer segments and a hydrophobic segment with diacetylene flanked by two urea moieties, were covalently fixated by topochemical photopolymerization to high degrees of polymerization by optimizing the hydrophobic core and...

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Pal A, Voudouris P, Koenigs MM, et al. Topochemical polymerization in self-assembled rodlike micelles of bisurea bolaamphiphiles. Soft Matter. 2014;10(7):952-6doi: 10.1039/c3sm52605d.
Pal, A., Voudouris, P., Koenigs, M. M., Besenius, P., Wyss, H. M., Degirmenci, V., & Sijbesma, R. P. (2014). Topochemical polymerization in self-assembled rodlike micelles of bisurea bolaamphiphiles. Soft matter, 10(7), 952-6. https://doi.org/10.1039/c3sm52605d
Pal, Asish, et al. "Topochemical polymerization in self-assembled rodlike micelles of bisurea bolaamphiphiles." Soft matter vol. 10,7 (2014): 952-6. doi: https://doi.org/10.1039/c3sm52605d
Pal A, Voudouris P, Koenigs MM, Besenius P, Wyss HM, Degirmenci V, Sijbesma RP. Topochemical polymerization in self-assembled rodlike micelles of bisurea bolaamphiphiles. Soft Matter. 2014 Feb 21;10(7):952-6. doi: 10.1039/c3sm52605d. PMID: 24983103.
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Synthesis of Amorphous Monomeric Glass Mixtures for Organic Electronic Applications.

The Journal of organic chemistry

Wu YC, Molaire MF, Weiss DS, Angel FA, DeBlase CR, Fors BP.
PMID: 26560445
J Org Chem. 2015 Dec 18;80(24):12740-5. doi: 10.1021/acs.joc.5b02459. Epub 2015 Nov 19.

We report a divergent synthetic strategy and novel design concept that exploit molecular mixtures to create amorphous organic charge-transporting glasses. Using Suzuki-Miyaura cross-coupling reactions, we synthesized well-defined molecular mixtures in a single step. These solution-processable materials are noncrystalline and...

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Wu YC, Molaire MF, Weiss DS, et al. Synthesis of Amorphous Monomeric Glass Mixtures for Organic Electronic Applications. J Org Chem. 2015;80(24):12740-5doi: 10.1021/acs.joc.5b02459.
Wu, Y. C., Molaire, M. F., Weiss, D. S., Angel, F. A., DeBlase, C. R., & Fors, B. P. (2015). Synthesis of Amorphous Monomeric Glass Mixtures for Organic Electronic Applications. The Journal of organic chemistry, 80(24), 12740-5. https://doi.org/10.1021/acs.joc.5b02459
Wu, You-Chi Mason, et al. "Synthesis of Amorphous Monomeric Glass Mixtures for Organic Electronic Applications." The Journal of organic chemistry vol. 80,24 (2015): 12740-5. doi: https://doi.org/10.1021/acs.joc.5b02459
Wu YC, Molaire MF, Weiss DS, Angel FA, DeBlase CR, Fors BP. Synthesis of Amorphous Monomeric Glass Mixtures for Organic Electronic Applications. J Org Chem. 2015 Dec 18;80(24):12740-5. doi: 10.1021/acs.joc.5b02459. Epub 2015 Nov 19. PMID: 26560445.
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Simulation of a suite of generic long-pulse neutron instruments to optimize the time structure of the European Spallation Source.

The Review of scientific instruments

Lefmann K, Klenø KH, Birk JO, Hansen BR, Holm SL, Knudsen E, Lieutenant K, von Moos L, Sales M, Willendrup PK, Andersen KH.
PMID: 23742588
Rev Sci Instrum. 2013 May;84(5):055106. doi: 10.1063/1.4803167.

We here describe the result of simulations of 15 generic neutron instruments for the long-pulsed European Spallation Source. All instruments have been simulated for 20 different settings of the source time structure, corresponding to pulse lengths between 1 ms...

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Lefmann K, Klenø KH, Birk JO, et al. Simulation of a suite of generic long-pulse neutron instruments to optimize the time structure of the European Spallation Source. Rev Sci Instrum. 2013;84(5):055106doi: 10.1063/1.4803167.
Lefmann, K., Klenø, K. H., Birk, J. O., Hansen, B. R., Holm, S. L., Knudsen, E., Lieutenant, K., von Moos, L., Sales, M., Willendrup, P. K., & Andersen, K. H. (2013). Simulation of a suite of generic long-pulse neutron instruments to optimize the time structure of the European Spallation Source. The Review of scientific instruments, 84(5), 055106. https://doi.org/10.1063/1.4803167
Lefmann, Kim, et al. "Simulation of a suite of generic long-pulse neutron instruments to optimize the time structure of the European Spallation Source." The Review of scientific instruments vol. 84,5 (2013): 055106. doi: https://doi.org/10.1063/1.4803167
Lefmann K, Klenø KH, Birk JO, Hansen BR, Holm SL, Knudsen E, Lieutenant K, von Moos L, Sales M, Willendrup PK, Andersen KH. Simulation of a suite of generic long-pulse neutron instruments to optimize the time structure of the European Spallation Source. Rev Sci Instrum. 2013 May;84(5):055106. doi: 10.1063/1.4803167. PMID: 23742588.
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One-step synthesis of unsymmetrical N-alkyl-N'-aryl perylene diimides.

The Journal of organic chemistry

Robb MJ, Newton B, Fors BP, Hawker CJ.
PMID: 24927297
J Org Chem. 2014 Jul 03;79(13):6360-5. doi: 10.1021/jo500945k. Epub 2014 Jun 13.

An efficient and facile protocol for the synthesis of unsymmetrical N-alkyl-N'-aryl perylene diimides is reported that circumvents the need for multiple reaction steps. A number of unsymmetrical perylene diimides containing a solubilizing swallowtail alkyl group and a variety of...

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Robb MJ, Newton B, Fors BP, et al. One-step synthesis of unsymmetrical N-alkyl-N'-aryl perylene diimides. J Org Chem. 2014;79(13):6360-5doi: 10.1021/jo500945k.
Robb, M. J., Newton, B., Fors, B. P., & Hawker, C. J. (2014). One-step synthesis of unsymmetrical N-alkyl-N'-aryl perylene diimides. The Journal of organic chemistry, 79(13), 6360-5. https://doi.org/10.1021/jo500945k
Robb, Maxwell J, et al. "One-step synthesis of unsymmetrical N-alkyl-N'-aryl perylene diimides." The Journal of organic chemistry vol. 79,13 (2014): 6360-5. doi: https://doi.org/10.1021/jo500945k
Robb MJ, Newton B, Fors BP, Hawker CJ. One-step synthesis of unsymmetrical N-alkyl-N'-aryl perylene diimides. J Org Chem. 2014 Jul 03;79(13):6360-5. doi: 10.1021/jo500945k. Epub 2014 Jun 13. PMID: 24927297.
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Showing 1 to 12 of 465 entries