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A framework for teaching the fundamentals of additive manufacturing and enabling rapid innovation

teaching innovation

Hart AJ.
GSID: ETwwuyZj1lAJ
J Go, AJ Hart - Additive Manufacturing, 2016 - Elsevier

… This paper presents our approach to teaching AM at the graduate and advanced undergraduate level, in the form of a 14-week course developed and taught at the Massachusetts Institute of Technology. The lectures begin with in-depth technical analysis...

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Go, J., & Hart, A. J. (2016). A framework for teaching the fundamentals of additive manufacturing and enabling rapid innovation. Additive Manufacturing, 10, 76-87.
Go, Jamison, and A. John Hart. "A framework for teaching the fundamentals of additive manufacturing and enabling rapid innovation." Additive Manufacturing 10 (2016): 76-87.
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Interactive case vignettes utilizing simulated pathologist-clinician encounters with whole slide imaging and video tutorials of whole slide scans improves student understanding of disease processes.

Journal of pathology informatics

Horn AJ, Czarnecki D, Lele SM.
PMID: 23243552
J Pathol Inform. 2012;3:34. doi: 10.4103/2153-3539.101786. Epub 2012 Sep 28.

BACKGROUND: One of the drawbacks of studying pathology in the second year of medical school in a classroom setting is the relatively limited exposure to patient encounters/clinical rotations, making it difficult to understand and fully appreciate the significance of...

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Horn AJ, Czarnecki D, Lele SM. Interactive case vignettes utilizing simulated pathologist-clinician encounters with whole slide imaging and video tutorials of whole slide scans improves student understanding of disease processes. J Pathol Inform. 2012;3:34doi: 10.4103/2153-3539.101786.
Horn, A. J., Czarnecki, D., & Lele, S. M. (2012). Interactive case vignettes utilizing simulated pathologist-clinician encounters with whole slide imaging and video tutorials of whole slide scans improves student understanding of disease processes. Journal of pathology informatics, 334. https://doi.org/10.4103/2153-3539.101786
Horn, Adam J, et al. "Interactive case vignettes utilizing simulated pathologist-clinician encounters with whole slide imaging and video tutorials of whole slide scans improves student understanding of disease processes." Journal of pathology informatics vol. 3 (2012): 34. doi: https://doi.org/10.4103/2153-3539.101786
Horn AJ, Czarnecki D, Lele SM. Interactive case vignettes utilizing simulated pathologist-clinician encounters with whole slide imaging and video tutorials of whole slide scans improves student understanding of disease processes. J Pathol Inform. 2012;3:34. doi: 10.4103/2153-3539.101786. Epub 2012 Sep 28. PMID: 23243552; PMCID: PMC3519009.
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TRIM21 Ubiquitylates SQSTM1/p62 and Suppresses Protein Sequestration to Regulate Redox Homeostasis.

Molecular cell

Pan JA, Sun Y, Jiang YP, Bott AJ, Jaber N, Dou Z, Yang B, Chen JS, Catanzaro JM, Du C, Ding WX, Diaz-Meco MT, Moscat J, Ozato K, Lin RZ, Zong WX.
PMID: 27058791
Mol Cell. 2016 Apr 07;62(1):149-51. doi: 10.1016/j.molcel.2016.03.015.

No abstract available.

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Pan JA, Sun Y, Jiang YP, et al. TRIM21 Ubiquitylates SQSTM1/p62 and Suppresses Protein Sequestration to Regulate Redox Homeostasis. Mol Cell. 2016;62(1):149-51doi: 10.1016/j.molcel.2016.03.015.
Pan, J. A., Sun, Y., Jiang, Y. P., Bott, A. J., Jaber, N., Dou, Z., Yang, B., Chen, J. S., Catanzaro, J. M., Du, C., Ding, W. X., Diaz-Meco, M. T., Moscat, J., Ozato, K., Lin, R. Z., & Zong, W. X. (2016). TRIM21 Ubiquitylates SQSTM1/p62 and Suppresses Protein Sequestration to Regulate Redox Homeostasis. Molecular cell, 62(1), 149-51. https://doi.org/10.1016/j.molcel.2016.03.015
Pan, Ji-An, et al. "TRIM21 Ubiquitylates SQSTM1/p62 and Suppresses Protein Sequestration to Regulate Redox Homeostasis." Molecular cell vol. 62,1 (2016): 149-51. doi: https://doi.org/10.1016/j.molcel.2016.03.015
Pan JA, Sun Y, Jiang YP, Bott AJ, Jaber N, Dou Z, Yang B, Chen JS, Catanzaro JM, Du C, Ding WX, Diaz-Meco MT, Moscat J, Ozato K, Lin RZ, Zong WX. TRIM21 Ubiquitylates SQSTM1/p62 and Suppresses Protein Sequestration to Regulate Redox Homeostasis. Mol Cell. 2016 Apr 07;62(1):149-51. doi: 10.1016/j.molcel.2016.03.015. PMID: 27058791.
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Non-covalent interactions in the multicomponent crystal of 1-aminocyclopentane carboxylic acid, oxalic acid and water: a crystallographic and a theoretical approach.

Acta crystallographica Section B, Structural science, crystal engineering and materials

Mora AJ, Belandria LM, Delgado GE, Seijas LE, Lunar A, Almeida R.
PMID: 28981004
Acta Crystallogr B Struct Sci Cryst Eng Mater. 2017 Oct 01;73:968-980. doi: 10.1107/S2052520617011775. Epub 2017 Sep 29.

Single-crystal X-ray diffraction and quantum mechanical theories were used to examine in detail the subtle nature of non-covalent interactions in the [2:1:1] multicomponent crystal of 1,1-aminocyclopentanecarboxylic acid:oxalic acid:water. The crystal, which is a hydrate salt of the amino acid...

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Mora AJ, Belandria LM, Delgado GE, et al. Non-covalent interactions in the multicomponent crystal of 1-aminocyclopentane carboxylic acid, oxalic acid and water: a crystallographic and a theoretical approach. Acta Crystallogr B Struct Sci Cryst Eng Mater. 2017;73:968-980doi: 10.1107/S2052520617011775.
Mora, A. J., Belandria, L. M., Delgado, G. E., Seijas, L. E., Lunar, A., & Almeida, R. (2017). Non-covalent interactions in the multicomponent crystal of 1-aminocyclopentane carboxylic acid, oxalic acid and water: a crystallographic and a theoretical approach. Acta crystallographica Section B, Structural science, crystal engineering and materials, 73968-980. https://doi.org/10.1107/S2052520617011775
Mora, Asiloé J, et al. "Non-covalent interactions in the multicomponent crystal of 1-aminocyclopentane carboxylic acid, oxalic acid and water: a crystallographic and a theoretical approach." Acta crystallographica Section B, Structural science, crystal engineering and materials vol. 73 (2017): 968-980. doi: https://doi.org/10.1107/S2052520617011775
Mora AJ, Belandria LM, Delgado GE, Seijas LE, Lunar A, Almeida R. Non-covalent interactions in the multicomponent crystal of 1-aminocyclopentane carboxylic acid, oxalic acid and water: a crystallographic and a theoretical approach. Acta Crystallogr B Struct Sci Cryst Eng Mater. 2017 Oct 01;73:968-980. doi: 10.1107/S2052520617011775. Epub 2017 Sep 29. PMID: 28981004.
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Management of metal-on-metal hip implant patients: Who, when and how to revise?.

World journal of orthopedics

Berber R, Skinner JA, Hart AJ.
PMID: 27190754
World J Orthop. 2016 May 18;7(5):272-9. doi: 10.5312/wjo.v7.i5.272. eCollection 2016 May 18.

The debate on how best to manage patients with metal-on-metal (MOM) hip implants continues. With over 1 million patients affected worldwide, the impact is far reaching. The majority of the aggressive failures of MOM hip implants have been dealt...

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Berber R, Skinner JA, Hart AJ. Management of metal-on-metal hip implant patients: Who, when and how to revise?. World J Orthop. 2016;7(5):272-9doi: 10.5312/wjo.v7.i5.272.
Berber, R., Skinner, J. A., & Hart, A. J. (2016). Management of metal-on-metal hip implant patients: Who, when and how to revise?. World journal of orthopedics, 7(5), 272-9. https://doi.org/10.5312/wjo.v7.i5.272
Berber, Reshid, et al. "Management of metal-on-metal hip implant patients: Who, when and how to revise?." World journal of orthopedics vol. 7,5 (2016): 272-9. doi: https://doi.org/10.5312/wjo.v7.i5.272
Berber R, Skinner JA, Hart AJ. Management of metal-on-metal hip implant patients: Who, when and how to revise?. World J Orthop. 2016 May 18;7(5):272-9. doi: 10.5312/wjo.v7.i5.272. eCollection 2016 May 18. PMID: 27190754; PMCID: PMC4865716.
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Conformal Robotic Stereolithography.

3D printing and additive manufacturing

Stevens AG, Oliver CR, Kirchmeyer M, Wu J, Chin L, Polsen ES, Archer C, Boyle C, Garber J, Hart AJ.
PMID: 29577062
3D Print Addit Manuf. 2016 Dec 01;3(4):226-235. doi: 10.1089/3dp.2016.0042.

Additive manufacturing by layerwise photopolymerization, commonly called stereolithography (SLA), is attractive due to its high resolution and diversity of materials chemistry. However, traditional SLA methods are restricted to planar substrates and planar layers that are perpendicular to a single-axis...

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Stevens AG, Oliver CR, Kirchmeyer M, et al. Conformal Robotic Stereolithography. 3D Print Addit Manuf. 2016;3(4):226-235doi: 10.1089/3dp.2016.0042.
Stevens, A. G., Oliver, C. R., Kirchmeyer, M., Wu, J., Chin, L., Polsen, E. S., Archer, C., Boyle, C., Garber, J., & Hart, A. J. (2016). Conformal Robotic Stereolithography. 3D printing and additive manufacturing, 3(4), 226-235. https://doi.org/10.1089/3dp.2016.0042
Stevens, Adam G, et al. "Conformal Robotic Stereolithography." 3D printing and additive manufacturing vol. 3,4 (2016): 226-235. doi: https://doi.org/10.1089/3dp.2016.0042
Stevens AG, Oliver CR, Kirchmeyer M, Wu J, Chin L, Polsen ES, Archer C, Boyle C, Garber J, Hart AJ. Conformal Robotic Stereolithography. 3D Print Addit Manuf. 2016 Dec 01;3(4):226-235. doi: 10.1089/3dp.2016.0042. PMID: 29577062; PMCID: PMC5363219.
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Design of Phthalazinone Amide Histamine H.

ACS medicinal chemistry letters

Procopiou PA, Ford AJ, Gore PM, Looker BE, Hodgson ST, Holmes DS, Vile S, Clark KL, Saunders KA, Slack RJ, Rowedder JE, Watts CJ.
PMID: 28523114
ACS Med Chem Lett. 2017 Apr 21;8(5):577-581. doi: 10.1021/acsmedchemlett.7b00112. eCollection 2017 May 11.

The synthesis of potent amide-containing phthalazinone H

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Procopiou PA, Ford AJ, Gore PM, et al. Design of Phthalazinone Amide Histamine H. ACS Med Chem Lett. 2017;8(5):577-581doi: 10.1021/acsmedchemlett.7b00112.
Procopiou, P. A., Ford, A. J., Gore, P. M., Looker, B. E., Hodgson, S. T., Holmes, D. S., Vile, S., Clark, K. L., Saunders, K. A., Slack, R. J., Rowedder, J. E., & Watts, C. J. (2017). Design of Phthalazinone Amide Histamine H. ACS medicinal chemistry letters, 8(5), 577-581. https://doi.org/10.1021/acsmedchemlett.7b00112
Procopiou, Panayiotis A, et al. "Design of Phthalazinone Amide Histamine H." ACS medicinal chemistry letters vol. 8,5 (2017): 577-581. doi: https://doi.org/10.1021/acsmedchemlett.7b00112
Procopiou PA, Ford AJ, Gore PM, Looker BE, Hodgson ST, Holmes DS, Vile S, Clark KL, Saunders KA, Slack RJ, Rowedder JE, Watts CJ. Design of Phthalazinone Amide Histamine H. ACS Med Chem Lett. 2017 Apr 21;8(5):577-581. doi: 10.1021/acsmedchemlett.7b00112. eCollection 2017 May 11. PMID: 28523114; PMCID: PMC5430406.
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Flavylium based dual photochromism: addressing cis-trans isomerization and ring opening-closure by different light inputs.

Chemical communications (Cambridge, England)

Gago S, Basílio N, Moro AJ, Pina F.
PMID: 25820365
Chem Commun (Camb). 2015 Apr 30;51(34):7349-51. doi: 10.1039/c5cc01677k.

The multistate system of 4',7-dihydroxy-3-methoxyflavylium is constituted by a multiequilibrium involving trans-chalcone, cis-chalcone, hemiketal, flavylium cation and quinoidal base. This system possesses two independently addressable inter-connected photochromic systems based on the cis-trans isomerization and ring opening-closure of the hemiketal.

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Gago S, Basílio N, Moro AJ, et al. Flavylium based dual photochromism: addressing cis-trans isomerization and ring opening-closure by different light inputs. Chem Commun (Camb). 2015;51(34):7349-51doi: 10.1039/c5cc01677k.
Gago, S., Basílio, N., Moro, A. J., & Pina, F. (2015). Flavylium based dual photochromism: addressing cis-trans isomerization and ring opening-closure by different light inputs. Chemical communications (Cambridge, England), 51(34), 7349-51. https://doi.org/10.1039/c5cc01677k
Gago, Sandra, et al. "Flavylium based dual photochromism: addressing cis-trans isomerization and ring opening-closure by different light inputs." Chemical communications (Cambridge, England) vol. 51,34 (2015): 7349-51. doi: https://doi.org/10.1039/c5cc01677k
Gago S, Basílio N, Moro AJ, Pina F. Flavylium based dual photochromism: addressing cis-trans isomerization and ring opening-closure by different light inputs. Chem Commun (Camb). 2015 Apr 30;51(34):7349-51. doi: 10.1039/c5cc01677k. PMID: 25820365.
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Direct fabrication of graphene on SiO2 enabled by thin film stress engineering.

Scientific reports

McNerny DQ, Viswanath B, Copic D, Laye FR, Prohoda C, Brieland-Shoultz AC, Polsen ES, Dee NT, Veerasamy VS, Hart AJ.
PMID: 24854632
Sci Rep. 2014 May 23;4:5049. doi: 10.1038/srep05049.

We demonstrate direct production of graphene on SiO2 by CVD growth of graphene at the interface between a Ni film and the SiO2 substrate, followed by dry mechanical delamination of the Ni using adhesive tape. This result is enabled...

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McNerny DQ, Viswanath B, Copic D, et al. Direct fabrication of graphene on SiO2 enabled by thin film stress engineering. Sci Rep. 2014;4:5049doi: 10.1038/srep05049.
McNerny, D. Q., Viswanath, B., Copic, D., Laye, F. R., Prohoda, C., Brieland-Shoultz, A. C., Polsen, E. S., Dee, N. T., Veerasamy, V. S., & Hart, A. J. (2014). Direct fabrication of graphene on SiO2 enabled by thin film stress engineering. Scientific reports, 45049. https://doi.org/10.1038/srep05049
McNerny, Daniel Q, et al. "Direct fabrication of graphene on SiO2 enabled by thin film stress engineering." Scientific reports vol. 4 (2014): 5049. doi: https://doi.org/10.1038/srep05049
McNerny DQ, Viswanath B, Copic D, Laye FR, Prohoda C, Brieland-Shoultz AC, Polsen ES, Dee NT, Veerasamy VS, Hart AJ. Direct fabrication of graphene on SiO2 enabled by thin film stress engineering. Sci Rep. 2014 May 23;4:5049. doi: 10.1038/srep05049. PMID: 24854632; PMCID: PMC4031480.
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Zwitterionic 4-piperidinecarboxylic acid monohydrate.

Acta crystallographica. Section C, Crystal structure communications

Delgado G, Mora AJ, Bahsas A.
PMID: 11498628
Acta Crystallogr C. 2001 Aug;57:965-7. doi: 10.1107/s0108270101007958. Epub 2001 Aug 09.

The title compound, 4-piperidiniocarboxylate (isonipecotic acid), crystallizes as a zwitterion and incorporates one water molecule, i.e. C(6)H(11)NO(2).H(2)O. The piperidine ring adopts a chair conformation and the alpha-carboxylate group is oriented in the equatorial position. The combination of the interactions...

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Delgado G, Mora AJ, Bahsas A. Zwitterionic 4-piperidinecarboxylic acid monohydrate. Acta Crystallogr C. 2001;57:965-7doi: 10.1107/s0108270101007958.
Delgado, G., Mora, A. J., & Bahsas, A. (2001). Zwitterionic 4-piperidinecarboxylic acid monohydrate. Acta crystallographica. Section C, Crystal structure communications, 57965-7. https://doi.org/10.1107/s0108270101007958
Delgado, G, et al. "Zwitterionic 4-piperidinecarboxylic acid monohydrate." Acta crystallographica. Section C, Crystal structure communications vol. 57 (2001): 965-7. doi: https://doi.org/10.1107/s0108270101007958
Delgado G, Mora AJ, Bahsas A. Zwitterionic 4-piperidinecarboxylic acid monohydrate. Acta Crystallogr C. 2001 Aug;57:965-7. doi: 10.1107/s0108270101007958. Epub 2001 Aug 09. PMID: 11498628.
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Solving larger molecular crystal structures from powder diffraction data by exploiting anisotropic thermal expansion.

Angewandte Chemie (International ed. in English)

Brunelli M, Wright JP, Vaughan GB, Mora AJ, Fitch AN.
PMID: 12746814
Angew Chem Int Ed Engl. 2003 May 09;42(18):2029-32. doi: 10.1002/anie.200250607.

No abstract available.

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Brunelli M, Wright JP, Vaughan GB, et al. Solving larger molecular crystal structures from powder diffraction data by exploiting anisotropic thermal expansion. Angew Chem Int Ed Engl. 2003;42(18):2029-32doi: 10.1002/anie.200250607.
Brunelli, M., Wright, J. P., Vaughan, G. B., Mora, A. J., & Fitch, A. N. (2003). Solving larger molecular crystal structures from powder diffraction data by exploiting anisotropic thermal expansion. Angewandte Chemie (International ed. in English), 42(18), 2029-32. https://doi.org/10.1002/anie.200250607
Brunelli, Michela, et al. "Solving larger molecular crystal structures from powder diffraction data by exploiting anisotropic thermal expansion." Angewandte Chemie (International ed. in English) vol. 42,18 (2003): 2029-32. doi: https://doi.org/10.1002/anie.200250607
Brunelli M, Wright JP, Vaughan GB, Mora AJ, Fitch AN. Solving larger molecular crystal structures from powder diffraction data by exploiting anisotropic thermal expansion. Angew Chem Int Ed Engl. 2003 May 09;42(18):2029-32. doi: 10.1002/anie.200250607. PMID: 12746814.
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Effects of temperature on the establishment potential of the predatory mite Amblyseius californicus McGregor (Acari: Phytoseiidae) in the UK.

Journal of insect physiology

Hart AJ, Bale JS, Tullett AG, Worland MR, Walters KF.
PMID: 12770070
J Insect Physiol. 2002 Jun;48(6):593-599. doi: 10.1016/s0022-1910(02)00087-2.

Amblyseius californicus was introduced into the UK in the early 1990s as a biocontrol agent against glasshouse red spider mite Tetranychus urticae. This study investigated the effects of temperature on the establishment potential of A. californicus in the UK...

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Hart AJ, Bale JS, Tullett AG, et al. Effects of temperature on the establishment potential of the predatory mite Amblyseius californicus McGregor (Acari: Phytoseiidae) in the UK. J Insect Physiol. 2002;48(6):593-599doi: 10.1016/s0022-1910(02)00087-2.
Hart, A. J., Bale, J. S., Tullett, A. G., Worland, M. R., & Walters, K. F. (2002). Effects of temperature on the establishment potential of the predatory mite Amblyseius californicus McGregor (Acari: Phytoseiidae) in the UK. Journal of insect physiology, 48(6), 593-599. https://doi.org/10.1016/s0022-1910(02)00087-2
Hart, A J., et al. "Effects of temperature on the establishment potential of the predatory mite Amblyseius californicus McGregor (Acari: Phytoseiidae) in the UK." Journal of insect physiology vol. 48,6 (2002): 593-599. doi: https://doi.org/10.1016/s0022-1910(02)00087-2
Hart AJ, Bale JS, Tullett AG, Worland MR, Walters KF. Effects of temperature on the establishment potential of the predatory mite Amblyseius californicus McGregor (Acari: Phytoseiidae) in the UK. J Insect Physiol. 2002 Jun;48(6):593-599. doi: 10.1016/s0022-1910(02)00087-2. PMID: 12770070.
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Showing 1 to 12 of 378 entries