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Shirley was the one bad apple on our unit.

NursingLife

Millen AH.
PMID: 3851216
Nurs Life. 1985 Nov-Dec;5(6):22-3.

No abstract available.

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Millen AH. Shirley was the one bad apple on our unit. Nurs Life. 1985;5(6):22-3
Millen, A. H. (1985). Shirley was the one bad apple on our unit. NursingLife, 5(6), 22-3.
Millen, A H. "Shirley was the one bad apple on our unit." NursingLife vol. 5,6 (1985): 22-3.
Millen AH. Shirley was the one bad apple on our unit. Nurs Life. 1985 Nov-Dec;5(6):22-3. PMID: 3851216.
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The evolutionary legacy of size-selective harvesting extends from genes to populations.

Evolutionary applications

Uusi-Heikkilä S, Whiteley AR, Kuparinen A, Matsumura S, Venturelli PA, Wolter C, Slate J, Primmer CR, Meinelt T, Killen SS, Bierbach D, Polverino G, Ludwig A, Arlinghaus R.
PMID: 26136825
Evol Appl. 2015 Jul;8(6):597-620. doi: 10.1111/eva.12268. Epub 2015 May 27.

Size-selective harvesting is assumed to alter life histories of exploited fish populations, thereby negatively affecting population productivity, recovery, and yield. However, demonstrating that fisheries-induced phenotypic changes in the wild are at least partly genetically determined has proved notoriously difficult....

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Uusi-Heikkilä S, Whiteley AR, Kuparinen A, et al. The evolutionary legacy of size-selective harvesting extends from genes to populations. Evol Appl. 2015;8(6):597-620doi: 10.1111/eva.12268.
Uusi-Heikkilä, S., Whiteley, A. R., Kuparinen, A., Matsumura, S., Venturelli, P. A., Wolter, C., Slate, J., Primmer, C. R., Meinelt, T., Killen, S. S., Bierbach, D., Polverino, G., Ludwig, A., & Arlinghaus, R. (2015). The evolutionary legacy of size-selective harvesting extends from genes to populations. Evolutionary applications, 8(6), 597-620. https://doi.org/10.1111/eva.12268
Uusi-Heikkilä, Silva, et al. "The evolutionary legacy of size-selective harvesting extends from genes to populations." Evolutionary applications vol. 8,6 (2015): 597-620. doi: https://doi.org/10.1111/eva.12268
Uusi-Heikkilä S, Whiteley AR, Kuparinen A, Matsumura S, Venturelli PA, Wolter C, Slate J, Primmer CR, Meinelt T, Killen SS, Bierbach D, Polverino G, Ludwig A, Arlinghaus R. The evolutionary legacy of size-selective harvesting extends from genes to populations. Evol Appl. 2015 Jul;8(6):597-620. doi: 10.1111/eva.12268. Epub 2015 May 27. PMID: 26136825; PMCID: PMC4479515.
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Draft Genome Sequence of Alteromonas macleodii Strain MIT1002, Isolated from an Enrichment Culture of the Marine Cyanobacterium Prochlorococcus.

Genome announcements

Biller SJ, Coe A, Martin-Cuadrado AB, Chisholm SW.
PMID: 26316635
Genome Announc. 2015 Aug 27;3(4). doi: 10.1128/genomeA.00967-15.

Alteromonas spp. are heterotrophic gammaproteobacteria commonly found in marine environments. We present here the draft genome sequence of Alteromonas macleodii MIT1002, which was isolated from an enrichment culture of the marine cyanobacterium Prochlorococcus NATL2A. This genome contains a mixture...

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Biller SJ, Coe A, Martin-Cuadrado AB, et al. Draft Genome Sequence of Alteromonas macleodii Strain MIT1002, Isolated from an Enrichment Culture of the Marine Cyanobacterium Prochlorococcus. Genome Announc. 2015;3(4)doi: 10.1128/genomeA.00967-15.
Biller, S. J., Coe, A., Martin-Cuadrado, A. B., & Chisholm, S. W. (2015). Draft Genome Sequence of Alteromonas macleodii Strain MIT1002, Isolated from an Enrichment Culture of the Marine Cyanobacterium Prochlorococcus. Genome announcements, 3(4), . https://doi.org/10.1128/genomeA.00967-15
Biller, Steven J, et al. "Draft Genome Sequence of Alteromonas macleodii Strain MIT1002, Isolated from an Enrichment Culture of the Marine Cyanobacterium Prochlorococcus." Genome announcements vol. 3,4 (2015). doi: https://doi.org/10.1128/genomeA.00967-15
Biller SJ, Coe A, Martin-Cuadrado AB, Chisholm SW. Draft Genome Sequence of Alteromonas macleodii Strain MIT1002, Isolated from an Enrichment Culture of the Marine Cyanobacterium Prochlorococcus. Genome Announc. 2015 Aug 27;3(4). doi: 10.1128/genomeA.00967-15. PMID: 26316635; PMCID: PMC4551879.
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A Synergistic Combinatorial and Chiroptical Study of Peptide Catalysts for Asymmetric Baeyer-Villiger Oxidation.

Advanced synthesis & catalysis

Giuliano MW, Lin CY, Romney DK, Miller SJ, Anslyn EV.
PMID: 26543444
Adv Synth Catal. 2015 Jul 06;357(10):2301-2309. doi: 10.1002/adsc.201500230. Epub 2015 Jul 14.

We report an approach to the asymmetric Baeyer-Villiger oxidation utilizing bioinformatics-inspired combinatorial screening for catalyst discovery. Scaled-up validation of our on-bead efforts with a circular dichroism-based assay of alcohols derived from the products of solution-phase reactions established the absolute...

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Giuliano MW, Lin CY, Romney DK, et al. A Synergistic Combinatorial and Chiroptical Study of Peptide Catalysts for Asymmetric Baeyer-Villiger Oxidation. Adv Synth Catal. 2015;357(10):2301-2309doi: 10.1002/adsc.201500230.
Giuliano, M. W., Lin, C. Y., Romney, D. K., Miller, S. J., & Anslyn, E. V. (2015). A Synergistic Combinatorial and Chiroptical Study of Peptide Catalysts for Asymmetric Baeyer-Villiger Oxidation. Advanced synthesis & catalysis, 357(10), 2301-2309. https://doi.org/10.1002/adsc.201500230
Giuliano, Michael W, et al. "A Synergistic Combinatorial and Chiroptical Study of Peptide Catalysts for Asymmetric Baeyer-Villiger Oxidation." Advanced synthesis & catalysis vol. 357,10 (2015): 2301-2309. doi: https://doi.org/10.1002/adsc.201500230
Giuliano MW, Lin CY, Romney DK, Miller SJ, Anslyn EV. A Synergistic Combinatorial and Chiroptical Study of Peptide Catalysts for Asymmetric Baeyer-Villiger Oxidation. Adv Synth Catal. 2015 Jul 06;357(10):2301-2309. doi: 10.1002/adsc.201500230. Epub 2015 Jul 14. PMID: 26543444; PMCID: PMC4629862.
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Cavity cooling a single charged levitated nanosphere.

Physical review letters

Millen J, Fonseca PZ, Mavrogordatos T, Monteiro TS, Barker PF.
PMID: 25860743
Phys Rev Lett. 2015 Mar 27;114(12):123602. doi: 10.1103/PhysRevLett.114.123602. Epub 2015 Mar 27.

Optomechanical cavity cooling of levitated objects offers the possibility for laboratory investigation of the macroscopic quantum behavior of systems that are largely decoupled from their environment. However, experimental progress has been hindered by particle loss mechanisms, which have prevented...

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Millen J, Fonseca PZ, Mavrogordatos T, et al. Cavity cooling a single charged levitated nanosphere. Phys Rev Lett. 2015;114(12):123602doi: 10.1103/PhysRevLett.114.123602.
Millen, J., Fonseca, P. Z., Mavrogordatos, T., Monteiro, T. S., & Barker, P. F. (2015). Cavity cooling a single charged levitated nanosphere. Physical review letters, 114(12), 123602. https://doi.org/10.1103/PhysRevLett.114.123602
Millen, J, et al. "Cavity cooling a single charged levitated nanosphere." Physical review letters vol. 114,12 (2015): 123602. doi: https://doi.org/10.1103/PhysRevLett.114.123602
Millen J, Fonseca PZ, Mavrogordatos T, Monteiro TS, Barker PF. Cavity cooling a single charged levitated nanosphere. Phys Rev Lett. 2015 Mar 27;114(12):123602. doi: 10.1103/PhysRevLett.114.123602. Epub 2015 Mar 27. PMID: 25860743.
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[Dual genetic encoding of acetyl-lysine and non-deacetylatablethioacetyl-lysine mediated by flexizyme].

Angewandte Chemie (Weinheim an der Bergstrasse, Germany)

Xiong H, Reynolds NM, Fan C, Englert M, Hoyer D, Miller SJ, Söll D.
PMID: 27330229
Angew Chem Weinheim Bergstr Ger. 2016 Mar 14;128(12):4151-4154. doi: 10.1002/ange.201511750. Epub 2016 Feb 23.

No abstract available.

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Xiong H, Reynolds NM, Fan C, et al. Duale genetische Kodierung von Acetyllysin und nicht-hydrolysierbarem Thioacetyllysin mittels Flexizym. [Dual genetic encoding of acetyl-lysine and non-deacetylatablethioacetyl-lysine mediated by flexizyme]. Angew Chem Weinheim Bergstr Ger. 2016;128(12):4151-4154doi: 10.1002/ange.201511750.
Xiong, H., Reynolds, N. M., Fan, C., Englert, M., Hoyer, D., Miller, S. J., & Söll, D. (2016). Duale genetische Kodierung von Acetyllysin und nicht-hydrolysierbarem Thioacetyllysin mittels Flexizym. [Dual genetic encoding of acetyl-lysine and non-deacetylatablethioacetyl-lysine mediated by flexizyme]. Angewandte Chemie (Weinheim an der Bergstrasse, Germany), 128(12), 4151-4154. https://doi.org/10.1002/ange.201511750
Xiong, Hai, et al. "Duale genetische Kodierung von Acetyllysin und nicht-hydrolysierbarem Thioacetyllysin mittels Flexizym." [Dual genetic encoding of acetyl-lysine and non-deacetylatablethioacetyl-lysine mediated by flexizyme]. Angewandte Chemie (Weinheim an der Bergstrasse, Germany) vol. 128,12 (2016): 4151-4154. doi: https://doi.org/10.1002/ange.201511750
Xiong H, Reynolds NM, Fan C, Englert M, Hoyer D, Miller SJ, Söll D. Duale genetische Kodierung von Acetyllysin und nicht-hydrolysierbarem Thioacetyllysin mittels Flexizym. [Dual genetic encoding of acetyl-lysine and non-deacetylatablethioacetyl-lysine mediated by flexizyme]. Angew Chem Weinheim Bergstr Ger. 2016 Mar 14;128(12):4151-4154. doi: 10.1002/ange.201511750. Epub 2016 Feb 23. German. PMID: 27330229; PMCID: PMC4909261.
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Fish swimming in schools save energy regardless of their spatial position.

Behavioral ecology and sociobiology

Marras S, Killen SS, Lindström J, McKenzie DJ, Steffensen JF, Domenici P.
PMID: 25620833
Behav Ecol Sociobiol. 2015;69:219-226. doi: 10.1007/s00265-014-1834-4. Epub 2014 Oct 30.

For animals, being a member of a group provides various advantages, such as reduced vulnerability to predators, increased foraging opportunities and reduced energetic costs of locomotion. In moving groups such as fish schools, there are benefits of group membership...

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Marras S, Killen SS, Lindström J, et al. Fish swimming in schools save energy regardless of their spatial position. Behav Ecol Sociobiol. 2014;69:219-226doi: 10.1007/s00265-014-1834-4.
Marras, S., Killen, S. S., Lindström, J., McKenzie, D. J., Steffensen, J. F., & Domenici, P. (2015). Fish swimming in schools save energy regardless of their spatial position. Behavioral ecology and sociobiology, 69219-226. https://doi.org/10.1007/s00265-014-1834-4
Marras, Stefano, et al. "Fish swimming in schools save energy regardless of their spatial position." Behavioral ecology and sociobiology vol. 69 (2015): 219-226. doi: https://doi.org/10.1007/s00265-014-1834-4
Marras S, Killen SS, Lindström J, McKenzie DJ, Steffensen JF, Domenici P. Fish swimming in schools save energy regardless of their spatial position. Behav Ecol Sociobiol. 2015;69:219-226. doi: 10.1007/s00265-014-1834-4. Epub 2014 Oct 30. PMID: 25620833; PMCID: PMC4293471.
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Production, analysis, and application of spatially resolved shells in solid-phase polymer spheres.

Journal of the American Chemical Society

Farrer RA, Copeland GT, Previte MJ, Okamoto MM, Miller SJ, Fourkas JT.
PMID: 11866613
J Am Chem Soc. 2002 Mar 06;124(9):1994-2003. doi: 10.1021/ja011675k.

Two-photon fluorescence microscopy has been used to interrogate the interior functionality of polymer resin beads. By employing this technique, the spatial distribution of the initial functionality contained within the polymer matrix has been determined. Spatially resolved, concentric shells were...

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Farrer RA, Copeland GT, Previte MJ, et al. Production, analysis, and application of spatially resolved shells in solid-phase polymer spheres. J Am Chem Soc. 2002;124(9):1994-2003doi: 10.1021/ja011675k.
Farrer, R. A., Copeland, G. T., Previte, M. J., Okamoto, M. M., Miller, S. J., & Fourkas, J. T. (2002). Production, analysis, and application of spatially resolved shells in solid-phase polymer spheres. Journal of the American Chemical Society, 124(9), 1994-2003. https://doi.org/10.1021/ja011675k
Farrer, Richard A, et al. "Production, analysis, and application of spatially resolved shells in solid-phase polymer spheres." Journal of the American Chemical Society vol. 124,9 (2002): 1994-2003. doi: https://doi.org/10.1021/ja011675k
Farrer RA, Copeland GT, Previte MJ, Okamoto MM, Miller SJ, Fourkas JT. Production, analysis, and application of spatially resolved shells in solid-phase polymer spheres. J Am Chem Soc. 2002 Mar 06;124(9):1994-2003. doi: 10.1021/ja011675k. PMID: 11866613.
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Commentary.

Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.]

Miller SJ.
PMID: 10691952
Dermatol Surg. 2000 Feb;26(2):165-6. doi: 10.1046/j.1524-4725.2000.00802-2.x.

No abstract available.

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Miller SJ. Commentary. Dermatol Surg. 2000;26(2):165-6doi: 10.1046/j.1524-4725.2000.00802-2.x.
Miller, S. J. (2000). Commentary. Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.], 26(2), 165-6. https://doi.org/10.1046/j.1524-4725.2000.00802-2.x
Miller. "Commentary." Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.] vol. 26,2 (2000): 165-6. doi: https://doi.org/10.1046/j.1524-4725.2000.00802-2.x
Miller SJ. Commentary. Dermatol Surg. 2000 Feb;26(2):165-6. doi: 10.1046/j.1524-4725.2000.00802-2.x. PMID: 10691952.
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Nucleophilic chiral amines as catalysts in asymmetric synthesis.

Chemical reviews

France S, Guerin DJ, Miller SJ, Lectka T.
PMID: 12914489
Chem Rev. 2003 Aug;103(8):2985-3012. doi: 10.1021/cr020061a.

No abstract available.

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France S, Guerin DJ, Miller SJ, et al. Nucleophilic chiral amines as catalysts in asymmetric synthesis. Chem Rev. 2003;103(8):2985-3012doi: 10.1021/cr020061a.
France, S., Guerin, D. J., Miller, S. J., & Lectka, T. (2003). Nucleophilic chiral amines as catalysts in asymmetric synthesis. Chemical reviews, 103(8), 2985-3012. https://doi.org/10.1021/cr020061a
France, Stefan, et al. "Nucleophilic chiral amines as catalysts in asymmetric synthesis." Chemical reviews vol. 103,8 (2003): 2985-3012. doi: https://doi.org/10.1021/cr020061a
France S, Guerin DJ, Miller SJ, Lectka T. Nucleophilic chiral amines as catalysts in asymmetric synthesis. Chem Rev. 2003 Aug;103(8):2985-3012. doi: 10.1021/cr020061a. PMID: 12914489.
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Amine-catalyzed coupling of allenic esters to alpha,beta-unsaturated carbonyls.

Journal of the American Chemical Society

Evans CA, Miller SJ.
PMID: 14531667
J Am Chem Soc. 2003 Oct 15;125(41):12394-5. doi: 10.1021/ja0377798.

Nucleophilic amines catalyze the 1,4-addition of allenic esters to alpha,beta-unsaturated carbonyl compounds. The reactions proceed under mild conditions. In addition, Baylis-Hillman products serve as appropriate electrophiles for the process such that a one-pot, three-component coupling of aldehydes, acrylates, and...

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Evans CA, Miller SJ. Amine-catalyzed coupling of allenic esters to alpha,beta-unsaturated carbonyls. J Am Chem Soc. 2003;125(41):12394-5doi: 10.1021/ja0377798.
Evans, C. A., & Miller, S. J. (2003). Amine-catalyzed coupling of allenic esters to alpha,beta-unsaturated carbonyls. Journal of the American Chemical Society, 125(41), 12394-5. https://doi.org/10.1021/ja0377798
Evans, Catherine A, and Miller, Scott J. "Amine-catalyzed coupling of allenic esters to alpha,beta-unsaturated carbonyls." Journal of the American Chemical Society vol. 125,41 (2003): 12394-5. doi: https://doi.org/10.1021/ja0377798
Evans CA, Miller SJ. Amine-catalyzed coupling of allenic esters to alpha,beta-unsaturated carbonyls. J Am Chem Soc. 2003 Oct 15;125(41):12394-5. doi: 10.1021/ja0377798. PMID: 14531667.
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Catalytic enantioselective synthesis of sulfinate esters through the dynamic resolution of tert-butanesulfinyl chloride.

Journal of the American Chemical Society

Evans JW, Fierman MB, Miller SJ, Ellman JA.
PMID: 15225052
J Am Chem Soc. 2004 Jul 07;126(26):8134-5. doi: 10.1021/ja047845l.

Development of a new synthetic route to obtain enantiomerically enriched tert-butanesulfinate esters in excellent yields through catalytic enantioselective sulfinyl transfer is described. As little as 0.5 mol % of chiral amine catalysts was used to couple racemic tert-butanesulfinyl chloride...

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Evans JW, Fierman MB, Miller SJ, et al. Catalytic enantioselective synthesis of sulfinate esters through the dynamic resolution of tert-butanesulfinyl chloride. J Am Chem Soc. 2004;126(26):8134-5doi: 10.1021/ja047845l.
Evans, J. W., Fierman, M. B., Miller, S. J., & Ellman, J. A. (2004). Catalytic enantioselective synthesis of sulfinate esters through the dynamic resolution of tert-butanesulfinyl chloride. Journal of the American Chemical Society, 126(26), 8134-5. https://doi.org/10.1021/ja047845l
Evans, Jared W, et al. "Catalytic enantioselective synthesis of sulfinate esters through the dynamic resolution of tert-butanesulfinyl chloride." Journal of the American Chemical Society vol. 126,26 (2004): 8134-5. doi: https://doi.org/10.1021/ja047845l
Evans JW, Fierman MB, Miller SJ, Ellman JA. Catalytic enantioselective synthesis of sulfinate esters through the dynamic resolution of tert-butanesulfinyl chloride. J Am Chem Soc. 2004 Jul 07;126(26):8134-5. doi: 10.1021/ja047845l. PMID: 15225052.
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Showing 1 to 12 of 340 entries