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Nonlocal response functions for predicting shear flow of strongly inhomogeneous fluids. I. Sinusoidally driven shear and sinusoidally driven inhomogeneity.

Physical review. E, Statistical, nonlinear, and soft matter physics

Glavatskiy KS, Dalton BA, Daivis PJ, Todd BD.
PMID: 26172686
Phys Rev E Stat Nonlin Soft Matter Phys. 2015 Jun;91(6):062132. doi: 10.1103/PhysRevE.91.062132. Epub 2015 Jun 22.

We present theoretical expressions for the density, strain rate, and shear pressure profiles in strongly inhomogeneous fluids undergoing steady shear flow with periodic boundary conditions. The expressions that we obtain take the form of truncated functional expansions. In these...

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Glavatskiy KS, Dalton BA, Daivis PJ, et al. Nonlocal response functions for predicting shear flow of strongly inhomogeneous fluids. I. Sinusoidally driven shear and sinusoidally driven inhomogeneity. Phys Rev E Stat Nonlin Soft Matter Phys. 2015;91(6):062132doi: 10.1103/PhysRevE.91.062132.
Glavatskiy, K. S., Dalton, B. A., Daivis, P. J., & Todd, B. D. (2015). Nonlocal response functions for predicting shear flow of strongly inhomogeneous fluids. I. Sinusoidally driven shear and sinusoidally driven inhomogeneity. Physical review. E, Statistical, nonlinear, and soft matter physics, 91(6), 062132. https://doi.org/10.1103/PhysRevE.91.062132
Glavatskiy, Kirill S, et al. "Nonlocal response functions for predicting shear flow of strongly inhomogeneous fluids. I. Sinusoidally driven shear and sinusoidally driven inhomogeneity." Physical review. E, Statistical, nonlinear, and soft matter physics vol. 91,6 (2015): 062132. doi: https://doi.org/10.1103/PhysRevE.91.062132
Glavatskiy KS, Dalton BA, Daivis PJ, Todd BD. Nonlocal response functions for predicting shear flow of strongly inhomogeneous fluids. I. Sinusoidally driven shear and sinusoidally driven inhomogeneity. Phys Rev E Stat Nonlin Soft Matter Phys. 2015 Jun;91(6):062132. doi: 10.1103/PhysRevE.91.062132. Epub 2015 Jun 22. PMID: 26172686.
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Guidelines for pharmacists integrating into primary care teams.

Canadian pharmacists journal : CPJ = Revue des pharmaciens du Canada : RPC

Jorgenson D, Dalton D, Farrell B, Tsuyuki RT, Dolovich L.
PMID: 24228050
Can Pharm J (Ott). 2013 Nov;146(6):342-52. doi: 10.1177/1715163513504528.

No abstract available.

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Jorgenson D, Dalton D, Farrell B, et al. Guidelines for pharmacists integrating into primary care teams. Can Pharm J (Ott). 2013;146(6):342-52doi: 10.1177/1715163513504528.
Jorgenson, D., Dalton, D., Farrell, B., Tsuyuki, R. T., & Dolovich, L. (2013). Guidelines for pharmacists integrating into primary care teams. Canadian pharmacists journal : CPJ = Revue des pharmaciens du Canada : RPC, 146(6), 342-52. https://doi.org/10.1177/1715163513504528
Jorgenson, Derek, et al. "Guidelines for pharmacists integrating into primary care teams." Canadian pharmacists journal : CPJ = Revue des pharmaciens du Canada : RPC vol. 146,6 (2013): 342-52. doi: https://doi.org/10.1177/1715163513504528
Jorgenson D, Dalton D, Farrell B, Tsuyuki RT, Dolovich L. Guidelines for pharmacists integrating into primary care teams. Can Pharm J (Ott). 2013 Nov;146(6):342-52. doi: 10.1177/1715163513504528. PMID: 24228050; PMCID: PMC3819955.
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Orthogonal breaking and forming of dynamic covalent imine and disulfide bonds in aqueous solution.

Chemical communications (Cambridge, England)

Bracchi ME, Fulton DA.
PMID: 26067447
Chem Commun (Camb). 2015 Jul 14;51(55):11052-5. doi: 10.1039/c5cc02716k.

Orthogonal bond-breaking and forming of dynamic covalent disulfide and imine bonds in aqueous solution is demonstrated. Through judicious choice of reaction partners and conditions, it is possible to cleave and reform selectively these bonds in the presence of each...

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Bracchi ME, Fulton DA. Orthogonal breaking and forming of dynamic covalent imine and disulfide bonds in aqueous solution. Chem Commun (Camb). 2015;51(55):11052-5doi: 10.1039/c5cc02716k.
Bracchi, M. E., & Fulton, D. A. (2015). Orthogonal breaking and forming of dynamic covalent imine and disulfide bonds in aqueous solution. Chemical communications (Cambridge, England), 51(55), 11052-5. https://doi.org/10.1039/c5cc02716k
Bracchi, Michael E, and Fulton, David A. "Orthogonal breaking and forming of dynamic covalent imine and disulfide bonds in aqueous solution." Chemical communications (Cambridge, England) vol. 51,55 (2015): 11052-5. doi: https://doi.org/10.1039/c5cc02716k
Bracchi ME, Fulton DA. Orthogonal breaking and forming of dynamic covalent imine and disulfide bonds in aqueous solution. Chem Commun (Camb). 2015 Jul 14;51(55):11052-5. doi: 10.1039/c5cc02716k. PMID: 26067447.
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The Efficient, Enantioselective Synthesis of Aza Sugars from Amino Acids. 1. The Polyhydroxylated Pyrrolidines.

The Journal of organic chemistry

Huang Y, Dalton DR, Carroll PJ.
PMID: 11671412
J Org Chem. 1997 Jan 24;62(2):372-376. doi: 10.1021/jo962028s.

Beginning with (+)-serine or (-)-serine, as appropriate, convenient, high-yield, enantioselective synthesis of all eight stereoisomeric 2-hydroxymethyl-3,4-dihydroxypyrrolidines (the enantiomeric pairs of iminoribitol, -arabinitol, -xylitol, and -lyxitol) can be effected. The absolute configuration of the starting amino acid defines the set...

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Huang Y, Dalton DR, Carroll PJ. The Efficient, Enantioselective Synthesis of Aza Sugars from Amino Acids. 1. The Polyhydroxylated Pyrrolidines. J Org Chem. 1997;62(2):372-376doi: 10.1021/jo962028s.
Huang, Y., Dalton, D. R., & Carroll, P. J. (1997). The Efficient, Enantioselective Synthesis of Aza Sugars from Amino Acids. 1. The Polyhydroxylated Pyrrolidines. The Journal of organic chemistry, 62(2), 372-376. https://doi.org/10.1021/jo962028s
Huang, Yifang, et al. "The Efficient, Enantioselective Synthesis of Aza Sugars from Amino Acids. 1. The Polyhydroxylated Pyrrolidines." The Journal of organic chemistry vol. 62,2 (1997): 372-376. doi: https://doi.org/10.1021/jo962028s
Huang Y, Dalton DR, Carroll PJ. The Efficient, Enantioselective Synthesis of Aza Sugars from Amino Acids. 1. The Polyhydroxylated Pyrrolidines. J Org Chem. 1997 Jan 24;62(2):372-376. doi: 10.1021/jo962028s. PMID: 11671412.
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British Empire Cancer Campaign.

Nature

GALTON DA.
PMID: 18888169
Nature. 1948 Oct 23;162(4121):664. doi: 10.1038/162664a0.

No abstract available.

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GALTON DA. British Empire Cancer Campaign. Nature. 1948;162(4121):664doi: 10.1038/162664a0.
GALTON, D. A. (1948). British Empire Cancer Campaign. Nature, 162(4121), 664. https://doi.org/10.1038/162664a0
GALTON, D A G. "British Empire Cancer Campaign." Nature vol. 162,4121 (1948): 664. doi: https://doi.org/10.1038/162664a0
GALTON DA. British Empire Cancer Campaign. Nature. 1948 Oct 23;162(4121):664. doi: 10.1038/162664a0. PMID: 18888169.
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On the role of the counter-ion in defining water structure and dynamics: order, structure and dynamics in hydrophilic and hydrophobic gadolinium salt complexes.

Dalton transactions (Cambridge, England : 2003)

Thompson AL, Parker D, Fulton DA, Howard JA, Pandya SU, Puschmann H, Senanayake K, Stenson PA, Badari A, Botta M, Avedano S, Aime S.
PMID: 17225897
Dalton Trans. 2006 Dec 21;(47):5605-16. doi: 10.1039/b606206g. Epub 2006 Aug 25.

The crystal structures of the hydrated salts of [Gd.DOTAM]3+ and its more hydrophobic derivative [Gd.]3+, bearing 4 alpha-phenylethyl groups, (both Gd and Yb salts) are reported and compared. The nature of the anion determines the degree of ordering in...

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Thompson AL, Parker D, Fulton DA, et al. On the role of the counter-ion in defining water structure and dynamics: order, structure and dynamics in hydrophilic and hydrophobic gadolinium salt complexes. Dalton Trans. 2006;(47):5605-16doi: 10.1039/b606206g.
Thompson, A. L., Parker, D., Fulton, D. A., Howard, J. A., Pandya, S. U., Puschmann, H., Senanayake, K., Stenson, P. A., Badari, A., Botta, M., Avedano, S., & Aime, S. (2006). On the role of the counter-ion in defining water structure and dynamics: order, structure and dynamics in hydrophilic and hydrophobic gadolinium salt complexes. Dalton transactions (Cambridge, England : 2003), (47), 5605-16. https://doi.org/10.1039/b606206g
Thompson, Amber L, et al. "On the role of the counter-ion in defining water structure and dynamics: order, structure and dynamics in hydrophilic and hydrophobic gadolinium salt complexes." Dalton transactions (Cambridge, England : 2003) vol. ,47 (2006): 5605-16. doi: https://doi.org/10.1039/b606206g
Thompson AL, Parker D, Fulton DA, Howard JA, Pandya SU, Puschmann H, Senanayake K, Stenson PA, Badari A, Botta M, Avedano S, Aime S. On the role of the counter-ion in defining water structure and dynamics: order, structure and dynamics in hydrophilic and hydrophobic gadolinium salt complexes. Dalton Trans. 2006 Dec 21;(47):5605-16. doi: 10.1039/b606206g. Epub 2006 Aug 25. PMID: 17225897.
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Specificity of Reductive Dehalogenation of Substituted ortho-Chlorophenols by Desulfitobacterium dehalogenans JW/IU-DC1.

Applied and environmental microbiology

Utkin I, Dalton DD, Wiegel J.
PMID: 16535014
Appl Environ Microbiol. 1995 Apr;61(4):1677. doi: 10.1128/aem.61.4.1677-1677c.1995.

Volume 61, no. 1, abstract, lines 4 and 5: "2,6-dichloro-4-R-phenols, where . . ." should read "2,6-dichloro-4-R-phenols (2,6-DCl-4-RPs, where R is -H, -F, -Cl, -NO(inf2), -CO(inf2)(sup-), or -COOCH(inf3)) . . ." Line 6: ". . . bromophenols (2-BrP, 2,6-DBrP,...

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Utkin I, Dalton DD, Wiegel J. Specificity of Reductive Dehalogenation of Substituted ortho-Chlorophenols by Desulfitobacterium dehalogenans JW/IU-DC1. Appl Environ Microbiol. 1995;61(4):1677doi: 10.1128/aem.61.4.1677-1677c.1995.
Utkin, I., Dalton, D. D., & Wiegel, J. (1995). Specificity of Reductive Dehalogenation of Substituted ortho-Chlorophenols by Desulfitobacterium dehalogenans JW/IU-DC1. Applied and environmental microbiology, 61(4), 1677. https://doi.org/10.1128/aem.61.4.1677-1677c.1995
Utkin, I, et al. "Specificity of Reductive Dehalogenation of Substituted ortho-Chlorophenols by Desulfitobacterium dehalogenans JW/IU-DC1." Applied and environmental microbiology vol. 61,4 (1995): 1677. doi: https://doi.org/10.1128/aem.61.4.1677-1677c.1995
Utkin I, Dalton DD, Wiegel J. Specificity of Reductive Dehalogenation of Substituted ortho-Chlorophenols by Desulfitobacterium dehalogenans JW/IU-DC1. Appl Environ Microbiol. 1995 Apr;61(4):1677. doi: 10.1128/aem.61.4.1677-1677c.1995. PMID: 16535014; PMCID: PMC1388432.
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Narrowing down the role of common variants in the genetic predisposition to obesity.

Genome medicine

Calton MA, Vaisse C.
PMID: 19341502
Genome Med. 2009 Mar 11;1(3):31. doi: 10.1186/gm31.

The extent to which common variants contribute to common phenotypes and disease in humans has important consequences for the future of medical genomics. Two reports have recently clarified this issue for one of the most pressing public health concerns,...

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Calton MA, Vaisse C. Narrowing down the role of common variants in the genetic predisposition to obesity. Genome Med. 2009;1(3):31doi: 10.1186/gm31.
Calton, M. A., & Vaisse, C. (2009). Narrowing down the role of common variants in the genetic predisposition to obesity. Genome medicine, 1(3), 31. https://doi.org/10.1186/gm31
Calton, Melissa A, and Vaisse, Christian. "Narrowing down the role of common variants in the genetic predisposition to obesity." Genome medicine vol. 1,3 (2009): 31. doi: https://doi.org/10.1186/gm31
Calton MA, Vaisse C. Narrowing down the role of common variants in the genetic predisposition to obesity. Genome Med. 2009 Mar 11;1(3):31. doi: 10.1186/gm31. PMID: 19341502; PMCID: PMC2664942.
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X-ray diffraction in the pulsed laser heated diamond anvil cell.

The Review of scientific instruments

Goncharov AF, Prakapenka VB, Struzhkin VV, Kantor I, Rivers ML, Dalton DA.
PMID: 21133481
Rev Sci Instrum. 2010 Nov;81(11):113902. doi: 10.1063/1.3499358.

We have developed in situ x-ray synchrotron diffraction measurements of samples heated by a pulsed laser in the diamond anvil cell at pressure up to 60 GPa. We used an electronically modulated 2-10 kHz repetition rate, 1064-1075 nm fiber...

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Goncharov AF, Prakapenka VB, Struzhkin VV, et al. X-ray diffraction in the pulsed laser heated diamond anvil cell. Rev Sci Instrum. 2010;81(11):113902doi: 10.1063/1.3499358.
Goncharov, A. F., Prakapenka, V. B., Struzhkin, V. V., Kantor, I., Rivers, M. L., & Dalton, D. A. (2010). X-ray diffraction in the pulsed laser heated diamond anvil cell. The Review of scientific instruments, 81(11), 113902. https://doi.org/10.1063/1.3499358
Goncharov, Alexander F, et al. "X-ray diffraction in the pulsed laser heated diamond anvil cell." The Review of scientific instruments vol. 81,11 (2010): 113902. doi: https://doi.org/10.1063/1.3499358
Goncharov AF, Prakapenka VB, Struzhkin VV, Kantor I, Rivers ML, Dalton DA. X-ray diffraction in the pulsed laser heated diamond anvil cell. Rev Sci Instrum. 2010 Nov;81(11):113902. doi: 10.1063/1.3499358. PMID: 21133481.
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The formation of core cross-linked star polymers containing cores cross-linked by dynamic covalent imine bonds.

Chemical communications (Cambridge, England)

Jackson AW, Fulton DA.
PMID: 20652193
Chem Commun (Camb). 2010 Sep 07;46(33):6051-3. doi: 10.1039/c0cc00691b. Epub 2010 Jul 23.

Diblock copolymers possessing amino or aldehyde functions within one of their blocks were prepared using RAFT polymerization techniques. These polymers were shown to cross-link through dynamic imine bonds to form core cross-linked star polymers which display a size-dependency upon...

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Jackson AW, Fulton DA. The formation of core cross-linked star polymers containing cores cross-linked by dynamic covalent imine bonds. Chem Commun (Camb). 2010;46(33):6051-3doi: 10.1039/c0cc00691b.
Jackson, A. W., & Fulton, D. A. (2010). The formation of core cross-linked star polymers containing cores cross-linked by dynamic covalent imine bonds. Chemical communications (Cambridge, England), 46(33), 6051-3. https://doi.org/10.1039/c0cc00691b
Jackson, Alexander W, and Fulton, David A. "The formation of core cross-linked star polymers containing cores cross-linked by dynamic covalent imine bonds." Chemical communications (Cambridge, England) vol. 46,33 (2010): 6051-3. doi: https://doi.org/10.1039/c0cc00691b
Jackson AW, Fulton DA. The formation of core cross-linked star polymers containing cores cross-linked by dynamic covalent imine bonds. Chem Commun (Camb). 2010 Sep 07;46(33):6051-3. doi: 10.1039/c0cc00691b. Epub 2010 Jul 23. PMID: 20652193.
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Origins of nonword phonological errors in aphasic picture naming.

Cognitive neuropsychology

Schwartz MF, Wilshire CE, Gagnon DA, Polansky M.
PMID: 21038198
Cogn Neuropsychol. 2004 Mar 01;21(2):159-86. doi: 10.1080/02643290342000519.

A recent theory of lexical access in picture naming maintains that all nonword errors are generated during the retrieval of phonemic segments from the lexicon (Dell, Schwartz, Martin, Saffran, & Gagnon, 1997b). This theory is challenged by "dual origin"...

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Schwartz MF, Wilshire CE, Gagnon DA, et al. Origins of nonword phonological errors in aphasic picture naming. Cogn Neuropsychol. 2004;21(2):159-86doi: 10.1080/02643290342000519.
Schwartz, M. F., Wilshire, C. E., Gagnon, D. A., & Polansky, M. (2004). Origins of nonword phonological errors in aphasic picture naming. Cognitive neuropsychology, 21(2), 159-86. https://doi.org/10.1080/02643290342000519
Schwartz, Myrna F, et al. "Origins of nonword phonological errors in aphasic picture naming." Cognitive neuropsychology vol. 21,2 (2004): 159-86. doi: https://doi.org/10.1080/02643290342000519
Schwartz MF, Wilshire CE, Gagnon DA, Polansky M. Origins of nonword phonological errors in aphasic picture naming. Cogn Neuropsychol. 2004 Mar 01;21(2):159-86. doi: 10.1080/02643290342000519. PMID: 21038198.
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Chk-ing in and Chk-ing out: kinase compartmentalization comes to checkpoint control.

Molecular cell

Canton DA, Scott JD.
PMID: 20932468
Mol Cell. 2010 Oct 08;40(1):1-2. doi: 10.1016/j.molcel.2010.09.020.

Checkpoints are the sentinels of cell-cycle progression. In this issue of Molecular Cell, Yaffe and colleagues (Reinhardt et al., 2010) show that spatial and temporal resolution of Chk1 and MK2, checkpoint kinases with identical substrate specificity, are necessary to...

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Canton DA, Scott JD. Chk-ing in and Chk-ing out: kinase compartmentalization comes to checkpoint control. Mol Cell. 2010;40(1):1-2doi: 10.1016/j.molcel.2010.09.020.
Canton, D. A., & Scott, J. D. (2010). Chk-ing in and Chk-ing out: kinase compartmentalization comes to checkpoint control. Molecular cell, 40(1), 1-2. https://doi.org/10.1016/j.molcel.2010.09.020
Canton, David A, and Scott, John D. "Chk-ing in and Chk-ing out: kinase compartmentalization comes to checkpoint control." Molecular cell vol. 40,1 (2010): 1-2. doi: https://doi.org/10.1016/j.molcel.2010.09.020
Canton DA, Scott JD. Chk-ing in and Chk-ing out: kinase compartmentalization comes to checkpoint control. Mol Cell. 2010 Oct 08;40(1):1-2. doi: 10.1016/j.molcel.2010.09.020. PMID: 20932468; PMCID: PMC3014293.
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Showing 1 to 12 of 134 entries