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'More than boy, girl, male, female': exploring young people's views on gender diversity within and beyond school contexts

gender (e.g., male, women, girls, transgender)

Bragg S, Renold E, Ringrose J, Jackson C.
GSID: nbtDBKiM8FMJ
S Bragg, E Renold, J Ringrose, C Jackson - Sex education, 2018 - Taylor & Francis

… only the views of trans* 1 young people, our project included participants who identified with and used trans* categories (eg gender fluid, agender, non-binary and gender diverse) and …

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Bragg, S., Renold, E., Ringrose, J., & Jackson, C. (2018). ‘More than boy, girl, male, female’: exploring young people’s views on gender diversity within and beyond school contexts. Sex education, 18(4), 420-434.
Bragg, Sara, et al. "‘More than boy, girl, male, female’: exploring young people’s views on gender diversity within and beyond school contexts." Sex education 18.4 (2018): 420-434.
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[How to deliver a lecture].

Yngre laeger

Bragg L.
PMID: 5584981
Yngre Laeger. 1967 Mar 30;13(7):61-4.

No abstract available.

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Bragg L. Om at holde foredrag. [How to deliver a lecture]. Yngre Laeger. 1967;13(7):61-4
Bragg, L. (1967). Om at holde foredrag. [How to deliver a lecture]. Yngre laeger, 13(7), 61-4.
Bragg, L. "Om at holde foredrag." [How to deliver a lecture]. Yngre laeger vol. 13,7 (1967): 61-4.
Bragg L. Om at holde foredrag. [How to deliver a lecture]. Yngre Laeger. 1967 Mar 30;13(7):61-4. Danish. PMID: 5584981.
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Mechanochemical preparation of co-crystals.

Chemical Society reviews

Braga D, Maini L, Grepioni F.
PMID: 23549606
Chem Soc Rev. 2013 Sep 21;42(18):7638-48. doi: 10.1039/c3cs60014a. Epub 2013 Apr 03.

The preparation of co-crystals via mechanochemistry combines the quest for clean and green processes with the investigation of multicomponent new materials, among the currently most fashionable systems in the crystal engineering field: the physico-chemical properties of the components add,...

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Braga D, Maini L, Grepioni F. Mechanochemical preparation of co-crystals. Chem Soc Rev. 2013;42(18):7638-48doi: 10.1039/c3cs60014a.
Braga, D., Maini, L., & Grepioni, F. (2013). Mechanochemical preparation of co-crystals. Chemical Society reviews, 42(18), 7638-48. https://doi.org/10.1039/c3cs60014a
Braga, Dario, et al. "Mechanochemical preparation of co-crystals." Chemical Society reviews vol. 42,18 (2013): 7638-48. doi: https://doi.org/10.1039/c3cs60014a
Braga D, Maini L, Grepioni F. Mechanochemical preparation of co-crystals. Chem Soc Rev. 2013 Sep 21;42(18):7638-48. doi: 10.1039/c3cs60014a. Epub 2013 Apr 03. PMID: 23549606.
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2,8-Disubstituted-1,6-Naphthyridines and 4,6-Disubstituted-Isoquinolines with Potent, Selective Affinity for CDK8/19.

ACS medicinal chemistry letters

Mallinger A, Schiemann K, Rink C, Sejberg J, Honey MA, Czodrowski P, Stubbs M, Poeschke O, Busch M, Schneider R, Schwarz D, Musil D, Burke R, Urbahns K, Workman P, Wienke D, Clarke PA, Raynaud FI, Eccles SA, Esdar C, Rohdich F, Blagg J.
PMID: 27326329
ACS Med Chem Lett. 2016 Mar 28;7(6):573-8. doi: 10.1021/acsmedchemlett.6b00022. eCollection 2016 Jun 09.

We demonstrate a designed scaffold-hop approach to the discovery of 2,8-disubstituted-1,6-naphthyridine- and 4,6-disubstituted-isoquinoline-based dual CDK8/19 ligands. Optimized compounds in both series exhibited rapid aldehyde oxidase-mediated metabolism, which could be abrogated by introduction of an amino substituent at C5 of...

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Mallinger A, Schiemann K, Rink C, et al. 2,8-Disubstituted-1,6-Naphthyridines and 4,6-Disubstituted-Isoquinolines with Potent, Selective Affinity for CDK8/19. ACS Med Chem Lett. 2016;7(6):573-8doi: 10.1021/acsmedchemlett.6b00022.
Mallinger, A., Schiemann, K., Rink, C., Sejberg, J., Honey, M. A., Czodrowski, P., Stubbs, M., Poeschke, O., Busch, M., Schneider, R., Schwarz, D., Musil, D., Burke, R., Urbahns, K., Workman, P., Wienke, D., Clarke, P. A., Raynaud, F. I., Eccles, S. A., Esdar, C., Rohdich, F., & Blagg, J. (2016). 2,8-Disubstituted-1,6-Naphthyridines and 4,6-Disubstituted-Isoquinolines with Potent, Selective Affinity for CDK8/19. ACS medicinal chemistry letters, 7(6), 573-8. https://doi.org/10.1021/acsmedchemlett.6b00022
Mallinger, Aurélie, et al. "2,8-Disubstituted-1,6-Naphthyridines and 4,6-Disubstituted-Isoquinolines with Potent, Selective Affinity for CDK8/19." ACS medicinal chemistry letters vol. 7,6 (2016): 573-8. doi: https://doi.org/10.1021/acsmedchemlett.6b00022
Mallinger A, Schiemann K, Rink C, Sejberg J, Honey MA, Czodrowski P, Stubbs M, Poeschke O, Busch M, Schneider R, Schwarz D, Musil D, Burke R, Urbahns K, Workman P, Wienke D, Clarke PA, Raynaud FI, Eccles SA, Esdar C, Rohdich F, Blagg J. 2,8-Disubstituted-1,6-Naphthyridines and 4,6-Disubstituted-Isoquinolines with Potent, Selective Affinity for CDK8/19. ACS Med Chem Lett. 2016 Mar 28;7(6):573-8. doi: 10.1021/acsmedchemlett.6b00022. eCollection 2016 Jun 09. PMID: 27326329; PMCID: PMC4904262.
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Nonequilibrium molecular dynamics simulations of nanoconfined fluids at solid-liquid interfaces.

The Journal of chemical physics

Morciano M, Fasano M, Nold A, Braga C, Yatsyshin P, Sibley DN, Goddard BD, Chiavazzo E, Asinari P, Kalliadasis S.
PMID: 28668055
J Chem Phys. 2017 Jun 28;146(24):244507. doi: 10.1063/1.4986904.

We investigate the hydrodynamic properties of a Lennard-Jones fluid confined to a nanochannel using molecular dynamics simulations. For channels of different widths and hydrophilic-hydrophobic surface wetting properties, profiles of the fluid density, stress, and viscosity across the channel are...

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Morciano M, Fasano M, Nold A, et al. Nonequilibrium molecular dynamics simulations of nanoconfined fluids at solid-liquid interfaces. J Chem Phys. 2017;146(24):244507doi: 10.1063/1.4986904.
Morciano, M., Fasano, M., Nold, A., Braga, C., Yatsyshin, P., Sibley, D. N., Goddard, B. D., Chiavazzo, E., Asinari, P., & Kalliadasis, S. (2017). Nonequilibrium molecular dynamics simulations of nanoconfined fluids at solid-liquid interfaces. The Journal of chemical physics, 146(24), 244507. https://doi.org/10.1063/1.4986904
Morciano, M, et al. "Nonequilibrium molecular dynamics simulations of nanoconfined fluids at solid-liquid interfaces." The Journal of chemical physics vol. 146,24 (2017): 244507. doi: https://doi.org/10.1063/1.4986904
Morciano M, Fasano M, Nold A, Braga C, Yatsyshin P, Sibley DN, Goddard BD, Chiavazzo E, Asinari P, Kalliadasis S. Nonequilibrium molecular dynamics simulations of nanoconfined fluids at solid-liquid interfaces. J Chem Phys. 2017 Jun 28;146(24):244507. doi: 10.1063/1.4986904. PMID: 28668055.
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Genome Sequences of Newly Isolated Mycobacteriophages Forming Cluster S.

Genome announcements

Mills ML, Bragg J, Bruce A, Dehn A, Drouin J, Hefner M, Katon D, McHugh D, Zeba F, Bowman CA, Cresawn SG, Jacobs-Sera D, Russell DA, Pope WH, Hatfull GF, Dunbar DA, Zegers GP, Page ST.
PMID: 27688332
Genome Announc. 2016 Sep 29;4(5). doi: 10.1128/genomeA.00933-16.

We describe the genomes of two mycobacteriophages, MosMoris and Gattaca, newly isolated on Mycobacterium smegmatis The two phages are very similar to each other, differing in 61 single nucleotide polymorphisms and six small insertion/deletions. Both have extensive nucleotide sequence...

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Mills ML, Bragg J, Bruce A, et al. Genome Sequences of Newly Isolated Mycobacteriophages Forming Cluster S. Genome Announc. 2016;4(5)doi: 10.1128/genomeA.00933-16.
Mills, M. L., Bragg, J., Bruce, A., Dehn, A., Drouin, J., Hefner, M., Katon, D., McHugh, D., Zeba, F., Bowman, C. A., Cresawn, S. G., Jacobs-Sera, D., Russell, D. A., Pope, W. H., Hatfull, G. F., Dunbar, D. A., Zegers, G. P., & Page, S. T. (2016). Genome Sequences of Newly Isolated Mycobacteriophages Forming Cluster S. Genome announcements, 4(5), . https://doi.org/10.1128/genomeA.00933-16
Mills, Monique L, et al. "Genome Sequences of Newly Isolated Mycobacteriophages Forming Cluster S." Genome announcements vol. 4,5 (2016). doi: https://doi.org/10.1128/genomeA.00933-16
Mills ML, Bragg J, Bruce A, Dehn A, Drouin J, Hefner M, Katon D, McHugh D, Zeba F, Bowman CA, Cresawn SG, Jacobs-Sera D, Russell DA, Pope WH, Hatfull GF, Dunbar DA, Zegers GP, Page ST. Genome Sequences of Newly Isolated Mycobacteriophages Forming Cluster S. Genome Announc. 2016 Sep 29;4(5). doi: 10.1128/genomeA.00933-16. PMID: 27688332; PMCID: PMC5043550.
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Relaxation dynamics of functionalized colloids on attractive substrates.

Soft matter

Dias CS, Braga C, Araújo NA, Telo da Gama MM.
PMID: 26661327
Soft Matter. 2016 Feb 07;12(5):1550-7. doi: 10.1039/c5sm02754c. Epub 2015 Dec 11.

Particle-based simulations are performed to study the post-relaxation dynamics of functionalized (patchy) colloids adsorbed on an attractive substrate. Kinetically arrested structures that depend on the number of adsorbed particles and the strength of the particle-particle and particle-substrate interactions are...

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Dias CS, Braga C, Araújo NA, et al. Relaxation dynamics of functionalized colloids on attractive substrates. Soft Matter. 2015;12(5):1550-7doi: 10.1039/c5sm02754c.
Dias, C. S., Braga, C., Araújo, N. A., & Telo da Gama, M. M. (2016). Relaxation dynamics of functionalized colloids on attractive substrates. Soft matter, 12(5), 1550-7. https://doi.org/10.1039/c5sm02754c
Dias, C S, et al. "Relaxation dynamics of functionalized colloids on attractive substrates." Soft matter vol. 12,5 (2016): 1550-7. doi: https://doi.org/10.1039/c5sm02754c
Dias CS, Braga C, Araújo NA, Telo da Gama MM. Relaxation dynamics of functionalized colloids on attractive substrates. Soft Matter. 2016 Feb 07;12(5):1550-7. doi: 10.1039/c5sm02754c. Epub 2015 Dec 11. PMID: 26661327.
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Interanionic (-)O-H...O(-) interactions: a solid-state and computational study of the ring and chain motifs.

Chemistry (Weinheim an der Bergstrasse, Germany)

Braga D, Maini L, Grepioni F, Mota F, Rovira C, Novoa JJ.
PMID: 11192087
Chemistry. 2000 Dec 15;6(24):4536-51. doi: 10.1002/1521-3765(20001215)6:24<4536::aid-chem4536>3.0.co;2-m.

The (-)O-H...O(-) interaction formed by the anions HCO3-, HCO4, HC4O4 and HC5O5- (HA-), obtained upon monodeprotonation of the corresponding carbonic, oxalic, squaric and croconic acids (H2A), has been investigated theoretically and experimentally. The ring (RING) and chain (CHAIN) hydrogen...

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Braga D, Maini L, Grepioni F, et al. Interanionic (-)O-H...O(-) interactions: a solid-state and computational study of the ring and chain motifs. Chemistry. 2000;6(24):4536-51doi: 10.1002/1521-3765(20001215)6:24<4536::aid-chem4536>3.0.co;2-m.
Braga, D., Maini, L., Grepioni, F., Mota, F., Rovira, C., & Novoa, J. J. (2000). Interanionic (-)O-H...O(-) interactions: a solid-state and computational study of the ring and chain motifs. Chemistry (Weinheim an der Bergstrasse, Germany), 6(24), 4536-51. https://doi.org/10.1002/1521-3765(20001215)6:24<4536::aid-chem4536>3.0.co;2-m
Braga, D, et al. "Interanionic (-)O-H...O(-) interactions: a solid-state and computational study of the ring and chain motifs." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 6,24 (2000): 4536-51. doi: https://doi.org/10.1002/1521-3765(20001215)6:24<4536::aid-chem4536>3.0.co;2-m
Braga D, Maini L, Grepioni F, Mota F, Rovira C, Novoa JJ. Interanionic (-)O-H...O(-) interactions: a solid-state and computational study of the ring and chain motifs. Chemistry. 2000 Dec 15;6(24):4536-51. doi: 10.1002/1521-3765(20001215)6:24<4536::aid-chem4536>3.0.co;2-m. PMID: 11192087.
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Mechanochemical assembly of hydrogen bonded organic-organometallic solid compounds.

Chemical communications (Cambridge, England)

Braga D, Maini L, Polito M, Mirolo L, Grepioni F.
PMID: 12536766
Chem Commun (Camb). 2002 Dec 21;(24):2960-1. doi: 10.1039/b209861j.

Solvent-free reactions with molecular systems have been exploited to prepare hybrid organic-organometallic solids: grinding of the complex [Fe(eta 5-C5H4COOH)2] with solid bases B generates quantitatively the corresponding hydrogen bonded salts [Fe(eta 5-C5H4COOH)(eta 5-C5H4COO)][HB] (B = 1,4-diazabicyclo[2.2.2]octane, 1,4-phenylenediamine); gas-solid reactions...

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Braga D, Maini L, Polito M, et al. Mechanochemical assembly of hydrogen bonded organic-organometallic solid compounds. Chem Commun (Camb). 2002;(24):2960-1doi: 10.1039/b209861j.
Braga, D., Maini, L., Polito, M., Mirolo, L., & Grepioni, F. (2002). Mechanochemical assembly of hydrogen bonded organic-organometallic solid compounds. Chemical communications (Cambridge, England), (24), 2960-1. https://doi.org/10.1039/b209861j
Braga, Dario, et al. "Mechanochemical assembly of hydrogen bonded organic-organometallic solid compounds." Chemical communications (Cambridge, England) vol. ,24 (2002): 2960-1. doi: https://doi.org/10.1039/b209861j
Braga D, Maini L, Polito M, Mirolo L, Grepioni F. Mechanochemical assembly of hydrogen bonded organic-organometallic solid compounds. Chem Commun (Camb). 2002 Dec 21;(24):2960-1. doi: 10.1039/b209861j. PMID: 12536766.
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[Raul Briquet].

Resenha clinico-cientifica

BRAGA E.
PMID: 13121369
Resen Clin Cient. 1953 Sep;22(9):310.

No abstract available.

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BRAGA E. [Raul Briquet]. Resen Clin Cient. 1953;22(9):310
BRAGA, E. (1953). [Raul Briquet]. Resenha clinico-cientifica, 22(9), 310.
BRAGA, E. "[Raul Briquet]." Resenha clinico-cientifica vol. 22,9 (1953): 310.
BRAGA E. [Raul Briquet]. Resen Clin Cient. 1953 Sep;22(9):310. Undetermined. PMID: 13121369.
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1,4-hydroxybiradical behavior revealed through crystal structure-solid-state reactivity correlations.

Journal of the American Chemical Society

Braga D, Chen S, Filson H, Maini L, Netherton MR, Patrick BO, Scheffer JR, Scott C, Xia W.
PMID: 15025478
J Am Chem Soc. 2004 Mar 24;126(11):3511-20. doi: 10.1021/ja039076w.

Structure-reactivity correlations for triplet 1,4-hydroxybiradicals in solution are made difficult by the presence of multiple reactive conformers and the possibility of conformation-dependent intersystem crossing. These problems can be overcome by working in the crystalline state, where the conformations of...

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Braga D, Chen S, Filson H, et al. 1,4-hydroxybiradical behavior revealed through crystal structure-solid-state reactivity correlations. J Am Chem Soc. 2004;126(11):3511-20doi: 10.1021/ja039076w.
Braga, D., Chen, S., Filson, H., Maini, L., Netherton, M. R., Patrick, B. O., Scheffer, J. R., Scott, C., & Xia, W. (2004). 1,4-hydroxybiradical behavior revealed through crystal structure-solid-state reactivity correlations. Journal of the American Chemical Society, 126(11), 3511-20. https://doi.org/10.1021/ja039076w
Braga, Dario, et al. "1,4-hydroxybiradical behavior revealed through crystal structure-solid-state reactivity correlations." Journal of the American Chemical Society vol. 126,11 (2004): 3511-20. doi: https://doi.org/10.1021/ja039076w
Braga D, Chen S, Filson H, Maini L, Netherton MR, Patrick BO, Scheffer JR, Scott C, Xia W. 1,4-hydroxybiradical behavior revealed through crystal structure-solid-state reactivity correlations. J Am Chem Soc. 2004 Mar 24;126(11):3511-20. doi: 10.1021/ja039076w. PMID: 15025478.
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Mechanochemical preparation of hydrogen-bonded adducts between the diamine 1,4-diazabicyclo[2.2.2]octane and dicarboxylic acids of variable chain length: an X-ray diffraction and solid-state NMR study.

Chemistry (Weinheim an der Bergstrasse, Germany)

Braga D, Maini L, de Sanctis G, Rubini K, Grepioni F, Chierotti MR, Gobetto R.
PMID: 14639637
Chemistry. 2003 Nov 21;9(22):5538-48. doi: 10.1002/chem.200304940.

Mechanical mixing of solid dicarboxylic acids of variable chain length HOOC(CH(2))(n)COOH (n = 1-7) with solid 1,4-diazabicyclo[2.2.2]octane generates the corresponding salts or co-crystals of the formula [N(CH(2)CH(2))(3)N]-H-[OOC(CH(2))(n)COOH] (n=1-7). Preparation of the same systems from solution has been instrumental for...

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Braga D, Maini L, de Sanctis G, et al. Mechanochemical preparation of hydrogen-bonded adducts between the diamine 1,4-diazabicyclo[2.2.2]octane and dicarboxylic acids of variable chain length: an X-ray diffraction and solid-state NMR study. Chemistry. 2003;9(22):5538-48doi: 10.1002/chem.200304940.
Braga, D., Maini, L., de Sanctis, G., Rubini, K., Grepioni, F., Chierotti, M. R., & Gobetto, R. (2003). Mechanochemical preparation of hydrogen-bonded adducts between the diamine 1,4-diazabicyclo[2.2.2]octane and dicarboxylic acids of variable chain length: an X-ray diffraction and solid-state NMR study. Chemistry (Weinheim an der Bergstrasse, Germany), 9(22), 5538-48. https://doi.org/10.1002/chem.200304940
Braga, Dario, et al. "Mechanochemical preparation of hydrogen-bonded adducts between the diamine 1,4-diazabicyclo[2.2.2]octane and dicarboxylic acids of variable chain length: an X-ray diffraction and solid-state NMR study." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 9,22 (2003): 5538-48. doi: https://doi.org/10.1002/chem.200304940
Braga D, Maini L, de Sanctis G, Rubini K, Grepioni F, Chierotti MR, Gobetto R. Mechanochemical preparation of hydrogen-bonded adducts between the diamine 1,4-diazabicyclo[2.2.2]octane and dicarboxylic acids of variable chain length: an X-ray diffraction and solid-state NMR study. Chemistry. 2003 Nov 21;9(22):5538-48. doi: 10.1002/chem.200304940. PMID: 14639637.
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Showing 1 to 12 of 342 entries