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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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The optimal organization of gynecologic oncology services: a systematic review.

Current oncology (Toronto, Ont.)

Fung-Kee-Fung M, Kennedy EB, Biagi J, Colgan T, D'Souza D, Elit LM, Hunter A, Irish J, McLeod R, Rosen B.
PMID: 26300679
Curr Oncol. 2015 Aug;22(4):e282-93. doi: 10.3747/co.22.2482.

BACKGROUND: A system-level organizational guideline for gynecologic oncology was identified by a provincial cancer agency as a key priority based on input from stakeholders, data showing more limited availability of multidisciplinary or specialist care in lower-volume than in higher-volume...

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Fung-Kee-Fung M, Kennedy EB, Biagi J, et al. The optimal organization of gynecologic oncology services: a systematic review. Curr Oncol. 2015;22(4):e282-93doi: 10.3747/co.22.2482.
Fung-Kee-Fung, M., Kennedy, E. B., Biagi, J., Colgan, T., D'Souza, D., Elit, L. M., Hunter, A., Irish, J., McLeod, R., & Rosen, B. (2015). The optimal organization of gynecologic oncology services: a systematic review. Current oncology (Toronto, Ont.), 22(4), e282-93. https://doi.org/10.3747/co.22.2482
Fung-Kee-Fung, M, et al. "The optimal organization of gynecologic oncology services: a systematic review." Current oncology (Toronto, Ont.) vol. 22,4 (2015): e282-93. doi: https://doi.org/10.3747/co.22.2482
Fung-Kee-Fung M, Kennedy EB, Biagi J, Colgan T, D'Souza D, Elit LM, Hunter A, Irish J, McLeod R, Rosen B. The optimal organization of gynecologic oncology services: a systematic review. Curr Oncol. 2015 Aug;22(4):e282-93. doi: 10.3747/co.22.2482. PMID: 26300679; PMCID: PMC4530826.
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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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Chromosomal Speciation in the Genomics Era: Disentangling Phylogenetic Evolution of Rock-wallabies.

Frontiers in genetics

Potter S, Bragg JG, Blom MP, Deakin JE, Kirkpatrick M, Eldridge MD, Moritz C.
PMID: 28265284
Front Genet. 2017 Feb 10;8:10. doi: 10.3389/fgene.2017.00010. eCollection 2017.

The association of chromosome rearrangements (CRs) with speciation is well established, and there is a long history of theory and evidence relating to "chromosomal speciation." Genomic sequencing has the potential to provide new insights into how reorganization of genome...

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Potter S, Bragg JG, Blom MP, et al. Chromosomal Speciation in the Genomics Era: Disentangling Phylogenetic Evolution of Rock-wallabies. Front Genet. 2017;8:10doi: 10.3389/fgene.2017.00010.
Potter, S., Bragg, J. G., Blom, M. P., Deakin, J. E., Kirkpatrick, M., Eldridge, M. D., & Moritz, C. (2017). Chromosomal Speciation in the Genomics Era: Disentangling Phylogenetic Evolution of Rock-wallabies. Frontiers in genetics, 810. https://doi.org/10.3389/fgene.2017.00010
Potter, Sally, et al. "Chromosomal Speciation in the Genomics Era: Disentangling Phylogenetic Evolution of Rock-wallabies." Frontiers in genetics vol. 8 (2017): 10. doi: https://doi.org/10.3389/fgene.2017.00010
Potter S, Bragg JG, Blom MP, Deakin JE, Kirkpatrick M, Eldridge MD, Moritz C. Chromosomal Speciation in the Genomics Era: Disentangling Phylogenetic Evolution of Rock-wallabies. Front Genet. 2017 Feb 10;8:10. doi: 10.3389/fgene.2017.00010. eCollection 2017. PMID: 28265284; PMCID: PMC5301020.
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Non-covalent graphene nanobuds from mono- and tripodal binding motifs.

Chemical communications (Cambridge, England)

Garrido M, Calbo J, Rodríguez-Pérez L, Aragó J, Ortí E, Herranz M, Martín N.
PMID: 29082988
Chem Commun (Camb). 2017 Nov 16;53(92):12402-12405. doi: 10.1039/c7cc07836f.

Graphene nanobuds were prepared via the non-covalent anchoring of C

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Garrido M, Calbo J, Rodríguez-Pérez L, et al. Non-covalent graphene nanobuds from mono- and tripodal binding motifs. Chem Commun (Camb). 2017;53(92):12402-12405doi: 10.1039/c7cc07836f.
Garrido, M., Calbo, J., Rodríguez-Pérez, L., Aragó, J., Ortí, E., Herranz, M., & Martín, N. (2017). Non-covalent graphene nanobuds from mono- and tripodal binding motifs. Chemical communications (Cambridge, England), 53(92), 12402-12405. https://doi.org/10.1039/c7cc07836f
Garrido, Marina, et al. "Non-covalent graphene nanobuds from mono- and tripodal binding motifs." Chemical communications (Cambridge, England) vol. 53,92 (2017): 12402-12405. doi: https://doi.org/10.1039/c7cc07836f
Garrido M, Calbo J, Rodríguez-Pérez L, Aragó J, Ortí E, Herranz M, Martín N. Non-covalent graphene nanobuds from mono- and tripodal binding motifs. Chem Commun (Camb). 2017 Nov 16;53(92):12402-12405. doi: 10.1039/c7cc07836f. PMID: 29082988.
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P24. Study of C677T methylene tetrahydrofolate reductase (MTHFR) polymorphism in preeclampsia.

Pregnancy hypertension

Matos A, Ferreira J, Portelinha A, Cerdeira AS, Braga J, Patrício B, Rebelo I, Bicho M, Marinho C.
PMID: 26009115
Pregnancy Hypertens. 2011 Jul-Oct;1(3):284. doi: 10.1016/j.preghy.2011.08.085. Epub 2011 Sep 29.

No abstract available.

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Matos A, Ferreira J, Portelinha A, et al. P24. Study of C677T methylene tetrahydrofolate reductase (MTHFR) polymorphism in preeclampsia. Pregnancy Hypertens. 2011;1(3):284doi: 10.1016/j.preghy.2011.08.085.
Matos, A., Ferreira, J., Portelinha, A., Cerdeira, A. S., Braga, J., Patrício, B., Rebelo, I., Bicho, M., & Marinho, C. (2011). P24. Study of C677T methylene tetrahydrofolate reductase (MTHFR) polymorphism in preeclampsia. Pregnancy hypertension, 1(3), 284. https://doi.org/10.1016/j.preghy.2011.08.085
Matos, Andreia, et al. "P24. Study of C677T methylene tetrahydrofolate reductase (MTHFR) polymorphism in preeclampsia." Pregnancy hypertension vol. 1,3 (2011): 284. doi: https://doi.org/10.1016/j.preghy.2011.08.085
Matos A, Ferreira J, Portelinha A, Cerdeira AS, Braga J, Patrício B, Rebelo I, Bicho M, Marinho C. P24. Study of C677T methylene tetrahydrofolate reductase (MTHFR) polymorphism in preeclampsia. Pregnancy Hypertens. 2011 Jul-Oct;1(3):284. doi: 10.1016/j.preghy.2011.08.085. Epub 2011 Sep 29. PMID: 26009115.
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Helical supramolecular polymerization of C3-symmetric amides and retroamides: on the origin of cooperativity and handedness.

Chemical communications (Cambridge, England)

Buendía J, Calbo J, García F, Aragó J, Viruela PM, Ortí E, Sánchez L.
PMID: 27142262
Chem Commun (Camb). 2016 May 25;52(42):6907-10. doi: 10.1039/c6cc02681h. Epub 2016 May 04.

The cooperative supramolecular polymerization of 1 and 2 yields P- or M-type helical aggregates depending on the absolute configuration (S or R) of the stereogenic centres attached to the side chains. The connectivity of the amide group does not...

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Buendía J, Calbo J, García F, et al. Helical supramolecular polymerization of C3-symmetric amides and retroamides: on the origin of cooperativity and handedness. Chem Commun (Camb). 2016;52(42):6907-10doi: 10.1039/c6cc02681h.
Buendía, J., Calbo, J., García, F., Aragó, J., Viruela, P. M., Ortí, E., & Sánchez, L. (2016). Helical supramolecular polymerization of C3-symmetric amides and retroamides: on the origin of cooperativity and handedness. Chemical communications (Cambridge, England), 52(42), 6907-10. https://doi.org/10.1039/c6cc02681h
Buendía, Julia, et al. "Helical supramolecular polymerization of C3-symmetric amides and retroamides: on the origin of cooperativity and handedness." Chemical communications (Cambridge, England) vol. 52,42 (2016): 6907-10. doi: https://doi.org/10.1039/c6cc02681h
Buendía J, Calbo J, García F, Aragó J, Viruela PM, Ortí E, Sánchez L. Helical supramolecular polymerization of C3-symmetric amides and retroamides: on the origin of cooperativity and handedness. Chem Commun (Camb). 2016 May 25;52(42):6907-10. doi: 10.1039/c6cc02681h. Epub 2016 May 04. PMID: 27142262.
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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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DLPNO-CCSD(T) scaled methods for the accurate treatment of large supramolecular complexes.

Journal of computational chemistry

Calbo J, Sancho-García JC, Ortí E, Aragó J.
PMID: 28558123
J Comput Chem. 2017 Jun 05;38(21):1869-1878. doi: 10.1002/jcc.24835. Epub 2017 May 30.

In this work, we present scaled variants of the DLPNO-CCSD(T) method, dubbed as (LS)DLPNO-CCSD(T) and (NS)DLPNO-CCSD(T), to obtain accurate interaction energies in supramolecular complexes governed by noncovalent interactions. The novel scaled schemes are based on the linear combination of...

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Calbo J, Sancho-García JC, Ortí E, et al. DLPNO-CCSD(T) scaled methods for the accurate treatment of large supramolecular complexes. J Comput Chem. 2017;38(21):1869-1878doi: 10.1002/jcc.24835.
Calbo, J., Sancho-García, J. C., Ortí, E., & Aragó, J. (2017). DLPNO-CCSD(T) scaled methods for the accurate treatment of large supramolecular complexes. Journal of computational chemistry, 38(21), 1869-1878. https://doi.org/10.1002/jcc.24835
Calbo, Joaquín, et al. "DLPNO-CCSD(T) scaled methods for the accurate treatment of large supramolecular complexes." Journal of computational chemistry vol. 38,21 (2017): 1869-1878. doi: https://doi.org/10.1002/jcc.24835
Calbo J, Sancho-García JC, Ortí E, Aragó J. DLPNO-CCSD(T) scaled methods for the accurate treatment of large supramolecular complexes. J Comput Chem. 2017 Jun 05;38(21):1869-1878. doi: 10.1002/jcc.24835. Epub 2017 May 30. PMID: 28558123.
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Desymmetrization of a meso-diol complex derived from [Cr(CO)3(eta6-5,8-naphthoquinone)]: use of new diamine acylation catalysts.

Chemical communications (Cambridge, England)

Kündig EP, Lomberget T, Bragg R, Poulard C, Bernardinelli G.
PMID: 15216374
Chem Commun (Camb). 2004 Jul 07;(13):1548-9. doi: 10.1039/b404006f. Epub 2004 May 21.

[Cr(CO)3(naphthoquinone)](1), prepared in a three-step sequence starting from 1,4-dihydroxynaphthalene, was reduced to the corresponding meso-dihydronaphthalene syn-diol complex and the latter was desymmetrized to give the mono-acyl complex with 99% ee via asymmetric acylation catalyzed by the two new and...

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Kündig EP, Lomberget T, Bragg R, et al. Desymmetrization of a meso-diol complex derived from [Cr(CO)3(eta6-5,8-naphthoquinone)]: use of new diamine acylation catalysts. Chem Commun (Camb). 2004;(13):1548-9doi: 10.1039/b404006f.
Kündig, E. P., Lomberget, T., Bragg, R., Poulard, C., & Bernardinelli, G. (2004). Desymmetrization of a meso-diol complex derived from [Cr(CO)3(eta6-5,8-naphthoquinone)]: use of new diamine acylation catalysts. Chemical communications (Cambridge, England), (13), 1548-9. https://doi.org/10.1039/b404006f
Kündig, E Peter, et al. "Desymmetrization of a meso-diol complex derived from [Cr(CO)3(eta6-5,8-naphthoquinone)]: use of new diamine acylation catalysts." Chemical communications (Cambridge, England) vol. ,13 (2004): 1548-9. doi: https://doi.org/10.1039/b404006f
Kündig EP, Lomberget T, Bragg R, Poulard C, Bernardinelli G. Desymmetrization of a meso-diol complex derived from [Cr(CO)3(eta6-5,8-naphthoquinone)]: use of new diamine acylation catalysts. Chem Commun (Camb). 2004 Jul 07;(13):1548-9. doi: 10.1039/b404006f. Epub 2004 May 21. PMID: 15216374.
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FUNCTIONAL ACTIVITY OF THE MAMMARY GLAND IN RELATION TO EXTRA-CHROMOSOMAL INFLUENCE IN THE INCIDENCE OF MAMMARY TUMORS.

Science (New York, N.Y.)

Bagg HJ.
PMID: 17837894
Science. 1936 Apr 17;83(2155):374-5. doi: 10.1126/science.83.2155.374.

No abstract available.

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Bagg HJ. FUNCTIONAL ACTIVITY OF THE MAMMARY GLAND IN RELATION TO EXTRA-CHROMOSOMAL INFLUENCE IN THE INCIDENCE OF MAMMARY TUMORS. Science. 1936;83(2155):374-5doi: 10.1126/science.83.2155.374.
Bagg, H. J. (1936). FUNCTIONAL ACTIVITY OF THE MAMMARY GLAND IN RELATION TO EXTRA-CHROMOSOMAL INFLUENCE IN THE INCIDENCE OF MAMMARY TUMORS. Science (New York, N.Y.), 83(2155), 374-5. https://doi.org/10.1126/science.83.2155.374
Bagg, H J. "FUNCTIONAL ACTIVITY OF THE MAMMARY GLAND IN RELATION TO EXTRA-CHROMOSOMAL INFLUENCE IN THE INCIDENCE OF MAMMARY TUMORS." Science (New York, N.Y.) vol. 83,2155 (1936): 374-5. doi: https://doi.org/10.1126/science.83.2155.374
Bagg HJ. FUNCTIONAL ACTIVITY OF THE MAMMARY GLAND IN RELATION TO EXTRA-CHROMOSOMAL INFLUENCE IN THE INCIDENCE OF MAMMARY TUMORS. Science. 1936 Apr 17;83(2155):374-5. doi: 10.1126/science.83.2155.374. PMID: 17837894.
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Showing 1 to 12 of 262 entries