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Binding of transcription factor sp1 to exon-1 of C-myc is altered in burkitts-lymphoma.

International journal of oncology

Bryans M, Lucas J, Wilkie N, Burrow K, Clark A, Lang J.
PMID: 21584528
Int J Oncol. 1992 Jul;1(2):175-80. doi: 10.3892/ijo.1.2.175.

In Burkitt's lymphoma (BL) a consistent chromosomal translocation involving the c-myc proto-oncogene locus on chromosome 8 and one of the immunoglobulin loci located on chromosomes 14, 22 or 2 results in the aberrant expression of c-myc. In six out...

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Bryans M, Lucas J, Wilkie N, et al. Binding of transcription factor sp1 to exon-1 of C-myc is altered in burkitts-lymphoma. Int J Oncol. 1992;1(2):175-80doi: 10.3892/ijo.1.2.175.
Bryans, M., Lucas, J., Wilkie, N., Burrow, K., Clark, A., & Lang, J. (1992). Binding of transcription factor sp1 to exon-1 of C-myc is altered in burkitts-lymphoma. International journal of oncology, 1(2), 175-80. https://doi.org/10.3892/ijo.1.2.175
Bryans, M, et al. "Binding of transcription factor sp1 to exon-1 of C-myc is altered in burkitts-lymphoma." International journal of oncology vol. 1,2 (1992): 175-80. doi: https://doi.org/10.3892/ijo.1.2.175
Bryans M, Lucas J, Wilkie N, Burrow K, Clark A, Lang J. Binding of transcription factor sp1 to exon-1 of C-myc is altered in burkitts-lymphoma. Int J Oncol. 1992 Jul;1(2):175-80. doi: 10.3892/ijo.1.2.175. PMID: 21584528.
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Delivery of health care in the far north.

Canadian family physician Medecin de famille canadien

Bryans AM.
PMID: 20468329
Can Fam Physician. 1968 Dec;14(12):55-61.

No abstract available.

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Bryans AM. Delivery of health care in the far north. Can Fam Physician. 1968;14(12):55-61
Bryans, A. M. (1968). Delivery of health care in the far north. Canadian family physician Medecin de famille canadien, 14(12), 55-61.
Bryans, A M. "Delivery of health care in the far north." Canadian family physician Medecin de famille canadien vol. 14,12 (1968): 55-61.
Bryans AM. Delivery of health care in the far north. Can Fam Physician. 1968 Dec;14(12):55-61. PMID: 20468329; PMCID: PMC2281195.
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Contract sterilization and validation companies offer new options for sterile compounded preparations.

International journal of pharmaceutical compounding

Latta KS, Howard B, Gordon K, Foster L, Nichols L, Floyd DB, Winters M, Bryans T.
PMID: 23970003
Int J Pharm Compd. 2009 Mar-Apr;13(2):106-19.

To ensure patient safety, adhere to good compounding practices, and safeguard against professional liability, the sterility of some compounded preparations must be assured. When in-house sterilization capabilities do not suffice, the intervention of a contract sterilization and/or validation company...

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Latta KS, Howard B, Gordon K, et al. Contract sterilization and validation companies offer new options for sterile compounded preparations. Int J Pharm Compd. 2009;13(2):106-19
Latta, K. S., Howard, B., Gordon, K., Foster, L., Nichols, L., Floyd, D. B., Winters, M., & Bryans, T. (2009). Contract sterilization and validation companies offer new options for sterile compounded preparations. International journal of pharmaceutical compounding, 13(2), 106-19.
Latta, Kenneth S, et al. "Contract sterilization and validation companies offer new options for sterile compounded preparations." International journal of pharmaceutical compounding vol. 13,2 (2009): 106-19.
Latta KS, Howard B, Gordon K, Foster L, Nichols L, Floyd DB, Winters M, Bryans T. Contract sterilization and validation companies offer new options for sterile compounded preparations. Int J Pharm Compd. 2009 Mar-Apr;13(2):106-19. PMID: 23970003.
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Pd-catalyzed allylic alkylation cascade with dihydropyrans: regioselective synthesis of furo[3,2-c]pyrans.

Organic letters

Bartlett MJ, Turner CA, Harvey JE.
PMID: 23621816
Org Lett. 2013 May 17;15(10):2430-3. doi: 10.1021/ol400902d. Epub 2013 Apr 26.

A regioselective palladium-catalyzed allylic alkylation cascade forms furo[3,2-c]pyrans from various cyclic β-dicarbonyl bis-nucleophiles and 3,6-dihydro-2H-pyran bis-electrophiles. The combination of allylic carbonate and anomeric siloxy leaving groups in the dihydropyran substrate allows control of the many regiochemical possibilities in this...

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Bartlett MJ, Turner CA, Harvey JE. Pd-catalyzed allylic alkylation cascade with dihydropyrans: regioselective synthesis of furo[3,2-c]pyrans. Org Lett. 2013;15(10):2430-3doi: 10.1021/ol400902d.
Bartlett, M. J., Turner, C. A., & Harvey, J. E. (2013). Pd-catalyzed allylic alkylation cascade with dihydropyrans: regioselective synthesis of furo[3,2-c]pyrans. Organic letters, 15(10), 2430-3. https://doi.org/10.1021/ol400902d
Bartlett, Mark J, et al. "Pd-catalyzed allylic alkylation cascade with dihydropyrans: regioselective synthesis of furo[3,2-c]pyrans." Organic letters vol. 15,10 (2013): 2430-3. doi: https://doi.org/10.1021/ol400902d
Bartlett MJ, Turner CA, Harvey JE. Pd-catalyzed allylic alkylation cascade with dihydropyrans: regioselective synthesis of furo[3,2-c]pyrans. Org Lett. 2013 May 17;15(10):2430-3. doi: 10.1021/ol400902d. Epub 2013 Apr 26. PMID: 23621816.
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Academia-industry partnerships in drug discovery.

Expert opinion on drug discovery

Dalrymple M, Taylor D, Kettleborough C, Bryans J, Solari R.
PMID: 23506026
Expert Opin Drug Discov. 2006 Jun;1(1):1-6. doi: 10.1517/17460441.1.1.1.

The movement of ideas and innovation from academia into the world of business has a long and fruitful history. Ironically, it might be argued that the recent pressure put on universities and basic research organisations to protect and exploit...

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Dalrymple M, Taylor D, Kettleborough C, et al. Academia-industry partnerships in drug discovery. Expert Opin Drug Discov. 2006;1(1):1-6doi: 10.1517/17460441.1.1.1.
Dalrymple, M., Taylor, D., Kettleborough, C., Bryans, J., & Solari, R. (2006). Academia-industry partnerships in drug discovery. Expert opinion on drug discovery, 1(1), 1-6. https://doi.org/10.1517/17460441.1.1.1
Dalrymple, Michael, et al. "Academia-industry partnerships in drug discovery." Expert opinion on drug discovery vol. 1,1 (2006): 1-6. doi: https://doi.org/10.1517/17460441.1.1.1
Dalrymple M, Taylor D, Kettleborough C, Bryans J, Solari R. Academia-industry partnerships in drug discovery. Expert Opin Drug Discov. 2006 Jun;1(1):1-6. doi: 10.1517/17460441.1.1.1. PMID: 23506026.
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Oxidative Prins and Prins/Friedel-Crafts cyclizations for the stereoselective synthesis of dioxabicycles and hexahydro-1H-benzo[f]isochromenes via the benzylic C-H activation.

Organic & biomolecular chemistry

Reddy BV, Borkar P, Yadav JS, Reddy PP, Kunwar AC, Sridhar B, Grée R.
PMID: 22187046
Org Biomol Chem. 2012 Feb 21;10(7):1349-58. doi: 10.1039/c1ob06489d. Epub 2011 Dec 20.

1-Benzyl ethers of (E)- and (Z)-hex-3-en-1,6-diols and hept-3-en-1,7-diols undergo a smooth oxidative cyclization with DDQ in the presence of In(OTf)(3) through a sequential C-H bond activation and an intramolecular Prins cyclization to afford the corresponding trans- and cis-fused hexahydro-2H-furo[3,2-c]pyrans...

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Reddy BV, Borkar P, Yadav JS, et al. Oxidative Prins and Prins/Friedel-Crafts cyclizations for the stereoselective synthesis of dioxabicycles and hexahydro-1H-benzo[f]isochromenes via the benzylic C-H activation. Org Biomol Chem. 2011;10(7):1349-58doi: 10.1039/c1ob06489d.
Reddy, B. V., Borkar, P., Yadav, J. S., Reddy, P. P., Kunwar, A. C., Sridhar, B., & Grée, R. (2012). Oxidative Prins and Prins/Friedel-Crafts cyclizations for the stereoselective synthesis of dioxabicycles and hexahydro-1H-benzo[f]isochromenes via the benzylic C-H activation. Organic & biomolecular chemistry, 10(7), 1349-58. https://doi.org/10.1039/c1ob06489d
Reddy, B V Subba, et al. "Oxidative Prins and Prins/Friedel-Crafts cyclizations for the stereoselective synthesis of dioxabicycles and hexahydro-1H-benzo[f]isochromenes via the benzylic C-H activation." Organic & biomolecular chemistry vol. 10,7 (2012): 1349-58. doi: https://doi.org/10.1039/c1ob06489d
Reddy BV, Borkar P, Yadav JS, Reddy PP, Kunwar AC, Sridhar B, Grée R. Oxidative Prins and Prins/Friedel-Crafts cyclizations for the stereoselective synthesis of dioxabicycles and hexahydro-1H-benzo[f]isochromenes via the benzylic C-H activation. Org Biomol Chem. 2012 Feb 21;10(7):1349-58. doi: 10.1039/c1ob06489d. Epub 2011 Dec 20. PMID: 22187046.
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Stress-induced cardiomyopathy: a syndrome of the susceptible patient?.

Expert review of cardiovascular therapy

Friedrich MG, Cocker MS.
PMID: 22390796
Expert Rev Cardiovasc Ther. 2012 Mar;10(3):271-3. doi: 10.1586/erc.12.9.

No abstract available.

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Friedrich MG, Cocker MS. Stress-induced cardiomyopathy: a syndrome of the susceptible patient?. Expert Rev Cardiovasc Ther. 2012;10(3):271-3doi: 10.1586/erc.12.9.
Friedrich, M. G., & Cocker, M. S. (2012). Stress-induced cardiomyopathy: a syndrome of the susceptible patient?. Expert review of cardiovascular therapy, 10(3), 271-3. https://doi.org/10.1586/erc.12.9
Friedrich, Matthias G, and Cocker, Myra S. "Stress-induced cardiomyopathy: a syndrome of the susceptible patient?." Expert review of cardiovascular therapy vol. 10,3 (2012): 271-3. doi: https://doi.org/10.1586/erc.12.9
Friedrich MG, Cocker MS. Stress-induced cardiomyopathy: a syndrome of the susceptible patient?. Expert Rev Cardiovasc Ther. 2012 Mar;10(3):271-3. doi: 10.1586/erc.12.9. PMID: 22390796.
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Regio- and diastereoselective stepwise [8 + 3]-Cycloaddition reaction between tropone derivatives and donor-acceptor cyclopropanes.

Organic letters

Rivero AR, Fernández I, Sierra MÁ.
PMID: 24040858
Org Lett. 2013 Oct 04;15(19):4928-31. doi: 10.1021/ol4020656. Epub 2013 Sep 16.

A novel SnCl4-catalyzed [8 + 3]-cycloaddition reaction between tropone derivatives and donor-acceptor aminocyclopropanes is described. The process leads to the formation of amino-substituted tetrahydrocyclohepta[b]pyrans with complete regio- and diastereoselectivity. Density functional theory calculations suggest that the cycloaddition occurs stepwise...

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Rivero AR, Fernández I, Sierra MÁ. Regio- and diastereoselective stepwise [8 + 3]-Cycloaddition reaction between tropone derivatives and donor-acceptor cyclopropanes. Org Lett. 2013;15(19):4928-31doi: 10.1021/ol4020656.
Rivero, A. R., Fernández, I., & Sierra, M. �. �. (2013). Regio- and diastereoselective stepwise [8 + 3]-Cycloaddition reaction between tropone derivatives and donor-acceptor cyclopropanes. Organic letters, 15(19), 4928-31. https://doi.org/10.1021/ol4020656
Rivero, Alexandra R, et al. "Regio- and diastereoselective stepwise [8 + 3]-Cycloaddition reaction between tropone derivatives and donor-acceptor cyclopropanes." Organic letters vol. 15,19 (2013): 4928-31. doi: https://doi.org/10.1021/ol4020656
Rivero AR, Fernández I, Sierra MÁ. Regio- and diastereoselective stepwise [8 + 3]-Cycloaddition reaction between tropone derivatives and donor-acceptor cyclopropanes. Org Lett. 2013 Oct 04;15(19):4928-31. doi: 10.1021/ol4020656. Epub 2013 Sep 16. PMID: 24040858.
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X-ray-absorption study of rhenium L3 and L1 edges in ReO3: Multiple-scattering approach.

Physical review. B, Condensed matter

Benfatto M, Kuzmin A, Natoli CR, Purans J.
PMID: 10006298
Phys Rev B Condens Matter. 1993 Feb 01;47(5):2480-2486. doi: 10.1103/physrevb.47.2480.

No abstract available.

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Benfatto M, Kuzmin A, Natoli CR, et al. X-ray-absorption study of rhenium L3 and L1 edges in ReO3: Multiple-scattering approach. Phys Rev B Condens Matter. 1993;47(5):2480-2486doi: 10.1103/physrevb.47.2480.
Benfatto, M., Kuzmin, A., Natoli, C. R., & Purans, J. (1993). X-ray-absorption study of rhenium L3 and L1 edges in ReO3: Multiple-scattering approach. Physical review. B, Condensed matter, 47(5), 2480-2486. https://doi.org/10.1103/physrevb.47.2480
Benfatto, et al. "X-ray-absorption study of rhenium L3 and L1 edges in ReO3: Multiple-scattering approach." Physical review. B, Condensed matter vol. 47,5 (1993): 2480-2486. doi: https://doi.org/10.1103/physrevb.47.2480
Benfatto M, Kuzmin A, Natoli CR, Purans J. X-ray-absorption study of rhenium L3 and L1 edges in ReO3: Multiple-scattering approach. Phys Rev B Condens Matter. 1993 Feb 01;47(5):2480-2486. doi: 10.1103/physrevb.47.2480. PMID: 10006298.
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X-ray-absorption spectroscopy of Nd3+-exchanged beta -alumina crystal.

Physical review. B, Condensed matter

Kuzmin A, Mariotto G, Purans J, Rocca F.
PMID: 9982762
Phys Rev B Condens Matter. 1996 May 01;53(17):11444-11450. doi: 10.1103/physrevb.53.11444.

No abstract available.

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Kuzmin A, Mariotto G, Purans J, et al. X-ray-absorption spectroscopy of Nd3+-exchanged beta -alumina crystal. Phys Rev B Condens Matter. 1996;53(17):11444-11450doi: 10.1103/physrevb.53.11444.
Kuzmin, A., Mariotto, G., Purans, J., & Rocca, F. (1996). X-ray-absorption spectroscopy of Nd3+-exchanged beta -alumina crystal. Physical review. B, Condensed matter, 53(17), 11444-11450. https://doi.org/10.1103/physrevb.53.11444
Kuzmin, et al. "X-ray-absorption spectroscopy of Nd3+-exchanged beta -alumina crystal." Physical review. B, Condensed matter vol. 53,17 (1996): 11444-11450. doi: https://doi.org/10.1103/physrevb.53.11444
Kuzmin A, Mariotto G, Purans J, Rocca F. X-ray-absorption spectroscopy of Nd3+-exchanged beta -alumina crystal. Phys Rev B Condens Matter. 1996 May 01;53(17):11444-11450. doi: 10.1103/physrevb.53.11444. PMID: 9982762.
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Analysis of the Expression of Repetitive DNA Elements in Osteosarcoma.

Frontiers in genetics

Ho XD, Nguyen HG, Trinh LH, Reimann E, Prans E, Kõks G, Maasalu K, Le VQ, Nguyen VH, Le NTN, Phung P, Märtson A, Lattekivi F, Kõks S.
PMID: 29250102
Front Genet. 2017 Nov 30;8:193. doi: 10.3389/fgene.2017.00193. eCollection 2017.

Osteosarcoma (OS) is a rare malignant bone tumor. It affects mostly young persons and has poor outcome with the present treatment. No improvement was observed since the introduction of chemotherapy. The better understanding of osteosarcoma development could indicate better...

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Ho XD, Nguyen HG, Trinh LH, et al. Analysis of the Expression of Repetitive DNA Elements in Osteosarcoma. Front Genet. 2017;8:193doi: 10.3389/fgene.2017.00193.
Ho, X. D., Nguyen, H. G., Trinh, L. H., Reimann, E., Prans, E., Kõks, G., Maasalu, K., Le, V. Q., Nguyen, V. H., Le, N. T. N., Phung, P., Märtson, A., Lattekivi, F., & Kõks, S. (2017). Analysis of the Expression of Repetitive DNA Elements in Osteosarcoma. Frontiers in genetics, 8193. https://doi.org/10.3389/fgene.2017.00193
Ho, Xuan D, et al. "Analysis of the Expression of Repetitive DNA Elements in Osteosarcoma." Frontiers in genetics vol. 8 (2017): 193. doi: https://doi.org/10.3389/fgene.2017.00193
Ho XD, Nguyen HG, Trinh LH, Reimann E, Prans E, Kõks G, Maasalu K, Le VQ, Nguyen VH, Le NTN, Phung P, Märtson A, Lattekivi F, Kõks S. Analysis of the Expression of Repetitive DNA Elements in Osteosarcoma. Front Genet. 2017 Nov 30;8:193. doi: 10.3389/fgene.2017.00193. eCollection 2017. PMID: 29250102; PMCID: PMC5714928.
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Total Synthesis of Bryostatin 8 Using an Organosilane-Based Strategy.

Angewandte Chemie (International ed. in English)

Zhang Y, Guo Q, Sun X, Lu J, Cao Y, Pu Q, Chu Z, Gao L, Song Z.
PMID: 29210495
Angew Chem Int Ed Engl. 2018 Jan 22;57(4):942-946. doi: 10.1002/anie.201711452. Epub 2017 Dec 20.

Convergent total synthesis of bryostatin 8 has been accomplished by an organosilane-based strategy. The C ring is constructed stereoselectively through a geminal bis(silane)-based [1,5]-Brook rearrangement, and the B ring through geminal bis(silane)-based Prins cyclization, thus efficiently joining the northern...

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Zhang Y, Guo Q, Sun X, et al. Total Synthesis of Bryostatin 8 Using an Organosilane-Based Strategy. Angew Chem Int Ed Engl. 2017;57(4):942-946doi: 10.1002/anie.201711452.
Zhang, Y., Guo, Q., Sun, X., Lu, J., Cao, Y., Pu, Q., Chu, Z., Gao, L., & Song, Z. (2018). Total Synthesis of Bryostatin 8 Using an Organosilane-Based Strategy. Angewandte Chemie (International ed. in English), 57(4), 942-946. https://doi.org/10.1002/anie.201711452
Zhang, Yuebao, et al. "Total Synthesis of Bryostatin 8 Using an Organosilane-Based Strategy." Angewandte Chemie (International ed. in English) vol. 57,4 (2018): 942-946. doi: https://doi.org/10.1002/anie.201711452
Zhang Y, Guo Q, Sun X, Lu J, Cao Y, Pu Q, Chu Z, Gao L, Song Z. Total Synthesis of Bryostatin 8 Using an Organosilane-Based Strategy. Angew Chem Int Ed Engl. 2018 Jan 22;57(4):942-946. doi: 10.1002/anie.201711452. Epub 2017 Dec 20. PMID: 29210495.
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Showing 25 to 36 of 299 entries