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Multimorbidity among people with HIV in regional New South Wales, Australia.

Sexual health

Edmiston N, Passmore E, Smith DJ, Petoumenos K.
PMID: 26144504
Sex Health. 2015 Oct;12(5):425-32. doi: 10.1071/SH14070.

UNLABELLED: Background Multimorbidity is the co-occurrence of more than one chronic health condition in addition to HIV. Higher multimorbidity increases mortality, complexity of care and healthcare costs while decreasing quality of life. The prevalence of and factors associated with...

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Edmiston N, Passmore E, Smith DJ, et al. Multimorbidity among people with HIV in regional New South Wales, Australia. Sex Health. 2015;12(5):425-32doi: 10.1071/SH14070.
Edmiston, N., Passmore, E., Smith, D. J., & Petoumenos, K. (2015). Multimorbidity among people with HIV in regional New South Wales, Australia. Sexual health, 12(5), 425-32. https://doi.org/10.1071/SH14070
Edmiston, Natalie, et al. "Multimorbidity among people with HIV in regional New South Wales, Australia." Sexual health vol. 12,5 (2015): 425-32. doi: https://doi.org/10.1071/SH14070
Edmiston N, Passmore E, Smith DJ, Petoumenos K. Multimorbidity among people with HIV in regional New South Wales, Australia. Sex Health. 2015 Oct;12(5):425-32. doi: 10.1071/SH14070. PMID: 26144504.
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Synthesis of novel N-cyclopentenyl-lactams using the Aubé reaction.

Beilstein journal of organic chemistry

Shinde MV, Ople RS, Sangtani E, Gonnade R, Reddy DS.
PMID: 26199661
Beilstein J Org Chem. 2015 Jun 23;11:1060-7. doi: 10.3762/bjoc.11.119. eCollection 2015.

A novel and convenient method utilizing the Aubé reaction to access a new class of compounds that are similar to carbocyclic nucleosides is reported. The azido alcohol derived from Vince lactam undergoes the Aubé reaction with various cyclic ketones...

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Shinde MV, Ople RS, Sangtani E, et al. Synthesis of novel N-cyclopentenyl-lactams using the Aubé reaction. Beilstein J Org Chem. 2015;11:1060-7doi: 10.3762/bjoc.11.119.
Shinde, M. V., Ople, R. S., Sangtani, E., Gonnade, R., & Reddy, D. S. (2015). Synthesis of novel N-cyclopentenyl-lactams using the Aubé reaction. Beilstein journal of organic chemistry, 111060-7. https://doi.org/10.3762/bjoc.11.119
Shinde, Madhuri V, et al. "Synthesis of novel N-cyclopentenyl-lactams using the Aubé reaction." Beilstein journal of organic chemistry vol. 11 (2015): 1060-7. doi: https://doi.org/10.3762/bjoc.11.119
Shinde MV, Ople RS, Sangtani E, Gonnade R, Reddy DS. Synthesis of novel N-cyclopentenyl-lactams using the Aubé reaction. Beilstein J Org Chem. 2015 Jun 23;11:1060-7. doi: 10.3762/bjoc.11.119. eCollection 2015. PMID: 26199661; PMCID: PMC4505090.
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Tautomerization lowers the activation barriers for N-glycosidic bond cleavage of protonated uridine and 2'-deoxyuridine.

Physical chemistry chemical physics : PCCP

Wu RR, Rodgers MT.
PMID: 27536972
Phys Chem Chem Phys. 2016 Sep 21;18(35):24451-9. doi: 10.1039/c6cp03620a. Epub 2016 Aug 18.

The gas-phase conformations of protonated uridine, [Urd+H](+), and its 2'-deoxy form, protonated 2'-deoxyuridine, [dUrd+H](+), have been examined in detail previously by infrared multiple photon dissociation action spectroscopy techniques. Both 2,4-dihydroxy tautomers and O4 protonated conformers of [Urd+H](+) and [dUrd+H](+)...

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Wu RR, Rodgers MT. Tautomerization lowers the activation barriers for N-glycosidic bond cleavage of protonated uridine and 2'-deoxyuridine. Phys Chem Chem Phys. 2016;18(35):24451-9doi: 10.1039/c6cp03620a.
Wu, R. R., & Rodgers, M. T. (2016). Tautomerization lowers the activation barriers for N-glycosidic bond cleavage of protonated uridine and 2'-deoxyuridine. Physical chemistry chemical physics : PCCP, 18(35), 24451-9. https://doi.org/10.1039/c6cp03620a
Wu, R R, and Rodgers, M T. "Tautomerization lowers the activation barriers for N-glycosidic bond cleavage of protonated uridine and 2'-deoxyuridine." Physical chemistry chemical physics : PCCP vol. 18,35 (2016): 24451-9. doi: https://doi.org/10.1039/c6cp03620a
Wu RR, Rodgers MT. Tautomerization lowers the activation barriers for N-glycosidic bond cleavage of protonated uridine and 2'-deoxyuridine. Phys Chem Chem Phys. 2016 Sep 21;18(35):24451-9. doi: 10.1039/c6cp03620a. Epub 2016 Aug 18. PMID: 27536972.
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A Positive Selection for Nucleoside Kinases in E. coli.

PloS one

Shelat NY, Parhi S, Ostermeier M.
PMID: 27677184
PLoS One. 2016 Sep 27;11(9):e0162921. doi: 10.1371/journal.pone.0162921. eCollection 2016.

Engineering heterologous nucleoside kinases inside E. coli is a difficult process due to the integral role nucleosides play in cell division and transcription. Nucleoside analogs are used in many kinase screens that depend on cellular metabolization of the analogs....

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Shelat NY, Parhi S, Ostermeier M. A Positive Selection for Nucleoside Kinases in E. coli. PLoS One. 2016;11(9):e0162921doi: 10.1371/journal.pone.0162921.
Shelat, N. Y., Parhi, S., & Ostermeier, M. (2016). A Positive Selection for Nucleoside Kinases in E. coli. PloS one, 11(9), e0162921. https://doi.org/10.1371/journal.pone.0162921
Shelat, Nirav Y, et al. "A Positive Selection for Nucleoside Kinases in E. coli." PloS one vol. 11,9 (2016): e0162921. doi: https://doi.org/10.1371/journal.pone.0162921
Shelat NY, Parhi S, Ostermeier M. A Positive Selection for Nucleoside Kinases in E. coli. PLoS One. 2016 Sep 27;11(9):e0162921. doi: 10.1371/journal.pone.0162921. eCollection 2016. PMID: 27677184; PMCID: PMC5038940.
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TEMPO-derived spin labels linked to the nucleobases adenine and cytosine for probing local structural perturbations in DNA by EPR spectroscopy.

Beilstein journal of organic chemistry

Gophane DB, Sigurdsson ST.
PMID: 25815073
Beilstein J Org Chem. 2015 Feb 09;11:219-27. doi: 10.3762/bjoc.11.24. eCollection 2015.

Three 2´-deoxynucleosides containing semi-flexible spin labels, namely (T)A, (U)A and (U)C, were prepared and incorporated into deoxyoligonucleotides using the phosphoramidite method. All three nucleosides contain 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) connected to the exocyclic amino group; (T)A directly and (U)A as well...

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Gophane DB, Sigurdsson ST. TEMPO-derived spin labels linked to the nucleobases adenine and cytosine for probing local structural perturbations in DNA by EPR spectroscopy. Beilstein J Org Chem. 2015;11:219-27doi: 10.3762/bjoc.11.24.
Gophane, D. B., & Sigurdsson, S. T. (2015). TEMPO-derived spin labels linked to the nucleobases adenine and cytosine for probing local structural perturbations in DNA by EPR spectroscopy. Beilstein journal of organic chemistry, 11219-27. https://doi.org/10.3762/bjoc.11.24
Gophane, Dnyaneshwar B, and Sigurdsson, Snorri Th. "TEMPO-derived spin labels linked to the nucleobases adenine and cytosine for probing local structural perturbations in DNA by EPR spectroscopy." Beilstein journal of organic chemistry vol. 11 (2015): 219-27. doi: https://doi.org/10.3762/bjoc.11.24
Gophane DB, Sigurdsson ST. TEMPO-derived spin labels linked to the nucleobases adenine and cytosine for probing local structural perturbations in DNA by EPR spectroscopy. Beilstein J Org Chem. 2015 Feb 09;11:219-27. doi: 10.3762/bjoc.11.24. eCollection 2015. PMID: 25815073; PMCID: PMC4362019.
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Enzymatic synthesis and phosphorolysis of 4(2)-thioxo- and 6(5)-azapyrimidine nucleosides by .

Beilstein journal of organic chemistry

Stepchenko VA, Miroshnikov AI, Seela F, Mikhailopulo IA.
PMID: 28144328
Beilstein J Org Chem. 2016 Dec 01;12:2588-2601. doi: 10.3762/bjoc.12.254. eCollection 2016.

The

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Stepchenko VA, Miroshnikov AI, Seela F, et al. Enzymatic synthesis and phosphorolysis of 4(2)-thioxo- and 6(5)-azapyrimidine nucleosides by . Beilstein J Org Chem. 2016;12:2588-2601doi: 10.3762/bjoc.12.254.
Stepchenko, V. A., Miroshnikov, A. I., Seela, F., & Mikhailopulo, I. A. (2016). Enzymatic synthesis and phosphorolysis of 4(2)-thioxo- and 6(5)-azapyrimidine nucleosides by . Beilstein journal of organic chemistry, 122588-2601. https://doi.org/10.3762/bjoc.12.254
Stepchenko, Vladimir A, et al. "Enzymatic synthesis and phosphorolysis of 4(2)-thioxo- and 6(5)-azapyrimidine nucleosides by ." Beilstein journal of organic chemistry vol. 12 (2016): 2588-2601. doi: https://doi.org/10.3762/bjoc.12.254
Stepchenko VA, Miroshnikov AI, Seela F, Mikhailopulo IA. Enzymatic synthesis and phosphorolysis of 4(2)-thioxo- and 6(5)-azapyrimidine nucleosides by . Beilstein J Org Chem. 2016 Dec 01;12:2588-2601. doi: 10.3762/bjoc.12.254. eCollection 2016. PMID: 28144328; PMCID: PMC5238616.
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Proton irradiation: a key to the challenge of N-glycosidic bond formation in a prebiotic context.

Scientific reports

Saladino R, Bizzarri BM, Botta L, Šponer J, Šponer JE, Georgelin T, Jaber M, Rigaud B, Kapralov M, Timoshenko GN, Rozanov A, Krasavin E, Timperio AM, Mauro ED.
PMID: 29116184
Sci Rep. 2017 Nov 07;7(1):14709. doi: 10.1038/s41598-017-15392-8.

The formation of nucleosides in abiotic conditions is a major hurdle in origin-of-life studies. We have determined the pathway of a general reaction leading to the one-pot synthesis of ribo- and 2'-deoxy-ribonucleosides from sugars and purine nucleobases under proton...

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Saladino R, Bizzarri BM, Botta L, et al. Proton irradiation: a key to the challenge of N-glycosidic bond formation in a prebiotic context. Sci Rep. 2017;7(1):14709doi: 10.1038/s41598-017-15392-8.
Saladino, R., Bizzarri, B. M., Botta, L., Šponer, J., Šponer, J. E., Georgelin, T., Jaber, M., Rigaud, B., Kapralov, M., Timoshenko, G. N., Rozanov, A., Krasavin, E., Timperio, A. M., & Mauro, E. D. (2017). Proton irradiation: a key to the challenge of N-glycosidic bond formation in a prebiotic context. Scientific reports, 7(1), 14709. https://doi.org/10.1038/s41598-017-15392-8
Saladino, Raffaele, et al. "Proton irradiation: a key to the challenge of N-glycosidic bond formation in a prebiotic context." Scientific reports vol. 7,1 (2017): 14709. doi: https://doi.org/10.1038/s41598-017-15392-8
Saladino R, Bizzarri BM, Botta L, Šponer J, Šponer JE, Georgelin T, Jaber M, Rigaud B, Kapralov M, Timoshenko GN, Rozanov A, Krasavin E, Timperio AM, Mauro ED. Proton irradiation: a key to the challenge of N-glycosidic bond formation in a prebiotic context. Sci Rep. 2017 Nov 07;7(1):14709. doi: 10.1038/s41598-017-15392-8. PMID: 29116184; PMCID: PMC5677017.
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Complex Thermodynamic Behavior of Single-Stranded Nucleic Acid Adsorption to Graphene Surfaces.

Langmuir : the ACS journal of surfaces and colloids

Ranganathan SV, Halvorsen K, Myers CA, Robertson NM, Yigit MV, Chen AA.
PMID: 27219463
Langmuir. 2016 Jun 21;32(24):6028-34. doi: 10.1021/acs.langmuir.6b00456. Epub 2016 Jun 06.

In just over a decade since its discovery, research on graphene has exploded due to a number of potential applications in electronics, materials, and medicine. In its water-soluble form of graphene oxide, the material has shown promise as a...

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Ranganathan SV, Halvorsen K, Myers CA, et al. Complex Thermodynamic Behavior of Single-Stranded Nucleic Acid Adsorption to Graphene Surfaces. Langmuir. 2016;32(24):6028-34doi: 10.1021/acs.langmuir.6b00456.
Ranganathan, S. V., Halvorsen, K., Myers, C. A., Robertson, N. M., Yigit, M. V., & Chen, A. A. (2016). Complex Thermodynamic Behavior of Single-Stranded Nucleic Acid Adsorption to Graphene Surfaces. Langmuir : the ACS journal of surfaces and colloids, 32(24), 6028-34. https://doi.org/10.1021/acs.langmuir.6b00456
Ranganathan, Srivathsan V, et al. "Complex Thermodynamic Behavior of Single-Stranded Nucleic Acid Adsorption to Graphene Surfaces." Langmuir : the ACS journal of surfaces and colloids vol. 32,24 (2016): 6028-34. doi: https://doi.org/10.1021/acs.langmuir.6b00456
Ranganathan SV, Halvorsen K, Myers CA, Robertson NM, Yigit MV, Chen AA. Complex Thermodynamic Behavior of Single-Stranded Nucleic Acid Adsorption to Graphene Surfaces. Langmuir. 2016 Jun 21;32(24):6028-34. doi: 10.1021/acs.langmuir.6b00456. Epub 2016 Jun 06. PMID: 27219463.
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Efficient microwave-assisted solid phase coupling of nucleosides, small library generation and mild conditions for release of nucleoside derivatives.

Tetrahedron letters

Paritala H, Suzuki Y, Carroll KS.
PMID: 23794759
Tetrahedron Lett. 2013 Apr 01;54(14):1869-1872. doi: 10.1016/j.tetlet.2013.01.109.

Nucleosides are essential bio-molecules that participate in a wide array of biological processes involved in maintaining physiologic homeostasis. Recent efforts geared towards the synthesis of nucleoside analogues and development of nucleoside combinatorial libraries using solid phase synthesis has contributed...

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Paritala H, Suzuki Y, Carroll KS. Efficient microwave-assisted solid phase coupling of nucleosides, small library generation and mild conditions for release of nucleoside derivatives. Tetrahedron Lett. 2013;54(14):1869-1872doi: 10.1016/j.tetlet.2013.01.109.
Paritala, H., Suzuki, Y., & Carroll, K. S. (2013). Efficient microwave-assisted solid phase coupling of nucleosides, small library generation and mild conditions for release of nucleoside derivatives. Tetrahedron letters, 54(14), 1869-1872. https://doi.org/10.1016/j.tetlet.2013.01.109
Paritala, Hanumantharao, et al. "Efficient microwave-assisted solid phase coupling of nucleosides, small library generation and mild conditions for release of nucleoside derivatives." Tetrahedron letters vol. 54,14 (2013): 1869-1872. doi: https://doi.org/10.1016/j.tetlet.2013.01.109
Paritala H, Suzuki Y, Carroll KS. Efficient microwave-assisted solid phase coupling of nucleosides, small library generation and mild conditions for release of nucleoside derivatives. Tetrahedron Lett. 2013 Apr 01;54(14):1869-1872. doi: 10.1016/j.tetlet.2013.01.109. PMID: 23794759; PMCID: PMC3684988.
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Purinergic signaling: a common pathway for neural and mesenchymal stem cell maintenance and differentiation.

Frontiers in cellular neuroscience

Cavaliere F, Donno C, D'Ambrosi N.
PMID: 26082684
Front Cell Neurosci. 2015 Jun 02;9:211. doi: 10.3389/fncel.2015.00211. eCollection 2015.

Extracellular ATP, related nucleotides and adenosine are among the earliest signaling molecules, operating in virtually all tissues and cells. Through their specific receptors, namely purinergic P1 for nucleosides and P2 for nucleotides, they are involved in a wide array...

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Cavaliere F, Donno C, D'Ambrosi N. Purinergic signaling: a common pathway for neural and mesenchymal stem cell maintenance and differentiation. Front Cell Neurosci. 2015;9:211doi: 10.3389/fncel.2015.00211.
Cavaliere, F., Donno, C., & D'Ambrosi, N. (2015). Purinergic signaling: a common pathway for neural and mesenchymal stem cell maintenance and differentiation. Frontiers in cellular neuroscience, 9211. https://doi.org/10.3389/fncel.2015.00211
Cavaliere, Fabio, et al. "Purinergic signaling: a common pathway for neural and mesenchymal stem cell maintenance and differentiation." Frontiers in cellular neuroscience vol. 9 (2015): 211. doi: https://doi.org/10.3389/fncel.2015.00211
Cavaliere F, Donno C, D'Ambrosi N. Purinergic signaling: a common pathway for neural and mesenchymal stem cell maintenance and differentiation. Front Cell Neurosci. 2015 Jun 02;9:211. doi: 10.3389/fncel.2015.00211. eCollection 2015. PMID: 26082684; PMCID: PMC4451364.
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Discovery of New Acid Ceramidase-Targeted Acyclic 5-Alkynyl and 5-Heteroaryl Uracil Nucleosides.

ACS medicinal chemistry letters

Meščić A, Harej A, Klobučar M, Glavač D, Cetina M, Pavelić SK, Raić-Malić S.
PMID: 26617970
ACS Med Chem Lett. 2015 Oct 05;6(11):1150-5. doi: 10.1021/acsmedchemlett.5b00298. eCollection 2015 Nov 12.

A series of novel N-acyclic uracil analogs with linear, branched, aromatic, and cyclopropyl-alkynyl as well as heteroaryl moieties at C-5 were prepared using palladium catalyzed Sonogashira and Stille cross-coupling and evaluated against malignant tumor cell lines. C-5-Furan-2-yl uracil derivative...

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Meščić A, Harej A, Klobučar M, et al. Discovery of New Acid Ceramidase-Targeted Acyclic 5-Alkynyl and 5-Heteroaryl Uracil Nucleosides. ACS Med Chem Lett. 2015;6(11):1150-5doi: 10.1021/acsmedchemlett.5b00298.
Meščić, A., Harej, A., Klobučar, M., Glavač, D., Cetina, M., Pavelić, S. K., & Raić-Malić, S. (2015). Discovery of New Acid Ceramidase-Targeted Acyclic 5-Alkynyl and 5-Heteroaryl Uracil Nucleosides. ACS medicinal chemistry letters, 6(11), 1150-5. https://doi.org/10.1021/acsmedchemlett.5b00298
Meščić, Andrijana, et al. "Discovery of New Acid Ceramidase-Targeted Acyclic 5-Alkynyl and 5-Heteroaryl Uracil Nucleosides." ACS medicinal chemistry letters vol. 6,11 (2015): 1150-5. doi: https://doi.org/10.1021/acsmedchemlett.5b00298
Meščić A, Harej A, Klobučar M, Glavač D, Cetina M, Pavelić SK, Raić-Malić S. Discovery of New Acid Ceramidase-Targeted Acyclic 5-Alkynyl and 5-Heteroaryl Uracil Nucleosides. ACS Med Chem Lett. 2015 Oct 05;6(11):1150-5. doi: 10.1021/acsmedchemlett.5b00298. eCollection 2015 Nov 12. PMID: 26617970; PMCID: PMC4645252.
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A SURVEY OF NONXANTHINE DERIVATIVES AS ADENOSINE RECEPTOR LIGANDS.

Nucleosides & nucleotides

Siddiqi SM, Ji XD, Melman N, Olah ME, Jain R, Evans P, Glashofer M, Padgett WL, Cohen LA, Daly JW, Stiles GL, Jacobson KA.
PMID: 27043138
Nucleosides Nucleotides. 1996;15(1):693-717. doi: 10.1080/07328319608002416.

The binding affinities at rat A

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Siddiqi SM, Ji XD, Melman N, et al. A SURVEY OF NONXANTHINE DERIVATIVES AS ADENOSINE RECEPTOR LIGANDS. Nucleosides Nucleotides. 1996;15(1):693-717doi: 10.1080/07328319608002416.
Siddiqi, S. M., Ji, X. D., Melman, N., Olah, M. E., Jain, R., Evans, P., Glashofer, M., Padgett, W. L., Cohen, L. A., Daly, J. W., Stiles, G. L., & Jacobson, K. A. (1996). A SURVEY OF NONXANTHINE DERIVATIVES AS ADENOSINE RECEPTOR LIGANDS. Nucleosides & nucleotides, 15(1), 693-717. https://doi.org/10.1080/07328319608002416
Siddiqi, Suhaib M, et al. "A SURVEY OF NONXANTHINE DERIVATIVES AS ADENOSINE RECEPTOR LIGANDS." Nucleosides & nucleotides vol. 15,1 (1996): 693-717. doi: https://doi.org/10.1080/07328319608002416
Siddiqi SM, Ji XD, Melman N, Olah ME, Jain R, Evans P, Glashofer M, Padgett WL, Cohen LA, Daly JW, Stiles GL, Jacobson KA. A SURVEY OF NONXANTHINE DERIVATIVES AS ADENOSINE RECEPTOR LIGANDS. Nucleosides Nucleotides. 1996;15(1):693-717. doi: 10.1080/07328319608002416. PMID: 27043138; PMCID: PMC4817726.
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Showing 1 to 12 of 998 entries