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Influenza vaccine recommendations for children and youth for the 2011/2012 season.

Paediatrics & child health

Salvadori MI.
PMID: 23115500
Paediatr Child Health. 2011 Nov;16(9):570-3. doi: 10.1093/pch/16.9.570.

No abstract available.

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Salvadori MI. Influenza vaccine recommendations for children and youth for the 2011/2012 season. Paediatr Child Health. 2011;16(9):570-3doi: 10.1093/pch/16.9.570.
Salvadori, M. I. (2011). Influenza vaccine recommendations for children and youth for the 2011/2012 season. Paediatrics & child health, 16(9), 570-3. https://doi.org/10.1093/pch/16.9.570
Salvadori, Marina I. "Influenza vaccine recommendations for children and youth for the 2011/2012 season." Paediatrics & child health vol. 16,9 (2011): 570-3. doi: https://doi.org/10.1093/pch/16.9.570
Salvadori MI. Influenza vaccine recommendations for children and youth for the 2011/2012 season. Paediatr Child Health. 2011 Nov;16(9):570-3. doi: 10.1093/pch/16.9.570. French. PMID: 23115500; PMCID: PMC3223899.
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Continuous Glucose Monitoring During Basal-Bolus Therapy Using Insulin Glargine 300 U mL(-1) and Glargine 100 U mL (-1) in Japanese People with Type 1 Diabetes Mellitus: A Crossover Pilot Study.

Diabetes therapy : research, treatment and education of diabetes and related disorders

Jinnouchi H, Koyama M, Amano A, Takahashi Y, Yoshida A, Hieshima K, Sugiyama S, Kurinami N, Jinnouchi T, Becker R.
PMID: 26055218
Diabetes Ther. 2015 Jun;6(2):143-52. doi: 10.1007/s13300-015-0115-1. Epub 2015 Jun 09.

INTRODUCTION: New insulin glargine 300 U mL(-1) (Gla-300) is a basal insulin that shows more stable and prolonged pharmacokinetic and pharmacodynamic profiles than insulin glargine 100 U mL(-1) (Gla-100). This study used continuous glucose monitoring (CGM) to compare 24-h...

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Jinnouchi H, Koyama M, Amano A, et al. Continuous Glucose Monitoring During Basal-Bolus Therapy Using Insulin Glargine 300 U mL(-1) and Glargine 100 U mL (-1) in Japanese People with Type 1 Diabetes Mellitus: A Crossover Pilot Study. Diabetes Ther. 2015;6(2):143-52doi: 10.1007/s13300-015-0115-1.
Jinnouchi, H., Koyama, M., Amano, A., Takahashi, Y., Yoshida, A., Hieshima, K., Sugiyama, S., Kurinami, N., Jinnouchi, T., & Becker, R. (2015). Continuous Glucose Monitoring During Basal-Bolus Therapy Using Insulin Glargine 300 U mL(-1) and Glargine 100 U mL (-1) in Japanese People with Type 1 Diabetes Mellitus: A Crossover Pilot Study. Diabetes therapy : research, treatment and education of diabetes and related disorders, 6(2), 143-52. https://doi.org/10.1007/s13300-015-0115-1
Jinnouchi, Hideaki, et al. "Continuous Glucose Monitoring During Basal-Bolus Therapy Using Insulin Glargine 300 U mL(-1) and Glargine 100 U mL (-1) in Japanese People with Type 1 Diabetes Mellitus: A Crossover Pilot Study." Diabetes therapy : research, treatment and education of diabetes and related disorders vol. 6,2 (2015): 143-52. doi: https://doi.org/10.1007/s13300-015-0115-1
Jinnouchi H, Koyama M, Amano A, Takahashi Y, Yoshida A, Hieshima K, Sugiyama S, Kurinami N, Jinnouchi T, Becker R. Continuous Glucose Monitoring During Basal-Bolus Therapy Using Insulin Glargine 300 U mL(-1) and Glargine 100 U mL (-1) in Japanese People with Type 1 Diabetes Mellitus: A Crossover Pilot Study. Diabetes Ther. 2015 Jun;6(2):143-52. doi: 10.1007/s13300-015-0115-1. Epub 2015 Jun 09. PMID: 26055218; PMCID: PMC4478173.
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A direct approach to a 6-hetarylamino[1,2,4]triazolo[4,3-b][1,2,4,5]tetrazine library.

Organic letters

Palysaeva NV, Kumpan KP, Struchkova MI, Dalinger IL, Kormanov AV, Aleksandrova NS, Chernyshev VM, Pyreu DF, Suponitsky KY, Sheremetev AB.
PMID: 24377749
Org Lett. 2014 Jan 17;16(2):406-9. doi: 10.1021/ol403308h. Epub 2013 Dec 30.

The synthesis of 6-hetarylamino[1,2,4]triazolo[4,3-b][1,2,4,5]tetrazines is reported. The functionalized secondary amines were constructed via a K2CO3-mediated SNAr reaction of weakly basic hetarylamines with 3-(3,5-dimethylpyrazol-1-yl)[1,2,4]triazolo[4,3-b][1,2,4,5]tetrazines, which allowed displacement 3,5-dimethylpyrazolyl leaving group. Significantly, the reaction exhibited a broad substrate scope and proceeded...

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Palysaeva NV, Kumpan KP, Struchkova MI, et al. A direct approach to a 6-hetarylamino[1,2,4]triazolo[4,3-b][1,2,4,5]tetrazine library. Org Lett. 2013;16(2):406-9doi: 10.1021/ol403308h.
Palysaeva, N. V., Kumpan, K. P., Struchkova, M. I., Dalinger, I. L., Kormanov, A. V., Aleksandrova, N. S., Chernyshev, V. M., Pyreu, D. F., Suponitsky, K. Y., & Sheremetev, A. B. (2014). A direct approach to a 6-hetarylamino[1,2,4]triazolo[4,3-b][1,2,4,5]tetrazine library. Organic letters, 16(2), 406-9. https://doi.org/10.1021/ol403308h
Palysaeva, Nadezhda V, et al. "A direct approach to a 6-hetarylamino[1,2,4]triazolo[4,3-b][1,2,4,5]tetrazine library." Organic letters vol. 16,2 (2014): 406-9. doi: https://doi.org/10.1021/ol403308h
Palysaeva NV, Kumpan KP, Struchkova MI, Dalinger IL, Kormanov AV, Aleksandrova NS, Chernyshev VM, Pyreu DF, Suponitsky KY, Sheremetev AB. A direct approach to a 6-hetarylamino[1,2,4]triazolo[4,3-b][1,2,4,5]tetrazine library. Org Lett. 2014 Jan 17;16(2):406-9. doi: 10.1021/ol403308h. Epub 2013 Dec 30. PMID: 24377749.
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Reactions of gem-Difluorinated Phosphonium Salts Induced by Light.

Organic letters

Panferova LI, Tsymbal AV, Levin VV, Struchkova MI, Dilman AD.
PMID: 26862998
Org Lett. 2016 Mar 04;18(5):996-9. doi: 10.1021/acs.orglett.6b00117. Epub 2016 Feb 10.

gem-Difluorinated phosphonium salts, which are readily obtained from aldehydes and difluoromethylene phosphobetaine, can serve as a source of radicals under reductive conditions. An iridium complex or Hantzsch ester was used as a one-electron reducing agent when irradiated with visible...

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Panferova LI, Tsymbal AV, Levin VV, et al. Reactions of gem-Difluorinated Phosphonium Salts Induced by Light. Org Lett. 2016;18(5):996-9doi: 10.1021/acs.orglett.6b00117.
Panferova, L. I., Tsymbal, A. V., Levin, V. V., Struchkova, M. I., & Dilman, A. D. (2016). Reactions of gem-Difluorinated Phosphonium Salts Induced by Light. Organic letters, 18(5), 996-9. https://doi.org/10.1021/acs.orglett.6b00117
Panferova, Liubov I, et al. "Reactions of gem-Difluorinated Phosphonium Salts Induced by Light." Organic letters vol. 18,5 (2016): 996-9. doi: https://doi.org/10.1021/acs.orglett.6b00117
Panferova LI, Tsymbal AV, Levin VV, Struchkova MI, Dilman AD. Reactions of gem-Difluorinated Phosphonium Salts Induced by Light. Org Lett. 2016 Mar 04;18(5):996-9. doi: 10.1021/acs.orglett.6b00117. Epub 2016 Feb 10. PMID: 26862998.
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Editorial: Microbial and Environmental Factors in Autoimmune and Inflammatory Diseases.

Frontiers in immunology

Arleevskaya MI, Manukyan G, Inoue R, Aminov R.
PMID: 28321226
Front Immunol. 2017 Mar 06;8:243. doi: 10.3389/fimmu.2017.00243. eCollection 2017.

No abstract available.

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Arleevskaya MI, Manukyan G, Inoue R, et al. Editorial: Microbial and Environmental Factors in Autoimmune and Inflammatory Diseases. Front Immunol. 2017;8:243doi: 10.3389/fimmu.2017.00243.
Arleevskaya, M. I., Manukyan, G., Inoue, R., & Aminov, R. (2017). Editorial: Microbial and Environmental Factors in Autoimmune and Inflammatory Diseases. Frontiers in immunology, 8243. https://doi.org/10.3389/fimmu.2017.00243
Arleevskaya, Marina I, et al. "Editorial: Microbial and Environmental Factors in Autoimmune and Inflammatory Diseases." Frontiers in immunology vol. 8 (2017): 243. doi: https://doi.org/10.3389/fimmu.2017.00243
Arleevskaya MI, Manukyan G, Inoue R, Aminov R. Editorial: Microbial and Environmental Factors in Autoimmune and Inflammatory Diseases. Front Immunol. 2017 Mar 06;8:243. doi: 10.3389/fimmu.2017.00243. eCollection 2017. PMID: 28321226; PMCID: PMC5337519.
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Lithium and beryllium hypophosphites.

Acta crystallographica. Section C, Crystal structure communications

Naumov DY, Naumova MI, Podberezskaya NV, Kuratieva NV.
PMID: 15295160
Acta Crystallogr C. 2004 Aug;60:i73-5. doi: 10.1107/S0108270104013691. Epub 2004 Jul 21.

No abstract available.

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Naumov DY, Naumova MI, Podberezskaya NV, et al. Lithium and beryllium hypophosphites. Acta Crystallogr C. 2004;60:i73-5doi: 10.1107/S0108270104013691.
Naumov, D. Y., Naumova, M. I., Podberezskaya, N. V., & Kuratieva, N. V. (2004). Lithium and beryllium hypophosphites. Acta crystallographica. Section C, Crystal structure communications, 60i73-5. https://doi.org/10.1107/S0108270104013691
Naumov, Dmitry Yu, et al. "Lithium and beryllium hypophosphites." Acta crystallographica. Section C, Crystal structure communications vol. 60 (2004): i73-5. doi: https://doi.org/10.1107/S0108270104013691
Naumov DY, Naumova MI, Podberezskaya NV, Kuratieva NV. Lithium and beryllium hypophosphites. Acta Crystallogr C. 2004 Aug;60:i73-5. doi: 10.1107/S0108270104013691. Epub 2004 Jul 21. PMID: 15295160.
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Dithiocarbamates: functional and versatile linkers for the formation of self-assembled monolayers.

Langmuir : the ACS journal of surfaces and colloids

Morf P, Raimondi F, Nothofer HG, Schnyder B, Yasuda A, Wessels JM, Jung TA.
PMID: 16401114
Langmuir. 2006 Jan 17;22(2):658-63. doi: 10.1021/la052952u.

Self-assembled monolayers have evolved into one of the best established self-assembly systems with high relevance in a scientific and applied context. So far, however, virtually exclusively thiol functional groups have been used for the investigation of fundamental processes on...

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Morf P, Raimondi F, Nothofer HG, et al. Dithiocarbamates: functional and versatile linkers for the formation of self-assembled monolayers. Langmuir. 2006;22(2):658-63doi: 10.1021/la052952u.
Morf, P., Raimondi, F., Nothofer, H. G., Schnyder, B., Yasuda, A., Wessels, J. M., & Jung, T. A. (2006). Dithiocarbamates: functional and versatile linkers for the formation of self-assembled monolayers. Langmuir : the ACS journal of surfaces and colloids, 22(2), 658-63. https://doi.org/10.1021/la052952u
Morf, Peter, et al. "Dithiocarbamates: functional and versatile linkers for the formation of self-assembled monolayers." Langmuir : the ACS journal of surfaces and colloids vol. 22,2 (2006): 658-63. doi: https://doi.org/10.1021/la052952u
Morf P, Raimondi F, Nothofer HG, Schnyder B, Yasuda A, Wessels JM, Jung TA. Dithiocarbamates: functional and versatile linkers for the formation of self-assembled monolayers. Langmuir. 2006 Jan 17;22(2):658-63. doi: 10.1021/la052952u. PMID: 16401114.
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Synthesis of pentafluorophenylmethylamines via silicon Mannich reaction.

Organic letters

Dilman AD, Belyakov PA, Korlyukov AA, Struchkova MI, Tartakovsky VA.
PMID: 15987168
Org Lett. 2005 Jul 07;7(14):2913-5. doi: 10.1021/ol050845l.

[reaction: see text] The three-component coupling of aldehydes, secondary amines, and methoxytris(pentafluorophenyl)silane, MeOSi(C(6)F(5))(3), affording pentafluorophenylmethylamines has been described. The generation of the five-coordinate silicate intermediate is believed to be the key feature responsible for the efficiency of the reaction.

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Dilman AD, Belyakov PA, Korlyukov AA, et al. Synthesis of pentafluorophenylmethylamines via silicon Mannich reaction. Org Lett. 2005;7(14):2913-5doi: 10.1021/ol050845l.
Dilman, A. D., Belyakov, P. A., Korlyukov, A. A., Struchkova, M. I., & Tartakovsky, V. A. (2005). Synthesis of pentafluorophenylmethylamines via silicon Mannich reaction. Organic letters, 7(14), 2913-5. https://doi.org/10.1021/ol050845l
Dilman, Alexander D, et al. "Synthesis of pentafluorophenylmethylamines via silicon Mannich reaction." Organic letters vol. 7,14 (2005): 2913-5. doi: https://doi.org/10.1021/ol050845l
Dilman AD, Belyakov PA, Korlyukov AA, Struchkova MI, Tartakovsky VA. Synthesis of pentafluorophenylmethylamines via silicon Mannich reaction. Org Lett. 2005 Jul 07;7(14):2913-5. doi: 10.1021/ol050845l. PMID: 15987168.
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Geminal silicon/zinc reagent as an equivalent of difluoromethylene bis-carbanion.

Organic letters

Kosobokov MD, Levin VV, Zemtsov AA, Struchkova MI, Korlyukov AA, Arkhipov DE, Dilman AD.
PMID: 24552348
Org Lett. 2014 Mar 07;16(5):1438-41. doi: 10.1021/ol5002297. Epub 2014 Feb 19.

A new difluorinated reagent, [difluoro(trimethylsilyl)methyl]zinc bromide, bearing C-Zn and C-Si bonds is described. The reagent is conveniently prepared by cobalt-catalyzed halogen/zinc exchange. It can be coupled with two different C-electrophiles in a stepwise manner (with allylic halides for C-Zn...

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Kosobokov MD, Levin VV, Zemtsov AA, et al. Geminal silicon/zinc reagent as an equivalent of difluoromethylene bis-carbanion. Org Lett. 2014;16(5):1438-41doi: 10.1021/ol5002297.
Kosobokov, M. D., Levin, V. V., Zemtsov, A. A., Struchkova, M. I., Korlyukov, A. A., Arkhipov, D. E., & Dilman, A. D. (2014). Geminal silicon/zinc reagent as an equivalent of difluoromethylene bis-carbanion. Organic letters, 16(5), 1438-41. https://doi.org/10.1021/ol5002297
Kosobokov, Mikhail D, et al. "Geminal silicon/zinc reagent as an equivalent of difluoromethylene bis-carbanion." Organic letters vol. 16,5 (2014): 1438-41. doi: https://doi.org/10.1021/ol5002297
Kosobokov MD, Levin VV, Zemtsov AA, Struchkova MI, Korlyukov AA, Arkhipov DE, Dilman AD. Geminal silicon/zinc reagent as an equivalent of difluoromethylene bis-carbanion. Org Lett. 2014 Mar 07;16(5):1438-41. doi: 10.1021/ol5002297. Epub 2014 Feb 19. PMID: 24552348.
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One-year antibody persistence and safety of a 4-dose schedule of MenACWY-CRM in healthy infants from South Korea.

Clinical and experimental vaccine research

Lee HJ, Jo DS, Kim YK, Lee H, Kim KH, Lee D, Curina C, Costantini M, Barbi S, Miao Y, Pellegrini M.
PMID: 31406690
Clin Exp Vaccine Res. 2019 Jul;8(2):94-102. doi: 10.7774/cevr.2019.8.2.94. Epub 2019 Jul 31.

PURPOSE: Results from a post-marketing study to generate evidence on 1-year antibody persistence and safety following vaccination of infants from South Korea with the quadrivalent meningococcal conjugate vaccine MenACWY-CRM.MATERIALS AND METHODS: In this phase IV, open-label, multi-center study (NCT02446691),...

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Lee HJ, Jo DS, Kim YK, et al. One-year antibody persistence and safety of a 4-dose schedule of MenACWY-CRM in healthy infants from South Korea. Clin Exp Vaccine Res. 2019;8(2):94-102doi: 10.7774/cevr.2019.8.2.94.
Lee, H. J., Jo, D. S., Kim, Y. K., Lee, H., Kim, K. H., Lee, D., Curina, C., Costantini, M., Barbi, S., Miao, Y., & Pellegrini, M. (2019). One-year antibody persistence and safety of a 4-dose schedule of MenACWY-CRM in healthy infants from South Korea. Clinical and experimental vaccine research, 8(2), 94-102. https://doi.org/10.7774/cevr.2019.8.2.94
Lee, Hoan-Jong, et al. "One-year antibody persistence and safety of a 4-dose schedule of MenACWY-CRM in healthy infants from South Korea." Clinical and experimental vaccine research vol. 8,2 (2019): 94-102. doi: https://doi.org/10.7774/cevr.2019.8.2.94
Lee HJ, Jo DS, Kim YK, Lee H, Kim KH, Lee D, Curina C, Costantini M, Barbi S, Miao Y, Pellegrini M. One-year antibody persistence and safety of a 4-dose schedule of MenACWY-CRM in healthy infants from South Korea. Clin Exp Vaccine Res. 2019 Jul;8(2):94-102. doi: 10.7774/cevr.2019.8.2.94. Epub 2019 Jul 31. PMID: 31406690; PMCID: PMC6689500.
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New species and new records of .

ZooKeys

Kurina O, Hippa H, Amorim DS.
PMID: 28769645
Zookeys. 2017 Apr 13;(668):83-105. doi: 10.3897/zookeys.668.11350. eCollection 2017.

The following five species are described as new:

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Kurina O, Hippa H, Amorim DS. New species and new records of . Zookeys. 2017;(668):83-105doi: 10.3897/zookeys.668.11350.
Kurina, O., Hippa, H., & Amorim, D. S. (2017). New species and new records of . ZooKeys, (668), 83-105. https://doi.org/10.3897/zookeys.668.11350
Kurina, Olavi, et al. "New species and new records of ." ZooKeys vol. ,668 (2017): 83-105. doi: https://doi.org/10.3897/zookeys.668.11350
Kurina O, Hippa H, Amorim DS. New species and new records of . Zookeys. 2017 Apr 13;(668):83-105. doi: 10.3897/zookeys.668.11350. eCollection 2017. PMID: 28769645; PMCID: PMC5538008.
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Bioactivity-Guided Isolation of Totarane-Derived Diterpenes from Podocarpus neriifolius and Structure Revision of 3-Deoxy-2α-hydroxynagilactone E.

Natural products and bioprospecting

Benatrehina PA, Chen WL, Czarnecki AA, Kurina S, Chai HB, Lantvit DD, Ninh TN, Zhang X, Soejarto DD, Burdette JE, Kinghorn AD, Rakotondraibe LH.
PMID: 30783922
Nat Prod Bioprospect. 2019 Apr;9(2):157-163. doi: 10.1007/s13659-019-0198-x. Epub 2019 Feb 19.

Bioactivity-guided phytochemical investigation of Podocarpus neriifolius D. Don. (Podocarpaceae) has led to the isolation of one new (2) and three known (1, 3, and 4) B-type podolactones, along with three totarane-type diterpenes (5-7). Their structures were determined by interpretation...

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Benatrehina PA, Chen WL, Czarnecki AA, et al. Bioactivity-Guided Isolation of Totarane-Derived Diterpenes from Podocarpus neriifolius and Structure Revision of 3-Deoxy-2α-hydroxynagilactone E. Nat Prod Bioprospect. 2019;9(2):157-163doi: 10.1007/s13659-019-0198-x.
Benatrehina, P. A., Chen, W. L., Czarnecki, A. A., Kurina, S., Chai, H. B., Lantvit, D. D., Ninh, T. N., Zhang, X., Soejarto, D. D., Burdette, J. E., Kinghorn, A. D., & Rakotondraibe, L. H. (2019). Bioactivity-Guided Isolation of Totarane-Derived Diterpenes from Podocarpus neriifolius and Structure Revision of 3-Deoxy-2α-hydroxynagilactone E. Natural products and bioprospecting, 9(2), 157-163. https://doi.org/10.1007/s13659-019-0198-x
Benatrehina, P Annécie, et al. "Bioactivity-Guided Isolation of Totarane-Derived Diterpenes from Podocarpus neriifolius and Structure Revision of 3-Deoxy-2α-hydroxynagilactone E." Natural products and bioprospecting vol. 9,2 (2019): 157-163. doi: https://doi.org/10.1007/s13659-019-0198-x
Benatrehina PA, Chen WL, Czarnecki AA, Kurina S, Chai HB, Lantvit DD, Ninh TN, Zhang X, Soejarto DD, Burdette JE, Kinghorn AD, Rakotondraibe LH. Bioactivity-Guided Isolation of Totarane-Derived Diterpenes from Podocarpus neriifolius and Structure Revision of 3-Deoxy-2α-hydroxynagilactone E. Nat Prod Bioprospect. 2019 Apr;9(2):157-163. doi: 10.1007/s13659-019-0198-x. Epub 2019 Feb 19. PMID: 30783922; PMCID: PMC6426912.
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Showing 1 to 12 of 250 entries