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[The feldshers in the U.S.S.R].

Revue de l'infirmiere et de l'assistante sociale

Christoforov B.
PMID: 4183666
Rev Infirm Assist Soc. 1969 Jun;19(6):659-62.

No abstract available.

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Christoforov B. Les feldshers en U.R.S.S. [The feldshers in the U.S.S.R]. Rev Infirm Assist Soc. 1969;19(6):659-62
Christoforov, B. (1969). Les feldshers en U.R.S.S. [The feldshers in the U.S.S.R]. Revue de l'infirmiere et de l'assistante sociale, 19(6), 659-62.
Christoforov, B. "Les feldshers en U.R.S.S." [The feldshers in the U.S.S.R]. Revue de l'infirmiere et de l'assistante sociale vol. 19,6 (1969): 659-62.
Christoforov B. Les feldshers en U.R.S.S. [The feldshers in the U.S.S.R]. Rev Infirm Assist Soc. 1969 Jun;19(6):659-62. French. PMID: 4183666.
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CD45+ Cells Present Within Mesenchymal Stem Cell Populations Affect Network Formation of Blood-Derived Endothelial Outgrowth Cells.

BioResearch open access

Peters EB, Christoforou N, Moore E, West JL, Truskey GA.
PMID: 26309784
Biores Open Access. 2015 Jan 01;4(1):75-88. doi: 10.1089/biores.2014.0029. eCollection 2015.

Mesenchymal stem cells (MSCs) and endothelial progenitor cells (EPCs) represent promising cell sources for angiogenic therapies. There are, however, conflicting reports regarding the ability of MSCs to support network formation of endothelial cells. The goal of this study was...

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Peters EB, Christoforou N, Moore E, et al. CD45+ Cells Present Within Mesenchymal Stem Cell Populations Affect Network Formation of Blood-Derived Endothelial Outgrowth Cells. Biores Open Access. 2015;4(1):75-88doi: 10.1089/biores.2014.0029.
Peters, E. B., Christoforou, N., Moore, E., West, J. L., & Truskey, G. A. (2015). CD45+ Cells Present Within Mesenchymal Stem Cell Populations Affect Network Formation of Blood-Derived Endothelial Outgrowth Cells. BioResearch open access, 4(1), 75-88. https://doi.org/10.1089/biores.2014.0029
Peters, Erica B, et al. "CD45+ Cells Present Within Mesenchymal Stem Cell Populations Affect Network Formation of Blood-Derived Endothelial Outgrowth Cells." BioResearch open access vol. 4,1 (2015): 75-88. doi: https://doi.org/10.1089/biores.2014.0029
Peters EB, Christoforou N, Moore E, West JL, Truskey GA. CD45+ Cells Present Within Mesenchymal Stem Cell Populations Affect Network Formation of Blood-Derived Endothelial Outgrowth Cells. Biores Open Access. 2015 Jan 01;4(1):75-88. doi: 10.1089/biores.2014.0029. eCollection 2015. PMID: 26309784; PMCID: PMC4497669.
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Poly(ethylene glycol) Hydrogel Scaffolds Containing Cell-Adhesive and Protease-Sensitive Peptides Support Microvessel Formation by Endothelial Progenitor Cells.

Cellular and molecular bioengineering

Peters EB, Christoforou N, Leong KW, Truskey GA, West JL.
PMID: 27042236
Cell Mol Bioeng. 2016 Mar 01;9(1):38-54. doi: 10.1007/s12195-015-0423-6. Epub 2015 Oct 20.

The development of stable, functional microvessels remains an important obstacle to overcome for tissue engineered organs and treatment of ischemia. Endothelial progenitor cells (EPCs) are a promising cell source for vascular tissue engineering as they are readily obtainable and...

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Peters EB, Christoforou N, Leong KW, et al. Poly(ethylene glycol) Hydrogel Scaffolds Containing Cell-Adhesive and Protease-Sensitive Peptides Support Microvessel Formation by Endothelial Progenitor Cells. Cell Mol Bioeng. 2015;9(1):38-54doi: 10.1007/s12195-015-0423-6.
Peters, E. B., Christoforou, N., Leong, K. W., Truskey, G. A., & West, J. L. (2016). Poly(ethylene glycol) Hydrogel Scaffolds Containing Cell-Adhesive and Protease-Sensitive Peptides Support Microvessel Formation by Endothelial Progenitor Cells. Cellular and molecular bioengineering, 9(1), 38-54. https://doi.org/10.1007/s12195-015-0423-6
Peters, Erica B, et al. "Poly(ethylene glycol) Hydrogel Scaffolds Containing Cell-Adhesive and Protease-Sensitive Peptides Support Microvessel Formation by Endothelial Progenitor Cells." Cellular and molecular bioengineering vol. 9,1 (2016): 38-54. doi: https://doi.org/10.1007/s12195-015-0423-6
Peters EB, Christoforou N, Leong KW, Truskey GA, West JL. Poly(ethylene glycol) Hydrogel Scaffolds Containing Cell-Adhesive and Protease-Sensitive Peptides Support Microvessel Formation by Endothelial Progenitor Cells. Cell Mol Bioeng. 2016 Mar 01;9(1):38-54. doi: 10.1007/s12195-015-0423-6. Epub 2015 Oct 20. PMID: 27042236; PMCID: PMC4812433.
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Hemiaminals as substrates for sulfur ylides: direct asymmetric syntheses of functionalised pyrrolidines and piperidines.

Chemical communications (Cambridge, England)

Kokotos CG, Aggarwal VK.
PMID: 16703139
Chem Commun (Camb). 2006 May 28;(20):2156-8. doi: 10.1039/b602226j. Epub 2006 Apr 13.

Phenyl stabilised chiral sulfur ylides react with five-membered-ring hemiaminals to give functionalised pyrrolidines directly with high enantioselectivity. The reaction can be diverted to give piperidines instead by isolation of the intermediate epoxide and treatment with TMSOTf.

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Kokotos CG, Aggarwal VK. Hemiaminals as substrates for sulfur ylides: direct asymmetric syntheses of functionalised pyrrolidines and piperidines. Chem Commun (Camb). 2006;(20):2156-8doi: 10.1039/b602226j.
Kokotos, C. G., & Aggarwal, V. K. (2006). Hemiaminals as substrates for sulfur ylides: direct asymmetric syntheses of functionalised pyrrolidines and piperidines. Chemical communications (Cambridge, England), (20), 2156-8. https://doi.org/10.1039/b602226j
Kokotos, Christoforos G, and Aggarwal, Varinder K. "Hemiaminals as substrates for sulfur ylides: direct asymmetric syntheses of functionalised pyrrolidines and piperidines." Chemical communications (Cambridge, England) vol. ,20 (2006): 2156-8. doi: https://doi.org/10.1039/b602226j
Kokotos CG, Aggarwal VK. Hemiaminals as substrates for sulfur ylides: direct asymmetric syntheses of functionalised pyrrolidines and piperidines. Chem Commun (Camb). 2006 May 28;(20):2156-8. doi: 10.1039/b602226j. Epub 2006 Apr 13. PMID: 16703139.
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Aminals as substrates for sulfur ylides: a synthesis of functionalized aziridines and N-heterocycles.

Organic letters

Kokotos CG, Aggarwal VK.
PMID: 17465558
Org Lett. 2007 May 24;9(11):2099-102. doi: 10.1021/ol070507f. Epub 2007 Apr 28.

Sulfur ylides stabilized by Ar, vinyl, or amide groups react with five-membered-ring tert-butylsulfinyl aminals to give functionalized chiral, nonracemic aziridines in high yield and with good selectivities (up to 15:1 trans:cis, up to >95:5 trans dr, always >95:5 cis...

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Kokotos CG, Aggarwal VK. Aminals as substrates for sulfur ylides: a synthesis of functionalized aziridines and N-heterocycles. Org Lett. 2007;9(11):2099-102doi: 10.1021/ol070507f.
Kokotos, C. G., & Aggarwal, V. K. (2007). Aminals as substrates for sulfur ylides: a synthesis of functionalized aziridines and N-heterocycles. Organic letters, 9(11), 2099-102. https://doi.org/10.1021/ol070507f
Kokotos, Christoforos G, and Aggarwal, Varinder K. "Aminals as substrates for sulfur ylides: a synthesis of functionalized aziridines and N-heterocycles." Organic letters vol. 9,11 (2007): 2099-102. doi: https://doi.org/10.1021/ol070507f
Kokotos CG, Aggarwal VK. Aminals as substrates for sulfur ylides: a synthesis of functionalized aziridines and N-heterocycles. Org Lett. 2007 May 24;9(11):2099-102. doi: 10.1021/ol070507f. Epub 2007 Apr 28. PMID: 17465558.
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Magnetic Resonance Measurement of Transient Shear Wave Propagation in a Viscoelastic Gel Cylinder.

Journal of the mechanics and physics of solids

Bayly PV, Massouros PG, Christoforou E, Sabet A, Genin GM.
PMID: 18568090
J Mech Phys Solids. 2008 May;56(5):2036-2049. doi: 10.1016/j.jmps.2007.10.012.

A magnetic resonance measurement technique was developed to characterize the transient mechanical response of a gel cylinder subjected to angular acceleration. The technique employs tagged magnetic resonance imaging (MRI) synchronized to periodic impact excitation of a bulk specimen. The...

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Bayly PV, Massouros PG, Christoforou E, et al. Magnetic Resonance Measurement of Transient Shear Wave Propagation in a Viscoelastic Gel Cylinder. J Mech Phys Solids. 2008;56(5):2036-2049doi: 10.1016/j.jmps.2007.10.012.
Bayly, P. V., Massouros, P. G., Christoforou, E., Sabet, A., & Genin, G. M. (2008). Magnetic Resonance Measurement of Transient Shear Wave Propagation in a Viscoelastic Gel Cylinder. Journal of the mechanics and physics of solids, 56(5), 2036-2049. https://doi.org/10.1016/j.jmps.2007.10.012
Bayly, P V, et al. "Magnetic Resonance Measurement of Transient Shear Wave Propagation in a Viscoelastic Gel Cylinder." Journal of the mechanics and physics of solids vol. 56,5 (2008): 2036-2049. doi: https://doi.org/10.1016/j.jmps.2007.10.012
Bayly PV, Massouros PG, Christoforou E, Sabet A, Genin GM. Magnetic Resonance Measurement of Transient Shear Wave Propagation in a Viscoelastic Gel Cylinder. J Mech Phys Solids. 2008 May;56(5):2036-2049. doi: 10.1016/j.jmps.2007.10.012. PMID: 18568090; PMCID: PMC2435052.
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Green Photo-Organocatalytic C-H Activation of Aldehydes: Selective Hydroacylation of Electron-Deficient Alkenes.

Chemistry (Weinheim an der Bergstrasse, Germany)

Papadopoulos GN, Voutyritsa E, Kaplaneris N, Kokotos CG.
PMID: 29194813
Chemistry. 2018 Feb 01;24(7):1726-1731. doi: 10.1002/chem.201705634. Epub 2018 Jan 04.

Selective C-H activation is an area of growing importance. Metal-free C-H activation of branched aldehydes mediating the hydroacylation of electron-deficient alkenes is an attractive transformation, but is limited by selectivity issues, especially in the case of α,α-disubstituted aldehydes. Herein,...

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Papadopoulos GN, Voutyritsa E, Kaplaneris N, et al. Green Photo-Organocatalytic C-H Activation of Aldehydes: Selective Hydroacylation of Electron-Deficient Alkenes. Chemistry. 2018;24(7):1726-1731doi: 10.1002/chem.201705634.
Papadopoulos, G. N., Voutyritsa, E., Kaplaneris, N., & Kokotos, C. G. (2018). Green Photo-Organocatalytic C-H Activation of Aldehydes: Selective Hydroacylation of Electron-Deficient Alkenes. Chemistry (Weinheim an der Bergstrasse, Germany), 24(7), 1726-1731. https://doi.org/10.1002/chem.201705634
Papadopoulos, Giorgos N, et al. "Green Photo-Organocatalytic C-H Activation of Aldehydes: Selective Hydroacylation of Electron-Deficient Alkenes." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 24,7 (2018): 1726-1731. doi: https://doi.org/10.1002/chem.201705634
Papadopoulos GN, Voutyritsa E, Kaplaneris N, Kokotos CG. Green Photo-Organocatalytic C-H Activation of Aldehydes: Selective Hydroacylation of Electron-Deficient Alkenes. Chemistry. 2018 Feb 01;24(7):1726-1731. doi: 10.1002/chem.201705634. Epub 2018 Jan 04. PMID: 29194813.
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Photoorganocatalysis, small organic molecules and light in the service of organic synthesis: the awakening of a sleeping giant.

Organic & biomolecular chemistry

Sideri IK, Voutyritsa E, Kokotos CG.
PMID: 29888357
Org Biomol Chem. 2018 Jul 07;16(25):4596-4614. doi: 10.1039/c8ob00725j. Epub 2018 Jun 11.

Photocatalysis, the use of light to promote organic transformations, is a field of catalysis that has received limited attention despite existing for over 100 years. With the revolution of photoredox catalysis in 2008, the rebirth or awakening of the...

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Sideri IK, Voutyritsa E, Kokotos CG. Photoorganocatalysis, small organic molecules and light in the service of organic synthesis: the awakening of a sleeping giant. Org Biomol Chem. 2018;16(25):4596-4614doi: 10.1039/c8ob00725j.
Sideri, I. K., Voutyritsa, E., & Kokotos, C. G. (2018). Photoorganocatalysis, small organic molecules and light in the service of organic synthesis: the awakening of a sleeping giant. Organic & biomolecular chemistry, 16(25), 4596-4614. https://doi.org/10.1039/c8ob00725j
Sideri, Ioanna K, et al. "Photoorganocatalysis, small organic molecules and light in the service of organic synthesis: the awakening of a sleeping giant." Organic & biomolecular chemistry vol. 16,25 (2018): 4596-4614. doi: https://doi.org/10.1039/c8ob00725j
Sideri IK, Voutyritsa E, Kokotos CG. Photoorganocatalysis, small organic molecules and light in the service of organic synthesis: the awakening of a sleeping giant. Org Biomol Chem. 2018 Jul 07;16(25):4596-4614. doi: 10.1039/c8ob00725j. Epub 2018 Jun 11. PMID: 29888357.
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Development of Photocatalytic Coatings by Thermal Hydrolysis of TiCl.

Materials (Basel, Switzerland)

Christogerou A, Koumpouri D, Angelopoulos GN.
PMID: 32019232
Materials (Basel). 2020 Jan 30;13(3). doi: 10.3390/ma13030620.

The development of new, environmental friendly building materials with photocatalytic properties remain still on the top of the investigations both for academy and industry. The main drive is the increasing air pollution and the greenhouse gas emissions that have...

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Christogerou A, Koumpouri D, Angelopoulos GN. Development of Photocatalytic Coatings by Thermal Hydrolysis of TiCl. Materials (Basel). 2020;13(3)doi: 10.3390/ma13030620.
Christogerou, A., Koumpouri, D., & Angelopoulos, G. N. (2020). Development of Photocatalytic Coatings by Thermal Hydrolysis of TiCl. Materials (Basel, Switzerland), 13(3), . https://doi.org/10.3390/ma13030620
Christogerou, Angeliki, et al. "Development of Photocatalytic Coatings by Thermal Hydrolysis of TiCl." Materials (Basel, Switzerland) vol. 13,3 (2020). doi: https://doi.org/10.3390/ma13030620
Christogerou A, Koumpouri D, Angelopoulos GN. Development of Photocatalytic Coatings by Thermal Hydrolysis of TiCl. Materials (Basel). 2020 Jan 30;13(3). doi: 10.3390/ma13030620. PMID: 32019232; PMCID: PMC7040661.
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Erratum to: Umbilical Cord Blood-Derived Mononuclear Cells Exhibit Pericyte-Like Phenotype and Support Network Formation of Endothelial Progenitor Cells In Vitro.

Annals of biomedical engineering

Peters EB, Liu B, Christoforou N, West JL, Truskey GA.
PMID: 25877461
Ann Biomed Eng. 2015 Aug;43(8):2022. doi: 10.1007/s10439-015-1321-8.

No abstract available.

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Peters EB, Liu B, Christoforou N, et al. Erratum to: Umbilical Cord Blood-Derived Mononuclear Cells Exhibit Pericyte-Like Phenotype and Support Network Formation of Endothelial Progenitor Cells In Vitro. Ann Biomed Eng. 2015;43(8):2022doi: 10.1007/s10439-015-1321-8.
Peters, E. B., Liu, B., Christoforou, N., West, J. L., & Truskey, G. A. (2015). Erratum to: Umbilical Cord Blood-Derived Mononuclear Cells Exhibit Pericyte-Like Phenotype and Support Network Formation of Endothelial Progenitor Cells In Vitro. Annals of biomedical engineering, 43(8), 2022. https://doi.org/10.1007/s10439-015-1321-8
Peters, Erica B, et al. "Erratum to: Umbilical Cord Blood-Derived Mononuclear Cells Exhibit Pericyte-Like Phenotype and Support Network Formation of Endothelial Progenitor Cells In Vitro." Annals of biomedical engineering vol. 43,8 (2015): 2022. doi: https://doi.org/10.1007/s10439-015-1321-8
Peters EB, Liu B, Christoforou N, West JL, Truskey GA. Erratum to: Umbilical Cord Blood-Derived Mononuclear Cells Exhibit Pericyte-Like Phenotype and Support Network Formation of Endothelial Progenitor Cells In Vitro. Ann Biomed Eng. 2015 Aug;43(8):2022. doi: 10.1007/s10439-015-1321-8. PMID: 25877461.
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Penetrating Atherosclerotic Ulcers of the Abdominal Aorta: A Case Report and Review of the Literature.

Vascular specialist international

Kotsis T, Spyropoulos BG, Asaloumidis N, Christoforou P, Katseni K, Papaconstantinou I.
PMID: 31620401
Vasc Specialist Int. 2019 Sep;35(3):152-159. doi: 10.5758/vsi.2019.35.3.152. Epub 2019 Sep 30.

Penetrating atherosclerotic ulcers (PAUs) of the aorta are defined as atherosclerotic lesions with aortic intima and media ulceration, which may lead to a complete rupture of the adventitial wall. The present article aimed to report an unusual case of...

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Kotsis T, Spyropoulos BG, Asaloumidis N, et al. Penetrating Atherosclerotic Ulcers of the Abdominal Aorta: A Case Report and Review of the Literature. Vasc Specialist Int. 2019;35(3):152-159doi: 10.5758/vsi.2019.35.3.152.
Kotsis, T., Spyropoulos, B. G., Asaloumidis, N., Christoforou, P., Katseni, K., & Papaconstantinou, I. (2019). Penetrating Atherosclerotic Ulcers of the Abdominal Aorta: A Case Report and Review of the Literature. Vascular specialist international, 35(3), 152-159. https://doi.org/10.5758/vsi.2019.35.3.152
Kotsis, Thomas, et al. "Penetrating Atherosclerotic Ulcers of the Abdominal Aorta: A Case Report and Review of the Literature." Vascular specialist international vol. 35,3 (2019): 152-159. doi: https://doi.org/10.5758/vsi.2019.35.3.152
Kotsis T, Spyropoulos BG, Asaloumidis N, Christoforou P, Katseni K, Papaconstantinou I. Penetrating Atherosclerotic Ulcers of the Abdominal Aorta: A Case Report and Review of the Literature. Vasc Specialist Int. 2019 Sep;35(3):152-159. doi: 10.5758/vsi.2019.35.3.152. Epub 2019 Sep 30. PMID: 31620401; PMCID: PMC6774427.
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Photochemical Activation of Aromatic Aldehydes: Synthesis of Amides, Hydroxamic Acids and Esters.

Chemistry (Weinheim an der Bergstrasse, Germany)

Nikitas NF, Apostolopoulou MK, Skolia E, Tsoukaki A, Kokotos CG.
PMID: 33772903
Chemistry. 2021 May 20;27(29):7915-7922. doi: 10.1002/chem.202100655. Epub 2021 Apr 22.

A cheap, facile and metal-free photochemical protocol for the activation of aromatic aldehydes has been developed. Utilizing thioxanthen-9-one as the photocatalyst and cheap household lamps as the light source, a variety of aromatic aldehydes have been activated and subsequently...

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Nikitas NF, Apostolopoulou MK, Skolia E, et al. Photochemical Activation of Aromatic Aldehydes: Synthesis of Amides, Hydroxamic Acids and Esters. Chemistry. 2021;27(29):7915-7922doi: 10.1002/chem.202100655.
Nikitas, N. F., Apostolopoulou, M. K., Skolia, E., Tsoukaki, A., & Kokotos, C. G. (2021). Photochemical Activation of Aromatic Aldehydes: Synthesis of Amides, Hydroxamic Acids and Esters. Chemistry (Weinheim an der Bergstrasse, Germany), 27(29), 7915-7922. https://doi.org/10.1002/chem.202100655
Nikitas, Nikolaos F, et al. "Photochemical Activation of Aromatic Aldehydes: Synthesis of Amides, Hydroxamic Acids and Esters." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 27,29 (2021): 7915-7922. doi: https://doi.org/10.1002/chem.202100655
Nikitas NF, Apostolopoulou MK, Skolia E, Tsoukaki A, Kokotos CG. Photochemical Activation of Aromatic Aldehydes: Synthesis of Amides, Hydroxamic Acids and Esters. Chemistry. 2021 May 20;27(29):7915-7922. doi: 10.1002/chem.202100655. Epub 2021 Apr 22. PMID: 33772903.
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Showing 1 to 12 of 132 entries