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Pro-angiogenic Role of Insulin: From Physiology to Pathology.

Frontiers in physiology

Escudero CA, Herlitz K, Troncoso F, Guevara K, Acurio J, Aguayo C, Godoy AS, González M.
PMID: 28424632
Front Physiol. 2017 Apr 05;8:204. doi: 10.3389/fphys.2017.00204. eCollection 2017.

The underlying molecular mechanisms involve in the regulation of the angiogenic process by insulin are not well understood. In this review article, we aim to describe the role of insulin and insulin receptor activation on the control of angiogenesis...

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Escudero CA, Herlitz K, Troncoso F, et al. Pro-angiogenic Role of Insulin: From Physiology to Pathology. Front Physiol. 2017;8:204doi: 10.3389/fphys.2017.00204.
Escudero, C. A., Herlitz, K., Troncoso, F., Guevara, K., Acurio, J., Aguayo, C., Godoy, A. S., & González, M. (2017). Pro-angiogenic Role of Insulin: From Physiology to Pathology. Frontiers in physiology, 8204. https://doi.org/10.3389/fphys.2017.00204
Escudero, Carlos A, et al. "Pro-angiogenic Role of Insulin: From Physiology to Pathology." Frontiers in physiology vol. 8 (2017): 204. doi: https://doi.org/10.3389/fphys.2017.00204
Escudero CA, Herlitz K, Troncoso F, Guevara K, Acurio J, Aguayo C, Godoy AS, González M. Pro-angiogenic Role of Insulin: From Physiology to Pathology. Front Physiol. 2017 Apr 05;8:204. doi: 10.3389/fphys.2017.00204. eCollection 2017. PMID: 28424632; PMCID: PMC5380736.
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Features of alpha-synuclein that could explain the progression and irreversibility of Parkinson's disease.

Frontiers in neuroscience

Gallegos S, Pacheco C, Peters C, Opazo CM, Aguayo LG.
PMID: 25805964
Front Neurosci. 2015 Mar 09;9:59. doi: 10.3389/fnins.2015.00059. eCollection 2015.

Alpha-synuclein is a presynaptic protein expressed throughout the central nervous system, and it is the main component of Lewy bodies, one of the histopathological features of Parkinson's disease (PD) which is a progressive and irreversible neurodegenerative disorder. The conformational...

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Gallegos S, Pacheco C, Peters C, et al. Features of alpha-synuclein that could explain the progression and irreversibility of Parkinson's disease. Front Neurosci. 2015;9:59doi: 10.3389/fnins.2015.00059.
Gallegos, S., Pacheco, C., Peters, C., Opazo, C. M., & Aguayo, L. G. (2015). Features of alpha-synuclein that could explain the progression and irreversibility of Parkinson's disease. Frontiers in neuroscience, 959. https://doi.org/10.3389/fnins.2015.00059
Gallegos, Scarlet, et al. "Features of alpha-synuclein that could explain the progression and irreversibility of Parkinson's disease." Frontiers in neuroscience vol. 9 (2015): 59. doi: https://doi.org/10.3389/fnins.2015.00059
Gallegos S, Pacheco C, Peters C, Opazo CM, Aguayo LG. Features of alpha-synuclein that could explain the progression and irreversibility of Parkinson's disease. Front Neurosci. 2015 Mar 09;9:59. doi: 10.3389/fnins.2015.00059. eCollection 2015. PMID: 25805964; PMCID: PMC4353246.
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Potentiation of Gamma Aminobutyric Acid Receptors (GABAAR) by Ethanol: How Are Inhibitory Receptors Affected?.

Frontiers in cellular neuroscience

Förstera B, Castro PA, Moraga-Cid G, Aguayo LG.
PMID: 27199667
Front Cell Neurosci. 2016 May 06;10:114. doi: 10.3389/fncel.2016.00114. eCollection 2016.

In recent years there has been an increase in the understanding of ethanol actions on the type A γ-aminobutyric acid chloride channel (GABAAR), a member of the pentameric ligand gated ion channels (pLGICs). However, the mechanism by which ethanol...

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Förstera B, Castro PA, Moraga-Cid G, et al. Potentiation of Gamma Aminobutyric Acid Receptors (GABAAR) by Ethanol: How Are Inhibitory Receptors Affected?. Front Cell Neurosci. 2016;10:114doi: 10.3389/fncel.2016.00114.
Förstera, B., Castro, P. A., Moraga-Cid, G., & Aguayo, L. G. (2016). Potentiation of Gamma Aminobutyric Acid Receptors (GABAAR) by Ethanol: How Are Inhibitory Receptors Affected?. Frontiers in cellular neuroscience, 10114. https://doi.org/10.3389/fncel.2016.00114
Förstera, Benjamin, et al. "Potentiation of Gamma Aminobutyric Acid Receptors (GABAAR) by Ethanol: How Are Inhibitory Receptors Affected?." Frontiers in cellular neuroscience vol. 10 (2016): 114. doi: https://doi.org/10.3389/fncel.2016.00114
Förstera B, Castro PA, Moraga-Cid G, Aguayo LG. Potentiation of Gamma Aminobutyric Acid Receptors (GABAAR) by Ethanol: How Are Inhibitory Receptors Affected?. Front Cell Neurosci. 2016 May 06;10:114. doi: 10.3389/fncel.2016.00114. eCollection 2016. PMID: 27199667; PMCID: PMC4858537.
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Polyol specificity of recombinant Arabidopsis thaliana sorbitol dehydrogenase studied by enzyme kinetics and in silico modeling.

Frontiers in plant science

Aguayo MF, Cáceres JC, Fuentealba M, Muñoz R, Stange C, Cabrera R, Handford M.
PMID: 25755662
Front Plant Sci. 2015 Feb 23;6:91. doi: 10.3389/fpls.2015.00091. eCollection 2015.

Polyols are enzymatically-produced plant compounds which can act as compatible solutes during periods of abiotic stress. Nicotinamide adenine dinucleotide(+)-dependent SORBITOL DEHYDROGENASE (SDH, E. C. 1.1.1.14) from Arabidopsis thaliana L. sorbitol dehydrogenase (AtSDH) is capable of oxidizing several polyols including...

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Aguayo MF, Cáceres JC, Fuentealba M, et al. Polyol specificity of recombinant Arabidopsis thaliana sorbitol dehydrogenase studied by enzyme kinetics and in silico modeling. Front Plant Sci. 2015;6:91doi: 10.3389/fpls.2015.00091.
Aguayo, M. F., Cáceres, J. C., Fuentealba, M., Muñoz, R., Stange, C., Cabrera, R., & Handford, M. (2015). Polyol specificity of recombinant Arabidopsis thaliana sorbitol dehydrogenase studied by enzyme kinetics and in silico modeling. Frontiers in plant science, 691. https://doi.org/10.3389/fpls.2015.00091
Aguayo, M Francisca, et al. "Polyol specificity of recombinant Arabidopsis thaliana sorbitol dehydrogenase studied by enzyme kinetics and in silico modeling." Frontiers in plant science vol. 6 (2015): 91. doi: https://doi.org/10.3389/fpls.2015.00091
Aguayo MF, Cáceres JC, Fuentealba M, Muñoz R, Stange C, Cabrera R, Handford M. Polyol specificity of recombinant Arabidopsis thaliana sorbitol dehydrogenase studied by enzyme kinetics and in silico modeling. Front Plant Sci. 2015 Feb 23;6:91. doi: 10.3389/fpls.2015.00091. eCollection 2015. PMID: 25755662; PMCID: PMC4337239.
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Fe(AsO4): a new iron(III) arsenate synthesized from thermal treatment of (NH4)[Fe(AsO4)F].

Chemical communications (Cambridge, England)

Bazán B, Mesa JL, Pizarro JL, Aguayo AT, Arriortua MI, Rojo T.
PMID: 12669855
Chem Commun (Camb). 2003 Mar 07;(5):622-3. doi: 10.1039/b210998k.

The new orthorhombic Fe(AsO4) phase has been synthesized by thermal treatment at 525 degrees C of a new (NH4)[Fe(AsO4)F] compound, with a [Fe(AsO4)F]- skeleton showing channels where the ammonium cations are located. The crystal structure of Fe(AsO4) has been...

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Bazán B, Mesa JL, Pizarro JL, et al. Fe(AsO4): a new iron(III) arsenate synthesized from thermal treatment of (NH4)[Fe(AsO4)F]. Chem Commun (Camb). 2003;(5):622-3doi: 10.1039/b210998k.
Bazán, B., Mesa, J. L., Pizarro, J. L., Aguayo, A. T., Arriortua, M. I., & Rojo, T. (2003). Fe(AsO4): a new iron(III) arsenate synthesized from thermal treatment of (NH4)[Fe(AsO4)F]. Chemical communications (Cambridge, England), (5), 622-3. https://doi.org/10.1039/b210998k
Bazán, Begoña, et al. "Fe(AsO4): a new iron(III) arsenate synthesized from thermal treatment of (NH4)[Fe(AsO4)F]." Chemical communications (Cambridge, England) vol. ,5 (2003): 622-3. doi: https://doi.org/10.1039/b210998k
Bazán B, Mesa JL, Pizarro JL, Aguayo AT, Arriortua MI, Rojo T. Fe(AsO4): a new iron(III) arsenate synthesized from thermal treatment of (NH4)[Fe(AsO4)F]. Chem Commun (Camb). 2003 Mar 07;(5):622-3. doi: 10.1039/b210998k. PMID: 12669855.
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Kinetic investigation of the reactions of S-4-nitrophenyl 4-substituted thiobenzoates with secondary alicyclic amines in aqueous ethanol.

The Journal of organic chemistry

Castro EA, Bessolo J, Aguayo R, Santos JG.
PMID: 14535798
J Org Chem. 2003 Oct 17;68(21):8157-61. doi: 10.1021/jo0348120.

The reactions of S-4-nitrophenyl 4-X-substituted thiobenzoates (X = H, Cl, and NO(2): 1, 2, and 3, respectively) with a series of secondary alicyclic amines (SAA) were subjected to a kinetic investigation in 44 wt % ethanol-water, at 25.0 degrees...

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Castro EA, Bessolo J, Aguayo R, et al. Kinetic investigation of the reactions of S-4-nitrophenyl 4-substituted thiobenzoates with secondary alicyclic amines in aqueous ethanol. J Org Chem. 2003;68(21):8157-61doi: 10.1021/jo0348120.
Castro, E. A., Bessolo, J., Aguayo, R., & Santos, J. G. (2003). Kinetic investigation of the reactions of S-4-nitrophenyl 4-substituted thiobenzoates with secondary alicyclic amines in aqueous ethanol. The Journal of organic chemistry, 68(21), 8157-61. https://doi.org/10.1021/jo0348120
Castro, Enrique A, et al. "Kinetic investigation of the reactions of S-4-nitrophenyl 4-substituted thiobenzoates with secondary alicyclic amines in aqueous ethanol." The Journal of organic chemistry vol. 68,21 (2003): 8157-61. doi: https://doi.org/10.1021/jo0348120
Castro EA, Bessolo J, Aguayo R, Santos JG. Kinetic investigation of the reactions of S-4-nitrophenyl 4-substituted thiobenzoates with secondary alicyclic amines in aqueous ethanol. J Org Chem. 2003 Oct 17;68(21):8157-61. doi: 10.1021/jo0348120. PMID: 14535798.
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Why Ni3Al is an itinerant ferromagnet but Ni3Ga is not.

Physical review letters

Aguayo A, Mazin II, Singh DJ.
PMID: 15089568
Phys Rev Lett. 2004 Apr 09;92(14):147201. doi: 10.1103/PhysRevLett.92.147201. Epub 2004 Apr 05.

Ni3Al and Ni3Ga are closely related materials on opposite sides of a ferromagnetic quantum critical point. The Stoner factor of Ni is virtually the same in both compounds and the density of states is larger in Ni3Ga. Thus in...

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Aguayo A, Mazin II, Singh DJ. Why Ni3Al is an itinerant ferromagnet but Ni3Ga is not. Phys Rev Lett. 2004;92(14):147201doi: 10.1103/PhysRevLett.92.147201.
Aguayo, A., Mazin, I. I., & Singh, D. J. (2004). Why Ni3Al is an itinerant ferromagnet but Ni3Ga is not. Physical review letters, 92(14), 147201. https://doi.org/10.1103/PhysRevLett.92.147201
Aguayo, A, et al. "Why Ni3Al is an itinerant ferromagnet but Ni3Ga is not." Physical review letters vol. 92,14 (2004): 147201. doi: https://doi.org/10.1103/PhysRevLett.92.147201
Aguayo A, Mazin II, Singh DJ. Why Ni3Al is an itinerant ferromagnet but Ni3Ga is not. Phys Rev Lett. 2004 Apr 09;92(14):147201. doi: 10.1103/PhysRevLett.92.147201. Epub 2004 Apr 05. PMID: 15089568.
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Kinetics and mechanism of the pyridinolysis of s-4-nitrophenyl 4-substituted thiobenzoates in aqueous ethanol.

The Journal of organic chemistry

Castro EA, Vivanco M, Aguayo R, Santos JG.
PMID: 15287788
J Org Chem. 2004 Aug 06;69(16):5399-404. doi: 10.1021/jo049260f.

The pyridinolysis of S-4-nitrophenyl 4-X-substituted thiobenzoates (X = H, Cl, and NO2; 1, 2, and 3, respectively) is studied kinetically in 44 wt % ethanol-water, at 25.0 degrees C and an ionic strength of 0.2 M (KCl). The reactions...

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Castro EA, Vivanco M, Aguayo R, et al. Kinetics and mechanism of the pyridinolysis of s-4-nitrophenyl 4-substituted thiobenzoates in aqueous ethanol. J Org Chem. 2004;69(16):5399-404doi: 10.1021/jo049260f.
Castro, E. A., Vivanco, M., Aguayo, R., & Santos, J. G. (2004). Kinetics and mechanism of the pyridinolysis of s-4-nitrophenyl 4-substituted thiobenzoates in aqueous ethanol. The Journal of organic chemistry, 69(16), 5399-404. https://doi.org/10.1021/jo049260f
Castro, Enrique A, et al. "Kinetics and mechanism of the pyridinolysis of s-4-nitrophenyl 4-substituted thiobenzoates in aqueous ethanol." The Journal of organic chemistry vol. 69,16 (2004): 5399-404. doi: https://doi.org/10.1021/jo049260f
Castro EA, Vivanco M, Aguayo R, Santos JG. Kinetics and mechanism of the pyridinolysis of s-4-nitrophenyl 4-substituted thiobenzoates in aqueous ethanol. J Org Chem. 2004 Aug 06;69(16):5399-404. doi: 10.1021/jo049260f. PMID: 15287788.
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Laminated diatomaceous sediments from the guaymas basin slope (central gulf of california): 250,000-year climate record.

Science (New York, N.Y.)

Schrader H, Kelts K, Curray J, Moore D, Aguayo E, Aubry MP, Einsele G, Fornari D, Gieskes J, Guerrero J, Kastner M, Lyle M, Matoba Y, Molina-Cruz A, Niemitz J, Rueda J, Saunders A, Simoneit B, Vaquier V.
PMID: 17776858
Science. 1980 Mar 14;207(4436):1207-9. doi: 10.1126/science.207.4436.1207.

During Deep Sea Drilling Project-International Program of Ocean Drilling leg 64, December 1978 to January 1979, the initial test of the Deep Sea Drilling Project's hydraulic piston corer obtained an almost undisturbed section from a 152-meter hole into the...

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Schrader H, Kelts K, Curray J, et al. Laminated diatomaceous sediments from the guaymas basin slope (central gulf of california): 250,000-year climate record. Science. 1980;207(4436):1207-9doi: 10.1126/science.207.4436.1207.
Schrader, H., Kelts, K., Curray, J., Moore, D., Aguayo, E., Aubry, M. P., Einsele, G., Fornari, D., Gieskes, J., Guerrero, J., Kastner, M., Lyle, M., Matoba, Y., Molina-Cruz, A., Niemitz, J., Rueda, J., Saunders, A., Simoneit, B., & Vaquier, V. (1980). Laminated diatomaceous sediments from the guaymas basin slope (central gulf of california): 250,000-year climate record. Science (New York, N.Y.), 207(4436), 1207-9. https://doi.org/10.1126/science.207.4436.1207
Schrader, H, et al. "Laminated diatomaceous sediments from the guaymas basin slope (central gulf of california): 250,000-year climate record." Science (New York, N.Y.) vol. 207,4436 (1980): 1207-9. doi: https://doi.org/10.1126/science.207.4436.1207
Schrader H, Kelts K, Curray J, Moore D, Aguayo E, Aubry MP, Einsele G, Fornari D, Gieskes J, Guerrero J, Kastner M, Lyle M, Matoba Y, Molina-Cruz A, Niemitz J, Rueda J, Saunders A, Simoneit B, Vaquier V. Laminated diatomaceous sediments from the guaymas basin slope (central gulf of california): 250,000-year climate record. Science. 1980 Mar 14;207(4436):1207-9. doi: 10.1126/science.207.4436.1207. PMID: 17776858.
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Method of achieving phase delay with wide optical bandwidth in multimode interference devices.

Optics letters

Lorenzo RM, Llorente C, Abril EJ, Aguado JC, López M.
PMID: 18091902
Opt Lett. 1998 Nov 15;23(22):1748-50. doi: 10.1364/ol.23.001748.

A completely passive method of achieving phase delays inside multimode interference devices is presented. The desired relative phase is obtained by adjustment of the width of the waveguides in conjunction with the tapers to avoid interference inside the multimode...

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Lorenzo RM, Llorente C, Abril EJ, et al. Method of achieving phase delay with wide optical bandwidth in multimode interference devices. Opt Lett. 1998;23(22):1748-50doi: 10.1364/ol.23.001748.
Lorenzo, R. M., Llorente, C., Abril, E. J., Aguado, J. C., & López, M. (1998). Method of achieving phase delay with wide optical bandwidth in multimode interference devices. Optics letters, 23(22), 1748-50. https://doi.org/10.1364/ol.23.001748
Lorenzo, R M, et al. "Method of achieving phase delay with wide optical bandwidth in multimode interference devices." Optics letters vol. 23,22 (1998): 1748-50. doi: https://doi.org/10.1364/ol.23.001748
Lorenzo RM, Llorente C, Abril EJ, Aguado JC, López M. Method of achieving phase delay with wide optical bandwidth in multimode interference devices. Opt Lett. 1998 Nov 15;23(22):1748-50. doi: 10.1364/ol.23.001748. PMID: 18091902.
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[Multiresistant Acinetobacter baumannii: an universal challenge].

Medicina clinica

Catalán M, Aguado JM.
PMID: 20605030
Med Clin (Barc). 2010 Sep 18;135(9):406-7. doi: 10.1016/j.medcli.2010.04.003. Epub 2010 Jul 06.

No abstract available.

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Catalán M, Aguado JM. Acinetobacter baumannii multirresistente: "un reto universal". [Multiresistant Acinetobacter baumannii: an universal challenge]. Med Clin (Barc). 2010;135(9):406-7doi: 10.1016/j.medcli.2010.04.003.
Catalán, M., & Aguado, J. M. (2010). Acinetobacter baumannii multirresistente: "un reto universal". [Multiresistant Acinetobacter baumannii: an universal challenge]. Medicina clinica, 135(9), 406-7. https://doi.org/10.1016/j.medcli.2010.04.003
Catalán, Mercedes, and Aguado, José María. "Acinetobacter baumannii multirresistente: "un reto universal"." [Multiresistant Acinetobacter baumannii: an universal challenge]. Medicina clinica vol. 135,9 (2010): 406-7. doi: https://doi.org/10.1016/j.medcli.2010.04.003
Catalán M, Aguado JM. Acinetobacter baumannii multirresistente: "un reto universal". [Multiresistant Acinetobacter baumannii: an universal challenge]. Med Clin (Barc). 2010 Sep 18;135(9):406-7. doi: 10.1016/j.medcli.2010.04.003. Epub 2010 Jul 06. Spanish. PMID: 20605030.
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Effect of posterior pituitary lobectomy on in vivo and in vitro secretion of prolactin in lactating rats.

Endocrine

Mena F, Aguayo D, Vigueras M, Quintanar-Stephano A, Perera G, Morales T.
PMID: 21153079
Endocrine. 1996 Dec;5(3):285-90. doi: 10.1007/BF02739061.

The effect of removing the posterior and neuro-intermediate lobes (PLX) of the pituitary gland of lactating rats was determined on both suckling-induced release and transformation of prolactin (PRL), and on regionalization of PRL release. Sixteen hours, or 1 or...

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Mena F, Aguayo D, Vigueras M, et al. Effect of posterior pituitary lobectomy on in vivo and in vitro secretion of prolactin in lactating rats. Endocrine. 1996;5(3):285-90doi: 10.1007/BF02739061.
Mena, F., Aguayo, D., Vigueras, M., Quintanar-Stephano, A., Perera, G., & Morales, T. (1996). Effect of posterior pituitary lobectomy on in vivo and in vitro secretion of prolactin in lactating rats. Endocrine, 5(3), 285-90. https://doi.org/10.1007/BF02739061
Mena, F, et al. "Effect of posterior pituitary lobectomy on in vivo and in vitro secretion of prolactin in lactating rats." Endocrine vol. 5,3 (1996): 285-90. doi: https://doi.org/10.1007/BF02739061
Mena F, Aguayo D, Vigueras M, Quintanar-Stephano A, Perera G, Morales T. Effect of posterior pituitary lobectomy on in vivo and in vitro secretion of prolactin in lactating rats. Endocrine. 1996 Dec;5(3):285-90. doi: 10.1007/BF02739061. PMID: 21153079.
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Showing 1 to 12 of 280 entries