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Dive into the research topics where Jorge Alberto Castañón-González is active.

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Featured researches published by Jorge Alberto Castañón-González.


Computational and Mathematical Methods in Medicine | 2013

Detection of Severe Respiratory Disease Epidemic Outbreaks by CUSUM-Based Overcrowd-Severe-Respiratory-Disease-Index Model

Carlos Polanco; Jorge Alberto Castañón-González; Alejandro Macias; José Lino Samaniego; Thomas Buhse; Sebastián Villanueva-Martínez

A severe respiratory disease epidemic outbreak correlates with a high demand of specific supplies and specialized personnel to hold it back in a wide region or set of regions; these supplies would be beds, storage areas, hemodynamic monitors, and mechanical ventilators, as well as physicians, respiratory technicians, and specialized nurses. We describe an online cumulative sum based model named Overcrowd-Severe-Respiratory-Disease-Index based on the Modified Overcrowd Index that simultaneously monitors and informs the demand of those supplies and personnel in a healthcare network generating early warnings of severe respiratory disease epidemic outbreaks through the interpretation of such variables. A post hoc historical archive is generated, helping physicians in charge to improve the transit and future allocation of supplies in the entire hospital network during the outbreak. The model was thoroughly verified in a virtual scenario, generating multiple epidemic outbreaks in a 6-year span for a 13-hospital network. When it was superimposed over the H1N1 influenza outbreak census (2008–2010) taken by the National Institute of Medical Sciences and Nutrition Salvador Zubiran in Mexico City, it showed that it is an effective algorithm to notify early warnings of severe respiratory disease epidemic outbreaks with a minimal rate of false alerts.


Cell Biochemistry and Biophysics | 2014

Polar Profile of Antiviral Peptides from AVPpred Database

Carlos Polanco; José Lino Samaniego; Jorge Alberto Castañón-González; Thomas Buhse

Diseases of viral origin in humans are among the most serious threats to health and the global economy. As recent history has shown the virus has a high pandemic potential, among other reasons, due to its ability to spread by air, hence the identification, investigation, containment, and treatment of viral diseases should be considered of paramount importance. In this sense, the bioinformatics research has focused on finding fast and efficient algorithms that can identify highly toxic antiviral peptides and to serve as a first filter, so that trials in the laboratory are substantially reduced. The work presented here contributes to this effort through the use of an algorithm already published by this team, called polarity index method, which identifies with high efficiency antiviral peptides from the exhaustive analysis of the polar profile, using the linear sequence of the peptide. The test carried out included all peptides in APD2 Database and 60 antiviral peptides identified by Kumar and co-workers (Nucleic Acids Res 40:W199–204, 2012), to build its AVPpred algorithm. The validity of the method was focused on its discriminating capacity so we included the 15 sub-classifications of both Databases.


Acta Biochimica Polonica | 2016

Classifying lipoproteins based on their polar profiles.

Carlos Polanco; Jorge Alberto Castañón-González; Thomas Buhse; Vladimir N. Uversky; Rafael Zonana Amkie

The lipoproteins are an important group of cargo proteins known for their unique capability to transport lipids. By applying the Polarity index algorithm, which has a metric that only considers the polar profile of the linear sequences of the lipoprotein group, we obtained an analytical and structural differentiation of all the lipoproteins found in UniProt Database. Also, the functional groups of lipoproteins, and particularly of the set of lipoproteins relevant to atherosclerosis, were analyzed with the same method to reveal their structural preference, and the results of Polarity index analysis were verified by an alternate test, the Cumulative Distribution Function algorithm, applied to the same groups of lipoproteins.


Acta Biochimica Polonica | 2017

Electronegativity and intrinsic disorder of preeclampsia-related proteins

Carlos Polanco; Jorge Alberto Castañón-González; Vladimir N. Uversky; Thomas Buhse; José Lino Samaniego Mendoza; Juan J. Calva

Preeclampsia, hemorrhage, and infection are the leading causes of maternal death in underdeveloped countries. Since several proteins associated with preeclampsia are known, we conducted a computational study which evaluated the commonness and potential functionality of intrinsic disorder of these proteins and also made an attempt to characterize their origin. The origin of the preeclampsia-related proteins was assessed with a supervised technique, a Polarity Index Method (PIM), which evaluates the electronegativity of proteins based solely on their sequence. The commonness of intrinsic disorder was evaluated using several disorder predictors from the PONDR family, the charge-hydropathy plot (CH-plot) and cumulative distribution function (CDF) analyses, and using the MobiDB web-based tool, whereas potential functionality of intrinsic disorder was studied with the D2P2 resource and ANCHOR predictor of disorder-based binding sites, and the STRING tool was used to build the interactivity networks of the preeclampsia-related proteins. Peculiarities of the PIM-derived polar profile of the group of preeclampsia-related proteins were then compared with profiles of a group of lipoproteins, antimicrobial peptides, angiogenesis-related proteins, and the intrinsically disordered proteins. Our results showed a high graphical correlation between preeclampsia proteins, lipoproteins, and the angiogenesis proteins. We also showed that many preeclampsia-related proteins contain numerous functional disordered regions. Therefore, these bioinformatics results led us to assume that the preeclampsia proteins are highly associated with the lipoproteins group, and that some preeclampsia-related proteins contain significant amounts of functional disorders.


Acta Biochimica Polonica | 2013

Detection of selective antibacterial peptides by the Polarity Profile method

Carlos Polanco; Thomas Buhse; José Lino Samaniego; Jorge Alberto Castañón-González


Acta Biochimica Polonica | 2013

Characterization of a possible uptake mechanism of selective antibacterial peptides

Carlos Polanco; José Lino Samaniego; Jorge Alberto Castañón-González; Thomas Buhse; Marili Leopold Sordo


Gaceta Medica De Mexico | 2013

Indice de saturación modificado en el servicio de urgencias médicas

Carlos Polanco-González; Jorge Alberto Castañón-González; Thomas Buhse; José Lino Samaniego-Mendoza; Rocío Arreguín-Nava; Sebastián Villanueva-Martínez


Cell Biochemistry and Biophysics | 2014

Polar Characterization of Antifungal Peptides from APD2 Database

Carlos Polanco; José Lino Samaniego-Mendoza; Thomas Buhse; Jorge Alberto Castañón-González; Marili Leopold-Sordo


Cirugia Y Cirujanos | 2014

La sobresaturación de los servicios de urgencias médicas

Jorge Alberto Castañón-González; Carlos Polanco-González; Sergio Camacho-Juárez


Gaceta Medica De Mexico | 2012

Encuesta sobre la capacidad de respuesta de los hospitales de alta especialidad ante un desastre médico: después de la influenza pandémica en México

Juan Carlos Serna-Ojeda; Jorge Alberto Castañón-González; Alejandro E. Macías; Armando Mansilla-Olivares; Guillermo Domínguez-Cherit; Carlos Polanco-González

Collaboration


Dive into the Jorge Alberto Castañón-González's collaboration.

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Carlos Polanco-González

National Autonomous University of Mexico

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Thomas Buhse

Universidad Autónoma del Estado de Morelos

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Carlos Polanco

National Autonomous University of Mexico

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José Lino Samaniego-Mendoza

National Autonomous University of Mexico

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Angélica Carbajal-Ramírez

Mexican Social Security Institute

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Armando Mansilla-Olivares

Mexican Social Security Institute

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Haiko Nellen-Hummel

Mexican Social Security Institute

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José Halabe-Cherem

Mexican Social Security Institute

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