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  1. Article ; Online: Murine experimental models of amyotrophic lateral sclerosis: an update.

    Moreno-Jiménez, L / Benito-Martín, M S / Sanclemente-Alamán, I / Matías-Guiu, J A / Sancho-Bielsa, F / Canales-Aguirre, A / Mateos-Díaz, J C / Matías-Guiu, J / Aguilar, J / Gómez-Pinedo, U

    Neurologia

    2023  Volume 39, Issue 3, Page(s) 282–291

    Abstract: Introduction: Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease whose aetiology is unknown. It is characterised by upper and lower motor neuron degeneration. Approximately 90% of cases of ALS are sporadic, whereas the other ... ...

    Abstract Introduction: Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease whose aetiology is unknown. It is characterised by upper and lower motor neuron degeneration. Approximately 90% of cases of ALS are sporadic, whereas the other 10% are familial. Regardless of whether the case is familial o sporadic, patients will develop progressive weakness, muscle atrophy with spasticity, and muscle contractures. Life expectancy of these patients is generally 2 to 5 years after diagnosis.
    Development: In vivo models have helped to clarify the aetiology and pathogenesis of ALS, as well as the mechanisms of the disease. However, as these mechanisms are not yet fully understood, experimental models are essential to the continued study of the pathogenesis of ALS, as well as in the search for possible therapeutic targets. Although 90% of cases are sporadic, most of the models used to study ALS pathogenesis are based on genetic mutations associated with the familial form of the disease; the pathogenesis of sporadic ALS remains unknown. Therefore, it would be critical to establish models based on the sporadic form.
    Conclusions: This article reviews the main genetic and sporadic experimental models used in the study of this disease, focusing on those that have been developed using rodents.
    MeSH term(s) Humans ; Animals ; Mice ; Amyotrophic Lateral Sclerosis/pathology ; Neurodegenerative Diseases ; DNA-Binding Proteins/genetics ; Mutation
    Chemical Substances DNA-Binding Proteins
    Language English
    Publishing date 2023-04-26
    Publishing country Spain
    Document type Journal Article ; Review
    ZDB-ID 2654369-2
    ISSN 2173-5808 ; 2173-5808
    ISSN (online) 2173-5808
    ISSN 2173-5808
    DOI 10.1016/j.nrleng.2021.07.004
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: A New Microplate Screening Method for the Simultaneous Activity Quantification of Feruloyl Esterases, Tannases, and Chlorogenate Esterases

    Ramírez, L / Arrizon, J / Sandoval, G / Cardador, A / Bello-Mendoza, R / Lappe, P / Mateos-Díaz, J. C

    Applied biochemistry and biotechnology ABAB. 2008 Dec., v. 151, no. 2-3

    2008  

    Abstract: Feruloyl, chlorogenate esterases, and tannases are enzymes useful in phenolic modifications of pharmaceutical relevance as protectors against several degenerative human diseases. Therefore, there is a growing interest in discovering new sources of these ... ...

    Abstract Feruloyl, chlorogenate esterases, and tannases are enzymes useful in phenolic modifications of pharmaceutical relevance as protectors against several degenerative human diseases. Therefore, there is a growing interest in discovering new sources of these enzymes. However, traditional methods for their activity measurements are time-consuming and poorly adapted for high-throughput screening. In this study, a successful new microplate high-throughput screening method for the simultaneous quantification of all mentioned activities is demonstrated. This method allows the detection of activities as low as 1.7 mU ml⁻¹. Furthermore, reaction rates increased proportionally with the amount of enzyme added, and no interferences with the other commercial hydrolases tested were found. The utility of the method was demonstrated after simultaneously screening feruloyl, chlorogenate esterase, and tannase activities in solid state fermentation extracts obtained during the kinetics of production of 20 fungal strains. Among these, seven strains were positive for at least one of the esterase activities tested. This result shows the potential for the rapid routine screening assays for multiple samples of moderate low to high enzymatic levels.
    Keywords enzyme activity ; esterases ; tannase ; strains ; kinetics ; solid state fermentation ; Coffea ; solid wastes ; fungi
    Language English
    Dates of publication 2008-12
    Size p. 711-723.
    Publisher Humana Press Inc
    Publishing place New York
    Document type Article
    Note In the special issue: New horizons in biotechnology 2007/ edited by A.Pandey, C.Larroche, C.R. Socol. Paper presented at the International conference "New horizons in biotechnology", November 26-29, 2007, Trivandrum, India.
    ZDB-ID 392344-7
    ISSN 0273-2289
    ISSN 0273-2289
    DOI 10.1007/s12010-008-8319-8
    Database NAL-Catalogue (AGRICOLA)

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  3. Article ; Online: A new microplate screening method for the simultaneous activity quantification of feruloyl esterases, tannases, and chlorogenate esterases.

    Ramírez, L / Arrizon, J / Sandoval, G / Cardador, A / Bello-Mendoza, R / Lappe, P / Mateos-Díaz, J C

    Applied biochemistry and biotechnology

    2008  Volume 151, Issue 2-3, Page(s) 711–723

    Abstract: Feruloyl, chlorogenate esterases, and tannases are enzymes useful in phenolic modifications of pharmaceutical relevance as protectors against several degenerative human diseases. Therefore, there is a growing interest in discovering new sources of these ... ...

    Abstract Feruloyl, chlorogenate esterases, and tannases are enzymes useful in phenolic modifications of pharmaceutical relevance as protectors against several degenerative human diseases. Therefore, there is a growing interest in discovering new sources of these enzymes. However, traditional methods for their activity measurements are time-consuming and poorly adapted for high-throughput screening. In this study, a successful new microplate high-throughput screening method for the simultaneous quantification of all mentioned activities is demonstrated. This method allows the detection of activities as low as 1.7 mU ml(-1). Furthermore, reaction rates increased proportionally with the amount of enzyme added, and no interferences with the other commercial hydrolases tested were found. The utility of the method was demonstrated after simultaneously screening feruloyl, chlorogenate esterase, and tannase activities in solid state fermentation extracts obtained during the kinetics of production of 20 fungal strains. Among these, seven strains were positive for at least one of the esterase activities tested. This result shows the potential for the rapid routine screening assays for multiple samples of moderate low to high enzymatic levels.
    MeSH term(s) Aspergillus/enzymology ; Carboxylic Ester Hydrolases/analysis ; Coffee/microbiology ; Drug Evaluation, Preclinical/methods ; Fermentation ; Microchemistry/methods
    Chemical Substances Coffee ; Carboxylic Ester Hydrolases (EC 3.1.1.-) ; chlorogenic acid esterase (EC 3.1.1.-) ; tannase (EC 3.1.1.20) ; feruloyl esterase (EC 3.1.1.73)
    Language English
    Publishing date 2008-12
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Validation Studies
    ZDB-ID 392344-7
    ISSN 1559-0291 ; 0273-2289
    ISSN (online) 1559-0291
    ISSN 0273-2289
    DOI 10.1007/s12010-008-8319-8
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Use of inulinases to improve fermentable carbohydrate recovery during tequila production

    Waleckx, E. / Mateos-Diaz, J. C. / Gschaedler, A. / Colonna-Ceccaldi, B. / Brin, N. / Garcia-Quezada, G. / Villanueva-Rodriguez, S. / Monsan, P.

    Food chemistry

    2010  Volume 124, Issue 4, Page(s) 1533

    Language English
    Document type Article
    ZDB-ID 243123-3
    ISSN 0308-8146
    Database Current Contents Nutrition, Environment, Agriculture

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