Hasil Pencarian - Giulia Babbi

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  1. 1
    PhenPath: a tool for characterizing biological functions underlying different phenotypes

    PhenPath: a tool for characterizing biological functions underlying different phenotypes oleh Giulia Babbi, Pier Luigi Martelli, Rita Casadio

    Diterbitkan 2019-07-01
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  2. 2
    Huntingtin: A Protein with a Peculiar Solvent Accessible Surface

    Huntingtin: A Protein with a Peculiar Solvent Accessible Surface oleh Giulia Babbi, Castrense Savojardo, Pier Luigi Martelli, Rita Casadio

    Diterbitkan 2021-03-01
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  3. 3
    Functional and Structural Features of Disease-Related Protein Variants

    Functional and Structural Features of Disease-Related Protein Variants oleh Castrense Savojardo, Giulia Babbi, Pier Luigi Martelli, Rita Casadio

    Diterbitkan 2019-03-01
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  4. 4
    Mapping OMIM Disease–Related Variations on Protein Domains Reveals an Association Among Variation Type, Pfam Models, and Disease Classes

    Mapping OMIM Disease–Related Variations on Protein Domains Reveals an Association Among Variation Type, Pfam Models, and Disease Classes oleh Castrense Savojardo, Giulia Babbi, Pier Luigi Martelli, Rita Casadio, Rita Casadio

    Diterbitkan 2021-05-01
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  5. 5
    A Glance into MTHFR Deficiency at a Molecular Level

    A Glance into MTHFR Deficiency at a Molecular Level oleh Castrense Savojardo, Giulia Babbi, Davide Baldazzi, Pier Luigi Martelli, Rita Casadio

    Diterbitkan 2021-12-01
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  6. 6
    Highlighting Human Enzymes Active in Different Metabolic Pathways and Diseases: The Case Study of EC 1.2.3.1 and EC 2.3.1.9

    Highlighting Human Enzymes Active in Different Metabolic Pathways and Diseases: The Case Study of EC 1.2.3.1 and EC 2.3.1.9 oleh Giulia Babbi, Davide Baldazzi, Castrense Savojardo, Pier Luigi Martelli, Rita Casadio

    Diterbitkan 2020-07-01
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  7. 7
    Mapping human disease-associated enzymes into Reactome allows characterization of disease groups and their interactions

    Mapping human disease-associated enzymes into Reactome allows characterization of disease groups and their interactions oleh Castrense Savojardo, Davide Baldazzi, Giulia Babbi, Pier Luigi Martelli, Rita Casadio

    Diterbitkan 2022-10-01
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  8. 8
    Editorial: Omics integration and network medicine to decipher human complex diseases

    Editorial: Omics integration and network medicine to decipher human complex diseases oleh Mario Zanfardino, Giulia Babbi, Kazim Yalcin Arga, Kazim Yalcin Arga, Katia Pane

    Diterbitkan 2023-03-01
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  9. 9
    Pathogenic variation types in human genes relate to diseases through Pfam and InterPro mapping

    Pathogenic variation types in human genes relate to diseases through Pfam and InterPro mapping oleh Giulia Babbi, Castrense Savojardo, Davide Baldazzi, Pier Luigi Martelli, Rita Casadio, Rita Casadio

    Diterbitkan 2022-09-01
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  10. 10
    eDGAR: a database of Disease-Gene Associations with annotated Relationships among genes

    eDGAR: a database of Disease-Gene Associations with annotated Relationships among genes oleh Giulia Babbi, Pier Luigi Martelli, Giuseppe Profiti, Samuele Bovo, Castrense Savojardo, Rita Casadio

    Diterbitkan 2017-08-01
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  11. 11
    Dispersion of antimicrobial resistant bacteria in pig farms and in the surrounding environment

    Dispersion of antimicrobial resistant bacteria in pig farms and in the surrounding environment oleh Daniel Scicchitano, Daniela Leuzzi, Giulia Babbi, Giorgia Palladino, Silvia Turroni, Cédric Christian Laczny, Paul Wilmes, Federico Correa, Pimlapas Leekitcharoenphon, Castrense Savojardo, Diana Luise, Pierluigi Martelli, Paolo Trevisi, Frank Møller Aarestrup, Marco Candela, Simone Rampelli

    Diterbitkan 2024-03-01
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  12. 12
    Resources and tools for rare disease variant interpretation

    Resources and tools for rare disease variant interpretation oleh Luana Licata, Allegra Via, Paola Turina, Giulia Babbi, Silvia Benevenuta, Claudio Carta, Rita Casadio, Andrea Cicconardi, Andrea Cicconardi, Angelo Facchiano, Piero Fariselli, Deborah Giordano, Federica Isidori, Anna Marabotti, Pier Luigi Martelli, Stefano Pascarella, Michele Pinelli, Tommaso Pippucci, Roberta Russo, Roberta Russo, Castrense Savojardo, Bernardina Scafuri, Lucrezia Valeriani, Emidio Capriotti

    Diterbitkan 2023-05-01
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  13. 13
    Critical assessment of variant prioritization methods for rare disease diagnosis within the rare genomes project

    Critical assessment of variant prioritization methods for rare disease diagnosis within the rare genomes project oleh Sarah L. Stenton, Melanie C. O’Leary, Gabrielle Lemire, Grace E. VanNoy, Stephanie DiTroia, Vijay S. Ganesh, Emily Groopman, Emily O’Heir, Brian Mangilog, Ikeoluwa Osei-Owusu, Lynn S. Pais, Jillian Serrano, Moriel Singer-Berk, Ben Weisburd, Michael W. Wilson, Christina Austin-Tse, Marwa Abdelhakim, Azza Althagafi, Giulia Babbi, Riccardo Bellazzi, Samuele Bovo, Maria Giulia Carta, Rita Casadio, Pieter-Jan Coenen, Federica De Paoli, Matteo Floris, Manavalan Gajapathy, Robert Hoehndorf, Julius O. B. Jacobsen, Thomas Joseph, Akash Kamandula, Panagiotis Katsonis, Cyrielle Kint, Olivier Lichtarge, Ivan Limongelli, Yulan Lu, Paolo Magni, Tarun Karthik Kumar Mamidi, Pier Luigi Martelli, Marta Mulargia, Giovanna Nicora, Keith Nykamp, Vikas Pejaver, Yisu Peng, Thi Hong Cam Pham, Maurizio S. Podda, Aditya Rao, Ettore Rizzo, Vangala G. Saipradeep, Castrense Savojardo, Peter Schols, Yang Shen, Naveen Sivadasan, Damian Smedley, Dorian Soru, Rajgopal Srinivasan, Yuanfei Sun, Uma Sunderam, Wuwei Tan, Naina Tiwari, Xiao Wang, Yaqiong Wang, Amanda Williams, Elizabeth A. Worthey, Rujie Yin, Yuning You, Daniel Zeiberg, Susanna Zucca, Constantina Bakolitsa, Steven E. Brenner, Stephanie M. Fullerton, Predrag Radivojac, Heidi L. Rehm, Anne O’Donnell-Luria

    Diterbitkan 2024-04-01
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