Search Results - "Vitale, Lorenza"

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  1. 1

    On the length, weight and GC content of the human genome by Piovesan, Allison, Pelleri, Maria Chiara, Antonaros, Francesca, Strippoli, Pierluigi, Caracausi, Maria, Vitale, Lorenza

    Published in BMC research notes (27-02-2019)
    “…Basic parameters commonly used to describe genomes including length, weight and relative guanine-cytosine (GC) content are widely cited in absence of a primary…”
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    An estimation of the number of cells in the human body by Bianconi, Eva, Piovesan, Allison, Facchin, Federica, Beraudi, Alina, Casadei, Raffaella, Frabetti, Flavia, Vitale, Lorenza, Pelleri, Maria Chiara, Tassani, Simone, Piva, Francesco, Perez-Amodio, Soledad, Strippoli, Pierluigi, Canaider, Silvia

    Published in Annals of human biology (01-11-2013)
    “…Abstract Background: All living organisms are made of individual and identifiable cells, whose number, together with their size and type, ultimately defines…”
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    GeneBase 1.1: a tool to summarize data from NCBI gene datasets and its application to an update of human gene statistics by Piovesan, Allison, Caracausi, Maria, Antonaros, Francesca, Pelleri, Maria Chiara, Vitale, Lorenza

    “…We release GeneBase 1.1, a local tool with a graphical interface useful for parsing, structuring and indexing data from the National Center for Biotechnology…”
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    Systematic identification of human housekeeping genes possibly useful as references in gene expression studies by Caracausi, Maria, Piovesan, Allison, Antonaros, Francesca, Strippoli, Pierluigi, Vitale, Lorenza, Pelleri, Maria Chiara

    Published in Molecular medicine reports (01-09-2017)
    “…The ideal reference, or control, gene for the study of gene expression in a given organism should be expressed at a medium-high level for easy detection,…”
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    A molecular view of the normal human thyroid structure and function reconstructed from its reference transcriptome map by Vitale, Lorenza, Piovesan, Allison, Antonaros, Francesca, Strippoli, Pierluigi, Pelleri, Maria Chiara, Caracausi, Maria

    Published in BMC genomics (18-09-2017)
    “…The thyroid is the earliest endocrine structure to appear during human development, and thyroid hormones are necessary for proper organism development, in…”
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    Human protein-coding genes and gene feature statistics in 2019 by Piovesan, Allison, Antonaros, Francesca, Vitale, Lorenza, Strippoli, Pierluigi, Pelleri, Maria Chiara, Caracausi, Maria

    Published in BMC research notes (04-06-2019)
    “…A well-known limit of genome browsers is that the large amount of genome and gene data is not organized in the form of a searchable database, hampering full…”
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    Identification of minimal eukaryotic introns through GeneBase, a user-friendly tool for parsing the NCBI Gene databank by Piovesan, Allison, Caracausi, Maria, Ricci, Marco, Strippoli, Pierluigi, Vitale, Lorenza, Pelleri, Maria Chiara

    Published in DNA research (01-12-2015)
    “…We have developed GeneBase, a full parser of the National Center for Biotechnology Information (NCBI) Gene database, which generates a fully structured local…”
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    Integrated Quantitative Transcriptome Maps of Human Trisomy 21 Tissues and Cells by Pelleri, Maria Chiara, Cattani, Chiara, Vitale, Lorenza, Antonaros, Francesca, Strippoli, Pierluigi, Locatelli, Chiara, Cocchi, Guido, Piovesan, Allison, Caracausi, Maria

    Published in Frontiers in genetics (24-04-2018)
    “…Down syndrome (DS) is due to the presence of an extra full or partial chromosome 21 (Hsa21). The identification of genes contributing to DS pathogenesis could…”
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    Structural Characterization of the Highly Restricted Down Syndrome Critical Region on 21q22.13: New KCNJ6 and DSCR4 Transcript Isoforms by Antonaros, Francesca, Pitocco, Margherita, Abete, Domenico, Vione, Beatrice, Piovesan, Allison, Vitale, Lorenza, Strippoli, Pierluigi, Caracausi, Maria, Pelleri, Maria Chiara

    Published in Frontiers in genetics (08-12-2021)
    “…Down syndrome (DS) is caused by trisomy of chromosome 21 and it is the most common genetic cause of intellectual disability (ID) in humans. Subjects with DS…”
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    The transcriptome profile of human trisomy 21 blood cells by Antonaros, Francesca, Zenatelli, Rossella, Guerri, Giulia, Bertelli, Matteo, Locatelli, Chiara, Vione, Beatrice, Catapano, Francesca, Gori, Alice, Vitale, Lorenza, Pelleri, Maria Chiara, Ramacieri, Giuseppe, Cocchi, Guido, Strippoli, Pierluigi, Caracausi, Maria, Piovesan, Allison

    Published in Human genomics (01-05-2021)
    “…Trisomy 21 (T21) is a genetic alteration characterised by the presence of an extra full or partial human chromosome 21 (Hsa21) leading to Down syndrome (DS),…”
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    Identification of housekeeping genes suitable for gene expression analysis in the zebrafish by Casadei, Raffaella, Pelleri, Maria Chiara, Vitale, Lorenza, Facchin, Federica, Lenzi, Luca, Canaider, Silvia, Strippoli, Pierluigi, Frabetti, Flavia

    Published in Gene Expression Patterns (01-03-2011)
    “…Housekeeping (HK) genes are constitutively expressed in order to maintain cellular function. They produce the minimal essential transcripts necessary for…”
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    A quantitative transcriptome reference map of the normal human brain by Caracausi, Maria, Vitale, Lorenza, Pelleri, Maria Chiara, Piovesan, Allison, Bruno, Samantha, Strippoli, Pierluigi

    Published in Neurogenetics (01-10-2014)
    “…We performed an innovative systematic meta-analysis of 60 gene expression profiles of whole normal human brain, to provide a quantitative transcriptome…”
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