Resultados de procura - Enzo Di Iorio

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  1. 1
    C/EBPδ regulates cell cycle and self-renewal of human limbal stem cells

    C/EBPδ regulates cell cycle and self-renewal of human limbal stem cells por V. Barbaro, Anna Testa, Enzo Di Iorio, Fulvio Mavilio, Graziella Pellegrini, Michele De Luca

    Publicado 2007
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  2. 2
    Retinitis Pigmentosa: Genes and Disease Mechanisms

    Retinitis Pigmentosa: Genes and Disease Mechanisms por Francesco Parmeggiani, Francesco Saverio Sorrentino, Diego Ponzin, V. Barbaro, Stefano Ferrari, Enzo Di Iorio

    Publicado 2011
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  3. 3
    Isoforms of ΔNp63 and the migration of ocular limbal cells in human corneal regeneration

    Isoforms of ΔNp63 and the migration of ocular limbal cells in human corneal regeneration por Enzo Di Iorio, V. Barbaro, Alessandro Ruzza, Diego Ponzin, Graziella Pellegrini, Michele De Luca

    Publicado 2005
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  4. 4
    Visualization of DNA G-quadruplexes in herpes simplex virus 1-infected cells

    Visualization of DNA G-quadruplexes in herpes simplex virus 1-infected cells por Sara Artusi, Rosalba Perrone, Sara Lago, Paolo Raffa, Enzo Di Iorio, Giorgio Palù, Sara N. Richter

    Publicado 2016
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  5. 5
    Limbal Stem Cell Deficiency and Ocular Phenotype in Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome Caused by p63 Mutations

    Limbal Stem Cell Deficiency and Ocular Phenotype in Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome Caused by p63 Mutations por Enzo Di Iorio, Stephen B. Kaye, Diego Ponzin, V. Barbaro, Stefano Ferrari, Elisabetta Böhm, Paola Nardiello, Giuseppe Castaldo, John A. McGrath, Colin E. Willoughby

    Publicado 2011
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  6. 6
    Correction of Laminin-5 Deficiency in Human Epidermal Stem Cells by Transcriptionally Targeted Lentiviral Vectors

    Correction of Laminin-5 Deficiency in Human Epidermal Stem Cells by Transcriptionally Targeted Lentiviral Vectors por Francesca Di Nunzio, Giulietta Maruggi, Stefano Ferrari, Enzo Di Iorio, Valentina Poletti, Marta García, Marcela Del Río, Michele De Luca, Fernando Larcher, Graziella Pellegrini, Fulvio Mavilio

    Publicado 2008
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  7. 7
    MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell’s Waltzer Mice, Is Mutated in Autosomal Dominant Nonsyndromic Hearing Loss

    MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell’s Waltzer Mice, Is Mutated in Autosomal Dominant Nonsyndromic Hearing Loss por Salvatore Melchionda, Nadav Ahituv, Luigi Bisceglia, Tama Sobe, Fabian Glaser, Raquel Rabionet, María L. Arbonés, Angelo Notarangelo, Enzo Di Iorio, Massimo Carella, Leopoldo Zelante, Xavier Estivill, Karen B. Avraham, Paolo Gasparini

    Publicado 2001
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