Hasil Pencarian - Sandro Banfi

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  1. 1
    Sophisticated Gene Regulation for a Complex Physiological System: The Role of Non-coding RNAs in Photoreceptor Cells

    Sophisticated Gene Regulation for a Complex Physiological System: The Role of Non-coding RNAs in Photoreceptor Cells oleh Sabrina Carrella, Sabrina Carrella, Sandro Banfi, Sandro Banfi, Marianthi Karali, Marianthi Karali

    Diterbitkan 2021-01-01
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  2. 2
    Mutation-Independent Therapies for Retinal Diseases: Focus on Gene-Based Approaches

    Mutation-Independent Therapies for Retinal Diseases: Focus on Gene-Based Approaches oleh Sabrina Carrella, Sabrina Carrella, Alessia Indrieri, Alessia Indrieri, Brunella Franco, Brunella Franco, Sandro Banfi, Sandro Banfi

    Diterbitkan 2020-09-01
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  3. 3
    The Pervasive Role of the miR-181 Family in Development, Neurodegeneration, and Cancer

    The Pervasive Role of the miR-181 Family in Development, Neurodegeneration, and Cancer oleh Alessia Indrieri, Sabrina Carrella, Pietro Carotenuto, Sandro Banfi, Brunella Franco

    Diterbitkan 2020-03-01
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  4. 4
    Impact of age at administration, lysosomal storage, and transgene regulatory elements on AAV2/8-mediated rat liver transduction.

    Impact of age at administration, lysosomal storage, and transgene regulatory elements on AAV2/8-mediated rat liver transduction. oleh Gabriella Cotugno, Patrizia Annunziata, Maria Vittoria Barone, Marianthi Karali, Sandro Banfi, Alberto Auricchio

    Diterbitkan 2012-01-01
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  5. 5
    TGF-β Controls miR-181/ERK Regulatory Network during Retinal Axon Specification and Growth.

    TGF-β Controls miR-181/ERK Regulatory Network during Retinal Axon Specification and Growth. oleh Sabrina Carrella, Sara Barbato, Ylenia D'Agostino, Francesco Giuseppe Salierno, Anna Manfredi, Sandro Banfi, Ivan Conte

    Diterbitkan 2015-01-01
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  6. 6
    Definition of the transcriptional units of inherited retinal disease genes by meta-analysis of human retinal transcriptome data

    Definition of the transcriptional units of inherited retinal disease genes by meta-analysis of human retinal transcriptome data oleh Karla Alejandra Ruiz-Ceja, Dalila Capasso, Michele Pinelli, Eugenio Del Prete, Diego Carrella, Diego di Bernardo, Sandro Banfi

    Diterbitkan 2023-04-01
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  7. 7
    miR-204 targeting of Ankrd13A controls both mesenchymal neural crest and lens cell migration.

    miR-204 targeting of Ankrd13A controls both mesenchymal neural crest and lens cell migration. oleh Raffaella Avellino, Sabrina Carrella, Marinella Pirozzi, Maurizio Risolino, Francesco Giuseppe Salierno, Paola Franco, Patrizia Stoppelli, Pasquale Verde, Sandro Banfi, Ivan Conte

    Diterbitkan 2013-01-01
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  8. 8
    RPE65-associated inherited retinal diseases: consensus recommendations for eligibility to gene therapy

    RPE65-associated inherited retinal diseases: consensus recommendations for eligibility to gene therapy oleh Andrea Sodi, Sandro Banfi, Francesco Testa, Michele Della Corte, Ilaria Passerini, Elisabetta Pelo, Settimio Rossi, Francesca Simonelli, Italian IRD Working Group

    Diterbitkan 2021-06-01
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  9. 9
    Inherited Retinal Diseases Due to <i>RPE65</i> Variants: From Genetic Diagnostic Management to Therapy

    Inherited Retinal Diseases Due to <i>RPE65</i> Variants: From Genetic Diagnostic Management to Therapy oleh Manar Aoun, Ilaria Passerini, Pietro Chiurazzi, Marianthi Karali, Irene De Rienzo, Giovanna Sartor, Vittoria Murro, Natalia Filimonova, Marco Seri, Sandro Banfi

    Diterbitkan 2021-07-01
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  10. 10
    Clinical and Molecular Characterization of Achromatopsia Patients: A Longitudinal Study

    Clinical and Molecular Characterization of Achromatopsia Patients: A Longitudinal Study oleh Raffaella Brunetti-Pierri, Marianthi Karali, Paolo Melillo, Valentina Di Iorio, Antonella De Benedictis, Gennarfrancesco Iaccarino, Francesco Testa, Sandro Banfi, Francesca Simonelli

    Diterbitkan 2021-02-01
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  11. 11
    Visual function and retinal changes after voretigene neparvovec treatment in children with biallelic RPE65-related inherited retinal dystrophy

    Visual function and retinal changes after voretigene neparvovec treatment in children with biallelic RPE65-related inherited retinal dystrophy oleh Francesco Testa, Paolo Melillo, Valentina Di Iorio, Claudio Iovino, Francesco Farinaro, Marianthi Karali, Sandro Banfi, Settimio Rossi, Michele Della Corte, Francesca Simonelli

    Diterbitkan 2022-10-01
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  12. 12
    Retinal dystrophy in an individual carrying a de novo missense variant of SMARCA4

    Retinal dystrophy in an individual carrying a de novo missense variant of SMARCA4 oleh Gerarda Cappuccio, Raffaella Brunetti‐Pierri, Annalaura Torella, Michele Pinelli, Raffaele Castello, Giorgio Casari, Vincenzo Nigro, Sandro Banfi, Francesca Simonelli, TUDP, Nicola Brunetti‐Pierri

    Diterbitkan 2019-06-01
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  13. 13
    Novel and Recurrent Copy Number Variants in <i>ABCA4</i>-Associated Retinopathy

    Novel and Recurrent Copy Number Variants in <i>ABCA4</i>-Associated Retinopathy oleh Zelia Corradi, Claire-Marie Dhaenens, Olivier Grunewald, Ipek Selen Kocabaş, Isabelle Meunier, Sandro Banfi, Marianthi Karali, Frans P. M. Cremers, Rebekkah J. Hitti-Malin

    Diterbitkan 2024-05-01
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  14. 14
    Cardiomyogenesis is controlled by the miR-99a/let-7c cluster and epigenetic modifications

    Cardiomyogenesis is controlled by the miR-99a/let-7c cluster and epigenetic modifications oleh Antonietta Coppola, Antonio Romito, Christelle Borel, Corinne Gehrig, Maryline Gagnebin, Emilie Falconnet, Antonella Izzo, Lucia Altucci, Sandro Banfi, Stylianos E. Antonarakis, Gabriella Minchiotti, Gilda Cobellis

    Diterbitkan 2014-03-01
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  15. 15
    Mild Clinical Presentation of Joubert Syndrome in a Male Adult Carrying Biallelic <i>MKS1</i> Truncating Variants

    Mild Clinical Presentation of Joubert Syndrome in a Male Adult Carrying Biallelic <i>MKS1</i> Truncating Variants oleh Raffaella Brunetti-Pierri, Marianthi Karali, Francesco Testa, Gerarda Cappuccio, Maria Elena Onore, Francesca Romano, Giuseppe De Rosa, Enrico Tedeschi, Nicola Brunetti-Pierri, Sandro Banfi, Francesca Simonelli

    Diterbitkan 2021-07-01
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  16. 16
    Mild form of Zellweger Spectrum Disorders (ZSD) due to variants in PEX1: Detailed clinical investigation in a 9-years-old female

    Mild form of Zellweger Spectrum Disorders (ZSD) due to variants in PEX1: Detailed clinical investigation in a 9-years-old female oleh Maria Rosaria Barillari, Marianthi Karali, Valentina Di Iorio, Maria Contaldo, Vincenzo Piccolo, Maria Esposito, Giuseppe Costa, Giuseppe Argenziano, Rosario Serpico, Marco Carotenuto, Gerarda Cappuccio, Sandro Banfi, Paolo Melillo, Francesca Simonelli

    Diterbitkan 2020-09-01
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  17. 17
    MicroRNA-restricted transgene expression in the retina.

    MicroRNA-restricted transgene expression in the retina. oleh Marianthi Karali, Anna Manfredi, Agostina Puppo, Elena Marrocco, Annagiusi Gargiulo, Mariacarmela Allocca, Michele Della Corte, Settimio Rossi, Massimo Giunti, Maria Laura Bacci, Francesca Simonelli, Enrico Maria Surace, Sandro Banfi, Alberto Auricchio

    Diterbitkan 2011-01-01
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  18. 18
    A multidisciplinary approach to inherited retinal dystrophies from diagnosis to initial care: a narrative review with inputs from clinical practice

    A multidisciplinary approach to inherited retinal dystrophies from diagnosis to initial care: a narrative review with inputs from clinical practice oleh Vittoria Murro, Sandro Banfi, Francesco Testa, Giancarlo Iarossi, Benedetto Falsini, Andrea Sodi, Sabrina Signorini, Achille Iolascon, Roberta Russo, Dario Pasquale Mucciolo, Roberto Caputo, Giacomo Maria Bacci, Sara Bargiacchi, Simona Turco, Stefania Fortini, Francesca Simonelli

    Diterbitkan 2023-07-01
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  19. 19
    Molecular diagnosis of Usher syndrome: application of two different next generation sequencing-based procedures.

    Molecular diagnosis of Usher syndrome: application of two different next generation sequencing-based procedures. oleh Danilo Licastro, Margherita Mutarelli, Ivana Peluso, Kornelia Neveling, Nienke Wieskamp, Rossella Rispoli, Diego Vozzi, Emmanouil Athanasakis, Angela D'Eustacchio, Mariateresa Pizzo, Francesca D'Amico, Carmela Ziviello, Francesca Simonelli, Antonella Fabretto, Hans Scheffer, Paolo Gasparini, Sandro Banfi, Vincenzo Nigro

    Diterbitkan 2012-01-01
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  20. 20
    Whole genome sequencing identifies elusive variants in genetically unsolved Italian inherited retinal disease patients

    Whole genome sequencing identifies elusive variants in genetically unsolved Italian inherited retinal disease patients oleh Roberta Zeuli, Marianthi Karali, Suzanne E. de Bruijn, Kim Rodenburg, Margherita Scarpato, Dalila Capasso, Galuh D.N. Astuti, Christian Gilissen, María Rodríguez-Hidalgo, Javier Ruiz-Ederra, Francesco Testa, Francesca Simonelli, Frans P.M. Cremers, Sandro Banfi, Susanne Roosing

    Diterbitkan 2024-07-01
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