Resultados de procura - Sandro Banfi
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microRNAs and genetic diseases por Nicola Meola, Vincenzo A. Gennarino, Sandro Banfi
Publicado 2009Artigo -
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RPE65-associated inherited retinal diseases: consensus recommendations for eligibility to gene therapy por Andrea Sodi, Sandro Banfi, Francesco Testa, Michele Della Corte, Ilaria Passerini, Elisabetta Pelo, Settimio Rossi, Francesca Simonelli
Publicado 2021Artigo -
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miR-340 inhibits tumor cell proliferation and induces apoptosis by targeting multiple negative regulators of p27 in non-small cell lung cancer por Serena Fernandez, Maurizio Risolino, Nadia Mandia, Francesco Talotta, Ylermi Soini, Mariarosaria Incoronato, Gerolama Condorelli, Sandro Banfi, Pasquale Verde
Publicado 2014Artigo -
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A Novel Variant in <scp><i>TUBB4B</i></scp> Causes Progressive Cone‐Rod Dystrophy and Early Onset Sensorineural Hearing Loss por Margherita Scarpato, Francesco Testa, Anna Nesti, Roberta Zeuli, Rosa Boccia, Gennaro Auletta, Sandro Banfi, Francesca Simonelli, Marianthi Karali
Publicado 2025Artigo -
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Lysoplex: An efficient toolkit to detect DNA sequence variations in the autophagy-lysosomal pathway por Giuseppina Di Fruscio, Angela Schulz, Rossella De Cegli, Marco Savarese, Margherita Mutarelli, Giancarlo Parenti, Sandro Banfi, Thomas Braulke, Vincenzo Nigro, Andrea Ballabio
Publicado 2015Artigo -
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An Autoregulatory Loop Directs the Tissue-Specific Expression of <i>p63</i> through a Long-Range Evolutionarily Conserved Enhancer por Dario Antonini, Barbara Rossi, Rong Han, Annunziata Minichiello, Tina Di Palma, Marcella Corrado, Sandro Banfi, Mariastella Zannini, Janice L. Brissette, Caterina Missero
Publicado 2006Artigo -
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AAV-miR-204 Protects from Retinal Degeneration by Attenuation of Microglia Activation and Photoreceptor Cell Death por Marianthi Karali, Irene Guadagnino, Elena Marrocco, Rossella De Cegli, Annamaria Carissimo, Mariateresa Pizzo, Simona Casarosa, Iván Conte, Enrico Maria Surace, Sandro Banfi
Publicado 2019Artigo -
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A Homozygous Missense Mutation in the<i>IRBP</i>Gene (<i>RBP3</i>) Associated with Autosomal Recessive Retinitis Pigmentosa por Anneke I. den Hollander, Terri L. McGee, Carmela Ziviello, Sandro Banfi, Thaddeus P. Dryja, Federico Gonzalez‐Fernandez, Debashis Ghosh, Eliot L. Berson
Publicado 2009Artigo -
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UTRdb and UTRsite (RELEASE 2010): a collection of sequences and regulatory motifs of the untranslated regions of eukaryotic mRNAs por Giorgio Grillo, Antonio Turi, Flavio Licciulli, Flavio Mignone, Sabino Liuni, Sandro Banfi, Vincenzo A. Gennarino, David S. Horner, Giulio Pavesi, Ernesto Picardi, Graziano Pesole
Publicado 2009Artigo -
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Cardiomyogenesis is controlled by the miR-99a/let-7c cluster and epigenetic modifications por 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
Publicado 2013Artigo
Ferramentas de procura:
Materias Relacionadas
Biology
Genetics
Gene
Medicine
Cell biology
Neuroscience
Computational biology
Phenotype
microRNA
Gene expression
Retinal
Retina
Retinitis pigmentosa
Mutation
Ophthalmology
Internal medicine
Regulation of gene expression
ABCA4
Exome sequencing
Transcription factor
Biochemistry
Retinal degeneration
Retinal pigment epithelium
Bioinformatics
Eye development
Function (biology)
Genetic enhancement
Genome
Missense mutation
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