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Sandro Banfi

Showing results (51-60 of 136) with videos related to

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International Journal of Molecular Sciences|June 19, 2024
Novel and Recurrent Copy Number Variants in <i>ABCA4</i>-Associated RetinopathyZelia Corradi, Claire-Marie Dhaenens, Olivier Grunewald, et al.
Nucleic Acids Research|November 28, 2012
Reverse engineering a mouse embryonic stem cell-specific transcriptional network reveals a new modulator of neuronal differentiationRossella De Cegli, Simona Iacobacci, Gemma Flore, et al.
Investigative Ophthalmology & Visual Science|June 5, 2012
Correlation between photoreceptor layer integrity and visual function in patients with Stargardt disease: implications for gene therapyFrancesco Testa, Settimio Rossi, Andrea Sodi, et al.
Stem Cell Research|December 25, 2013
Cardiomyogenesis is controlled by the miR-99a/let-7c cluster and epigenetic modificationsAntonietta Coppola, Antonio Romito, Christelle Borel, et al.
Genes|October 21, 2017
Clinical and Genetic Evaluation of a Cohort of Pediatric Patients with Severe Inherited Retinal DystrophiesValentina Di Iorio, Marianthi Karali, Raffaella Brunetti-Pierri, et al.
Investigative Ophthalmology & Visual Science|July 1, 2021
Spectrum of Disease Severity in Nonsyndromic Patients With Mutations in the CEP290 Gene: A Multicentric Longitudinal StudyFrancesco Testa, Andrea Sodi, Sabrina Signorini, et al.
Translational Vision Science & Technology|May 12, 2026
Voretigene Neparvovec Gene Therapy in Clinical Practice: A 12-Month, Single-Center, In-Depth Analysis of Beneficial and Adverse Drug EffectsFrancesco Testa, Valentina Di Iorio, Paolo Melillo, et al.
Genome Research|February 21, 2012
Identification of microRNA-regulated gene networks by expression analysis of target genesVincenzo Alessandro Gennarino, Giovanni D'Angelo, Gopuraja Dharmalingam, et al.
European Journal of Medical Genetics|September 3, 2008
Sonic Hedgehog deletion and distal trisomy 3p in a patient with microphthalmia and microcephaly, lacking cerebral anomalies typical of holoprosencephalyVirginia M Ginocchio, Daniele De Brasi, Rita Genesio, et al.
Investigative Ophthalmology & Visual Science|December 29, 2020
Spectrum of Disease Severity in Patients With X-Linked Retinitis Pigmentosa Due to RPGR MutationsValentina Di Iorio, Marianthi Karali, Paolo Melillo, et al.
Pageof 14

Showing results (51-60 of 136) with videos related to

Sort By:
Pageof 14
International Journal of Molecular Sciences|June 19, 2024
Novel and Recurrent Copy Number Variants in <i>ABCA4</i>-Associated RetinopathyZelia Corradi, Claire-Marie Dhaenens, Olivier Grunewald, et al.
Nucleic Acids Research|November 28, 2012
Reverse engineering a mouse embryonic stem cell-specific transcriptional network reveals a new modulator of neuronal differentiationRossella De Cegli, Simona Iacobacci, Gemma Flore, et al.
Investigative Ophthalmology & Visual Science|June 5, 2012
Correlation between photoreceptor layer integrity and visual function in patients with Stargardt disease: implications for gene therapyFrancesco Testa, Settimio Rossi, Andrea Sodi, et al.
Stem Cell Research|December 25, 2013
Cardiomyogenesis is controlled by the miR-99a/let-7c cluster and epigenetic modificationsAntonietta Coppola, Antonio Romito, Christelle Borel, et al.
Genes|October 21, 2017
Clinical and Genetic Evaluation of a Cohort of Pediatric Patients with Severe Inherited Retinal DystrophiesValentina Di Iorio, Marianthi Karali, Raffaella Brunetti-Pierri, et al.
Investigative Ophthalmology & Visual Science|July 1, 2021
Spectrum of Disease Severity in Nonsyndromic Patients With Mutations in the CEP290 Gene: A Multicentric Longitudinal StudyFrancesco Testa, Andrea Sodi, Sabrina Signorini, et al.
Translational Vision Science & Technology|May 12, 2026
Voretigene Neparvovec Gene Therapy in Clinical Practice: A 12-Month, Single-Center, In-Depth Analysis of Beneficial and Adverse Drug EffectsFrancesco Testa, Valentina Di Iorio, Paolo Melillo, et al.
Genome Research|February 21, 2012
Identification of microRNA-regulated gene networks by expression analysis of target genesVincenzo Alessandro Gennarino, Giovanni D'Angelo, Gopuraja Dharmalingam, et al.
European Journal of Medical Genetics|September 3, 2008
Sonic Hedgehog deletion and distal trisomy 3p in a patient with microphthalmia and microcephaly, lacking cerebral anomalies typical of holoprosencephalyVirginia M Ginocchio, Daniele De Brasi, Rita Genesio, et al.
Investigative Ophthalmology & Visual Science|December 29, 2020
Spectrum of Disease Severity in Patients With X-Linked Retinitis Pigmentosa Due to RPGR MutationsValentina Di Iorio, Marianthi Karali, Paolo Melillo, et al.
Pageof 14