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Sandro Banfi

Showing results (31-40 of 136) with videos related to

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Ophthalmology. Retina|January 31, 2024
Objective Outcomes to Evaluate Voretigene Neparvovec Treatment Effects in Clinical PracticePaolo Melillo, Francesco Testa, Valentina Di Iorio, et al.
Human Molecular Genetics|February 11, 2005
Natural antisense transcripts associated with genes involved in eye developmentGiovanna Alfano, Carmen Vitiello, Cristina Caccioppoli, et al.
Genes|December 24, 2021
VarGenius-HZD Allows Accurate Detection of Rare Homozygous or Hemizygous Deletions in Targeted Sequencing Leveraging Breadth of CoverageFrancesco Musacchia, Marianthi Karali, Annalaura Torella, et al.
Plos One|April 27, 2013
miR-204 targeting of Ankrd13A controls both mesenchymal neural crest and lens cell migrationRaffaella Avellino, Sabrina Carrella, Marinella Pirozzi, et al.
International Journal of Molecular Sciences|July 20, 2021
Inherited Retinal Diseases Due to <i>RPE65</i> Variants: From Genetic Diagnostic Management to TherapyManar Aoun, Ilaria Passerini, Pietro Chiurazzi, et al.
International Journal of Molecular Sciences|February 10, 2021
Clinical and Molecular Characterization of Achromatopsia Patients: A Longitudinal StudyRaffaella Brunetti-Pierri, Marianthi Karali, Paolo Melillo, et al.
European Journal of Human Genetics : EJHG|March 14, 2003
Identification and characterisation of the retinitis pigmentosa 1-like1 gene (RP1L1): a novel candidate for retinal degenerationsIvan Conte, Marta Lestingi, Anneke den Hollander, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 12, 2005
Novel mutation of SACS gene in a Spanish family with autosomal recessive spastic ataxiaChiara Criscuolo, Francesco Saccà, Giuseppe De Michele, et al.
Autophagy|June 16, 2015
Lysoplex: An efficient toolkit to detect DNA sequence variations in the autophagy-lysosomal pathwayGiuseppina Di Fruscio, Angela Schulz, Rossella De Cegli, et al.
Scientific Reports|October 22, 2022
Visual function and retinal changes after voretigene neparvovec treatment in children with biallelic RPE65-related inherited retinal dystrophyFrancesco Testa, Paolo Melillo, Valentina Di Iorio, et al.
Pageof 14

Showing results (31-40 of 136) with videos related to

Sort By:
Pageof 14
Ophthalmology. Retina|January 31, 2024
Objective Outcomes to Evaluate Voretigene Neparvovec Treatment Effects in Clinical PracticePaolo Melillo, Francesco Testa, Valentina Di Iorio, et al.
Human Molecular Genetics|February 11, 2005
Natural antisense transcripts associated with genes involved in eye developmentGiovanna Alfano, Carmen Vitiello, Cristina Caccioppoli, et al.
Genes|December 24, 2021
VarGenius-HZD Allows Accurate Detection of Rare Homozygous or Hemizygous Deletions in Targeted Sequencing Leveraging Breadth of CoverageFrancesco Musacchia, Marianthi Karali, Annalaura Torella, et al.
Plos One|April 27, 2013
miR-204 targeting of Ankrd13A controls both mesenchymal neural crest and lens cell migrationRaffaella Avellino, Sabrina Carrella, Marinella Pirozzi, et al.
International Journal of Molecular Sciences|July 20, 2021
Inherited Retinal Diseases Due to <i>RPE65</i> Variants: From Genetic Diagnostic Management to TherapyManar Aoun, Ilaria Passerini, Pietro Chiurazzi, et al.
International Journal of Molecular Sciences|February 10, 2021
Clinical and Molecular Characterization of Achromatopsia Patients: A Longitudinal StudyRaffaella Brunetti-Pierri, Marianthi Karali, Paolo Melillo, et al.
European Journal of Human Genetics : EJHG|March 14, 2003
Identification and characterisation of the retinitis pigmentosa 1-like1 gene (RP1L1): a novel candidate for retinal degenerationsIvan Conte, Marta Lestingi, Anneke den Hollander, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 12, 2005
Novel mutation of SACS gene in a Spanish family with autosomal recessive spastic ataxiaChiara Criscuolo, Francesco Saccà, Giuseppe De Michele, et al.
Autophagy|June 16, 2015
Lysoplex: An efficient toolkit to detect DNA sequence variations in the autophagy-lysosomal pathwayGiuseppina Di Fruscio, Angela Schulz, Rossella De Cegli, et al.
Scientific Reports|October 22, 2022
Visual function and retinal changes after voretigene neparvovec treatment in children with biallelic RPE65-related inherited retinal dystrophyFrancesco Testa, Paolo Melillo, Valentina Di Iorio, et al.
Pageof 14