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Francesco Vetrini

Showing results (1-10 of 57) with videos related to

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Viruses|October 14, 2011
Gene therapy with helper-dependent adenoviral vectors: current advances and future perspectivesFrancesco Vetrini, Philip Ng
Current Pharmaceutical Design|July 22, 2011
Liver-directed gene therapy with helper-dependent adenoviral vectors: current state of the art and future challengesFrancesco Vetrini, Philip Ng
Journal of Genetic Syndromes & Gene Therapy|February 18, 2014
Helper-Dependent Adenoviral VectorsAmanda Rosewell, Francesco Vetrini, Philip Ng
Molecular Vision|October 26, 2007
Fibroblast growth factor and epidermal growth factor differently affect differentiation of murine retinal stem cells in vitroFrancesca Giordano, Anna De Marzo, Francesco Vetrini, et al.
Clinical Genetics|February 12, 2024
Further evidence of involvement of ITSN1 in autosomal dominant neurodevelopmental disorderKhurram Liaqat, Kayla Treat, Theodore E Wilson, et al.
Clinical Case Reports|February 14, 2022
Exome sequencing identified a novel HIST1H1E heterozygous protein-truncating variant in a 6-month-old male patient with Rahman syndrome: A case reportSubba Rao Indugula, Sofia Saenz Ayala, Francesco Vetrini, et al.
Cold Spring Harbor Molecular Case Studies|January 29, 2022
Reanalysis of a novel variant in the <i>IGF1R</i> gene in a family with variable prenatal and postnatal growth retardation and dysmorphic features: benefits and feasibility of IUSM-URDC (Undiagnosed Rare Disease Clinic) programAnnalise Jacobs, Catherine Burns, Purva Patel, et al.
Molecular and Cellular Biology|July 16, 2004
The microphthalmia transcription factor (Mitf) controls expression of the ocular albinism type 1 gene: link between melanin synthesis and melanosome biogenesisFrancesco Vetrini, Alberto Auricchio, Jinyan Du, et al.
Genetic Testing and Molecular Biomarkers|April 18, 2025
Uncovering a Diagnosis Through Reanalysis of <i>UBA2</i> Variants in a Patient with Syndactyly, Polydactyly, and Aplasia Cutis Congenita: A Short Report and a Review of the LiteratureKhurram Liaqat, Kimberly Felipe, Kayla Treat, et al.
American Journal of Medical Genetics. Part A|December 22, 2023
A case of MBTPS1-related disorder due to compound heterozygous variants in MBTPS1 gene: Genotype-phenotype expansion and the emergence of a novel syndromeKhurram Liaqat, Kayla Treat, Lili Mantcheva, et al.
Pageof 6

Showing results (1-10 of 57) with videos related to

Sort By:
Pageof 6
Viruses|October 14, 2011
Gene therapy with helper-dependent adenoviral vectors: current advances and future perspectivesFrancesco Vetrini, Philip Ng
Current Pharmaceutical Design|July 22, 2011
Liver-directed gene therapy with helper-dependent adenoviral vectors: current state of the art and future challengesFrancesco Vetrini, Philip Ng
Journal of Genetic Syndromes & Gene Therapy|February 18, 2014
Helper-Dependent Adenoviral VectorsAmanda Rosewell, Francesco Vetrini, Philip Ng
Molecular Vision|October 26, 2007
Fibroblast growth factor and epidermal growth factor differently affect differentiation of murine retinal stem cells in vitroFrancesca Giordano, Anna De Marzo, Francesco Vetrini, et al.
Clinical Genetics|February 12, 2024
Further evidence of involvement of ITSN1 in autosomal dominant neurodevelopmental disorderKhurram Liaqat, Kayla Treat, Theodore E Wilson, et al.
Clinical Case Reports|February 14, 2022
Exome sequencing identified a novel HIST1H1E heterozygous protein-truncating variant in a 6-month-old male patient with Rahman syndrome: A case reportSubba Rao Indugula, Sofia Saenz Ayala, Francesco Vetrini, et al.
Cold Spring Harbor Molecular Case Studies|January 29, 2022
Reanalysis of a novel variant in the <i>IGF1R</i> gene in a family with variable prenatal and postnatal growth retardation and dysmorphic features: benefits and feasibility of IUSM-URDC (Undiagnosed Rare Disease Clinic) programAnnalise Jacobs, Catherine Burns, Purva Patel, et al.
Molecular and Cellular Biology|July 16, 2004
The microphthalmia transcription factor (Mitf) controls expression of the ocular albinism type 1 gene: link between melanin synthesis and melanosome biogenesisFrancesco Vetrini, Alberto Auricchio, Jinyan Du, et al.
Genetic Testing and Molecular Biomarkers|April 18, 2025
Uncovering a Diagnosis Through Reanalysis of <i>UBA2</i> Variants in a Patient with Syndactyly, Polydactyly, and Aplasia Cutis Congenita: A Short Report and a Review of the LiteratureKhurram Liaqat, Kimberly Felipe, Kayla Treat, et al.
American Journal of Medical Genetics. Part A|December 22, 2023
A case of MBTPS1-related disorder due to compound heterozygous variants in MBTPS1 gene: Genotype-phenotype expansion and the emergence of a novel syndromeKhurram Liaqat, Kayla Treat, Lili Mantcheva, et al.
Pageof 6