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Malo Serafini

Showing results (1-10 of 6) with videos related to

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Nature Protocols|July 26, 2023
Precise mutagenesis in zebrafish using cytosine base editorsMarion Rosello, Malo Serafini, Jean-Paul Concordet, et al.
Scientific Reports|December 30, 2022
A minimally invasive fin scratching protocol for fast genotyping and early selection of zebrafish embryosMartina Venditti, Catia Pedalino, Marion Rosello, et al.
Nature Communications|June 14, 2022
Disease modeling by efficient genome editing using a near PAM-less base editor in vivoMarion Rosello, Malo Serafini, Luca Mignani, et al.
The Journal of Clinical Investigation|July 9, 2024
De novo monoallelic Reelin missense variants cause dominant neuronal migration disorders via a dominant-negative mechanismMartina Riva, Sofia Ferreira, Kotaro Hayashi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 31, 2024
Variants in UBAP1L lead to autosomal recessive rod-cone and cone-rod dystrophyChristina Zeitz, Julien Navarro, Leila Azizzadeh Pormehr, et al.
American Journal of Human Genetics|February 5, 2026
Bi-allelic loss-of-function variants in JKAMP cause a neurodevelopmental syndrome associated with dysregulation of GPR37 traffickingPilar Chacon-Millan, Antonella Delicato, Arif Mahmood, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Nature Protocols|July 26, 2023
Precise mutagenesis in zebrafish using cytosine base editorsMarion Rosello, Malo Serafini, Jean-Paul Concordet, et al.
Scientific Reports|December 30, 2022
A minimally invasive fin scratching protocol for fast genotyping and early selection of zebrafish embryosMartina Venditti, Catia Pedalino, Marion Rosello, et al.
Nature Communications|June 14, 2022
Disease modeling by efficient genome editing using a near PAM-less base editor in vivoMarion Rosello, Malo Serafini, Luca Mignani, et al.
The Journal of Clinical Investigation|July 9, 2024
De novo monoallelic Reelin missense variants cause dominant neuronal migration disorders via a dominant-negative mechanismMartina Riva, Sofia Ferreira, Kotaro Hayashi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 31, 2024
Variants in UBAP1L lead to autosomal recessive rod-cone and cone-rod dystrophyChristina Zeitz, Julien Navarro, Leila Azizzadeh Pormehr, et al.
American Journal of Human Genetics|February 5, 2026
Bi-allelic loss-of-function variants in JKAMP cause a neurodevelopmental syndrome associated with dysregulation of GPR37 traffickingPilar Chacon-Millan, Antonella Delicato, Arif Mahmood, et al.
Pageof 1