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Lucia Susani

Showing results (1-10 of 19) with videos related to

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Hepatology (Baltimore, Md.)|October 18, 2008
Cell fusion is a physiological process in mouse liverFrancesca Faggioli, Maria Grazia Sacco, Lucia Susani, et al.
Stem Cell Research|June 20, 2025
Generation and characterization of human iPSC lines from two patients with therapy-resistant epilepsy carrying nonsense heterozygous variants in the SMC1A geneMarianna Paulis, Maddalena Di Nardo, Lucia Susani, et al.
The CRISPR Journal|April 26, 2019
Correction of a Recessive Genetic Defect by CRISPR-Cas9-Mediated Endogenous RepairLucia Susani, Alessandra Castelli, Michela Lizier, et al.
Scientific Reports|July 25, 2015
A pre-screening FISH-based method to detect CRISPR/Cas9 off-targets in mouse embryonic stem cellsMarianna Paulis, Alessandra Castelli, Michela Lizier, et al.
Cytogenetic and Genome Research|October 24, 2025
Chromosomal Instability in Mouse-Induced Pluripotent Stem Cells: Insights into X and Y AneuploidiesMarianna Paulis, Paola Rebuzzini, Lucia Susani, et al.
Cells|April 26, 2024
Chromosome Transplantation: Opportunities and LimitationsAngela La Grua, Ilaria Rao, Lucia Susani, et al.
Calcified Tissue International|August 1, 2012
A homozygous contiguous gene deletion in chromosome 16p13.3 leads to autosomal recessive osteopetrosis in a Jordanian patientAlessandra Pangrazio, Annalisa Frattini, Roberto Valli, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|July 29, 2016
Synonymous Mutations Add a Layer of Complexity in the Diagnosis of Human OsteopetrosisEleonora Palagano, Lucia Susani, Ciro Menale, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|February 19, 2014
As little as needed: the extraordinary case of a mild recessive osteopetrosis owing to a novel splicing hypomorphic mutation in the TCIRG1 geneCristina Sobacchi, Alessandra Pangrazio, Antonio González-Meneses Lopez, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 22, 2008
Characterization of a novel Alu-Alu recombination-mediated genomic deletion in the TCIRG1 gene in five osteopetrotic patientsAlessandra Pangrazio, Maria Elena Caldana, Cristina Sobacchi, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Hepatology (Baltimore, Md.)|October 18, 2008
Cell fusion is a physiological process in mouse liverFrancesca Faggioli, Maria Grazia Sacco, Lucia Susani, et al.
Stem Cell Research|June 20, 2025
Generation and characterization of human iPSC lines from two patients with therapy-resistant epilepsy carrying nonsense heterozygous variants in the SMC1A geneMarianna Paulis, Maddalena Di Nardo, Lucia Susani, et al.
The CRISPR Journal|April 26, 2019
Correction of a Recessive Genetic Defect by CRISPR-Cas9-Mediated Endogenous RepairLucia Susani, Alessandra Castelli, Michela Lizier, et al.
Scientific Reports|July 25, 2015
A pre-screening FISH-based method to detect CRISPR/Cas9 off-targets in mouse embryonic stem cellsMarianna Paulis, Alessandra Castelli, Michela Lizier, et al.
Cytogenetic and Genome Research|October 24, 2025
Chromosomal Instability in Mouse-Induced Pluripotent Stem Cells: Insights into X and Y AneuploidiesMarianna Paulis, Paola Rebuzzini, Lucia Susani, et al.
Cells|April 26, 2024
Chromosome Transplantation: Opportunities and LimitationsAngela La Grua, Ilaria Rao, Lucia Susani, et al.
Calcified Tissue International|August 1, 2012
A homozygous contiguous gene deletion in chromosome 16p13.3 leads to autosomal recessive osteopetrosis in a Jordanian patientAlessandra Pangrazio, Annalisa Frattini, Roberto Valli, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|July 29, 2016
Synonymous Mutations Add a Layer of Complexity in the Diagnosis of Human OsteopetrosisEleonora Palagano, Lucia Susani, Ciro Menale, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|February 19, 2014
As little as needed: the extraordinary case of a mild recessive osteopetrosis owing to a novel splicing hypomorphic mutation in the TCIRG1 geneCristina Sobacchi, Alessandra Pangrazio, Antonio González-Meneses Lopez, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 22, 2008
Characterization of a novel Alu-Alu recombination-mediated genomic deletion in the TCIRG1 gene in five osteopetrotic patientsAlessandra Pangrazio, Maria Elena Caldana, Cristina Sobacchi, et al.
Pageof 2