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Lucia Susani

Showing results (11-20 of 19) with videos related to

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Human Mutation|August 10, 2004
TCIRG1-dependent recessive osteopetrosis: mutation analysis, functional identification of the splicing defects, and in vitro rescue by U1 snRNALucia Susani, Alessandra Pangrazio, Cristina Sobacchi, et al.
Stem Cells (Dayton, Ohio)|March 22, 2019
Chromosome Transplantation: Correction of the Chronic Granulomatous Disease Defect in Mouse Induced Pluripotent Stem CellsAlessandra Castelli, Lucia Susani, Ciro Menale, et al.
Human Molecular Genetics|November 11, 2008
Cornelia de Lange syndrome mutations in SMC1A or SMC3 affect binding to DNAEkaterina Revenkova, Maria Luisa Focarelli, Lucia Susani, et al.
Molecular Therapy. Methods & Clinical Development|February 27, 2020
Chromosome Transplantation: A Possible Approach to Treat Human X-linked DisordersMarianna Paulis, Lucia Susani, Alessandra Castelli, et al.
Stem Cell Reports|May 14, 2021
Human iPSC-based neurodevelopmental models of globoid cell leukodystrophy uncover patient- and cell type-specific disease phenotypesElisabeth Mangiameli, Anna Cecchele, Francesco Morena, et al.
Oncotarget|October 21, 2015
Chromosome transplantation as a novel approach for correcting complex genomic disordersMarianna Paulis, Alessandra Castelli, Lucia Susani, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 31, 2003
Chloride channel ClCN7 mutations are responsible for severe recessive, dominant, and intermediate osteopetrosisAnnalisa Frattini, Alessandra Pangrazio, Lucia Susani, et al.
Nature Genetics|July 17, 2007
Osteoclast-poor human osteopetrosis due to mutations in the gene encoding RANKLCristina Sobacchi, Annalisa Frattini, Matteo M Guerrini, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 3, 2013
SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severityAlessandra Pangrazio, Anders Fasth, Andrea Sbardellati, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Human Mutation|August 10, 2004
TCIRG1-dependent recessive osteopetrosis: mutation analysis, functional identification of the splicing defects, and in vitro rescue by U1 snRNALucia Susani, Alessandra Pangrazio, Cristina Sobacchi, et al.
Stem Cells (Dayton, Ohio)|March 22, 2019
Chromosome Transplantation: Correction of the Chronic Granulomatous Disease Defect in Mouse Induced Pluripotent Stem CellsAlessandra Castelli, Lucia Susani, Ciro Menale, et al.
Human Molecular Genetics|November 11, 2008
Cornelia de Lange syndrome mutations in SMC1A or SMC3 affect binding to DNAEkaterina Revenkova, Maria Luisa Focarelli, Lucia Susani, et al.
Molecular Therapy. Methods & Clinical Development|February 27, 2020
Chromosome Transplantation: A Possible Approach to Treat Human X-linked DisordersMarianna Paulis, Lucia Susani, Alessandra Castelli, et al.
Stem Cell Reports|May 14, 2021
Human iPSC-based neurodevelopmental models of globoid cell leukodystrophy uncover patient- and cell type-specific disease phenotypesElisabeth Mangiameli, Anna Cecchele, Francesco Morena, et al.
Oncotarget|October 21, 2015
Chromosome transplantation as a novel approach for correcting complex genomic disordersMarianna Paulis, Alessandra Castelli, Lucia Susani, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 31, 2003
Chloride channel ClCN7 mutations are responsible for severe recessive, dominant, and intermediate osteopetrosisAnnalisa Frattini, Alessandra Pangrazio, Lucia Susani, et al.
Nature Genetics|July 17, 2007
Osteoclast-poor human osteopetrosis due to mutations in the gene encoding RANKLCristina Sobacchi, Annalisa Frattini, Matteo M Guerrini, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 3, 2013
SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severityAlessandra Pangrazio, Anders Fasth, Andrea Sbardellati, et al.
Pageof 2