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Nadia Passon

Showing results (11-20 of 27) with videos related to

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Genetic Testing and Molecular Biomarkers|March 25, 2009
A simple multiplex real-time PCR methodology for the SMN1 gene copy number quantificationNadia Passon, Federico Pozzo, Cristiano Molinis, et al.
Minerva Endocrinologica|September 8, 2017
Evaluation of somatic genomic imbalances in thyroid carcinomas of follicular origin by CGH-based approachesFederica Baldan, Catia Mio, Lorenzo Allegri, et al.
European Journal of Medical Genetics|January 19, 2020
CACNA1C haploinsufficiency accounts for the common features of interstitial 12p13.33 deletion carriersCatia Mio, Nadia Passon, Federica Baldan, et al.
Journal of Clinical Pathology|January 20, 2012
Expression of Dicer and Drosha in triple-negative breast cancerNadia Passon, Anna Gerometta, Cinzia Puppin, et al.
Cytogenetic and Genome Research|May 11, 2016
Microdeletion 15q26.2qter and Microduplication 18q23 in a Patient with Prader-Willi-Like Syndrome: Clinical FindingsPatrizia Dello Russo, Eliana Demori, Annalisa Sechi, et al.
Biochemical and Biophysical Research Communications|July 19, 2011
Levels of histone acetylation in thyroid tumorsCinzia Puppin, Nadia Passon, Elisa Lavarone, et al.
Endocrine|November 8, 2022
Novel IGFALS mutations with predicted pathogenetic effects by the analysis of AlphaFold structureAlessandra Franzoni, Federica Baldan, Nadia Passon, et al.
Molecular and Cellular Probes|July 28, 2010
Quick MLPA test for quantification of SMN1 and SMN2 copy numbersNadia Passon, Giorgia Dubsky de Wittenau, Irena Jurman, et al.
Molecular and Cellular Biochemistry|February 19, 2009
Down-regulation of SM22/transgelin gene expression during H9c2 cells differentiationElisa Bregant, Giovanni Renzone, Renata Lonigro, et al.
Endocrine|April 13, 2015
Somatic amplifications and deletions in genome of papillary thyroid carcinomasNadia Passon, Elisa Bregant, Marialuisa Sponziello, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Genetic Testing and Molecular Biomarkers|March 25, 2009
A simple multiplex real-time PCR methodology for the SMN1 gene copy number quantificationNadia Passon, Federico Pozzo, Cristiano Molinis, et al.
Minerva Endocrinologica|September 8, 2017
Evaluation of somatic genomic imbalances in thyroid carcinomas of follicular origin by CGH-based approachesFederica Baldan, Catia Mio, Lorenzo Allegri, et al.
European Journal of Medical Genetics|January 19, 2020
CACNA1C haploinsufficiency accounts for the common features of interstitial 12p13.33 deletion carriersCatia Mio, Nadia Passon, Federica Baldan, et al.
Journal of Clinical Pathology|January 20, 2012
Expression of Dicer and Drosha in triple-negative breast cancerNadia Passon, Anna Gerometta, Cinzia Puppin, et al.
Cytogenetic and Genome Research|May 11, 2016
Microdeletion 15q26.2qter and Microduplication 18q23 in a Patient with Prader-Willi-Like Syndrome: Clinical FindingsPatrizia Dello Russo, Eliana Demori, Annalisa Sechi, et al.
Biochemical and Biophysical Research Communications|July 19, 2011
Levels of histone acetylation in thyroid tumorsCinzia Puppin, Nadia Passon, Elisa Lavarone, et al.
Endocrine|November 8, 2022
Novel IGFALS mutations with predicted pathogenetic effects by the analysis of AlphaFold structureAlessandra Franzoni, Federica Baldan, Nadia Passon, et al.
Molecular and Cellular Probes|July 28, 2010
Quick MLPA test for quantification of SMN1 and SMN2 copy numbersNadia Passon, Giorgia Dubsky de Wittenau, Irena Jurman, et al.
Molecular and Cellular Biochemistry|February 19, 2009
Down-regulation of SM22/transgelin gene expression during H9c2 cells differentiationElisa Bregant, Giovanni Renzone, Renata Lonigro, et al.
Endocrine|April 13, 2015
Somatic amplifications and deletions in genome of papillary thyroid carcinomasNadia Passon, Elisa Bregant, Marialuisa Sponziello, et al.
Pageof 3