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Rosa Romano

Showing results (21-30 of 37) with videos related to

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Biomolecules|February 26, 2025
The Role of Circulating Biomarkers in Patients with Coronary Microvascular DiseaseRossella Quarta, Giovanni Martino, Letizia Rosa Romano, et al.
Journal of Clinical Medicine|June 26, 2026
Strategies and Timing of Complete Revascularization in STEMI Patients with Multivessel Coronary Artery DiseaseDomenico Simone Castiello, Claudia Rocca, Letizia Rosa Romano, et al.
Journal of Clinical Medicine|February 15, 2022
Non-Invasive Myocardial Work in Patients with Severe Aortic StenosisSalvatore De Rosa, Jolanda Sabatino, Antonio Strangio, et al.
Italian Journal of Pediatrics|February 16, 2013
The R156H variation in IL-12Rβ1 is not a mutationEsther van de Vosse, Jaap T van Dissel, Loredana Palamaro, et al.
American Journal of Medical Genetics. Part A|August 21, 2012
De novo 13q12.3-q14.11 deletion involving BRCA2 gene in a patient with developmental delay, elevated IgM levels, transient ataxia, and cerebellar hypoplasia, mimicking an A-T like phenotypeEmilia Cirillo, Rosa Romano, Alfonso Romano, et al.
International Immunology|September 17, 2013
Human skin-derived keratinocytes and fibroblasts co-cultured on 3D poly ε-caprolactone scaffold support in vitro HSC differentiation into T-lineage committed cellsLoredana Palamaro, Vincenzo Guarino, Giulia Scalia, et al.
Plos One|December 19, 2013
Molecular evidence for a thymus-independent partial T cell development in a FOXN1-/- athymic human fetusAnna Fusco, Luigi Panico, Marisa Gorrese, et al.
Frontiers in Immunology|July 26, 2021
BHLHE40 Regulates IL-10 and IFN-<i>γ</i> Production in T Cells but Does Not Interfere With Human Type 1 Regulatory T Cell DifferentiationMolly Javier Uyeda, Robert A Freeborn, Brandon Cieniewicz, et al.
Blood Advances|November 7, 2025
Novel humanized loss-of-function NF1 mouse model of juvenile myelomonocytic leukemiaRoshani Sinha, Rachana V Patil, Rosa Romano, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 20, 2021
Correction of recessive dystrophic epidermolysis bullosa by homology-directed repair-mediated genome editingJose Bonafont, Angeles Mencía, Esteban Chacón-Solano, et al.
Pageof 4

Showing results (21-30 of 37) with videos related to

Sort By:
Pageof 4
Biomolecules|February 26, 2025
The Role of Circulating Biomarkers in Patients with Coronary Microvascular DiseaseRossella Quarta, Giovanni Martino, Letizia Rosa Romano, et al.
Journal of Clinical Medicine|June 26, 2026
Strategies and Timing of Complete Revascularization in STEMI Patients with Multivessel Coronary Artery DiseaseDomenico Simone Castiello, Claudia Rocca, Letizia Rosa Romano, et al.
Journal of Clinical Medicine|February 15, 2022
Non-Invasive Myocardial Work in Patients with Severe Aortic StenosisSalvatore De Rosa, Jolanda Sabatino, Antonio Strangio, et al.
Italian Journal of Pediatrics|February 16, 2013
The R156H variation in IL-12Rβ1 is not a mutationEsther van de Vosse, Jaap T van Dissel, Loredana Palamaro, et al.
American Journal of Medical Genetics. Part A|August 21, 2012
De novo 13q12.3-q14.11 deletion involving BRCA2 gene in a patient with developmental delay, elevated IgM levels, transient ataxia, and cerebellar hypoplasia, mimicking an A-T like phenotypeEmilia Cirillo, Rosa Romano, Alfonso Romano, et al.
International Immunology|September 17, 2013
Human skin-derived keratinocytes and fibroblasts co-cultured on 3D poly ε-caprolactone scaffold support in vitro HSC differentiation into T-lineage committed cellsLoredana Palamaro, Vincenzo Guarino, Giulia Scalia, et al.
Plos One|December 19, 2013
Molecular evidence for a thymus-independent partial T cell development in a FOXN1-/- athymic human fetusAnna Fusco, Luigi Panico, Marisa Gorrese, et al.
Frontiers in Immunology|July 26, 2021
BHLHE40 Regulates IL-10 and IFN-<i>γ</i> Production in T Cells but Does Not Interfere With Human Type 1 Regulatory T Cell DifferentiationMolly Javier Uyeda, Robert A Freeborn, Brandon Cieniewicz, et al.
Blood Advances|November 7, 2025
Novel humanized loss-of-function NF1 mouse model of juvenile myelomonocytic leukemiaRoshani Sinha, Rachana V Patil, Rosa Romano, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 20, 2021
Correction of recessive dystrophic epidermolysis bullosa by homology-directed repair-mediated genome editingJose Bonafont, Angeles Mencía, Esteban Chacón-Solano, et al.
Pageof 4