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Carolina Belli

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Human Mutation|January 29, 2003
Rapid detection of exon 1 NRAS gene mutations using universal heteroduplex generator technologyCarolina Belli, Carlos De Brasi, Irene Larripa
British Journal of Haematology|August 4, 2004
A single, multiplex analysis for all relevant activating NRAS gene mutations using heteroduplex generatorsCarolina Belli, Derrick J Bowen, Carlos De Brasi, et al.
Leukemia & Lymphoma|August 9, 2012
Early detection and quantification of mutations in the tyrosine kinase domain of chimerical BCR-ABL1 gene combining high-resolution melting analysis and mutant-allele specific quantitative polymerase chain reactionCristian Ferri, Michele Bianchini, Gustavo Icardi, et al.
Cancer Genetics and Cytogenetics|May 30, 2002
Evaluation of constitutional chromosome aberrations in hematologic disordersRoxana Cerretini, Susana Acevedo, Christian Chena, et al.
Archives of Medical Research|May 14, 2025
Human Voltage-Activated H<sup>+</sup> Channel is Highly Expressed in Acute Myeloid Leukemia and is Associated With the Blast Differentiated StageDiego Issouribehere, Nicolás Enrique, Paulina Finochietto, et al.
Stem Cell Research|January 20, 2024
Derivation of two human induced pluripotent stem cell lines carrying a missense mutation in FHL1 (c.377G > A, p.C126Y) linked to familial muscular dystrophyFederico Zabalegui, Sheila Lucia Castañeda, Guadalupe Amin, et al.
Stem Cell Research|July 2, 2023
Generation of two edited iPSCs lines by CRISPR/Cas9 with point mutations in PKP2 gene for arrhythmogenic cardiomyopathy in vitro modelingGuadalupe Amin, Sheila Lucía Castañeda, Federico Zabalegui, et al.
Leukemia & Lymphoma|September 25, 2014
Polymorphisms in TNF and IFNG are associated with clinical characteristics of aplastic anemia in Argentinean populationYesica Bestach, Yamila Sieza, Myriam Attie, et al.
Haematologica|January 22, 2002
Detection of risk groups in myelodysplastic syndromes. A multicenter studyCarolina Belli, Susana Acevedo, Raquel Bengio, et al.
Annals of Hematology|June 12, 2017
Influence of TNF and IL6 gene polymorphisms on the severity of cytopenias in Argentine patients with myelodysplastic syndromesYesica Bestach, Virginia Palau Nagore, María G Flores, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Human Mutation|January 29, 2003
Rapid detection of exon 1 NRAS gene mutations using universal heteroduplex generator technologyCarolina Belli, Carlos De Brasi, Irene Larripa
British Journal of Haematology|August 4, 2004
A single, multiplex analysis for all relevant activating NRAS gene mutations using heteroduplex generatorsCarolina Belli, Derrick J Bowen, Carlos De Brasi, et al.
Leukemia & Lymphoma|August 9, 2012
Early detection and quantification of mutations in the tyrosine kinase domain of chimerical BCR-ABL1 gene combining high-resolution melting analysis and mutant-allele specific quantitative polymerase chain reactionCristian Ferri, Michele Bianchini, Gustavo Icardi, et al.
Cancer Genetics and Cytogenetics|May 30, 2002
Evaluation of constitutional chromosome aberrations in hematologic disordersRoxana Cerretini, Susana Acevedo, Christian Chena, et al.
Archives of Medical Research|May 14, 2025
Human Voltage-Activated H<sup>+</sup> Channel is Highly Expressed in Acute Myeloid Leukemia and is Associated With the Blast Differentiated StageDiego Issouribehere, Nicolás Enrique, Paulina Finochietto, et al.
Stem Cell Research|January 20, 2024
Derivation of two human induced pluripotent stem cell lines carrying a missense mutation in FHL1 (c.377G > A, p.C126Y) linked to familial muscular dystrophyFederico Zabalegui, Sheila Lucia Castañeda, Guadalupe Amin, et al.
Stem Cell Research|July 2, 2023
Generation of two edited iPSCs lines by CRISPR/Cas9 with point mutations in PKP2 gene for arrhythmogenic cardiomyopathy in vitro modelingGuadalupe Amin, Sheila Lucía Castañeda, Federico Zabalegui, et al.
Leukemia & Lymphoma|September 25, 2014
Polymorphisms in TNF and IFNG are associated with clinical characteristics of aplastic anemia in Argentinean populationYesica Bestach, Yamila Sieza, Myriam Attie, et al.
Haematologica|January 22, 2002
Detection of risk groups in myelodysplastic syndromes. A multicenter studyCarolina Belli, Susana Acevedo, Raquel Bengio, et al.
Annals of Hematology|June 12, 2017
Influence of TNF and IL6 gene polymorphisms on the severity of cytopenias in Argentine patients with myelodysplastic syndromesYesica Bestach, Virginia Palau Nagore, María G Flores, et al.
Pageof 2