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Carlos De Brasi

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

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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
Molecular Diagnosis : a Journal Devoted to the Understanding of Human Disease Through the Clinical Application of Molecular Biology|November 6, 2004
Feasibility of a cost-effective approach to evaluate short tandem repeat markers suitable for chimerism follow-upAriela F Fundia, 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.
Blood Cells, Molecules & Diseases|February 6, 2004
Incidence of BCL-2 gene rearrangements in Argentinean non-Hodgkin lymphoma patients: increased frequency of breakpoints outside of MBR and MCRMaría Fernanda Noriega, Carlos De Brasi, Marina Narbaitz, et al.
European Journal of Haematology|February 5, 2009
Specific assessment of BCR-ABL transcript overexpression and imatinib resistance in chronic myeloid leukemia patientsMichele Bianchini, Carlos De Brasi, Patricia Gargallo, et al.
Leukemia & Lymphoma|November 12, 2013
CAMKIIγ, HSP70 and HSP90 transcripts are differentially expressed in chronic myeloid leukemia cells from patients with resistant mutated diseaseMariana Gonzalez, Carlos De Brasi, Cristian Ferri, et al.
Journal of the Neurological Sciences|October 19, 2013
Symptomatic female carriers of Duchenne muscular dystrophy (DMD): genetic and clinical characterizationFlorencia Giliberto, Claudia Pamela Radic, Leonela Luce, et al.
Molecular Immunology|February 19, 2019
Cytokines use different intracellular mechanisms to upregulate the membrane expression of CX<sub>3</sub>CR1 in human monocytesCecilia Analia Panek, Andrea Cecilia Bruballa, Gonzalo Ezequiel Pineda, et al.
Neuromuscular Disorders : NMD|January 16, 2021
Analysis of complex structural variants in the DMD gene in one familyLeonela Luce, Martín M Abelleyro, Micaela Carcione, et al.
Journal of Medical Genetics|May 8, 2024
Comprehensive genomic filtering algorithm to expose the cause of skewed X chromosome inactivation. The proof of concept in female haemophilia expressionBetiana Michelle Ziegler, Miguel Martin Abelleyro, Vanina Daniela Marchione, et al.
Pageof 1

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

Sort By:
Pageof 1
Human Mutation|January 29, 2003
Rapid detection of exon 1 NRAS gene mutations using universal heteroduplex generator technologyCarolina Belli, Carlos De Brasi, Irene Larripa
Molecular Diagnosis : a Journal Devoted to the Understanding of Human Disease Through the Clinical Application of Molecular Biology|November 6, 2004
Feasibility of a cost-effective approach to evaluate short tandem repeat markers suitable for chimerism follow-upAriela F Fundia, 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.
Blood Cells, Molecules & Diseases|February 6, 2004
Incidence of BCL-2 gene rearrangements in Argentinean non-Hodgkin lymphoma patients: increased frequency of breakpoints outside of MBR and MCRMaría Fernanda Noriega, Carlos De Brasi, Marina Narbaitz, et al.
European Journal of Haematology|February 5, 2009
Specific assessment of BCR-ABL transcript overexpression and imatinib resistance in chronic myeloid leukemia patientsMichele Bianchini, Carlos De Brasi, Patricia Gargallo, et al.
Leukemia & Lymphoma|November 12, 2013
CAMKIIγ, HSP70 and HSP90 transcripts are differentially expressed in chronic myeloid leukemia cells from patients with resistant mutated diseaseMariana Gonzalez, Carlos De Brasi, Cristian Ferri, et al.
Journal of the Neurological Sciences|October 19, 2013
Symptomatic female carriers of Duchenne muscular dystrophy (DMD): genetic and clinical characterizationFlorencia Giliberto, Claudia Pamela Radic, Leonela Luce, et al.
Molecular Immunology|February 19, 2019
Cytokines use different intracellular mechanisms to upregulate the membrane expression of CX<sub>3</sub>CR1 in human monocytesCecilia Analia Panek, Andrea Cecilia Bruballa, Gonzalo Ezequiel Pineda, et al.
Neuromuscular Disorders : NMD|January 16, 2021
Analysis of complex structural variants in the DMD gene in one familyLeonela Luce, Martín M Abelleyro, Micaela Carcione, et al.
Journal of Medical Genetics|May 8, 2024
Comprehensive genomic filtering algorithm to expose the cause of skewed X chromosome inactivation. The proof of concept in female haemophilia expressionBetiana Michelle Ziegler, Miguel Martin Abelleyro, Vanina Daniela Marchione, et al.
Pageof 1