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Elena Manara

Showing results (31-40 of 45) with videos related to

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Journal of Hematology & Oncology|June 13, 2015
Identification of the NUP98-PHF23 fusion gene in pediatric cytogenetically normal acute myeloid leukemia by whole-transcriptome sequencingMarco Togni, Riccardo Masetti, Martina Pigazzi, et al.
International Journal of Molecular Sciences|January 5, 2021
Expanding the Clinical and Genetic Spectrum of <i>RAB28</i>-Related Cone-Rod Dystrophy: Pathogenicity of Novel Variants in Italian FamiliesGiancarlo Iarossi, Valerio Marino, Paolo Enrico Maltese, et al.
International Journal of Molecular Sciences|September 3, 2020
Aldo-Keto Reductase 1C1 (<i>AKR1C1</i>) as the First Mutated Gene in a Family with Nonsyndromic Primary LipedemaSandro Michelini, Pietro Chiurazzi, Valerio Marino, et al.
Haematologica|October 27, 2012
MicroRNA-34b promoter hypermethylation induces CREB overexpression and contributes to myeloid transformationMartina Pigazzi, Elena Manara, Silvia Bresolin, et al.
Haematologica|December 7, 2014
Minimal residual disease monitored after induction therapy by RQ-PCR can contribute to tailor treatment of patients with t(8;21) RUNX1-RUNX1T1 rearrangementMartina Pigazzi, Elena Manara, Barbara Buldini, et al.
Human Genetics|November 25, 2021
A novel complex genomic rearrangement affecting the KCNJ2 regulatory region causes a variant of Cooks syndromeLuigia Cinque, Lucia Micale, Elena Manara, et al.
Eating and Weight Disorders : EWD|November 25, 2021
A next generation sequencing gene panel for use in the diagnosis of anorexia nervosaMaria Rachele Ceccarini, Vincenza Precone, Elena Manara, et al.
Leukemia|February 24, 2018
Epigenetic heterogeneity affects the risk of relapse in children with t(8;21)RUNX1-RUNX1T1-rearranged AMLMatteo Zampini, Claudia Tregnago, Valeria Bisio, et al.
Molecular Genetics & Genomic Medicine|March 30, 2026
Exclusion of CLIC5 as a Candidate Gene and Identification of NEFM as a Possible Novel Gene Correlated With Autosomal Recessive Pure Cerebellar Ataxia in a Highly Consanguineous FamilyPaolo Enrico Maltese, Gabriele Bonetti, Elena Manara, et al.
Acta Bio-Medica : Atenei Parmensis|November 10, 2020
Pilot study for the evaluation of safety profile of a potential inhibitor of SARS-CoV-2 endocytosisStefano Paolacci, Maria Rachele Ceccarini, Michela Codini, et al.
Pageof 5

Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
Journal of Hematology & Oncology|June 13, 2015
Identification of the NUP98-PHF23 fusion gene in pediatric cytogenetically normal acute myeloid leukemia by whole-transcriptome sequencingMarco Togni, Riccardo Masetti, Martina Pigazzi, et al.
International Journal of Molecular Sciences|January 5, 2021
Expanding the Clinical and Genetic Spectrum of <i>RAB28</i>-Related Cone-Rod Dystrophy: Pathogenicity of Novel Variants in Italian FamiliesGiancarlo Iarossi, Valerio Marino, Paolo Enrico Maltese, et al.
International Journal of Molecular Sciences|September 3, 2020
Aldo-Keto Reductase 1C1 (<i>AKR1C1</i>) as the First Mutated Gene in a Family with Nonsyndromic Primary LipedemaSandro Michelini, Pietro Chiurazzi, Valerio Marino, et al.
Haematologica|October 27, 2012
MicroRNA-34b promoter hypermethylation induces CREB overexpression and contributes to myeloid transformationMartina Pigazzi, Elena Manara, Silvia Bresolin, et al.
Haematologica|December 7, 2014
Minimal residual disease monitored after induction therapy by RQ-PCR can contribute to tailor treatment of patients with t(8;21) RUNX1-RUNX1T1 rearrangementMartina Pigazzi, Elena Manara, Barbara Buldini, et al.
Human Genetics|November 25, 2021
A novel complex genomic rearrangement affecting the KCNJ2 regulatory region causes a variant of Cooks syndromeLuigia Cinque, Lucia Micale, Elena Manara, et al.
Eating and Weight Disorders : EWD|November 25, 2021
A next generation sequencing gene panel for use in the diagnosis of anorexia nervosaMaria Rachele Ceccarini, Vincenza Precone, Elena Manara, et al.
Leukemia|February 24, 2018
Epigenetic heterogeneity affects the risk of relapse in children with t(8;21)RUNX1-RUNX1T1-rearranged AMLMatteo Zampini, Claudia Tregnago, Valeria Bisio, et al.
Molecular Genetics & Genomic Medicine|March 30, 2026
Exclusion of CLIC5 as a Candidate Gene and Identification of NEFM as a Possible Novel Gene Correlated With Autosomal Recessive Pure Cerebellar Ataxia in a Highly Consanguineous FamilyPaolo Enrico Maltese, Gabriele Bonetti, Elena Manara, et al.
Acta Bio-Medica : Atenei Parmensis|November 10, 2020
Pilot study for the evaluation of safety profile of a potential inhibitor of SARS-CoV-2 endocytosisStefano Paolacci, Maria Rachele Ceccarini, Michela Codini, et al.
Pageof 5