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Francesca Bruno

Showing results (1-10 of 67) with videos related to

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Haematologica|December 17, 2009
The -582A>G variant of the HAMP promoter is not associated with high serum ferritin levels in normal subjectsFrancesca Bruno, Sara Bonalumi, Clara Camaschella, et al.
Genes|August 26, 2023
Forensic DNA Phenotyping: Genes and Genetic Variants for Eye Color PredictionDesiree Brancato, Elvira Coniglio, Francesca Bruno, et al.
Genes|July 29, 2025
Cytogenetics and Cytogenomics in Clinical Diagnostics: Genome Architecture, Structural Variants, and Translational ApplicationsConcetta Federico, Desiree Brancato, Francesca Bruno, et al.
Journal of Clinical Immunology|September 19, 2014
Polyfunctional analysis of human cytomegalovirus (HCMV)-specific CD4(+) and CD8 (+) memory T-cells in HCMV-seropositive healthy subjects following different stimuliElisa Gabanti, Francesca Bruno, Chiara Fornara, et al.
International Journal of Molecular Sciences|June 27, 2024
The Chromatin Organization Close to SNP rs12913832, Involved in Eye Color Variation, Is Evolutionary Conserved in VertebratesDesiree Brancato, Francesca Bruno, Elvira Coniglio, et al.
Biomedicines|October 27, 2022
Hereditary Transthyretin-Related Amyloidosis: Genetic Heterogeneity and Early Personalized Gene TherapyKetty Dugo, Francesca Bruno, Valentina Sturiale, et al.
Internal and Emergency Medicine|August 24, 2012
Renal angiomyolipomatosis and Kaposi's sarcoma: a possible link disrupted by sirolimusGiovanni Stallone, Barbara Infante, Luciano Tartaglia, et al.
Genes|June 26, 2025
Origin and Evolution of Genes in Eukaryotes: Mechanisms, Dynamics, and Functional ImplicationsSalvatore Saccone, Desiree Brancato, Francesca Bruno, et al.
Genes|June 27, 2024
Robertsonian Translocation between Human Chromosomes 21 and 22, Inherited across Three Generations, without Any Phenotypic EffectConcetta Federico, Desiree Brancato, Francesca Bruno, et al.
Human Genetics|May 17, 2017
Somatic mosaicism with reversion to normality of a mutated transthyretin allele related to a familial amyloidotic polyneuropathyConcetta Federico, Ketty Dugo, Francesca Bruno, et al.
Pageof 7

Showing results (1-10 of 67) with videos related to

Sort By:
Pageof 7
Haematologica|December 17, 2009
The -582A>G variant of the HAMP promoter is not associated with high serum ferritin levels in normal subjectsFrancesca Bruno, Sara Bonalumi, Clara Camaschella, et al.
Genes|August 26, 2023
Forensic DNA Phenotyping: Genes and Genetic Variants for Eye Color PredictionDesiree Brancato, Elvira Coniglio, Francesca Bruno, et al.
Genes|July 29, 2025
Cytogenetics and Cytogenomics in Clinical Diagnostics: Genome Architecture, Structural Variants, and Translational ApplicationsConcetta Federico, Desiree Brancato, Francesca Bruno, et al.
Journal of Clinical Immunology|September 19, 2014
Polyfunctional analysis of human cytomegalovirus (HCMV)-specific CD4(+) and CD8 (+) memory T-cells in HCMV-seropositive healthy subjects following different stimuliElisa Gabanti, Francesca Bruno, Chiara Fornara, et al.
International Journal of Molecular Sciences|June 27, 2024
The Chromatin Organization Close to SNP rs12913832, Involved in Eye Color Variation, Is Evolutionary Conserved in VertebratesDesiree Brancato, Francesca Bruno, Elvira Coniglio, et al.
Biomedicines|October 27, 2022
Hereditary Transthyretin-Related Amyloidosis: Genetic Heterogeneity and Early Personalized Gene TherapyKetty Dugo, Francesca Bruno, Valentina Sturiale, et al.
Internal and Emergency Medicine|August 24, 2012
Renal angiomyolipomatosis and Kaposi's sarcoma: a possible link disrupted by sirolimusGiovanni Stallone, Barbara Infante, Luciano Tartaglia, et al.
Genes|June 26, 2025
Origin and Evolution of Genes in Eukaryotes: Mechanisms, Dynamics, and Functional ImplicationsSalvatore Saccone, Desiree Brancato, Francesca Bruno, et al.
Genes|June 27, 2024
Robertsonian Translocation between Human Chromosomes 21 and 22, Inherited across Three Generations, without Any Phenotypic EffectConcetta Federico, Desiree Brancato, Francesca Bruno, et al.
Human Genetics|May 17, 2017
Somatic mosaicism with reversion to normality of a mutated transthyretin allele related to a familial amyloidotic polyneuropathyConcetta Federico, Ketty Dugo, Francesca Bruno, et al.
Pageof 7