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Biomedicines
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September 27, 2025
Unraveling the Functional Impact of Splicing Variants in Inherited Hearing Disorders Through Minigene Splicing Assays
Lara Emily Rosso, Giulia Pianigiani, Anna Morgan, et al.
The Journal of Physiology
|
June 26, 2015
Ion channel and lipid scramblase activity associated with expression of TMEM16F/ANO6 isoforms
Paolo Scudieri, Emanuela Caci, Arianna Venturini, et al.
Human Molecular Genetics
|
April 28, 2018
Exon-specific U1 snRNAs improve ELP1 exon 20 definition and rescue ELP1 protein expression in a familial dysautonomia mouse model
Irving Donadon, Mirko Pinotti, Katarzyna Rajkowska, et al.
Nucleic Acids Research
|
May 26, 2019
Rescue of spinal muscular atrophy mouse models with AAV9-Exon-specific U1 snRNA
Irving Donadon, Erica Bussani, Federico Riccardi, et al.
Leukemia
|
August 25, 2022
Current status and future perspectives in targeted therapy of NPM1-mutated AML
Roberta Ranieri, Giulia Pianigiani, Sofia Sciabolacci, et al.
Leukemia
|
May 14, 2022
The absent/low expression of CD34 in NPM1-mutated AML is not related to cytoplasmic dislocation of NPM1 mutant protein
Giulia Pianigiani, Francesca Rocchio, Sara Peruzzi, et al.
BMC Genomics
|
November 11, 2025
Variability of transposable elements in six genetic isolates from North-Eastern Italy and their relationship with alcohol consumption, tobacco use and BMI
Giorgia Modenini, Giacomo Mercuri, Paolo Abondio, et al.
Pharmaceutics
|
November 27, 2025
Hacking Extracellular Vesicles: Using Vesicle-Related Tags to Engineer Mesenchymal Stromal Cell-Derived Extracellular Vesicles
Gabriele Scattini, Giulia Pianigiani, Stefano Capomaccio, et al.
Blood Advances
|
August 29, 2022
Prolonged XPO1 inhibition is essential for optimal antileukemic activity in NPM1-mutated AML
Giulia Pianigiani, Andrea Gagliardi, Federica Mezzasoma, et al.
Genes
|
October 29, 2025
Beyond the Curtains: Identification of the Genetic Cause of Foetal Developmental Abnormalities Through the Application of Molecular Autopsy
Beatrice Spedicati, Giulia Pianigiani, Aurora Santin, et al.
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Search research articles
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Showing results (11-20 of 29) with videos related to
Sort By:
Page
of 3
Biomedicines
|
September 27, 2025
Unraveling the Functional Impact of Splicing Variants in Inherited Hearing Disorders Through Minigene Splicing Assays
Lara Emily Rosso, Giulia Pianigiani, Anna Morgan, et al.
The Journal of Physiology
|
June 26, 2015
Ion channel and lipid scramblase activity associated with expression of TMEM16F/ANO6 isoforms
Paolo Scudieri, Emanuela Caci, Arianna Venturini, et al.
Human Molecular Genetics
|
April 28, 2018
Exon-specific U1 snRNAs improve ELP1 exon 20 definition and rescue ELP1 protein expression in a familial dysautonomia mouse model
Irving Donadon, Mirko Pinotti, Katarzyna Rajkowska, et al.
Nucleic Acids Research
|
May 26, 2019
Rescue of spinal muscular atrophy mouse models with AAV9-Exon-specific U1 snRNA
Irving Donadon, Erica Bussani, Federico Riccardi, et al.
Leukemia
|
August 25, 2022
Current status and future perspectives in targeted therapy of NPM1-mutated AML
Roberta Ranieri, Giulia Pianigiani, Sofia Sciabolacci, et al.
Leukemia
|
May 14, 2022
The absent/low expression of CD34 in NPM1-mutated AML is not related to cytoplasmic dislocation of NPM1 mutant protein
Giulia Pianigiani, Francesca Rocchio, Sara Peruzzi, et al.
BMC Genomics
|
November 11, 2025
Variability of transposable elements in six genetic isolates from North-Eastern Italy and their relationship with alcohol consumption, tobacco use and BMI
Giorgia Modenini, Giacomo Mercuri, Paolo Abondio, et al.
Pharmaceutics
|
November 27, 2025
Hacking Extracellular Vesicles: Using Vesicle-Related Tags to Engineer Mesenchymal Stromal Cell-Derived Extracellular Vesicles
Gabriele Scattini, Giulia Pianigiani, Stefano Capomaccio, et al.
Blood Advances
|
August 29, 2022
Prolonged XPO1 inhibition is essential for optimal antileukemic activity in NPM1-mutated AML
Giulia Pianigiani, Andrea Gagliardi, Federica Mezzasoma, et al.
Genes
|
October 29, 2025
Beyond the Curtains: Identification of the Genetic Cause of Foetal Developmental Abnormalities Through the Application of Molecular Autopsy
Beatrice Spedicati, Giulia Pianigiani, Aurora Santin, et al.
Page
of 3