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Carla Lintas

Showing results (21-30 of 52) with videos related to

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Human Molecular Genetics|December 12, 2018
Evidence that ITGB3 promoter variants increase serotonin blood levels by regulating platelet serotonin transporter traffickingStefano Gabriele, Marco Canali, Carla Lintas, et al.
Molecular Syndromology|March 22, 2016
Xp22.33p22.12 Duplication in a Patient with Intellectual Disability and Dysmorphic Facial FeaturesCarla Lintas, Chiara Picinelli, Ignazio S Piras, et al.
Biology|November 11, 2022
Genetic Characterization in Familial Rotator Cuff Tear: An Exome Sequencing StudyAlessia Azzarà, Laura Risi Ambrogioni, Ilaria Cassano, et al.
Gene Reports|November 9, 2022
Whole exome sequencing identifies a rare variant in MAS1 gene in a subject with lethal COVID-19Alessia Azzarà, Ilaria Cassano, Maria Cristina Tirindelli, et al.
Genes|December 23, 2022
Expanding the Spectrum of <i>KDM5C</i> Neurodevelopmental Disorder: A Novel De Novo Stop Variant in a Young Woman and Emerging Genotype-Phenotype CorrelationsCarla Lintas, Irene Bottillo, Roberto Sacco, et al.
International Journal of Cancer|September 10, 2005
Methylation profile in tumor and sputum samples of lung cancer patients detected by spiral computed tomography: a nested case-control studyRosalia Cirincione, Carla Lintas, Davide Conte, et al.
European Journal of Neurology|October 12, 2023
A new gene for autosomal dominant facial palsy/migraine identified in a family by whole exome sequencingAlessia Azzarà, Ilaria Cassano, Carla Lintas, et al.
Cancers|August 26, 2023
BRAF Mutations in Melanoma: Biological Aspects, Therapeutic Implications, and Circulating BiomarkersGiorgia Castellani, Mariachiara Buccarelli, Maria Beatrice Arasi, et al.
Plos One|October 13, 2022
Genetic variants determine intrafamilial variability of SARS-CoV-2 clinical outcomes in 19 Italian familiesAlessia Azzarà, Ilaria Cassano, Elisa Paccagnella, et al.
Genes|March 29, 2023
Maternal Epigenetic Dysregulation as a Possible Risk Factor for Neurodevelopmental DisordersCarla Lintas, Ilaria Cassano, Alessia Azzarà, et al.
Pageof 6

Showing results (21-30 of 52) with videos related to

Sort By:
Pageof 6
Human Molecular Genetics|December 12, 2018
Evidence that ITGB3 promoter variants increase serotonin blood levels by regulating platelet serotonin transporter traffickingStefano Gabriele, Marco Canali, Carla Lintas, et al.
Molecular Syndromology|March 22, 2016
Xp22.33p22.12 Duplication in a Patient with Intellectual Disability and Dysmorphic Facial FeaturesCarla Lintas, Chiara Picinelli, Ignazio S Piras, et al.
Biology|November 11, 2022
Genetic Characterization in Familial Rotator Cuff Tear: An Exome Sequencing StudyAlessia Azzarà, Laura Risi Ambrogioni, Ilaria Cassano, et al.
Gene Reports|November 9, 2022
Whole exome sequencing identifies a rare variant in MAS1 gene in a subject with lethal COVID-19Alessia Azzarà, Ilaria Cassano, Maria Cristina Tirindelli, et al.
Genes|December 23, 2022
Expanding the Spectrum of <i>KDM5C</i> Neurodevelopmental Disorder: A Novel De Novo Stop Variant in a Young Woman and Emerging Genotype-Phenotype CorrelationsCarla Lintas, Irene Bottillo, Roberto Sacco, et al.
International Journal of Cancer|September 10, 2005
Methylation profile in tumor and sputum samples of lung cancer patients detected by spiral computed tomography: a nested case-control studyRosalia Cirincione, Carla Lintas, Davide Conte, et al.
European Journal of Neurology|October 12, 2023
A new gene for autosomal dominant facial palsy/migraine identified in a family by whole exome sequencingAlessia Azzarà, Ilaria Cassano, Carla Lintas, et al.
Cancers|August 26, 2023
BRAF Mutations in Melanoma: Biological Aspects, Therapeutic Implications, and Circulating BiomarkersGiorgia Castellani, Mariachiara Buccarelli, Maria Beatrice Arasi, et al.
Plos One|October 13, 2022
Genetic variants determine intrafamilial variability of SARS-CoV-2 clinical outcomes in 19 Italian familiesAlessia Azzarà, Ilaria Cassano, Elisa Paccagnella, et al.
Genes|March 29, 2023
Maternal Epigenetic Dysregulation as a Possible Risk Factor for Neurodevelopmental DisordersCarla Lintas, Ilaria Cassano, Alessia Azzarà, et al.
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