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Isabella Ceccherini

Showing results (81-90 of 180) with videos related to

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European Journal of Medical Genetics|August 21, 2020
Targeted re-sequencing in pediatric and perinatal strokeAlice Grossi, Mariasavina Severino, Marta Rusmini, et al.
Oncotarget|April 2, 2016
Genetic and epigenetic factors affect RET gene expression in breast cancer cell lines and influence survival in patientsPaola Griseri, Ornella Garrone, Alessandra Lo Sardo, et al.
International Journal of Molecular Medicine|June 13, 2002
HOX11L1: a promoter study to evaluate possible expression defects in intestinal motility disordersMonica Fava, Silvia Borghini, Roberta Cinti, et al.
Rheumatology (Oxford, England)|September 10, 2024
Majeed syndrome: first description in a patient of central-European ancestryEnrico Drago, Arinna Bertoni, Alice Grossi, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|April 24, 2017
Common PHOX2B poly-alanine contractions impair RET gene transcription, predisposing to Hirschsprung diseaseEleonora Di Zanni, Annalisa Adamo, Elga Belligni, et al.
Brain : a Journal of Neurology|August 8, 2008
Adult-onset Alexander disease: a series of eleven unrelated cases with review of the literatureDavide Pareyson, Roberto Fancellu, Caterina Mariotti, et al.
Journal of Medical Genetics|August 6, 2017
Mutations in <i>MYO1H</i> cause a recessive form of central hypoventilation with autonomic dysfunctionMalte Spielmann, Luis R Hernandez-Miranda, Isabella Ceccherini, et al.
Clinical and Experimental Rheumatology|June 17, 2016
Gene expression profile in TNF receptor-associated periodic syndrome reveals constitutively enhanced pathways and new players in the underlying inflammationSilvia Borghini, Denise Ferrera, Ignazia Prigione, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 1, 2018
ABCC6 mutations and early onset stroke: Two cases of a typical Pseudoxanthoma ElasticumMarta Bertamino, Mariasavina Severino, Alice Grossi, et al.
Genes|December 24, 2021
The Genetic Landscape of Patent Foramen Ovale: A Systematic ReviewMatteo Paolucci, Chiara Vincenzi, Michele Romoli, et al.
Pageof 18

Showing results (81-90 of 180) with videos related to

Sort By:
Pageof 18
European Journal of Medical Genetics|August 21, 2020
Targeted re-sequencing in pediatric and perinatal strokeAlice Grossi, Mariasavina Severino, Marta Rusmini, et al.
Oncotarget|April 2, 2016
Genetic and epigenetic factors affect RET gene expression in breast cancer cell lines and influence survival in patientsPaola Griseri, Ornella Garrone, Alessandra Lo Sardo, et al.
International Journal of Molecular Medicine|June 13, 2002
HOX11L1: a promoter study to evaluate possible expression defects in intestinal motility disordersMonica Fava, Silvia Borghini, Roberta Cinti, et al.
Rheumatology (Oxford, England)|September 10, 2024
Majeed syndrome: first description in a patient of central-European ancestryEnrico Drago, Arinna Bertoni, Alice Grossi, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|April 24, 2017
Common PHOX2B poly-alanine contractions impair RET gene transcription, predisposing to Hirschsprung diseaseEleonora Di Zanni, Annalisa Adamo, Elga Belligni, et al.
Brain : a Journal of Neurology|August 8, 2008
Adult-onset Alexander disease: a series of eleven unrelated cases with review of the literatureDavide Pareyson, Roberto Fancellu, Caterina Mariotti, et al.
Journal of Medical Genetics|August 6, 2017
Mutations in <i>MYO1H</i> cause a recessive form of central hypoventilation with autonomic dysfunctionMalte Spielmann, Luis R Hernandez-Miranda, Isabella Ceccherini, et al.
Clinical and Experimental Rheumatology|June 17, 2016
Gene expression profile in TNF receptor-associated periodic syndrome reveals constitutively enhanced pathways and new players in the underlying inflammationSilvia Borghini, Denise Ferrera, Ignazia Prigione, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 1, 2018
ABCC6 mutations and early onset stroke: Two cases of a typical Pseudoxanthoma ElasticumMarta Bertamino, Mariasavina Severino, Alice Grossi, et al.
Genes|December 24, 2021
The Genetic Landscape of Patent Foramen Ovale: A Systematic ReviewMatteo Paolucci, Chiara Vincenzi, Michele Romoli, et al.
Pageof 18