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Arianna Tucci

Showing results (1-10 of 75) with videos related to

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Neurology|March 27, 2015
Author responseAndrea Cortese, Arianna Tucci
The New England Journal of Medicine|May 24, 2023
Deep Intronic FGF14 GAA Repeat Expansion in Late-Onset Cerebellar AtaxiaZhongbo Chen, Arianna Tucci, Mina Ryten
Neurology|February 11, 2015
Novel CLN3 mutation causing autophagic vacuolar myopathyPeter E Taschner, Andrea Cortese, Arianna Tucci
Molecular Cytogenetics|November 9, 2016
<i>MIR137</i> is the key gene mediator of the syndromic obesity phenotype of patients with 1p21.3 microdeletionsArianna Tucci, Claudia Ciaccio, Giulietta Scuvera, et al.
BMC Medical Genetics|March 13, 2016
The p.Phe174Ser mutation is associated with mild forms of Smith Lemli Opitz SyndromeArianna Tucci, Luisa Ronzoni, Carlo Arduino, et al.
American Journal of Medical Genetics. Part A|January 13, 2016
Interstitial 6q25 microdeletion syndrome: ARID1B is the key geneLuisa Ronzoni, Francesco Tagliaferri, Arianna Tucci, et al.
The Prostate|January 15, 2008
2-chloroadenosine modulates PAR-1 and IL-23 expression and enhances docetaxel effects on PC3 cellsAlba Minelli, Ilaria Bellezza, Arianna Tucci, et al.
European Journal of Medical Genetics|December 24, 2016
16p13 microduplication without CREBBP involvement: Moving toward a phenotype delineationClaudia Ciaccio, Arianna Tucci, Giulietta Scuvera, et al.
Journal of the Neurological Sciences|June 8, 2015
A novel ABCD1 mutation detected by next generation sequencing in presumed hereditary spastic paraplegia: A 30-year diagnostic delay caused by misleading biochemical findingsGeorgios Koutsis, David S Lynch, Arianna Tucci, et al.
The Prostate|December 25, 2008
Differential involvement of reactive oxygen species and nucleoside transporters in cytotoxicity induced by two adenosine analogues in human prostate cancer cellsAlba Minelli, Ilaria Bellezza, Arianna Tucci, et al.
Pageof 8

Showing results (1-10 of 75) with videos related to

Sort By:
Pageof 8
Neurology|March 27, 2015
Author responseAndrea Cortese, Arianna Tucci
The New England Journal of Medicine|May 24, 2023
Deep Intronic FGF14 GAA Repeat Expansion in Late-Onset Cerebellar AtaxiaZhongbo Chen, Arianna Tucci, Mina Ryten
Neurology|February 11, 2015
Novel CLN3 mutation causing autophagic vacuolar myopathyPeter E Taschner, Andrea Cortese, Arianna Tucci
Molecular Cytogenetics|November 9, 2016
<i>MIR137</i> is the key gene mediator of the syndromic obesity phenotype of patients with 1p21.3 microdeletionsArianna Tucci, Claudia Ciaccio, Giulietta Scuvera, et al.
BMC Medical Genetics|March 13, 2016
The p.Phe174Ser mutation is associated with mild forms of Smith Lemli Opitz SyndromeArianna Tucci, Luisa Ronzoni, Carlo Arduino, et al.
American Journal of Medical Genetics. Part A|January 13, 2016
Interstitial 6q25 microdeletion syndrome: ARID1B is the key geneLuisa Ronzoni, Francesco Tagliaferri, Arianna Tucci, et al.
The Prostate|January 15, 2008
2-chloroadenosine modulates PAR-1 and IL-23 expression and enhances docetaxel effects on PC3 cellsAlba Minelli, Ilaria Bellezza, Arianna Tucci, et al.
European Journal of Medical Genetics|December 24, 2016
16p13 microduplication without CREBBP involvement: Moving toward a phenotype delineationClaudia Ciaccio, Arianna Tucci, Giulietta Scuvera, et al.
Journal of the Neurological Sciences|June 8, 2015
A novel ABCD1 mutation detected by next generation sequencing in presumed hereditary spastic paraplegia: A 30-year diagnostic delay caused by misleading biochemical findingsGeorgios Koutsis, David S Lynch, Arianna Tucci, et al.
The Prostate|December 25, 2008
Differential involvement of reactive oxygen species and nucleoside transporters in cytotoxicity induced by two adenosine analogues in human prostate cancer cellsAlba Minelli, Ilaria Bellezza, Arianna Tucci, et al.
Pageof 8