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Michele Traversa

Showing results (1-10 of 12) with videos related to

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Oncology Letters|July 3, 2015
Long-term response of gemcitabine plus docetaxel chemotherapy regimen for extraskeletal osteosarcoma: A case reportSabino Strippoli, Michele Traversa, Antonio Cramarossa, et al.
International Journal of Oncology|June 1, 2017
Sorafenib induces variations of the DNA methylome in HA22T/VGH human hepatocellular carcinoma-derived cellsEdoardo Abeni, Alessandro Salvi, Eleonora Marchina, et al.
BMC Medical Genetics|July 8, 2015
SNP array and FISH analysis of a proband with a 22q13.2- 22qter duplication shed light on the molecular origin of the rearrangementChiara Magri, Eleonora Marchina, Valeria Bertini, et al.
Molecular Cytogenetics|April 17, 2014
De novo 1Mb interstitial deletion of 8p22 in a patient with slight mental retardation and speech delayGiovanna Piovani, Giulia Savio, Michele Traversa, et al.
Plos One|October 23, 2010
New copy number variations in schizophreniaChiara Magri, Emilio Sacchetti, Michele Traversa, et al.
Molecular Genetics and Metabolism Reports|June 27, 2017
Insights in the etiopathology of galactosyltransferase II (GalT-II) deficiency from transcriptome-wide expression profiling of skin fibroblasts of two sisters with compound heterozygosity for two novel <i>B3GALT6</i> mutationsMarco Ritelli, Nicola Chiarelli, Nicoletta Zoppi, et al.
Psychiatric Genetics|November 6, 2014
Copy number variants in attention-deficit hyperactive disorder: identification of the 15q13 deletion and its functional roleStefano Valbonesi, Chiara Magri, Michele Traversa, et al.
Plos One|August 9, 2017
Exome sequencing in schizophrenic patients with high levels of homozygosity identifies novel and extremely rare mutations in the GABA/glutamatergic pathwaysEdoardo Giacopuzzi, Massimo Gennarelli, Alessandra Minelli, et al.
Molecular Genetics and Genomics : MGG|April 6, 2010
Evidences for insulator activity of the 5'UTR of the Drosophila melanogaster LTR-retrotransposon ZAMCrescenzio Francesco Minervini, Simona Ruggieri, Michele Traversa, et al.
Orphanet Journal of Rare Diseases|April 17, 2013
Clinical and molecular characterization of 40 patients with classic Ehlers-Danlos syndrome: identification of 18 COL5A1 and 2 COL5A2 novel mutationsMarco Ritelli, Chiara Dordoni, Marina Venturini, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Oncology Letters|July 3, 2015
Long-term response of gemcitabine plus docetaxel chemotherapy regimen for extraskeletal osteosarcoma: A case reportSabino Strippoli, Michele Traversa, Antonio Cramarossa, et al.
International Journal of Oncology|June 1, 2017
Sorafenib induces variations of the DNA methylome in HA22T/VGH human hepatocellular carcinoma-derived cellsEdoardo Abeni, Alessandro Salvi, Eleonora Marchina, et al.
BMC Medical Genetics|July 8, 2015
SNP array and FISH analysis of a proband with a 22q13.2- 22qter duplication shed light on the molecular origin of the rearrangementChiara Magri, Eleonora Marchina, Valeria Bertini, et al.
Molecular Cytogenetics|April 17, 2014
De novo 1Mb interstitial deletion of 8p22 in a patient with slight mental retardation and speech delayGiovanna Piovani, Giulia Savio, Michele Traversa, et al.
Plos One|October 23, 2010
New copy number variations in schizophreniaChiara Magri, Emilio Sacchetti, Michele Traversa, et al.
Molecular Genetics and Metabolism Reports|June 27, 2017
Insights in the etiopathology of galactosyltransferase II (GalT-II) deficiency from transcriptome-wide expression profiling of skin fibroblasts of two sisters with compound heterozygosity for two novel <i>B3GALT6</i> mutationsMarco Ritelli, Nicola Chiarelli, Nicoletta Zoppi, et al.
Psychiatric Genetics|November 6, 2014
Copy number variants in attention-deficit hyperactive disorder: identification of the 15q13 deletion and its functional roleStefano Valbonesi, Chiara Magri, Michele Traversa, et al.
Plos One|August 9, 2017
Exome sequencing in schizophrenic patients with high levels of homozygosity identifies novel and extremely rare mutations in the GABA/glutamatergic pathwaysEdoardo Giacopuzzi, Massimo Gennarelli, Alessandra Minelli, et al.
Molecular Genetics and Genomics : MGG|April 6, 2010
Evidences for insulator activity of the 5'UTR of the Drosophila melanogaster LTR-retrotransposon ZAMCrescenzio Francesco Minervini, Simona Ruggieri, Michele Traversa, et al.
Orphanet Journal of Rare Diseases|April 17, 2013
Clinical and molecular characterization of 40 patients with classic Ehlers-Danlos syndrome: identification of 18 COL5A1 and 2 COL5A2 novel mutationsMarco Ritelli, Chiara Dordoni, Marina Venturini, et al.
Pageof 2