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Massimo Carella

Showing results (121-130 of 207) with videos related to

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Nucleic Acids Research|April 13, 2016
Multifaceted enrichment analysis of RNA-RNA crosstalk reveals cooperating micro-societies in human colorectal cancerTommaso Mazza, Gianluigi Mazzoccoli, Caterina Fusilli, et al.
The International Journal of Biological Markers|April 6, 2013
VHL gene alterations in Italian patients with isolated renal cell carcinomasLucia Anna Muscarella, Leonardo D'Agruma, Annamaria la Torre, et al.
Molecular Genetics & Genomic Medicine|November 23, 2019
Prenatal whole exome sequencing detects a new homozygous fukutin (FKTN) mutation in a fetus with an ultrasound suspicion of familial Dandy-Walker malformationAlice Traversa, Silvia Bernardo, Alessandro Paiardini, et al.
Journal of Electrocardiology|September 5, 2018
Sudden cardiac death in J wave syndrome with short QT associated to a novel mutation in Na<sub>v</sub> 1.8 coding gene SCN10A: First case report for a possible pharmacogenomic roleGiuseppe Di Stolfo, Pietro Palumbo, Stefano Castellana, et al.
Molecular Neurobiology|May 31, 2022
Potassium Channel KCNH1 Activating Variants Cause Altered Functional and Morphological CiliogenesisGiulia Napoli, Noemi Panzironi, Alice Traversa, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 19, 2014
Excess of runs of homozygosity is associated with severe cognitive impairment in intellectual disabilityIlaria Gandin, Flavio Faletra, Francesca Faletra, et al.
BMC Medical Genomics|March 5, 2009
Promoter methylation correlates with reduced NDRG2 expression in advanced colon tumourAda Piepoli, Rosa Cotugno, Giuseppe Merla, et al.
International Journal of Oncology|December 25, 2013
Establishment and genetic characterization of ANGM-CSS, a novel, immortal cell line derived from a human glioblastoma multiformeAngelantonio Notarangelo, Domenico Trombetta, Vincenzo D'Angelo, et al.
Cancer Research|December 25, 2016
Wnt5a Drives an Invasive Phenotype in Human Glioblastoma Stem-like CellsElena Binda, Alberto Visioli, Fabrizio Giani, et al.
Cancers|April 13, 2023
Co-Occurrence of Beckwith-Wiedemann Syndrome and Early-Onset Colorectal CancerFrancesco Cecere, Laura Pignata, Bruno Hay Mele, et al.
Pageof 21

Showing results (121-130 of 207) with videos related to

Sort By:
Pageof 21
Nucleic Acids Research|April 13, 2016
Multifaceted enrichment analysis of RNA-RNA crosstalk reveals cooperating micro-societies in human colorectal cancerTommaso Mazza, Gianluigi Mazzoccoli, Caterina Fusilli, et al.
The International Journal of Biological Markers|April 6, 2013
VHL gene alterations in Italian patients with isolated renal cell carcinomasLucia Anna Muscarella, Leonardo D'Agruma, Annamaria la Torre, et al.
Molecular Genetics & Genomic Medicine|November 23, 2019
Prenatal whole exome sequencing detects a new homozygous fukutin (FKTN) mutation in a fetus with an ultrasound suspicion of familial Dandy-Walker malformationAlice Traversa, Silvia Bernardo, Alessandro Paiardini, et al.
Journal of Electrocardiology|September 5, 2018
Sudden cardiac death in J wave syndrome with short QT associated to a novel mutation in Na<sub>v</sub> 1.8 coding gene SCN10A: First case report for a possible pharmacogenomic roleGiuseppe Di Stolfo, Pietro Palumbo, Stefano Castellana, et al.
Molecular Neurobiology|May 31, 2022
Potassium Channel KCNH1 Activating Variants Cause Altered Functional and Morphological CiliogenesisGiulia Napoli, Noemi Panzironi, Alice Traversa, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 19, 2014
Excess of runs of homozygosity is associated with severe cognitive impairment in intellectual disabilityIlaria Gandin, Flavio Faletra, Francesca Faletra, et al.
BMC Medical Genomics|March 5, 2009
Promoter methylation correlates with reduced NDRG2 expression in advanced colon tumourAda Piepoli, Rosa Cotugno, Giuseppe Merla, et al.
International Journal of Oncology|December 25, 2013
Establishment and genetic characterization of ANGM-CSS, a novel, immortal cell line derived from a human glioblastoma multiformeAngelantonio Notarangelo, Domenico Trombetta, Vincenzo D'Angelo, et al.
Cancer Research|December 25, 2016
Wnt5a Drives an Invasive Phenotype in Human Glioblastoma Stem-like CellsElena Binda, Alberto Visioli, Fabrizio Giani, et al.
Cancers|April 13, 2023
Co-Occurrence of Beckwith-Wiedemann Syndrome and Early-Onset Colorectal CancerFrancesco Cecere, Laura Pignata, Bruno Hay Mele, et al.
Pageof 21