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Massimo Carella

Showing results (161-170 of 207) with videos related to

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Inflammatory Bowel Diseases|April 23, 2015
Genome-wide Pathway Analysis Using Gene Expression Data of Colonic Mucosa in Patients with Inflammatory Bowel DiseaseOrazio Palmieri, Teresa M Creanza, Fabrizio Bossa, et al.
Human Molecular Genetics|September 17, 2011
The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome casesNicoletta Chiesa, Agostina De Crescenzo, Kankadeb Mishra, et al.
Human Mutation|August 31, 2018
A single-center study on 140 patients with cerebral cavernous malformations: 28 new pathogenic variants and functional characterization of a PDCD10 large deletionGrazia Nardella, Grazia Visci, Vito Guarnieri, et al.
International Journal of Infectious Diseases : IJID : Official Publication of the International Society for Infectious Diseases|December 31, 2020
False-positive results of SARS-CoV-2 IgM/IgG antibody tests in sera stored before the 2020 pandemic in ItalyAnna Latiano, Francesca Tavano, Anna Panza, et al.
Journal of Clinical Medicine|June 19, 2024
The Role of TOMM40 in Cardiovascular Mortality and Conduction Disorders: An Observational StudyGiuseppe Di Stolfo, Sandra Mastroianno, Nicolò Soldato, et al.
European Journal of Human Genetics : EJHG|August 5, 2004
Mitochondrial DNA mutations in patients with postlingual, nonsyndromic hearing impairmentHoward T Jacobs, Timothy P Hutchin, Timo Käppi, et al.
Scientific Reports|June 22, 2019
The levels of the NMDA receptor co-agonist D-serine are reduced in the substantia nigra of MPTP-lesioned macaques and in the cerebrospinal fluid of Parkinson's disease patientsTommaso Nuzzo, Daniela Punzo, Paola Devoto, et al.
Molecular Genetics & Genomic Medicine|June 11, 2020
Heterozygous nonsense ARX mutation in a family highlights the complexity of clinical and molecular diagnosis in case of chromosomal and single gene disorder co-inheritanceAlice Traversa, Enrica Marchionni, Agnese Giovannetti, et al.
Plos One|August 2, 2014
Evaluation of genome-wide expression profiles of blood and sputum neutrophils in cystic fibrosis patients before and after antibiotic therapyMassimo Conese, Stefano Castellani, Silvia Lepore, et al.
Clinical Epigenetics|December 13, 2019
The phenotypic variations of multi-locus imprinting disturbances associated with maternal-effect variants of NLRP5 range from overt imprinting disorder to apparently healthy phenotypeAngela Sparago, Ankit Verma, Maria Grazia Patricelli, et al.
Pageof 21

Showing results (161-170 of 207) with videos related to

Sort By:
Pageof 21
Inflammatory Bowel Diseases|April 23, 2015
Genome-wide Pathway Analysis Using Gene Expression Data of Colonic Mucosa in Patients with Inflammatory Bowel DiseaseOrazio Palmieri, Teresa M Creanza, Fabrizio Bossa, et al.
Human Molecular Genetics|September 17, 2011
The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome casesNicoletta Chiesa, Agostina De Crescenzo, Kankadeb Mishra, et al.
Human Mutation|August 31, 2018
A single-center study on 140 patients with cerebral cavernous malformations: 28 new pathogenic variants and functional characterization of a PDCD10 large deletionGrazia Nardella, Grazia Visci, Vito Guarnieri, et al.
International Journal of Infectious Diseases : IJID : Official Publication of the International Society for Infectious Diseases|December 31, 2020
False-positive results of SARS-CoV-2 IgM/IgG antibody tests in sera stored before the 2020 pandemic in ItalyAnna Latiano, Francesca Tavano, Anna Panza, et al.
Journal of Clinical Medicine|June 19, 2024
The Role of TOMM40 in Cardiovascular Mortality and Conduction Disorders: An Observational StudyGiuseppe Di Stolfo, Sandra Mastroianno, Nicolò Soldato, et al.
European Journal of Human Genetics : EJHG|August 5, 2004
Mitochondrial DNA mutations in patients with postlingual, nonsyndromic hearing impairmentHoward T Jacobs, Timothy P Hutchin, Timo Käppi, et al.
Scientific Reports|June 22, 2019
The levels of the NMDA receptor co-agonist D-serine are reduced in the substantia nigra of MPTP-lesioned macaques and in the cerebrospinal fluid of Parkinson's disease patientsTommaso Nuzzo, Daniela Punzo, Paola Devoto, et al.
Molecular Genetics & Genomic Medicine|June 11, 2020
Heterozygous nonsense ARX mutation in a family highlights the complexity of clinical and molecular diagnosis in case of chromosomal and single gene disorder co-inheritanceAlice Traversa, Enrica Marchionni, Agnese Giovannetti, et al.
Plos One|August 2, 2014
Evaluation of genome-wide expression profiles of blood and sputum neutrophils in cystic fibrosis patients before and after antibiotic therapyMassimo Conese, Stefano Castellani, Silvia Lepore, et al.
Clinical Epigenetics|December 13, 2019
The phenotypic variations of multi-locus imprinting disturbances associated with maternal-effect variants of NLRP5 range from overt imprinting disorder to apparently healthy phenotypeAngela Sparago, Ankit Verma, Maria Grazia Patricelli, et al.
Pageof 21