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Massimo Carella

Showing results (141-150 of 207) with videos related to

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American Journal of Medical Genetics. Part A|June 15, 2011
Mental retardation, congenital heart malformation, and myelodysplasia in a patient with a complex chromosomal rearrangement involving the critical region 21q22Daniela Melis, Rita Genesio, Gerarda Cappuccio, et al.
Lung Cancer (Amsterdam, Netherlands)|May 5, 2009
Molecular analysis of the HuD gene in neuroendocrine lung cancersVito D'Alessandro, Lucia Anna Muscarella, Annamaria la Torre, et al.
Frontiers in Pharmacology|June 22, 2026
Precision management of cenobamate in drug-resistant epilepsy: integrating pharmacogenetics, therapeutic drug monitoring, and real-world clinical strategiesGiuseppe d'Orsi, Maria Teresa Di Claudio, Alessia Cafaro, et al.
Chronobiology International|July 15, 2015
Systematic analysis of circadian genes using genome-wide cDNA microarrays in the inflammatory bowel disease transcriptomeOrazio Palmieri, Gianluigi Mazzoccoli, Fabrizio Bossa, et al.
Frontiers in Immunology|May 3, 2021
Genome-Wide Gene Expression Analysis of Mtb-Infected DC Highlights the Rapamycin-Driven Modulation of Regulatory Cytokines <i>via</i> the mTOR/GSK-3β AxisMarilena P Etna, Martina Severa, Valerio Licursi, et al.
European Journal of Human Genetics : EJHG|August 2, 2003
Juvenile hemochromatosis locus maps to chromosome 1q in a French Canadian populationSylvain R Rivard, Carmela Lanzara, Doria Grimard, et al.
Cancer Letters|May 15, 2007
Genomic instability and increased expression of BUB1B and MAD2L1 genes in ductal breast carcinomaMarina Scintu, Rita Vitale, Maria Prencipe, et al.
Neurogastroenterology and Motility|November 28, 2019
microRNA-mRNA network model in patients with achalasiaOrazio Palmieri, Tommaso Mazza, Gabrio Bassotti, et al.
Plos One|October 4, 2014
A miRNA signature for defining aggressive phenotype and prognosis in gliomasRaffaela Barbano, Orazio Palumbo, Barbara Pasculli, et al.
Journal of Medical Genetics|September 17, 2020
Biallelic variant in cyclin B3 is associated with failure of maternal meiosis II and recurrent digynic triploidyNayeralsadat Fatemi, Najmeh Salehi, Laura Pignata, et al.
Pageof 21

Showing results (141-150 of 207) with videos related to

Sort By:
Pageof 21
American Journal of Medical Genetics. Part A|June 15, 2011
Mental retardation, congenital heart malformation, and myelodysplasia in a patient with a complex chromosomal rearrangement involving the critical region 21q22Daniela Melis, Rita Genesio, Gerarda Cappuccio, et al.
Lung Cancer (Amsterdam, Netherlands)|May 5, 2009
Molecular analysis of the HuD gene in neuroendocrine lung cancersVito D'Alessandro, Lucia Anna Muscarella, Annamaria la Torre, et al.
Frontiers in Pharmacology|June 22, 2026
Precision management of cenobamate in drug-resistant epilepsy: integrating pharmacogenetics, therapeutic drug monitoring, and real-world clinical strategiesGiuseppe d'Orsi, Maria Teresa Di Claudio, Alessia Cafaro, et al.
Chronobiology International|July 15, 2015
Systematic analysis of circadian genes using genome-wide cDNA microarrays in the inflammatory bowel disease transcriptomeOrazio Palmieri, Gianluigi Mazzoccoli, Fabrizio Bossa, et al.
Frontiers in Immunology|May 3, 2021
Genome-Wide Gene Expression Analysis of Mtb-Infected DC Highlights the Rapamycin-Driven Modulation of Regulatory Cytokines <i>via</i> the mTOR/GSK-3β AxisMarilena P Etna, Martina Severa, Valerio Licursi, et al.
European Journal of Human Genetics : EJHG|August 2, 2003
Juvenile hemochromatosis locus maps to chromosome 1q in a French Canadian populationSylvain R Rivard, Carmela Lanzara, Doria Grimard, et al.
Cancer Letters|May 15, 2007
Genomic instability and increased expression of BUB1B and MAD2L1 genes in ductal breast carcinomaMarina Scintu, Rita Vitale, Maria Prencipe, et al.
Neurogastroenterology and Motility|November 28, 2019
microRNA-mRNA network model in patients with achalasiaOrazio Palmieri, Tommaso Mazza, Gabrio Bassotti, et al.
Plos One|October 4, 2014
A miRNA signature for defining aggressive phenotype and prognosis in gliomasRaffaela Barbano, Orazio Palumbo, Barbara Pasculli, et al.
Journal of Medical Genetics|September 17, 2020
Biallelic variant in cyclin B3 is associated with failure of maternal meiosis II and recurrent digynic triploidyNayeralsadat Fatemi, Najmeh Salehi, Laura Pignata, et al.
Pageof 21