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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 21q22
Daniela Melis, Rita Genesio, Gerarda Cappuccio, et al.
Lung Cancer (Amsterdam, Netherlands)
|
May 5, 2009
Molecular analysis of the HuD gene in neuroendocrine lung cancers
Vito 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 strategies
Giuseppe 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 transcriptome
Orazio 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 Axis
Marilena 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 population
Sylvain 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 carcinoma
Marina Scintu, Rita Vitale, Maria Prencipe, et al.
Neurogastroenterology and Motility
|
November 28, 2019
microRNA-mRNA network model in patients with achalasia
Orazio Palmieri, Tommaso Mazza, Gabrio Bassotti, et al.
Plos One
|
October 4, 2014
A miRNA signature for defining aggressive phenotype and prognosis in gliomas
Raffaela 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 triploidy
Nayeralsadat Fatemi, Najmeh Salehi, Laura Pignata, et al.
Page
of 21
Search research articles
Search
Showing results (141-150 of 207) with videos related to
Sort By:
Page
of 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 21q22
Daniela Melis, Rita Genesio, Gerarda Cappuccio, et al.
Lung Cancer (Amsterdam, Netherlands)
|
May 5, 2009
Molecular analysis of the HuD gene in neuroendocrine lung cancers
Vito 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 strategies
Giuseppe 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 transcriptome
Orazio 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 Axis
Marilena 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 population
Sylvain 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 carcinoma
Marina Scintu, Rita Vitale, Maria Prencipe, et al.
Neurogastroenterology and Motility
|
November 28, 2019
microRNA-mRNA network model in patients with achalasia
Orazio Palmieri, Tommaso Mazza, Gabrio Bassotti, et al.
Plos One
|
October 4, 2014
A miRNA signature for defining aggressive phenotype and prognosis in gliomas
Raffaela 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 triploidy
Nayeralsadat Fatemi, Najmeh Salehi, Laura Pignata, et al.
Page
of 21