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Giuseppe Merla

Showing results (81-90 of 129) with videos related to

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Clinical Genetics|April 30, 2025
A Novel Intronic Variant in the KH3 Domain of HNRNPK Leads to a Mild Form of Au-Kline SyndromeMaura Mingoia, Alessandra Meloni, Silvia Sedda, et al.
Blood Cells, Molecules & Diseases|September 28, 2011
Amplification of the G allele at SNP rs6983267 in 8q24 amplicons in myeloid malignancies as cause of the lack of MYC overexpression?Lucia Micale, Bartolomeo Augello, Giulia Daniele, et al.
International Journal of Molecular Sciences|August 27, 2021
Identification of a DNA Methylation Episignature in the 22q11.2 Deletion SyndromeKathleen Rooney, Michael A Levy, Sadegheh Haghshenas, et al.
BMC Cancer|June 17, 2015
TRIM8 downregulation in glioma affects cell proliferation and it is associated with patients survivalLucia Micale, Carmela Fusco, Andrea Fontana, et al.
Epigenetics|December 22, 2010
Regulation of KEAP1 expression by promoter methylation in malignant gliomas and association with patient's outcomeLucia Anna Muscarella, Raffaela Barbano, Vincenzo D'Angelo, et al.
Orphanet Journal of Rare Diseases|October 26, 2016
The alliance between genetic biobanks and patient organisations: the experience of the telethon network of genetic biobanksChiara Baldo, Lorena Casareto, Alessandra Renieri, et al.
Plos One|January 4, 2013
Influence of pentraxin 3 (PTX3) genetic variants on myocardial infarction risk and PTX3 plasma levelsElisa Barbati, Claudia Specchia, Massimo Villella, et al.
European Journal of Pediatrics|July 7, 2021
Clinical heterogeneity of Kabuki syndrome in a cohort of Italian patients and review of the literatureFrancesca Di Candia, Paolo Fontana, Pamela Paglia, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
DNA methylation episignature testing improves molecular diagnosis of Mendelian chromatinopathiesJennifer Kerkhof, Gabriella Maria Squeo, Haley McConkey, et al.
Epigenetics|May 26, 2011
Frequent epigenetics inactivation of KEAP1 gene in non-small cell lung cancerLucia Anna Muscarella, Paola Parrella, Vito D'Alessandro, et al.
Pageof 13

Showing results (81-90 of 129) with videos related to

Sort By:
Pageof 13
Clinical Genetics|April 30, 2025
A Novel Intronic Variant in the KH3 Domain of HNRNPK Leads to a Mild Form of Au-Kline SyndromeMaura Mingoia, Alessandra Meloni, Silvia Sedda, et al.
Blood Cells, Molecules & Diseases|September 28, 2011
Amplification of the G allele at SNP rs6983267 in 8q24 amplicons in myeloid malignancies as cause of the lack of MYC overexpression?Lucia Micale, Bartolomeo Augello, Giulia Daniele, et al.
International Journal of Molecular Sciences|August 27, 2021
Identification of a DNA Methylation Episignature in the 22q11.2 Deletion SyndromeKathleen Rooney, Michael A Levy, Sadegheh Haghshenas, et al.
BMC Cancer|June 17, 2015
TRIM8 downregulation in glioma affects cell proliferation and it is associated with patients survivalLucia Micale, Carmela Fusco, Andrea Fontana, et al.
Epigenetics|December 22, 2010
Regulation of KEAP1 expression by promoter methylation in malignant gliomas and association with patient's outcomeLucia Anna Muscarella, Raffaela Barbano, Vincenzo D'Angelo, et al.
Orphanet Journal of Rare Diseases|October 26, 2016
The alliance between genetic biobanks and patient organisations: the experience of the telethon network of genetic biobanksChiara Baldo, Lorena Casareto, Alessandra Renieri, et al.
Plos One|January 4, 2013
Influence of pentraxin 3 (PTX3) genetic variants on myocardial infarction risk and PTX3 plasma levelsElisa Barbati, Claudia Specchia, Massimo Villella, et al.
European Journal of Pediatrics|July 7, 2021
Clinical heterogeneity of Kabuki syndrome in a cohort of Italian patients and review of the literatureFrancesca Di Candia, Paolo Fontana, Pamela Paglia, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
DNA methylation episignature testing improves molecular diagnosis of Mendelian chromatinopathiesJennifer Kerkhof, Gabriella Maria Squeo, Haley McConkey, et al.
Epigenetics|May 26, 2011
Frequent epigenetics inactivation of KEAP1 gene in non-small cell lung cancerLucia Anna Muscarella, Paola Parrella, Vito D'Alessandro, et al.
Pageof 13