Search research articles
Contact Us
Filters
Showing results (41-50 of 129) with videos related to
Page
of 13
Sort By:
Cellular Signalling
|
December 7, 2013
HDAC6 mediates the acetylation of TRIM50
Carmela Fusco, Lucia Micale, Bartolomeo Augello, et al.
Neurogenetics
|
August 18, 2014
DPP6 gene disruption in a family with Gilles de la Tourette syndrome
Paolo Prontera, Valerio Napolioni, Valentina Ottaviani, et al.
Orphanet Journal of Rare Diseases
|
September 6, 2013
Telethon Network of Genetic Biobanks: a key service for diagnosis and research on rare diseases
Mirella Filocamo, Chiara Baldo, Stefano Goldwurm, et al.
The EMBO Journal
|
November 1, 2025
Non-cell-autonomous control of mouse gastruloid development by the ultra-conserved lncRNA T-UCstem1
Arianna Coppola, Filomena Amoroso, Federica Saracino, et al.
Stem Cell Research
|
September 4, 2019
Generation of the induced human pluripotent stem cell lines CSSi009-A from a patient with a GNB5 pathogenic variant, and CSSi010-A from a CRISPR/Cas9 engineered GNB5 knock-out human cell line
Natascia Malerba, Patrizia Benzoni, Gabriella Maria Squeo, et al.
Cell Death & Disease
|
August 5, 2023
The ubiquitin ligase TRIM32 promotes the autophagic response to Mycobacterium tuberculosis infection in macrophages
Alessandra Romagnoli, Martina Di Rienzo, Elisa Petruccioli, et al.
Biochimica Et Biophysica Acta
|
April 10, 2016
Clock-genes and mitochondrial respiratory activity: Evidence of a reciprocal interplay
Rosella Scrima, Olga Cela, Giuseppe Merla, et al.
European Journal of Human Genetics : EJHG
|
October 22, 2009
Identification and characterization of seven novel mutations of elastin gene in a cohort of patients affected by supravalvular aortic stenosis
Lucia Micale, Maria Giuseppina Turturo, Carmela Fusco, et al.
Cells
|
July 17, 2020
Loss of Function of the Gene Encoding the Histone Methyltransferase KMT2D Leads to Deregulation of Mitochondrial Respiration
Consiglia Pacelli, Iolanda Adipietro, Natascia Malerba, et al.
Molecular Genetics and Metabolism
|
July 31, 2012
Absence of deletion and duplication of MLL2 and KDM6A genes in a large cohort of patients with Kabuki syndrome
Manuela Priolo, Lucia Micale, Bartolomeo Augello, et al.
Page
of 13
Search research articles
Search
Showing results (41-50 of 129) with videos related to
Sort By:
Page
of 13
Cellular Signalling
|
December 7, 2013
HDAC6 mediates the acetylation of TRIM50
Carmela Fusco, Lucia Micale, Bartolomeo Augello, et al.
Neurogenetics
|
August 18, 2014
DPP6 gene disruption in a family with Gilles de la Tourette syndrome
Paolo Prontera, Valerio Napolioni, Valentina Ottaviani, et al.
Orphanet Journal of Rare Diseases
|
September 6, 2013
Telethon Network of Genetic Biobanks: a key service for diagnosis and research on rare diseases
Mirella Filocamo, Chiara Baldo, Stefano Goldwurm, et al.
The EMBO Journal
|
November 1, 2025
Non-cell-autonomous control of mouse gastruloid development by the ultra-conserved lncRNA T-UCstem1
Arianna Coppola, Filomena Amoroso, Federica Saracino, et al.
Stem Cell Research
|
September 4, 2019
Generation of the induced human pluripotent stem cell lines CSSi009-A from a patient with a GNB5 pathogenic variant, and CSSi010-A from a CRISPR/Cas9 engineered GNB5 knock-out human cell line
Natascia Malerba, Patrizia Benzoni, Gabriella Maria Squeo, et al.
Cell Death & Disease
|
August 5, 2023
The ubiquitin ligase TRIM32 promotes the autophagic response to Mycobacterium tuberculosis infection in macrophages
Alessandra Romagnoli, Martina Di Rienzo, Elisa Petruccioli, et al.
Biochimica Et Biophysica Acta
|
April 10, 2016
Clock-genes and mitochondrial respiratory activity: Evidence of a reciprocal interplay
Rosella Scrima, Olga Cela, Giuseppe Merla, et al.
European Journal of Human Genetics : EJHG
|
October 22, 2009
Identification and characterization of seven novel mutations of elastin gene in a cohort of patients affected by supravalvular aortic stenosis
Lucia Micale, Maria Giuseppina Turturo, Carmela Fusco, et al.
Cells
|
July 17, 2020
Loss of Function of the Gene Encoding the Histone Methyltransferase KMT2D Leads to Deregulation of Mitochondrial Respiration
Consiglia Pacelli, Iolanda Adipietro, Natascia Malerba, et al.
Molecular Genetics and Metabolism
|
July 31, 2012
Absence of deletion and duplication of MLL2 and KDM6A genes in a large cohort of patients with Kabuki syndrome
Manuela Priolo, Lucia Micale, Bartolomeo Augello, et al.
Page
of 13