Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Human Mutation|February 1, 2011
Allele-specific methylated multiplex real-time quantitative PCR (ASMM RTQ-PCR), a powerful method for diagnosing loss of imprinting of the 11p15 region in Russell Silver and Beckwith Wiedemann syndromesSalah Azzi, Virginie Steunou, Alexandra Rousseau, et al.
Science Advances|February 26, 2019
Transcriptional profiling at the <i>DLK1/MEG3</i> domain explains clinical overlap between imprinting disordersWalid Abi Habib, Frédéric Brioude, Salah Azzi, et al.
Human Molecular Genetics|September 17, 2009
Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted lociSalah Azzi, Sylvie Rossignol, Virginie Steunou, et al.
Human Mutation|May 8, 2013
Simultaneous hyper- and hypomethylation at imprinted loci in a subset of patients with GNAS epimutations underlies a complex and different mechanism of multilocus methylation defect in pseudohypoparathyroidism type 1bStéphanie Maupetit-Méhouas, Salah Azzi, Virginie Steunou, et al.
Nature Genetics|August 9, 2005
Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndromeChristine Gicquel, Sylvie Rossignol, Sylvie Cabrol, et al.
Journal of Medical Genetics|November 15, 2014
Exhaustive methylation analysis revealed uneven profiles of methylation at IGF2/ICR1/H19 11p15 loci in Russell Silver syndromeSalah Azzi, Virginie Steunou, Jörg Tost, et al.
Human Mutation|July 22, 2014
Complex tissue-specific epigenotypes in Russell-Silver Syndrome associated with 11p15 ICR1 hypomethylationSalah Azzi, Annick Blaise, Virginie Steunou, et al.
Human Molecular Genetics|June 12, 2014
Extensive investigation of the IGF2/H19 imprinting control region reveals novel OCT4/SOX2 binding site defects associated with specific methylation patterns in Beckwith-Wiedemann syndromeWalid Abi Habib, Salah Azzi, Frédéric Brioude, et al.
Plos One|August 5, 2014
IGF2 promotes growth of adrenocortical carcinoma cells, but its overexpression does not modify phenotypic and molecular features of adrenocortical carcinomaMarine Guillaud-Bataille, Bruno Ragazzon, Aurélien de Reyniès, et al.
Cell Death & Disease|October 6, 2025
Adipocyte-specific Mlkl knockout mitigates obesity-induced metabolic dysfunction by enhancing mitochondrial functionsJuliette Tokgozoglu, Valeria Pistorio, Mirko Minini, et al.
Pageof 2