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Biomolecules
|
December 23, 2023
ICF1-Syndrome-Associated <i>DNMT3B</i> Mutations Prevent De Novo Methylation at a Subset of Imprinted Loci during iPSC Reprogramming
Ankit Verma, Varsha Poondi Krishnan, Francesco Cecere, et al.
Genome Research
|
February 24, 2023
The aberrant epigenome of <i>DNMT3B</i>-mutated ICF1 patient iPSCs is amenable to correction, with the exception of a subset of regions with H3K4me3- and/or CTCF-based epigenetic memory
Varsha Poondi Krishnan, Barbara Morone, Shir Toubiana, et al.
Stem Cell Reports
|
December 9, 2020
MeCP2 and Major Satellite Forward RNA Cooperate for Pericentric Heterochromatin Organization
Salvatore Fioriniello, Eva Csukonyi, Domenico Marano, et al.
Genome Research
|
February 5, 2003
Complex events in the evolution of the human pseudoautosomal region 2 (PAR2)
Fadi J Charchar, Marta Svartman, Nisrine El-Mogharbel, et al.
Epigenetics
|
September 21, 2011
Variegated silencing through epigenetic modifications of a large Xq region in a case of balanced X;2 translocation with Incontinentia Pigmenti-like phenotype
Rita Genesio, Daniela Melis, Sole Gatto, et al.
Nucleic Acids Research
|
March 24, 2017
ICF-specific DNMT3B dysfunction interferes with intragenic regulation of mRNA transcription and alternative splicing
Sole Gatto, Miriam Gagliardi, Monica Franzese, et al.
Stem Cell Reports
|
December 10, 2013
L-Proline induces a mesenchymal-like invasive program in embryonic stem cells by remodeling H3K9 and H3K36 methylation
Stefania Comes, Miriam Gagliardi, Nicola Laprano, et al.
Frontiers in Immunology
|
July 23, 2024
A novel iPSC-based model of ICF syndrome subtype 2 recapitulates the molecular phenotype of ZBTB24 deficiency
Vincenzo Lullo, Francesco Cecere, Saveria Batti, et al.
Cancer Research
|
May 8, 2019
Collagen Prolyl Hydroxylation-Dependent Metabolic Perturbation Governs Epigenetic Remodeling and Mesenchymal Transition in Pluripotent and Cancer Cells
Cristina D'Aniello, Federica Cermola, Andrea Palamidessi, et al.
Epigenetics
|
May 19, 2012
Whole-genome bisulfite DNA sequencing of a DNMT3B mutant patient
Holger Heyn, Enrique Vidal, Sergi Sayols, et al.
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Search research articles
Search
Showing results (11-20 of 20) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 20 results.
Biomolecules
|
December 23, 2023
ICF1-Syndrome-Associated <i>DNMT3B</i> Mutations Prevent De Novo Methylation at a Subset of Imprinted Loci during iPSC Reprogramming
Ankit Verma, Varsha Poondi Krishnan, Francesco Cecere, et al.
Genome Research
|
February 24, 2023
The aberrant epigenome of <i>DNMT3B</i>-mutated ICF1 patient iPSCs is amenable to correction, with the exception of a subset of regions with H3K4me3- and/or CTCF-based epigenetic memory
Varsha Poondi Krishnan, Barbara Morone, Shir Toubiana, et al.
Stem Cell Reports
|
December 9, 2020
MeCP2 and Major Satellite Forward RNA Cooperate for Pericentric Heterochromatin Organization
Salvatore Fioriniello, Eva Csukonyi, Domenico Marano, et al.
Genome Research
|
February 5, 2003
Complex events in the evolution of the human pseudoautosomal region 2 (PAR2)
Fadi J Charchar, Marta Svartman, Nisrine El-Mogharbel, et al.
Epigenetics
|
September 21, 2011
Variegated silencing through epigenetic modifications of a large Xq region in a case of balanced X;2 translocation with Incontinentia Pigmenti-like phenotype
Rita Genesio, Daniela Melis, Sole Gatto, et al.
Nucleic Acids Research
|
March 24, 2017
ICF-specific DNMT3B dysfunction interferes with intragenic regulation of mRNA transcription and alternative splicing
Sole Gatto, Miriam Gagliardi, Monica Franzese, et al.
Stem Cell Reports
|
December 10, 2013
L-Proline induces a mesenchymal-like invasive program in embryonic stem cells by remodeling H3K9 and H3K36 methylation
Stefania Comes, Miriam Gagliardi, Nicola Laprano, et al.
Frontiers in Immunology
|
July 23, 2024
A novel iPSC-based model of ICF syndrome subtype 2 recapitulates the molecular phenotype of ZBTB24 deficiency
Vincenzo Lullo, Francesco Cecere, Saveria Batti, et al.
Cancer Research
|
May 8, 2019
Collagen Prolyl Hydroxylation-Dependent Metabolic Perturbation Governs Epigenetic Remodeling and Mesenchymal Transition in Pluripotent and Cancer Cells
Cristina D'Aniello, Federica Cermola, Andrea Palamidessi, et al.
Epigenetics
|
May 19, 2012
Whole-genome bisulfite DNA sequencing of a DNMT3B mutant patient
Holger Heyn, Enrique Vidal, Sergi Sayols, et al.
Page
of 2