Lista de obras -

3D genome architecture in the mammalian nucleus

artículo científico publicado en 2013

A Novel Epi-drug Therapy Based on the Suppression of BET Family Epigenetic Readers

artículo científico publicado en 2017

A central role of H3K4me3 extended chromatin domains in gene regulation

scientific article published on 13 July 2016

Alternative splicing and promoter use in TFII-I genes

artículo científico publicado en 2008

Cell-specific gene promoters are marked by broader spans of H3K4me3 and are associated with robust gene expression patterns

artículo científico publicado en 2015

ChIP-Chip Identifies SEC23A, CFDP1, and NSD1 as TFII-I Target Genes in Human Neural Crest Progenitor Cells

artículo científico publicado en 2012

Diversity and complexity in chromatin recognition by TFII-I transcription factors in pluripotent embryonic stem cells and embryonic tissues

artículo científico publicado en 2012

Epigenetic drug therapy based on bromodomain inhibition

artículo científico publicado en 2014

Epigenetic mechanisms involved in modulation of inflammatory diseases

artículo científico publicado en 2016

Epigenetic modulation by TFII-I during embryonic stem cell differentiation

artículo científico publicado en 2012

Essential functions of the Williams-Beuren syndrome-associated TFII-I genes in embryonic development

scholarly article

Expression of BEN, a member of TFII-I family of transcription factors, during mouse pre- and postimplantation development

scientific journal article

Expression profiling of BEN regulated genes in mouse embryonic fibroblasts

artículo científico publicado en 2007

GTF2IRD2 is located in the Williams-Beuren syndrome critical region 7q11.23 and encodes a protein with two TFII-I-like helix-loop-helix repeats

scholarly article

Gene expression analysis of TFII-I modulated genes in mouse embryonic fibroblasts

artículo científico publicado en 2007

Generation of a mouse model for a conditional inactivation of Gtf2i allele

artículo científico publicado en 2016

Generation of neural crest progenitors from human embryonic stem cells

artículo científico publicado en 2010

Genome-wide Chromatin Mapping Defines AP2α in the Etiology of Craniofacial Disorders

artículo científico publicado en 2014

Genomic organization of the genes Gtf2ird1, Gtf2i, and Ncf1 at the mouse chromosome 5 region syntenic to the human chromosome 7q11.23 Williams syndrome critical region.

artículo científico publicado en 2002

HnRNP A3 genes and pseudogenes in the vertebrate genomes

artículo científico publicado en 2005

Homez, a homeobox leucine zipper gene specific to the vertebrate lineage

artículo científico publicado en 2003

Identification of the TFII-I family target genes in the vertebrate genome

artículo científico publicado en 2008

Laser-assisted microdissection (LAM) in developmental biology

artículo científico publicado en 2007

Mesenchyme-specific loss of Dot1L histone methyltransferase leads to skeletal dysplasia phenotype in mice

artículo científico publicado en 2020

Modus operandi of COMPASS/MLL epigenetic writers in the mammalian genome

artículo científico publicado en 2018

Molecular basis of Williams-Beuren syndrome: TFII-I regulated targets involved in craniofacial development

artículo científico publicado en 2010

Neuronal deletion of Gtf2i, associated with Williams syndrome, causes behavioral and myelin alterations rescuable by a remyelinating drug

artículo científico publicado en 2019

New TFII-I family target genes involved in embryonic development

artículo científico publicado en 2009

PI3K/Akt-dependent functions of TFII-I transcription factors in mouse embryonic stem cells

artículo científico publicado en 2012

Physical and functional interactions of histone deacetylase 3 with TFII-I family proteins and PIASxbeta ⬇️

artículo científico publicado en 2002

Publisher Correction: Neuronal deletion of Gtf2i, associated with Williams syndrome, causes behavioral and myelin alterations rescuable by a remyelinating drug

scientific article published on 01 July 2019

SSDP1 gene encodes a protein with a conserved N-terminal FORWARD domain

artículo científico publicado en 2002

Ssdp proteins interact with the LIM-domain-binding protein Ldb1 to regulate development

artículo científico publicado en 2002

TFII-I and AP2α Co-occupy the Promoters of Key Regulatory Genes Associated With Craniofacial Development

artículo científico publicado en 2017

The early embryonic expression of TFII-I during mouse preimplantation development

artículo científico publicado en 2004

The role of the proline-rich domain of Ssdp1 in the modular architecture of the vertebrate head organizer

artículo científico publicado en 2006

Toward integrative annotation of cell type-specific epigenomes to better understand human biology and disease

artículo científico publicado en 2015

What role does TFII-I have to play in epigenetic modulation during embryogenesis?

artículo científico publicado en 2013

Lista de obras de

3D genome architecture in the mammalian nucleus

A Novel Epi-drug Therapy Based on the Suppression of BET Family Epigenetic Readers

A central role of H3K4me3 extended chromatin domains in gene regulation

Alternative splicing and promoter use in TFII-I genes

Cell-specific gene promoters are marked by broader spans of H3K4me3 and are associated with robust gene expression patterns

ChIP-Chip Identifies SEC23A, CFDP1, and NSD1 as TFII-I Target Genes in Human Neural Crest Progenitor Cells

Diversity and complexity in chromatin recognition by TFII-I transcription factors in pluripotent embryonic stem cells and embryonic tissues

Epigenetic drug therapy based on bromodomain inhibition

Epigenetic mechanisms involved in modulation of inflammatory diseases

Epigenetic modulation by TFII-I during embryonic stem cell differentiation

Essential functions of the Williams-Beuren syndrome-associated TFII-I genes in embryonic development

Expression of BEN, a member of TFII-I family of transcription factors, during mouse pre- and postimplantation development

Expression profiling of BEN regulated genes in mouse embryonic fibroblasts

GTF2IRD2 is located in the Williams-Beuren syndrome critical region 7q11.23 and encodes a protein with two TFII-I-like helix-loop-helix repeats

Gene expression analysis of TFII-I modulated genes in mouse embryonic fibroblasts

Generation of a mouse model for a conditional inactivation of Gtf2i allele

Generation of neural crest progenitors from human embryonic stem cells

Genome-wide Chromatin Mapping Defines AP2α in the Etiology of Craniofacial Disorders

Genomic organization of the genes Gtf2ird1, Gtf2i, and Ncf1 at the mouse chromosome 5 region syntenic to the human chromosome 7q11.23 Williams syndrome critical region.

HnRNP A3 genes and pseudogenes in the vertebrate genomes

Homez, a homeobox leucine zipper gene specific to the vertebrate lineage

Identification of the TFII-I family target genes in the vertebrate genome

Laser-assisted microdissection (LAM) in developmental biology

Mesenchyme-specific loss of Dot1L histone methyltransferase leads to skeletal dysplasia phenotype in mice

Modus operandi of COMPASS/MLL epigenetic writers in the mammalian genome

Molecular basis of Williams-Beuren syndrome: TFII-I regulated targets involved in craniofacial development

Neuronal deletion of Gtf2i, associated with Williams syndrome, causes behavioral and myelin alterations rescuable by a remyelinating drug

New TFII-I family target genes involved in embryonic development

PI3K/Akt-dependent functions of TFII-I transcription factors in mouse embryonic stem cells

Physical and functional interactions of histone deacetylase 3 with TFII-I family proteins and PIASxbeta ⬇️

Publisher Correction: Neuronal deletion of Gtf2i, associated with Williams syndrome, causes behavioral and myelin alterations rescuable by a remyelinating drug

SSDP1 gene encodes a protein with a conserved N-terminal FORWARD domain

Ssdp proteins interact with the LIM-domain-binding protein Ldb1 to regulate development

TFII-I and AP2α Co-occupy the Promoters of Key Regulatory Genes Associated With Craniofacial Development

The early embryonic expression of TFII-I during mouse preimplantation development

The role of the proline-rich domain of Ssdp1 in the modular architecture of the vertebrate head organizer

Toward integrative annotation of cell type-specific epigenomes to better understand human biology and disease

What role does TFII-I have to play in epigenetic modulation during embryogenesis?