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3D genome architecture in the mammalian nucleus

artículo científico publicado en 2013

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 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

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

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

artículo científico publicado en 2016

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

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

artículo científico publicado en 2012

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