Genetic Deletion of Hesx1 Promotes Exit from the Pluripotent State and Impairs Developmental Diapause
Author:
Funder
Wellcome Trust
Publisher
Elsevier BV
Subject
Cell Biology,Developmental Biology,Genetics,Biochemistry
Reference21 articles.
1. Insulin fine-tunes self-renewal pathways governing naive pluripotency and extra-embryonic endoderm;Anderson;Nat. Cell Biol.,2017
2. Lack of the murine homeobox gene Hesx1 leads to a posterior transformation of the anterior forebrain;Andoniadou;Development,2007
3. Lineage-specific profiling delineates the emergence and progression of naive pluripotency in mammalian embryogenesis;Boroviak;Dev. Cell,2015
4. Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse;Dattani;Nat. Genet.,1998
5. Characterization of cis-regulatory elements of the homeobox gene Xanf-1;Eroshkin;Gene,2002
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