Septo-optic dysplasia and other midline defects: The role of transcription factors: HESX1 and beyond
- 28 February 2011
- journal article
- review article
- Published by Elsevier BV in Best Practice & Research Clinical Endocrinology & Metabolism
- Vol. 25 (1), 115-124
- https://doi.org/10.1016/j.beem.2010.06.008
Abstract
No abstract availableKeywords
This publication has 80 references indexed in Scilit:
- OTX2 microphthalmia syndrome: four novel mutations and delineation of a phenotypeClinical Genetics, 2011
- The unfolding clinical spectrum of holoprosencephaly due to mutations in SHH, ZIC2, SIX3 and TGIF genesEuropean Journal of Human Genetics, 2010
- A role of the LIM-homeobox gene Lhx2 in the regulation of pituitary developmentDevelopmental Biology, 2010
- Genetic Regulation of Pituitary Gland Development in Human and MouseEndocrine Reviews, 2009
- Septo-optic dysplasiaEuropean Journal of Human Genetics, 2009
- A Novel Dominant Negative Mutation of OTX2 Associated with Combined Pituitary Hormone DeficiencyJournal of Clinical Endocrinology & Metabolism, 2008
- SOX2 Plays a Critical Role in the Pituitary, Forebrain, and Eye during Human Embryonic DevelopmentJournal of Clinical Endocrinology & Metabolism, 2008
- Mechanisms underlying pituitary hypoplasia and failed cell specification in Lhx3-deficient miceDevelopmental Biology, 2008
- Mutations within Sox2/SOX2 are associated with abnormalities in the hypothalamo-pituitary-gonadal axis in mice and humansJCI Insight, 2006
- SOX2 is a dose-dependent regulator of retinal neural progenitor competenceGenes & Development, 2006