The homeobox gene Otx2 in development and disease

F Beby, T Lamonerie - Experimental eye research, 2013 - Elsevier
The Otx2 gene encodes a transcription factor essential for the normal development of brain,
cerebellum, pineal gland, and eye. In the retina, Otx2 has essential functions from early …

Differentially expressed genes are marked by histone 3 lysine 9 trimethylation in human cancer cells

JK Wiencke, S Zheng, Z Morrison, RF Yeh - Oncogene, 2008 - nature.com
Histone H3 lysine 9 trimethylation (H3K9Me3) has been associated with transcriptional
repression, but recent findings implicate this chromatin modification in transcriptional …

A new GFP-tagged line reveals unexpected Otx2 protein localization in retinal photoreceptors

N Fossat, C Le Greneur, F Beby, S Vincent… - BMC developmental …, 2007 - Springer
Background Dynamic monitoring of protein expression and localization is fundamental to the
understanding of biological processes. The paired-class homeodomain-containing …

Developmental pathway genes and neural plasticity underlying emotional learning and stress-related disorders

ME Maheu, KJ Ressler - Learning & Memory, 2017 - learnmem.cshlp.org
The manipulation of neural plasticity as a means of intervening in the onset and progression
of stress-related disorders retains its appeal for many researchers, despite our limited …

Otx2 Gene Deletion in Adult Mouse Retina Induces Rapid RPE Dystrophy and Slow Photoreceptor Degeneration

F Béby, M Housset, N Fossat, C Le Greneur, F Flamant… - PloS one, 2010 - journals.plos.org
Background Many developmental genes are still active in specific tissues after development
is completed. This is the case for the homeobox gene Otx2, an essential actor of forebrain …

Molecular dissection reveals decreased activity and not dominant negative effect in human OTX2 mutants

G Chatelain, N Fossat, G Brun, T Lamonerie - Journal of molecular …, 2006 - Springer
The paired-type homeodomain transcription factor Otx2 is essential for forebrain and eye
development. Severe ocular malformations in humans have recently been associated with …

[HTML][HTML] Ectopic Mitf in the embryonic chick retina by co-transfection of β-catenin and Otx2

PD Westenskow, JB McKean, F Kubo… - … & visual science, 2010 - iovs.arvojournals.org
Purpose.: Development of the retinal pigment epithelium (RPE) is controlled by intrinsic and
extrinsic regulators including orthodenticle homeobox 2 (Otx2) and the Wnt/β-catenin …

Candidate genes for panhypopituitarism identified by gene expression profiling

AH Mortensen, JW MacDonald… - Physiological …, 2011 - journals.physiology.org
Mutations in the transcription factors PROP1 and PIT1 (POU1F1) lead to pituitary hormone
deficiency and hypopituitarism in mice and humans. The dysmorphology of developing …

Long-term culture and differentiation of CNS precursors derived from anterior human neural rosettes following exposure to ventralizing factors

S Colleoni, C Galli, SG Giannelli, MT Armentero… - Experimental cell …, 2010 - Elsevier
In this study we demonstrated that neural rosettes derived from human ES cells can give rise
either to neural crest precursors, following expansion in presence of bFGF and EGF, or to …

[HTML][HTML] Selective inactivation of Otx2 mRNA isoforms reveals isoform-specific requirement for visceral endoderm anteriorization and head morphogenesis and …

D Acampora, LG Di Giovannantonio, M Di Salvio… - Mechanisms of …, 2009 - Elsevier
Genetic and embryological experiments demonstrated that the visceral endoderm (VE) is
essential for positioning the primitive streak at one pole of the embryo and head …