Epilepsy and brain abnormalities in mice lacking the Otx1 gene. - Wikidata - awgldk - TriplyDB

Epilepsy and brain abnormalities in mice lacking the Otx1 gene.

Epilepsy and brain abnormalities in mice lacking the Otx1 gene.

http://www.wikidata.org/entity/Q34400653

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A symphony of inner ear developmental control genes.Insights into the urbilaterian brain: conserved genetic patterning mechanisms in insect and vertebrate brain development BEST1 expression in the retinal pigment epithelium is modulated by OTX family members Sequencing of 50 human exomes reveals adaptation to high altitude Expression of the homeobox genes OTX2 and OTX1 in the early developing human brain Developmental rescue of Drosophila cephalic defects by the human Otx genes Evolutionary conservation of otd/Otx2 transcription factor action: a genome-wide microarray analysis in Drosophila.Eye development and retinogenesis Origins of anteroposterior patterning and Hox gene regulation during chordate evolution.Otx dose-dependent integrated control of antero-posterior and dorso-ventral patterning of midbrain Identification, tissue expression, and functional characterization of Otx3, a novel member of the Otx family Pancreatic homeodomain transcription factor IDX1/IPF1 expressed in developing brain regulates somatostatin gene transcription in embryonic neural cells The essential haematopoietic transcription factor Scl is also critical for neuronal development The nuclear receptor Nor-1 is essential for proliferation of the semicircular canals of the mouse inner ear Notch2 regulates BMP signaling and epithelial morphogenesis in the ciliary body of the mouse eye Specification of the mammalian cochlea is dependent on Sonic hedgehog Role of the Bicoid-related homeodomain factor Pitx1 in specifying hindlimb morphogenesis and pituitary development Otx1 and Otx2 in the development and evolution of the mammalian brain.Developmental genetic evidence for a monophyletic origin of the bilaterian brain.Unsuspected role of the brain morphogenetic gene Otx1 in hematopoiesis.Otic ablation of smoothened reveals direct and indirect requirements for Hedgehog signaling in inner ear development.Molecular genetics of pattern formation in the inner ear: do compartment boundaries play a role?Delayed fusion and altered gene expression contribute to semicircular canal defects in Chd7 deficient mice Cortical malformations and epilepsy: new insights from animal models.Recent advances in the genetics of epilepsy: insights from human and animal studies.Genitourinary defects associated with genomic deletions in 2p15 encompassing OTX1.Regulation of mandibular growth and morphogenesis.The Bicoid class homeodomain factors ceh-36/OTX and unc-30/PITX cooperate in C. elegans embryonic progenitor cells to regulate robust development.The Nanoscale Observation of the Three-Dimensional Structures of Neurosynapses, Membranous Conjunctions Between Cultured Hippocampal Neurons and Their Significance in the Development of Epilepsy.Identification of Wnt/β-catenin modulated genes in the developing retina.Patterning of the mammalian cochlea.Planar relationships of the semicircular canals in two strains of mice.Combinatorial decoding of the invariant C. elegans embryonic lineage in space and time.Lacrimal gland development: From signaling interactions to regenerative medicine.2p15-p16.1 microdeletion syndrome: molecular characterization and association of the OTX1 and XPO1 genes with autism spectrum disorders.A specific box switches the cell fate determining activity of XOTX2 and XOTX5b in the Xenopus retina.Neuron-restricted expression of the rat gonadotropin-releasing hormone gene is conferred by a cell-specific protein complex that binds repeated CAATT elements Homeobox genes in embryogenesis and pathogenesis.Pallial patterning and the origin of the isocortex.Immunoprecipitation and mass spectrometry identify non-cell autonomous Otx2 homeoprotein in the granular and supragranular layers of mouse visual cortex.

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P2860

Epilepsy and brain abnormalities in mice lacking the Otx1 gene.

http://www.wikidata.org/entity/Q34400653

description

1996 nî lūn-bûn

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1996 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

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1996年の論文

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1996年論文

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1996年論文

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1996年論文

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1996年論文

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Epilepsy and brain abnormalities in mice lacking the Otx1 gene.

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Epilepsy and brain abnormalities in mice lacking the Otx1 gene.

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Epilepsy and brain abnormalities in mice lacking the Otx1 gene.

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type

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Epilepsy and brain abnormalities in mice lacking the Otx1 gene.

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Epilepsy and brain abnormalities in mice lacking the Otx1 gene.

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Epilepsy and brain abnormalities in mice lacking the Otx1 gene.

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prefLabel

Epilepsy and brain abnormalities in mice lacking the Otx1 gene.

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Epilepsy and brain abnormalities in mice lacking the Otx1 gene.

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Epilepsy and brain abnormalities in mice lacking the Otx1 gene.

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Nature Genetics

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Epilepsy and brain abnormalities in mice lacking the Otx1 gene.

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P2860

Localization of a gene for partial epilepsy to chromosome 10q

Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q 13.2

The Wnt-1 (int-1) proto-oncogene is required for development of a large region of the mouse brain

Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly.

Pax in development.

Ataxia and epileptic seizures in mice lacking type 1 inositol 1,4,5-trisphosphate receptor.

Targeting epilepsy genes.

Developmental defects in brain segmentation caused by mutations of the homeobox genes orthodenticle and empty spiracles in Drosophila.

Nested expression domains of four homeobox genes in developing rostral brain.

Periventricular Heterotopia: An X-Linked Dominant Epilepsy Locus Causing Aberrant Cerebral Cortical Development

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Antonio Simeone

Francesca Tuorto

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1996-10-01T00:00:00Z

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8841200

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