Eye and neural defects associated with loss of GDF6 - Test2 - elhamkhani - TriplyDB

Eye and neural defects associated with loss of GDF6

Eye and neural defects associated with loss of GDF6

http://www.wikidata.org/entity/Q21284140

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Genomic screening identifies novel linkages and provides further evidence for a role of MYH9 in nonsyndromic cleft lip and palate GDF6, a novel locus for a spectrum of ocular developmental anomalies gdf6a is required for cone photoreceptor subtype differentiation and for the actions of tbx2b in determining rod versus cone photoreceptor fate Incomplete penetrance and phenotypic variability characterize Gdf6-attributable oculo-skeletal phenotypes Pbx homeodomain proteins pattern both the zebrafish retina and tectum.Genetic defects of GDF6 in the zebrafish out of sight mutant and in human eye developmental anomalies A homolog of Subtilisin-like Proprotein Convertase 7 is essential to anterior neural development in Xenopus.Bone Morphogenetic Protein (BMP) signaling in development and human diseases Association of rs6982567 near GDF6 with neovascular age-related macular degeneration and polypoidal choroidal vasculopathy in a Han Chinese cohort.Smad4 is required predominantly in the developmental processes dependent on the BMP branch of the TGF-β signaling system in the embryonic mouse retina Eye development genes and known syndromes High temperature requirement factor A1 (HTRA1) gene regulates angiogenesis through transforming growth factor-β family member growth differentiation factor 6.Antagonism between Gdf6a and retinoic acid pathways controls timing of retinal neurogenesis and growth of the eye in zebrafish.An essential role for Radar (Gdf6a) in inducing dorsal fate in the zebrafish retina.Unveiling the bmp13 enigma: redundant morphogen or crucial regulator?The dynamic role of bone morphogenetic proteins in neural stem cell fate and maturation.Early development of the neural plate: new roles for apoptosis and for one of its main effectors caspase-3.Human Dental Pulp Stem Cells Are More Effective Than Human Bone Marrow-Derived Mesenchymal Stem Cells in Cerebral Ischemic Injury.Conserved genetic pathways associated with microphthalmia, anophthalmia, and coloboma.Canonical Wnt signaling is required for the maintenance of dorsal retinal identity.Extraocular ectoderm triggers dorsal retinal fate during optic vesicle evagination in zebrafish.Ligand-activated BMP signaling inhibits cell differentiation and death to promote melanoma.

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P2860

Eye and neural defects associated with loss of GDF6

http://www.wikidata.org/entity/Q21284140

description

2006 nî lūn-bûn

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2006 թուականին հրատարակուած գիտական յօդուած

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2006年の論文

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Eye and neural defects associated with loss of GDF6

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Eye and neural defects associated with loss of GDF6

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Eye and neural defects associated with loss of GDF6

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Eye and neural defects associated with loss of GDF6

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Eye and neural defects associated with loss of GDF6

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Eye and neural defects associated with loss of GDF6

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Eye and neural defects associated with loss of GDF6

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BMC Developmental Biology

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Eye and neural defects associated with loss of GDF6

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Carmel Hensey

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Meredith L Hanel

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P2860

Identification of receptors and signaling pathways for orphan bone morphogenetic protein/growth differentiation factor ligands based on genomic analyses

The Spemann organizer signal noggin binds and inactivates bone morphogenetic protein 4

Ectopic induction of tendon and ligament in rats by growth and differentiation factors 5, 6, and 7, members of the TGF-beta gene family

Neuronal patterning by BMPs: a requirement for GDF7 in the generation of a discrete class of commissural interneurons in the mouse spinal cord

Xenopus GDF6, a new antagonist of noggin and a partner of BMPs

Homology of the eyeless gene of Drosophila to the Small eye gene in mice and Aniridia in humans

Limb alterations in brachypodism mice due to mutations in a new member of the TGF beta-superfamily

Ventral mesodermal patterning in Xenopus embryos: expression patterns and activities of BMP-2 and BMP-4

BMP receptor 1b is required for axon guidance and cell survival in the developing retina

Overlapping expression domains of bone morphogenetic protein family members potentially account for limited tissue defects in BMP7 deficient embryos

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43

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scholarly article

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10.1186/1471-213X-6-43

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1013394359

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17010201

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1609107

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