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The Talpid3 gene (KIAA0586) encodes a centrosomal protein that is essential for primary cilia formationThe presence of PHOSPHO1 in matrix vesicles and its developmental expression prior to skeletal mineralizationGeneration of mice with functional inactivation of talpid3, a gene first identified in chickenMicro-magnetic resonance imaging of avian embryos.Foxj1 regulates floor plate cilia architecture and modifies the response of cells to sonic hedgehog signallingCanine Brachycephaly Is Associated with a Retrotransposon-Mediated Missplicing of SMOC2.The chicken talpid3 gene encodes a novel protein essential for Hedgehog signalingThe chicken left right organizer has nonmotile cilia which are lost in a stage-dependent manner in the talpid(3) ciliopathy.Utilizing the chicken as an animal model for human craniofacial ciliopathies.Loss of MACF1 Abolishes Ciliogenesis and Disrupts Apicobasal Polarity Establishment in the Retina.eChickAtlas: an introduction to the database.TALPID3 controls centrosome and cell polarity and the human ortholog KIAA0586 is mutated in Joubert syndrome (JBTS23)A recurrent de novo mutation in ACTG1 causes isolated ocular coloboma.Loss of cilia causes embryonic lung hypoplasia, liver fibrosis, and cholestasis in the talpid3 ciliopathy mutant.Direct functional consequences of ZRS enhancer mutation combine with secondary long range SHH signalling effects to cause preaxial polydactyly.Failure of centrosome migration causes a loss of motile cilia in talpid(3) mutants.Pivotal Advance: Avian colony-stimulating factor 1 (CSF-1), interleukin-34 (IL-34), and CSF-1 receptor genes and gene products.Identification of genes downstream of the Shh signalling in the developing chick wing and syn-expressed with Hoxd13 using microarray and 3D computational analysis.Analysis of talpid3 and wild-type chicken embryos reveals roles for Hedgehog signalling in development of the limb bud vasculature.Craniofacial development in the talpid3 chicken mutant.The chick limb: embryology, genetics and teratology.Feather arrays are patterned by interacting signalling and cell density wavesExperimental evidence that preaxial polydactyly and forearm radial deficiencies may share a common developmental originIlluminating the chicken model through genetic modification
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description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Megan G Davey
@ast
Megan G Davey
@en
Megan G Davey
@es
Megan G Davey
@nl
Megan G Davey
@sl
type
label
Megan G Davey
@ast
Megan G Davey
@en
Megan G Davey
@es
Megan G Davey
@nl
Megan G Davey
@sl
prefLabel
Megan G Davey
@ast
Megan G Davey
@en
Megan G Davey
@es
Megan G Davey
@nl
Megan G Davey
@sl
P108
P1053
C-7723-2013
P106
P21
P31
P3829
P496
0000-0003-0194-9229