Isolation of a new homeobox gene belonging to the Pitx/Rieg family: expression during lens development and mapping to the aphakia region on mouse chromosome 19.
about
Functional analysis of human mutations in homeodomain transcription factor PITX3A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMDPtx1 regulates SF-1 activity by an interaction that mimics the role of the ligand-binding domainDifferential regulation of gene expression by PITX2 isoformsPosterior polar cataract: genetic analysis of a large familyPitx3 controls multiple aspects of lens developmentAnalysis of three Ptx2 splice variants on transcriptional activity and differential expression pattern in the brainSequential activation of transcription factors in lens induction.Identification of differentially expressed genes in mouse Pax6 heterozygous lenses.Motor deficits and altered striatal gene expression in aphakia (ak) mice.Novel forms of Paired-like homeodomain transcription factor 2 (PITX2): generation by alternative translation initiation and mRNA splicing.The A9 dopamine neuron component in grafts of ventral mesencephalon is an important determinant for recovery of motor function in a rat model of Parkinson's disease.Pitx3-deficient aphakia mice display unique behavioral responses to psychostimulant and antipsychotic drugs.Absence of PITX3 mutation in a Tunisian family with congenital cataract and mental retardation.Mouse models of congenital cataract.The role of transcription factor Pitx3 in dopamine neuron development and Parkinson's disease.Multifunctional role of the Pitx2 homeodomain protein C-terminal tail.MIP/Aquaporin 0 represents a direct transcriptional target of PITX3 in the developing lens.The genetics of childhood cataractSpatial and temporal lineage analysis of a Pitx3-driven Cre-recombinase knock-in mouse model.Fine mapping of the split-hand/split-foot locus (SHFM3) at 10q24: evidence for anticipation and segregation distortion.Expression of truncated PITX3 in the developing lens leads to microphthalmia and aphakia in mice.Pleiotropic and isoform-specific functions for Pitx2 in superior colliculus and hypothalamic neuronal developmentPitx homeobox genes in Ciona and amphioxus show left-right asymmetry is a conserved chordate character and define the ascidian adenohypophysis.The cellular and molecular mechanisms of vertebrate lens development.Midbrain dopamine neurons associated with reward processing innervate the neurogenic subventricular zone.Parent-of-origin effects in SOX2 anophthalmia syndromeAP-2β Is a Downstream Effector of PITX2 Required to Specify Endothelium and Establish Angiogenic Privilege During Corneal Development.Paired-like homeodomain transcription factors 1 and 2 regulate follicle-stimulating hormone beta-subunit transcription through a conserved cis-element.Vesicular monoamine transporter 2 and dopamine transporter are molecular targets of Pitx3 in the ventral midbrain dopamine neuronsSelection of embryonic stem cell-derived enhanced green fluorescent protein-positive dopamine neurons using the tyrosine hydroxylase promoter is confounded by reporter gene expression in immature cell populations.Asymmetric lower-limb malformations in individuals with homeobox PITX1 gene mutationEmbryonic stem cell-derived Pitx3-enhanced green fluorescent protein midbrain dopamine neurons survive enrichment by fluorescence-activated cell sorting and function in an animal model of Parkinson's disease.Conservation of mechanisms mediating gonadotrophin-releasing hormone 1 stimulation of human luteinizing hormone beta subunit transcription.The lens in focus: a comparison of lens development in Drosophila and vertebrates.Neural crest derivatives in ocular development: discerning the eye of the stormNovel and recurrent PITX3 mutations in Belgian families with autosomal dominant congenital cataract and anterior segment dysgenesis have similar phenotypic and functional characteristics.Gestational restraint stress and the developing dopaminergic system: an overview.Conserved genetic pathways associated with microphthalmia, anophthalmia, and coloboma.Cyclin A1 is a transcriptional target of PITX2 and overexpressed in papillary thyroid carcinoma.
P2860
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P2860
Isolation of a new homeobox gene belonging to the Pitx/Rieg family: expression during lens development and mapping to the aphakia region on mouse chromosome 19.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
1997年论文
@zh
1997年论文
@zh-cn
name
Isolation of a new homeobox ge ...... region on mouse chromosome 19.
@en
type
label
Isolation of a new homeobox ge ...... region on mouse chromosome 19.
@en
prefLabel
Isolation of a new homeobox ge ...... region on mouse chromosome 19.
@en
P2093
P2860
P356
P1476
Isolation of a new homeobox ge ...... region on mouse chromosome 19.
@en
P2093
P2860
P304
P356
10.1093/HMG/6.12.2109
P577
1997-11-01T00:00:00Z