Analysis of FOXD3 sequence variation in human ocular disease.

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Definition of transcriptome-based indices for quantitative characterization of chemically disturbed stem cell development: introduction of the STOP-Toxukn and STOP-Toxukk tests.Integrated microarray analysis provided novel insights to the pathogenesis of glaucoma.

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Analysis of FOXD3 sequence variation in human ocular disease.

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2012 nî lūn-bûn

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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2012年论文

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Analysis of FOXD3 sequence variation in human ocular disease.

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Analysis of FOXD3 sequence variation in human ocular disease.

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Analysis of FOXD3 sequence variation in human ocular disease.

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Analysis of FOXD3 sequence variation in human ocular disease.

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Analysis of FOXD3 sequence variation in human ocular disease.

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Analysis of FOXD3 sequence variation in human ocular disease.

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Analysis of FOXD3 sequence variation in human ocular disease.

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Bethany A Volkmann Kloss

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Dominique Brémond-Gignac

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Linda M Reis

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Tom Glaser

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P2860

Analyses of the effects that disease-causing missense mutations have on the structure and function of the winged-helix protein FOXC1

Foxe3 haploinsufficiency in mice: a model for Peters' anomaly

Identification of dominant FOXE3 and PAX6 mutations in patients with congenital cataract and aniridia

FOXE3 plays a significant role in autosomal recessive microphthalmia

Dynamic DNA contacts observed in the NMR structure of winged helix protein-DNA complex

Co-crystal structure of the HNF-3/fork head DNA-recognition motif resembles histone H5

Structural changes in the region directly adjacent to the DNA-binding helix highlight a possible mechanism to explain the observed changes in the sequence-specific binding of winged helix proteins

Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene

The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25

Requirement for Foxd3 in maintaining pluripotent cells of the early mouse embryo

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1740-1749

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scholarly article

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Elena V Semina

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2012-06-27T00:00:00Z

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Analysis of FOXD3 sequence variation in human ocular disease.

about

P2860

P2860

Analysis of FOXD3 sequence variation in human ocular disease.

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P1433

P1476

P2093

P2860

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