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Journal Abstract Search

144 related items for PubMed ID: 10415461

  • 1. Sequence and location of SIX3, a homeobox gene expressed in the human eye.
    Leppert GS, Yang JM, Sundin OH.
    Ophthalmic Genet; 1999 Mar; 20(1):7-21. PubMed ID: 10415461
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  • 2. Six3, a medaka homologue of the Drosophila homeobox gene sine oculis is expressed in the anterior embryonic shield and the developing eye.
    Loosli F, Köster RW, Carl M, Krone A, Wittbrodt J.
    Mech Dev; 1998 Jun; 74(1-2):159-64. PubMed ID: 9651515
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  • 3. Six3, a murine homologue of the sine oculis gene, demarcates the most anterior border of the developing neural plate and is expressed during eye development.
    Oliver G, Mailhos A, Wehr R, Copeland NG, Jenkins NA, Gruss P.
    Development; 1995 Dec; 121(12):4045-55. PubMed ID: 8575305
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  • 4. Genomic cloning and characterization of the human homeobox gene SIX6 reveals a cluster of SIX genes in chromosome 14 and associates SIX6 hemizygosity with bilateral anophthalmia and pituitary anomalies.
    Gallardo ME, Lopez-Rios J, Fernaud-Espinosa I, Granadino B, Sanz R, Ramos C, Ayuso C, Seller MJ, Brunner HG, Bovolenta P, Rodríguez de Córdoba S.
    Genomics; 1999 Oct 01; 61(1):82-91. PubMed ID: 10512683
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  • 5. Genomic cloning, structure, expression pattern, and chromosomal location of the human SIX3 gene.
    Granadino B, Gallardo ME, López-Ríos J, Sanz R, Ramos C, Ayuso C, Bovolenta P, Rodríguez de Córdoba S.
    Genomics; 1999 Jan 01; 55(1):100-5. PubMed ID: 9889003
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  • 7. Overexpression of the forebrain-specific homeobox gene six3 induces rostral forebrain enlargement in zebrafish.
    Kobayashi M, Toyama R, Takeda H, Dawid IB, Kawakami K.
    Development; 1998 Aug 01; 125(15):2973-82. PubMed ID: 9655819
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  • 9. Six6 (Optx2) is a novel murine Six3-related homeobox gene that demarcates the presumptive pituitary/hypothalamic axis and the ventral optic stalk.
    Jean D, Bernier G, Gruss P.
    Mech Dev; 1999 Jun 01; 84(1-2):31-40. PubMed ID: 10473118
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  • 10. Six3 overexpression initiates the formation of ectopic retina.
    Loosli F, Winkler S, Wittbrodt J.
    Genes Dev; 1999 Mar 15; 13(6):649-54. PubMed ID: 10090721
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  • 11. A new mutation in the six-domain of SIX3 gene causes holoprosencephaly.
    Pasquier L, Dubourg C, Blayau M, Lazaro L, Le Marec B, David V, Odent S.
    Eur J Hum Genet; 2000 Oct 15; 8(10):797-800. PubMed ID: 11039582
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  • 13. Expression pattern of cSix3, a member of the Six/sine oculis family of transcription factors.
    Bovolenta P, Mallamaci A, Puelles L, Boncinelli E.
    Mech Dev; 1998 Jan 15; 70(1-2):201-3. PubMed ID: 9510037
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  • 14. Six3-mediated auto repression and eye development requires its interaction with members of the Groucho-related family of co-repressors.
    Zhu CC, Dyer MA, Uchikawa M, Kondoh H, Lagutin OV, Oliver G.
    Development; 2002 Jun 15; 129(12):2835-49. PubMed ID: 12050133
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  • 16. Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly.
    Wallis DE, Roessler E, Hehr U, Nanni L, Wiltshire T, Richieri-Costa A, Gillessen-Kaesbach G, Zackai EH, Rommens J, Muenke M.
    Nat Genet; 1999 Jun 15; 22(2):196-8. PubMed ID: 10369266
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  • 19. The homeobox protein Six3 interacts with the Groucho corepressor and acts as a transcriptional repressor in eye and forebrain formation.
    Kobayashi M, Nishikawa K, Suzuki T, Yamamoto M.
    Dev Biol; 2001 Apr 15; 232(2):315-26. PubMed ID: 11401394
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  • 20. Six3 promotes the formation of ectopic optic vesicle-like structures in mouse embryos.
    Lagutin O, Zhu CC, Furuta Y, Rowitch DH, McMahon AP, Oliver G.
    Dev Dyn; 2001 Jul 15; 221(3):342-9. PubMed ID: 11458394
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