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Journal Abstract Search

124 related items for PubMed ID: 15523651

  • 1. Functional characterization of SIX3 homeodomain mutations in holoprosencephaly: interaction with the nuclear receptor NR4A3/NOR1.
    Laflamme C, Filion C, Labelle Y.
    Hum Mutat; 2004 Dec; 24(6):502-8. PubMed ID: 15523651
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  • 3. EYA4, deleted in a case with middle interhemispheric variant of holoprosencephaly, interacts with SIX3 both physically and functionally.
    Abe Y, Oka A, Mizuguchi M, Igarashi T, Ishikawa S, Aburatani H, Yokoyama S, Asahara H, Nagao K, Yamada M, Miyashita T.
    Hum Mutat; 2009 Oct; 30(10):E946-55. PubMed ID: 19606496
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  • 4. The homeotic protein Six3 is a coactivator of the nuclear receptor NOR-1 and a corepressor of the fusion protein EWS/NOR-1 in human extraskeletal myxoid chondrosarcomas.
    Laflamme C, Filion C, Bridge JA, Ladanyi M, Goldring MB, Labelle Y.
    Cancer Res; 2003 Jan 15; 63(2):449-54. PubMed ID: 12543801
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  • 7. Molecular screening of SHH, ZIC2, SIX3, and TGIF genes in patients with features of holoprosencephaly spectrum: Mutation review and genotype-phenotype correlations.
    Dubourg C, Lazaro L, Pasquier L, Bendavid C, Blayau M, Le Duff F, Durou MR, Odent S, David V.
    Hum Mutat; 2004 Jul 15; 24(1):43-51. PubMed ID: 15221788
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  • 10. [Genetic study of holoprosencephaly].
    Dubourg C, Lazaro L, Blayau M, Pasquier L, Durou MR, Odent S, David V.
    Ann Biol Clin (Paris); 2003 Jul 15; 61(6):679-87. PubMed ID: 14711609
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  • 12. Mutations in the human SIX3 gene in holoprosencephaly are loss of function.
    Domené S, Roessler E, El-Jaick KB, Snir M, Brown JL, Vélez JI, Bale S, Lacbawan F, Muenke M, Feldman B.
    Hum Mol Genet; 2008 Dec 15; 17(24):3919-28. PubMed ID: 18791198
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  • 13. Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function.
    Lacbawan F, Solomon BD, Roessler E, El-Jaick K, Domené S, Vélez JI, Zhou N, Hadley D, Balog JZ, Long R, Fryer A, Smith W, Omar S, McLean SD, Clarkson K, Lichty A, Clegg NJ, Delgado MR, Levey E, Stashinko E, Potocki L, Vanallen MI, Clayton-Smith J, Donnai D, Bianchi DW, Juliusson PB, Njølstad PR, Brunner HG, Carey JC, Hehr U, Müsebeck J, Wieacker PF, Postra A, Hennekam RC, van den Boogaard MJ, van Haeringen A, Paulussen A, Herbergs J, Schrander-Stumpel CT, Janecke AR, Chitayat D, Hahn J, McDonald-McGinn DM, Zackai EH, Dobyns WB, Muenke M.
    J Med Genet; 2009 Jun 15; 46(6):389-98. PubMed ID: 19346217
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  • 14. A microarray model system identifies potential new target genes of the proto-oncogene HOX11.
    Hoffmann K, Dixon DN, Greene WK, Ford J, Taplin R, Kees UR.
    Genes Chromosomes Cancer; 2004 Dec 15; 41(4):309-20. PubMed ID: 15384172
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  • 16. Ectopic Six3 expression in the dragon eye goldfish.
    Ma DM, Zhu HP, Gui JF.
    Comp Biochem Physiol B Biochem Mol Biol; 2008 Feb 15; 149(2):303-13. PubMed ID: 18006349
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  • 19. Mutations in holoprosencephaly.
    Wallis D, Muenke M.
    Hum Mutat; 2000 Feb 15; 16(2):99-108. PubMed ID: 10923031
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