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Journal Abstract Search

129 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
    [Abstract] [Full Text] [Related]

  • 2. Coexpression of NOR1 and SIX3 proteins in extraskeletal myxoid chondrosarcomas without detectable NR4A3 fusion genes.
    Hisaoka M, Okamoto S, Yokoyama K, Hashimoto H.
    Cancer Genet Cytogenet; 2004 Jul 15; 152(2):101-7. PubMed ID: 15262426
    [Abstract] [Full Text] [Related]

  • 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 15; 30(10):E946-55. PubMed ID: 19606496
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 8. Autoregulatory binding sites in the zebrafish six3a promoter region define a new recognition sequence for Six3 proteins.
    Suh CS, Ellingsen S, Austbø L, Zhao XF, Seo HC, Fjose A.
    FEBS J; 2010 Apr 15; 277(7):1761-75. PubMed ID: 20193042
    [Abstract] [Full Text] [Related]

  • 9. First occurrence of aprosencephaly/atelencephaly and holoprosencephaly in a family with a SIX3 gene mutation and phenotype/genotype correlation in our series of SIX3 mutations.
    Pasquier L, Dubourg C, Gonzales M, Lazaro L, David V, Odent S, Encha-Razavi F.
    J Med Genet; 2005 Jan 15; 42(1):e4. PubMed ID: 15635066
    [No Abstract] [Full Text] [Related]

  • 10. [Genetic study of holoprosencephaly].
    Dubourg C, Lazaro L, Blayau M, Pasquier L, Durou MR, Odent S, David V.
    Ann Biol Clin (Paris); 2003 Jan 15; 61(6):679-87. PubMed ID: 14711609
    [Abstract] [Full Text] [Related]

  • 11. Single median maxillary central incisor: new data and mutation review.
    El-Jaick KB, Fonseca RF, Moreira MA, Ribeiro MG, Bolognese AM, Dias SO, Pereira ET, Castilla EE, Orioli IM.
    Birth Defects Res A Clin Mol Teratol; 2007 Aug 15; 79(8):573-80. PubMed ID: 17584896
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 15. A novel heterozygous missense mutation 377T > C (V126A) of TGIF gene in a family segregated with holoprosencephaly and moyamoya disease.
    Chen M, Kuo SJ, Liu CS, Chen WL, Ko TM, Chen TH, Chang SP, Huang CH, Chang YY, Wang BT.
    Prenat Diagn; 2006 Mar 15; 26(3):226-30. PubMed ID: 16475235
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 17. Six3 dosage mediates the pathogenesis of holoprosencephaly.
    Geng X, Acosta S, Lagutin O, Gil HJ, Oliver G.
    Development; 2016 Dec 01; 143(23):4462-4473. PubMed ID: 27770010
    [Abstract] [Full Text] [Related]

  • 18. Six3 controls the neural progenitor status in the murine CNS.
    Appolloni I, Calzolari F, Corte G, Perris R, Malatesta P.
    Cereb Cortex; 2008 Mar 01; 18(3):553-62. PubMed ID: 17576749
    [Abstract] [Full Text] [Related]

  • 19. Mutations in holoprosencephaly.
    Wallis D, Muenke M.
    Hum Mutat; 2000 Mar 01; 16(2):99-108. PubMed ID: 10923031
    [Abstract] [Full Text] [Related]

  • 20. SIX3 deletions and incomplete penetrance in families affected by holoprosencephaly.
    Stokes B, Berger SI, Hall BA, Weiss K, Martinez AF, Hadley DW, Murdock DR, Ramanathan S, Clark RD, Roessler E, Kruszka P, Muenke M.
    Congenit Anom (Kyoto); 2018 Jan 01; 58(1):29-32. PubMed ID: 28670735
    [Abstract] [Full Text] [Related]

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