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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

187 related items for PubMed ID: 16573733

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  • 4. her7 and hey1, but not lunatic fringe show dynamic expression during somitogenesis in medaka (Oryzias latipes).
    Elmasri H, Liedtke D, Lücking G, Volff JN, Gessler M, Winkler C.
    Gene Expr Patterns; 2004 Sep; 4(5):553-9. PubMed ID: 15261833
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  • 7. Oscillating expression of c-Hey2 in the presomitic mesoderm suggests that the segmentation clock may use combinatorial signaling through multiple interacting bHLH factors.
    Leimeister C, Dale K, Fischer A, Klamt B, Hrabe de Angelis M, Radtke F, McGrew MJ, Pourquié O, Gessler M.
    Dev Biol; 2000 Nov 01; 227(1):91-103. PubMed ID: 11076679
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  • 8. Identification of Epha4 enhancer required for segmental expression and the regulation by Mesp2.
    Nakajima Y, Morimoto M, Takahashi Y, Koseki H, Saga Y.
    Development; 2006 Jul 01; 133(13):2517-25. PubMed ID: 16728472
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  • 9. Comparative analysis of her genes during fish somitogenesis suggests a mouse/chick-like mode of oscillation in medaka.
    Gajewski M, Elmasri H, Girschick M, Sieger D, Winkler C.
    Dev Genes Evol; 2006 Jun 01; 216(6):315-32. PubMed ID: 16544152
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  • 10. The oscillation of Notch activation, but not its boundary, is required for somite border formation and rostral-caudal patterning within a somite.
    Oginuma M, Takahashi Y, Kitajima S, Kiso M, Kanno J, Kimura A, Saga Y.
    Development; 2010 May 01; 137(9):1515-22. PubMed ID: 20335362
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  • 17. Notch signaling is involved in the regulation of Id3 gene transcription during Xenopus embryogenesis.
    Reynaud-Deonauth S, Zhang H, Afouda A, Taillefert S, Beatus P, Kloc M, Etkin LD, Fischer-Lougheed J, Spohr G.
    Differentiation; 2002 Jan 01; 69(4-5):198-208. PubMed ID: 11841478
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  • 18. Differential contributions of Mesp1 and Mesp2 to the epithelialization and rostro-caudal patterning of somites.
    Takahashi Y, Hiraoka S, Kitajima S, Inoue T, Kanno J, Saga Y.
    Development; 2005 Feb 01; 132(4):787-96. PubMed ID: 15677726
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