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113 related items for PubMed ID: 12609048

  • 1. Interactions between gene activity and cell layers during floral development.
    Vincent CA, Carpenter R, Coen ES.
    Plant J; 2003 Feb; 33(4):765-74. PubMed ID: 12609048
    [Abstract] [Full Text] [Related]

  • 2. Quantitative levels of Deficiens and Globosa during late petal development show a complex transcriptional network topology of B function.
    Manchado-Rojo M, Delgado-Benarroch L, Roca MJ, Weiss J, Egea-Cortines M.
    Plant J; 2012 Oct; 72(2):294-307. PubMed ID: 22708513
    [Abstract] [Full Text] [Related]

  • 3. The duplicated B-class heterodimer model: whorl-specific effects and complex genetic interactions in Petunia hybrida flower development.
    Vandenbussche M, Zethof J, Royaert S, Weterings K, Gerats T.
    Plant Cell; 2004 Mar; 16(3):741-54. PubMed ID: 14973163
    [Abstract] [Full Text] [Related]

  • 4. Characterization of antirrhinum petal development and identification of target genes of the class B MADS box gene DEFICIENS.
    Bey M, Stüber K, Fellenberg K, Schwarz-Sommer Z, Sommer H, Saedler H, Zachgo S.
    Plant Cell; 2004 Dec; 16(12):3197-215. PubMed ID: 15539471
    [Abstract] [Full Text] [Related]

  • 5. Proliferating Floral Organs (Pfo), a Lotus japonicus gene required for specifying floral meristem determinacy and organ identity, encodes an F-box protein.
    Zhang S, Sandal N, Polowick PL, Stiller J, Stougaard J, Fobert PR.
    Plant J; 2003 Feb; 33(4):607-19. PubMed ID: 12609036
    [Abstract] [Full Text] [Related]

  • 6. To B or Not to B a flower: the role of DEFICIENS and GLOBOSA orthologs in the evolution of the angiosperms.
    Zahn LM, Leebens-Mack J, DePamphilis CW, Ma H, Theissen G.
    J Hered; 2005 Feb; 96(3):225-40. PubMed ID: 15695551
    [Abstract] [Full Text] [Related]

  • 7. The pollen-specific DEFH125 promoter from Antirrhinum is bound in vivo by the MADS-box proteins DEFICIENS and GLOBOSA.
    Lauri A, Xing S, Heidmann I, Saedler H, Zachgo S.
    Planta; 2006 Jun; 224(1):61-71. PubMed ID: 16374606
    [Abstract] [Full Text] [Related]

  • 8. Non-cell-autonomous function of the Antirrhinum floral homeotic proteins DEFICIENS and GLOBOSA is exerted by their polar cell-to-cell trafficking.
    Perbal MC, Haughn G, Saedler H, Schwarz-Sommer Z.
    Development; 1996 Nov; 122(11):3433-41. PubMed ID: 8951059
    [Abstract] [Full Text] [Related]

  • 9. The gene fimbriata interacts non-cell autonomously with floral regulatory genes.
    Schultz E, Carpenter R, Doyle S, Coen E.
    Plant J; 2001 Mar; 25(5):499-507. PubMed ID: 11309140
    [Abstract] [Full Text] [Related]

  • 10. The modified ABC model explains the development of the petaloid perianth of Agapanthus praecox ssp. orientalis (Agapanthaceae) flowers.
    Nakamura T, Fukuda T, Nakano M, Hasebe M, Kameya T, Kanno A.
    Plant Mol Biol; 2005 Jun; 58(3):435-45. PubMed ID: 16021405
    [Abstract] [Full Text] [Related]

  • 11. Ternary complex formation between the MADS-box proteins SQUAMOSA, DEFICIENS and GLOBOSA is involved in the control of floral architecture in Antirrhinum majus.
    Egea-Cortines M, Saedler H, Sommer H.
    EMBO J; 1999 Oct 01; 18(19):5370-9. PubMed ID: 10508169
    [Abstract] [Full Text] [Related]

  • 12. INCOMPOSITA: a MADS-box gene controlling prophyll development and floral meristem identity in Antirrhinum.
    Masiero S, Li MA, Will I, Hartmann U, Saedler H, Huijser P, Schwarz-Sommer Z, Sommer H.
    Development; 2004 Dec 01; 131(23):5981-90. PubMed ID: 15539492
    [Abstract] [Full Text] [Related]

  • 13. Multiple interactions amongst floral homeotic MADS box proteins.
    Davies B, Egea-Cortines M, de Andrade Silva E, Saedler H, Sommer H.
    EMBO J; 1996 Aug 15; 15(16):4330-43. PubMed ID: 8861961
    [Abstract] [Full Text] [Related]

  • 14. Epidermal control of floral organ identity by class B homeotic genes in Antirrhinum and Arabidopsis.
    Efremova N, Perbal MC, Yephremov A, Hofmann WA, Saedler H, Schwarz-Sommer Z.
    Development; 2001 Jul 15; 128(14):2661-71. PubMed ID: 11526073
    [Abstract] [Full Text] [Related]

  • 15. The S locus-linked Primula homeotic mutant sepaloid shows characteristics of a B-function mutant but does not result from mutation in a B-function gene.
    Li J, Webster M, Dudas B, Cook H, Manfield I, Davies B, Gilmartin PM.
    Plant J; 2008 Oct 15; 56(1):1-12. PubMed ID: 18564384
    [Abstract] [Full Text] [Related]

  • 16. Regulation of SUP expression identifies multiple regulators involved in arabidopsis floral meristem development.
    Sakai H, Krizek BA, Jacobsen SE, Meyerowitz EM.
    Plant Cell; 2000 Sep 15; 12(9):1607-18. PubMed ID: 11006335
    [Abstract] [Full Text] [Related]

  • 17. The gene FLORAL ORGAN NUMBER1 regulates floral meristem size in rice and encodes a leucine-rich repeat receptor kinase orthologous to Arabidopsis CLAVATA1.
    Suzaki T, Sato M, Ashikari M, Miyoshi M, Nagato Y, Hirano HY.
    Development; 2004 Nov 15; 131(22):5649-57. PubMed ID: 15509765
    [Abstract] [Full Text] [Related]

  • 18. ROSINA (RSI), a novel protein with DNA-binding capacity, acts during floral organ development in Antirrhinum majus.
    Roccaro M, Li Y, Masiero S, Saedler H, Sommer H.
    Plant J; 2005 Jul 15; 43(2):238-50. PubMed ID: 15998310
    [Abstract] [Full Text] [Related]

  • 19. Functional analysis of the Antirrhinum floral homeotic DEFICIENS gene in vivo and in vitro by using a temperature-sensitive mutant.
    Zachgo S, Silva Ede A, Motte P, Tröbner W, Saedler H, Schwarz-Sommer Z.
    Development; 1995 Sep 15; 121(9):2861-75. PubMed ID: 7555713
    [Abstract] [Full Text] [Related]

  • 20. Floral asymmetry involves an interplay between TCP and MYB transcription factors in Antirrhinum.
    Corley SB, Carpenter R, Copsey L, Coen E.
    Proc Natl Acad Sci U S A; 2005 Apr 05; 102(14):5068-73. PubMed ID: 15790677
    [Abstract] [Full Text] [Related]


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