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Recessive loci Pps-1 and OM differentially regulate PISTILLATA-1 and APETALA3-1 expression for sepal and petal development in Papaver somniferum.

Singh SK, Shukla AK, Dhawan OP, Shasany AK.

PLoS One. 2014 Jun 30;9(6):e101272. doi: 10.1371/journal.pone.0101272.


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;56(1):1-12. doi: 10.1111/j.1365-313X.2008.03584.x.


Poppy APETALA1/FRUITFULL orthologs control flowering time, branching, perianth identity, and fruit development.

Pabón-Mora N, Ambrose BA, Litt A.

Plant Physiol. 2012 Apr;158(4):1685-704. doi: 10.1104/pp.111.192104.


Characterization of the possible roles for B class MADS box genes in regulation of perianth formation in orchid.

Chang YY, Kao NH, Li JY, Hsu WH, Liang YL, Wu JW, Yang CH.

Plant Physiol. 2010 Feb;152(2):837-53. doi: 10.1104/pp.109.147116.


Co-modification of class B genes TfDEF and TfGLO in Torenia fournieri Lind. alters both flower morphology and inflorescence architecture.

Sasaki K, Yamaguchi H, Nakayama M, Aida R, Ohtsubo N.

Plant Mol Biol. 2014 Oct;86(3):319-34. doi: 10.1007/s11103-014-0231-8.


'Living stones' reveal alternative petal identity programs within the core eudicots.

Brockington SF, Rudall PJ, Frohlich MW, Oppenheimer DG, Soltis PS, Soltis DE.

Plant J. 2012 Jan;69(2):193-203. doi: 10.1111/j.1365-313X.2011.04797.x.


Petaloidy and petal identity MADS-box genes in the balsaminoid genera Impatiens and Marcgravia.

Geuten K, Becker A, Kaufmann K, Caris P, Janssens S, Viaene T, Theissen G, Smets E.

Plant J. 2006 Aug;47(4):501-18.


Mutation in Torenia fournieri Lind. UFO homolog confers loss of TfLFY interaction and results in a petal to sepal transformation.

Sasaki K, Yamaguchi H, Aida R, Shikata M, Abe T, Ohtsubo N.

Plant J. 2012 Sep;71(6):1002-14. doi: 10.1111/j.1365-313X.2012.05047.x.


The Petal-Specific InMYB1 Promoter Functions by Recognizing Petaloid Cells.

Azuma M, Mitsuda N, Goto K, Oshima Y, Ohme-Takagi M, Otagaki S, Matsumoto S, Shiratake K.

Plant Cell Physiol. 2016 Mar;57(3):580-7. doi: 10.1093/pcp/pcw017.


A soybean MADS-box protein modulates floral organ numbers, petal identity and sterility.

Huang F, Xu G, Chi Y, Liu H, Xue Q, Zhao T, Gai J, Yu D.

BMC Plant Biol. 2014 Apr 2;14:89. doi: 10.1186/1471-2229-14-89.


Heterotopic expression of class B floral homeotic genes supports a modified ABC model for tulip (Tulipa gesneriana).

Kanno A, Saeki H, Kameya T, Saedler H, Theissen G.

Plant Mol Biol. 2003 Jul;52(4):831-41.


Functional analyses of genetic pathways controlling petal specification in poppy.

Drea S, Hileman LC, de Martino G, Irish VF.

Development. 2007 Dec;134(23):4157-66.


Elaboration of B gene function to include the identity of novel floral organs in the lower eudicot Aquilegia.

Kramer EM, Holappa L, Gould B, Jaramillo MA, Setnikov D, Santiago PM.

Plant Cell. 2007 Mar;19(3):750-66.


A de novo floral transcriptome reveals clues into Phalaenopsis orchid flower development.

Huang JZ, Lin CP, Cheng TC, Chang BC, Cheng SY, Chen YW, Lee CY, Chin SW, Chen FC.

PLoS One. 2015 May 13;10(5):e0123474. doi: 10.1371/journal.pone.0123474.


"The usual suspects"- analysis of transcriptome sequences reveals deviating B gene activity in C. vulgaris bud bloomers.

Behrend A, Borchert T, Hohe A.

BMC Plant Biol. 2015 Jan 21;15:8. doi: 10.1186/s12870-014-0407-z.


The differentiation of sepal and petal morphologies in Commelinaceae.

Ochiai T, Nakamura T, Mashiko Y, Fukuda T, Yokoyama J, Kanno A, Kameya T.

Gene. 2004 Dec 22;343(2):253-62.

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