251 related articles for article (PubMed ID: 21527418)
1. A double-flowered variety of lesser periwinkle (Vinca minor fl. pl.) that has persisted in the wild for more than 160 years.
Wang YQ; Melzer R; Theissen G
Ann Bot; 2011 Jun; 107(9):1445-52. PubMed ID: 21527418
[TBL] [Abstract][Full Text] [Related]
2. Molecular characterisation of four double-flowered mutants of Silene dioica representing four centuries of variation.
Ingle EK; Gilmartin PM
J Exp Bot; 2015 Jun; 66(11):3297-307. PubMed ID: 25878355
[TBL] [Abstract][Full Text] [Related]
3. Floral visitation and reproductive traits of Stamenoid petals, a naturally occurring floral homeotic variant of Capsella bursa-pastoris (Brassicaceae).
Ziermann J; Ritz MS; Hameister S; Abel C; Hoffmann MH; Neuffer B; Theissen G
Planta; 2009 Nov; 230(6):1239-49. PubMed ID: 19784670
[TBL] [Abstract][Full Text] [Related]
4. A comparison of early floral ontogeny in wild-type and floral homeotic mutant phenotypes of Primula.
Webster MA; Gilmartin PA
Planta; 2003 Apr; 216(6):903-17. PubMed ID: 12687358
[TBL] [Abstract][Full Text] [Related]
5. Isolation and characterization of the C-class MADS-box gene involved in the formation of double flowers in Japanese gentian.
Nakatsuka T; Saito M; Yamada E; Fujita K; Yamagishi N; Yoshikawa N; Nishihara M
BMC Plant Biol; 2015 Jul; 15():182. PubMed ID: 26183329
[TBL] [Abstract][Full Text] [Related]
6. Morphological and molecular analysis of a double-flowered mutant of the dioecious plant white campion showing both meristic and homeotic effects.
Scutt CP; Oliveira M; Gilmartin PM; Negrutiu I
Dev Genet; 1999 Sep; 25(3):267-79. PubMed ID: 10528267
[TBL] [Abstract][Full Text] [Related]
7. 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. PubMed ID: 18564384
[TBL] [Abstract][Full Text] [Related]
8. Floral patterning defects induced by Arabidopsis APETALA2 and microRNA172 expression in Nicotiana benthamiana.
Mlotshwa S; Yang Z; Kim Y; Chen X
Plant Mol Biol; 2006 Jul; 61(4-5):781-93. PubMed ID: 16897492
[TBL] [Abstract][Full Text] [Related]
9. STYLOSA and FISTULATA: regulatory components of the homeotic control of Antirrhinum floral organogenesis.
Motte P; Saedler H; Schwarz-Sommer Z
Development; 1998 Jan; 125(1):71-84. PubMed ID: 9389665
[TBL] [Abstract][Full Text] [Related]
10. Exploring the evolutionary origin of floral organs of Erycina pusilla, an emerging orchid model system.
Dirks-Mulder A; Butôt R; van Schaik P; Wijnands JW; van den Berg R; Krol L; Doebar S; van Kooperen K; de Boer H; Kramer EM; Smets EF; Vos RA; Vrijdaghs A; Gravendeel B
BMC Evol Biol; 2017 Mar; 17(1):89. PubMed ID: 28335712
[TBL] [Abstract][Full Text] [Related]
11. The whorl-specific action of a petunia class B floral homeotic gene.
Tsuchimoto S; Mayama T; van der Krol A; Ohtsubo E
Genes Cells; 2000 Feb; 5(2):89-99. PubMed ID: 10672040
[TBL] [Abstract][Full Text] [Related]
12. 'Who's who' in two different flower types of Calluna vulgaris (Ericaceae): morphological and molecular analyses of flower organ identity.
Borchert T; Eckardt K; Fuchs J; Krüger K; Hohe A
BMC Plant Biol; 2009 Dec; 9():148. PubMed ID: 20003430
[TBL] [Abstract][Full Text] [Related]
13. The double-corolla phenotype in the Hawaiian lobelioid genus Clermontia involves ectopic expression of PISTILLATA B-function MADS box gene homologs.
Hofer KA; Ruonala R; Albert VA
Evodevo; 2012 Nov; 3(1):26. PubMed ID: 23116179
[TBL] [Abstract][Full Text] [Related]
14. Unique morphological changes in plant pathogenic phytoplasma-infected petunia flowers are related to transcriptional regulation of floral homeotic genes in an organ-specific manner.
Himeno M; Neriya Y; Minato N; Miura C; Sugawara K; Ishii Y; Yamaji Y; Kakizawa S; Oshima K; Namba S
Plant J; 2011 Sep; 67(6):971-9. PubMed ID: 21605209
[TBL] [Abstract][Full Text] [Related]
15. Separation of AG function in floral meristem determinacy from that in reproductive organ identity by expressing antisense AG RNA.
Mizukami Y; Ma H
Plant Mol Biol; 1995 Aug; 28(5):767-84. PubMed ID: 7640351
[TBL] [Abstract][Full Text] [Related]
16. Functional analysis of B and C class floral organ genes in spinach demonstrates their role in sexual dimorphism.
Sather DN; Jovanovic M; Golenberg EM
BMC Plant Biol; 2010 Mar; 10():46. PubMed ID: 20226063
[TBL] [Abstract][Full Text] [Related]
17. Loss of deeply conserved C-class floral homeotic gene function and C- and E-class protein interaction in a double-flowered ranunculid mutant.
Galimba KD; Tolkin TR; Sullivan AM; Melzer R; Theißen G; Di Stilio VS
Proc Natl Acad Sci U S A; 2012 Aug; 109(34):E2267-75. PubMed ID: 22853954
[TBL] [Abstract][Full Text] [Related]
18. Are petals sterile stamens or bracts? The origin and evolution of petals in the core eudicots.
Ronse De Craene LP
Ann Bot; 2007 Sep; 100(3):621-30. PubMed ID: 17513305
[TBL] [Abstract][Full Text] [Related]
19. Evolution and genetic control of the floral ground plan.
Smyth DR
New Phytol; 2018 Oct; 220(1):70-86. PubMed ID: 29959892
[TBL] [Abstract][Full Text] [Related]
20. 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
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
