205 related articles for article (PubMed ID: 23772833)
1. Molecular control of normal and acrocona mutant seed cone development in Norway spruce (Picea abies) and the evolution of conifer ovule-bearing organs.
Carlsbecker A; Sundström JF; Englund M; Uddenberg D; Izquierdo L; Kvarnheden A; Vergara-Silva F; Engström P
New Phytol; 2013 Oct; 200(1):261-275. PubMed ID: 23772833
[TBL] [Abstract][Full Text] [Related]
2. Early cone setting in Picea abies acrocona is associated with increased transcriptional activity of a MADS box transcription factor.
Uddenberg D; Reimegård J; Clapham D; Almqvist C; von Arnold S; Emanuelsson O; Sundström JF
Plant Physiol; 2013 Feb; 161(2):813-23. PubMed ID: 23221834
[TBL] [Abstract][Full Text] [Related]
3. When paleontology and molecular genetics meet: a genetic context for the evolution of conifer ovuliferous scales.
Ruelens P; Geuten K
New Phytol; 2013 Oct; 200(1):10-12. PubMed ID: 24032566
[No Abstract] [Full Text] [Related]
4. The DAL10 gene from Norway spruce (Picea abies) belongs to a potentially gymnosperm-specific subclass of MADS-box genes and is specifically active in seed cones and pollen cones.
Carlsbecker A; Sundström J; Tandre K; Englund M; Kvarnheden A; Johanson U; Engström P
Evol Dev; 2003; 5(6):551-61. PubMed ID: 14984037
[TBL] [Abstract][Full Text] [Related]
5. AGAMOUS subfamily MADS-box genes and the evolution of seed cone morphology in Cupressaceae and Taxodiaceae.
Groth E; Tandre K; Engström P; Vergara-Silva F
Evol Dev; 2011; 13(2):159-70. PubMed ID: 21410872
[TBL] [Abstract][Full Text] [Related]
6. Cone-setting in spruce is regulated by conserved elements of the age-dependent flowering pathway.
Akhter S; Westrin KJ; Zivi N; Nordal V; Kretzschmar WW; Delhomme N; Street NR; Nilsson O; Emanuelsson O; Sundström JF
New Phytol; 2022 Dec; 236(5):1951-1963. PubMed ID: 36076311
[TBL] [Abstract][Full Text] [Related]
7. MADS goes genomic in conifers: towards determining the ancestral set of MADS-box genes in seed plants.
Gramzow L; Weilandt L; Theißen G
Ann Bot; 2014 Nov; 114(7):1407-29. PubMed ID: 24854168
[TBL] [Abstract][Full Text] [Related]
8. Conservation of gene structure and activity in the regulation of reproductive organ development of conifers and angiosperms.
Tandre K; Svenson M; Svensson ME; Engström P
Plant J; 1998 Sep; 15(5):615-23. PubMed ID: 9778844
[TBL] [Abstract][Full Text] [Related]
9. The MADS-box gene DAL1 is a potential mediator of the juvenile-to-adult transition in Norway spruce (Picea abies).
Carlsbecker A; Tandre K; Johanson U; Englund M; Engström P
Plant J; 2004 Nov; 40(4):546-57. PubMed ID: 15500470
[TBL] [Abstract][Full Text] [Related]
10. Conifer homologues to genes that control floral development in angiosperms.
Tandre K; Albert VA; Sundås A; Engström P
Plant Mol Biol; 1995 Jan; 27(1):69-78. PubMed ID: 7865797
[TBL] [Abstract][Full Text] [Related]
11. APETALA2 like genes from Picea abies show functional similarities to their Arabidopsis homologues.
Nilsson L; Carlsbecker A; Sundås-Larsson A; Vahala T
Planta; 2007 Feb; 225(3):589-602. PubMed ID: 16953432
[TBL] [Abstract][Full Text] [Related]
12. MADS-box genes active in developing pollen cones of Norway spruce (Picea abies) are homologous to the B-class floral homeotic genes in angiosperms.
Sundström J; Carlsbecker A; Svensson ME; Svenson M; Johanson U; Theissen G; Engström P
Dev Genet; 1999 Sep; 25(3):253-66. PubMed ID: 10528266
[TBL] [Abstract][Full Text] [Related]
13. The WUSCHEL-RELATED HOMEOBOX 3 gene PaWOX3 regulates lateral organ formation in Norway spruce.
Alvarez JM; Sohlberg J; Engström P; Zhu T; Englund M; Moschou PN; von Arnold S
New Phytol; 2015 Dec; 208(4):1078-88. PubMed ID: 26115363
[TBL] [Abstract][Full Text] [Related]
14. Conifer reproductive development involves B-type MADS-box genes with distinct and different activities in male organ primordia.
Sundström J; Engström P
Plant J; 2002 Jul; 31(2):161-9. PubMed ID: 12121446
[TBL] [Abstract][Full Text] [Related]
15. Morphological "primary homology" and expression of AG-subfamily MADS-box genes in pines, podocarps, and yews.
Englund M; Carlsbecker A; Engström P; Vergara-Silva F
Evol Dev; 2011; 13(2):171-81. PubMed ID: 21410873
[TBL] [Abstract][Full Text] [Related]
16. Characterization of an AGAMOUS homologue from the conifer black spruce (Picea mariana) that produces floral homeotic conversions when expressed in Arabidopsis.
Rutledge R; Regan S; Nicolas O; Fobert P; Côté C; Bosnich W; Kauffeldt C; Sunohara G; Séguin A; Stewart D
Plant J; 1998 Sep; 15(5):625-34. PubMed ID: 9778845
[TBL] [Abstract][Full Text] [Related]
17. High expression of putative aquaporin genes in cells with transporting and nutritive functions during seed development in Norway spruce (Picea abies).
Hakman I; Oliviusson P
J Exp Bot; 2002 Apr; 53(369):639-49. PubMed ID: 11886883
[TBL] [Abstract][Full Text] [Related]
18. Evolution of AGL6-like MADS box genes in grasses (Poaceae): ovule expression is ancient and palea expression is new.
Reinheimer R; Kellogg EA
Plant Cell; 2009 Sep; 21(9):2591-605. PubMed ID: 19749151
[TBL] [Abstract][Full Text] [Related]
19. Characterization of MADS genes in the gymnosperm Gnetum parvifolium and its implication on the evolution of reproductive organs in seed plants.
Shindo S; Ito M; Ueda K; Kato M; Hasebe M
Evol Dev; 1999; 1(3):180-90. PubMed ID: 11324103
[TBL] [Abstract][Full Text] [Related]
20. The petunia AGL6 gene has a SEPALLATA-like function in floral patterning.
Rijpkema AS; Zethof J; Gerats T; Vandenbussche M
Plant J; 2009 Oct; 60(1):1-9. PubMed ID: 19453449
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
