scholarly article | Q13442814 |
P50 | author | Keiichi Mochida | Q55189009 |
Shigeo Takumi | Q60973216 | ||
Kanako Kawaura | Q114316276 | ||
Yasunari Ogihara | Q114316277 | ||
P2093 | author name string | Koji Murai | |
Naoki Shitsukawa | |||
Tomoaki Shimizu | |||
Chizuru Hirabayashi | |||
Chikako Tahira | |||
Ken-Ichiro Kassai | |||
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B and C floral organ identity functions require SEPALLATA MADS-box genes | Q28144934 | ||
The SEP4 gene of Arabidopsis thaliana functions in floral organ and meristem identity | Q28291983 | ||
Sequence elimination and cytosine methylation are rapid and reproducible responses of the genome to wide hybridization and allopolyploidy in wheat | Q28345504 | ||
Molecular and genetic mechanisms of floral control | Q28755419 | ||
Conservation of B class gene expression in the second whorl of a basal grass and outgroups links the origin of lodicules and petals | Q28763748 | ||
Stochastic and epigenetic changes of gene expression in Arabidopsis polyploids | Q28768687 | ||
Duplication and Diversification in the APETALA1/FRUITFULL Floral Homeotic Gene Lineage: Implications for the Evolution of Floral Development | Q28768947 | ||
Two rice MADS domain proteins interact with OsMADS1. | Q30654423 | ||
Allopolyploidy-induced rapid genome evolution in the wheat (Aegilops-Triticum) group | Q30657840 | ||
Cloning, mapping and expression analysis of barley MADS-box genes. | Q30885010 | ||
Correlated clustering and virtual display of gene expression patterns in the wheat life cycle by large-scale statistical analyses of expressed sequence tags | Q30895721 | ||
Expression of MADS box genes ZMM8 and ZMM14 during inflorescence development of Zea mays discriminates between the upper and the lower floret of each spikelet | Q33333825 | ||
Ternary complex formation between the MADS-box proteins SQUAMOSA, DEFICIENS and GLOBOSA is involved in the control of floral architecture in Antirrhinum majus | Q33334017 | ||
Redundant regulation of meristem identity and plant architecture by FRUITFULL, APETALA1 and CAULIFLOWER. | Q33334279 | ||
Spatially and temporally regulated expression of rice MADS box genes with similarity to Arabidopsis class A, B and C genes | Q33334886 | ||
Ectopic expression of rice OsMADS1 reveals a role in specifying the lemma and palea, grass floral organs analogous to sepals | Q33335769 | ||
Positional cloning of the wheat vernalization gene VRN1 | Q33338351 | ||
Two Lily SEPALLATA-Like Genes Cause Different Effects on Floral Formation and Floral Transition in Arabidopsis | Q33339298 | ||
The YABBY gene DROOPING LEAF regulates carpel specification and midrib development in Oryza sativa. | Q33339550 | ||
Heterogeneous expression patterns and separate roles of the SEPALLATA gene LEAFY HULL STERILE1 in grasses | Q33340139 | ||
Overexpression of TaMADS1, a SEPALLATA-like gene in wheat, causes early flowering and the abnormal development of floral organs in Arabidopsis | Q33341609 | ||
Conservation of the E-function for floral organ identity in rice revealed by the analysis of tissue culture-induced loss-of-function mutants of the OsMADS1 gene | Q33341682 | ||
Function and diversification of MADS-box genes in rice. | Q51997643 | ||
TaVRT-1, a putative transcription factor associated with vegetative to reproductive transition in cereals. | Q52101786 | ||
Identification of class B and class C floral organ identity genes from rice plants. | Q52228677 | ||
Complexes of MADS-box proteins are sufficient to convert leaves into floral organs | Q56836177 | ||
Functional characterization of OsMADS18, a member of the AP1/SQUA subfamily of MADS box genes | Q58675672 | ||
Ovule-specific MADS-box proteins have conserved protein-protein interactions in monocot and dicot plants | Q58675731 | ||
Allopolyploidy alters gene expression in the highly stable hexaploid wheat | Q73659220 | ||
Rapid genomic changes in newly synthesized amphiploids of Triticum and Aegilops. II. Changes in low-copy coding DNA sequences | Q77489554 | ||
SUPERWOMAN1 and DROOPING LEAF genes control floral organ identity in rice | Q78728638 | ||
Discrimination of homoeologous gene expression in hexaploid wheat by SNP analysis of contigs grouped from a large number of expressed sequence tags | Q79243428 | ||
Homoeologous gene silencing in hexaploid wheat | Q80086966 | ||
OsMADS1, a rice MADS-box factor, controls differentiation of specific cell types in the lemma and palea and is an early-acting regulator of inner floral organs | Q81175653 | ||
Sequence evidence for sporadic intergeneric DNA introgression from wheat into a wild Aegilops species | Q81880535 | ||
Functional diversification of the two C-class MADS box genes OSMADS3 and OSMADS58 in Oryza sativa | Q33341862 | ||
WFL, a wheat FLORICAULA/LEAFY ortholog, is associated with spikelet formation as lateral branch of the inflorescence meristem | Q33342312 | ||
Multiple interactions amongst floral homeotic MADS box proteins. | Q33367826 | ||
MADS box genes expressed in developing inflorescences of rice and sorghum. | Q33368022 | ||
Three genomes differentially contribute to the biosynthesis of benzoxazinones in hexaploid wheat | Q34132228 | ||
Genes duplicated by polyploidy show unequal contributions to the transcriptome and organ-specific reciprocal silencing | Q34532390 | ||
Gene loss, silencing and activation in a newly synthesized wheat allotetraploid. | Q34614890 | ||
Types and rates of sequence evolution at the high-molecular-weight glutenin locus in hexaploid wheat and its ancestral genomes | Q35176082 | ||
Allopolyploidy--a shaping force in the evolution of wheat genomes | Q36064549 | ||
MIKC-type MADS-domain proteins: structural modularity, protein interactions and network evolution in land plants | Q36074852 | ||
Flower development and evolution: gene duplication, diversification and redeployment | Q36167347 | ||
Protein-coding genes are epigenetically regulated in Arabidopsis polyploids | Q36234675 | ||
Functional conservation of MADS-box factors controlling floral organ identity in rice and Arabidopsis. | Q36591930 | ||
MADS box genes control vernalization-induced flowering in cereals. | Q36690232 | ||
Gene dosage and stochastic effects determine the severity and direction of uniparental ribosomal RNA gene silencing (nucleolar dominance) in Arabidopsis allopolyploids | Q36757679 | ||
Molecular and genetic analyses of the silky1 gene reveal conservation in floral organ specification between eudicots and monocots | Q41745278 | ||
Organ-specific silencing of duplicated genes in a newly synthesized cotton allotetraploid | Q41958784 | ||
leafy hull sterile1 is a homeotic mutation in a rice MADS box gene affecting rice flower development | Q42627903 | ||
Rapid elimination of low-copy DNA sequences in polyploid wheat: a possible mechanism for differentiation of homoeologous chromosomes | Q42968076 | ||
Conversion of leaves into petals in Arabidopsis | Q44908356 | ||
WAP1, a wheat APETALA1 homolog, plays a central role in the phase transition from vegetative to reproductive growth | Q45047462 | ||
Conservation of B-class floral homeotic gene function between maize and Arabidopsis | Q46493450 | ||
Patterns of sequence loss and cytosine methylation within a population of newly resynthesized Brassica napus allopolyploids | Q46868173 | ||
OsMADS13, a novel rice MADS-box gene expressed during ovule development | Q47918500 | ||
Early flowering and reduced apical dominance result from ectopic expression of a rice MADS box gene | Q48078625 | ||
Expression profile of two storage-protein gene families in hexaploid wheat revealed by large-scale analysis of expressed sequence tags | Q48111756 | ||
Molecular basis of evolutionary events that shaped the hardness locus in diploid and polyploid wheat species (Triticum and Aegilops). | Q48148034 | ||
Pistillody is caused by alterations to the class-B MADS-box gene expression pattern in alloplasmic wheats | Q48217912 | ||
Characterization and functional analysis of three wheat genes with homology to the CONSTANS flowering time gene in transgenic rice | Q48228445 | ||
The MADS box gene FBP2 is required for SEPALLATA function in petunia | Q48252729 | ||
Pistillody, homeotic transformation of stamens into pistil-like structures, caused by nuclear-cytoplasm interaction in wheat. | Q48317894 | ||
P275 | copyright license | Creative Commons Attribution-NonCommercial 4.0 International | Q34179348 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 6 | |
P921 | main subject | wheat | Q15645384 |
P304 | page(s) | 1723-1737 | |
P577 | publication date | 2007-06-22 | |
P1433 | published in | The Plant Cell | Q3988745 |
P1476 | title | Genetic and epigenetic alteration among three homoeologous genes of a class E MADS box gene in hexaploid wheat. | |
P478 | volume | 19 |
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Q47946244 | Altered expression of the TaRSL2 gene contributed to variation in root hair length during allopolyploid wheat evolution |
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Q38730733 | Creating Order from Chaos: Epigenome Dynamics in Plants with Complex Genomes. |
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Q45917133 | Ectopic expression of two MADS box genes from orchid (Oncidium Gower Ramsey) and lily (Lilium longiflorum) alters flower transition and formation in Eustoma grandiflorum. |
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