scholarly article | Q13442814 |
P50 | author | C. Robertson McClung | Q71155080 |
P2093 | author name string | Jian Wu | |
Xiaowu Wang | |||
Feng Cheng | |||
Ping Lou | |||
Laura G Cressman | |||
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Does the core circadian clock in the moss Physcomitrella patens (Bryophyta) comprise a single loop? | Q33605392 | ||
Following tetraploidy in maize, a short deletion mechanism removed genes preferentially from one of the two homologs. | Q33627522 | ||
An expanding universe of circadian networks in higher plants | Q33838338 | ||
REVEILLE8 and PSEUDO-REPONSE REGULATOR5 form a negative feedback loop within the Arabidopsis circadian clock | Q33869625 | ||
Modeling gene and genome duplications in eukaryotes | Q33936694 | ||
PSEUDO-RESPONSE REGULATORS 9, 7, and 5 are transcriptional repressors in the Arabidopsis circadian clock. | Q34104306 | ||
The ELF4-ELF3-LUX complex links the circadian clock to diurnal control of hypocotyl growth | Q34200239 | ||
Biased gene fractionation and dominant gene expression among the subgenomes of Brassica rapa | Q34261809 | ||
Quantitative analysis of regulatory flexibility under changing environmental conditions | Q34439915 | ||
Genomewide nonadditive gene regulation in Arabidopsis allotetraploids | Q34587400 | ||
Segmental structure of the Brassica napus genome based on comparative analysis with Arabidopsis thaliana | Q34589707 | ||
A functional genomics approach reveals CHE as a component of the Arabidopsis circadian clock | Q34651457 | ||
Differentiation of the maize subgenomes by genome dominance and both ancient and ongoing gene loss | Q34651956 | ||
Network news: prime time for systems biology of the plant circadian clock. | Q34993876 | ||
Gene and genome duplications: the impact of dosage-sensitivity on the fate of nuclear genes | Q35006352 | ||
Proteasome function is required for biological timing throughout the twenty-four hour cycle | Q35007639 | ||
Multiple light inputs to a simple clock circuit allow complex biological rhythms | Q35087694 | ||
Altered patterns of fractionation and exon deletions in Brassica rapa support a two-step model of paleohexaploidy | Q35863144 | ||
Gene-balanced duplications, like tetraploidy, provide predictable drive to increase morphological complexity | Q36526608 | ||
Systems approach identifies an organic nitrogen-responsive gene network that is regulated by the master clock control gene CCA1 | Q36534251 | ||
Phytochrome-mediated development in land plants: red light sensing evolves to meet the challenges of changing light environments | Q36619649 | ||
The gene balance hypothesis: from classical genetics to modern genomics | Q36733469 | ||
How to usefully compare homologous plant genes and chromosomes as DNA sequences | Q37082931 | ||
REVEILLE1, a Myb-like transcription factor, integrates the circadian clock and auxin pathways | Q37377360 | ||
Thinking outside the F-box: novel ligands for novel receptors | Q37414804 | ||
The circadian system in higher plants | Q37539967 | ||
Bias in plant gene content following different sorts of duplication: tandem, whole-genome, segmental, or by transposition | Q37539972 | ||
Insights from the comparison of plant genome sequences | Q37742162 | ||
The genetics of plant clocks | Q37933776 | ||
Comparative evolution of photosynthetic genes in response to polyploid and nonpolyploid duplication | Q38503509 | ||
Following tetraploidy in an Arabidopsis ancestor, genes were removed preferentially from one homeolog leaving clusters enriched in dose-sensitive genes | Q41626345 | ||
ZEITLUPE encodes a novel clock-associated PAS protein from Arabidopsis | Q41740671 | ||
LUX ARRHYTHMO encodes a nighttime repressor of circadian gene expression in the Arabidopsis core clock | Q42123195 | ||
Mapping loci controlling flowering time in Brassica oleracea | Q42625307 | ||
EARLY FLOWERING4 recruitment of EARLY FLOWERING3 in the nucleus sustains the Arabidopsis circadian clock | Q42635968 | ||
Robust circadian rhythms of gene expression in Brassica rapa tissue culture. | Q43091625 | ||
The novel MYB protein EARLY-PHYTOCHROME-RESPONSIVE1 is a component of a slave circadian oscillator in Arabidopsis | Q44605399 | ||
Finding and comparing syntenic regions among Arabidopsis and the outgroups papaya, poplar, and grape: CoGe with rosids | Q46064782 | ||
F-box proteins FKF1 and LKP2 act in concert with ZEITLUPE to control Arabidopsis clock progression | Q46225771 | ||
PRR3 Is a vascular regulator of TOC1 stability in the Arabidopsis circadian clock | Q46564014 | ||
CIRCADIAN CLOCK ASSOCIATED1 and LATE ELONGATED HYPOCOTYL function synergistically in the circadian clock of Arabidopsis. | Q46582099 | ||
Two-phase resolution of polyploidy in the Arabidopsis metabolic network gives rise to relative and absolute dosage constraints | Q47301236 | ||
FKF1, a clock-controlled gene that regulates the transition to flowering in Arabidopsis | Q47854429 | ||
Rates of nucleotide substitution in angiosperm mitochondrial DNA sequences and dates of divergence between Brassica and other angiosperm lineages | Q47972929 | ||
Comparative mapping, genomic structure, and expression analysis of eight pseudo-response regulator genes in Brassica rapa | Q48050825 | ||
Clocks in the green lineage: comparative functional analysis of the circadian architecture of the picoeukaryote ostreococcus | Q48066883 | ||
Evolution of the class III HD-Zip gene family in land plants | Q48086422 | ||
Constitutive expression of CIR1 (RVE2) affects several circadian-regulated processes and seed germination in Arabidopsis | Q50303861 | ||
PSEUDO-RESPONSE REGULATORS, PRR9, PRR7 and PRR5, together play essential roles close to the circadian clock of Arabidopsis thaliana. | Q50772147 | ||
The F-box protein ZEITLUPE confers dosage-dependent control on the circadian clock, photomorphogenesis, and flowering time. | Q51029209 | ||
Evolutionary rate variation, genomic dominance and duplicate gene expression evolution during allotetraploid cotton speciation. | Q51642803 | ||
The role of the Arabidopsis morning loop components CCA1, LHY, PRR7, and PRR9 in temperature compensation. | Q51895069 | ||
Highly specific gene silencing by artificial microRNAs in Arabidopsis. | Q52023593 | ||
Phylogenetic analysis of the plant-specific zinc finger-homeobox and mini zinc finger gene families. | Q53532383 | ||
Isolation of circadian-associated genes in Brassica rapa by comparative genomics with Arabidopsis thaliana. | Q53572047 | ||
Comparative genomics of Brassica oleracea and Arabidopsis thaliana reveal gene loss, fragmentation, and dispersal after polyploidy | Q57007961 | ||
Weather and seasons together demand complex biological clocks | Q57120497 | ||
Overlapping and Distinct Roles of PRR7 and PRR9 in the Arabidopsis Circadian Clock | Q58456872 | ||
Detection and resolution of genetic loci affecting circadian period in Brassica oleracea | Q59303571 | ||
Phylogenetic analysis of Brassiceae based on the nucleotide sequences of the S-locus related gene, SLR1 | Q78971639 | ||
PSEUDO-RESPONSE REGULATOR 7 and 9 are partially redundant genes essential for the temperature responsiveness of the Arabidopsis circadian clock | Q81391270 | ||
Functional implication of the MYB transcription factor RVE8/LCL5 in the circadian control of histone acetylation | Q83124407 | ||
Genetic architecture of the circadian clock and flowering time in Brassica rapa | Q83907647 | ||
Heterologous expression and functional characterization of a Physcomitrella Pseudo response regulator homolog, PpPRR2, in Arabidopsis | Q83930274 | ||
P433 | issue | 6 | |
P921 | main subject | Brassica rapa | Q3384 |
whole genome sequencing | Q2068526 | ||
P304 | page(s) | 2415-2426 | |
P577 | publication date | 2012-06-08 | |
P1433 | published in | The Plant Cell | Q3988745 |
P1476 | title | Preferential retention of circadian clock genes during diploidization following whole genome triplication in Brassica rapa | |
P478 | volume | 24 |
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