scholarly article | Q13442814 |
P50 | author | Trupti Joshi | Q42306087 |
Gunvant Patil | Q43285212 | ||
Henry T Nguyen | Q86166811 | ||
P2093 | author name string | Wei Chen | |
Song Li | |||
Saad Khan | |||
Raymond N Mutava | |||
Silvas J Prince | |||
Naeem H Syed | |||
Valliyodan Babu | |||
P2860 | cites work | Modelling the widespread effects of TOC1 signalling on the plant circadian clock and its outputs | Q21202768 |
LEA (late embryogenesis abundant) proteins and their encoding genes in Arabidopsis thaliana | Q21263184 | ||
LEA proteins prevent protein aggregation due to water stress | Q24535125 | ||
Arabidopsis circadian clock protein, TOC1, is a DNA-binding transcription factor | Q24630145 | ||
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Circadian Clock Genes Universally Control Key Agricultural Traits | Q26864980 | ||
Phylogeny.fr: robust phylogenetic analysis for the non-specialist | Q29547666 | ||
Alternative splicing mediates responses of the Arabidopsis circadian clock to temperature changes | Q30414157 | ||
Global transcriptome analysis reveals circadian regulation of key pathways in plant growth and development. | Q30440986 | ||
Genetic mechanisms conferring adaptation to submergence and drought in rice: simple or complex? | Q30596408 | ||
The circadian clock regulates auxin signaling and responses in Arabidopsis | Q33293377 | ||
RNA-seq analyses of multiple meristems of soybean: novel and alternative transcripts, evolutionary and functional implications | Q33358634 | ||
Integrating omic approaches for abiotic stress tolerance in soybean | Q33701336 | ||
Understanding abiotic stress tolerance mechanisms in soybean: a comparative evaluation of soybean response to drought and flooding stress | Q39284558 | ||
Thermoplasticity in the plant circadian clock: how plants tell the time-perature | Q41335948 | ||
Photosynthetic entrainment of the Arabidopsis thaliana circadian clock | Q41839335 | ||
Analysis of clock gene homologs using unifoliolates as target organs in soybean (Glycine max). | Q43445542 | ||
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CIRCADIAN CLOCK ASSOCIATED1 and LATE ELONGATED HYPOCOTYL function synergistically in the circadian clock of Arabidopsis. | Q46582099 | ||
Circadian rhythms confer a higher level of fitness to Arabidopsis plants. | Q46588457 | ||
Comparative transcriptome of diurnally oscillating genes and hormone-responsive genes in Arabidopsis thaliana: insight into circadian clock-controlled daily responses to common ambient stresses in plants | Q46803434 | ||
Global dissection of alternative splicing in paleopolyploid soybean | Q46912463 | ||
Overexpression of the vacuolar sugar carrier AtSWEET16 modifies germination, growth, and stress tolerance in Arabidopsis | Q48617947 | ||
Two splice variants of the IDD14 transcription factor competitively form nonfunctional heterodimers which may regulate starch metabolism. | Q50521048 | ||
Posttranslational regulation of CIRCADIAN CLOCK ASSOCIATED1 in the circadian oscillator of Arabidopsis. | Q50597962 | ||
Identification of two additional members of the tRNA isopentenyltransferase family in Physcomitrella patens. | Q50956719 | ||
Submergence tolerance in rice requires Sub1A, an ethylene-response-factor-like gene. | Q51997518 | ||
A Simple Analytical Method for High-Throughput Screening of Major Sugars from Soybean by Normal-Phase HPLC with Evaporative Light Scattering Detection | Q59104953 | ||
Circadian control of carbohydrate availability for growth in Arabidopsis plants at night | Q33927440 | ||
Reciprocal regulation between TOC1 and LHY/CCA1 within the Arabidopsis circadian clock. | Q34085869 | ||
Transcriptome survey reveals increased complexity of the alternative splicing landscape in Arabidopsis | Q34185155 | ||
Mapping the core of the Arabidopsis circadian clock defines the network structure of the oscillator | Q34259774 | ||
Plant circadian clocks increase photosynthesis, growth, survival, and competitive advantage | Q34436491 | ||
Circadian phase has profound effects on differential expression analysis | Q34490577 | ||
Sub1A is an ethylene-response-factor-like gene that confers submergence tolerance to rice | Q34555951 | ||
Abiotic stress and ABA-inducible Group 4 LEA from Brassica napus plays a key role in salt and drought tolerance | Q34600469 | ||
Biosynthesis of flavonoids and effects of stress | Q34605574 | ||
A functional genomics approach reveals CHE as a component of the Arabidopsis circadian clock | Q34651457 | ||
The ethylene response factors SNORKEL1 and SNORKEL2 allow rice to adapt to deep water | Q34998356 | ||
Natural diversity in daily rhythms of gene expression contributes to phenotypic variation | Q35031493 | ||
Allelic polymorphism of GIGANTEA is responsible for naturally occurring variation in circadian period in Brassica rapa | Q35229586 | ||
Soybean (Glycine max) SWEET gene family: insights through comparative genomics, transcriptome profiling and whole genome re-sequence analysis | Q35688445 | ||
Alternative splicing and nonsense-mediated decay modulate expression of important regulatory genes in Arabidopsis. | Q35860653 | ||
CCA1 alternative splicing as a way of linking the circadian clock to temperature response in Arabidopsis | Q36373179 | ||
Understanding regulatory networks and engineering for enhanced drought tolerance in plants | Q36398942 | ||
Loss of the circadian clock-associated protein 1 in Arabidopsis results in altered clock-regulated gene expression | Q36461391 | ||
Alternative splicing of pre-messenger RNAs in plants in the genomic era. | Q36707492 | ||
Submergence tolerance conferred by Sub1A is mediated by SLR1 and SLRL1 restriction of gibberellin responses in rice | Q36954993 | ||
Source-to-sink transport of sugar and regulation by environmental factors | Q37040996 | ||
Flooding stress: acclimations and genetic diversity | Q37150335 | ||
Physiological and molecular approaches to improve drought resistance in soybean | Q37527420 | ||
The circadian system in higher plants | Q37539967 | ||
Starch and the clock: the dark side of plant productivity | Q37826994 | ||
Abiotic stress and the plant circadian clock | Q37843253 | ||
Making sense of low oxygen sensing | Q37978973 | ||
Late Embryogenesis Abundant (LEA) proteins in legumes | Q38117371 | ||
Jasmonic acid transient accumulation is needed for abscisic acid increase in citrus roots under drought stress conditions. | Q38966661 | ||
The submergence tolerance regulator SUB1A mediates crosstalk between submergence and drought tolerance in rice | Q39013797 | ||
LEA proteins in higher plants: structure, function, gene expression and regulation | Q39076151 | ||
TOC1 functions as a molecular switch connecting the circadian clock with plant responses to drought | Q39168804 | ||
Diurnal oscillations of soybean circadian clock and drought responsive genes. | Q39214367 | ||
Arabidopsis transcriptome analysis under drought, cold, high-salinity and ABA treatment conditions using a tiling array | Q39225436 | ||
P433 | issue | 22 | |
P921 | main subject | drought | Q43059 |
alternative mRNA splicing, via spliceosome | Q21114084 | ||
P304 | page(s) | 7129-7149 | |
P577 | publication date | 2015-08-27 | |
P1433 | published in | Journal of Experimental Botany | Q6295179 |
P1476 | title | Core clock, SUB1, and ABAR genes mediate flooding and drought responses via alternative splicing in soybean | |
P478 | volume | 66 |
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Q38609470 | Evolutionarily Conserved Alternative Splicing Across Monocots. |
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Q57093123 | Molecular and physiological responses in roots of two full-sib poplars uncover mechanisms that contribute to differences in partial submergence tolerance |
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Q36991024 | Transcriptomic analysis of submergence-tolerant and sensitive Brachypodium distachyon ecotypes reveals oxidative stress as a major tolerance factor. |
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