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Genome-Wide Characterization and Expression of the Myb-Cc Gene Family in Salvia Miltiorrhiza Andsmmyb-Cc7-Mediated Response to Phosphate Starvation in Arabidopsis

https://doi.org/10.2139/ssrn.4837258
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inferredcites →https://doi.org/10.1002/tpg2.20041openalex-extracted
A high‐quality reference genome sequence of Salvia miltiorrhiza provides insights into tanshinone synthesis in its red rhizomes
inferredcites →https://doi.org/10.1007/978-94-011-0221-6_1openalex-extracted
Global extent, development and economic impact of acid soils
inferredcites →https://doi.org/10.1007/bf00009558openalex-extracted
Global extent, development and economic impact of acid soils
inferredcites →https://doi.org/10.1007/s00299-016-2007-xopenalex-extracted
Phosphate starvation promoted the accumulation of phenolic acids by inducing the key enzyme genes in Salvia miltiorrhiza hairy roots
inferredcites →https://doi.org/10.1007/s10709-018-0042-yopenalex-extracted
Genome-wide analysis of the MYB-CC gene family of maize
inferredcites →https://doi.org/10.1016/j.biochi.2006.05.007openalex-extracted
Phosphate deficiency promotes modification of iron distribution in Arabidopsis plants
inferredcites →https://doi.org/10.1016/j.cell.2021.09.030openalex-extracted
A phosphate starvation response-centered network regulates mycorrhizal symbiosis
inferredcites →https://doi.org/10.1016/j.molp.2020.06.009openalex-extracted
TBtools: An Integrative Toolkit Developed for Interactive Analyses of Big Biological Data
inferredcites →https://doi.org/10.1016/j.pbi.2017.07.006openalex-extracted
The world according to GARP transcription factors
inferredcites →https://doi.org/10.1016/j.plantsci.2018.12.025openalex-extracted
The FvPHR1 transcription factor control phosphate homeostasis by transcriptionally regulating miR399a in woodland strawberry
inferredcites →https://doi.org/10.1016/j.plaphy.2022.12.021openalex-extracted
Characterization of phosphate transporter genes and the function of SgPT1 involved in phosphate uptake in Stylosanthes guianensis
inferredcites →https://doi.org/10.1016/j.plaphy.2023.01.029openalex-extracted
Molecular mechanism of phosphorous signaling inducing anthocyanin accumulation in Arabidopsis
inferredcites →https://doi.org/10.1016/j.plaphy.2023.02.043openalex-extracted
Phosphorous fertilization alleviates shading stress by regulating leaf photosynthesis and the antioxidant system in mung bean (Vigna radiata L.)
inferredcites →https://doi.org/10.1016/j.plaphy.2023.03.008openalex-extracted
Arbuscular mycorrhiza fungus alleviates arsenic mediated disturbances in tricarboxylic acid cycle and nitrogen metabolism in Triticum aestivum L.
inferredcites →https://doi.org/10.1016/j.tplants.2006.10.007openalex-extracted
How do plants respond to nutrient shortage by biomass allocation?
inferredcites →https://doi.org/10.1038/aps.2017.191openalex-extracted
Different network pharmacology mechanisms of Danshen-based Fangjis in the treatment of stable angina
inferredcites →https://doi.org/10.1038/nature21417openalex-extracted
Root microbiota drive direct integration of phosphate stress and immunity
inferredcites →https://doi.org/10.1038/ncomms2512openalex-extracted
A new class of plant lipid is essential for protection against phosphorus depletion
inferredcites →https://doi.org/10.1038/nrmicro1987openalex-extracted
Arbuscular mycorrhiza: the mother of plant root endosymbioses
inferredcites →https://doi.org/10.1038/s41477-022-01231-wopenalex-extracted
SHORT-ROOT stabilizes PHOSPHATE1 to regulate phosphate allocation in Arabidopsis
inferredcites →https://doi.org/10.1038/srep43320openalex-extracted
Targeted mutagenesis in the medicinal plant Salvia miltiorrhiza
inferredcites →https://doi.org/10.1073/pnas.2535513100openalex-extracted
The early stages of duplicate gene evolution
inferredcites →https://doi.org/10.1093/jxb/ert238openalex-extracted
Soybean GmbZIP123 gene enhances lipid content in the seeds of transgenic Arabidopsis plants
inferredcites →https://doi.org/10.1093/jxb/eru535openalex-extracted
The transcription factor PHR1 regulates lipid remodeling and triacylglycerol accumulation in Arabidopsis thaliana during phosphorus starvation
inferredcites →https://doi.org/10.1093/pcp/pcab007openalex-extracted
A Citrus Phosphate Starvation Response Factor CsPHL3 Negatively Regulates Carotenoid Metabolism
inferredcites →https://doi.org/10.1093/plphys/kiaa115openalex-extracted
Phosphorus deprivation affects composition and spatial distribution of membrane lipids in legume nodules
inferredcites →https://doi.org/10.1093/plphys/kiac521openalex-extracted
PHOSPHATE RESPONSE 1 family members act distinctly to regulate transcriptional responses to phosphate starvation
inferredcites →https://doi.org/10.1101/gad.204401openalex-extracted
A conserved MYB transcription factor involved in phosphate starvation signaling both in vascular plants and in unicellular algae
inferredcites →https://doi.org/10.1101/gr.4197006openalex-extracted
Evolution of alternative splicing after gene duplication
inferredcites →https://doi.org/10.1104/pp.107.111443openalex-extracted
OsPHR2 Is Involved in Phosphate-Starvation Signaling and Excessive Phosphate Accumulation in Shoots of Plants
inferredcites →https://doi.org/10.1104/pp.111.175232openalex-extracted
Phosphorus Dynamics: From Soil to Plant
inferredcites →https://doi.org/10.1104/pp.15.00695openalex-extracted
Functional divergence of diterpene syntheses in the medicinal plant Salvia miltiorrhiza Bunge
inferredcites →https://doi.org/10.1104/pp.15.01336openalex-extracted
Arabidopsis PHL2 and PHR1 Act Redundantly as the Key Components of the Central Regulatory System Controlling Transcriptional Responses to Phosphate Starvation
inferredcites →https://doi.org/10.1104/pp.17.01713openalex-extracted
The ARF7 and ARF19 Transcription Factors Positively Regulate PHOSPHATE STARVATION RESPONSE1 in Arabidopsis Roots
inferredcites →https://doi.org/10.1105/tpc.114.123208openalex-extracted
SPX4 Negatively Regulates Phosphate Signaling and Homeostasis through Its Interaction with PHR2 in Rice
inferredcites →https://doi.org/10.1111/j.1365-3040.2007.01734.xopenalex-extracted
Increased expression of the MYB‐related transcription factor, PHR1, leads to enhanced phosphate uptake in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/jipb.13090openalex-extracted
Root developmental responses to phosphorus nutrition
inferredcites →https://doi.org/10.1111/ppl.13503openalex-extracted
SlPHL1 , a MYB‐CC transcription factor identified from tomato, positively regulates the phosphate starvation response
inferredcites →https://doi.org/10.1126/science.290.5499.2105openalex-extracted
Arabidopsis Transcription Factors: Genome-Wide Comparative Analysis Among Eukaryotes
inferredcites →https://doi.org/10.1126/science.aba0196openalex-extracted
A plant’s diet, surviving in a variable nutrient environment
inferredcites →https://doi.org/10.1371/journal.pgen.1001102openalex-extracted
A Central Regulatory System Largely Controls Transcriptional Activation and Repression Responses to Phosphate Starvation in Arabidopsis
inferredcites →https://doi.org/10.1371/journal.pone.0044005openalex-extracted
Brassica napus PHR1 Gene Encoding a MYB-Like Protein Functions in Response to Phosphate Starvation
inferredcites →https://doi.org/10.2144/05391rv01openalex-extracted
Real-Time PCR for mRNA Quantitation
inferredcites →https://doi.org/10.3389/fpls.2022.914648openalex-extracted
Involvement of PtPHR1 in phosphates starvation-induced alkaloid biosynthesis in Pinellia ternata (Thunb.) Breit
inferredcites →https://doi.org/10.3390/genes10121018openalex-extracted
Plant PHR Transcription Factors: Put on A Map
inferredcites →https://doi.org/10.3390/ijerph14070695openalex-extracted
Contrasting Eutrophication Risks and Countermeasures in Different Water Bodies: Assessments to Support Targeted Watershed Management
inferredcites →https://doi.org/10.3390/ijms24108461openalex-extracted
Genome-Wide Characterization and Expression of the Hsf Gene Family in Salvia miltiorrhiza (Danshen) and the Potential Thermotolerance of SmHsf1 and SmHsf7 in Yeast
inferredcites →https://doi.org/10.3390/molecules23051132openalex-extracted
Salvia castanea Hairy Roots are More Tolerant to Phosphate Deficiency than Salvia miltiorrhiza Hairy Roots Based on the Secondary Metabolism and Antioxidant Defenses
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