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Arabidopsis PPC2 is crucial for growth at low CO 2 by involvement in photorespiratory metabolism and integration of ABI5
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Effects of altered phosphoenolpyruvate carboxylase activities on transgenic C3 plant Solanum tuberosum
inferredcites →https://doi.org/10.1007/s00425-016-2556-9openalex-snapshot
Phosphoenolpyruvate carboxylase (PEPC) and PEPC-kinase (PEPC-k) isoenzymes in Arabidopsis thaliana: role in control and abiotic stress conditions
inferredcites →https://doi.org/10.1007/s13197-017-2838-7openalex-snapshot
Free amino acids profile of Polish and Slovak honeys based on LC–MS/MS method without the prior derivatisation
inferredcites →https://doi.org/10.1016/s1360-1385(97)01046-7openalex-snapshot
Positional cloning for pathogen resistance
inferredcites →https://doi.org/10.1016/s1360-1385(97)89548-9openalex-snapshot
Regulatory phosphorylation of C4 PEP carboxylase
inferredcites →https://doi.org/10.1038/ncomms5636openalex-snapshot
Phytochrome-interacting transcription factors PIF4 and PIF5 induce leaf senescence in Arabidopsis
inferredcites →https://doi.org/10.1038/nprot.2007.199openalex-snapshot
Arabidopsis mesophyll protoplasts: a versatile cell system for transient gene expression analysis
inferredcites →https://doi.org/10.1046/j.1365-3040.2002.00866.xopenalex-snapshot
How does photorespiration modulate leaf amino acid contents? A dual approach through modelling and metabolite analysis
inferredcites →https://doi.org/10.1046/j.1365-313x.1999.00591.xopenalex-snapshot
Glycine and serine catabolism in non‐photosynthetic higher plant cells: their role in C1 metabolism
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.01185.xopenalex-snapshot
ABA plays a central role in mediating the regulatory effects of nitrate on root branching in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0404388101openalex-snapshot
Nitrate assimilation in plant shoots depends on photorespiration
inferredcites →https://doi.org/10.1073/pnas.081594298openalex-snapshot
A postgermination developmental arrest checkpoint is mediated by abscisic acid and requires the ABI5 transcription factor in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0913127107openalex-snapshot
Phospho enol pyruvate carboxylase intrinsically located in the chloroplast of rice plays a crucial role in ammonium assimilation
inferredcites →https://doi.org/10.1073/pnas.1319485111openalex-snapshot
Isotopically nonstationary 13 C flux analysis of changes in Arabidopsis thaliana leaf metabolism due to high light acclimation
inferredcites →https://doi.org/10.1073/pnas.77.5.2684openalex-snapshot
Photorespiration mutants of Arabidopsis thaliana deficient in serine-glyoxylate aminotransferase activity
inferredcites →https://doi.org/10.1093/aob/mcn227openalex-snapshot
Transcription factors and regulation of photosynthetic and related metabolism under environmental stresses
inferredcites →https://doi.org/10.1093/jxb/erm121openalex-snapshot
Glutamate in plants: metabolism, regulation, and signalling
inferredcites →https://doi.org/10.1093/jxb/eru193openalex-snapshot
Was low CO2 a driving force of C4 evolution: Arabidopsis responses to long-term low CO2 stress
inferredcites →https://doi.org/10.1093/jxb/ery095openalex-snapshot
CO2 availability influences hydraulic function of C3 and C4 grass leaves
inferredcites →https://doi.org/10.1104/pp.008201openalex-snapshot
Bundle Sheath Diffusive Resistance to CO2 and Effectiveness of C4 Photosynthesis and Refixation of Photorespired CO2 in a C4 Cycle Mutant and Wild-Type Amaranthus edulis
inferredcites →https://doi.org/10.1104/pp.106.092320openalex-snapshot
Repression of theLEAFY COTYLEDON 1/B3Regulatory Network in Plant Embryo Development byVP1/ABSCISIC ACID INSENSITIVE 3-LIKEB3 Genes
inferredcites →https://doi.org/10.1104/pp.110.161612openalex-snapshot
Mitochondrial Malate Dehydrogenase Lowers Leaf Respiration and Alters Photorespiration and Plant Growth in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.111.175950openalex-snapshot
ABI4 Activates DGAT1 Expression in Arabidopsis Seedlings during Nitrogen Deficiency
inferredcites →https://doi.org/10.1104/pp.114.254474openalex-snapshot
Phosphoenolpyruvate Carboxylase in Arabidopsis Leaves Plays a Crucial Role in Carbon and Nitrogen Metabolism
inferredcites →https://doi.org/10.1104/pp.83.4.820openalex-snapshot
A Possible Role for Abscisic Acid in Regulation of Photosynthetic and Photorespiratory Carbon Metabolism in Barley Leaves
inferredcites →https://doi.org/10.1104/pp.84.3.696openalex-snapshot
The Effect of Abscisic Acid and Other Inhibitors on Photosynthetic Capacity and the Biochemistry of CO2 Assimilation
inferredcites →https://doi.org/10.1105/tpc.010441openalex-snapshot
Abscisic Acid Signaling in Seeds and Seedlings
inferredcites →https://doi.org/10.1105/tpc.10.6.1043openalex-snapshot
The Arabidopsis Abscisic Acid Response Locus ABI4 Encodes an APETALA2 Domain Protein
inferredcites →https://doi.org/10.1105/tpc.12.4.599openalex-snapshot
The Arabidopsis Abscisic Acid Response Gene ABI5 Encodes a Basic Leucine Zipper Transcription Factor
inferredcites →https://doi.org/10.1105/tpc.15.00105openalex-snapshot
Mitochondrial Dihydrolipoyl Dehydrogenase Activity Shapes Photosynthesis and Photorespiration of Arabidopsis thaliana
inferredcites →https://doi.org/10.1105/tpc.4.10.1251openalex-snapshot
Isolation of the Arabidopsis ABI3 Gene by Positional Cloning
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02617.xopenalex-snapshot
Gateway‐compatible vectors for plant functional genomics and proteomics
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03441.xopenalex-snapshot
Plant responses to low [CO2] of the past
inferredcites →https://doi.org/10.1111/nph.14719openalex-snapshot
Direct assessment of the metabolic origin of carbon atoms in glutamate from illuminated leaves using 13C‐ NMR
inferredcites →https://doi.org/10.1111/nph.15500openalex-snapshot
In vivo phospho enol pyruvate carboxylase activity is controlled by CO 2 and O 2 mole fractions and represents a major flux at high photorespiration rates
inferredcites →https://doi.org/10.1111/nph.15828openalex-snapshot
Net photosynthetic CO 2 assimilation: more than just CO 2 and O2 reduction cycles
inferredcites →https://doi.org/10.1111/pce.12098openalex-snapshot
Steady‐state models of photosynthesis
inferredcites →https://doi.org/10.1111/plb.12020openalex-snapshot
D ‐2‐hydroxyglutarate metabolism is linked to photorespiration in the shm1‐1 mutant
inferredcites →https://doi.org/10.1146/annurev.arplant.47.1.273openalex-snapshot
PHOSPHO ENOL PYRUVATE CARBOXYLASE: A Ubiquitous, Highly Regulated Enzyme in Plants
inferredcites →https://doi.org/10.1146/annurev.arplant.57.032905.105444openalex-snapshot
TRANSCRIPTIONAL REGULATORY NETWORKS IN CELLULAR RESPONSES AND TOLERANCE TO DEHYDRATION AND COLD STRESSES
inferredcites →https://doi.org/10.1146/annurev.arplant.59.032607.092759openalex-snapshot
Chlorophyll Fluorescence: A Probe of Photosynthesis In Vivo
inferredcites →https://doi.org/10.1186/1746-4811-1-13openalex-snapshot
Transient expression vectors for functional genomics, quantification of promoter activity and RNA silencing in plants
inferredcites →https://doi.org/10.1186/1746-4811-8-2openalex-snapshot
A convenient method for simultaneous quantification of multiple phytohormones and metabolites: application in study of rice-bacterium interaction
inferredcites →https://doi.org/10.1199/tab.0158openalex-snapshot
Carotenoid Biosynthesis in Arabidopsis: A Colorful Pathway
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