| Q41938841 | 2-Hydroxy Acids in Plant Metabolism |
| Q45341627 | A Common histone modification code on C4 genes in maize and its conservation in Sorghum and Setaria italica |
| Q39781110 | Analysis of gene expression and histone modification between C4 and non-C4 homologous genes of PPDK and PCK in maize. |
| Q39792239 | Arabidopsis uses two gluconeogenic gateways for organic acids to fuel seedling establishment |
| Q43199129 | Bundle-sheath aquaporins play a role in controlling Arabidopsis leaf hydraulic conductivity |
| Q34236863 | C4 cycles: past, present, and future research on C4 photosynthesis |
| Q54979735 | Changes in nitrogen availability lead to a reprogramming of pyruvate metabolism. |
| Q35182201 | Deep evolutionary comparison of gene expression identifies parallel recruitment of trans-factors in two independent origins of C4 photosynthesis |
| Q44495333 | Differential tissue-specific expression of NtAQP1 in Arabidopsis thaliana reveals a role for this protein in stomatal and mesophyll conductance of CO₂ under standard and salt-stress conditions |
| Q38761982 | Engineering C4 photosynthesis into C3 chassis in the synthetic biology age. |
| Q39347662 | Expression and manipulation of phosphoenolpyruvate carboxykinase 1 identifies a role for malate metabolism in stomatal closure. |
| Q60407079 | Fumarate and cytosolic pH as modulators of the synthesis or consumption of C4 organic acids through NADP-malic enzyme in Arabidopsis thaliana |
| Q46787460 | Genetic enablers underlying the clustered evolutionary origins of C4 photosynthesis in angiosperms |
| Q46885503 | High light acclimation of Oryza sativa L. leaves involves specific photosynthetic-sourced changes of NADPH/NADP⁺ in the midvein |
| Q45711958 | Light-regulated phosphorylation of maize phosphoenolpyruvate carboxykinase plays a vital role in its activity. |
| Q42504786 | Loss of cytosolic NADP-malic enzyme 2 in Arabidopsis thaliana is associated with enhanced susceptibility to Colletotrichum higginsianum. |
| Q38308757 | Members of the barley NAC transcription factor gene family show differential co-regulation with senescence-associated genes during senescence of flag leaves. |
| Q45386798 | Multiple Arabidopsis genes primed for recruitment into C₄ photosynthesis |
| Q43042682 | NAD-malic enzymes of Arabidopsis thaliana display distinct kinetic mechanisms that support differences in physiological control |
| Q59127748 | NADP-Dependent Malic Enzyme 1 Participates in the Abscisic Acid Response in |
| Q52313863 | Natural variation within a species for traits underpinning C4 photosynthesis. |
| Q41191781 | Nitrogen recycling from the xylem in rice leaves: dependence upon metabolism and associated changes in xylem hydraulics |
| Q38066595 | Perspectives on plant photorespiratory metabolism |
| Q36996069 | Photosynthesis-related characteristics of the midrib and the interveinal lamina in leaves of the C3-CAM intermediate plant Mesembryanthemum crystallinum. |
| Q33361010 | Photosynthetic Genes and Genes Associated with the C4 Trait in Maize Are Characterized by a Unique Class of Highly Regulated Histone Acetylation Peaks on Upstream Promoters |
| Q46321166 | Recruitment of pre-existing networks during the evolution of C4 photosynthesis |
| Q57340612 | Salicylic Acid: A Novel Plant Growth Regulator - Role in Physiological Processes and Abiotic Stresses Under Changing Environments |
| Q39016134 | Signal integration on plant promoters: a case study in maize |
| Q43057650 | Sinks for photosynthetic electron flow in green petioles and pedicels of Zantedeschia aethiopica: evidence for innately high photorespiration and cyclic electron flow rates |
| Q50462648 | Specific Arabidopsis thaliana malic enzyme isoforms can provide anaplerotic pyruvate carboxylation function in Saccharomyces cerevisiae |
| Q34627094 | Strategies for engineering a two-celled C(4) photosynthetic pathway into rice |
| Q64277665 | Synthetic biology approaches for improving photosynthesis |
| Q37802104 | Targeting mitochondrial metabolism and machinery as a means to enhance photosynthesis |
| Q30852839 | The complex character of photosynthesis in cucumber fruit |
| Q35283156 | The evolutionary ecology of C4 plants |
| Q36894787 | The existence of C4-bundle-sheath-like photosynthesis in the mid-vein of C3 rice |
| Q88153240 | The intracellular distribution of inorganic carbon fixing enzymes does not support the presence of a C4 pathway in the diatom Phaeodactylum tricornutum |
| Q54564018 | The pyruvate, orthophosphate dikinase regulatory proteins of Arabidopsis are both bifunctional and interact with the catalytic and nucleotide-binding domains of pyruvate, orthophosphate dikinase. |
| Q33920736 | The role of photorespiration during the evolution of C4 photosynthesis in the genus Flaveria. |
| Q34440924 | The role of plasma membrane aquaporins in regulating the bundle sheath-mesophyll continuum and leaf hydraulics |
| Q37842014 | The role of proteins in C(3) plants prior to their recruitment into the C(4) pathway |
| Q39982761 | Three different and tissue-specific NAD-malic enzymes generated by alternative subunit association in Arabidopsis thaliana |
| Q46920865 | Transcript residency on ribosomes reveals a key role for the Arabidopsis thaliana bundle sheath in sulfur and glucosinolate metabolism |
| Q31098935 | Transcriptomes of Eight Arabidopsis thaliana Accessions Reveal Core Conserved, Genotype- and Organ-Specific Responses to Flooding Stress. |
| Q46816880 | Transgenic perturbation of the decarboxylation phase of Crassulacean acid metabolism alters physiology and metabolism but has only a small effect on growth |
| Q35055929 | Two Rumex species from contrasting hydrological niches regulate flooding tolerance through distinct mechanisms. |
| Q36967548 | Using evolution as a guide to engineer kranz-type c4 photosynthesis |
| Q33860173 | Was low CO2 a driving force of C4 evolution: Arabidopsis responses to long-term low CO2 stress. |
| Q44834667 | You're so vein: bundle sheath physiology, phylogeny and evolution in C3 and C4 plants |