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The oxidative pentose phosphate pathway in photosynthesis: a tale of two shunts
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/1-4020-3589-6_4openalex-snapshot
Respiration in Photosynthetic Cells: Gas Exchange Components, Interactions with Photorespiration and the Operation of Mitochondria in the Light
inferredcites →https://doi.org/10.1007/bf00385601openalex-snapshot
Simultaneous requirement of carbon dioxide and abscisic acid for stomatal closing in Xanthium strumarium L.
inferredcites →https://doi.org/10.1007/bf00386231openalex-snapshot
A biochemical model of photosynthetic CO2 assimilation in leaves of C3 species
inferredcites →https://doi.org/10.1007/bf02139287openalex-snapshot
The path of carbon in photosynthesis
inferredcites →https://doi.org/10.1016/0003-9861(86)90598-9openalex-snapshot
Purification and properties of the cytoplasmic glucose-6-phosphate dehydrogenase from pea leaves
inferredcites →https://doi.org/10.1016/0003-9861(89)90104-5openalex-snapshot
Pyruvate kinase isozymes from the green alga, Selenastrum minutum
inferredcites →https://doi.org/10.1016/0003-9861(89)90441-4openalex-snapshot
Chloroplast glucose-6-phosphate dehydrogenase: Km shift upon light modulation and reduction
inferredcites →https://doi.org/10.1016/0014-5793(84)80335-xopenalex-snapshot
Metabolite‐mediated catalyst conversion of PFK and PFP: a mechanism of enyme regulation in green plants
inferredcites →https://doi.org/10.1016/0304-4165(85)90004-2openalex-snapshot
A possible rate-limiting function of chloroplast hexosemonophosphate isomerase in starch synthesis of leaves
inferredcites →https://doi.org/10.1016/j.febslet.2009.07.035openalex-snapshot
Redox regulation of chloroplastic glucose‐6‐phosphate dehydrogenase: A new role for f‐type thioredoxin
inferredcites →https://doi.org/10.1016/j.phytochem.2008.08.026openalex-snapshot
Putting plant hexokinases in their proper place
inferredcites →https://doi.org/10.1016/j.tplants.2010.05.006openalex-snapshot
Not just a circle: flux modes in the plant TCA cycle
inferredcites →https://doi.org/10.1016/s0005-2728(03)00106-3openalex-snapshot
Regulation of NAD- and NADP-dependent isocitrate dehydrogenases by reduction levels of pyridine nucleotides in mitochondria and cytosol of pea leaves
inferredcites →https://doi.org/10.1016/s0014-5793(99)01417-9openalex-snapshot
Spinach hexokinase I is located in the outer envelope membrane of plastids
inferredcites →https://doi.org/10.1016/s0021-9258(19)52402-4openalex-snapshot
THE PATH OF CARBON IN PHOTOSYNTHESIS
inferredcites →https://doi.org/10.1021/ja01150a545openalex-snapshot
IDENTIFICATION OF RIBULOSE IN C14O2 PHOTOSYNTHESIS PRODUCTS1
inferredcites →https://doi.org/10.1042/bcj20190234openalex-snapshot
Plastidic glucose-6-phosphate dehydrogenases are regulated to maintain activity in the light
inferredcites →https://doi.org/10.1042/bcj20200480openalex-snapshot
Source of 12C in Calvin–Benson cycle intermediates and isoprene emitted from plant leaves fed with 13CO2
inferredcites →https://doi.org/10.1042/bj20130337openalex-snapshot
Redox regulation of chloroplastic G6PDH activity by thioredoxin occurs through structural changes modifying substrate accessibility and cofactor binding
inferredcites →https://doi.org/10.1046/j.1365-3040.2000.00634.xopenalex-snapshot
Reciprocal diurnal changes of phosphoenolpyruvate carboxylase expression and cytosolic pyruvate kinase, citrate synthase and NADP‐isocitrate dehydrogenase expression regulate organic acid metabolism during nitrate assimilation in tobacco leaves
inferredcites →https://doi.org/10.1046/j.1432-1033.2003.03469.xopenalex-snapshot
Regulation of pyruvate dehydrogenase complex activity in plant cells
inferredcites →https://doi.org/10.1073/pnas.0914299107openalex-snapshot
Circadian control of carbohydrate availability for growth in Arabidopsis plants at night
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.2121531119openalex-snapshot
Reimport of carbon from cytosolic and vacuolar sugar pools into the Calvin–Benson cycle explains photosynthesis labeling anomalies
inferredcites →https://doi.org/10.1073/pnas.2309536120openalex-snapshot
Hydroxymethylbutenyl diphosphate accumulation reveals MEP pathway regulation for high CO 2 -induced suppression of isoprene emission
inferredcites →https://doi.org/10.1073/pnas.87.2.673openalex-snapshot
Pea leaf mitochondrial pyruvate dehydrogenase complex is inactivated in vivo in a light-dependent manner.
inferredcites →https://doi.org/10.1074/jbc.272.43.26985openalex-snapshot
Identification of the Cysteine Residues Involved in Redox Modification of Plant Plastidic Glucose-6-phosphate Dehydrogenase
inferredcites →https://doi.org/10.1074/mcp.m110.001214openalex-snapshot
Diurnal Changes in Mitochondrial Function Reveal Daily Optimization of Light and Dark Respiratory Metabolism in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/erp374openalex-snapshot
Metabolic turnover analysis by a combination of in vivo13C-labelling from 13CO2 and metabolic profiling with CE-MS/MS reveals rate-limiting steps of the C3 photosynthetic pathway in Nicotiana tabacum leaves
inferredcites →https://doi.org/10.1093/jxb/ert400openalex-snapshot
Substantial roles of hexokinase and fructokinase in the effects of sugars on plant physiology and development
inferredcites →https://doi.org/10.1093/jxb/erv484openalex-snapshot
The glucose 6-phosphate shunt around the Calvin–Benson cycle
inferredcites →https://doi.org/10.1093/plphys/kiab076openalex-snapshot
The metabolic origins of non-photorespiratory CO2 release during photosynthesis: a metabolic flux analysis
inferredcites →https://doi.org/10.1093/plphys/kiac582openalex-snapshot
Short- and long-term responses of leaf day respiration to elevated atmospheric CO2
inferredcites →https://doi.org/10.1093/plphys/kiad305openalex-snapshot
Laisk measurements in the nonsteady state: Tests in plants exposed to warming and variable CO2 concentrations
inferredcites →https://doi.org/10.1093/plphys/kiad601openalex-snapshot
The end game(s) of photosynthetic carbon metabolism
inferredcites →https://doi.org/10.1104/pp.010576openalex-snapshot
The Plastidic Pentose Phosphate Translocator Represents a Link between the Cytosolic and the Plastidic Pentose Phosphate Pathways in Plants
inferredcites →https://doi.org/10.1104/pp.105.062141openalex-snapshot
In Vivo Respiratory Metabolism of Illuminated Leaves
inferredcites →https://doi.org/10.1104/pp.109.142976openalex-snapshot
In Folio Respiratory Fluxomics Revealed by 13C Isotopic Labeling and H/D Isotope Effects Highlight the Noncyclic Nature of the Tricarboxylic Acid “Cycle” in Illuminated Leaves
inferredcites →https://doi.org/10.1104/pp.109.4.1327openalex-snapshot
Molecular Characterization of the Plastidic Glucose-6-Phosphate Dehydrogenase from Potato in Comparison to its Cytosolic Counterpart
inferredcites →https://doi.org/10.1104/pp.118.4.1439openalex-snapshot
Export of Carbon from Chloroplasts at Night
inferredcites →https://doi.org/10.1104/pp.18.01391openalex-snapshot
Isoprene Acts as a Signaling Molecule in Gene Networks Important for Stress Responses and Plant Growth
inferredcites →https://doi.org/10.1104/pp.83.2.399openalex-snapshot
Subcellular Metabolite Levels in Spinach Leaves
inferredcites →https://doi.org/10.1104/pp.90.2.385openalex-snapshot
Low Oxygen Inhibition of Photosynthesis Is Caused by Inhibition of Starch Synthesis
inferredcites →https://doi.org/10.1105/tpc.10.1.105openalex-snapshot
Molecular Characterization of a Carbon Transporter in Plastids from Heterotrophic Tissues: The Glucose 6-Phosphate/Phosphate Antiporter
inferredcites →https://doi.org/10.1105/tpc.108.063925openalex-snapshot
A Chloroplastic UDP-Glucose Pyrophosphorylase from Arabidopsis Is the Committed Enzyme for the First Step of Sulfolipid Biosynthesis
inferredcites →https://doi.org/10.1105/tpc.112.106989openalex-snapshot
Metabolic Fluxes in an Illuminated Arabidopsis Rosette
inferredcites →https://doi.org/10.1105/tpc.12.5.787openalex-snapshot
Identification, Purification, and Molecular Cloning of a Putative Plastidic Glucose Translocator
inferredcites →https://doi.org/10.1105/tpc.19.00959openalex-snapshot
The Arabidopsis Plastidial Glucose-6-Phosphate Transporter GPT1 is Dually Targeted to Peroxisomes via the Endoplasmic Reticulum
inferredcites →https://doi.org/10.1111/j.1365-3040.2009.01934.xopenalex-snapshot
Using combined measurements of gas exchange and chlorophyll fluorescence to estimate parameters of a biochemical C 3 photosynthesis model: a critical appraisal and a new integrated approach applied to leaves in a wheat ( Triticum aestivum ) canopy
inferredcites →https://doi.org/10.1111/j.1365-3040.2009.01946.xopenalex-snapshot
Isoprene synthesis protects transgenic tobacco plants from oxidative stress
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02293.xopenalex-snapshot
Genome‐wide analysis of glucose‐6‐phosphate dehydrogenases in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04535.xopenalex-snapshot
Alternative targeting of Arabidopsis plastidic glucose‐6‐phosphate dehydrogenase G6PD1 involves cysteine‐dependent interaction with G6PD4 in the cytosol
inferredcites →https://doi.org/10.1111/j.1438-8677.2010.00349.xopenalex-snapshot
The role of plastidial glucose‐6‐phosphate/phosphate translocators in vegetative tissues of Arabidopsis thaliana mutants impaired in starch biosynthesis
inferredcites →https://doi.org/10.1111/j.1469-8137.2008.02672.xopenalex-snapshot
On the metabolic origin of the carbon isotope composition of CO2 evolved from darkened light‐acclimated leaves in Ricinus communis
inferredcites →https://doi.org/10.1111/j.1469-8137.2009.03130.xopenalex-snapshot
In folio isotopic tracing demonstrates that nitrogen assimilation into glutamate is mostly independent from current CO2 assimilation in illuminated leaves of Brassica napus
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.14816openalex-snapshot
Leaf day respiration: low CO 2 flux but high significance for metabolism and carbon balance
inferredcites →https://doi.org/10.1111/nph.15126openalex-snapshot
Determination of leaf respiration in the light: comparison between an isotopic disequilibrium method and the Laisk method
inferredcites →https://doi.org/10.1111/nph.17957openalex-snapshot
Anaplerotic flux into the Calvin–Benson cycle: hydrogen isotope evidence for in vivo occurrence in C 3 metabolism
inferredcites →https://doi.org/10.1111/nph.18965openalex-snapshot
A model of photosynthetic CO 2 assimilation in C 3 leaves accounting for respiration and energy recycling by the plastidial oxidative pentose phosphate pathway
inferredcites →https://doi.org/10.1111/nph.19330openalex-snapshot
Estimating leaf day respiration from conventional gas exchange measurements
inferredcites →https://doi.org/10.1111/pce.14324openalex-snapshot
Drought exerts a greater influence than growth temperature on the temperature response of leaf day respiration in wheat ( Triticum aestivum )
inferredcites →https://doi.org/10.1146/annurev.pp.41.060190.001101openalex-snapshot
Fructose-2,6-Bisphosphate as a Regulatory Molecule in Plants
inferredcites →https://doi.org/10.1186/s12859-016-1360-7openalex-snapshot
FluxFix: automatic isotopologue normalization for metabolic tracer analysis
inferredcites →https://doi.org/10.18637/jss.v067.i01openalex-snapshot
Fitting Linear Mixed-Effects Models Using lme4
inferredcites →https://doi.org/10.18637/jss.v082.i13openalex-snapshot
lmerTest Package: Tests in Linear Mixed Effects Models
inferredcites →https://doi.org/10.3389/fpls.2018.00339openalex-snapshot
Plant Fructokinases: Evolutionary, Developmental, and Metabolic Aspects in Sink Tissues
inferredcites →https://doi.org/10.3389/fpls.2019.00280openalex-snapshot
Autophagic Turnover of Chloroplasts: Its Roles and Regulatory Mechanisms in Response to Sugar Starvation
inferredcites →https://doi.org/10.3389/fpls.2019.00827openalex-snapshot
Transcriptional Regulation of the Glucose-6-Phosphate/Phosphate Translocator 2 Is Related to Carbon Exchange Across the Chloroplast Envelope
inferredcites →https://doi.org/10.3389/fpls.2020.580726openalex-snapshot
Phosphoglucoisomerase Is an Important Regulatory Enzyme in Partitioning Carbon out of the Calvin-Benson Cycle
inferredcites →https://doi.org/10.3390/cells10061547openalex-snapshot
Pentose Phosphate Pathway Reactions in Photosynthesizing Cells
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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