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Pre-mature senescence in the oldest leaves of low nitrate-grown Atxdh1 mutant uncovers a role for purine catabolism in plant nitrogen metabolism
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9780470988855.ch5openalex-snapshot
Nutrient Remobilization During Leaf Senescence
inferredcites →https://doi.org/10.1006/abio.1976.9999openalex-snapshot
A Rapid and Sensitive Method for the Quantitation of Microgram Quantities of Protein Utilizing the Principle of Protein-Dye Binding
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Coordination of protein and mRNA abundances of stromal enzymes and mRNA abundances of the Clp protease subunits during senescence of Phaseolus vulgaris (L.) leaves
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Nutrient use efficiency in evergreen and deciduous species from heathlands
inferredcites →https://doi.org/10.1007/bf03030735openalex-snapshot
Protein degradation and nitrogen remobilization during leaf senescence
inferredcites →https://doi.org/10.1007/s00425-006-0236-xopenalex-snapshot
AtAAH encodes a protein with allantoate amidohydrolase activity from Arabidopsis thaliana
inferredcites →https://doi.org/10.1007/s00425-006-0315-zopenalex-snapshot
Comparative studies on Ureide Permeases in Arabidopsis thaliana and analysis of two alternative splice variants of AtUPS5
inferredcites →https://doi.org/10.1007/s004250000310openalex-snapshot
Characterization of the sink/source transition in tobacco ( Nicotiana tabacum L.) shoots in relation to nitrogen management and leaf senescence
inferredcites →https://doi.org/10.1007/s10863-012-9445-0openalex-snapshot
The peroxisomal NAD+ carrier of Arabidopsis thaliana transports coenzyme A and its derivatives
inferredcites →https://doi.org/10.1007/s11103-004-2331-3openalex-snapshot
Recent advances in chlorophyll biosynthesis and breakdown in higher plants
inferredcites →https://doi.org/10.1007/s11103-016-0490-7openalex-snapshot
Allantoin accumulation mediated by allantoinase downregulation and transport by Ureide Permease 5 confers salt stress tolerance to Arabidopsis plants
inferredcites →https://doi.org/10.1007/s11120-006-9065-9openalex-snapshot
Consistent Sets of Spectrophotometric Chlorophyll Equations for Acetone, Methanol and Ethanol Solvents
inferredcites →https://doi.org/10.1016/0003-2697(70)90448-3openalex-snapshot
Differential analyses of glyoxylate derivatives
inferredcites →https://doi.org/10.1016/0005-2744(79)90210-9openalex-snapshot
AMP deaminase from baker's yeast. Purification and some regulatory properties
inferredcites →https://doi.org/10.1016/0308-8146(94)90167-8openalex-snapshot
Leaf protein contents and nitrogen-to-protein conversion factors for 90 plant species
inferredcites →https://doi.org/10.1016/j.envexpbot.2005.07.002openalex-snapshot
Growth and stress conditions cause similar changes in xylem amino acids for different legume species
inferredcites →https://doi.org/10.1016/j.phytochem.2007.10.029openalex-snapshot
Caffeine and related purine alkaloids: Biosynthesis, catabolism, function and genetic engineering
inferredcites →https://doi.org/10.1016/j.plaphy.2003.07.002openalex-snapshot
Metabolism of purine bases, nucleosides and alkaloids in theobromine-forming Theobroma cacao leaves
inferredcites →https://doi.org/10.1016/j.tplants.2011.03.012openalex-snapshot
The biochemistry of nitrogen mobilization: purine ring catabolism
inferredcites →https://doi.org/10.1016/j.trac.2005.12.002openalex-snapshot
A guide for selecting the most appropriate method for ammonium determination in water analysis
inferredcites →https://doi.org/10.1016/s0168-9452(98)00075-2openalex-snapshot
The Mo-hydroxylases xanthine dehydrogenase and aldehyde oxidase in ryegrass as affected by nitrogen and salinity
inferredcites →https://doi.org/10.1016/s0168-9452(98)00084-3openalex-snapshot
The levels of nitrate reductase and MoCo in annual ryegrass as affected by nitrate and ammonium nutrition
inferredcites →https://doi.org/10.1016/s1360-1385(03)00103-1openalex-snapshot
Molecular genetics of leaf senescence in Arabidopsis
inferredcites →https://doi.org/10.1034/j.1399-3054.1997.990405.xopenalex-snapshot
Nitrate reductase and molybdenum cofactor in annual ryegrass as affected by salinity and nitrogen source
inferredcites →https://doi.org/10.1034/j.1399-3054.1998.1020206.xopenalex-snapshot
Influence of nitrogen deficiency on senescence and the amounts of RNA and proteins in wheat leaves
inferredcites →https://doi.org/10.1038/286257a0openalex-snapshot
Inhibition of photosynthesis in Arabidopsis mutants lacking leaf glutamate synthase activity
inferredcites →https://doi.org/10.1038/nchembio.265openalex-snapshot
Ureide catabolism in Arabidopsis thaliana and Escherichia coli
inferredcites →https://doi.org/10.1046/j.1365-3040.2002.00905.xopenalex-snapshot
Do anthocyanins function as antioxidants in leaves? Imaging of H 2 O 2 in red and green leaves after mechanical injury
inferredcites →https://doi.org/10.1046/j.1365-313x.2000.00833.xopenalex-snapshot
The Arabidopsis sugar‐insensitive mutants sis4 and sis5 are defective in abscisic acid synthesis and response
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01908.xopenalex-snapshot
Large‐scale identification of leaf senescence‐associated genes
inferredcites →https://doi.org/10.1071/fp03236openalex-snapshot
Die and let live: leaf senescence contributes to plant survival under drought stress
inferredcites →https://doi.org/10.1073/pnas.94.4.1579openalex-snapshot
Mechanism of photosystem II photoinactivation and D1 protein degradation at low light: The role of back electron flow
inferredcites →https://doi.org/10.1074/jbc.m405433200openalex-snapshot
UPS1 and UPS2 from Arabidopsis Mediate High Affinity Transport of Uracil and 5-Fluorouracil
inferredcites →https://doi.org/10.1080/00103627509366547openalex-snapshot
Rapid colorimetric determination of nitrate in plant tissue by nitration of salicylic acid
inferredcites →https://doi.org/10.1093/aob/mcq028openalex-snapshot
Nitrogen uptake, assimilation and remobilization in plants: challenges for sustainable and productive agriculture
inferredcites →https://doi.org/10.1093/jexbot/51.342.123openalex-snapshot
Bundle sheath proteins are more sensitive to oxidative damage than those of the mesophyll in maize leaves exposed to paraquat or low temperatures
inferredcites →https://doi.org/10.1093/jexbot/53.370.927openalex-snapshot
Nitrogen metabolism and remobilization during senescence
inferredcites →https://doi.org/10.1093/jxb/31.2.409openalex-snapshot
Ureide Metabolism in Non-nodulatedPhaseolus vulgarisL.
inferredcites →https://doi.org/10.1093/jxb/48.12.2031openalex-snapshot
The occurrence and gene expression of vegetative storage proteins and a Rubisco Complex Protein in several perennial soybean species
inferredcites →https://doi.org/10.1093/jxb/erh100openalex-snapshot
Soybean cultivars 'Williams 82' and 'Maple Arrow' produce both urea and ammonia during ureide degradation
inferredcites →https://doi.org/10.1093/jxb/erj013openalex-snapshot
Update on ureide degradation in legumes
inferredcites →https://doi.org/10.1093/jxb/erj035openalex-snapshot
The two senescence-related markers, GS1 (cytosolic glutamine synthetase) and GDH (glutamate dehydrogenase), involved in nitrogen mobilization, are differentially regulated during pathogen attack and by stress hormones and reactive oxygen species in Nicotiana tabacum L. leaves
inferredcites →https://doi.org/10.1093/jxb/err313openalex-snapshot
In Posidonia oceanica cadmium induces changes in DNA methylation and chromatin patterning
inferredcites →https://doi.org/10.1093/jxb/ers090openalex-snapshot
Developmental effects on ureide levels are mediated by tissue-specific regulation of allantoinase in Phaseolus vulgaris L.
inferredcites →https://doi.org/10.1093/jxb/erw071openalex-snapshot
Allantoin, a stress-related purine metabolite, can activate jasmonate signaling in a MYC2-regulated and abscisic acid-dependent manner
inferredcites →https://doi.org/10.1093/jxb/erw365openalex-snapshot
Nitrogen remobilisation during leaf senescence: lessons from Arabidopsis to crops
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a029622openalex-snapshot
Detection of Chlorophyll Breakdown Products in the Senescent Leaves of Higher Plants
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a075029openalex-snapshot
Aldehyde oxidase isoenzymes (E.C. 1.2.3.1) in potato tubers (Solanum tuberosum)
inferredcites →https://doi.org/10.1093/pcp/pcg172openalex-snapshot
The Arabidopsis-accelerated cell death Gene ACD1 is Involved in Oxygenation of Pheophorbide a: Inhibition of the Pheophorbide a Oxygenase Activity does not Lead to the “Stay-Green” Phenotype in Arabidopsis
inferredcites →https://doi.org/10.1093/pcp/pcm119openalex-snapshot
The RNAi-Mediated Silencing of Xanthine Dehydrogenase Impairs Growth and Fertility and Accelerates Leaf Senescence in Transgenic Arabidopsis Plants
inferredcites →https://doi.org/10.1093/treephys/15.10.679openalex-snapshot
Role of nitrogen remobilization from old leaves for new leaf growth of Eucalyptus globulus seedlings
inferredcites →https://doi.org/10.1093/treephys/18.6.403openalex-snapshot
Transport, storage and mobilization of nitrogen by trees and shrubs in the wet/dry tropics of northern Australia
inferredcites →https://doi.org/10.1104/pp.010912openalex-snapshot
Purine Biosynthesis. Big in Cell Division, Even Bigger in Nitrogen Assimilation
inferredcites →https://doi.org/10.1104/pp.105.060764openalex-snapshot
Characterization of Markers to Determine the Extent and Variability of Leaf Senescence in Arabidopsis. A Metabolic Profiling Approach
inferredcites →https://doi.org/10.1104/pp.105.065870openalex-snapshot
Chlorophyll Breakdown in Senescent Arabidopsis Leaves. Characterization of Chlorophyll Catabolites and of Chlorophyll Catabolic Enzymes Involved in the Degreening Reaction
inferredcites →https://doi.org/10.1104/pp.106.3.817openalex-snapshot
Posttranslational Regulation of Nitrate Reductase in Higher Plants
inferredcites →https://doi.org/10.1104/pp.107.096487openalex-snapshot
Adenine Nucleotide Pool Perturbation Is a Metabolic Trigger for AMP Deaminase Inhibitor-Based Herbicide Toxicity
inferredcites →https://doi.org/10.1104/pp.107.110809openalex-snapshot
Identification, Biochemical Characterization, and Subcellular Localization of Allantoate Amidohydrolases from Arabidopsis and Soybean
inferredcites →https://doi.org/10.1104/pp.107.114702openalex-snapshot
Functions of Chloroplastic Adenylate Kinases in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.109.1.169openalex-snapshot
Urease Is Not Essential for Ureide Degradation in Soybean
inferredcites →https://doi.org/10.1104/pp.111.179838openalex-snapshot
Arabidopsis Roots and Shoots Show Distinct Temporal Adaptation Patterns toward Nitrogen Starvation
inferredcites →https://doi.org/10.1104/pp.112.4.1403openalex-snapshot
Chlorophyll Breakdown in Senescent Leaves
inferredcites →https://doi.org/10.1104/pp.113.224261openalex-snapshot
The Ureide-Degrading Reactions of Purine Ring Catabolism Employ Three Amidohydrolases and One Aminohydrolase in Arabidopsis, Soybean, and Rice
inferredcites →https://doi.org/10.1104/pp.120.4.1015openalex-snapshot
Senescence-Associated Gene Expression during Ozone-Induced Leaf Senescence in Arabidopsis1
inferredcites →https://doi.org/10.1104/pp.126.3.1281openalex-snapshot
Superoxide Production by Plant Homologues of the gp91phox NADPH Oxidase. Modulation of Activity by Calcium and by Tobacco Mosaic Virus Infection
inferredcites →https://doi.org/10.1104/pp.16.01939openalex-snapshot
Aldehyde Oxidase 4 Plays a Critical Role in Delaying Silique Senescence by Catalyzing Aldehyde Detoxification
inferredcites →https://doi.org/10.1104/pp.68.5.1115openalex-snapshot
Enzymes of Purine Biosynthesis and Catabolism in Glycine max
inferredcites →https://doi.org/10.1104/pp.70.1.55openalex-snapshot
De Novo Purine Synthesis in Nitrogen-Fixing Nodules of Cowpea (Vigna unguiculata [L.] Walp.) and Soybean (Glycine max [L.] Merr.)
inferredcites →https://doi.org/10.1104/pp.71.1.7openalex-snapshot
Nitrogen Redistribution during Grain Growth in Wheat (Triticum aestivum L.)
inferredcites →https://doi.org/10.1105/tpc.010458openalex-snapshot
A Novel Superfamily of Transporters for Allantoin and Other Oxo Derivatives of Nitrogen Heterocyclic Compounds in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.106.044891openalex-snapshot
The Senescence-Induced Staygreen Protein Regulates Chlorophyll Degradation
inferredcites →https://doi.org/10.1105/tpc.107.050989openalex-snapshot
Proteome Analysis ofArabidopsisLeaf Peroxisomes Reveals Novel Targeting Peptides, Metabolic Pathways, and Defense Mechanisms
inferredcites →https://doi.org/10.1105/tpc.114.124008openalex-snapshot
Uric Acid Accumulation in an Arabidopsis Urate Oxidase Mutant Impairs Seedling Establishment by Blocking Peroxisome Maintenance
inferredcites →https://doi.org/10.1105/tpc.15.00880openalex-snapshot
Dual and Opposing Roles of Xanthine Dehydrogenase in Defense-Associated Reactive Oxygen Species Metabolism in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.5.5.553openalex-snapshot
Developmental and age-related processes that influence the longevity and senescence of photosynthetic tissues in arabidopsis.
inferredcites →https://doi.org/10.1111/j.1365-3040.2010.02187.xopenalex-snapshot
Molecular analysis of ureide accumulation under drought stress in Phaseolus vulgaris L.
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02411.xopenalex-snapshot
EMBRYONIC FACTOR 1 encodes an AMP deaminase and is essential for the zygote to embryo transition in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02422.xopenalex-snapshot
The plant Mo‐hydroxylases aldehyde oxidase and xanthine dehydrogenase have distinct reactive oxygen species signatures and are induced by drought and abscisic acid
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03223.xopenalex-snapshot
AtDUR3 represents the major transporter for high‐affinity urea transport across the plasma membrane of nitrogen‐deficient Arabidopsis roots
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03440.xopenalex-snapshot
A critical role for ureides in dark and senescence‐induced purine remobilization is unmasked in the Atxdh1 Arabidopsis mutant
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03632.xopenalex-snapshot
The effects of the loss of TIP1;1 and TIP1;2 aquaporins in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1365-313x.2012.05086.xopenalex-snapshot
Soybean ureide transporters play a critical role in nodule development, function and nitrogen export
inferredcites →https://doi.org/10.1111/j.1399-3054.1962.tb08052.xopenalex-snapshot
A Revised Medium for Rapid Growth and Bio Assays with Tobacco Tissue Cultures
inferredcites →https://doi.org/10.1111/j.1399-3054.1986.tb05075.xopenalex-snapshot
Nucleotide pools in leaf and root tissue of tobacco plants: Influence of leaf senescence
inferredcites →https://doi.org/10.1111/j.1399-3054.1988.tb04965.xopenalex-snapshot
Nitrate reductase and its role in nitrate assimilation in plants
inferredcites →https://doi.org/10.1111/j.1438-8677.2008.00097.xopenalex-snapshot
Leaf nitrogen remobilisation for plant development and grain filling
inferredcites →https://doi.org/10.1111/j.1751-1097.1999.tb01944.xopenalex-snapshot
Environmental Significance of Anthocyanins in Plant Stress Responses
inferredcites →https://doi.org/10.1111/nph.14782openalex-snapshot
The ribokinases of Arabidopsis thaliana and Saccharomyces cerevisiae are required for ribose recycling from nucleotide catabolism, which in plants is not essential to survive prolonged dark stress
inferredcites →https://doi.org/10.1111/pce.12218openalex-snapshot
The purine metabolite allantoin enhances abiotic stress tolerance through synergistic activation of abscisic acid metabolism
inferredcites →https://doi.org/10.1139/b88-288openalex-snapshot
Ammonia, glutamine, and asparagine: a carbon–nitrogen interface
inferredcites →https://doi.org/10.1146/annurev.arplant.37.1.539openalex-snapshot
Products of Biological Nitrogen Fixation in Higher Plants: Synthesis, Transport, and Metabolism
inferredcites →https://doi.org/10.1146/annurev.arplant.57.032905.105316openalex-snapshot
Leaf Senescence
inferredcites →https://doi.org/10.1146/annurev.arplant.57.032905.105421openalex-snapshot
PYRIMIDINE AND PURINE BIOSYNTHESIS AND DEGRADATION IN PLANTS
inferredcites →https://doi.org/10.1146/annurev.pp.31.060180.001525openalex-snapshot
Transport and Partitioning of Nitrogenous Solutes
inferredcites →https://doi.org/10.1146/annurev.pp.37.060186.002543openalex-snapshot
Products of Biological Nitrogen Fixation in Higher Plants: Synthesis, Transport, and Metabolism
inferredcites →https://doi.org/10.1199/tab.0010openalex-snapshot
Primary N-assimilation into Amino Acids in Arabidopsis
inferredcites →https://doi.org/10.2135/cropsci1992.0011183x003200020032xopenalex-snapshot
Nitrogen Partitioning in Maize during Ear Development
inferredcites →https://doi.org/10.2135/cropsci1995.0011183x003500010034xopenalex-snapshot
Nitrogen and Carbon Accumulation and Remobilization during Grain Filling in Maize under Different Source/Sink Ratios
inferredcites →https://doi.org/10.3390/plants4030573openalex-snapshot
Sulfite Oxidase Activity Is Essential for Normal Sulfur, Nitrogen and Carbon Metabolism in Tomato Leaves
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inferred← citeshttps://doi.org/10.1002/agg2.20079openalex-snapshot
Temporal biological nitrogen fixation pattern in soybean inoculated with Bradyrhizobium
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