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Advances in Asparagine Metabolism
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/fes3.85openalex-snapshot
Reducing the acrylamide‐forming potential of wheat
inferredcites →https://doi.org/10.1002/j.1460-2075.1990.tb08114.xopenalex-snapshot
Dark‐induced and organ‐specific expression of two asparagine synthetase genes in Pisum sativum.
inferredcites →https://doi.org/10.1007/0-387-24980-x_14openalex-snapshot
Mechanisms of Acrylamide Formation
inferredcites →https://doi.org/10.1007/bf00395182openalex-snapshot
Two routes for asparagine metabolism in Pisum sativum L.
inferredcites →https://doi.org/10.1007/bf00403035openalex-snapshot
Photorespiratory N donors, aminotransferase specificity and photosynthesis in a mutant of barley deficient in serine: glyoxylate aminotransferase activity
inferredcites →https://doi.org/10.1007/s000180050145openalex-snapshot
The mechanism of glutamine-dependent amidotransferases
inferredcites →https://doi.org/10.1007/s00425-005-0196-6openalex-snapshot
High levels of asparagine synthetase in hypocotyls of pine seedlings suggest a role of the enzyme in re-allocation of seed-stored nitrogen
inferredcites →https://doi.org/10.1007/s00425-006-0245-9openalex-snapshot
Co-occurrence of both l-asparaginase subtypes in Arabidopsis: At3g16150 encodes a K+-dependent l-asparaginase
inferredcites →https://doi.org/10.1007/s00425-006-0431-9openalex-snapshot
Coordination of PsAS1 and PsASPG expression controls timing of re-allocated N utilization in hypocotyls of pine seedlings
inferredcites →https://doi.org/10.1007/s00425-011-1557-yopenalex-snapshot
Role of asparaginase variable loop at the carboxyl terminal of the alpha subunit in the determination of substrate preference in plants
inferredcites →https://doi.org/10.1007/s004250000420openalex-snapshot
Enzymatic characterization of the recombinant Arabidopsis thaliana nitrilase subfamily encoded by the NIT 2/ NIT 1/ NIT 3-gene cluster
inferredcites →https://doi.org/10.1007/s004250000513openalex-snapshot
Cloning, characterization and mRNA expression analysis of PVAS1 , a type I asparagine synthetase gene from Phaseolus vulgaris
inferredcites →https://doi.org/10.1007/s004250050310openalex-snapshot
Transport of amino acids with special emphasis on the synthesis and transport of asparagine in the Illinois Low Protein and Illinois High Protein strains of maize
inferredcites →https://doi.org/10.1007/s00726-011-0973-4openalex-snapshot
Arabidopsis mutants lacking asparaginases develop normally but exhibit enhanced root inhibition by exogenous asparagine
inferredcites →https://doi.org/10.1007/s11103-005-6217-9openalex-snapshot
Cyanide Metabolism in Higher Plants: Cyanoalanine Hydratase is a NIT4 Homolog
inferredcites →https://doi.org/10.1007/s11103-016-0463-xopenalex-snapshot
Hormones and nitrate: a two-way connection
inferredcites →https://doi.org/10.1007/s11120-004-9366-9openalex-snapshot
Molecular aspects of nitrogen mobilization and recycling in trees
inferredcites →https://doi.org/10.1007/s12230-015-9485-1openalex-snapshot
Biotech Potatoes in the 21st Century: 20 Years Since the First Biotech Potato
inferredcites →https://doi.org/10.1016/0003-9861(83)90594-5openalex-snapshot
Purification and properties of an asparagine aminotransferase from Pisum sativum leaves
inferredcites →https://doi.org/10.1016/0006-291x(78)91647-9openalex-snapshot
2-hydroxysuccinamic acid: A product of asparagine metabolism in plants
inferredcites →https://doi.org/10.1016/0031-9422(88)84071-8openalex-snapshot
The metabolism of asparagine in plants
inferredcites →https://doi.org/10.1016/0031-9422(90)87085-9openalex-snapshot
Asparaginase, allantoinase and glutamine synthetase activities in soybean cotyledons grown in vitro
inferredcites →https://doi.org/10.1016/j.biochi.2009.07.002openalex-snapshot
Molecular identification of ω-amidase, the enzyme that is functionally coupled with glutamine transaminases, as the putative tumor suppressor Nit2
inferredcites →https://doi.org/10.1016/j.biochi.2009.07.003openalex-snapshot
Identification of the putative tumor suppressor Nit2 as ω-amidase, an enzyme metabolically linked to glutamine and asparagine transamination
inferredcites →https://doi.org/10.1016/j.cell.2014.10.015openalex-snapshot
A Widespread Glutamine-Sensing Mechanism in the Plant Kingdom
inferredcites →https://doi.org/10.1016/j.celrep.2016.11.015openalex-snapshot
L-Met Activates Arabidopsis GLR Ca2+ Channels Upstream of ROS Production and Regulates Stomatal Movement
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.jcs.2016.01.010openalex-snapshot
Food safety: Structure and expression of the asparagine synthetase gene family of wheat
inferredcites →https://doi.org/10.1016/j.jmb.2006.04.066openalex-snapshot
Crystal Structure of Plant Asparaginase
inferredcites →https://doi.org/10.1016/j.jplph.2013.06.002openalex-snapshot
Molecular characterization of PVAS3: An asparagine synthetase gene from common bean prevailing in developing organs
inferredcites →https://doi.org/10.1016/j.phytochem.2012.09.017openalex-snapshot
Characterization of Arabidopsis serine:glyoxylate aminotransferase, AGT1, as an asparagine aminotransferase
inferredcites →https://doi.org/10.1016/j.phytochem.2013.12.020openalex-snapshot
Identification and characterization of omega-amidase as an enzyme metabolically linked to asparagine transamination in Arabidopsis
inferredcites →https://doi.org/10.1016/j.phytochem.2014.04.012openalex-snapshot
Evidence that glutamine transaminase and omega-amidase potentially act in tandem to close the methionine salvage cycle in bacteria and plants
inferredcites →https://doi.org/10.1016/j.plantsci.2010.04.010openalex-snapshot
Biological functions of asparagine synthetase in plants
inferredcites →https://doi.org/10.1016/j.plaphy.2010.12.006openalex-snapshot
A kinetic comparison of asparagine synthetase isozymes from higher plants
inferredcites →https://doi.org/10.1016/j.plaphy.2011.03.010openalex-snapshot
An Arabidopsis mutant disrupted in ASN2 encoding asparagine synthetase 2 exhibits low salt stress tolerance
inferredcites →https://doi.org/10.1016/j.tplants.2006.07.004openalex-snapshot
Interactions between nitrogen and cytokinin in the regulation of metabolism and development
inferredcites →https://doi.org/10.1016/s0021-9258(18)45003-xopenalex-snapshot
THE PREPARATION OF ASPARAGINE
inferredcites →https://doi.org/10.1016/s0021-9258(18)66019-3openalex-snapshot
ASPARTATE METABOLISM AND ASPARAGINE SYNTHESIS IN PLANT SYSTEMS
inferredcites →https://doi.org/10.1016/s0021-9258(19)45861-4openalex-snapshot
Structure of the Dimeric α-Keto Acid Analogue of Asparagine
inferredcites →https://doi.org/10.1016/s0076-6879(85)13048-xopenalex-snapshot
[45] α-keto acid ω-amidase from rat liver
inferredcites →https://doi.org/10.1016/s0168-9452(03)00251-6openalex-snapshot
N-stress alters aspartate and asparagine levels of xylem sap in soybean
inferredcites →https://doi.org/10.1016/s0959-440x(02)00387-1openalex-snapshot
Catalysis in the nitrilase superfamily
inferredcites →https://doi.org/10.1021/bi300870gopenalex-snapshot
Structures of Apo and Product-Bound Human l -Asparaginase: Insights into the Mechanism of Autoproteolysis and Substrate Hydrolysis
inferredcites →https://doi.org/10.1021/bi9915768openalex-snapshot
Three-Dimensional Structure of Escherichia coli Asparagine Synthetase B: A Short Journey from Substrate to Product,
inferredcites →https://doi.org/10.1021/jf991006eopenalex-snapshot
Measuring Asparagine Synthetase Activity in Crude Plant Extracts
inferredcites →https://doi.org/10.1023/a:1005998918418openalex-snapshot
Structural analysis of the nit2/nit1/nit3 gene cluster encoding nitrilases, enzymes catalyzing the terminal activation step in indole-acetic acid biosynthesis in Arabidopsis thaliana
inferredcites →https://doi.org/10.1023/a:1026772627998openalex-snapshot
Singh B.K. (Ed.): Plant Amino Acids. Biochemistry and Biotechnology
inferredcites →https://doi.org/10.1034/j.1399-3054.2001.1110312.xopenalex-snapshot
Dark‐inducible genes from Arabidopsisthaliana are associated with leaf senescence and repressed by sugars
inferredcites →https://doi.org/10.1038/263703a0openalex-snapshot
Ammonia assimilation in lupin nodules
inferredcites →https://doi.org/10.1038/378416a0openalex-snapshot
A protein catalytic framework with an N-terminal nucleophile is capable of self-activation
inferredcites →https://doi.org/10.1038/nature19079openalex-snapshot
Mechanism of arginine sensing by CASTOR1 upstream of mTORC1
inferredcites →https://doi.org/10.1038/nchembio.1520openalex-snapshot
Plant perception of β-aminobutyric acid is mediated by an aspartyl-tRNA synthetase
inferredcites →https://doi.org/10.1038/ncomms11457openalex-snapshot
Asparagine promotes cancer cell proliferation through use as an amino acid exchange factor
inferredcites →https://doi.org/10.1039/c6np00122jopenalex-snapshot
A tale of four kingdoms – isoxazolin-5-one- and 3-nitropropanoic acid-derived natural products
inferredcites →https://doi.org/10.1042/bj0180395openalex-snapshot
Investigations on the Nitrogenous Metabolism of the Higher Plants. Part VI
inferredcites →https://doi.org/10.1046/j.1365-313x.1996.09010001.xopenalex-snapshot
Metabolic regulation of asparagine synthetase gene expression in maize (Zea mays L.) root tips
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00302.xopenalex-snapshot
Reciprocal regulation of distinct asparagine synthetase genes by light and metabolites in Arabidopsis thaliana
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01618.xopenalex-snapshot
Reduced amino acid content in transgenic potato tubers due to antisense inhibition of the leaf H+/amino acid symporter StAAP1
inferredcites →https://doi.org/10.1055/s-2006-923876openalex-snapshot
Correlation between AS1 Gene Expression and Seed Protein Contents in Different Soybean (Glycine Max [L.] Merr.) Cultivars
inferredcites →https://doi.org/10.1071/fp03198openalex-snapshot
Distinct cis-elements in the Asparagus officinalis asparagine synthetase promoter respond to carbohydrate and senescence signals
inferredcites →https://doi.org/10.1073/pnas.0800211105openalex-snapshot
Systems approach identifies an organic nitrogen-responsive gene network that is regulated by the master clock control gene CCA1
inferredcites →https://doi.org/10.1073/pnas.0910097107openalex-snapshot
Chloroplast acetyl-CoA carboxylase activity is 2-oxoglutarate–regulated by interaction of PII with the biotin carboxyl carrier subunit
inferredcites →https://doi.org/10.1073/pnas.1404657111openalex-snapshot
Hit-and-run transcriptional control by bZIP1 mediates rapid nutrient signaling in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1613736114openalex-snapshot
Nit1 is a metabolite repair enzyme that hydrolyzes deaminated glutathione
inferredcites →https://doi.org/10.1073/pnas.78.10.5978openalex-snapshot
Asparagine amide metabolism in developing cotyledons of soybean
inferredcites →https://doi.org/10.1073/pnas.81.10.3059openalex-snapshot
Formation of cyanide from carbon 1 of 1-aminocyclopropane-1-carboxylic acid during its conversion to ethylene
inferredcites →https://doi.org/10.1074/jbc.m007890200openalex-snapshot
The Arabidopsis thaliana Isogene NIT4 and Its Orthologs in Tobacco Encode β-Cyano-l-alanine Hydratase/Nitrilase
inferredcites →https://doi.org/10.1074/jbc.m116.732511openalex-snapshot
Amino Acids Regulate mTORC1 by an Obligate Two-step Mechanism
inferredcites →https://doi.org/10.1074/jbc.m205699200openalex-snapshot
Plant C-N Hydrolases and the Identification of a Plant N-Carbamoylputrescine Amidohydrolase Involved in Polyamine Biosynthesis
inferredcites →https://doi.org/10.1074/jbc.m504501200openalex-snapshot
Crystal Structure of Isoaspartyl Aminopeptidase in Complex with l-Aspartate
inferredcites →https://doi.org/10.1080/01140671.1997.9514006openalex-snapshot
Asparagine synthetase gene expression increases as sucrose declines in broccoli after harvest
inferredcites →https://doi.org/10.1093/jexbot/53.370.905openalex-snapshot
Enzyme redundancy and the importance of 2‐oxoglutarate in plant ammonium assimilation
inferredcites →https://doi.org/10.1093/jxb/39.6.695openalex-snapshot
Diurnal Changes in Asparaginase Activity in Pea Leaves
inferredcites →https://doi.org/10.1093/jxb/39.6.707openalex-snapshot
Diurnal Changes in Asparaginase Activity in Pea Leaves
inferredcites →https://doi.org/10.1093/jxb/eri191openalex-snapshot
Free amino acid profiles suggest a possible role for asparagine in the control of storage-product accumulation in developing seeds of low- and high-protein soybean lines
inferredcites →https://doi.org/10.1093/jxb/ers039openalex-snapshot
Relationship between asparagine metabolism and protein concentration in soybean seed
inferredcites →https://doi.org/10.1093/jxb/eru236openalex-snapshot
The challenges of commercializing second-generation transgenic crop traits necessitate the development of international public sector research infrastructure
inferredcites →https://doi.org/10.1093/jxb/eru323openalex-snapshot
Nitrogen metabolism meets phytopathology
inferredcites →https://doi.org/10.1093/jxb/erw145openalex-snapshot
Perspectives for a better understanding of the metabolic integration of photorespiration within a complex plant primary metabolism network
inferredcites →https://doi.org/10.1093/jxb/erw467openalex-snapshot
High serine:glyoxylate aminotransferase activity lowers leaf daytime serine levels, inducing the phosphoserine pathway in Arabidopsis
inferredcites →https://doi.org/10.1093/mp/sst110openalex-snapshot
Increased β-Cyanoalanine Nitrilase Activity Improves Cyanide Tolerance and Assimilation in Arabidopsis
inferredcites →https://doi.org/10.1093/oxfordjournals.aob.a087355openalex-snapshot
Utilization of Nitrogen Sources by Immature Soybean Cotyledons in Culture
inferredcites →https://doi.org/10.1093/pcp/pch092openalex-snapshot
Up-Regulation and Localization of Asparagine Synthetase in Tomato Leaves Infected by the Bacterial Pathogen Pseudomonas syringae
inferredcites →https://doi.org/10.1093/pcp/pch192openalex-snapshot
Cadmium Toxicity Induced Changes in Nitrogen Management in Lycopersicon esculentum Leading to a Metabolic Safeguard Through an Amino Acid Storage Strategy
inferredcites →https://doi.org/10.1093/pcp/pcs156openalex-snapshot
The K+-Dependent Asparaginase, NSE1, is Crucial for Plant Growth and Seed Production in Lotus japonicus
inferredcites →https://doi.org/10.1093/pcp/pcv005openalex-snapshot
Asparagine Synthetase1, but not Asparagine Synthetase2, is Responsible for the Biosynthesis of Asparagine Following the Supply of Ammonium to Rice Roots
inferredcites →https://doi.org/10.1093/pcp/pcv184openalex-snapshot
Asparagine Metabolic Pathways in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.10.3.447openalex-snapshot
PHYSIOLOGICAL RÔLE OF ASPARAGINE AND RELATED SUBSTANCES IN NITROGEN METABOLISM OF PLANTS
inferredcites →https://doi.org/10.1104/pp.103.020123openalex-snapshot
Overexpression of the ASN1 Gene Enhances Nitrogen Status in Seeds of Arabidopsis
inferredcites →https://doi.org/10.1104/pp.103.021253openalex-snapshot
Microarray Analysis of the Nitrate Response in Arabidopsis Roots and Shoots Reveals over 1,000 Rapidly Responding Genes and New Linkages to Glucose, Trehalose-6-Phosphate, Iron, and Sulfate Metabolism
inferredcites →https://doi.org/10.1104/pp.103.033126openalex-snapshot
Correlation of ASN2 Gene Expression with Ammonium Metabolism in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.104.043778openalex-snapshot
Amino Acid Metabolism in Maize Earshoots. Implications for Assimilate Preconditioning and Nitrogen Signaling
inferredcites →https://doi.org/10.1104/pp.104.044610openalex-snapshot
Genomic Analysis of the Nitrate Response Using a Nitrate Reductase-Null Mutant of Arabidopsis
inferredcites →https://doi.org/10.1104/pp.104.047019openalex-snapshot
Genome-Wide Reprogramming of Primary and Secondary Metabolism, Protein Synthesis, Cellular Growth Processes, and the Regulatory Infrastructure of Arabidopsis in Response to Nitrogen
inferredcites →https://doi.org/10.1104/pp.106.086694openalex-snapshot
Arabidopsis Seed Development and Germination Is Associated with Temporally Distinct Metabolic Switches
inferredcites →https://doi.org/10.1104/pp.106.4.1347openalex-snapshot
Metabolic Regulation of the Gene Encoding Glutamine-Dependent Asparagine Synthetase in Arabidopsis thaliana
inferredcites →https://doi.org/10.1104/pp.111.3.877openalex-snapshot
Sugar Regulation of Harvest-Related Genes in Asparagus
inferredcites →https://doi.org/10.1104/pp.112.203299openalex-snapshot
Carbon and Nitrogen Provisions Alter the Metabolic Flux in Developing Soybean Embryos
inferredcites →https://doi.org/10.1104/pp.16.00950openalex-snapshot
Histidine Regulates Seed Oil Deposition through Abscisic Acid Biosynthesis and β-oxidation
inferredcites →https://doi.org/10.1104/pp.56.6.807openalex-snapshot
Asparagine Metabolism—Key to the Nitrogen Nutrition of Developing Legume Seeds
inferredcites →https://doi.org/10.1104/pp.60.2.235openalex-snapshot
Asparaginase and Asparagine Transaminase in Soybean Leaves and Root Nodules
inferredcites →https://doi.org/10.1104/pp.65.1.22openalex-snapshot
Distribution and Properties of a Potassium-dependent Asparaginase Isolated from Developing Seeds of Pisum sativum and Other Plants
inferredcites →https://doi.org/10.1104/pp.67.1.37openalex-snapshot
Synthesis, Storage, and Utilization of Amino Compounds in White Lupin (Lupinus albus L.)
inferredcites →https://doi.org/10.1104/pp.69.2.308openalex-snapshot
[15N]NMR Determination of Asparagine and Glutamine Nitrogen Utilization for Synthesis of Storage Protein in Developing Cotyledons of Soybean in Culture
inferredcites →https://doi.org/10.1104/pp.71.4.841openalex-snapshot
Amino Acid Transport and Metabolism in Relation to the Nitrogen Economy of a Legume Leaf
inferredcites →https://doi.org/10.1104/pp.72.4.1127openalex-snapshot
Subcellular Localization of Asparaginase and Asparagine Aminotransferase in Pisum sativum Leaves
inferredcites →https://doi.org/10.1104/pp.74.4.822openalex-snapshot
Amino Acid Metabolism in Pea Leaves
inferredcites →https://doi.org/10.1104/pp.75.3.527openalex-snapshot
Utilization of the Amide Groups of Asparagine and 2-Hydroxysuccinamic Acid by Young Pea Leaves
inferredcites →https://doi.org/10.1104/pp.77.2.506openalex-snapshot
Diurnal Variation of Asparaginase in Developing Pea Leaves
inferredcites →https://doi.org/10.1104/pp.78.2.334openalex-snapshot
Role of Asparagine in the Photorespiratory Nitrogen Metabolism of Pea Leaves
inferredcites →https://doi.org/10.1104/pp.87.4.806openalex-snapshot
A Mutant of Nicotiana sylvestris Lacking Serine:Glyoxylate Aminotransferase
inferredcites →https://doi.org/10.1105/tpc.108.058479openalex-snapshot
Protein Repair l -Isoaspartyl Methyltransferase1 Is Involved in Both Seed Longevity and Germination Vigor in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.110.073833openalex-snapshot
Altered Xylem-Phloem Transfer of Amino Acids Affects Metabolism and Leads to Increased Seed Yield and Oil Content in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.7.7.887openalex-snapshot
Use of Arabidopsis mutants and genes to study amide amino acid biosynthesis.
inferredcites →https://doi.org/10.1107/s0907444913009347openalex-snapshot
Structures of enzyme–intermediate complexes of yeast Nit2: insights into its catalytic mechanism and different substrate specificity compared with mammalian Nit2
inferredcites →https://doi.org/10.1107/s1399004714008700openalex-snapshot
Na+/K+exchange switches the catalytic apparatus of potassium-dependent plant L -asparaginase
inferredcites →https://doi.org/10.1111/j.1365-3040.2012.02576.xopenalex-snapshot
Arabidopsis thaliana ASN2 encoding asparagine synthetase is involved in the control of nitrogen assimilation and export during vegetative growth
inferredcites →https://doi.org/10.1111/j.1365-313x.1994.00695.xopenalex-snapshot
Asparaginase gene expression is regulated in a complex spatial and temporal pattern in nitrogen‐sink tissues
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02530.xopenalex-snapshot
Immediate‐early and delayed cytokinin response genes of Arabidopsis thaliana identified by genome‐wide expression profiling reveal novel cytokinin‐sensitive processes and suggest cytokinin action through transcriptional cascades
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03385.xopenalex-snapshot
The sucrose regulated transcription factor bZIP11 affects amino acid metabolism by regulating the expression of ASPARAGINE SYNTHETASE1 and PROLINE DEHYDROGENASE2
inferredcites →https://doi.org/10.1111/j.1365-313x.2009.03890.xopenalex-snapshot
AAP1 regulates import of amino acids into developing Arabidopsis embryos
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04622.xopenalex-snapshot
Pepper asparagine synthetase 1 ( CaAS1 ) is required for plant nitrogen assimilation and defense responses to microbial pathogens
inferredcites →https://doi.org/10.1111/j.1399-3054.2008.01092.xopenalex-snapshot
Nitrogen stress and the expression of asparagine synthetase in roots and nodules of soybean (Glycine max)
inferredcites →https://doi.org/10.1111/j.1399-3054.2012.01712.xopenalex-snapshot
Changes in the C/N balance caused by increasing external ammonium concentrations are driven by carbon and energy availabilities during ammonium nutrition in pea plants: the key roles of asparagine synthetase and anaplerotic enzymes
inferredcites →https://doi.org/10.1111/j.1432-1033.2004.04254.xopenalex-snapshot
Expression, purification and catalytic activity of Lupinus luteus asparagine β‐amidohydrolase and its Escherichia coli homolog
inferredcites →https://doi.org/10.1111/j.1438-8677.2012.00606.xopenalex-snapshot
The GCN2 homologue in Arabidopsis thaliana interacts with uncharged tRNA and uses Arabidopsis eIF2α molecules as direct substrates
inferredcites →https://doi.org/10.1111/j.1467-7652.2008.00363.xopenalex-snapshot
Low‐acrylamide French fries and potato chips
inferredcites →https://doi.org/10.1111/j.1467-7652.2012.00720.xopenalex-snapshot
Tuber‐specific silencing of asparagine synthetase‐1 reduces the acrylamide‐forming potential of potatoes grown in the field without affecting tuber shape and yield
inferredcites →https://doi.org/10.1111/j.1744-7348.2006.00104.xopenalex-snapshot
Asparagine in plants
inferredcites →https://doi.org/10.1111/pbi.12421openalex-snapshot
Silencing of vacuolar invertase and asparagine synthetase genes and its impact on acrylamide formation of fried potato products
inferredcites →https://doi.org/10.1111/pce.12692openalex-snapshot
Deciphering the molecular basis of ammonium uptake and transport in maritime pine
inferredcites →https://doi.org/10.1111/pce.12755openalex-snapshot
The β‐cyanoalanine synthase pathway: beyond cyanide detoxification
inferredcites →https://doi.org/10.1111/pce.12826openalex-snapshot
The inhibition of protein translation mediated by AtGCN1 is essential for cold tolerance in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/ppl.12341openalex-snapshot
Soybean seeds overexpressing asparaginase exhibit reduced nitrogen concentration
inferredcites →https://doi.org/10.1111/risa.12709openalex-snapshot
Reduction in Dietary Acrylamide Exposure—Impact of Potatoes with Low Acrylamide Potential
inferredcites →https://doi.org/10.1111/tpj.13567openalex-snapshot
ASN 1 ‐encoded asparagine synthetase in floral organs contributes to nitrogen filling in Arabidopsis seeds
inferredcites →https://doi.org/10.1126/science.aab2674openalex-snapshot
Sestrin2 is a leucine sensor for the mTORC1 pathway
inferredcites →https://doi.org/10.1146/annurev-arplant-043014-114648openalex-snapshot
TOR Signaling and Nutrient Sensing
inferredcites →https://doi.org/10.1152/physrev.00008.2006openalex-snapshot
Role of Na + and K + in Enzyme Function
inferredcites →https://doi.org/10.1182/blood-2013-10-535112openalex-snapshot
The glutaminase activity of l-asparaginase is not required for anticancer activity against ASNS-negative cells
inferredcites →https://doi.org/10.1186/s12284-017-0143-8openalex-snapshot
A temporal and spatial contribution of asparaginase to asparagine catabolism during development of rice grains
inferredcites →https://doi.org/10.1199/tab.0010openalex-snapshot
Primary N-assimilation into Amino Acids in Arabidopsis
inferredcites →https://doi.org/10.18388/abp.2006_3291openalex-snapshot
Structural aspects of L-asparaginases, their friends and relations.
inferredcites →https://doi.org/10.3109/07388551.2015.1120705openalex-snapshot
Therapeutic l -asparaginase: upstream, downstream and beyond
inferredcites →https://doi.org/10.3389/fpls.2014.00437openalex-snapshot
Soybean seed proteome rebalancing
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Handbuch der biochemischen Arbeitsmethoden
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