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Isolation and characterisation of two MATE genes in rye

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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/s00122-001-0782-3openalex-snapshot
AFLP markers tightly linked to the aluminum-tolerance gene Alt3 in rye (Secale cereale L.)
inferredcites →https://doi.org/10.1007/s00122-005-2029-1openalex-snapshot
A new aluminum tolerance gene located on rye chromosome arm 7RS
inferredcites →https://doi.org/10.1007/s00122-006-0427-7openalex-snapshot
Candidate gene identification of an aluminum-activated organic acid transporter gene at the Alt4 locus for aluminum tolerance in rye (Secale cereale L.)
inferredcites →https://doi.org/10.1007/s00122-007-0562-9openalex-snapshot
High-resolution mapping of the Alp locus and identification of a candidate gene HvMATE controlling aluminium tolerance in barley (Hordeum vulgare L.)
inferredcites →https://doi.org/10.1007/s001220050575openalex-snapshot
Genetic control of aluminium tolerance in rye (Secale cereale L.)
inferredcites →https://doi.org/10.1007/s00425-003-1043-2openalex-snapshot
Differential Al resistance and citrate secretion in barley ( Hordeum vulgare L.)
inferredcites →https://doi.org/10.1007/s11104-009-0035-9openalex-snapshot
From the rye Alt3 and Alt4 aluminum tolerance loci to orthologous genes in other cereals
inferredcites →https://doi.org/10.1016/j.jplph.2009.02.009openalex-snapshot
Two MATE proteins play a role in iron efficiency in soybean
inferredcites →https://doi.org/10.1016/j.pbi.2005.03.011openalex-snapshot
Transporters of secondary metabolites
inferredcites →https://doi.org/10.1016/j.tips.2006.09.001openalex-snapshot
The MATE proteins as fundamental transporters of metabolic and xenobiotic organic cations
inferredcites →https://doi.org/10.1016/s1360-1385(01)01961-6openalex-snapshot
Aluminium tolerance in plants and the complexing role of organic acids
inferredcites →https://doi.org/10.1038/ng2074openalex-snapshot
A gene in the multidrug and toxic compound extrusion (MATE) family confers aluminum tolerance in sorghum
inferredcites →https://doi.org/10.1046/j.1432-1033.2003.03418.xopenalex-snapshot
The multidrug/oligosaccharidyl‐lipid/polysaccharide (MOP) exporter superfamily
inferredcites →https://doi.org/10.1073/pnas.0700117104openalex-snapshot
Zinc finger protein STOP1 is critical for proton tolerance in Arabidopsis and coregulates a key gene in aluminum tolerance
inferredcites →https://doi.org/10.1073/pnas.0812512106openalex-snapshot
Vacuolar transport of nicotine is mediated by a multidrug and toxic compound extrusion (MATE) transporter in Nicotiana tabacum
inferredcites →https://doi.org/10.1074/jbc.m108777200openalex-snapshot
Functional Cloning and Characterization of a Plant Efflux Carrier for Multidrug and Heavy Metal Detoxification
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a029266openalex-snapshot
Specific Secretion of Citric Acid Induced by Al Stress in Cassia tora L.
inferredcites →https://doi.org/10.1093/pcp/pcm091openalex-snapshot
An Aluminum-Activated Citrate Transporter in Barley
inferredcites →https://doi.org/10.1104/pp.103.3.695openalex-snapshot
Aluminum Tolerance in Wheat (Triticum aestivum L.) (II. Aluminum-Stimulated Excretion of Malic Acid from Root Apices)
inferredcites →https://doi.org/10.1104/pp.104.045633openalex-snapshot
FRD3 Controls Iron Localization in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.105.064352openalex-snapshot
Characterization of Vacuolar Transport of the Endogenous Alkaloid Berberine in Coptis japonica
inferredcites →https://doi.org/10.1104/pp.106.093005openalex-snapshot
Spatial Distribution and Temporal Variation of the Rice Silicon Transporter Lsi1
inferredcites →https://doi.org/10.1104/pp.107.097162openalex-snapshot
The FRD3-Mediated Efflux of Citrate into the Root Vasculature Is Necessary for Efficient Iron Translocation
inferredcites →https://doi.org/10.1104/pp.108.128132openalex-snapshot
OsFRDL1 Is a Citrate Transporter Required for Efficient Translocation of Iron in Rice
inferredcites →https://doi.org/10.1104/pp.108.129155openalex-snapshot
A Second Mechanism for Aluminum Resistance in Wheat Relies on the Constitutive Efflux of Citrate from Roots
inferredcites →https://doi.org/10.1104/pp.122.3.687openalex-snapshot
Aluminum Tolerance Genes on the Short Arm of Chromosome 3R Are Linked to Organic Acid Release in Triticale
inferredcites →https://doi.org/10.1104/pp.123.4.1537openalex-snapshot
Pattern of Aluminum-Induced Secretion of Organic Acids Differs between Rye and Wheat
inferredcites →https://doi.org/10.1105/tpc.001495openalex-snapshot
FRD3, a Member of the Multidrug and Toxin Efflux Family, Controls Iron Deficiency Responses in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.010035openalex-snapshot
Arabidopsis ALF5 , a Multidrug Efflux Transporter Gene Family Member, Confers Resistance to Toxins
inferredcites →https://doi.org/10.1105/tpc.106.046029openalex-snapshot
TheArabidopsisMATE Transporter TT12 Acts as a Vacuolar Flavonoid/H+-Antiporter Active in Proanthocyanidin-Accumulating Cells of the Seed Coat
inferredcites →https://doi.org/10.1105/tpc.109.070771openalex-snapshot
A Zinc Finger Transcription Factor ART1 Regulates Multiple Genes Implicated in Aluminum Tolerance in Rice
inferredcites →https://doi.org/10.1105/tpc.13.4.853openalex-snapshot
The TRANSPARENT TESTA12 Gene of Arabidopsis Encodes a Multidrug Secondary Transporter-like Protein Required for Flavonoid Sequestration in Vacuoles of the Seed Coat Endothelium
inferredcites →https://doi.org/10.1111/j.1365-313x.2003.01991.xopenalex-snapshot
A wheat gene encoding an aluminum‐activated malate transporter
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02573.xopenalex-snapshot
Transgenic proteoid roots of white lupin: a vehicle for characterizing and silencing root genes involved in adaptation to P stress
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03696.xopenalex-snapshot
Aluminum‐activated citrate and malate transporters from the MATE and ALMT families function independently to confer Arabidopsis aluminum tolerance
inferredcites →https://doi.org/10.1128/aac.42.7.1778openalex-snapshot
NorM, a Putative Multidrug Efflux Protein, of Vibrio parahaemolyticus and Its Homolog in Escherichia coli
inferredcites →https://doi.org/10.1128/jb.184.2.572-576.2002openalex-snapshot
VmrA, a Member of a Novel Class of Na + -Coupled Multidrug Efflux Pumps from Vibrio parahaemolyticus
inferredcites →https://doi.org/10.1186/1471-2229-8-89openalex-snapshot
Physiological and molecular characterization of aluminum resistance in Medicago truncatula
inferredcites →https://doi.org/10.1534/genetics.107.083451openalex-snapshot
AnALMT1Gene Cluster Controlling Aluminum Tolerance at theAlt4Locus of Rye (Secale cerealeL.)
inferredcites →https://doi.org/10.2307/3871345openalex-snapshot
The TRANSPARENT TESTA12 Gene of Arabidopsis Encodes a Multidrug Secondary Transporter-Like Protein Required for Flavonoid Sequestration in Vacuoles of the Seed Coat Endothelium
inferredcites →https://doi.org/10.2307/3871390openalex-snapshot
Arabidopsis ALF5, a Multidrug Efflux Transporter Gene Family Member, Confers Resistance to Toxins

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Unravelling Aluminium Toxicity in Barley: Understanding Physiological and Molecular Insights into Altered Stomatal Kinetics Caused by the Accumulation of Aluminium in Guard Cells
inferred← citeshttps://doi.org/10.2139/ssrn.4890341openalex-extracted
Unravelling Aluminium Toxicity in Barley: Understanding Physiological and Molecular Insights into Altered Stomatal Kinetics Caused by the Accumulation of Aluminium in Guard Cells
inferred← citeshttps://doi.org/10.1002/9781118728482.ch6openalex-snapshot
Aluminum Tolerance in Sorghum and Maize
inferred← citeshttps://doi.org/10.1002/9781118860526.ch4openalex-snapshot
The “Gatekeeper” Concept: Cell‐Type Specific Molecular Mechanisms of Plant Adaptation to Abiotic Stress
inferred← citeshttps://doi.org/10.1002/9781119691419.ch6openalex-snapshot
Aluminium Stress in Plants
inferred← citeshttps://doi.org/10.1007/978-3-030-83383-1_11openalex-snapshot
Genetics and Genomics of Stress Tolerance
inferred← citeshttps://doi.org/10.1007/978-3-030-83383-1_9openalex-snapshot
Bridging the Genotype–Phenotype Gap for Precision Breeding in Rye
inferred← citeshttps://doi.org/10.1007/978-3-319-13368-3_2openalex-snapshot
Physiology and Biochemistry of Aluminum Toxicity and Tolerance in Crops
inferred← citeshttps://doi.org/10.1007/978-3-319-14526-6_10openalex-snapshot
Heavy Metal Uptake and Transport in Plants
inferred← citeshttps://doi.org/10.1007/978-3-319-19968-9_2openalex-snapshot
Transcriptional Regulation of Al Tolerance in Plants
inferred← citeshttps://doi.org/10.1007/978-94-007-7575-6_8openalex-snapshot
Genetic Dissection of Aluminium Tolerance in the Triticeae
inferred← citeshttps://doi.org/10.1007/978-981-19-6103-8_8openalex-snapshot
The Multidrug and Toxic Compound Extrusion (MATE) Family in Plants and Their Significance in Metal Transport
inferred← citeshttps://doi.org/10.1007/978-981-19-6103-8_9openalex-snapshot
Molecular Mechanism of Aluminum Tolerance in Plants: An Overview
inferred← citeshttps://doi.org/10.1007/s10534-016-9910-zopenalex-snapshot
Toxicity and tolerance of aluminum in plants: tailoring plants to suit to acid soils
inferred← citeshttps://doi.org/10.1007/s10535-015-0537-7openalex-snapshot
Signal transduction during aluminum-induced secretion of organic acids in plants
inferred← citeshttps://doi.org/10.1007/s10535-017-0749-0openalex-snapshot
Characterization, genetic diversity, phylogenetic relationships, and expression of the aluminum tolerance MATE1 gene in Secale species
inferred← citeshttps://doi.org/10.1007/s10535-018-0804-5openalex-snapshot
Transcriptional profiling of wheat and wheat-rye addition lines to identify candidate genes for aluminum tolerance
inferred← citeshttps://doi.org/10.1007/s10661-013-3443-5openalex-snapshot
The secretion of organic acids is also regulated by factors other than aluminum
inferred← citeshttps://doi.org/10.1007/s11032-011-9668-5openalex-snapshot
The ScAACT1 gene at the Q alt5 locus as a candidate for increased aluminum tolerance in rye (Secale cereale L.)
inferred← citeshttps://doi.org/10.1007/s11104-012-1289-1openalex-snapshot
Dual effects of transgenic Brassica napus overexpressing CS gene on tolerances to aluminum toxicity and phosphorus deficiency
inferred← citeshttps://doi.org/10.1007/s11104-014-2073-1openalex-snapshot
Molecular mechanisms of Al tolerance in gramineous plants
inferred← citeshttps://doi.org/10.1007/s11104-014-2325-0openalex-snapshot
Possible involvement of heterotrimeric G-protein signaling in Al-induced secretion of organic acid anions in Arabidopsis and rye
inferred← citeshttps://doi.org/10.1007/s11104-018-3746-yopenalex-snapshot
Natural variation ofCsSTOP1in tea plant (Camellia sinensis) related to aluminum tolerance
inferred← citeshttps://doi.org/10.1007/s11104-019-04192-wopenalex-snapshot
Functional characterization of three MATE genes in relation to aluminum-induced citrate efflux from soybean root
inferred← citeshttps://doi.org/10.1007/s11738-012-1067-yopenalex-snapshot
Al-induced secretion of organic acid, gene expression and root elongation in soybean roots
inferred← citeshttps://doi.org/10.1007/s12041-016-0686-2openalex-snapshot
Genomewide analysis of MATE-type gene family in maize reveals microsynteny and their expression patterns under aluminum treatment
inferred← citeshttps://doi.org/10.1007/s12374-020-09280-4openalex-snapshot
Aluminium Toxicity and Its Tolerance in Plant: A Review
inferred← citeshttps://doi.org/10.1016/b978-0-12-802922-0.00007-8openalex-snapshot
Exploration and Utilization of Aluminum-Tolerant Barley Germplasm
inferred← citeshttps://doi.org/10.1016/b978-0-323-98332-7.00003-2openalex-snapshot
Role of low molecular organic acids in regulating physiological and molecular aspects of plants under abiotic stress
inferred← citeshttps://doi.org/10.1016/j.bbrc.2024.150821openalex-snapshot
MATE transporter OsMATE2 mediates root growth, grain size and weight by interacting with Mn-SOD and PABP in rice
inferred← citeshttps://doi.org/10.1016/j.cj.2026.01.010openalex-snapshot
HvMATE-mediated aluminium exclusion sustains stomatal function and photosynthesis in barley under acidic soils
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2018.08.087openalex-snapshot
Mechanisms of organic acids and boron induced tolerance of aluminum toxicity: A review
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2024.116558openalex-snapshot
Genome-wide identification of MATE and ALMT genes and their expression profiling in mungbean (Vigna radiata L.) under aluminium stress
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2024.117001openalex-snapshot
Physiological and comprehensive transcriptome analysis reveals distinct regulatory mechanisms for aluminum tolerance of Trifolium repens
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2019.02.011openalex-snapshot
Biochemical, physiological and genetic analysis of aluminum tolerance of different rye species
inferred← citeshttps://doi.org/10.1016/j.fmre.2023.03.004openalex-snapshot
Towards sustainable use of acidic soils: Deciphering aluminum-resistant mechanisms in plants
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2024.135011openalex-snapshot
Comparative transcriptome analyses reveal regulatory network and hub genes of aluminum response in roots of elephant grass (Cenchrus purpureus)
inferred← citeshttps://doi.org/10.1016/j.jplph.2012.01.011openalex-snapshot
Zonal responses of sensitive vs. tolerant wheat roots during Al exposure and recovery
inferred← citeshttps://doi.org/10.1016/j.ncrops.2024.100034openalex-snapshot
Research progress on the physiological and molecular mechanisms underlying soybean aluminum resistance
inferred← citeshttps://doi.org/10.1016/j.pedsph.2022.10.001openalex-snapshot
Molecular mechanisms of plant adaptation to acid soils: A review
inferred← citeshttps://doi.org/10.1016/j.plantsci.2017.05.010openalex-snapshot
Functional characterization of the SbNrat1 gene in sorghum
inferred← citeshttps://doi.org/10.1016/j.plantsci.2021.110951openalex-snapshot
The rye transcription factor ScSTOP1 regulates the tolerance to aluminum by activating the ALMT1 transporter
inferred← citeshttps://doi.org/10.1016/j.plaphy.2011.01.026openalex-snapshot
Towards a knowledge-based correction of iron chlorosis
inferred← citeshttps://doi.org/10.1016/j.tplants.2012.02.008openalex-snapshot
Transcriptional regulation of aluminium tolerance genes
inferred← citeshttps://doi.org/10.1038/s41598-017-18146-8openalex-snapshot
Functional characterization and discovery of modulators of SbMATE, the agronomically important aluminium tolerance transporter from Sorghum bicolor
inferred← citeshttps://doi.org/10.1071/fp13362openalex-snapshot
Brachypodium distachyon: a model species for aluminium tolerance in Poaceae
inferred← citeshttps://doi.org/10.1071/fpv37n4_foopenalex-snapshot
Foreword : Understanding how plants cope with acid soils
inferred← citeshttps://doi.org/10.1080/02571862.2017.1335891openalex-snapshot
The potential of omics technologies as tools to understand the environmental factors influencing okra (Abelmoschus esculentus) growth and adaptation
inferred← citeshttps://doi.org/10.1080/07388551.2021.1874282openalex-snapshot
Aluminum toxicity and aluminum stress-induced physiological tolerance responses in higher plants
inferred← citeshttps://doi.org/10.1080/10643389.2020.1859306openalex-snapshot
The aluminum tolerance and detoxification mechanisms in plants; recent advances and prospects
inferred← citeshttps://doi.org/10.1080/14620316.2024.2340578openalex-snapshot
Genome-wide analysis of the MATE gene family and expression analysis of subfamily III genes in response to aluminium toxicity in pineapple
inferred← citeshttps://doi.org/10.1080/15592324.2022.2057060openalex-snapshot
Aluminum stress signaling, response, and adaptive mechanisms in plants
inferred← citeshttps://doi.org/10.1093/jxb/erab019openalex-snapshot
Organic acids: versatile stress-response roles in plants
inferred← citeshttps://doi.org/10.1093/jxb/erq272openalex-snapshot
The identification of aluminium-resistance genes provides opportunities for enhancing crop production on acid soils
inferred← citeshttps://doi.org/10.1093/jxb/ert039openalex-snapshot
The role of VuMATE1 expression in aluminium-inducible citrate secretion in rice bean (Vigna umbellata) roots
inferred← citeshttps://doi.org/10.1093/jxb/erv364openalex-snapshot
Phosphorus and iron deficiencies induce a metabolic reprogramming and affect the exudation traits of the woody plantFragaria×ananassa
inferred← citeshttps://doi.org/10.1093/jxb/ery357openalex-snapshot
The role of transposable elements in the evolution of aluminium resistance in plants
inferred← citeshttps://doi.org/10.1093/jxb/erz089openalex-snapshot
AhFRDL1-mediated citrate secretion contributes to adaptation to iron deficiency and aluminum stress in peanuts
inferred← citeshttps://doi.org/10.1093/jxb/erz246openalex-snapshot
The multitasking abilities of MATE transporters in plants
inferred← citeshttps://doi.org/10.1093/pcp/pct019openalex-snapshot
LjMATE1: A Citrate Transporter Responsible for Iron Supply to the Nodule Infection Zone of Lotus japonicus
inferred← citeshttps://doi.org/10.1093/pcp/pcw026openalex-snapshot
Functional Analysis of a MATE GeneOsFRDL2Revealed its Involvement in Al-Induced Secretion of Citrate, but a Lower Contribution to Al Tolerance in Rice
inferred← citeshttps://doi.org/10.1093/pcp/pcx152openalex-snapshot
Two MATE Transporters with Different Subcellular Localization are Involved in Al Tolerance in Buckwheat
inferred← citeshttps://doi.org/10.1093/treephys/tpt011openalex-snapshot
Metabolic responses to iron deficiency in roots of Carrizo citrange [Citrus sinensis (L.) Osbeck. x Poncirus trifoliata (L.) Raf.]
inferred← citeshttps://doi.org/10.1104/pp.19.00598openalex-snapshot
A Vacuolar Phytosiderophore Transporter Alters Iron and Zinc Accumulation in Polished Rice Grains
inferred← citeshttps://doi.org/10.1105/tpc.112.096925openalex-snapshot
Nramp5 Is a Major Transporter Responsible for Manganese and Cadmium Uptake in Rice
inferred← citeshttps://doi.org/10.1111/j.1365-3040.2011.02410.xopenalex-snapshot
A de novo synthesis citrate transporter, Vigna umbellata multidrug and toxic compound extrusion, implicates in Al‐activated citrate efflux in rice bean (Vigna umbellata) root apex
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2011.04757.xopenalex-snapshot
An Al‐inducible MATE gene is involved in external detoxification of Al in rice
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2011.04837.xopenalex-snapshot
A tonoplast‐localized half‐size ABC transporter is required for internal detoxification of aluminum in rice
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2012.04994.xopenalex-snapshot
A promoter‐swap strategy between the AtALMT and AtMATE genes increased Arabidopsis aluminum resistance and improved carbon‐use efficiency for aluminum resistance
inferred← citeshttps://doi.org/10.1111/jipb.12041openalex-snapshot
The Plant Vascular System: Evolution, Development and Functions F
inferred← citeshttps://doi.org/10.1111/jipb.12162openalex-snapshot
The role of aluminum sensing and signaling in plant aluminum resistance
inferred← citeshttps://doi.org/10.1111/plb.12219openalex-snapshot
On the consequences of aluminium stress in rye: repression of two mitochondrial malate dehydrogenase mRNA s
inferred← citeshttps://doi.org/10.1111/plb.12864openalex-snapshot
Molecular cloning of TaMATE2 homoeologues potentially related to aluminium tolerance in bread wheat (Triticum aestivum L.)
inferred← citeshttps://doi.org/10.1111/plb.13107openalex-snapshot
Isolation and characterization of a new MATE gene located in the same chromosome arm of the aluminium tolerance (Alt1) rye locus
inferred← citeshttps://doi.org/10.1111/ppl.12179openalex-snapshot
Molecular characterization of the citrate transporter gene TaMATE1 and expression analysis of upstream genes involved in organic acid transport under Al stress in bread wheat (Triticum aestivum)
inferred← citeshttps://doi.org/10.1111/ppl.13382openalex-snapshot
Alleviating aluminum toxicity in plants: Implications of reactive oxygen species signaling and crosstalk with other signaling pathways
inferred← citeshttps://doi.org/10.1111/tpj.12266openalex-snapshot
Adaptation to acidic soil is achieved by increased numbers of cis‐acting elements regulating ALMT1 expression in H olcus lanatus
inferred← citeshttps://doi.org/10.1111/tpj.12337openalex-snapshot
WRKY 46 functions as a transcriptional repressor of ALMT 1, regulating aluminum‐induced malate secretion in A rabidopsis
inferred← citeshttps://doi.org/10.1111/tpj.16463openalex-snapshot
A citrate efflux transporter important for manganese distribution and phosphorus uptake in rice
inferred← citeshttps://doi.org/10.1139/g11-060openalex-snapshot
Transcriptomic responses to aluminum stress in soybean roots
inferred← citeshttps://doi.org/10.1146/annurev-arplant-043014-114822openalex-snapshot
Plant Adaptation to Acid Soils: The Molecular Basis for Crop Aluminum Resistance
inferred← citeshttps://doi.org/10.1155/2013/173682openalex-snapshot
Roles of Organic Acid Anion Secretion in Aluminium Tolerance of Higher Plants
inferred← citeshttps://doi.org/10.1186/1471-2164-15-153openalex-snapshot
Genetic dissection of Al tolerance QTLs in the maize genome by high density SNP scan
inferred← citeshttps://doi.org/10.1186/1471-2229-13-134openalex-snapshot
Molecular characterization of TaSTOP1 homoeologues and their response to aluminium and proton (H+) toxicity in bread wheat (Triticum aestivum L.)
inferred← citeshttps://doi.org/10.1186/s12870-016-0895-0openalex-snapshot
The similar and different evolutionary trends of MATE family occurred between rice and Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1186/s12870-017-1115-2openalex-snapshot
Global analysis of the MATE gene family of metabolite transporters in tomato
inferred← citeshttps://doi.org/10.1201/b15553-12openalex-snapshot
Genetics
inferred← citeshttps://doi.org/10.1271/kagakutoseibutsu.53.529openalex-snapshot
inferred← citeshttps://doi.org/10.1371/journal.pone.0020830openalex-snapshot
The Relationship between Population Structure and Aluminum Tolerance in Cultivated Sorghum
inferred← citeshttps://doi.org/10.1534/g3.115.025791openalex-snapshot
Back to Acid Soil Fields: The Citrate Transporter SbMATE Is a Major Asset for Sustainable Grain Yield for Sorghum Cultivated on Acid Soils
inferred← citeshttps://doi.org/10.1631/jzus.b1900188openalex-snapshot
Mechanisms and regulation of aluminum-induced secretion of organic acid anions from plant roots
inferred← citeshttps://doi.org/10.18699/vj20.655openalex-snapshot
Genetic diversity of VIR Raphanus sativus L. collections on aluminum tolerance
inferred← citeshttps://doi.org/10.25959/23206100openalex-snapshot
Enhancing aluminium resistance in barley through over-expression of MATE genes
inferred← citeshttps://doi.org/10.32615/bp.2019.099openalex-snapshot
Expression profile analysis of MATE gene family in rice
inferred← citeshttps://doi.org/10.3389/fgene.2021.675260openalex-snapshot
Aluminum or Low pH – Which Is the Bigger Enemy of Barley? Transcriptome Analysis of Barley Root Meristem Under Al and Low pH Stress
inferred← citeshttps://doi.org/10.3389/fphys.2014.00201openalex-snapshot
Beyond cellular detoxification: a plethora of physiological roles for MDR transporter homologs in plants
inferred← citeshttps://doi.org/10.3389/fpls.2015.00192openalex-snapshot
Jacks of metal/metalloid chelation trade in plants—an overview
inferred← citeshttps://doi.org/10.3389/fpls.2016.00685openalex-snapshot
Oxidative Metabolism of Rye (Secale cereale L.) after Short Term Exposure to Aluminum: Uncovering the Glutathione–Ascorbate Redox Network
inferred← citeshttps://doi.org/10.3389/fpls.2018.01334openalex-snapshot
Assessing How the Aluminum-Resistance Traits in Wheat and Rye Transfer to Hexaploid and Octoploid Triticale
inferred← citeshttps://doi.org/10.3389/fpls.2022.1027560openalex-snapshot
Characterization of GmMATE13 in its contribution of citrate efflux and aluminum resistance in soybeans
inferred← citeshttps://doi.org/10.3389/fpls.2022.832981openalex-snapshot
Repression of Mitochondrial Citrate Synthase Genes by Aluminum Stress in Roots of Secale cereale and Brachypodium distachyon
inferred← citeshttps://doi.org/10.3390/agriculture14020285openalex-snapshot
Ability of Nutrient Management and Molecular Physiology Advancements to Overcome Abiotic Stress: A Study on Sub-Saharan African Crops
inferred← citeshttps://doi.org/10.3390/agronomy9090498openalex-snapshot
Physical Location of New Stripe Rust Resistance Gene(s) and PCR-Based Markers on Rye (Secale cereale L.) Chromosome 5 Using 5R Dissection Lines
inferred← citeshttps://doi.org/10.3390/horticulturae12010022openalex-snapshot
Comparative Transcriptional Analysis and Functional Validation of Aluminum Stress-Responsive RsALS3 Gene in Two Rhododendron Cultivars
inferred← citeshttps://doi.org/10.3390/ijms20071551openalex-snapshot
Molecular Mechanisms for Coping with Al Toxicity in Plants
inferred← citeshttps://doi.org/10.3390/ijms21124316openalex-snapshot
Comparative Transcriptome Analysis of Two Contrasting Soybean Varieties in Response to Aluminum Toxicity
inferred← citeshttps://doi.org/10.3390/ijms21228869openalex-snapshot
Wild Soybean Oxalyl-CoA Synthetase Degrades Oxalate and Affects the Tolerance to Cadmium and Aluminum Stresses
inferred← citeshttps://doi.org/10.3390/ijms22137235openalex-snapshot
Citric Acid-Mediated Abiotic Stress Tolerance in Plants
inferred← citeshttps://doi.org/10.3390/ijms25179542openalex-snapshot
The Role of Low-Molecular-Weight Organic Acids in Metal Homeostasis in Plants
inferred← citeshttps://doi.org/10.3390/microorganisms12122433openalex-snapshot
Multidrug and Toxic Compound Extrusion Transporters: Ubiquitous Multifaceted Proteins in Microbes, Plants, and Their Interactions
inferred← citeshttps://doi.org/10.3390/plants9111448openalex-snapshot
Identification and Expression of the Multidrug and Toxic Compound Extrusion (MATE) Gene Family in Capsicum annuum and Solanum tuberosum
inferred← citeshttps://doi.org/10.4238/2012.july.19.14openalex-snapshot
Review Genetic and molecular mechanisms of aluminum tolerance in plants
inferred← citeshttps://doi.org/10.5511/plantbiotechnology.14.0904aopenalex-snapshot
The multidrug and toxic compound extrusion (MATE) family in plants
inferred← citeshttps://doi.org/10.5772/25187openalex-snapshot
Biotechnological Solutions for Enhancing the Aluminium Resistance of Crop Plants
inferred← citeshttps://doi.org/10.5772/7943openalex-snapshot
Concentration-Dependent Laser Performance of Yb:YAG Ceramics and Passively Q-switched Yb:YAG/Cr,Ca:YAG Lasers
inferred← citeshttps://doi.org/10.7287/peerj.11461v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Physiological, nutritional, and molecular responses of Brazilian sugarcane cultivars under stress by aluminum (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.11461v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Physiological, nutritional, and molecular responses of Brazilian sugarcane cultivars under stress by aluminum (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.11461v0.1/reviews/3openalex-snapshot
Peer Review #3 of "Physiological, nutritional, and molecular responses of Brazilian sugarcane cultivars under stress by aluminum (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.11461v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Physiological, nutritional, and molecular responses of Brazilian sugarcane cultivars under stress by aluminum (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.11461v0.2/reviews/3openalex-snapshot
Peer Review #3 of "Physiological, nutritional, and molecular responses of Brazilian sugarcane cultivars under stress by aluminum (v0.2)"
inferred← citeshttps://doi.org/10.7717/peerj.11461openalex-snapshot
Physiological, nutritional, and molecular responses of Brazilian sugarcane cultivars under stress by aluminum
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.