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Full title: Label free quantitative proteomics of Qualea grandiflora Mart. (Vochysiaceae) roots indicates an aluminium requirement for growth and development

https://doi.org/10.1101/396093
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/pmic.200600703openalex-snapshot
Identification of aluminum‐responsive proteins in rice roots by a proteomic approach: Cysteine synthase as a key player in Al response
inferredcites →https://doi.org/10.1007/1-4020-4099-7_9openalex-snapshot
The physiology, genetics and molecular biology of plant aluminum resistance and toxicity
inferredcites →https://doi.org/10.1007/bf00197346openalex-snapshot
Organic acid exudation as an aluminum-tolerance mechanism in maize (Zea mays L.)
inferredcites →https://doi.org/10.1007/bf01106775openalex-snapshot
Organic acid exudation as an aluminum-tolerance mechanism in maize (Zea mays L.)
inferredcites →https://doi.org/10.1007/bf02374657openalex-snapshot
Aluminium accumulation by some cerrado native species of central Brazil
inferredcites →https://doi.org/10.1007/s00018-008-8516-1openalex-snapshot
Structure-function relationships in methionine adenosyltransferases
inferredcites →https://doi.org/10.1007/s00425-006-0350-9openalex-snapshot
An α-galactosidase with an essential function during leaf development
inferredcites →https://doi.org/10.1007/s00425-007-0668-yopenalex-snapshot
Physiological roles of plant glycoside hydrolases
inferredcites →https://doi.org/10.1007/s004250000277openalex-snapshot
Arabidopsis thaliana germin-like proteins: common and specific features point to a variety of functions
inferredcites →https://doi.org/10.1007/s00449-011-0640-xopenalex-snapshot
Structural and functional characterization of S-adenosylmethionine (SAM) synthetase from Pichia ciferrii
inferredcites →https://doi.org/10.1007/s11104-004-1158-7openalex-snapshot
The Physiology, Genetics and Molecular Biology of Plant Aluminum Resistance and Toxicity
inferredcites →https://doi.org/10.1007/s11270-005-8682-9openalex-snapshot
Toxic Effects, Oxidative Stress and Ultrastructural Changes in Moss Taxithelium Nepalense (Schwaegr.) Broth. Under Chromium and Lead Phytotoxicity
inferredcites →https://doi.org/10.1016/0167-4838(92)90476-topenalex-snapshot
Malate dehydrogenase isoenzymes: Cellular locations and role in the flow of metabolites between the cytoplasm and cell organelles
inferredcites →https://doi.org/10.1016/b978-0-12-803158-2.00002-3openalex-snapshot
Copper Stress and Responses in Plants
inferredcites →https://doi.org/10.1016/j.envexpbot.2010.05.013openalex-snapshot
Al-hyperaccumulator Vochysiaceae from the Brazilian Cerrado store aluminum in their chloroplasts without apparent damage
inferredcites →https://doi.org/10.1016/j.jmb.2015.11.006openalex-snapshot
BlastKOALA and GhostKOALA: KEGG Tools for Functional Characterization of Genome and Metagenome Sequences
inferredcites →https://doi.org/10.1016/j.jprot.2012.09.035openalex-snapshot
Root protein profile changes induced by Al exposure in two rice cultivars differing in Al tolerance
inferredcites →https://doi.org/10.1016/j.jprot.2013.12.023openalex-snapshot
Root proteome of rice studied by iTRAQ provides integrated insight into aluminum stress tolerance mechanisms in plants
inferredcites →https://doi.org/10.1016/j.plantsci.2005.06.006openalex-snapshot
Signs of oxidative stress in the chlorotic leaves of iron starved plants
inferredcites →https://doi.org/10.1016/j.plaphy.2007.12.014openalex-snapshot
Structure and function of plant acyl-CoA oxidases
inferredcites →https://doi.org/10.1016/j.tplants.2012.02.008openalex-snapshot
Transcriptional regulation of aluminium tolerance genes
inferredcites →https://doi.org/10.1016/s0959-440x(03)00098-8openalex-snapshot
Formate dehydrogenase – a versatile enzyme in changing environments
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/10.1021/acs.jproteome.6b00128openalex-snapshot
Proteome Modification in Tomato Plants upon Long-Term Aluminum Treatment
inferredcites →https://doi.org/10.1034/j.1399-3054.2001.1120308.xopenalex-snapshot
Changes in cell‐wall properties of wheat (Triticum aestivum) roots during aluminum‐induced growth inhibition
inferredcites →https://doi.org/10.1034/j.1399-3054.2001.1130401.xopenalex-snapshot
Sustaining S‐adenosyl‐ l ‐methionine‐dependent methyltransferase activity in plant cells
inferredcites →https://doi.org/10.1038/35002501openalex-snapshot
Biodiversity hotspots for conservation priorities
inferredcites →https://doi.org/10.1038/nrm1746openalex-snapshot
Growth of the plant cell wall
inferredcites →https://doi.org/10.1038/srep10343openalex-snapshot
The mitochondrial malate dehydrogenase 1 gene GhmMDH1 is involved in plant and root growth under phosphorus deficiency conditions in cotton
inferredcites →https://doi.org/10.1042/bj3010625openalex-snapshot
NAD+-dependent formate dehydrogenase
inferredcites →https://doi.org/10.1073/pnas.0602868103openalex-snapshot
AtALMT1 , which encodes a malate transporter, is identified as one of several genes critical for aluminum tolerance in Arabidopsis
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/10.1081/css-120003885openalex-snapshot
Mechanisms of adaptation to high aluminum condition in native plant species growing in acid soils: a review
inferredcites →https://doi.org/10.1093/aob/mcl005openalex-snapshot
Citrate Transporters Play a Critical Role in Aluminium-stimulated Citrate Efflux in Rice Bean (Vigna umbellata) Roots
inferredcites →https://doi.org/10.1093/jxb/erl275openalex-snapshot
Methyl recycling activities are co-ordinately regulated during plant development
inferredcites →https://doi.org/10.1093/jxb/erq028openalex-snapshot
Glyoxylate rather than ascorbate is an efficient precursor for oxalate biosynthesis in rice
inferredcites →https://doi.org/10.1093/jxb/err045openalex-snapshot
Identification of genes involved in cell wall biogenesis in grasses by differential gene expression profiling of elongating and non-elongating maize internodes
inferredcites →https://doi.org/10.1093/jxb/erw019openalex-snapshot
Enhancing cytokinin synthesis by overexpressing ipt alleviated drought inhibition of root growth through activating ROS-scavenging systems in Agrostis stolonifera
inferredcites →https://doi.org/10.1093/nar/gku1003openalex-snapshot
STRING v10: protein–protein interaction networks, integrated over the tree of life
inferredcites →https://doi.org/10.1093/pcp/41.4.383openalex-snapshot
Role of Organic Acids in Detoxification of Aluminum in Higher Plants
inferredcites →https://doi.org/10.1093/pcp/pcu135openalex-snapshot
Global Transcriptome Analysis of Al-Induced Genes in an Al-Accumulating Species, Common Buckwheat (Fagopyrum esculentum Moench)
inferredcites →https://doi.org/10.1096/fj.09-130187openalex-snapshot
Conformational signals in the C‐terminal domain of methionine adenosyltransferase I/III determine its nucleocytoplasmic distribution
inferredcites →https://doi.org/10.1104/pp.102.2.685openalex-snapshot
cDNA Encoding a Putative 10-Kilodalton Chaperonin from Arabidopsis thaliana
inferredcites →https://doi.org/10.1104/pp.103.022129openalex-snapshot
Aluminum-Induced Gene Expression and Protein Localization of a Cell Wall-Associated Receptor Kinase in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.103.031237openalex-snapshot
The Fasciclin-Like Arabinogalactan Proteins of Arabidopsis. A Multigene Family of Putative Cell Adhesion Molecules
inferredcites →https://doi.org/10.1104/pp.103.3.685openalex-snapshot
Aluminum Tolerance in Wheat (Triticum aestivum L.) (I. Uptake and Distribution of Aluminum in Root Apices)
inferredcites →https://doi.org/10.1104/pp.106.083824openalex-snapshot
The Multigene Family Encoding Germin-Like Proteins of Barley. Regulation and Function in Basal Host Resistance
inferredcites →https://doi.org/10.1104/pp.108.134700openalex-snapshot
STOP1 Regulates Multiple Genes That Protect Arabidopsis from Proton and Aluminum Toxicities
inferredcites →https://doi.org/10.1104/pp.113.4.1033openalex-snapshot
Internal Detoxification Mechanism of Al in Hydrangea (Identification of Al Form in the Leaves)
inferredcites →https://doi.org/10.1104/pp.117.3.745openalex-snapshot
High Aluminum Resistance in Buckwheat1
inferredcites →https://doi.org/10.1104/pp.68.3.703openalex-snapshot
Formate Oxidation and Oxygen Reduction by Leaf Mitochondria
inferredcites →https://doi.org/10.1104/pp.96.3.737openalex-snapshot
Mechanism of Aluminum Tolerance in Snapbeans
inferredcites →https://doi.org/10.1105/tpc.007872openalex-snapshot
The Arabidopsis SOS5 Locus Encodes a Putative Cell Surface Adhesion Protein and Is Required for Normal Cell Expansion
inferredcites →https://doi.org/10.1105/tpc.106.041541openalex-snapshot
Rice NTRC Is a High-Efficiency Redox System for Chloroplast Protection against Oxidative Damage
inferredcites →https://doi.org/10.1105/tpc.15.00452openalex-snapshot
MicroRNA miR396 Regulates the Switch between Stem Cells and Transit-Amplifying Cells in Arabidopsis Roots
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.1399-3054.2010.01355.xopenalex-snapshot
Spatial characteristics of aluminum uptake and translocation in roots of buckwheat (Fagopyrum esculentum)
inferredcites →https://doi.org/10.1111/j.1567-1364.2008.00387.xopenalex-snapshot
The alcohol dehydrogenases ofSaccharomyces cerevisiae: a comprehensive review
inferredcites →https://doi.org/10.1126/science.276.5318.1566openalex-snapshot
Aluminum Tolerance in Transgenic Plants by Alteration of Citrate Synthesis
inferredcites →https://doi.org/10.1146/annurev.arplant.56.032604.144106openalex-snapshot
CALCIUM OXALATE IN PLANTS: Formation and Function
inferredcites →https://doi.org/10.1186/1471-2164-11-620openalex-snapshot
Identification and analysis of the germin-like gene family in soybean
inferredcites →https://doi.org/10.1199/tab.0121openalex-snapshot
Aspartate-Derived Amino Acid Biosynthesis inArabidopsis thaliana
inferredcites →https://doi.org/10.1199/tab.0168openalex-snapshot
Cytokinins
inferredcites →https://doi.org/10.1242/dev.142331openalex-snapshot
Control of root cap maturation and cell detachment by BEARSKIN transcription factors in Arabidopsis
inferredcites →https://doi.org/10.1371/journal.pone.0144927openalex-snapshot
Global Transcriptome Analysis Reveals Distinct Aluminum-Tolerance Pathways in the Al-Accumulating Species Hydrangea macrophylla and Marker Identification
inferredcites →https://doi.org/10.1371/journal.pone.0150583openalex-snapshot
AtGRP3 Is Implicated in Root Size and Aluminum Response Pathways in Arabidopsis
inferredcites →https://doi.org/10.1590/s1677-04202005000100013openalex-snapshot
Metabolism and root exudation of organic acid anions under aluminium stress
inferredcites →https://doi.org/10.2134/agronj1977.00021962006900050025xopenalex-snapshot
Cerrado Vegetation in Brazil: An Edaphic Gradient1
inferredcites →https://doi.org/10.2307/2845050openalex-snapshot
Soil Resources and Plant Communities of the Central Brazilian Cerrado and Their Development
inferredcites →https://doi.org/10.32607/20758251-2011-3-4-38-54openalex-snapshot
NAD+-dependent Formate Dehydrogenase from Plants
inferredcites →https://doi.org/10.3389/fpls.2015.01140openalex-snapshot
Genome-Wide Analysis of the Fasciclin-Like Arabinogalactan Protein Gene Family Reveals Differential Expression Patterns, Localization, and Salt Stress Response in Populus
inferredcites →https://doi.org/10.3390/microorganisms5010003openalex-snapshot
Using Network Extracted Ontologies to Identify Novel Genes with Roles in Appressorium Development in the Rice Blast Fungus Magnaporthe oryzae
inferredcites →https://doi.org/10.4061/2011/352538openalex-snapshot
The Catalytic Machinery of a Key Enzyme in Amino Acid Biosynthesis
inferredcites →https://doi.org/10.4172/2155-9821.1000227openalex-snapshot
Pectin Methylesterases: A Review

What points at this work

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

inferred← citeshttps://doi.org/10.1002/cbf.3497openalex-snapshot
Proteomic changes in skeletal muscle of aged rats in response to resistance training
inferred← citeshttps://doi.org/10.3389/fcell.2020.00380openalex-snapshot
Paternal Resistance Training Modulates Calcaneal Tendon Proteome in the Offspring Exposed to High-Fat Diet
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