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ALFIN ‐ LIKE 6 is involved in root hair elongation during phosphate deficiency in Arabidopsis
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-1-4020-8435-5_5openalex-snapshot
Root strategies for phosphorus acquisition
inferredcites →https://doi.org/10.1007/bf00333575openalex-snapshot
Auxin-resistant mutants of Arabidopsis thaliana with an altered morphology
inferredcites →https://doi.org/10.1007/pl00008150openalex-snapshot
Alfin1 transcription factor overexpression enhances plant root growth under normal and saline conditions and improves salt tolerance in alfalfa
inferredcites →https://doi.org/10.1007/s00018-012-1090-6openalex-snapshot
Transcriptional regulation of phosphate acquisition by higher plants
inferredcites →https://doi.org/10.1007/s00425-004-1296-4openalex-snapshot
The MsPRP2 promoter enables strong heterologous gene expression in a root-specific manner and is enhanced by overexpression of Alfin�1
inferredcites →https://doi.org/10.1016/b978-0-12-473542-2.x5000-7openalex-snapshot
Mineral Nutrition of Higher Plants
inferredcites →https://doi.org/10.1016/j.bbagen.2010.11.006openalex-snapshot
The Arabidopsis thaliana phosphate starvation responsive gene AtPPsPase1 encodes a novel type of inorganic pyrophosphatase
inferredcites →https://doi.org/10.1016/j.biochi.2006.05.007openalex-snapshot
Phosphate deficiency promotes modification of iron distribution in Arabidopsis plants
inferredcites →https://doi.org/10.1016/j.cell.2005.01.001openalex-snapshot
Genomic Maps and Comparative Analysis of Histone Modifications in Human and Mouse
inferredcites →https://doi.org/10.1016/j.molcel.2006.10.026openalex-snapshot
Yng1 PHD Finger Binding to H3 Trimethylated at K4 Promotes NuA3 HAT Activity at K14 of H3 and Transcription at a Subset of Targeted ORFs
inferredcites →https://doi.org/10.1016/j.molcel.2007.11.010openalex-snapshot
Recognition of Trimethylated Histone H3 Lysine 4 Facilitates the Recruitment of Transcription Postinitiation Factors and Pre-mRNA Splicing
inferredcites →https://doi.org/10.1016/j.tplants.2004.09.003openalex-snapshot
Short on phosphate: plant surveillance and countermeasures
inferredcites →https://doi.org/10.1016/j.tplants.2011.05.006openalex-snapshot
Root developmental adaptation to phosphate starvation: better safe than sorry
inferredcites →https://doi.org/10.1016/j.ydbio.2003.12.037openalex-snapshot
The ENHANCER OF TRY AND CPC1 gene acts redundantly with TRIPTYCHON and CAPRICE in trichome and root hair cell patterning in Arabidopsis
inferredcites →https://doi.org/10.1023/a:1006081926699openalex-snapshot
Alfin1, a novel zinc-finger protein in alfalfa roots that binds to promoter elements in the salt-inducible MsPRP2 gene
inferredcites →https://doi.org/10.1023/a:1013324727040openalex-snapshot
Topsoil foraging – an architectural adaptation of plants to low phosphorus availability
inferredcites →https://doi.org/10.1038/nature01080openalex-snapshot
Active genes are tri-methylated at K4 of histone H3
inferredcites →https://doi.org/10.1038/nature04814openalex-snapshot
Molecular mechanism of histone H3K4me3 recognition by plant homeodomain of ING2
inferredcites →https://doi.org/10.1038/nature04815openalex-snapshot
A PHD finger of NURF couples histone H3 lysine 4 trimethylation with chromatin remodelling
inferredcites →https://doi.org/10.1038/ncb1076openalex-snapshot
Histone H3 lysine 4 methylation patterns in higher eukaryotic genes
inferredcites →https://doi.org/10.1038/ng.529openalex-snapshot
A basic helix-loop-helix transcription factor controls cell growth and size in root hairs
inferredcites →https://doi.org/10.1038/nsmb0706-572openalex-snapshot
It takes a PHD to interpret histone methylation
inferredcites →https://doi.org/10.1042/bj20070102openalex-snapshot
BHLH32 modulates several biochemical and morphological processes that respond to Pi starvation in Arabidopsis
inferredcites →https://doi.org/10.1046/j.1365-3040.2001.00695.xopenalex-snapshot
Regulation of root hair density by phosphorus availability in Arabidopsis thaliana
inferredcites →https://doi.org/10.1046/j.1365-313x.1995.08030457.xopenalex-snapshot
Efficient isolation and mapping of Arabidopsis thaliana T‐DNA insert junctions by thermal asymmetric interlaced PCR
inferredcites →https://doi.org/10.1046/j.1365-313x.1997.11040841.xopenalex-snapshot
Mutants of Arabidopsis thaliana with pleiotropic effects on the expression of the gene for β‐amylase and on the accumulation of anthocyanin that are inducible by sugars
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00343.xopenalex-snapshot
Floral dip: a simplified method for Agrobacterium ‐mediated transformation of Arabidopsis thaliana
inferredcites →https://doi.org/10.1046/j.1469-8137.2003.00695.xopenalex-snapshot
Phosphorus acquisition and use: critical adaptations by plants for securing a nonrenewable resource
inferredcites →https://doi.org/10.1073/pnas.0505266102openalex-snapshot
A genome-wide transcriptional analysis using Arabidopsis thaliana Affymetrix gene chips determined plant responses to phosphate deprivation
inferredcites →https://doi.org/10.1073/pnas.082696499openalex-snapshot
Arabidopsis disrupted in SQD2 encoding sulfolipid synthase is impaired in phosphate-limited growth
inferredcites →https://doi.org/10.1074/jbc.m408799200openalex-snapshot
A Novel Phosphatidylcholine-hydrolyzing Phospholipase C Induced by Phosphate Starvation in Arabidopsis
inferredcites →https://doi.org/10.1074/mcp.m112.020461openalex-snapshot
Complementary Proteome and Transcriptome Profiling in Phosphate-deficient Arabidopsis Roots Reveals Multiple Levels of Gene Regulation
inferredcites →https://doi.org/10.1093/genetics/120.3.621openalex-snapshot
Genetic applications of an inverse polymerase chain reaction.
inferredcites →https://doi.org/10.1093/jxb/ern195openalex-snapshot
Manganese deficiency alters the patterning and development of root hairs in Arabidopsis
inferredcites →https://doi.org/10.1093/mp/ssp086openalex-snapshot
Ubiquitin-Specific Protease 14 (UBP14) Is Involved in Root Responses to Phosphate Deficiency in Arabidopsis
inferredcites →https://doi.org/10.1093/pcp/pcn157openalex-snapshot
Identification of an F-Box Protein that Negatively Regulates Pi Starvation Responses
inferredcites →https://doi.org/10.1104/pp.010934openalex-snapshot
Phosphate Availability Alters Architecture and Causes Changes in Hormone Sensitivity in the Arabidopsis Root System
inferredcites →https://doi.org/10.1104/pp.103.029066openalex-snapshot
Environmentally Induced Plasticity of Root Hair Development in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.105.073825openalex-snapshot
Characterization of low phosphorus insensitive Mutants Reveals a Crosstalk between Low Phosphorus-Induced Determinate Root Development and the Activation of Genes Involved in the Adaptation of Arabidopsis to Phosphorus Deficiency
inferredcites →https://doi.org/10.1104/pp.106.093971openalex-snapshot
WRKY75 Transcription Factor Is a Modulator of Phosphate Acquisition and Root Development in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.110.166520openalex-snapshot
Coexpression-Based Clustering of Arabidopsis Root Genes Predicts Functional Modules in Early Phosphate Deficiency Signaling
inferredcites →https://doi.org/10.1104/pp.126.2.875openalex-snapshot
Phosphate Availability Regulates Root System Architecture in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.105.038943openalex-snapshot
Regulation of Phosphate Homeostasis by MicroRNA in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-3040.1996.tb00386.xopenalex-snapshot
Stimulation of root hair elongation in Arabidopsis thaliana by low phosphorus availability
inferredcites →https://doi.org/10.1111/j.1365-313x.2009.03795.xopenalex-snapshot
Arabidopsis ING and Alfin1‐like protein families localize to the nucleus and bind to H3K4me3/2 via plant homeodomain fingers
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04375.xopenalex-snapshot
Dissection of local and systemic transcriptional responses to phosphate starvation in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1469-8137.1975.tb01409.xopenalex-snapshot
COMPARISON OF THE EFFECTS OF A LOCALISED SUPPLY OF PHOSPHATE, NITRATE, AMMONIUM AND POTASSIUM ON THE GROWTH OF THE SEMINAL ROOT SYSTEM, AND THE SHOOT, IN BARLEY
inferredcites →https://doi.org/10.1126/science.1105373openalex-snapshot
Positional Signaling Mediated by a Receptor-like Kinase in Arabidopsis
inferredcites →https://doi.org/10.1146/annurev-arplant-042110-103849openalex-snapshot
Signaling Network in Sensing Phosphate Availability in Plants
inferredcites →https://doi.org/10.1146/annurev.arplant.50.1.665openalex-snapshot
PHOSPHATE ACQUISITION
inferredcites →https://doi.org/10.1371/journal.pgen.1001102openalex-snapshot
A Central Regulatory System Largely Controls Transcriptional Activation and Repression Responses to Phosphate Starvation in Arabidopsis
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4766567openalex-extracted
Egphl7, Egphr1 and Egphr2 Bind to P1bs and a Unique Motif, Agatwc, for Phosphate Starvation Transcriptional Regulation in Oil Palm
inferred← citeshttps://doi.org/10.1002/9781118958841.ch2openalex-snapshot
Sensing, signaLling, and CONTROL of phosphate starvation in plants: molecular players and applications
inferred← citeshttps://doi.org/10.1002/9781118958841.ch3openalex-snapshot
‘Omics’ Approaches Towards Understanding Plant Phosphorus Acquisition and Use
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0517openalex-snapshot
Sensing, Signalling, and Control of Phosphate Starvation in Plants: Molecular Players and Applications
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0518openalex-snapshot
‘Omics’ Approaches Towards Understanding Plant Phosphorus Acquisition and Use
inferred← citeshttps://doi.org/10.1007/978-1-0716-3183-6_9openalex-snapshot
Comprehensive Survey of ChIP-Seq Datasets to Identify Candidate Iron Homeostasis Genes Regulated by Chromatin Modifications
inferred← citeshttps://doi.org/10.1007/978-3-030-84985-6_11openalex-snapshot
Role of Nitric Oxide as a Double Edged Sword in Root Growth and Development
inferred← citeshttps://doi.org/10.1007/978-981-96-9859-2_5openalex-snapshot
Epigenetic Regulation of Abiotic Stress Responses
inferred← citeshttps://doi.org/10.1007/s00299-026-03964-wopenalex-snapshot
ASP1-mediated deSUMOylation of AL6 controls seed dormancy in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s00425-020-03520-0openalex-snapshot
H3K4 trimethylation dynamics impact diverse developmental and environmental responses in plants
inferred← citeshttps://doi.org/10.1007/s00438-015-0993-yopenalex-snapshot
Characterization and stress-induced expression analysis of Alfin-like transcription factors in Brassica rapa
inferred← citeshttps://doi.org/10.1007/s10142-015-0454-zopenalex-snapshot
Versatility of germin-like proteins in their sequences, expressions, and functions
inferred← citeshttps://doi.org/10.1007/s10265-019-01100-2openalex-snapshot
A gene regulatory network for root hair development
inferred← citeshttps://doi.org/10.1007/s10725-024-01152-yopenalex-snapshot
Broadening the epigenetic horizon of abiotic stress response in plants
inferred← citeshttps://doi.org/10.1007/s11103-019-00937-4openalex-snapshot
Zinc finger protein 5 (ZFP5) associates with ethylene signaling to regulate the phosphate and potassium deficiency-induced root hair development in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s11738-016-2139-1openalex-snapshot
Alfin-like transcription factor family: characterization and expression profiling against stresses in Brassica oleracea
inferred← citeshttps://doi.org/10.1007/s13237-016-0159-2openalex-snapshot
Transcription factors involved in acid stress responses in plants
inferred← citeshttps://doi.org/10.1007/s13258-016-0491-6openalex-snapshot
Genome-wide identification and comparative analysis of Alfin-like transcription factors in maize
inferred← citeshttps://doi.org/10.1007/s13258-023-01383-9openalex-snapshot
Genomic survey of high-throughput RNA-Seq data implicates involvement of long intergenic non-coding RNAs (lincRNAs) in cytoplasmic male-sterility and fertility restoration in pigeon pea
inferred← citeshttps://doi.org/10.1007/s40626-021-00223-zopenalex-snapshot
The Conringia planisiliqua Alfin-like2 gene enhances drought and salt tolerance in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s44154-022-00039-0openalex-snapshot
Plant phosphate nutrition: sensing the stress
inferred← citeshttps://doi.org/10.1016/b978-0-323-91861-9.00013-6openalex-snapshot
Use of microbial inoculants against biotic stress in vegetable crops: physiological and molecular aspect
inferred← citeshttps://doi.org/10.1016/b978-0-443-18675-2.00001-8openalex-snapshot
Molecular basis of plant nutrient use efficiency - concepts and challenges for its improvement
inferred← citeshttps://doi.org/10.1016/j.bbagen.2024.130580openalex-snapshot
Epigenetic regulation influenced by soil microbiota and nutrients: Paving road to epigenome editing in plants
inferred← citeshttps://doi.org/10.1016/j.bbrc.2015.06.015openalex-snapshot
Arabidopsis RING E3 ubiquitin ligase AtATL80 is negatively involved in phosphate mobilization and cold stress response in sufficient phosphate growth conditions
inferred← citeshttps://doi.org/10.1016/j.btre.2024.e00845openalex-snapshot
Alfin-like (AL) transcription factor family in Oryza sativa L.: Genome-wide analysis and expression profiling under different stresses
inferred← citeshttps://doi.org/10.1016/j.cj.2024.07.012openalex-snapshot
PHD17 acts as a target of miR1320 to negatively control cold tolerance via JA-activated signaling in rice
inferred← citeshttps://doi.org/10.1016/j.cj.2026.06.017openalex-snapshot
Activation of GmGCS1 by GmPHR1 modulates root architecture and phosphorus acquisition in soybean
inferred← citeshttps://doi.org/10.1016/j.csbj.2021.09.014openalex-snapshot
Efficient and accurate identification of protein complexes from protein-protein interaction networks based on the clustering coefficient
inferred← citeshttps://doi.org/10.1016/j.devcel.2019.01.002openalex-snapshot
Tackling Plant Phosphate Starvation by the Roots
inferred← citeshttps://doi.org/10.1016/j.hal.2022.102323openalex-snapshot
Identification of epigenetic histone modifications and analysis of histone lysine methyltransferases in Alexandrium pacificum
inferred← citeshttps://doi.org/10.1016/j.hpj.2024.07.001openalex-snapshot
Investigating the role of MpAL1 in drought stress responses in Malus prunifolia: insights into AL gene family functionality
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.144539openalex-snapshot
Optimizing plant phosphate uptake: Advances in the core regulatory mechanisms of phosphate starvation response proteins and their macromolecular partners: A review
inferred← citeshttps://doi.org/10.1016/j.jmb.2018.08.021openalex-snapshot
Structural Analysis of the Arabidopsis AL2-PAL and PRC1 Complex Provides Mechanistic Insight into Active-to-Repressive Chromatin State Switch
inferred← citeshttps://doi.org/10.1016/j.jplph.2021.153363openalex-snapshot
Epigenetic regulation of nitrogen and phosphorus responses in plants
inferred← citeshttps://doi.org/10.1016/j.jprot.2018.06.006openalex-snapshot
iTRAQ-based analysis of the Arabidopsis proteome reveals insights into the potential mechanisms of anthocyanin accumulation regulation in response to phosphate deficiency
inferred← citeshttps://doi.org/10.1016/j.ncrna.2020.10.002openalex-snapshot
Genome-wide analysis of PHD finger gene family and identification of potential miRNA and their PHD finger gene specific targets in Oryza sativa indica
inferred← citeshttps://doi.org/10.1016/j.pbi.2017.04.001openalex-snapshot
Nutrient stress-induced chromatin changes in plants
inferred← citeshttps://doi.org/10.1016/j.plantsci.2015.06.020openalex-snapshot
miRNA778 and SUVH6 are involved in phosphate homeostasis in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plantsci.2021.111060openalex-snapshot
PERK13 modulates phosphate deficiency-induced root hair elongation in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plipres.2021.101091openalex-snapshot
Headgroup biosynthesis of phosphatidylcholine and phosphatidylethanolamine in seed plants
inferred← citeshttps://doi.org/10.1016/j.rhisph.2024.100922openalex-snapshot
Physiological, hormonal and molecular dynamics of root system architectural response to drought stress signaling in crops
inferred← citeshttps://doi.org/10.1016/j.scienta.2020.109459openalex-snapshot
Genome-wide identification and testing of superior reference genes for transcript normalization during analyses of flesh development in Asian pear cultivars
inferred← citeshttps://doi.org/10.1016/j.semcdb.2019.03.010openalex-snapshot
The potential application of genome editing by using CRISPR/Cas9, and its engineered and ortholog variants for studying the transcription factors involved in the maintenance of phosphate homeostasis in model plants
inferred← citeshttps://doi.org/10.1016/j.stress.2023.100168openalex-snapshot
Genome-wide identification of Alfin Like (AL) transcription factors and their regulatory role in abiotic stress responses in Poplar (Populus trichocarpa)
inferred← citeshttps://doi.org/10.1038/s41598-018-21148-9openalex-snapshot
An Alfin-like gene from Atriplex hortensis enhances salt and drought tolerance and abscisic acid response in transgenic Arabidopsis
inferred← citeshttps://doi.org/10.1038/srep15708openalex-snapshot
The histone deacetylase HDA19 controls root cell elongation and modulates a subset of phosphate starvation responses in Arabidopsis
inferred← citeshttps://doi.org/10.1038/srep26820openalex-snapshot
Discriminative gene co-expression network analysis uncovers novel modules involved in the formation of phosphate deficiency-induced root hairs in Arabidopsis
inferred← citeshttps://doi.org/10.1080/15592324.2019.1686236openalex-snapshot
Epigenetic regulation: another layer in plant nutrition
inferred← citeshttps://doi.org/10.1093/hr/uhad104openalex-snapshot
CG hypermethylation of the bHLH39 promoter regulates its expression and Fe deficiency responses in tomato roots
inferred← citeshttps://doi.org/10.1093/jxb/eru014openalex-snapshot
Characteristics of a root hair-less line of Arabidopsis thaliana under physiological stresses
inferred← citeshttps://doi.org/10.1093/jxb/erv259openalex-snapshot
The paralogous R3 MYB proteins CAPRICE, TRIPTYCHON and ENHANCER OF TRY AND CPC1 play pleiotropic and partly non-redundant roles in the phosphate starvation response of Arabidopsis roots
inferred← citeshttps://doi.org/10.1093/jxb/erv512openalex-snapshot
Gene expression regulation in roots under drought
inferred← citeshttps://doi.org/10.1093/jxb/erz218openalex-snapshot
Epigenetic regulation of sulfur homeostasis in plants
inferred← citeshttps://doi.org/10.1093/jxb/erz359openalex-snapshot
Histone acetyltransferase GCN5-mediated regulation of long non-coding RNA At4 contributes to phosphate starvation response in Arabidopsis
inferred← citeshttps://doi.org/10.1093/pcp/pcw063openalex-snapshot
Arabidopsis MYB-Related HHO2 Exerts a Regulatory Influence on a Subset of Root Traits and Genes Governing Phosphate Homeostasis
inferred← citeshttps://doi.org/10.1093/plcell/koaa054openalex-snapshot
Nonspecific phospholipase C4 hydrolyzes phosphosphingolipids and sustains plant root growth during phosphate deficiency
inferred← citeshttps://doi.org/10.1093/plcell/koab107openalex-snapshot
Length variation in short tandem repeats affects gene expression in natural populations of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1093/plphys/kiad170openalex-snapshot
Transcription factors GmERF1 and GmWRKY6 synergistically regulate low phosphorus tolerance in soybean
inferred← citeshttps://doi.org/10.1093/plphys/kiae317openalex-snapshot
Transcription factor GmAlfin09 regulates endoplasmic reticulum stress in soybean via peroxidase GmPRDX6
inferred← citeshttps://doi.org/10.1101/2020.05.26.117002openalex-snapshot
Genome-wide Association Studies Reveal Important Candidate Genes for the Bacillus pumilus TUAT-1- Arabidopsis thaliana Interaction
inferred← citeshttps://doi.org/10.1101/2021.04.21.440803openalex-snapshot
NAC transcription factor RD26 is a regulator of root hair morphogenic plasticity
inferred← citeshttps://doi.org/10.1101/2022.07.20.500783openalex-snapshot
KAI2 -KL signalling regulates root hair elongation under magnesium deficiency by activating auxin, ethylene, and nitric oxide biosynthesis and signalling genes
inferred← citeshttps://doi.org/10.1101/2023.01.13.523841openalex-snapshot
SUMO protease FUG1, histone reader AL3 and the PRC1 Complex are integral to repeat-expansion induced epigenetic silencing in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1101/2023.02.05.527234openalex-snapshot
The Alfin-like transcription factor GmAlfin09 regulates endoplasmic reticulum stress in soybean via a peroxidase GmPRDX6
inferred← citeshttps://doi.org/10.1101/706507openalex-snapshot
Defining chromatin state transitions predicts a network that modulates cell wall remodeling in phosphate-starved rice shoots
inferred← citeshttps://doi.org/10.1104/pp.16.00786openalex-snapshot
The Chloroplast Protease AMOS1/EGY1 Affects Phosphate Homeostasis under Phosphate Stress
inferred← citeshttps://doi.org/10.1104/pp.16.01764openalex-snapshot
A Histone Code Reader and a Transcriptional Activator Interact to Regulate Genes for Salt Tolerance
inferred← citeshttps://doi.org/10.1104/pp.16.01945openalex-snapshot
ABA Suppresses Root Hair Growth via the OBP4 Transcriptional Regulator
inferred← citeshttps://doi.org/10.1104/pp.17.01188openalex-snapshot
Deubiquitinating Enzyme OTU5 Contributes to DNA Methylation Patterns and Is Critical for Phosphate Nutrition Signals
inferred← citeshttps://doi.org/10.1104/pp.17.01246openalex-snapshot
The Phosphate Fast-Responsive Genes PECP1 and PPsPase1 Affect Phosphocholine and Phosphoethanolamine Content
inferred← citeshttps://doi.org/10.1104/pp.17.01525openalex-snapshot
The Deubiquitinase OTU5 Regulates Root Responses to Phosphate Starvation
inferred← citeshttps://doi.org/10.1104/pp.19.01153openalex-snapshot
Low-Phosphate Chromatin Dynamics Predict a Cell Wall Remodeling Network in Rice Shoots
inferred← citeshttps://doi.org/10.1111/jipb.12163openalex-snapshot
Molecular mechanisms underlying phosphate sensing, signaling, and adaptation in plants
inferred← citeshttps://doi.org/10.1111/jipb.12901openalex-snapshot
Epigenetic regulation in plant abiotic stress responses
inferred← citeshttps://doi.org/10.1111/jipb.13368openalex-snapshot
Dynamic regulation of DNA methylation and histone modifications in response to abiotic stresses in plants
inferred← citeshttps://doi.org/10.1111/mpp.13280openalex-snapshot
Alfin‐like transcription factor VqAL4 regulates a stilbene synthase to enhance powdery mildew resistance in grapevine
inferred← citeshttps://doi.org/10.1111/nph.12491openalex-snapshot
Trait‐directed de novo population transcriptome dissects genetic regulation of a balanced polymorphism in phosphorus nutrition/arsenate tolerance in a wild grass, H olcus lanatus
inferred← citeshttps://doi.org/10.1111/nph.14259openalex-snapshot
Ethylene and nitric oxide interact to regulate the magnesium deficiency‐induced root hair development in Arabidopsis
inferred← citeshttps://doi.org/10.1111/nph.14887openalex-snapshot
Dual‐flow‐RootChip reveals local adaptations of roots towards environmental asymmetry at the physiological and genetic levels
inferred← citeshttps://doi.org/10.1111/nph.20264openalex-snapshot
Machine learning‐based identification of general transcriptional predictors for plant disease
inferred← citeshttps://doi.org/10.1111/nph.70570openalex-snapshot
Arabidopsis thaliana exhibits wide within‐species variation in tolerance to boron limitation and root and shoot trait resilience associate with a pleiotropic locus
inferred← citeshttps://doi.org/10.1111/pbi.12461openalex-snapshot
Simultaneous expression of regulatory genes associated with specific drought‐adaptive traits improves drought adaptation in peanut
inferred← citeshttps://doi.org/10.1111/pce.12988openalex-snapshot
Enhanced root growth in phosphate‐starved Arabidopsis by stimulating de novo phospholipid biosynthesis through the overexpression of LYSOPHOSPHATIDIC ACID ACYLTRANSFERASE 2 (LPAT2)
inferred← citeshttps://doi.org/10.1111/pce.15122openalex-snapshot
Non‐specific Phospholipase C4 Improves Phosphorus Remobilization From Old to Young Leaves in Camelina
inferred← citeshttps://doi.org/10.1111/tpj.12741openalex-snapshot
Phosphatidylinositol phosphate 5‐kinase genes respond to phosphate deficiency for root hair elongation in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1111/tpj.12773openalex-snapshot
The A lfin‐like homeodomain finger protein AL 5 suppresses multiple negative factors to confer abiotic stress tolerance in A rabidopsis
inferred← citeshttps://doi.org/10.1111/tpj.13858openalex-snapshot
Different effects of phospholipase Dζ2 and non‐specific phospholipase C4 on lipid remodeling and root hair growth in Arabidopsis response to phosphate deficiency
inferred← citeshttps://doi.org/10.1111/tpj.16003openalex-snapshot
Natural variation of Alfin‐like family affects seed size and drought tolerance in rice
inferred← citeshttps://doi.org/10.1186/s12864-019-5905-9openalex-snapshot
Evolution and conservation of polycomb repressive complex 1 core components and putative associated factors in the green lineage
inferred← citeshttps://doi.org/10.1186/s12864-021-08160-6openalex-snapshot
Chromatin enrichment for proteomics in plants (ChEP-P) implicates the histone reader ALFIN-LIKE 6 in jasmonate signalling
inferred← citeshttps://doi.org/10.1186/s12864-024-10557-yopenalex-snapshot
Comprehensive analysis of Alfin-like transcription factors associated with drought and salt stresses in wheat (Triticum aestivum L.)
inferred← citeshttps://doi.org/10.1186/s12870-014-0194-6openalex-snapshot
Global transcriptomics identification and analysis of transcriptional factors in different tissues of the paper mulberry
inferred← citeshttps://doi.org/10.1186/s13059-025-03605-7openalex-snapshot
H3K4me3 binding ALFIN-LIKE proteins recruit SWR1 for gene-body deposition of H2A.Z
inferred← citeshttps://doi.org/10.1242/dev.132845openalex-snapshot
The regulation and plasticity of root hair patterning and morphogenesis
inferred← citeshttps://doi.org/10.1371/journal.pone.0075452openalex-snapshot
Positional Signaling and Expression of ENHANCER OF TRY AND CPC1 Are Tuned to Increase Root Hair Density in Response to Phosphate Deficiency in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.21769/bioprotoc.3010openalex-snapshot
Fabrication and Use of the Dual-Flow-RootChip for the Imaging of Arabidopsis Roots in Asymmetric Microenvironments
inferred← citeshttps://doi.org/10.3389/fgene.2022.874648openalex-snapshot
Moving Beyond DNA Sequence to Improve Plant Stress Responses
inferred← citeshttps://doi.org/10.3389/fmars.2026.1948236openalex-snapshot
Mangrove-derived marine actinobacteria as sustainable biostimulants: exploring functional diversity and plant growth promotion in paddy (Oryza sativa)
inferred← citeshttps://doi.org/10.3389/fpls.2018.01164openalex-snapshot
High Auxin and High Phosphate Impact on RSL2 Expression and ROS-Homeostasis Linked to Root Hair Growth in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3389/fpls.2018.01372openalex-snapshot
Molecular Background of Pi Deficiency-Induced Root Hair Growth in Brassica carinata – A Fasciclin-Like Arabinogalactan Protein Is Involved
inferred← citeshttps://doi.org/10.3389/fpls.2018.01509openalex-snapshot
Chromatin-Based Regulation of Plant Root Development
inferred← citeshttps://doi.org/10.3389/fpls.2019.00362openalex-snapshot
Recent Advances in the Cellular and Developmental Biology of Phospholipases in Plants
inferred← citeshttps://doi.org/10.3389/fpls.2019.00662openalex-snapshot
Expression Profiles of 2 Phosphate Starvation-Inducible Phosphocholine/Phosphoethanolamine Phosphatases, PECP1 and PS2, in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2021.658787openalex-snapshot
Abscisic Acid Mediates Drought-Enhanced Rhizosheath Formation in Tomato
inferred← citeshttps://doi.org/10.3389/fpls.2022.893610openalex-snapshot
The Genetic Architecture of Nitrogen Use Efficiency in Switchgrass (Panicum virgatum L.)
inferred← citeshttps://doi.org/10.3389/fpls.2022.959840openalex-snapshot
Minireview: Chromatin-based regulation of iron homeostasis in plants
inferred← citeshttps://doi.org/10.3389/fpls.2026.1749944openalex-snapshot
Functional characterization of BrPHD58, an Alfin-like PHD finger protein from Brassica rapa, reveals its negative role in salt stress tolerance in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3390/genes12081106openalex-snapshot
Plants’ Epigenetic Mechanisms and Abiotic Stress
inferred← citeshttps://doi.org/10.3390/genes15020184openalex-snapshot
Involvement of Alfin-Like Transcription Factors in Plant Development and Stress Response
inferred← citeshttps://doi.org/10.3390/ijms21207457openalex-snapshot
Epigenetic Mechanisms of Plant Adaptation to Biotic and Abiotic Stresses
inferred← citeshttps://doi.org/10.3390/ijms22179311openalex-snapshot
Genetic Dissection of Phosphorus Use Efficiency in a Maize Association Population under Two P Levels in the Field
inferred← citeshttps://doi.org/10.3390/ijms232012157openalex-snapshot
Carrot DcALFIN4 and DcALFIN7 Transcription Factors Boost Carotenoid Levels and Participate Differentially in Salt Stress Tolerance When Expressed in Arabidopsis thaliana and Actinidia deliciosa
inferred← citeshttps://doi.org/10.3390/ijms24065107openalex-snapshot
Phenotypes and Molecular Mechanisms Underlying the Root Response to Phosphate Deprivation in Plants
inferred← citeshttps://doi.org/10.3390/ijms26073188openalex-snapshot
Harnessing Apple Cell Suspension Cultures in Bioreactors for Triterpene Production: Transcriptomic Insights into Biomass and Triterpene Biosynthesis
inferred← citeshttps://doi.org/10.3390/ijms27156824openalex-snapshot
Coordinated MBW, GIS, and RSL Regulatory Networks in Plant Epidermal Patterning Under Environmental Cues
inferred← citeshttps://doi.org/10.3390/plants12152829openalex-snapshot
Identification and Expression Analysis of the Alfin-like Gene Family in Tomato and the Role of SlAL3 in Salt and Drought Stresses
inferred← citeshttps://doi.org/10.3390/plants13111489openalex-snapshot
Genome-Wide Identification and Expression Analysis of the PHD Finger Gene Family in Pea (Pisum sativum)
inferred← citeshttps://doi.org/10.3390/plants13172493openalex-snapshot
Genome-Wide Characterization of Alfin-like Genes in Brassica napus and Functional Analyses of BnaAL02 and BnaAL28 in Response to Nitrogen and Phosphorus Deficiency
inferred← citeshttps://doi.org/10.4161/15592324.2014.993253openalex-snapshot
PHDs govern plant development
inferred← citeshttps://doi.org/10.6084/m9.figshare.17066058openalex-snapshot
Additional file 1 of Chromatin enrichment for proteomics in plants (ChEP-P) implicates the histone reader ALFIN-LIKE 6 in jasmonate signalling
inferred← citeshttps://doi.org/10.6084/m9.figshare.17066061openalex-snapshot
Additional file 2 of Chromatin enrichment for proteomics in plants (ChEP-P) implicates the histone reader ALFIN-LIKE 6 in jasmonate signalling
inferred← citeshttps://doi.org/10.6084/m9.figshare.17066064openalex-snapshot
Additional file 3 of Chromatin enrichment for proteomics in plants (ChEP-P) implicates the histone reader ALFIN-LIKE 6 in jasmonate signalling
inferred← citeshttps://doi.org/10.6084/m9.figshare.26322693openalex-snapshot
Additional file 1 of Comprehensive analysis of Alfin-like transcription factors associated with drought and salt stresses in wheat (Triticum aestivum L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.26322774openalex-snapshot
Additional file 2 of Comprehensive analysis of Alfin-like transcription factors associated with drought and salt stresses in wheat (Triticum aestivum L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.26750384openalex-snapshot
Additional file 3 of Comprehensive analysis of Alfin-like transcription factors associated with drought and salt stresses in wheat (Triticum aestivum L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.26750387openalex-snapshot
Additional file 4 of Comprehensive analysis of Alfin-like transcription factors associated with drought and salt stresses in wheat (Triticum aestivum L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.26750390openalex-snapshot
Additional file 5 of Comprehensive analysis of Alfin-like transcription factors associated with drought and salt stresses in wheat (Triticum aestivum L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.26750393openalex-snapshot
Additional file 6 of Comprehensive analysis of Alfin-like transcription factors associated with drought and salt stresses in wheat (Triticum aestivum L.)
inferred← citeshttps://doi.org/10.70675/311d0d15za80ez4dd9z96aezabcbb99b7532openalex-snapshot
Caractérisation in vivo du rôle de phosphatases de la famille PS2;1 à 3, marqueurs précoces de la carence en phosphate chez Arabidopsis thaliana
inferred← citeshttps://doi.org/10.70675/40f401b4z5e3cz4dfaza070z77c95a145f2eopenalex-snapshot
Glutathione and glutaredoxins, major regulators of root system architecture
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