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A Noncanonical Role for the CKI-RB-E2F Cell-Cycle Signaling Pathway in Plant Effector-Triggered Immunity
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/j.chom.2014.03.007openalex-snapshot
Atypical E2F Transcriptional Repressor DEL1 Acts at the Intersection of Plant Growth and Immunity by Controlling the Hormone Salicylic Acid
inferredcites →https://doi.org/10.1016/j.cub.2011.12.015openalex-snapshot
The HSF-like Transcription Factor TBF1 Is a Major Molecular Switch for Plant Growth-to-Defense Transition
inferredcites →https://doi.org/10.1016/j.devcel.2008.01.013openalex-snapshot
CDK Inhibitors: Cell Cycle Regulators and Beyond
inferredcites →https://doi.org/10.1016/j.tcb.2008.08.003openalex-snapshot
E2F – at the crossroads of life and death
inferredcites →https://doi.org/10.1016/j.tcb.2011.10.004openalex-snapshot
Multiple degradation pathways regulate versatile CIP/KIP CDK inhibitors
inferredcites →https://doi.org/10.1016/j.tcb.2013.03.002openalex-snapshot
Cell cycle control across the eukaryotic kingdom
inferredcites →https://doi.org/10.1016/s0092-8674(02)00661-xopenalex-snapshot
RIN4 Interacts with Pseudomonas syringae Type III Effector Molecules and Is Required for RPM1-Mediated Resistance in Arabidopsis
inferredcites →https://doi.org/10.1016/s0960-9822(01)00590-5openalex-snapshot
CPR5 is involved in cell proliferation and cell death control and encodes a novel transmembrane protein
inferredcites →https://doi.org/10.1038/386451a0openalex-snapshot
A plant cyclin-dependent kinase inhibitor gene
inferredcites →https://doi.org/10.1038/emboj.2012.13openalex-snapshot
Arabidopsis E2FA stimulates proliferation and endocycle separately through RBR‐bound and RBR‐free complexes
inferredcites →https://doi.org/10.1038/nature09766openalex-snapshot
Timing of plant immune responses by a central circadian regulator
inferredcites →https://doi.org/10.1038/nature11162openalex-snapshot
NPR3 and NPR4 are receptors for the immune signal salicylic acid in plants
inferredcites →https://doi.org/10.1038/ni1253openalex-snapshot
Are innate immune signaling pathways in plants and animals conserved?
inferredcites →https://doi.org/10.1038/nrc2718openalex-snapshot
p53 and E2f: partners in life and death
inferredcites →https://doi.org/10.1038/nri2296openalex-snapshot
NLRs at the intersection of cell death and immunity
inferredcites →https://doi.org/10.1038/nrm2227openalex-snapshot
The ins and outs of the plant cell cycle
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.2641041.xopenalex-snapshot
Constitutive disease resistance requires EDS1 in the Arabidopsis mutants cpr1 and cpr6 and is partially EDS1‐dependent in cpr5
inferredcites →https://doi.org/10.1073/pnas.1005978107openalex-snapshot
Arabidopsis BRCA2 and RAD51 proteins are specifically involved in defense gene transcription during plant immune responses
inferredcites →https://doi.org/10.1073/pnas.1113726108openalex-snapshot
Expanded functions for a family of plant intracellular immune receptors beyond specific recognition of pathogen effectors
inferredcites →https://doi.org/10.1073/pnas.1217024110openalex-snapshot
Perturbation of cell cycle regulation triggers plant immune response via activation of disease resistance genes
inferredcites →https://doi.org/10.1093/emboj/20.19.5400openalex-snapshot
Direct interaction between the Arabidopsis disease resistance signaling proteins, EDS1 and PAD4
inferredcites →https://doi.org/10.1101/gad.13.12.1501openalex-snapshot
CDK inhibitors: positive and negative regulators of G1-phase progression
inferredcites →https://doi.org/10.1101/gad.813200openalex-snapshot
The Rb/E2F pathway: expanding roles and emerging paradigms
inferredcites →https://doi.org/10.1104/pp.105.066290openalex-snapshot
Genome-Wide Identification of Potential Plant E2F Target Genes
inferredcites →https://doi.org/10.1104/pp.107.111740openalex-snapshot
Firefly Luciferase Complementation Imaging Assay for Protein-Protein Interactions in Plants
inferredcites →https://doi.org/10.1104/pp.112.194035openalex-snapshot
Structure-Function Analysis of the Coiled-Coil and Leucine-Rich Repeat Domains of the RPS5 Disease Resistance Protein
inferredcites →https://doi.org/10.1105/tpc.008342openalex-snapshot
Misexpression of the Cyclin-Dependent Kinase Inhibitor ICK1/KRP1 in Single-Celled Arabidopsis Trichomes Reduces Endoreduplication and Cell Size and Induces Cell Death
inferredcites →https://doi.org/10.1105/tpc.010085openalex-snapshot
The Disease Resistance Signaling Components EDS1 and PAD4 Are Essential Regulators of the Cell Death Pathway Controlled by LSD1 in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.010087openalex-snapshot
Functional Analysis of Cyclin-Dependent Kinase Inhibitors of Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.105.032383openalex-snapshot
The Cyclin-Dependent Kinase Inhibitor KRP2 Controls the Onset of the Endoreduplication Cycle during Arabidopsis Leaf Development through Inhibition of Mitotic CDKA;1 Kinase Complexes
inferredcites →https://doi.org/10.1105/tpc.108.064519openalex-snapshot
Nuclear Pore Complex Component MOS7/Nup88 Is Required for Innate Immunity and Nuclear Accumulation of Defense Regulators inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.12.11.2175openalex-snapshot
Roles of Salicylic Acid, Jasmonic Acid, and Ethylene in cpr-Induced Resistance in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.13.10.2211openalex-snapshot
The Disease Resistance Signaling Components EDS1 and PAD4 Are Essential Regulators of the Cell Death Pathway Controlled by LSD1 in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.13.7.1653openalex-snapshot
Functional Analysis of Cyclin-Dependent Kinase Inhibitors of Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.8.11.2033openalex-snapshot
Characterization of eds1, a mutation in Arabidopsis suppressing resistance to Peronospora parasitica specified by several different RPP genes.
inferredcites →https://doi.org/10.1105/tpc.9.9.1573openalex-snapshot
The cpr5 mutant of Arabidopsis expresses both NPR1-dependent and NPR1-independent resistance.
inferredcites →https://doi.org/10.1126/science.1194980openalex-snapshot
Arabidopsis Type I Metacaspases Control Cell Death
inferredcites →https://doi.org/10.1126/science.1211592openalex-snapshot
Pathogen Effectors Target Arabidopsis EDS1 and Alter Its Interactions with Immune Regulators
inferredcites →https://doi.org/10.1126/science.1211641openalex-snapshot
Arabidopsis EDS1 Connects Pathogen Effector Recognition to Cell Compartment–Specific Immune Responses
inferredcites →https://doi.org/10.1146/annurev.phyto.050908.135202openalex-snapshot
Salicylic Acid, a Multifaceted Hormone to Combat Disease
inferredcites →https://doi.org/10.1146/annurev.phyto.42.040803.140421openalex-snapshot
SYSTEMIC ACQUIRED RESISTANCE
inferredcites →https://doi.org/10.1242/dev.127.18.3931openalex-snapshot
SIAMESE, a gene controlling the endoreduplication cell cycle in Arabidopsis thaliana trichomes
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.4181443openalex-extracted
Function of Two Splicing Variants of RcCPR5 in the Resistance of Rosa Chinensis to Powdery Mildew
inferred← citeshttps://doi.org/10.1002/advs.202516380openalex-snapshot
Single‐Cell Transcriptomics Reveals FLS2‐Dependent Hypoxia Signaling and ERF13‐Mediated Transcription During flg22‐Triggered Immunity
inferred← citeshttps://doi.org/10.1007/s00122-017-2853-0openalex-snapshot
Fine mapping of RYMV3: a new resistance gene to Rice yellow mottle virus from Oryza glaberrima
inferred← citeshttps://doi.org/10.1007/s00425-023-04312-yopenalex-snapshot
Arabidopsis nucleoporin NUP96 mediates plant salt tolerance by modulating the transcription of salt-responsive genes
inferred← citeshttps://doi.org/10.1007/s10265-020-01177-0openalex-snapshot
Nuclear pore complex-mediated gene expression in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s10658-017-1286-6openalex-snapshot
Functional analysis of spinach CONSTITUTIVE EXPRESSOR OF PATHOGENESIS-RELATED GENES5 (SoCPR5) in plant immunity
inferred← citeshttps://doi.org/10.1007/s10658-022-02584-wopenalex-snapshot
Characterization of rice and maize CONSTITUTIVE EXPRESSER OF PATHOGENESIS-RELATED GENES 5 in plant immunity
inferred← citeshttps://doi.org/10.1007/s11105-020-01236-9openalex-snapshot
Core Cell Cycle–Related Gene Identification and Expression Analysis in Maize
inferred← citeshttps://doi.org/10.1007/s44154-023-00086-1openalex-snapshot
A necessary considering factor for breeding: growth-defense tradeoff in plants
inferred← citeshttps://doi.org/10.1016/j.cell.2016.07.042openalex-snapshot
Nuclear Pore Permeabilization Is a Convergent Signaling Event in Effector-Triggered Immunity
inferred← citeshttps://doi.org/10.1016/j.cell.2016.08.026openalex-snapshot
Gating Immunity and Death at the Nuclear Pore Complex
inferred← citeshttps://doi.org/10.1016/j.chom.2014.11.015openalex-snapshot
Co-opting the Cell-Cycle Machinery for Plant Immunity
inferred← citeshttps://doi.org/10.1016/j.chom.2015.10.001openalex-snapshot
Cell-Cycle Regulators and Cell Death in Immunity
inferred← citeshttps://doi.org/10.1016/j.chom.2025.02.006openalex-snapshot
Plant cell-cycle regulators control the nuclear environment for viral pathogenesis
inferred← citeshttps://doi.org/10.1016/j.chom.2026.02.007openalex-snapshot
Immune activation reprograms growth mRNA stability to shape plant growth-defense trade-offs
inferred← citeshttps://doi.org/10.1016/j.chom.2026.07.009openalex-snapshot
Cell-type-specific activation of broadly perceived effector-triggered immunity restricts pathogen invasion in plants
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2018.03.047openalex-snapshot
Redox regulation of cell proliferation: Bioinformatics and redox proteomics approaches to identify redox-sensitive cell cycle regulators
inferred← citeshttps://doi.org/10.1016/j.genrep.2020.100598openalex-snapshot
In-silico identification and differential expressions of LepR4-syntenic disease resistance related domain containing genes against blackleg causal fungus Leptosphaeria maculans in Brassica oleracea
inferred← citeshttps://doi.org/10.1016/j.gpb.2018.08.002openalex-snapshot
PlaD: A Transcriptomics Database for Plant Defense Responses to Pathogens, Providing New Insights into Plant Immune System
inferred← citeshttps://doi.org/10.1016/j.jgg.2025.06.002openalex-snapshot
The nucleoporin CPR5 and histone chaperone NAP1 form a complex to negatively modulate plant immunity
inferred← citeshttps://doi.org/10.1016/j.mib.2023.102284openalex-snapshot
Plant pathogens and symbionts target the plant nucleus
inferred← citeshttps://doi.org/10.1016/j.molp.2015.03.013openalex-snapshot
Linking the Cell Cycle with Innate Immunity in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.molp.2017.07.001openalex-snapshot
Membrane Trafficking in Plant Immunity
inferred← citeshttps://doi.org/10.1016/j.molp.2021.06.011openalex-snapshot
A karyopherin constrains nuclear activity of the NLR protein SNC1 and is essential to prevent autoimmunity in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.pbi.2015.06.006openalex-snapshot
Growth versus immunity — a redirection of the cell cycle?
inferred← citeshttps://doi.org/10.1016/j.pbi.2015.12.003openalex-snapshot
Integration of developmental and environmental signals into cell proliferation and differentiation through RETINOBLASTOMA-RELATED 1
inferred← citeshttps://doi.org/10.1016/j.pbi.2016.10.002openalex-snapshot
DREAMs make plant cells to cycle or to become quiescent
inferred← citeshttps://doi.org/10.1016/j.pbi.2019.04.003openalex-snapshot
Endoreplication as a potential driver of cell wall modifications
inferred← citeshttps://doi.org/10.1016/j.pbi.2026.102949openalex-snapshot
Cell cycle reprogramming in plant symbiotic and pathogenic interactions
inferred← citeshttps://doi.org/10.1016/j.plantsci.2018.03.007openalex-snapshot
ZmSMR4, a novel cyclin-dependent kinase inhibitor (CKI) gene in maize (Zea mays L.), functions as a key player in plant growth, development and tolerance to abiotic stress
inferred← citeshttps://doi.org/10.1016/j.plantsci.2023.111678openalex-snapshot
Function of two splicing variants of RcCPR5 in the resistance of Rosa chinensis to powdery mildew
inferred← citeshttps://doi.org/10.1016/j.plantsci.2026.113482openalex-snapshot
Nucleocytoplasmic trafficking of immune signals in plants
inferred← citeshttps://doi.org/10.1016/j.tplants.2016.04.008openalex-snapshot
The SnRK1 Energy Sensor in Plant Biotic Interactions
inferred← citeshttps://doi.org/10.1016/s2095-3119(21)63728-0openalex-snapshot
Recent advances in plant immunity with cell death: A review
inferred← citeshttps://doi.org/10.1038/s41477-020-0700-9openalex-snapshot
Global profiling of plant nuclear membrane proteome in Arabidopsis
inferred← citeshttps://doi.org/10.1038/s41559-019-1036-6openalex-snapshot
Genomic basis of European ash tree resistance to ash dieback fungus
inferred← citeshttps://doi.org/10.1038/s42003-023-05259-2openalex-snapshot
The canonical E2Fs together with RETINOBLASTOMA-RELATED are required to establish quiescence during plant development
inferred← citeshttps://doi.org/10.1038/s44318-024-00282-3openalex-snapshot
Developmental cues are encoded by the combinatorial phosphorylation of Arabidopsis RETINOBLASTOMA-RELATED protein RBR1
inferred← citeshttps://doi.org/10.1042/ebc20210100openalex-snapshot
Transcriptional regulation of plant innate immunity
inferred← citeshttps://doi.org/10.1073/pnas.1720094115openalex-snapshot
Negative regulator of E2F transcription factors links cell cycle checkpoint and DNA damage repair
inferred← citeshttps://doi.org/10.1080/07060661.2017.1347202openalex-snapshot
Identification of spinach SIAMESE and analysis of its function in plant immunity
inferred← citeshttps://doi.org/10.1080/11263504.2020.1869118openalex-snapshot
Comparative transcriptomics and metabolomics in Vitis vinifera ‘Malvasia’ and Vitis rupestris ‘Du Lot’ cultured cells provide insights in possible innate resistance against pathogens
inferred← citeshttps://doi.org/10.1080/15592324.2017.1282021openalex-snapshot
Why do plants need so many cyclin-dependent kinase inhibitors?
inferred← citeshttps://doi.org/10.1080/19491034.2023.2178201openalex-snapshot
Plant nuclear envelope as a hub connecting genome organization with regulation of gene expression
inferred← citeshttps://doi.org/10.1093/aob/mcw211openalex-snapshot
Should I fight or should I grow now? The role of cytokinins in plant growth and immunity and in the growth–defence trade-off
inferred← citeshttps://doi.org/10.1093/bfgp/elv013openalex-snapshot
Nuclear processes associated with plant immunity and pathogen susceptibility
inferred← citeshttps://doi.org/10.1093/hr/uhag184openalex-snapshot
A transposon insertion in the promoter of BcCPR5 impairs trichome formation in wucai ( Brassica campestris L.)
inferred← citeshttps://doi.org/10.1093/jxb/erv106openalex-snapshot
Hormone activities and the cell cycle machinery in immunity-triggered growth inhibition
inferred← citeshttps://doi.org/10.1093/jxb/erv564openalex-snapshot
The Arabidopsis microtubule-associated protein MAP65-3 supports infection by filamentous biotrophic pathogens by down-regulating salicylic acid-dependent defenses
inferred← citeshttps://doi.org/10.1093/plcell/koaa047openalex-snapshot
Exportin-4 coordinates nuclear shuttling of TOPLESS family transcription corepressors to regulate plant immunity
inferred← citeshttps://doi.org/10.1093/plcell/koac037openalex-snapshot
CONSTITUTIVE EXPRESSER OF PATHOGENESIS-RELATED GENES 5 is an RNA-binding protein controlling plant immunity via an RNA processing complex
inferred← citeshttps://doi.org/10.1093/plcell/koac060openalex-snapshot
CPR5 modulates plant immunity via RNA processing
inferred← citeshttps://doi.org/10.1093/plcell/koaf186openalex-snapshot
Defense strategies for plant health: Disease resistance and tolerance
inferred← citeshttps://doi.org/10.1101/2021.12.20.472892openalex-snapshot
A phosphorylation code regulates the multi-functional protein RETINOBLASTOMA-RELATED1 in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1101/2021.12.22.473497openalex-snapshot
The dual role of the RETINOBLASTOMA-RELATED protein in the DNA damage response is spatio-temporally coordinated by the interaction with LXCXE-containing proteins
inferred← citeshttps://doi.org/10.1101/2024.05.28.596227openalex-snapshot
Retinoblastoma-related (RBR) has both canonical and non-canonical regulatory functions during thermo-morphogenic responses in Arabidopsis seedlings
inferred← citeshttps://doi.org/10.1101/2024.09.02.610746openalex-snapshot
Identification of nuclear pore proteins at plasmodesmata: potential role in intercellular transport?
inferred← citeshttps://doi.org/10.1101/2025.06.28.662111openalex-snapshot
Cell-type-specific execution of effector-triggered immunity
inferred← citeshttps://doi.org/10.1101/742742openalex-snapshot
Transcriptional Dynamics of the Salicylic Acid Response and its Interplay with the Jasmonic Acid Pathway
inferred← citeshttps://doi.org/10.1104/pp.15.01466openalex-snapshot
Differential Roles of Two Homologous Cyclin-Dependent Kinase Inhibitor Genes in Regulating Cell Cycle and Innate Immunity in Arabidopsis
inferred← citeshttps://doi.org/10.1104/pp.16.00950openalex-snapshot
Histidine Regulates Seed Oil Deposition through Abscisic Acid Biosynthesis and β-oxidation
inferred← citeshttps://doi.org/10.1104/pp.17.00788openalex-snapshot
Dynamic Changes in Plant Nuclear Organization in Response to Environmental and Developmental Signals
inferred← citeshttps://doi.org/10.1104/pp.17.01461openalex-snapshot
STOREKEEPER RELATED1/G-Element Binding Protein (STKR1) Interacts with Protein Kinase SnRK1
inferred← citeshttps://doi.org/10.1104/pp.18.00147openalex-snapshot
Functional Analysis of Short Linear Motifs in the Plant Cyclin-Dependent Kinase Inhibitor SIAMESE
inferred← citeshttps://doi.org/10.1104/pp.19.00212openalex-snapshot
E2FB Interacts with RETINOBLASTOMA RELATED and Regulates Cell Proliferation during Leaf Development
inferred← citeshttps://doi.org/10.1105/tpc.15.00489openalex-snapshot
Functional Conservation in the SIAMESE-RELATED Family of Cyclin-Dependent Kinase Inhibitors in Land Plants
inferred← citeshttps://doi.org/10.1105/tpc.17.00983openalex-snapshot
A Spatiotemporal DNA Endoploidy Map of the Arabidopsis Root Reveals Roles for the Endocycle in Root Development and Stress Adaptation
inferred← citeshttps://doi.org/10.1111/jipb.13472openalex-snapshot
CPR5 positively regulates pattern‐triggered immunity via a mediator protein
inferred← citeshttps://doi.org/10.1111/mpp.70059openalex-snapshot
Identification and Application of the Heptad Repeat Domain in the CPR5 Protein for Enhancing Plant Immunity
inferred← citeshttps://doi.org/10.1111/mpp.70086openalex-snapshot
The Nucleoporin CPR5 Modulates Plant Immunity via Guanylate‐Binding Proteins
inferred← citeshttps://doi.org/10.1111/mpp.70319openalex-snapshot
The Transcription Factor DPB Confers Antiviral Defence Against Potato Virus X by Modulating MYB ‐Dependent Signalling
inferred← citeshttps://doi.org/10.1111/nph.14756openalex-snapshot
The nuclear pore complex: a strategic platform for regulating cell signaling
inferred← citeshttps://doi.org/10.1111/nph.14959openalex-snapshot
Plant–microbe interactions: organelles and the cytoskeleton in action
inferred← citeshttps://doi.org/10.1111/nph.18359openalex-snapshot
NLR we there yet? Nucleocytoplasmic coordination of NLR ‐mediated immunity
inferred← citeshttps://doi.org/10.1111/nph.70524openalex-snapshot
Guanylate‐binding proteins: emerging critical functions in plant development, immunity and stress response
inferred← citeshttps://doi.org/10.1111/pbi.14043openalex-snapshot
Phytophthora sojae effector PsAvh113 associates with the soybean transcription factor GmDPB to inhibit catalase‐mediated immunity
inferred← citeshttps://doi.org/10.1111/pbi.70662openalex-snapshot
Unfolding Plant Defence: Endoplasmic Reticulum Stress Signalling at the Plant‐Pathogen Interface
inferred← citeshttps://doi.org/10.1111/pce.15202openalex-snapshot
RETINOBLASTOMA‐RELATED Has Both Canonical and Noncanonical Regulatory Functions During Thermo‐Morphogenic Responses in Arabidopsis Seedlings
inferred← citeshttps://doi.org/10.1111/pce.70489openalex-snapshot
Complex Regulation of RETINOBLASTOMA‐RELATED's Interactions With E2Fs via Phosphorylation
inferred← citeshttps://doi.org/10.1111/plb.13068openalex-snapshot
Arabidopsis nucleoporin CPR5 controls trichome cell death through the core cell cycle regulator CKI
inferred← citeshttps://doi.org/10.1111/ppl.13771openalex-snapshot
Transcriptomic and methylation analysis of susceptible and tolerant grapevine genotypes following Plasmopara viticola infection
inferred← citeshttps://doi.org/10.1111/tpj.13397openalex-snapshot
CPR 5 modulates salicylic acid and the unfolded protein response to manage tradeoffs between plant growth and stress responses
inferred← citeshttps://doi.org/10.1111/tpj.13757openalex-snapshot
MOS 1 functions closely with TCP transcription factors to modulate immunity and cell cycle in Arabidopsis
inferred← citeshttps://doi.org/10.1139/cjps-2017-0005openalex-snapshot
The CPR5-CKI signaling pathway plays a central role in integrating plant stress responses
inferred← citeshttps://doi.org/10.1186/s12864-017-3848-6openalex-snapshot
The biocontrol agent Pseudomonas chlororaphis PA23 primes Brassica napus defenses through distinct gene networks
inferred← citeshttps://doi.org/10.1186/s12870-019-1759-1openalex-snapshot
Genome-wide association analysis for fumonisin content in maize kernels
inferred← citeshttps://doi.org/10.1186/s12870-020-02485-2openalex-snapshot
Putative alternative translation start site-encoding nucleotides of CPR5 regulate growth and resistance
inferred← citeshttps://doi.org/10.1186/s13059-025-03814-0openalex-snapshot
A nucleoporin-associated signaling cascade controls plant immunity via histone modification
inferred← citeshttps://doi.org/10.1242/dev.179333openalex-snapshot
E2FA and E2FB transcription factors coordinate cell proliferation with seed maturation
inferred← citeshttps://doi.org/10.1371/journal.pbio.2004122openalex-snapshot
Active photosynthetic inhibition mediated by MPK3/MPK6 is critical to effector-triggered immunity
inferred← citeshttps://doi.org/10.1371/journal.pone.0162840openalex-snapshot
Influence of Human p53 on Plant Development
inferred← citeshttps://doi.org/10.1371/journal.pone.0183870openalex-snapshot
Involvement of Arabidopsis thaliana endoplasmic reticulum KDEL-tailed cysteine endopeptidase 1 (AtCEP1) in powdery mildew-induced and AtCPR5-controlled cell death
inferred← citeshttps://doi.org/10.14232/phd.10705openalex-snapshot
Az Arabidopsis E2FB transzkripciós faktor funkcionális jellemzése
inferred← citeshttps://doi.org/10.14232/phd.10739openalex-snapshot
A növényi (Arabidopsis) aktivátor E2F transzkripciós faktorok szerepe a magfejlődésben és a sejtciklus szabályozásában
inferred← citeshttps://doi.org/10.15252/embj.201694571openalex-snapshot
The retinoblastoma homolog RBR1 mediates localization of the repair protein RAD51 to DNA lesions in Arabidopsis
inferred← citeshttps://doi.org/10.15252/embj.2020105802openalex-snapshot
Roles of plant retinoblastoma protein: cell cycle and beyond
inferred← citeshttps://doi.org/10.18174/551711openalex-snapshot
Roles and regulation of the RETINOBLASTOMA-RELATED protein in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.18388/pb.2019_258openalex-snapshot
Immunoreceptory wewnątrzkomórkowe NB-LRR/NLR rozpoznające białka efektorowe fitopatogenów i aktywujące drugą linię obrony układu odpornościowego roślin
inferred← citeshttps://doi.org/10.2139/ssrn.4879052openalex-snapshot
A Study of the Origin and Function of the Cpr5 Protein in Arabidopsis
inferred← citeshttps://doi.org/10.26508/lsa.202101141openalex-snapshot
The DREAM complex represses growth in response to DNA damage in Arabidopsis
inferred← citeshttps://doi.org/10.31390/gradschool_dissertations.2135openalex-snapshot
Functional Motifs in SIAMESE, a Plant Cyclin-Dependent Kinase Inhibitor
inferred← citeshttps://doi.org/10.31390/gradschool_dissertations.5173openalex-snapshot
Functions of CDK/cyclin Complexes in Endoreplication Regulation by the CDK Inhibitor SIAMESE
inferred← citeshttps://doi.org/10.32604/phyton.2021.014967openalex-snapshot
Non-Canonical Functions of the E2F/DP Pathway with Emphasis in Plants
inferred← citeshttps://doi.org/10.3389/fimmu.2021.771065openalex-snapshot
Regulation of Plant Immunity by Nuclear Membrane-Associated Mechanisms
inferred← citeshttps://doi.org/10.3389/fpls.2016.01717openalex-snapshot
Mighty Dwarfs: Arabidopsis Autoimmune Mutants and Their Usages in Genetic Dissection of Plant Immunity
inferred← citeshttps://doi.org/10.3389/fpls.2016.01744openalex-snapshot
Transcriptomic Effects of the Cell Cycle Regulator LGO in Arabidopsis Sepals
inferred← citeshttps://doi.org/10.3389/fpls.2016.01779openalex-snapshot
Mutations in Rice yellow mottle virus Polyprotein P2a Involved in RYMV2 Gene Resistance Breakdown
inferred← citeshttps://doi.org/10.3389/fpls.2017.00574openalex-snapshot
Roles of Nuclear Pores and Nucleo-cytoplasmic Trafficking in Plant Stress Responses
inferred← citeshttps://doi.org/10.3389/fpls.2018.00638openalex-snapshot
The Canonical E2Fs Are Required for Germline Development in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2021.652570openalex-snapshot
Molecular Analysis of the E2F/DP Gene Family of Daucus carota and Involvement of the DcE2F1 Factor in Cell Proliferation
inferred← citeshttps://doi.org/10.3389/fpls.2021.719453openalex-snapshot
Nucleocytoplasmic Communication in Healthy and Diseased Plant Tissues
inferred← citeshttps://doi.org/10.3389/fpls.2022.1030247openalex-snapshot
Rice microtubule-associated protein OsMAP65-3.1, but not OsMAP65-3.2, plays a critical role in phragmoplast microtubule organization in cytokinesis
inferred← citeshttps://doi.org/10.3389/fpls.2024.1362460openalex-snapshot
The SIAMESE family of cell-cycle inhibitors in the response of plants to environmental stresses
inferred← citeshttps://doi.org/10.3390/antiox12020301openalex-snapshot
Overexpression of an Antioxidant Enzyme APX1 in cpr5 Mutant Restores its Pleiotropic Growth Phenotype
inferred← citeshttps://doi.org/10.3390/ijms25063356openalex-snapshot
ZmSMR10 Increases the Level of Endoreplication of Plants through Its Interactions with ZmPCNA2 and ZmCSN5B
inferred← citeshttps://doi.org/10.3889/oamjms.2020.3328openalex-snapshot
Polyisoprenoids from Avicennia marina induces on P13k, Akt1, Mammalian target of rapamycin, Egfr, and P53 Gene Expression Using Reverse Transcription-Polymerase Chain Reaction
inferred← citeshttps://doi.org/10.70675/42cb6fcfze078z4cf3zacc3zc1312590fc21openalex-snapshot
TCTP and CSN4 interact to control cell cycle progression and development in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.70675/44036f37za290z4af7za534zd4c8f8f0d7ddopenalex-snapshot
Rôles du gène SMR5 et de son inducteur, l'acide β-cyclocitrique, dans le développement racinaire et la tolérance des plantes à la sécheresse
inferred← citeshttps://doi.org/10.7554/elife.108676openalex-snapshot
Identification of nuclear pore proteins at plasmodesmata: potential role in intercellular transport?
inferred← citeshttps://doi.org/10.7554/elife.108676.1openalex-snapshot
Identification of nuclear pore proteins at plasmodesmata: potential role in intercellular transport?
inferred← citeshttps://doi.org/10.7717/peerj.21666openalex-snapshot
Advances and prospects in fungal disease resistance breeding of roses
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