On the public citation graph

Integrative analysis in Pinus revealed long‐term heat stress splicing memory

0 signed · 77 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

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

inferredcites →https://doi.org/10.1016/j.cell.2010.11.056openalex-snapshot

Epigenetics in Alternative Pre-mRNA Splicing

inferredcites →https://doi.org/10.1016/j.cell.2016.02.058openalex-snapshot

SnapShot: Timescales in Cell Biology

inferredcites →https://doi.org/10.1016/j.gene.2020.144961openalex-snapshot

Full-length sequencing of ginkgo transcriptomes for an in-depth understanding of flavonoid and terpenoid trilactone biosynthesis

inferredcites →https://doi.org/10.1016/j.heliyon.2023.e16811openalex-snapshot

Seiðr: Efficient calculation of robust ensemble gene networks

inferredcites →https://doi.org/10.1016/j.molp.2019.01.003openalex-snapshot

MapMan4: A Refined Protein Classification and Annotation Framework Applicable to Multi-Omics Data Analysis

inferredcites →https://doi.org/10.1016/j.molp.2020.07.007openalex-snapshot

Phytophthora Effectors Modulate Genome-wide Alternative Splicing of Host mRNAs to Reprogram Plant Immunity

inferredcites →https://doi.org/10.1016/j.tplants.2017.09.019openalex-snapshot

Alternative Splicing Control of Abiotic Stress Responses

inferredcites →https://doi.org/10.1016/j.tplants.2019.02.006openalex-snapshot

Perspective on Alternative Splicing and Proteome Complexity in Plants

inferredcites →https://doi.org/10.1016/j.tplants.2020.08.007openalex-snapshot

Emerging Plant Thermosensors: From RNA to Protein

inferredcites →https://doi.org/10.1038/nmeth.1923openalex-snapshot

Fast gapped-read alignment with Bowtie 2

inferredcites →https://doi.org/10.1038/nmeth.2016openalex-snapshot

Wisdom of crowds for robust gene network inference

inferredcites →https://doi.org/10.1038/nrm3953openalex-snapshot

Getting up to speed with transcription elongation by RNA polymerase II

inferredcites →https://doi.org/10.1038/s41467-020-17896-wopenalex-snapshot

Natural variation at FLM splicing has pleiotropic effects modulating ecological strategies in Arabidopsis thaliana

inferredcites →https://doi.org/10.1038/s41477-017-0097-2openalex-snapshot

A genome for gnetophytes and early evolution of seed plants

inferredcites →https://doi.org/10.1038/s41477-018-0176-zopenalex-snapshot

PORCUPINE regulates development in response to temperature through alternative splicing

inferredcites →https://doi.org/10.1038/s41477-020-0688-1openalex-snapshot

Post-transcriptional splicing of nascent RNA contributes to widespread intron retention in plants

inferredcites →https://doi.org/10.1038/s41586-019-1693-2openalex-snapshot

One thousand plant transcriptomes and the phylogenomics of green plants

inferredcites →https://doi.org/10.1073/pnas.0706851105openalex-snapshot

Maps of random walks on complex networks reveal community structure

inferredcites →https://doi.org/10.1073/pnas.1803361115openalex-snapshot

Genetics of alternative splicing evolution during sunflower domestication

inferredcites →https://doi.org/10.1073/pnas.2022302118openalex-snapshot

Phylogenomic and ecological analyses reveal the spatiotemporal evolution of global pines

inferredcites →https://doi.org/10.1073/pnas.2026330118openalex-snapshot

Predicting transcriptional responses to cold stress across plant species

inferredcites →https://doi.org/10.1093/bib/bbaa045openalex-snapshot

CodAn: predictive models for precise identification of coding regions in eukaryotic transcripts

inferredcites →https://doi.org/10.1093/bioinformatics/btu031openalex-snapshot

InterProScan 5: genome-scale protein function classification

inferredcites →https://doi.org/10.1093/jxb/erae033openalex-snapshot

Multiomics analyses reveal the central role of the nucleolus and its machinery during heat stress acclimation in Pinus radiata

inferredcites →https://doi.org/10.1093/jxb/erx198openalex-snapshot

System-wide analysis of short-term response to high temperature in Pinus radiata

inferredcites →https://doi.org/10.1093/jxb/ery062openalex-snapshot

Thermopriming triggers splicing memory in Arabidopsis

inferredcites →https://doi.org/10.1093/jxb/erz524openalex-snapshot

Integrative analysis of the nuclear proteome in Pinus radiata reveals thermopriming coupled to epigenetic regulation

inferredcites →https://doi.org/10.1093/nar/gkaa1100openalex-snapshot

UniProt: the universal protein knowledgebase in 2021

inferredcites →https://doi.org/10.1093/nar/gkaa1113openalex-snapshot

The Gene Ontology resource: enriching a GOld mine

inferredcites →https://doi.org/10.1093/nar/gkaa464openalex-snapshot

Comprehensive database and evolutionary dynamics of U12-type introns

inferredcites →https://doi.org/10.1093/nar/gkab1038openalex-snapshot

The PRIDE database resources in 2022: a hub for mass spectrometry-based proteomics evidences

inferredcites →https://doi.org/10.1093/nar/gkv007openalex-snapshot

limma powers differential expression analyses for RNA-sequencing and microarray studies

inferredcites →https://doi.org/10.1093/nar/gkz1068openalex-snapshot

The changing paradigm of intron retention: regulation, ramifications and recipes

inferredcites →https://doi.org/10.1093/nargab/lqaa095openalex-snapshot

Influenza virus infection induces widespread alterations of host cell splicing

inferredcites →https://doi.org/10.1101/2022.07.08.499117openalex-snapshot

Multiomics analyses reveal the central role of nucleolus and nucleoid machinery during heat stress acclimation in Pinus radiata

inferredcites →https://doi.org/10.1101/250696openalex-snapshot

Seiðr: Efficient Calculation of Robust Ensemble Gene Networks

inferredcites →https://doi.org/10.1104/pp.110.157370openalex-snapshot

Functional Analysis of the Arabidopsis PAL Gene Family in Plant Growth, Development, and Response to Environmental Stress

inferredcites →https://doi.org/10.1104/pp.114.248708openalex-snapshot

Insights into Conifer Giga-Genomes

inferredcites →https://doi.org/10.1105/tpc.113.117523openalex-snapshot

Complexity of the Alternative Splicing Landscape in Plants

inferredcites →https://doi.org/10.1105/tpc.114.135939openalex-snapshot

The Endosomal Protein CHARGED MULTIVESICULAR BODY PROTEIN1 Regulates the Autophagic Turnover of Plastids in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.18.00177openalex-snapshot

Rapid and Dynamic Alternative Splicing Impacts the Arabidopsis Cold Response Transcriptome

inferredcites →https://doi.org/10.1105/tpc.19.00344openalex-snapshot

Questionomics: Using Big Data to Ask and Answer Big Questions

inferredcites →https://doi.org/10.1111/eva.12839openalex-snapshot

Functional and morphological evolution in gymnosperms: A portrait of implicated gene families

inferredcites →https://doi.org/10.1111/pbi.12659openalex-snapshot

The heat‐shock protein/chaperone network and multiple stress resistance

inferredcites →https://doi.org/10.1111/pce.14238openalex-snapshot

Nucleus and chloroplast: A necessary understanding to overcome heat stress in Pinus radiata

inferredcites →https://doi.org/10.1111/tpj.12546openalex-snapshot

A universal protocol for the combined isolation of metabolites, DNA , long RNA s, small RNA s, and proteins from plants and microorganisms

inferredcites →https://doi.org/10.1126/sciadv.1501340openalex-snapshot

Reconsidering plant memory: Intersections between stress recovery, RNA turnover, and epigenetics

inferredcites →https://doi.org/10.1186/1471-2105-13-s6-s5openalex-snapshot

KIS SPLICE: de-novo calling alternative splicing events from RNA-seq data

inferredcites →https://doi.org/10.1186/s13059-014-0550-8openalex-snapshot

Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2

inferredcites →https://doi.org/10.1371/journal.pone.0021800openalex-snapshot

REVIGO Summarizes and Visualizes Long Lists of Gene Ontology Terms

inferredcites →https://doi.org/10.15252/msb.20178124openalex-snapshot

Multi‐Omics Factor Analysis—a framework for unsupervised integration of multi‐omics data sets

inferredcites →https://doi.org/10.3390/ijms20246350openalex-snapshot

Single-Molecule Long-Read Sequencing Reveals the Diversity of Full-Length Transcripts in Leaves of Gnetum (Gnetales)

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.4837256openalex-extracted

Physiological and Molecular Response to Drought in Somatic Plants from Pinus Radiata Embryonal Masses Induced at High Temperatures

inferred← citeshttps://doi.org/10.1007/978-981-95-5183-5_2openalex-snapshot

RNA Sequencing Platforms and Bioinformatics Tools

inferred← citeshttps://doi.org/10.1007/s00122-025-05010-xopenalex-snapshot

Climate change and plant genomic plasticity

inferred← citeshttps://doi.org/10.1007/s11103-024-01528-8openalex-snapshot

Hydrogen peroxide priming triggers splicing memory in grape berries

inferred← citeshttps://doi.org/10.1007/s13280-024-02008-5openalex-snapshot

While clearing the forests: The social–ecological memory of trees in the Anthropocene

inferred← citeshttps://doi.org/10.1016/j.envexpbot.2024.105828openalex-snapshot

An analysis of natural variation in Pinus pinaster through the lens of systems biology

inferred← citeshttps://doi.org/10.1016/j.indcrop.2025.121826openalex-snapshot

JA regulates the impact of combined heat stress and drought stress on the GA-mediated response of Pinus yunnanensis

inferred← citeshttps://doi.org/10.1016/j.pbi.2024.102590openalex-snapshot

Mechanisms of heat stress-induced transcriptional memory

inferred← citeshttps://doi.org/10.1016/j.plantsci.2024.112056openalex-snapshot

Transcription and splicing variations of SR genes accompany with genome-wide accumulation of long-introns in pine

inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.109886openalex-snapshot

Physiological and molecular response to drought in somatic plants from Pinus radiata embryonal masses induced at high temperatures

inferred← citeshttps://doi.org/10.1016/j.stress.2025.100796openalex-snapshot

Functional analyses revealed Pinus radiata CHLOROPLAST SENSOR KINASE as a key component in UV-B stress and development

inferred← citeshttps://doi.org/10.1016/j.tibs.2026.07.014openalex-snapshot

The expanding functional landscape of alternative splicing in plants

inferred← citeshttps://doi.org/10.1016/j.tig.2026.01.006openalex-snapshot

Alternative splicing and climate-resilient crops

inferred← citeshttps://doi.org/10.1016/j.tplants.2026.04.001openalex-snapshot

Alternative splicing in plants: emerging order from chaos

inferred← citeshttps://doi.org/10.1093/jxb/erae033openalex-snapshot

Multiomics analyses reveal the central role of the nucleolus and its machinery during heat stress acclimation in Pinus radiata

inferred← citeshttps://doi.org/10.1093/plphys/kiae051openalex-snapshot

Epigenetic stress memory in gymnosperms

inferred← citeshttps://doi.org/10.1101/2024.01.29.577781openalex-snapshot

An analysis of natural variation in Pinus pinaster through the lens of systems biology

inferred← citeshttps://doi.org/10.1111/pce.14836openalex-snapshot

Like mother like son: Transgenerational memory and cross‐tolerance from drought to heat stress are identified in chloroplast proteome and seed provisioning in Pinus radiata

inferred← citeshttps://doi.org/10.3389/fmolb.2023.1122201openalex-snapshot

Co-expression network of heat-response transcripts: A glimpse into how splicing factors impact rice basal thermotolerance

inferred← citeshttps://doi.org/10.3389/fpls.2023.1130665openalex-snapshot

Proteomics research in forest trees: A 2012-2022 update

inferred← citeshttps://doi.org/10.3389/fpls.2024.1387575openalex-snapshot

The multifaceted role of RNA-based regulation in plant stress memory

inferred← citeshttps://doi.org/10.3390/ijms25168976openalex-snapshot

Establishment and Maintenance of Heat-Stress Memory in Plants

inferred← citeshttps://doi.org/10.3390/plants12030511openalex-snapshot

The Integration of Data from Different Long-Read Sequencing Platforms Enhances Proteoform Characterization in Arabidopsis

inferred← citeshttps://doi.org/10.3390/plants14132021openalex-snapshot

Molecular Mechanisms of Plant Stress Memory: Roles of Non-Coding RNAs and Alternative Splicing

inferred← citeshttps://doi.org/10.5565/rev/brumal.968openalex-snapshot

Morir en árbol para matar al monstruo. Lo fantástico como resistencia a la violencia y el androcentrismo en La vegetariana de Han Kang.

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.