On the public citation graph

Rice LTG 1 is involved in adaptive growth and fitness under low ambient temperature

https://doi.org/10.1111/tpj.12487
0 signed · 154 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1002/j.1460-2075.1987.tb02730.xopenalex-snapshot
GUS fusions: beta‐glucuronidase as a sensitive and versatile gene fusion marker in higher plants.
inferredcites →https://doi.org/10.1006/meth.2001.1262openalex-snapshot
Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method
inferredcites →https://doi.org/10.1007/978-1-60761-702-0_3openalex-snapshot
Gene Regulation During Cold Stress Acclimation in Plants
inferredcites →https://doi.org/10.1007/978-94-007-0394-0_27openalex-snapshot
Cold Stress Tolerance Mechanisms in Plants
inferredcites →https://doi.org/10.1007/bf00033276openalex-snapshot
Genetic divergence among cold tolerant rices (Oryza sativa L.)
inferredcites →https://doi.org/10.1007/pl00013882openalex-snapshot
Cold Acclimation in Plants: Relationship Between the Lipid Composition and the Cryostability of the Plasma Membrane
inferredcites →https://doi.org/10.1007/s00122-002-0908-2openalex-snapshot
Molecular dissection of seedling-vigor and associated physiological traits in rice
inferredcites →https://doi.org/10.1007/s00122-002-1126-7openalex-snapshot
QTLs conferring cold tolerance at the booting stage of rice using recombinant inbred lines from a japonica × indica cross
inferredcites →https://doi.org/10.1007/s00122-003-1509-4openalex-snapshot
Mapping of quantitative trait loci controlling low-temperature germinability in rice (Oryza sativa L.)
inferredcites →https://doi.org/10.1007/s00122-004-1667-zopenalex-snapshot
Physical mapping and putative candidate gene identification of a quantitative trait locus Ctb1 for cold tolerance at the booting stage of rice
inferredcites →https://doi.org/10.1007/s00122-004-1744-3openalex-snapshot
QTL detection for eating quality of cooked rice in a population of chromosome segment substitution lines
inferredcites →https://doi.org/10.1007/s00122-007-0589-yopenalex-snapshot
A quantitative trait locus for cold tolerance at the booting stage on rice chromosome 8
inferredcites →https://doi.org/10.1007/s001220100661openalex-snapshot
Identification of two closely linked quantitative trait loci for cold tolerance on chromosome 4 of rice and their association with anther length
inferredcites →https://doi.org/10.1007/s00344-012-9314-4openalex-snapshot
Protein Kinase LTRPK1 Influences Cold Adaptation and Microtubule Stability in Rice
inferredcites →https://doi.org/10.1007/s00425-012-1641-yopenalex-snapshot
Physiological and molecular changes in plants grown at low temperatures
inferredcites →https://doi.org/10.1007/s11427-012-4300-4openalex-snapshot
Interaction between temperature and photoperiod in regulation of flowering time in rice
inferredcites →https://doi.org/10.1016/j.envexpbot.2010.05.011openalex-snapshot
How plants sense temperature
inferredcites →https://doi.org/10.1016/j.fcr.2005.12.015openalex-snapshot
Analysis of QTLs for seed low temperature germinability and anoxia germinability in rice (Oryza sativa L.)
inferredcites →https://doi.org/10.1016/j.fcr.2007.03.001openalex-snapshot
Opportunities to increasing dry season rice productivity in low temperature affected areas
inferredcites →https://doi.org/10.1016/j.pbi.2010.08.016openalex-snapshot
Regulation of flowering in rice: two florigen genes, a complex gene network, and natural variation
inferredcites →https://doi.org/10.1016/j.plantsci.2004.09.021openalex-snapshot
A major QTL conferring cold tolerance at the early seedling stage using recombinant inbred lines of rice (Oryza sativa L.)
inferredcites →https://doi.org/10.1016/j.plantsci.2007.12.003openalex-snapshot
Identification and mapping of quantitative trait loci for cold tolerance at the booting stage in a japonica rice near-isogenic line
inferredcites →https://doi.org/10.1016/j.plantsci.2013.01.008openalex-snapshot
Post-translational regulation of cold acclimation response
inferredcites →https://doi.org/10.1016/j.tplants.2007.07.002openalex-snapshot
Cold stress regulation of gene expression in plants
inferredcites →https://doi.org/10.1016/s0021-9258(18)53265-8openalex-snapshot
Molecular cloning, expression, and characterization of a 49-kilodalton casein kinase I isoform from rat testis.
inferredcites →https://doi.org/10.1016/s0074-7696(07)56006-7openalex-snapshot
Daylength Measurements by Rice Plants in Photoperiodic Short‐Day Flowering
inferredcites →https://doi.org/10.1016/s1875-2780(08)60021-8openalex-snapshot
QTL and Epistasis for Low Temperature Germinability in Rice
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01661.xopenalex-snapshot
OsDREB genes in rice, Oryza sativa L., encode transcription activators that function in drought‐, high‐salt‐ and cold‐responsive gene expression
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01866.xopenalex-snapshot
Roles of OsCKI1, a rice casein kinase I, in root development and plant hormone sensitivity
inferredcites →https://doi.org/10.1051/agro/2009050openalex-snapshot
Cold stress tolerance mechanisms in plants. A review
inferredcites →https://doi.org/10.1073/pnas.0805303105openalex-snapshot
Molecular identification of a major quantitative trait locus, qLTG3–1 , controlling low-temperature germinability in rice
inferredcites →https://doi.org/10.1073/pnas.1110682108openalex-snapshot
PHYTOCHROME-INTERACTING FACTOR 4 (PIF4) regulates auxin biosynthesis at high temperature
inferredcites →https://doi.org/10.1073/pnas.95.12.7197openalex-snapshot
High temperature promotes auxin-mediated hypocotyl elongation in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/err013openalex-snapshot
Cold affects the transcription of fatty acid desaturases and oil quality in the fruit of Olea europaea L. genotypes with different cold hardiness
inferredcites →https://doi.org/10.1093/pcp/pci230openalex-snapshot
Functional Analysis of Rice DREB1/CBF-type Transcription Factors Involved in Cold-responsive Gene Expression in Transgenic Rice
inferredcites →https://doi.org/10.1101/cshperspect.a001479openalex-snapshot
Auxin and Monocot Development
inferredcites →https://doi.org/10.1104/pp.105.072645openalex-snapshot
Transcriptome Analysis of Cold Acclimation in Barley Albina and Xantha Mutants
inferredcites →https://doi.org/10.1104/pp.110.156943openalex-snapshot
DTH8 Suppresses Flowering in Rice, Influencing Plant Height and Yield Potential Simultaneously
inferredcites →https://doi.org/10.1104/pp.110.161794openalex-snapshot
Molecular Basis of Plant Cold Acclimation: Insights Gained from Studying the CBF Cold Response Pathway
inferredcites →https://doi.org/10.1105/tpc.109.069906openalex-snapshot
Auxin Response inArabidopsisunder Cold Stress: Underlying Molecular Mechanisms
inferredcites →https://doi.org/10.1111/j.1364-3703.2006.00346.xopenalex-snapshot
A highly efficient transient protoplast system for analyzing defence gene expression and protein–protein interactions in rice
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02359.xopenalex-snapshot
The etr1‐2 mutation in Arabidopsis thaliana affects the abscisic acid, auxin, cytokinin and gibberellin metabolic pathways during maintenance of seed dormancy, moist‐chilling and germination
inferredcites →https://doi.org/10.1111/j.1469-8137.2008.02478.xopenalex-snapshot
Temperature perception and signal transduction in plants
inferredcites →https://doi.org/10.1126/science.3291115openalex-snapshot
The Protein Kinase Family: Conserved Features and Deduced Phylogeny of the Catalytic Domains
inferredcites →https://doi.org/10.1242/dev.008631openalex-snapshot
Hd3a and RFT1 are essential for flowering in rice
inferredcites →https://doi.org/10.1270/jsbbs.51.191openalex-snapshot
Mapping Quantitative Trait Loci Controlling Cool-temperature Tolerance at Booting Stage in Temperate Japonica Rice.
inferredcites →https://doi.org/10.1270/jsbbs.51.293openalex-snapshot
Mapping Quantitative Trait Loci Controlling Low Temperature Germinability in Rice (Oryza sativa L.).
inferredcites →https://doi.org/10.1371/journal.pgen.1002594openalex-snapshot
PIF4–Mediated Activation of YUCCA8 Expression Integrates Temperature into the Auxin Pathway in Regulating Arabidopsis Hypocotyl Growth
inferredcites →https://doi.org/10.1371/journal.pone.0005891openalex-snapshot
The Effect of the Crosstalk between Photoperiod and Temperature on the Heading-Date in Rice
inferredcites →https://doi.org/10.1626/jcs.39.468openalex-snapshot
Male Sterility Caused by Cooling Treatment at the Young Microspore Stage in Rice Plants : V. Estimations of pollen developmental stage and the most sensitive stage to coolness
inferredcites →https://doi.org/10.1626/jcs.58.240openalex-snapshot
Male sterility caused by cooling treatment at the young microspore stage in rice plants. XXIX. The mechanism of enhancement in cool tolerance by raising water temperature before the critical stage.
inferredcites →https://doi.org/10.2135/cropsci1997.0011183x003700040051xopenalex-snapshot
Genetic Variation for Traits Related to Temperate Adaptation of Rice Cultivars
inferredcites →https://doi.org/10.3390/ijms14035312openalex-snapshot
Cold Signaling and Cold Response in Plants
inferredcites →https://doi.org/10.3724/sp.j.1006.2008.00551openalex-snapshot
QTL and Epistasis for Low Temperature Germinability in Rice

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.4675953openalex-extracted
Sub4 Encoding Subtilisin-Like Protease Modulates Cold Tolerance in Rice Seedlings Through Cell Wall Modification
inferred← citeshttps://doi.org/10.1007/978-3-032-01704-8_1openalex-snapshot
Unveiling Abiotic Stress Sensing and Regulatory Pathways for Enhanced Crop Resilience
inferred← citeshttps://doi.org/10.1007/s00122-023-04362-6openalex-snapshot
QTL-seq and transcriptomic integrative analyses reveal two positively regulated genes that control the low-temperature germination ability of MTP–maize introgression lines
inferred← citeshttps://doi.org/10.1007/s00122-023-04388-wopenalex-snapshot
qCTB7 positively regulates cold tolerance at booting stage in rice
inferred← citeshttps://doi.org/10.1007/s00122-026-05246-1openalex-snapshot
Discovery of cold tolerance genes and favorable alleles in Kam sweet rice across various growth stages
inferred← citeshttps://doi.org/10.1007/s10681-014-1260-8openalex-snapshot
Genetic analysis and molecular mapping of a high threshold and low temperature-sensitive mutant in rice (Oryza sativa L.) at the seedling stage
inferred← citeshttps://doi.org/10.1007/s10681-019-2410-9openalex-snapshot
Mapping quantitative trait loci and meta-analysis for cold tolerance in rice at booting stage
inferred← citeshttps://doi.org/10.1007/s10681-019-2524-0openalex-snapshot
QTL mapping and validation of a segment responsible for early-seedling cold tolerance in rice
inferred← citeshttps://doi.org/10.1007/s10722-015-0262-2openalex-snapshot
Morphological and molecular genetics of ancient remains and modern rice (Oryza sativa) confirm diversity in ancient Japan
inferred← citeshttps://doi.org/10.1007/s10722-024-02004-4openalex-snapshot
Genetic assessment of diverse rice germplasm for yield-related and stress tolerance traits
inferred← citeshttps://doi.org/10.1007/s11032-022-01297-6openalex-snapshot
Combined QTL mapping and RNA-Seq pro-filing reveal candidate genes related to low-temperature tolerance in maize
inferred← citeshttps://doi.org/10.1007/s11032-025-01543-7openalex-snapshot
Integrating molecular markers and phenotypic analysis to assess cold tolerance in rice germplasm
inferred← citeshttps://doi.org/10.1007/s11427-021-2024-0openalex-snapshot
Rice functional genomics: decades’ efforts and roads ahead
inferred← citeshttps://doi.org/10.1007/s11816-017-0466-3openalex-snapshot
Global analysis of differentially expressed genes between japonica and indica rice roots reveals the molecular basis for enhanced cold tolerance in japonic a rice
inferred← citeshttps://doi.org/10.1007/s13258-018-0731-zopenalex-snapshot
Locating QTLs controlling overwintering seedling rate in perennial glutinous rice 89-1 (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1007/s13258-023-01394-6openalex-snapshot
QTL mapping and identification of candidate genes for cold tolerance at the germination stage in wild rice
inferred← citeshttps://doi.org/10.1007/s42976-021-00214-5openalex-snapshot
Challenges and opportunities in productivity and sustainability of rice cultivation system: a critical review in Indian perspective
inferred← citeshttps://doi.org/10.1016/j.bbrc.2014.10.083openalex-snapshot
Cell cycle transcription factor E2F2 mediates non-stress temperature response of AtHSP70-4 in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.114965openalex-snapshot
Domestication-selected COG4-OsbZIP23 module regulates chilling tolerance in rice
inferred← citeshttps://doi.org/10.1016/j.cj.2021.02.005openalex-snapshot
What happened during domestication of wild to cultivated rice
inferred← citeshttps://doi.org/10.1016/j.cj.2023.01.007openalex-snapshot
The road toward Cd-safe rice: From mass selection to marker-assisted selection and genetic manipulation
inferred← citeshttps://doi.org/10.1016/j.cj.2024.02.005openalex-snapshot
MIR1868 negatively regulates rice cold tolerance at both the seedling and booting stages
inferred← citeshttps://doi.org/10.1016/j.cj.2024.07.016openalex-snapshot
The dual role of casein kinase 1, DTG1, in regulating tillering and grain size in rice
inferred← citeshttps://doi.org/10.1016/j.cj.2025.04.012openalex-snapshot
ZmBARK1 as a low-temperature tolerance gene in maize germination
inferred← citeshttps://doi.org/10.1016/j.cj.2025.05.014openalex-snapshot
qLTS5/OsALA4 encodes a P4-ATPase that positively regulates cold tolerance in rice seedlings
inferred← citeshttps://doi.org/10.1016/j.gene.2025.149600openalex-snapshot
Haplotype analysis and molecular marker development of the COLD1 for cold stress tolerance at the germination stage in rice
inferred← citeshttps://doi.org/10.1016/j.genrep.2025.102201openalex-snapshot
Mechanisms underpinning cold tolerance in indica hybrid rice: Insights for northern adaptation
inferred← citeshttps://doi.org/10.1016/j.gpb.2018.12.002openalex-snapshot
From Basic Research to Molecular Breeding — Chinese Scientists Play A Central Role in Boosting World Rice Production
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2023.126877openalex-snapshot
The G protein-coupled receptor COLD1 promotes chilling tolerance in maize during germination
inferred← citeshttps://doi.org/10.1016/j.jcs.2020.102980openalex-snapshot
Low temperature increased the biosynthesis of 2-AP, cooked rice elongation percentage and amylose content percentage in rice
inferred← citeshttps://doi.org/10.1016/j.jplph.2021.153576openalex-snapshot
Chilling tolerance in rice: Past and present
inferred← citeshttps://doi.org/10.1016/j.molp.2020.02.004openalex-snapshot
Molecular Regulation of Plant Responses to Environmental Temperatures
inferred← citeshttps://doi.org/10.1016/j.molp.2021.12.001openalex-snapshot
From Green Super Rice to green agriculture: Reaping the promise of functional genomics research
inferred← citeshttps://doi.org/10.1016/j.molp.2022.12.020openalex-snapshot
Genomic footprints of Kam Sweet Rice domestication indicate possible migration routes of the Dong people in China and provide resources for future rice breeding
inferred← citeshttps://doi.org/10.1016/j.molp.2024.08.006openalex-snapshot
The OsSRO1c-OsDREB2B complex undergoes protein phase transition to enhance cold tolerance in rice
inferred← citeshttps://doi.org/10.1016/j.plantsci.2026.113070openalex-snapshot
Fine mapping of the qSCT12 locus conferring seedling cold tolerance in Oryza nivara
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.108086openalex-snapshot
Genetic dissection of cold tolerance at the budding stage of rice in an indica-japonica recombination inbred line population
inferred← citeshttps://doi.org/10.1038/ncomms14788openalex-snapshot
Natural variation in CTB4a enhances rice adaptation to cold habitats
inferred← citeshttps://doi.org/10.1038/s41467-018-05753-wopenalex-snapshot
Early selection of bZIP73 facilitated adaptation of japonica rice to cold climates
inferred← citeshttps://doi.org/10.1038/s41467-021-25001-yopenalex-snapshot
Natural variation in a type-A response regulator confers maize chilling tolerance
inferred← citeshttps://doi.org/10.1038/s41467-023-38860-4openalex-snapshot
The COG1-OsSERL2 complex senses cold to trigger signaling network for chilling tolerance in japonica rice
inferred← citeshttps://doi.org/10.1038/s41467-025-56992-7openalex-snapshot
Natural variation of indels in the CTB3 promoter confers cold tolerance in japonica rice
inferred← citeshttps://doi.org/10.1038/s41467-025-59449-zopenalex-snapshot
Suppressing an auxin efflux transporter enhances rice adaptation to temperate habitats
inferred← citeshttps://doi.org/10.1038/s41576-018-0024-zopenalex-snapshot
The rice genome revolution: from an ancient grain to Green Super Rice
inferred← citeshttps://doi.org/10.1038/s41598-024-84491-0openalex-snapshot
Subtilisin-like protease 4 regulates cold tolerance through cell wall modification in rice
inferred← citeshttps://doi.org/10.1071/cp17329openalex-snapshot
Mapping quantitative trait loci for cold tolerance at the booting stage in rice by using chromosome segment substitution lines
inferred← citeshttps://doi.org/10.1093/jxb/erab334openalex-snapshot
Cold response and tolerance in cereal roots
inferred← citeshttps://doi.org/10.1093/plcell/koae039openalex-snapshot
Pan-transcriptomic analysis reveals alternative splicing control of cold tolerance in rice
inferred← citeshttps://doi.org/10.1093/plcell/koaf140openalex-snapshot
Translational insights into abiotic interactions: From Arabidopsis to crop plants
inferred← citeshttps://doi.org/10.1093/plphys/kiab284openalex-snapshot
Plant casein kinases phosphorylate and destabilize a cyclin-dependent kinase inhibitor to promote cell division
inferred← citeshttps://doi.org/10.1093/plphys/kiae130openalex-snapshot
CALMODULIN-LIKE16 and PIN-LIKES7a cooperatively regulate rice seedling primary root elongation under chilling
inferred← citeshttps://doi.org/10.1104/pp.17.01714openalex-snapshot
Ribosomal RNA Biogenesis and Its Response to Chilling Stress in Oryza sativa
inferred← citeshttps://doi.org/10.1104/pp.19.00034openalex-snapshot
The Amino Acid Permease 5 (OsAAP5) Regulates Tiller Number and Grain Yield in Rice
inferred← citeshttps://doi.org/10.1105/tpc.16.00218openalex-snapshot
The Rice Receptor-Like Kinases DWARF AND RUNTISH SPIKELET1 and 2 Repress Cell Death and Affect Sugar Utilization during Reproductive Development
inferred← citeshttps://doi.org/10.1111/jipb.70086openalex-snapshot
Cold tolerance in rice: Insights into genetic basis, molecular mechanisms, and adaptive strategies
inferred← citeshttps://doi.org/10.1111/jipb.70148openalex-snapshot
The receptor‐like pseudokinase LENG stimulates chilling tolerance in rice by inhibiting the activity of the OsCRPK1‐OsGF14d module
inferred← citeshttps://doi.org/10.1111/nph.19514openalex-snapshot
COG3 confers the chilling tolerance to mediate OsFtsH2‐D1 module in rice
inferred← citeshttps://doi.org/10.1111/nph.19696openalex-snapshot
A major gene for chilling tolerance variation in Indica rice codes for a kinase OsCTK1 that phosphorylates multiple substrates under cold
inferred← citeshttps://doi.org/10.1111/pbi.13243openalex-snapshot
The lipid transfer protein Os LTPL 159 is involved in cold tolerance at the early seedling stage in rice
inferred← citeshttps://doi.org/10.1111/pbi.13938openalex-snapshot
Time‐ordering japonica/geng genomes analysis indicates the importance of large structural variants in rice breeding
inferred← citeshttps://doi.org/10.1111/pce.12635openalex-snapshot
New insights into the genetic basis of natural chilling and cold shock tolerance in rice by genome‐wide association analysis
inferred← citeshttps://doi.org/10.1111/pce.13717openalex-snapshot
A point mutation in LTT1 enhances cold tolerance at the booting stage in rice
inferred← citeshttps://doi.org/10.1111/tpj.12939openalex-snapshot
OsPIN5b modulates rice (Oryza sativa) plant architecture and yield by changing auxin homeostasis, transport and distribution
inferred← citeshttps://doi.org/10.1111/tpj.15095openalex-snapshot
SHORT‐ROOT 1 is critical to cell division and tracheary element development in rice roots
inferred← citeshttps://doi.org/10.1111/tpj.16194openalex-snapshot
Ornithine δ‐aminotransferase OsOAT is critical for male fertility and cold tolerance during rice plant development
inferred← citeshttps://doi.org/10.1186/s12284-023-00682-9openalex-snapshot
OsVPE2, a Member of Vacuolar Processing Enzyme Family, Decreases Chilling Tolerance of Rice
inferred← citeshttps://doi.org/10.1186/s12284-024-00749-1openalex-snapshot
Identification of the Cold-Related Genes COLD11 and OsCTS11 via BSA-seq and Fine Mapping at the Rice Seedling Stage
inferred← citeshttps://doi.org/10.1186/s12870-020-02569-zopenalex-snapshot
Transcriptomic profiling of germinating seeds under cold stress and characterization of the cold-tolerant gene LTG5 in rice
inferred← citeshttps://doi.org/10.1186/s12870-021-03317-7openalex-snapshot
Identification of cold tolerance QTLs at the bud burst stage in 211 rice landraces by GWAS
inferred← citeshttps://doi.org/10.1186/s12870-022-03510-2openalex-snapshot
Integration of transcriptomic and proteomic analyses reveals several levels of metabolic regulation in the excess starch and early senescent leaf mutant lses1 in rice
inferred← citeshttps://doi.org/10.1186/s12870-025-07585-5openalex-snapshot
Functional characterization of PcMYB25, a candidate regulator of Patchouli alcohol biosynthesis in Pogostemon cablin, via exogenous hormone-elicited transcriptome analysis
inferred← citeshttps://doi.org/10.1360/tb-2024-1407openalex-snapshot
Gene mining and breeding utilization of important agronomic traits in rice
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1727782/v1openalex-snapshot
Genome-wide dissection of Quan9311A breeding and application
inferred← citeshttps://doi.org/10.21203/rs.3.rs-207385/v1openalex-snapshot
Coexpression Analysis Identified PcMYB25 as a Patchoulol Synthase Gene Activator to Enhance Patchouli Alcohol Biosynthesis in Pogostemon Cablin
inferred← citeshttps://doi.org/10.21203/rs.3.rs-207385/v2openalex-snapshot
Coexpression Analysis Identified PcMYB25 as a Patchoulol Synthase Gene Activator to Enhance Patchouli Alcohol Biosynthesis in Pogostemon Cablin
inferred← citeshttps://doi.org/10.3389/fpls.2018.00065openalex-snapshot
QTL Mapping in Three Connected Populations Reveals a Set of Consensus Genomic Regions for Low Temperature Germination Ability in Zea mays L.
inferred← citeshttps://doi.org/10.3389/fpls.2022.1110724openalex-snapshot
Multi-omics approach reveals the contribution of OsSEH1 to rice cold tolerance
inferred← citeshttps://doi.org/10.3389/fpls.2024.1326606openalex-snapshot
Micrometeorological monitoring reveals that canopy temperature is a reliable trait for the screening of heat tolerance in rice
inferred← citeshttps://doi.org/10.3389/fpls.2024.1390603openalex-snapshot
Integration of molecular breeding and multi-resistance screening for developing a promising restorer line Guihui5501 with heavy grain, good grain quality, and endurance to biotic and abiotic stresses
inferred← citeshttps://doi.org/10.3389/fpls.2025.1716845openalex-snapshot
Divergent genetic architecture of cold stress tolerance in aus and tropical japonica rice
inferred← citeshttps://doi.org/10.3390/agronomy11122416openalex-snapshot
Starch Morphology and Metabolomic Analyses Reveal That the Effect of High Temperature on Cooked Rice Elongation and Expansion Varied in Indica and Japonica Rice Cultivars
inferred← citeshttps://doi.org/10.3390/agronomy13071902openalex-snapshot
Bacillus methylotrophicus Could Improve the Tolerance and Recovery Ability of the Tomato to Low-Temperature Stress and Improve Fruit Quality
inferred← citeshttps://doi.org/10.3390/agronomy15112601openalex-snapshot
LSES1, Encoding a Member of the Casein Kinase 1 Family, Is Involved in the Regulation of Leaf Senescence in Rice
inferred← citeshttps://doi.org/10.3390/beverages12060068openalex-snapshot
Optimizing Milled Rice Utilization in the Brewing Industry by Overcoming Equipment Barriers Through Cultivar Characterization
inferred← citeshttps://doi.org/10.3390/genes8070179openalex-snapshot
Overexpression of the OsIMP Gene Increases the Accumulation of Inositol and Confers Enhanced Cold Tolerance in Tobacco through Modulation of the Antioxidant Enzymes’ Activities
inferred← citeshttps://doi.org/10.3390/ijms21041284openalex-snapshot
Genetic Dissection of Germinability under Low Temperature by Building a Resequencing Linkage Map in japonica Rice
inferred← citeshttps://doi.org/10.3390/ijms21051562openalex-snapshot
Mut9p-LIKE KINASE Family Members: New Roles of the Plant-Specific Casein Kinase I in Plant Growth and Development
inferred← citeshttps://doi.org/10.3390/ijms21228567openalex-snapshot
Natural Genetic Resources from Diverse Plants to Improve Abiotic Stress Tolerance in Plants
inferred← citeshttps://doi.org/10.3390/plants10091864openalex-snapshot
Convergence and Divergence: Signal Perception and Transduction Mechanisms of Cold Stress in Arabidopsis and Rice
inferred← citeshttps://doi.org/10.3390/plants12040871openalex-snapshot
Transcriptomic and QTL Analysis of Seed Germination Vigor under Low Temperature in Weedy Rice WR04-6
inferred← citeshttps://doi.org/10.3390/plants12102019openalex-snapshot
Recent Molecular Aspects and Integrated Omics Strategies for Understanding the Abiotic Stress Tolerance of Rice
inferred← citeshttps://doi.org/10.3390/plants15040540openalex-snapshot
Transcriptome Analysis Identifies OsWRKY26 as a Key Regulator for Cold Tolerance at the Seedling Stage in Rice
inferred← citeshttps://doi.org/10.5010/jpb.2024.51.029.294openalex-snapshot
Haplotype analysis of Tongil-type rice varieties through sequence polymorphism analysis of cold tolerance-enhancing genes
inferred← citeshttps://doi.org/10.6084/m9.figshare.17056682openalex-snapshot
Additional file 1 of Identification of cold tolerance QTLs at the bud burst stage in 211 rice landraces by GWAS
inferred← citeshttps://doi.org/10.6084/m9.figshare.17056685openalex-snapshot
Additional file 2 of Identification of cold tolerance QTLs at the bud burst stage in 211 rice landraces by GWAS
inferred← citeshttps://doi.org/10.6084/m9.figshare.17056688openalex-snapshot
Additional file 3 of Identification of cold tolerance QTLs at the bud burst stage in 211 rice landraces by GWAS
inferred← citeshttps://doi.org/10.6084/m9.figshare.17056691openalex-snapshot
Additional file 4 of Identification of cold tolerance QTLs at the bud burst stage in 211 rice landraces by GWAS
inferred← citeshttps://doi.org/10.6084/m9.figshare.24971303openalex-snapshot
Additional file 1 of OsVPE2, a Member of Vacuolar Processing Enzyme Family, Decreases Chilling Tolerance of Rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.24971626openalex-snapshot
Additional file 2 of OsVPE2, a Member of Vacuolar Processing Enzyme Family, Decreases Chilling Tolerance of Rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.26665666openalex-snapshot
Additional file 3 of OsVPE2, a Member of Vacuolar Processing Enzyme Family, Decreases Chilling Tolerance of Rice
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.