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Natural variation in CTB4a enhances rice adaptation to cold habitats

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What this work says

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

inferredcites →https://doi.org/10.1002/fes3.25openalex-snapshot

Avoiding damage and achieving cold tolerance in rice plants

inferredcites →https://doi.org/10.1002/pmic.200401148openalex-snapshot

A proteomic analysis of cold stress responses in rice seedlings

inferredcites →https://doi.org/10.1007/bf02772683openalex-snapshot

A practical vector for efficient knockdown of gene expression in rice (Oryza sativa L.)

inferredcites →https://doi.org/10.1007/bf03191147openalex-snapshot

QTLs of cold tolerance-related traits at the booting stage for NIL-RILs in rice revealed by SSR

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/s00122-007-0589-yopenalex-snapshot

A quantitative trait locus for cold tolerance at the booting stage on rice chromosome 8

inferredcites →https://doi.org/10.1007/s00122-010-1358-xopenalex-snapshot

Fine mapping a QTL qCTB7 for cold tolerance at the booting stage on rice chromosome 7 using a near-isogenic line

inferredcites →https://doi.org/10.1007/s00122-011-1758-6openalex-snapshot

Delimitation of a QTL region controlling cold tolerance at booting stage of a cultivar, ‘Lijiangxintuanheigu’, in rice, Oryza sativa L.

inferredcites →https://doi.org/10.1007/s00122-015-2654-2openalex-snapshot

Detection of QTLs for cold tolerance of rice cultivar ‘Kuchum’ and effect of QTL pyramiding

inferredcites →https://doi.org/10.1007/s10681-010-0226-8openalex-snapshot

A QTL controlling low temperature induced spikelet sterility at booting stage in rice

inferredcites →https://doi.org/10.1007/s11032-015-0425-zopenalex-snapshot

TaTGW6-A1, an ortholog of rice TGW6, is associated with grain weight and yield in bread wheat

inferredcites →https://doi.org/10.1007/s11032-016-0498-3openalex-snapshot

Hybrid lethality caused by two complementary dominant genes in cabbage (Brassica oleracea L.)

inferredcites →https://doi.org/10.1007/s11032-016-0520-9openalex-snapshot

Identification and pyramiding of QTLs for cold tolerance at the bud bursting and the seedling stages by use of single segment substitution lines in rice (Oryza sativa L.)

inferredcites →https://doi.org/10.1007/s11120-006-9078-4openalex-snapshot

Multiple phosphorylation sites in the β subunit of thylakoid ATP synthase

inferredcites →https://doi.org/10.1007/s11434-009-0348-3openalex-snapshot

Stamen specification and anther development in rice

inferredcites →https://doi.org/10.1016/j.cell.2006.12.006openalex-snapshot

The Molecular Genetics of Crop Domestication

inferredcites →https://doi.org/10.1016/j.cell.2015.01.046openalex-snapshot

COLD1 Confers Chilling Tolerance 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.pbi.2009.09.011openalex-snapshot

Receptor endocytosis and signaling in plants

inferredcites →https://doi.org/10.1016/j.pbi.2013.03.003openalex-snapshot

Understanding rice domestication and implications for cultivar improvement

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.2010.04.004openalex-snapshot

Map-based cloning of the rice cold tolerance gene Ctb1

inferredcites →https://doi.org/10.1016/s1360-1385(00)01808-2openalex-snapshot

Impacts of chilling temperatures on photosynthesis in warm-climate plants

inferredcites →https://doi.org/10.1016/s1369-5266(99)00047-3openalex-snapshot

International Rice Genome Sequencing Project: the effort to completely sequence the rice genome

inferredcites →https://doi.org/10.1038/ncomms1716openalex-snapshot

Rice APC/CTE controls tillering by mediating the degradation of MONOCULM 1

inferredcites →https://doi.org/10.1038/nrg2187openalex-snapshot

Recent and ongoing selection in the human genome

inferredcites →https://doi.org/10.1046/j.1365-313x.1994.6020271.xopenalex-snapshot

Efficient transformation of rice ( Oryza sativa L.) mediated by Agrobacterium and sequence analysis of the boundaries of the T‐DNA

inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01753.xopenalex-snapshot

Two cis‐ acting elements necessary and sufficient for gibberellin‐upregulated proteinase expression in rice seeds

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/10.1080/15216549800203602openalex-snapshot

The β subunit of chloroplast ATP synthase (CF0CF1‐ATPase) is phosphorylated by casein kinase II

inferredcites →https://doi.org/10.1093/aob/mci219openalex-snapshot

Detection and Preliminary Analysis of Motifs in Promoters of Anaerobically Induced Genes of Different Plant Species

inferredcites →https://doi.org/10.1093/bioinformatics/btp187openalex-snapshot

DnaSP v5: a software for comprehensive analysis of DNA polymorphism data

inferredcites →https://doi.org/10.1093/genetics/123.3.585openalex-snapshot

Statistical method for testing the neutral mutation hypothesis by DNA polymorphism.

inferredcites →https://doi.org/10.1093/jxb/erg243openalex-snapshot

Mapping of QTLs associated with cold tolerance during the vegetative stage in rice

inferredcites →https://doi.org/10.1093/molbev/msm005openalex-snapshot

Multilocus Analysis of Nucleotide Variation of Oryza sativa and Its Wild Relatives: Severe Bottleneck during Domestication of Rice

inferredcites →https://doi.org/10.1093/molbev/msr121openalex-snapshot

MEGA5: Molecular Evolutionary Genetics Analysis Using Maximum Likelihood, Evolutionary Distance, and Maximum Parsimony Methods

inferredcites →https://doi.org/10.1093/nar/gks576openalex-snapshot

EvolView, an online tool for visualizing, annotating and managing phylogenetic trees

inferredcites →https://doi.org/10.1098/rstb.2009.0219openalex-snapshot

Genome-wide scans for footprints of natural selection

inferredcites →https://doi.org/10.1104/pp.014357openalex-snapshot

T-DNA Insertional Mutagenesis for Activation Tagging in Rice

inferredcites →https://doi.org/10.1104/pp.103.027979openalex-snapshot

A Gateway Cloning Vector Set for High-Throughput Functional Analysis of Genes in Planta

inferredcites →https://doi.org/10.1104/pp.109.138677openalex-snapshot

Large-Scale Arabidopsis Phosphoproteome Profiling Reveals Novel Chloroplast Kinase Substrates and Phosphorylation Networks

inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03212.xopenalex-snapshot

A multicolored set of in vivo organelle markers for co‐localization studies in Arabidopsis and other plants

inferredcites →https://doi.org/10.1111/j.1755-0998.2010.02847.xopenalex-snapshot

Arlequin suite ver 3.5: a new series of programs to perform population genetics analyses under Linux and Windows

inferredcites →https://doi.org/10.1111/j.1755-0998.2010.02890.xopenalex-snapshot

HapStar: automated haplotype network layout and visualization

inferredcites →https://doi.org/10.1111/tpj.12487openalex-snapshot

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

inferredcites →https://doi.org/10.1186/s12284-016-0133-2openalex-snapshot

Genome-wide Association Mapping of Cold Tolerance Genes at the Seedling Stage 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/10.1360/n972014-01231openalex-snapshot

Rice functional genomics and breeding database (RFGB)-3K-rice SNP and InDel sub-database

inferredcites →https://doi.org/10.1371/journal.pone.0120590openalex-snapshot

Genetic Analysis of Cold Tolerance at the Germination and Booting Stages in Rice by Association Mapping

inferredcites →https://doi.org/10.1371/journal.pone.0145704openalex-snapshot

Identification and Fine Mapping of a Stably Expressed QTL for Cold Tolerance at the Booting Stage Using an Interconnected Breeding Population in Rice

inferredcites →https://doi.org/10.1534/genetics.104.026500openalex-snapshot

The HKA Test Revisited

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/10.3390/ijms14034885openalex-snapshot

Metabolomics as a Tool to Investigate Abiotic Stress Tolerance in Plants

inferredcites →https://doi.org/10.5511/plantbiotechnology.12.1015aopenalex-snapshot

High-temperature stress susceptibility of representative japonica rice cultivars derived from Norin-22: Inadequate ATP supply during seed development may lead to severe damage

inferredcites →https://doi.org/10.5511/plantbiotechnology.27.67openalex-snapshot

Reduced rice grain production under high-temperature stress closely correlates with ATP shortage during seed development

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/10.1002/advs.202411357openalex-snapshot

CTB6 Confers Cold Tolerance at the Booting Stage by Maintaining Tapetum Development in Rice

inferred← citeshttps://doi.org/10.1002/advs.76225openalex-snapshot

Natural Variation of COLD and CATECHINS REGULATOR 1 Coordinately Fine‐Tunes Cold Tolerance and Tea Quality in Tea Plants

inferred← citeshttps://doi.org/10.1002/fes3.70283openalex-snapshot

Identification of qCTB2 for Booting‐Stage Cold Tolerance From the Highly Tolerant Rice Landrace “Lijiangxintuanheigu” ( Oryza sativa L.)

inferred← citeshttps://doi.org/10.1002/tpg2.20402openalex-snapshot

Advances and opportunities in unraveling cold‐tolerance mechanisms in the world's primary staple food crops

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Mapping of Quantitative Trait Loci (QTL) Associated with Plant Freezing Tolerance and Cold Acclimation

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Green Super Rice (GSR) Traits: Breeding and Genetics for Multiple Biotic and Abiotic Stress Tolerance in Rice

inferred← citeshttps://doi.org/10.1007/978-3-030-66530-2_8openalex-snapshot

Genetics and Breeding of Low-Temperature Stress Tolerance in Rice

inferred← citeshttps://doi.org/10.1007/978-981-15-4120-9_23openalex-snapshot

Biotechnological Approaches to Develop Rice Tolerance to Low and High Temperature Stress

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Importance of Genetic Variability, Breeding, and Associative Transcriptomics in Rapeseed Genetic Resources

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Cellulases from Psychrophilic and Psychrotrophic Microorganisms and their Potential Applications

inferred← citeshttps://doi.org/10.1007/s00122-017-2992-3openalex-snapshot

Fine mapping of QTL qCTB10-2 that confers cold tolerance at the booting stage in rice

inferred← citeshttps://doi.org/10.1007/s00122-019-03516-9openalex-snapshot

Genomic Breeding of Green Super Rice Varieties and Their Deployment in Asia and Africa

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Whole-genome sequencing reveals uniqueness of black-hulled and straw-hulled weedy rice genomes

inferred← citeshttps://doi.org/10.1007/s00122-023-04261-wopenalex-snapshot

COG2 negatively regulates chilling tolerance through cell wall components altered in rice

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/s00122-024-04733-7openalex-snapshot

Identification of transcription factor BnHDG4-A08 as a novel candidate associated with the accumulation of oleic, linoleic, linolenic, and erucic acid in Brassica napus

inferred← citeshttps://doi.org/10.1007/s00122-025-05071-yopenalex-snapshot

Haplotype analysis and molecular marker development for the cold tolerance gene OsCTS11 at the seedling stage of rice

inferred← citeshttps://doi.org/10.1007/s00122-026-05339-xopenalex-snapshot

Natural variation in WRKY53 confers cold tolerance at the booting stage between japonica and indica rice

inferred← citeshttps://doi.org/10.1007/s00122-026-05385-5openalex-snapshot

OsERF5 enhances cold tolerance and is associated with GA‑mediated antioxidant defence in rice

inferred← citeshttps://doi.org/10.1007/s00299-023-03093-8openalex-snapshot

Identification of hub genes that variate the qCSS12-mediated cold tolerance between indica and japonica rice using WGCNA

inferred← citeshttps://doi.org/10.1007/s00299-026-03997-1openalex-snapshot

OsbHLH6 regulates OsMADS57 and amino acid metabolism to impair cold tolerance in rice

inferred← citeshttps://doi.org/10.1007/s00425-020-03488-xopenalex-snapshot

Whole-genome mining of abiotic stress gene loci in rice

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/s10681-019-2507-1openalex-snapshot

QTL analysis of main agronomic traits in rice under low temperature stress

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/s10681-021-02898-6openalex-snapshot

Identification of QTLs for cold tolerance at the booting and flowering stages in rice (Oryza sativa L.)

inferred← citeshttps://doi.org/10.1007/s10681-022-03044-6openalex-snapshot

Survey of overwintering trait in Chinese rice cultivars (Oryza sativa L)

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Physical mapping of qDTH3 for heading date reveals the evolution of cultivated rice (Oryza sativa L.)

inferred← citeshttps://doi.org/10.1007/s10722-024-02004-4openalex-snapshot

Genetic assessment of diverse rice germplasm for yield-related and stress tolerance traits

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GhRH32 negatively regulates cold tolerance in upland cotton (Gossypium hirsutum L.)

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Current understanding of genetic and molecular basis of cold tolerance in rice

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Genetic analysis of rice seed recovery under low-temperature conditions using a new CSSL population with a high-density genetic map in rice

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Combined QTL mapping and RNA-Seq pro-filing reveal candidate genes related to low-temperature tolerance in maize

inferred← citeshttps://doi.org/10.1007/s11032-024-01488-3openalex-snapshot

QTL detection and candidate gene identification of qCTB1 for cold tolerance in the Yunnan plateau landrace rice

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Transcriptomic profiling of the cold stress and recovery responsiveness of two contrasting Guizhou HE rice genotypes

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/s40502-023-00709-9openalex-snapshot

microRNA-marker based genetic diversity analysis for drought tolerance in rice (Oryza sativa L.)

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Challenges and opportunities in productivity and sustainability of rice cultivation system: a critical review in Indian perspective

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CRISPR-Cas9-mediated genome editing technology for abiotic stress tolerance in crop plant

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Roles of plant receptor-like kinases in response to abiotic stress

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CRISPR/Cas-mediated genome editing for improved stress tolerance in plants

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Advancement in the understanding of the different abiotic stresses using “omics”

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Pangenomics for developing cold stress-tolerant plants

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QTL mapping by GWAS and functional analysis of OsbZIP72 for cold tolerance at rice seedling stage

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ZmBARK1 as a low-temperature tolerance gene in maize germination

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A missense mutation in TaBGLU1-5D confers early heading in wheat

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Effects of root characteristics on panicle formation in japonica rice under low temperature water stress at the reproductive stage

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Prescreening rice for cold tolerance at the reproductive stage using anther length

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Utilization of natural alleles and haplotypes of Ctb1 for rice cold adaptability

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Haplotype analysis and molecular marker development of the COLD1 for cold stress tolerance at the germination stage in rice

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From Basic Research to Molecular Breeding — Chinese Scientists Play A Central Role in Boosting World Rice Production

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The G protein-coupled receptor COLD1 promotes chilling tolerance in maize during germination

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Integrated genomics, QTL mapping, and co-expression analyses identifying candidates of low-temperature tolerance in Brassica napus L.

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Polyamine oxidase 3 is involved in salt tolerance at the germination stage in rice

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Genotype of pioneer plant Miscanthus is not a key factor in the structure of rhizosphere bacterial community in heavy metal polluted sites

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Abscisic acid alleviates photosynthetic damage in the tomato abscisic acid-deficient mutant sitiens and protects photosystem II from damage via the WRKY22–PsbA under low-temperature stress

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Chilling tolerance in rice: Past and present

inferred← citeshttps://doi.org/10.1016/j.jplph.2021.153602openalex-snapshot

Cold responses in rice: From physiology to molecular biology

inferred← citeshttps://doi.org/10.1016/j.molcel.2024.09.031openalex-snapshot

COLD6-OSM1 module senses chilling for cold tolerance via 2′,3′-cAMP signaling in rice

inferred← citeshttps://doi.org/10.1016/j.molp.2018.01.007openalex-snapshot

Rice Functional Genomics Research: Past Decade and Future

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

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Twenty years of rice genomics research: From sequencing and functional genomics to quantitative genomics

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The OsSRO1c-OsDREB2B complex undergoes protein phase transition to enhance cold tolerance in rice

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The OsNAC41-RoLe1-OsAGAP module promotes root development and drought resistance in upland rice

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Facing chilling, kinase-transcription factors relay cold tolerance signals

inferred← citeshttps://doi.org/10.1016/j.plantsci.2020.110669openalex-snapshot

Genome-wide association study reveals novel genetic loci contributing to cold tolerance at the germination stage in indica rice

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GPA1 is a determinant of leaf width and fruit size in tomato

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Fine mapping of the qSCT12 locus conferring seedling cold tolerance in Oryza nivara

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Genetic dissection of cold tolerance at the budding stage of rice in an indica-japonica recombination inbred line population

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Transcriptomic and functional analyzes reveal that the brassinosteroid insensitive 1 receptor (OsBRI1) regulates cold tolerance in rice

inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.109455openalex-snapshot

OsNCED5 confers cold stress tolerance through regulating ROS homeostasis in rice

inferred← citeshttps://doi.org/10.1016/j.rsci.2021.08.003openalex-snapshot

Conservation and Utilization of Genetic Resources of Wild Rice in China

inferred← citeshttps://doi.org/10.1016/j.rsci.2024.12.003openalex-snapshot

Leucine-Rich Repeat Protein Family Regulates Stress Tolerance and Development in Plants

inferred← citeshttps://doi.org/10.1016/j.scienta.2022.111689openalex-snapshot

QTL analysis for low temperature tolerance of wild potato species Solanum commersonii in natural field trials

inferred← citeshttps://doi.org/10.1016/j.scienta.2023.112523openalex-snapshot

Transcriptome reveals molecular mechanism of cabbage response to low temperature stress and functional study of BoPYL8 gene

inferred← citeshttps://doi.org/10.1016/j.stress.2024.100700openalex-snapshot

Anther transcriptomes in cold-tolerant rice cultivars tend to show insensitive responses

inferred← citeshttps://doi.org/10.1016/j.ygeno.2022.110285openalex-snapshot

Comparative physiological and transcriptomic analyses reveal key regulatory networks and potential hub genes controlling peanut chilling tolerance

inferred← citeshttps://doi.org/10.1021/acs.jafc.6c04159openalex-snapshot

The E3 Ubiquitin-Protein Ligase ZmBOIR3 Is a Key Regulator of Low-Temperature Tolerance in Maize Seedlings

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/s41467-020-19320-9openalex-snapshot

Natural variations of SLG1 confer high-temperature tolerance in indica rice

inferred← citeshttps://doi.org/10.1038/s41467-021-22564-8openalex-snapshot

O-linked N-acetylglucosamine transferase is involved in fine regulation of flowering time in winter wheat

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/s41467-024-52510-3openalex-snapshot

A point mutation in VIG1 boosts development and chilling tolerance in rice

inferred← citeshttps://doi.org/10.1038/s41467-025-56174-5openalex-snapshot

Natural variation of CTB5 confers cold adaptation in plateau 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/s41477-019-0582-xopenalex-snapshot

Introducing selective agrochemical manipulation of gibberellin metabolism into a cereal crop

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/10.1071/fp20046openalex-snapshot

Identification and characterisation of cold stress-related proteins in Oryza rufipogon at the seedling stage using label-free quantitative proteomic analysis

inferred← citeshttps://doi.org/10.1073/pnas.1819769116openalex-snapshot

Natural variation in the HAN1 gene confers chilling tolerance in rice and allowed adaptation to a temperate climate

inferred← citeshttps://doi.org/10.1073/pnas.2514614122openalex-snapshot

Evolutionary histories of functional mutations during the domestication and spread of japonica rice in Asia

inferred← citeshttps://doi.org/10.1073/pnas.2529950123openalex-snapshot

Natural variation of CTS1 confers cold tolerance and blast resistance in rice

inferred← citeshttps://doi.org/10.1079/pavsnnr201914050openalex-snapshot

CRISPR-Cas technology in modifying food crops.

inferred← citeshttps://doi.org/10.1080/07388551.2026.2680427openalex-snapshot

A step forward toward improved cold tolerance in rice: integrating physiological insights with cutting-edge genomic approaches

inferred← citeshttps://doi.org/10.1080/1343943x.2026.2676573openalex-snapshot

Floral traits associated with low temperature tolerance at the young microspore stage in rice

inferred← citeshttps://doi.org/10.1080/1343943x.2026.2706782openalex-snapshot

Cold damage to rice during the reproductive stage: a review

inferred← citeshttps://doi.org/10.1080/15592324.2022.2025678openalex-snapshot

Functional verification and screening of protein interacting with the slPHB3

inferred← citeshttps://doi.org/10.1080/15592324.2024.2318514openalex-snapshot

Insights on the enhancement of chilling tolerance in Rice through over-expression and knock-out studies of OsRBCS3

inferred← citeshttps://doi.org/10.1093/aob/mcab091openalex-snapshot

Revision of the relationship between anther morphology and pollen sterility by cold stress at the booting stage in rice

inferred← citeshttps://doi.org/10.1093/aobpla/plad075openalex-snapshot

Genetics of chilling response at early growth stage in rice: a recessive gene for tolerance and importance of acclimation

inferred← citeshttps://doi.org/10.1093/hr/uhab088openalex-snapshot

The novel leucine-rich repeat receptor-like kinase MRK1 regulates resistance to multiple stresses in tomato

inferred← citeshttps://doi.org/10.1093/hr/uhad001openalex-snapshot

The class B heat shock factor HSFB1 regulates heat tolerance in grapevine

inferred← citeshttps://doi.org/10.1093/jxb/erad120openalex-snapshot

Genome-wide association study identifies a novel BMI1A QTL allele that confers FLC expression diversity in Arabidopsis thaliana

inferred← citeshttps://doi.org/10.1093/jxb/ery256openalex-snapshot

Gnp4/LAX2, a RAWUL protein, interferes with the OsIAA3–OsARF25 interaction to regulate grain length via the auxin signaling pathway in rice

inferred← citeshttps://doi.org/10.1093/plcell/koac253openalex-snapshot

WRKY53 negatively regulates rice cold tolerance at the booting stage by fine-tuning anther gibberellin levels

inferred← citeshttps://doi.org/10.1093/plcell/koae100openalex-snapshot

Methyltransferase TaSAMT1 mediates wheat freezing tolerance by integrating brassinosteroid and salicylic acid signaling

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/plcell/koag086openalex-snapshot

Natural variation in the ORL4 promoter regulates rice leaf rolling to modulate leaf architecture and yield

inferred← citeshttps://doi.org/10.1093/plphys/kiac208openalex-snapshot

Osa-miR1320 targets the ERF transcription factor OsERF096 to regulate cold tolerance via JA-mediated signaling

inferred← citeshttps://doi.org/10.1093/plphys/kiad420openalex-snapshot

Natural variation in OsSEC13 HOMOLOG 1 modulates redox homeostasis to confer cold tolerance in rice

inferred← citeshttps://doi.org/10.1093/plphys/kiae118openalex-snapshot

Acyl carrier protein OsMTACP2 confers rice cold tolerance at the booting stage

inferred← citeshttps://doi.org/10.1098/rsos.201081openalex-snapshot

Identification of candidate genes controlling chilling tolerance of rice in the cold region at the booting stage by BSA-Seq and RNA-Seq

inferred← citeshttps://doi.org/10.1101/2025.11.23.690040openalex-snapshot

Stage-specific screening reveals complex resilience pathways to cold stress in rice

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.18.00209openalex-snapshot

Identification of Genes Related to Cold Tolerance and a Functional Allele That Confers Cold Tolerance

inferred← citeshttps://doi.org/10.1111/jac.12663openalex-snapshot

Responses of rice cultivars with different cold tolerance to chilling in booting and flowering stages: An experiment in Northeast China

inferred← citeshttps://doi.org/10.1111/jipb.12852openalex-snapshot

Coordination of light, circadian clock with temperature: The potential mechanisms regulating chilling tolerance in rice

inferred← citeshttps://doi.org/10.1111/jipb.13061openalex-snapshot

Protein kinases in plant responses to drought, salt, and cold stress

inferred← citeshttps://doi.org/10.1111/jipb.13489openalex-snapshot

The basic helix‐loop‐helix transcription factor gene, OsbHLH38, plays a key role in controlling rice salt tolerance

inferred← citeshttps://doi.org/10.1111/jipb.13571openalex-snapshot

Natural variation in STAYGREEN contributes to low‐temperature tolerance in cucumber

inferred← citeshttps://doi.org/10.1111/jipb.13585openalex-snapshot

OsNAC5 orchestrates OsABI5 to fine‐tune cold tolerance in rice

inferred← citeshttps://doi.org/10.1111/jipb.13674openalex-snapshot

Natural variation in MORE GRAINS 1 regulates grain number and grain weight in rice

inferred← citeshttps://doi.org/10.1111/jipb.13726openalex-snapshot

BTA2 regulates tiller angle and the shoot gravity response through controlling auxin content and distribution in rice

inferred← citeshttps://doi.org/10.1111/jipb.13830openalex-snapshot

The MYB61–STRONG2 module regulates culm diameter and lodging resistance in rice

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/jipb.70260openalex-snapshot

Temperature regulation in plants: From molecular mechanisms to climate‐resilient crop improvement

inferred← citeshttps://doi.org/10.1111/jipb.70322openalex-snapshot

Natural variation in the promoter of OsPDX1.2 enhances vitamin B6 accumulation and cold tolerance in rice

inferred← citeshttps://doi.org/10.1111/nph.17407openalex-snapshot

Stepwise selection of natural variations at CTB2 and CTB4a improves cold adaptation during domestication of japonica rice

inferred← citeshttps://doi.org/10.1111/nph.17515openalex-snapshot

Natural variations of BrHISN2 provide a genetic basis for growth‐flavour trade‐off in different Brassica rapa subspecies

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/pbi.13080openalex-snapshot

Natural alleles of GLA for grain length and awn development were differently domesticated in rice subspecies japonica and indica

inferred← citeshttps://doi.org/10.1111/pbi.13104openalex-snapshot

The bZIP 73 transcription factor controls rice cold tolerance at the reproductive stage

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.13424openalex-snapshot

Differentiation, evolution and utilization of natural alleles for cold adaptability at the reproductive stage in rice

inferred← citeshttps://doi.org/10.1111/pbi.14017openalex-snapshot

Natural variation in Tiller Number 1 affects its interaction with TIF1 to regulate tillering in rice

inferred← citeshttps://doi.org/10.1111/pbi.14308openalex-snapshot

A natural variation in OsDSK2a modulates plant growth and salt tolerance through phosphorylation by SnRK1A in rice

inferred← citeshttps://doi.org/10.1111/pbi.14600openalex-snapshot

Natural variation in CTF1 conferring cold tolerance at the flowering stage in rice

inferred← citeshttps://doi.org/10.1111/pbi.70195openalex-snapshot

Co‐domestication of cold tolerance and female flower is determined by CsEIN2 in cucumber

inferred← citeshttps://doi.org/10.1111/pbi.70293openalex-snapshot

Natural Variation of a Specific NLR Gene RGA4L Confers Strong Chilling Tolerance in Rice

inferred← citeshttps://doi.org/10.1111/pbr.12603openalex-snapshot

Deployment of cold tolerance loci from Oryza sativa ssp. Japonica cv. ‘Nipponbare’ in a high‐yielding Indica rice cultivar ‘93‐11’

inferred← citeshttps://doi.org/10.1111/pbr.70053openalex-snapshot

Comprehensive Evaluation of Cold and Anaerobic Tolerance in Rice Oryza sativa L. and Screening of Multistress‐Resistant Germplasm

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/pce.14513openalex-snapshot

bHLH57 confers chilling tolerance and grain yield improvement in rice

inferred← citeshttps://doi.org/10.1111/pce.14900openalex-snapshot

OsEIN2‐OsEIL1/2 pathway negatively regulates chilling tolerance by attenuating OsICE1 function in rice

inferred← citeshttps://doi.org/10.1111/pce.15053openalex-snapshot

The invertase gene PWIN1 confers chilling tolerance of rice at the booting stage via mediating pollen development

inferred← citeshttps://doi.org/10.1111/pce.15665openalex-snapshot

Small G Protein OsRab6a Confers Cold Tolerance by Cooperating With OsRAN2 and Suppressing ABA Signalling in Rice

inferred← citeshttps://doi.org/10.1111/pce.70122openalex-snapshot

Natural Variations in the Promoter of CHILLING TOLERANCE DIVERGENCE 8 Contribute to the Functional Divergence in the Chilling Tolerance of Rice

inferred← citeshttps://doi.org/10.1111/pce.70190openalex-snapshot

Root‐Derived Trans‐ Zeatin‐Type Cytokinins Increase Cold Tolerance in Rice Seedlings by Regulating Energy Metabolism

inferred← citeshttps://doi.org/10.1111/ppl.70895openalex-snapshot

HSP101 Polymorphism Is Related to Heat Tolerance and Seedling Growth in Wild‐Type Arabidopsis Accessions From Diverse Geographical Locations

inferred← citeshttps://doi.org/10.1111/tpj.15870openalex-snapshot

Cold‐adaptive evolution at the reproductive stage in Geng / japonica subspecies reveals the role of OsMAPK3 and OsLEA9

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/10.1111/tpj.70145openalex-snapshot

Exploring genomic regions and genes modulating plant height and flag leaf morphology in rice

inferred← citeshttps://doi.org/10.1111/tpj.70246openalex-snapshot

OsPPR8 , a pentatricopeptide repeat protein, regulates splicing of mitochondrial nad2 intron 3 to affect grain quality and high‐temperature tolerance in rice

inferred← citeshttps://doi.org/10.1111/tpj.70256openalex-snapshot

RsWRKY49 promotes cold tolerance via activating the expression of RsCBF2 and RsNR2 in radish ( Raphanus sativus L.)

inferred← citeshttps://doi.org/10.1111/tpj.70382openalex-snapshot

Genomics control of biostimulant‐induced stress tolerance and crop yield enhancement

inferred← citeshttps://doi.org/10.1126/sciadv.abq5506openalex-snapshot

Natural variation of codon repeats in COLD11 endows rice with chilling resilience

inferred← citeshttps://doi.org/10.1139/gen-2019-0160openalex-snapshot

Construction of three half-sib SSR linkage maps derived from overwintering cultivated rice and segregation distortion loci mapping

inferred← citeshttps://doi.org/10.1155/2018/5480617openalex-snapshot

Overexpression of a New Zinc Finger Protein Transcription FactorOsCTZFP8Improves Cold Tolerance in Rice

inferred← citeshttps://doi.org/10.1186/s12284-018-0218-1openalex-snapshot

Identification of a cold-tolerant locus in rice (Oryza sativa L.) using bulked segregant analysis with a next-generation sequencing strategy

inferred← citeshttps://doi.org/10.1186/s12284-019-0363-1openalex-snapshot

Comprehensive Evaluation and Analysis of the Mechanism of Cold Tolerance Based on the Transcriptome of Weedy Rice Seedlings

inferred← citeshttps://doi.org/10.1186/s12284-021-00485-wopenalex-snapshot

OsGATA16, a GATA Transcription Factor, Confers Cold Tolerance by Repressing OsWRKY45–1 at the Seedling Stage in 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/s12284-025-00846-9openalex-snapshot

Engineering non-coding DNA Elements in Rice: an Elegant Approach To fine-tune Agronomical Advantageous Traits

inferred← citeshttps://doi.org/10.1186/s12284-026-00916-6openalex-snapshot

The Pentatricopeptide Repeat Protein OsPPR7 Confers Cold Tolerance at the Booting Stage in Rice by Regulating ABA and ROS Homeostasis

inferred← citeshttps://doi.org/10.1186/s12863-021-00995-yopenalex-snapshot

Genome-wide association studies of yield-related traits in high-latitude japonica rice

inferred← citeshttps://doi.org/10.1186/s12864-020-07342-yopenalex-snapshot

Physical mapping and InDel marker development for the restorer gene Rf2 in cytoplasmic male sterile CMS-D8 cotton

inferred← citeshttps://doi.org/10.1186/s12864-020-6711-0openalex-snapshot

GWAS and co-expression network combination uncovers multigenes with close linkage effects on the oleic acid content accumulation in Brassica napus

inferred← citeshttps://doi.org/10.1186/s12864-021-07958-8openalex-snapshot

Genome-wide identification and expression profile under abiotic stress of the barley non-specific lipid transfer protein gene family and its Qingke Orthologues

inferred← citeshttps://doi.org/10.1186/s12864-023-09262-zopenalex-snapshot

Comparative transcriptomic analysis of germinating rice seedlings to individual and combined anaerobic and cold stress

inferred← citeshttps://doi.org/10.1186/s12864-024-10219-zopenalex-snapshot

Integrated meta-analysis and transcriptomics pinpoint genomic loci and novel candidate genes associated with submergence tolerance in rice

inferred← citeshttps://doi.org/10.1186/s12864-025-11937-8openalex-snapshot

Combining QTL mapping and transcriptomics to identify candidate genes for cold tolerance during the budding and seedling stages in rice

inferred← citeshttps://doi.org/10.1186/s12870-018-1616-7openalex-snapshot

Molecular mapping of the Cf-10 gene by combining SNP/InDel-index and linkage analysis in tomato (Solanum lycopersicum)

inferred← citeshttps://doi.org/10.1186/s12870-020-02543-9openalex-snapshot

Identification of candidate tolerance genes to low-temperature during maize germination by GWAS and RNA-seq approaches

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/s12870-021-03076-5openalex-snapshot

Combining QTL-seq and linkage mapping to fine map a candidate gene in qCTS6 for cold tolerance at the seedling stage in rice

inferred← citeshttps://doi.org/10.1186/s12870-021-03089-0openalex-snapshot

Genetic basis of maize kernel oil-related traits revealed by high-density SNP markers in a recombinant inbred line population

inferred← citeshttps://doi.org/10.1186/s12870-022-03437-8openalex-snapshot

Transcriptional and physiological data revealed cold tolerance in a photo-thermo sensitive genic male sterile line Yu17S

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