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Avoiding damage and achieving cold tolerance in rice plants
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/joc.1584openalex-snapshot
Surface air temperature trends in Southern Brazil for 1960–2002
inferredcites →https://doi.org/10.1002/pmic.200401148openalex-snapshot
A proteomic analysis of cold stress responses in rice seedlings
inferredcites →https://doi.org/10.1002/pmic.200600921openalex-snapshot
Proteomic analysis of rice seedlings during cold stress
inferredcites →https://doi.org/10.1007/978-1-4020-6635-1_31openalex-snapshot
The Molecular Basis of Cold-Induced Pollen Sterility in Rice
inferredcites →https://doi.org/10.1007/bf00028303openalex-snapshot
Feasibility of selection for traits associated with cold tolerance in rice under rapid generation advance method
inferredcites →https://doi.org/10.1007/bf00033276openalex-snapshot
Genetic divergence among cold tolerant rices (Oryza sativa L.)
inferredcites →https://doi.org/10.1007/bf00034606openalex-snapshot
Evaluation of chilling sensitivity in different rice varieties. Relationship between screening procedures applied during germination and vegetative growth
inferredcites →https://doi.org/10.1007/bf02884949openalex-snapshot
QTL analysis of the rice seedling cold tolerance in a double haploid population derived from anther culture of a hybrid betweenindica andjaponica 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/s00122-003-1346-5openalex-snapshot
An AP2/EREBP-type transcription-factor gene from rice is cold-inducible and encodes a nuclear-localized protein
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/s00122-006-0311-5openalex-snapshot
Fine mapping of the qCTS12 locus, a major QTL for seedling cold tolerance in rice
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/s00122-009-1226-8openalex-snapshot
Identification and analysis of QTLs controlling cold tolerance at the reproductive stage and validation of effective QTLs in cold-tolerant genotypes of rice (Oryza sativa L.)
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/s001220050667openalex-snapshot
Genetic basis of low-temperature-sensitive sterility in indica-japonica hybrids of rice as determined by RFLP analysis
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/s00299-010-0985-7openalex-snapshot
Enhanced chilling tolerance at the booting stage in rice by transgenic overexpression of the ascorbate peroxidase gene, OsAPXa
inferredcites →https://doi.org/10.1007/s00299-011-1103-1openalex-snapshot
ZmCBF3 overexpression improves tolerance to abiotic stress in transgenic rice (Oryza sativa) without yield penalty
inferredcites →https://doi.org/10.1007/s00425-007-0548-5openalex-snapshot
Overexpression of OsCOIN, a putative cold inducible zinc finger protein, increased tolerance to chilling, salt and drought, and enhanced proline level in rice
inferredcites →https://doi.org/10.1007/s00425-011-1403-2openalex-snapshot
Physiological mechanisms underlying OsNAC5-dependent tolerance of rice plants to abiotic stress
inferredcites →https://doi.org/10.1007/s00425-011-1458-0openalex-snapshot
Overexpression of the trehalose-6-phosphate synthase gene OsTPS1 enhances abiotic stress tolerance 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/s00438-010-0548-1openalex-snapshot
Identification and fine mapping of a major quantitative trait locus originating from wild rice, controlling cold tolerance at the seedling stage
inferredcites →https://doi.org/10.1007/s10059-009-0055-6openalex-snapshot
Ectopic Expression of a Cold-Responsive OsAsr1 cDNA Gives Enhanced Cold Tolerance in Transgenic Rice Plants
inferredcites →https://doi.org/10.1007/s10059-011-0186-4openalex-snapshot
Quantitative Trait Loci for Cold Tolerance of Rice Recombinant Inbred Lines in Low Temperature Environments
inferredcites →https://doi.org/10.1007/s10681-007-9431-5openalex-snapshot
A major QTL associated with cold tolerance at seedling stage in rice (Oryza sativa L.)
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/s11103-007-9213-4openalex-snapshot
T-DNA tagged knockout mutation of rice OsGSK1, an orthologue of Arabidopsis BIN2, with enhanced tolerance to various abiotic stresses
inferredcites →https://doi.org/10.1007/s11103-008-9309-5openalex-snapshot
Characterization of transcription factor gene SNAC2 conferring cold and salt tolerance in rice
inferredcites →https://doi.org/10.1007/s11103-008-9340-6openalex-snapshot
Overexpression of a rice OsDREB1F gene increases salt, drought, and low temperature tolerance in both Arabidopsis and rice
inferredcites →https://doi.org/10.1007/s11103-009-9524-8openalex-snapshot
Identification and expression profiling analysis of TIFY family genes involved in stress and phytohormone responses in rice
inferredcites →https://doi.org/10.1007/s11103-009-9557-zopenalex-snapshot
OsPRP3, a flower specific proline-rich protein of rice, determines extracellular matrix structure of floral organs and its overexpression confers cold-tolerance
inferredcites →https://doi.org/10.1007/s11103-009-9559-xopenalex-snapshot
Genome-wide analysis of genes targeted by qLTG3-1 controlling low-temperature germinability in rice
inferredcites →https://doi.org/10.1007/s11103-009-9560-4openalex-snapshot
Improved drought and salt stress tolerance in transgenic tobacco overexpressing a novel A20/AN1 zinc-finger “AlSAP” gene isolated from the halophyte grass Aeluropus littoralis
inferredcites →https://doi.org/10.1007/s11103-010-9609-4openalex-snapshot
Enhanced tolerance to freezing in tobacco and tomato overexpressing transcription factor TERF2/LeERF2 is modulated by ethylene biosynthesis
inferredcites →https://doi.org/10.1007/s11103-012-9955-5openalex-snapshot
A TFIIIA-type zinc finger protein confers multiple abiotic stress tolerances in transgenic rice (Oryza sativa L.)
inferredcites →https://doi.org/10.1007/s11248-010-9463-9openalex-snapshot
Overexpression of ethylene response factor TERF2 confers cold tolerance in rice seedlings
inferredcites →https://doi.org/10.1007/s12284-008-9006-7openalex-snapshot
Toward Understanding Molecular Mechanisms of Abiotic Stress Responses in Rice
inferredcites →https://doi.org/10.1007/s12374-009-9017-yopenalex-snapshot
Ectopic Expression of a Cold-Responsive CuZn Superoxide Dismutase Gene, SodCc1, in Transgenic Rice (Oryza sativa L.)
inferredcites →https://doi.org/10.1016/0168-9452(95)04156-oopenalex-snapshot
Effect of chilling on activated oxygen-scavenging enzymes in low temperature-sensitive and -tolerant cultivars of rice (Oryza sativa L.)
inferredcites →https://doi.org/10.1016/b978-0-444-99615-2.50007-7openalex-snapshot
Differentiation of Ecotypes in Oryza Sativa L.
inferredcites →https://doi.org/10.1016/j.bbrc.2009.09.032openalex-snapshot
Increased tolerance of rice to cold, drought and oxidative stresses mediated by the overexpression of a gene that encodes the zinc finger protein ZFP245
inferredcites →https://doi.org/10.1016/j.crvi.2007.01.001openalex-snapshot
An approach to identify cold-induced low-abundant proteins in rice leaf
inferredcites →https://doi.org/10.1016/j.fcr.2006.11.010openalex-snapshot
Low temperature-induced sterility in rice: Evidence for the effects of temperature before panicle initiation
inferredcites →https://doi.org/10.1016/j.gene.2008.05.019openalex-snapshot
Expression analysis of rice A20/AN1-type zinc finger genes and characterization of ZFP177 that contributes to temperature stress tolerance
inferredcites →https://doi.org/10.1016/j.jcs.2007.08.013openalex-snapshot
QTL analysis of cold tolerance at seedling stage in rice (Oryza sativa L.) using recombination inbred lines
inferredcites →https://doi.org/10.1016/j.jphotobiol.2010.12.010openalex-snapshot
On the relation between the Kautsky effect (chlorophyll a fluorescence induction) and Photosystem II: Basics and applications of the OJIP fluorescence transient
inferredcites →https://doi.org/10.1016/j.jplph.2005.12.004openalex-snapshot
Alteration of oxidative and carbohydrate metabolism under abiotic stress in two rice (Oryza sativa L.) genotypes contrasting in chilling tolerance
inferredcites →https://doi.org/10.1016/j.jplph.2008.02.001openalex-snapshot
Chilling stress-induced proteomic changes in rice roots
inferredcites →https://doi.org/10.1016/j.jplph.2010.05.008openalex-snapshot
The ABRE-binding bZIP transcription factor OsABF2 is a positive regulator of abiotic stress and ABA signaling in rice
inferredcites →https://doi.org/10.1016/j.plantsci.2003.08.008openalex-snapshot
Trapping and characterization of cold-responsive genes from T-DNA tagging lines in rice
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.2010.04.004openalex-snapshot
Map-based cloning of the rice cold tolerance gene Ctb1
inferredcites →https://doi.org/10.1016/j.plantsci.2011.01.023openalex-snapshot
Response to photoxidative stress induced by cold in japonica rice is genotype dependent
inferredcites →https://doi.org/10.1016/j.plaphy.2009.05.003openalex-snapshot
Heat shock factor gene family in rice: Genomic organization and transcript expression profiling in response to high temperature, low temperature and oxidative stresses
inferredcites →https://doi.org/10.1016/j.plaphy.2010.09.014openalex-snapshot
OVP1, a Vacuolar H+-translocating inorganic pyrophosphatase (V-PPase), overexpression improved rice cold tolerance
inferredcites →https://doi.org/10.1016/j.tibtech.2009.05.006openalex-snapshot
Next-generation sequencing technologies and their implications for crop genetics and breeding
inferredcites →https://doi.org/10.1016/s0168-9452(97)04602-5openalex-snapshot
High-temperature induced chlorophyll fluorescence changes in barley leaves Comparison of the critical temperatures determined from fluorescence induction and from fluorescence temperature curve
inferredcites →https://doi.org/10.1016/s0958-1669(03)00030-2openalex-snapshot
Molecular responses to drought, salinity and frost: common and different paths for plant protection
inferredcites →https://doi.org/10.1016/s1016-8478(23)13088-3openalex-snapshot
Ectopic Expression of a Cold-inducible Transcription Factor, CBF1/DREB1b, in Transgenic Rice (Oryza sativa L.)
inferredcites →https://doi.org/10.1016/s1016-8478(23)13158-xopenalex-snapshot
Characterization of an Abiotic Stress-inducible Dehydrin Gene, OsDhn1, in Rice (Oryza sativa L.)
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/10.1023/a:1026718308155openalex-snapshot
Over-expression of ζ glutathione S-transferase in transgenic rice enhances germination and growth at low temperature
inferredcites →https://doi.org/10.1038/nature03895openalex-snapshot
The map-based sequence of the rice genome
inferredcites →https://doi.org/10.1042/bj20101610openalex-snapshot
Cold sensitivity in rice (Oryza sativa L.) is strongly correlated with a naturally occurring I99V mutation in the multifunctional glutathione transferase isoenzyme GSTZ2
inferredcites →https://doi.org/10.1042/bj20111792openalex-snapshot
Biochemical identification of the OsMKK6–OsMPK3 signalling pathway for chilling stress tolerance in rice
inferredcites →https://doi.org/10.1046/j.1365-313x.2000.00787.xopenalex-snapshot
Over‐expression of a single Ca 2+ ‐dependent protein kinase confers both cold and salt/drought tolerance on rice plants
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/10.1071/ea9840255openalex-snapshot
Low-temperature induced floret sterility in the rice cultivars Calrose and Inga as influenced by nitrogen supply
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.1302265110openalex-snapshot
Arabidopsis AHP2, AHP3, and AHP5 histidine phosphotransfer proteins function as redundant negative regulators of drought stress response
inferredcites →https://doi.org/10.1074/mcp.m500251-mcp200openalex-snapshot
Comparative Proteomic Analysis Provides New Insights into Chilling Stress Responses in Rice
inferredcites →https://doi.org/10.1080/10425170500061590openalex-snapshot
Identification of a rice zinc finger protein whose expression is transiently induced by drought, cold but not by salinity and abscisic acid
inferredcites →https://doi.org/10.1093/aob/mcm128openalex-snapshot
The Complex History of the Domestication of Rice
inferredcites →https://doi.org/10.1093/dnares/9.6.199openalex-snapshot
Development and Mapping of 2240 New SSR Markers for Rice (Oryza sativa L.)
inferredcites →https://doi.org/10.1093/genetics/148.1.479openalex-snapshot
A High-Density Rice Genetic Linkage Map with 2275 Markers Using a Single F2 Population
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/jxb/erm367openalex-snapshot
Genetic engineering of rice capable of synthesizing fructans and enhancing chilling tolerance
inferredcites →https://doi.org/10.1093/jxb/err144openalex-snapshot
OsWRKY45 alleles play different roles in abscisic acid signalling and salt stress tolerance but similar roles in drought and cold tolerance in rice
inferredcites →https://doi.org/10.1093/jxb/err431openalex-snapshot
A R2R3-type MYB gene, OsMYB2, is involved in salt, cold, and dehydration tolerance in rice
inferredcites →https://doi.org/10.1093/pcp/pch075openalex-snapshot
Changes in the Thermal Dissipation and the Electron Flow in the Water–Water Cycle in Rice Grown Under Conditions of Physiologically Low Temperature
inferredcites →https://doi.org/10.1093/pcp/pch198openalex-snapshot
Comparative Studies on the Arabidopsis Aldehyde Oxidase (AAO) Gene Family Revealed a Major Role of AAO3 in ABA Biosynthesis in Seeds
inferredcites →https://doi.org/10.1093/pcp/pci149openalex-snapshot
The Photosynthetic Properties of Rice Leaves Treated with Low Temperature and High Irradiance
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/10.1093/pcp/pcq190openalex-snapshot
RiceFOX: A Database of Arabidopsis Mutant Lines Overexpressing Rice Full-Length cDNA that Contains a Wide Range of Trait Information to Facilitate Analysis of Gene Function
inferredcites →https://doi.org/10.1104/pp.006072openalex-snapshot
Two Novel Mitogen-Activated Protein Signaling Components, OsMEK1 and OsMAP1, Are Involved in a Moderate Low-Temperature Signaling Pathway in Rice
inferredcites →https://doi.org/10.1104/pp.103.036970openalex-snapshot
Tissue-Specific Localization of an Abscisic Acid Biosynthetic Enzyme, AAO3, in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.108.133454openalex-snapshot
Enhanced Tolerance to Chilling Stress in OsMYB3R-2 Transgenic Rice Is Mediated by Alteration in Cell Cycle and Ectopic Expression of Stress Genes
inferredcites →https://doi.org/10.1104/pp.110.153015openalex-snapshot
A Novel MYBS3-Dependent Pathway Confers Cold Tolerance in Rice
inferredcites →https://doi.org/10.1104/pp.111.176164openalex-snapshot
Control of Abscisic Acid Catabolism and Abscisic Acid Homeostasis Is Important for Reproductive Stage Stress Tolerance in Cereals1
inferredcites →https://doi.org/10.1104/pp.120.4.945openalex-snapshot
Betaines and Related Osmoprotectants. Targets for Metabolic Engineering of Stress Resistance1
inferredcites →https://doi.org/10.1105/tpc.008714openalex-snapshot
Disease Resistance and Abiotic Stress Tolerance in Rice Are Inversely Modulated by an Abscisic Acid–Inducible Mitogen-Activated Protein Kinase[W]
inferredcites →https://doi.org/10.1111/j.1365-3040.2005.01390.xopenalex-snapshot
Cold‐induced repression of the rice anther‐specific cell wall invertase gene OSINV4 is correlated with sucrose accumulation and pollen sterility
inferredcites →https://doi.org/10.1111/j.1365-3040.2008.01811.xopenalex-snapshot
Functional characterization of two cold shock domain proteins from Oryza sativa
inferredcites →https://doi.org/10.1111/j.1365-3040.2010.02225.xopenalex-snapshot
OsRAN2, essential for mitosis, enhances cold tolerance in rice by promoting export of intranuclear tubulin and maintaining cell division under cold stress
inferredcites →https://doi.org/10.1111/j.1365-3040.2011.02441.xopenalex-snapshot
Expression of the Aeluropus littoralis AlSAP gene in rice confers broad tolerance to abiotic stresses through maintenance of photosynthesis
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03168.xopenalex-snapshot
Functional analysis of a NAC‐type transcription factor OsNAC6 involved in abiotic and biotic stress‐responsive gene expression in rice
inferredcites →https://doi.org/10.1146/annurev.arplant.53.100201.160729openalex-snapshot
A CCLIMATIVE R ESPONSE TO T EMPERATURE S TRESS IN H IGHER P LANTS : Approaches of Gene Engineering for Temperature Tolerance
inferredcites →https://doi.org/10.1155/2012/831460openalex-snapshot
SNP Discovery through Next-Generation Sequencing and Its Applications
inferredcites →https://doi.org/10.1186/1471-2164-13-426openalex-snapshot
SNPs in stress-responsive rice genes: validation, genotyping, functional relevance and population structure
inferredcites →https://doi.org/10.1266/ggs.80.135openalex-snapshot
OsNAC6, a member of the NAC gene family, is induced by various stresses 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/10.1270/jsbbs.54.253openalex-snapshot
Identification of Quantitative Trait Loci Controlling Cold Tolerance at the Reproductive Stage in Yunnan Landrace of Rice, Kunmingxiaobaigu
inferredcites →https://doi.org/10.1270/jsbbs1951.41.35openalex-snapshot
Genic control of tolerance to chilling injury at seedling stage in rice, Oryza sativa L.
inferredcites →https://doi.org/10.1371/journal.pone.0035995openalex-snapshot
ERF5 and ERF6 Play Redundant Roles as Positive Regulators of JA/Et-Mediated Defense against Botrytis cinerea in Arabidopsis
inferredcites →https://doi.org/10.1590/s0101-31222009000200031openalex-snapshot
Alterações fisiológicas em sementes de arroz expostas ao frio na fase de germinação
inferredcites →https://doi.org/10.1590/s0103-84782000000500031openalex-snapshot
Melhoramento genético para tolerância ao frio em arroz irrigado
inferredcites →https://doi.org/10.1590/s0103-90162004000100001openalex-snapshot
Cold tolerance at the germination stage of rice: methods of evaluation and characterization of genotypes
inferredcites →https://doi.org/10.1590/s0103-90162006000300007openalex-snapshot
Rice cold tolerance at the reproductive stage in a controlled environment
inferredcites →https://doi.org/10.1590/s1415-47572006000200020openalex-snapshot
Inheritance of rice cold tolerance at the germination stage
inferredcites →https://doi.org/10.1590/s1677-04202010000300007openalex-snapshot
Alterations in fatty acid composition due to cold exposure at the vegetative stage in rice
inferredcites →https://doi.org/10.1626/jcs.38.706openalex-snapshot
Male Sterility Caused by Cooling Treatment at the Meiotic Stage in Rice Plants : II. The most sensitive stage to cooling and the fertilizing ability of pistils
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.39.60openalex-snapshot
Male Sterility Caused by Cooling Treatment at the Meiotic Stage in Rice Plants : III. Male abnormalities at anthesis
inferredcites →https://doi.org/10.1626/jcs.45.558openalex-snapshot
Male Sterility Caused by Cooling Treatment at the Young Microspore Stage in Rice Plants : XV. Effect of moderate cooling before or after the critical stage on the sterility induced by cooling at the critical stage
inferredcites →https://doi.org/10.1626/jcs.47.318openalex-snapshot
Male Sterility Caused by Cooling Treatment at the Young Microspore Stage in Rice Plants : XVI. Changes in carbohydrates, nitrogenous and phosphorous compounds in rice anthers after cooling treatment
inferredcites →https://doi.org/10.1626/jcs.47.551openalex-snapshot
Male Sterility Caused by Cooling Treatment at the Young Microspore Stage in Rice Plants : XVIII. Some enzyme activities in anthers during and after the cooling
inferredcites →https://doi.org/10.1626/pps.3.299openalex-snapshot
Number of Pollen Grains in Rice Cultivars with Different Cool-Weather Resistance at the Young Microspore Stage
inferredcites →https://doi.org/10.2135/cropsci1989.0011183x002900050042xopenalex-snapshot
Implication of Fatty Acids and Seed Dormancy in a New Screening Procedure for Cold Tolerance in Rice
inferredcites →https://doi.org/10.2135/cropsci1997.0011183x003700040051xopenalex-snapshot
Genetic Variation for Traits Related to Temperate Adaptation of Rice Cultivars
inferredcites →https://doi.org/10.2135/cropsci1998.0011183x003800030007xopenalex-snapshot
Inheritance of Tolerance to Chilling Stress in Rice during Germination and Plumule Greening
inferredcites →https://doi.org/10.2135/cropsci2003.2109openalex-snapshot
Antioxidative Enzymes Offer Protection from Chilling Damage in Rice Plants
inferredcites →https://doi.org/10.2135/cropsci2010.12.0733openalex-snapshot
Identification of Cold‐Tolerant Breeding Lines by Quantitative Trait Loci Associated with Cold Tolerance in Rice
inferredcites →https://doi.org/10.2174/138920211794520178openalex-snapshot
Engineering Cold Stress Tolerance in Crop Plants
inferredcites →https://doi.org/10.22004/ag.econ.126549openalex-snapshot
Economic Analysis of Breeding for Improved Cold Tolerance in Rice in Australia
inferredcites →https://doi.org/10.3724/sp.j.1006.2008.00551openalex-snapshot
QTL and Epistasis for Low Temperature Germinability in Rice
inferredcites →https://doi.org/10.4025/actascibiolsci.v34i4.8535openalex-snapshot
Enzyme expression in indica and japonica rice cultivars under saline stress
inferredcites →https://doi.org/10.4238/2012.october.9.8openalex-snapshot
Chloroplast DNA polymorphism and evolutional relationships between Asian cultivated rice (Oryza sativa) and its wild relatives (O. rufipogon)
inferredcites →https://doi.org/10.5483/bmbrep.2009.42.8.486openalex-snapshot
Expression of a rice DREB1 gene, OsDREB1D, enhances cold and high-salt tolerance in transgenic Arabidopsis
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4675953openalex-extracted
Sub4 Encoding Subtilisin-Like Protease Modulates Cold Tolerance in Rice Seedlings Through Cell Wall Modification
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0739openalex-snapshot
ToColdlyGo Where No Grass has Gone Before: A Multidisciplinary Review of Cold Adaptation in Poaceae
inferred← citeshttps://doi.org/10.1002/cche.10268openalex-snapshot
Effects of dynamic low temperature during the grain filling stage on starch morphological structure, physicochemical properties, and eating quality of soft japonica rice
inferred← citeshttps://doi.org/10.1002/fes3.359openalex-snapshot
Nitrogen limits zinc‐mediated stimulation of tillering in rice by modifying phytohormone balance under low‐temperature stress
inferred← citeshttps://doi.org/10.1002/fes3.372openalex-snapshot
Will temperature and rainfall changes prevent yield progress in Europe?
inferred← citeshttps://doi.org/10.1002/fes3.452openalex-snapshot
Identification of QTLs and candidate genes for rice seed germinability under low temperature using high‐density genetic mapping and RNA‐seq
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/rse2.320openalex-snapshot
Time‐series remote sensing of rice paddy expansion in the Yellow River Delta: Towards sustainable ecological conservation in the context of water scarcity
inferred← citeshttps://doi.org/10.1002/tpg2.20020openalex-snapshot
Genome‐wide lncRNAs identification and association analysis for cold‐responsive genes at the booting stage in rice ( Oryza sativa L.)
inferred← citeshttps://doi.org/10.1007/978-3-030-21687-0_2openalex-snapshot
Genome Editing and Abiotic Stress Tolerance in Crop Plants
inferred← citeshttps://doi.org/10.1007/978-3-030-66530-2_3openalex-snapshot
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_7openalex-snapshot
Genomic Approaches to Understand Varietal Differences in Rice Species and Genotypes with Respect to Stress Response and Quality Traits
inferred← citeshttps://doi.org/10.1007/978-981-16-9720-3_13openalex-snapshot
Role of Mutation Breeding in Crop Improvement with Special Reference to Indian Subcontinent
inferred← citeshttps://doi.org/10.1007/s00122-015-2540-yopenalex-snapshot
High-resolution mapping of a major effect QTL from wild tomato Solanum habrochaites that influences water relations under root chilling
inferred← citeshttps://doi.org/10.1007/s00299-016-2073-0openalex-snapshot
Breeding approaches and genomics technologies to increase crop yield under low-temperature stress
inferred← citeshttps://doi.org/10.1007/s00299-017-2234-9openalex-snapshot
Deep RNAseq indicates protective mechanisms of cold-tolerant indica rice plants during early vegetative stage
inferred← citeshttps://doi.org/10.1007/s00344-019-10009-yopenalex-snapshot
Seed Priming with Spermidine and Trehalose Enhances Chilling Tolerance of Rice via Different Mechanisms
inferred← citeshttps://doi.org/10.1007/s00344-025-12025-7openalex-snapshot
Genome-Wide Association Study Reveals Marker-Trait Associations and Genes Linked To Cold Tolerance during Developmental Stages in Rice
inferred← citeshttps://doi.org/10.1007/s00425-017-2838-xopenalex-snapshot
Oryza sativa salt-induced RING E3 ligase 2 (OsSIRP2) acts as a positive regulator of transketolase in plant response to salinity and osmotic stress
inferred← citeshttps://doi.org/10.1007/s00425-026-05173-xopenalex-snapshot
Cold-sensitive chloroplast development: advances from chloroplast ribosome-deficient mutants
inferred← citeshttps://doi.org/10.1007/s00709-026-02262-2openalex-snapshot
Metabolic acclimation of rice cultivars via cold stress-induced carbohydrate accumulation
inferred← citeshttps://doi.org/10.1007/s10142-021-00790-zopenalex-snapshot
The NAC-type transcription factor GmNAC20 improves cold, salinity tolerance, and lateral root formation in transgenic rice plants
inferred← citeshttps://doi.org/10.1007/s10457-015-9835-5openalex-snapshot
Trees and agroforestry for coping with extreme weather events: experiences from northern and central Viet Nam
inferred← citeshttps://doi.org/10.1007/s10535-016-0648-9openalex-snapshot
Some key physiological and molecular processes of cold acclimation
inferred← citeshttps://doi.org/10.1007/s10681-015-1584-zopenalex-snapshot
Genetic analysis of germinating ability and seedling vigor under cold stress in US weedy rice
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/s10681-020-02661-3openalex-snapshot
Phenotyping and QTL mapping for cold tolerance at the germination and seedling stages in Argentine temperate 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/s10722-024-02004-4openalex-snapshot
Genetic assessment of diverse rice germplasm for yield-related and stress tolerance traits
inferred← citeshttps://doi.org/10.1007/s10725-020-00577-5openalex-snapshot
Lsi1 plays an active role in enhancing the chilling tolerance of rice roots
inferred← citeshttps://doi.org/10.1007/s11032-019-1090-4openalex-snapshot
Identification of main-effect quantitative trait loci (QTLs) for low-temperature stress tolerance germination- and early seedling vigor-related traits in rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1007/s11033-025-10507-1openalex-snapshot
Upregulated expression of MYB4, DREB1 and AP37 transcription factors modulates cold stress response in high-altitude Himalayan rice via time-dependent ROS regulation
inferred← citeshttps://doi.org/10.1007/s11103-020-00989-xopenalex-snapshot
Oryza sativa drought-, heat-, and salt-induced RING finger protein 1 (OsDHSRP1) negatively regulates abiotic stress-responsive gene expression
inferred← citeshttps://doi.org/10.1007/s11240-014-0475-7openalex-snapshot
The effect of molybdenum on the molecular control of cold tolerance in cauliflower (Brassica oleracea var. botrytis) artificial seeds
inferred← citeshttps://doi.org/10.1007/s11738-016-2291-7openalex-snapshot
Correlation of proline content and gene expression involved in the metabolism of this amino acid under abiotic stress
inferred← citeshttps://doi.org/10.1007/s11738-019-2864-3openalex-snapshot
Chitooligosaccharide plays essential roles in regulating proline metabolism and cold stress tolerance in rice seedlings
inferred← citeshttps://doi.org/10.1007/s12298-020-00792-4openalex-snapshot
Photosynthetic activity of indica rice sister lines with contrasting cold tolerance
inferred← citeshttps://doi.org/10.1007/s12298-024-01412-1openalex-snapshot
Meta-QTL and ortho analysis unravels the genetic architecture and key candidate genes for cold tolerance at seedling stage in rice
inferred← citeshttps://doi.org/10.1007/s12355-022-01118-2openalex-snapshot
Overexpression of α-Tubulin Gene of Sugarcane (Saccharum spp. hybrids), SoTUA, Enhances Tobacco Tolerance to Cold Stress
inferred← citeshttps://doi.org/10.1007/s12374-016-0461-1openalex-snapshot
Development of functional modules based on co-expression patterns for cell-wall biosynthesis related genes in rice
inferred← citeshttps://doi.org/10.1007/s12374-016-0901-yopenalex-snapshot
Erratum to Development of functional modules based on co-expression patterns for cell-wall biosynthesis related genes in rice
inferred← citeshttps://doi.org/10.1007/s12892-022-00175-zopenalex-snapshot
An optimized index for cold tolerance assessment in rice during germination and early seedling stage
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/s40626-018-0131-4openalex-snapshot
Transcript analysis of abscisic acid-inducible genes in response to different abiotic disturbances in two indica rice varieties
inferred← citeshttps://doi.org/10.1007/s42535-021-00235-9openalex-snapshot
Screening of boro rice varieties of Assam, India to estimate their potential resistance to cold and heat stresses
inferred← citeshttps://doi.org/10.1007/s42729-021-00496-yopenalex-snapshot
Rhizospheric Soil from Rice Paddy Presents Isolable Bacteria Able to Induce Cold Tolerance in Rice Plants
inferred← citeshttps://doi.org/10.1007/s42977-026-00326-1openalex-snapshot
CRISPR-Cas systems for enhancing chilling tolerance in rice: recent advances and future prospects
inferred← citeshttps://doi.org/10.1016/b978-0-12-814332-2.00006-xopenalex-snapshot
Deciphering Strategies for Salt Stress Tolerance in Rice in the Context of Climate Change
inferred← citeshttps://doi.org/10.1016/b978-0-12-814332-2.00011-3openalex-snapshot
Scope and Progress of Rice Research Harnessing Cold Tolerance
inferred← citeshttps://doi.org/10.1016/b978-0-12-814332-2.00036-8openalex-snapshot
Genomic Footprints Uncovering Abiotic Stress Tolerance in Rice
inferred← citeshttps://doi.org/10.1016/b978-0-443-33465-8.00019-0openalex-snapshot
Growth and morphological alterations of rice under major abiotic stresses
inferred← citeshttps://doi.org/10.1016/bs.agron.2017.11.002openalex-snapshot
Rice in Saline Soils: Physiology, Biochemistry, Genetics, and Management
inferred← citeshttps://doi.org/10.1016/j.agrformet.2024.110087openalex-snapshot
Simulating the effects of low-temperature stress during flowering stage on leaf-level photosynthesis with current rice models
inferred← citeshttps://doi.org/10.1016/j.cell.2015.02.037openalex-snapshot
Cold Tolerance Encoded in One SNP
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2021.112816openalex-snapshot
Addressing the challenge of cold stress resilience with the synergistic effect of Rhizobium inoculation and exogenous melatonin application in Medicago truncatula
inferred← citeshttps://doi.org/10.1016/j.egg.2022.100128openalex-snapshot
Screening of rice germplasms (Oryza sativa L.) for seedling stage cold tolerance utilizing morphological and molecular markers
inferred← citeshttps://doi.org/10.1016/j.eja.2023.126901openalex-snapshot
Localized phosphorus application via P-dipping doubles applied P use efficiency and avoids weather-induced stresses for rice production on P-deficient lowlands
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2018.11.001openalex-snapshot
Nitrogen application after low-temperature exposure alleviates tiller decrease in rice
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2024.105932openalex-snapshot
CRISPR/Cas9-mediated genome editing of OsCS511 enhances cold tolerance in Oryza sativa L.
inferred← citeshttps://doi.org/10.1016/j.fcr.2015.07.024openalex-snapshot
Field phenomics for response of a rice diversity panel to ten environments in Senegal and Madagascar. 2. Chilling-induced spikelet sterility
inferred← citeshttps://doi.org/10.1016/j.fcr.2021.108395openalex-snapshot
Effects of root characteristics on panicle formation in japonica rice under low temperature water stress at the reproductive stage
inferred← citeshttps://doi.org/10.1016/j.fcr.2023.109140openalex-snapshot
Crop productivity in a rice–ratoon-rice system vs. a single-crop system in central Japan
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2026.150517openalex-snapshot
The Oryza sativa programmed cell death 5 - Oryza sativa WRKY DNA-binding protein 76 module regulates chilling tolerance by suppressing the Oryza sativa dehydration-responsive element binding protein 1B transcription in rice seedlings
inferred← citeshttps://doi.org/10.1016/j.jplph.2020.153153openalex-snapshot
WITHDRAWN: Cold tolerance in rice plants is partially controlled by root responses
inferred← citeshttps://doi.org/10.1016/j.jplph.2020.153307openalex-snapshot
Root responses of contrasting rice genotypes to low temperature stress
inferred← citeshttps://doi.org/10.1016/j.phyplu.2021.100185openalex-snapshot
Cold Stress-induced Seed Germination and Biosynthesis of Polyphenolics Content in Medicinally Important Brassica rapa
inferred← citeshttps://doi.org/10.1016/j.plantsci.2015.05.009openalex-snapshot
Cold tolerance in rice germinating seeds revealed by deep RNAseq analysis of contrasting indica genotypes
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
inferred← citeshttps://doi.org/10.1016/j.plantsci.2022.111395openalex-snapshot
STRIPE3, encoding a human dNTPase SAMHD1 homolog, regulates chloroplast development in rice
inferred← citeshttps://doi.org/10.1016/j.plaphy.2014.06.007openalex-snapshot
Salinity and drought tolerant OsACA6 enhances cold tolerance in transgenic tobacco by interacting with stress-inducible proteins
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.108954openalex-snapshot
Phytochrome interacting factor ZmPIF6 simultaneously enhances chilling tolerance and grain size in rice
inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111422openalex-snapshot
Rice cold tolerance: Physiological responses, molecular regulatory networks, and improvement strategies
inferred← citeshttps://doi.org/10.1016/j.plgene.2017.05.014openalex-snapshot
Marker assisted selection (MAS) towards generating stress tolerant crop plants
inferred← citeshttps://doi.org/10.1016/j.sajb.2023.01.025openalex-snapshot
Antioxidative response of Stevia leaves to night chilling temperature
inferred← citeshttps://doi.org/10.1016/j.scienta.2022.111486openalex-snapshot
SlNPR1 modulates chilling stress resistance in tomato plant by alleviating oxidative damage and affecting the synthesis of ferulic acid
inferred← citeshttps://doi.org/10.1016/j.stress.2024.100707openalex-snapshot
Deciphering the genomic regions associated with seedling cold tolerance traits in rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1016/j.ympev.2020.106737openalex-snapshot
Phylogeny and highland adaptation of Chinese species in Allium section Daghestanica (Amaryllidaceae) revealed by transcriptome sequencing
inferred← citeshttps://doi.org/10.1016/s2095-3119(15)61214-xopenalex-snapshot
Combining QTL mapping and expression profile analysis to identify candidate genes of cold tolerance from Dongxiang common wild rice (Oryza rufipogon Griff.)
inferred← citeshttps://doi.org/10.1017/s002185961400046xopenalex-snapshot
Characterization of tetraploid wheat landraces for cold tolerance and agronomic traits under rainfed conditions of Iran
inferred← citeshttps://doi.org/10.1017/s0021859621000186openalex-snapshot
Evaluating irrigated rice yields in Japan within the Climate Zonation Scheme of the Global Yield Gap Atlas
inferred← citeshttps://doi.org/10.1038/hortres.2015.51openalex-snapshot
Tomato expressing Arabidopsis glutaredoxin gene AtGRXS17 confers tolerance to chilling stress via modulating cold responsive components
inferred← citeshttps://doi.org/10.1038/ncomms14788openalex-snapshot
Natural variation in CTB4a enhances rice adaptation to cold habitats
inferred← citeshttps://doi.org/10.1038/s41467-025-62887-4openalex-snapshot
Pangenome analysis of transposable element insertion polymorphisms reveals features underlying cold tolerance in rice
inferred← citeshttps://doi.org/10.1038/s41598-018-32513-zopenalex-snapshot
Genome-wide discovery of DNA polymorphisms by whole genome sequencing differentiates weedy and cultivated rice
inferred← citeshttps://doi.org/10.1038/s41598-022-16116-3openalex-snapshot
Subtercola endophyticus sp. nov., a cold-adapted bacterium isolated from Abies koreana
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/cp15331openalex-snapshot
Rice-cold tolerance across reproductive stages
inferred← citeshttps://doi.org/10.1071/cp21135openalex-snapshot
Decreased night temperature affects development and grain yield only in cold-susceptible rice (Oryza sativa) plants
inferred← citeshttps://doi.org/10.1073/pnas.2306338120openalex-snapshot
NTRC regulates CP12 to activate Calvin–Benson cycle during cold acclimation
inferred← citeshttps://doi.org/10.1080/13102818.2014.978539openalex-snapshot
Mapping QTLs for cold tolerance at germination and the early seedling stage in rice (Oryza sativaL.)
inferred← citeshttps://doi.org/10.1080/1343943x.2020.1727752openalex-snapshot
Analysis of rice yield response to various cropping seasons to develop optimal cropping calendars in Mwea, Kenya
inferred← citeshttps://doi.org/10.1080/1343943x.2020.1777877openalex-snapshot
A method for evaluating cold tolerance in rice during reproductive growth stages under natural low-temperature conditions in tropical highlands in Kenya
inferred← citeshttps://doi.org/10.1080/15592324.2015.1057369openalex-snapshot
Ubiquitination pathway as a target to develop abiotic stress tolerance in rice
inferred← citeshttps://doi.org/10.1080/17429145.2017.1308568openalex-snapshot
Advances in physiological and molecular aspects of plant cold tolerance
inferred← citeshttps://doi.org/10.1088/1755-1315/374/1/012021openalex-snapshot
Identification of gene action on rice tolerance to low temperature stress
inferred← citeshttps://doi.org/10.1088/1755-1315/484/1/012085openalex-snapshot
Adaptation of new superior rice varieties at the altitude of 1600 masl in Jayawijaya Papua
inferred← citeshttps://doi.org/10.1093/aobpla/plaf043openalex-snapshot
Physiological and molecular responses to high-temperature stress at anthesis in Brazilian flooded rice
inferred← citeshttps://doi.org/10.1093/jxb/eraa025openalex-snapshot
Glycosyltransferase OsUGT90A1 helps protect the plasma membrane during chilling stress in rice
inferred← citeshttps://doi.org/10.1093/jxb/erab334openalex-snapshot
Cold response and tolerance in cereal roots
inferred← citeshttps://doi.org/10.1093/jxb/erac045openalex-snapshot
Can we improve the chilling tolerance of maize photosynthesis through breeding?
inferred← citeshttps://doi.org/10.1093/jxb/erx250openalex-snapshot
Crop-model assisted phenomics and genome-wide association study for climate adaptation of indica rice. 2. Thermal stress and spikelet sterility
inferred← citeshttps://doi.org/10.1093/lambio/ovac035openalex-snapshot
Effect of seed biopriming with selected endophytes on the growth and chilling tolerance of rice plants
inferred← citeshttps://doi.org/10.1093/pcp/pcaa146openalex-snapshot
The Rice Plastidial Phosphorylase Participates Directly in Both Sink and Source Processes
inferred← citeshttps://doi.org/10.1093/pcp/pcw151openalex-snapshot
Differential Regulation of Protochlorophyllide Oxidoreductase Abundances by VIRESCENT 5A (OsV5A) and VIRESCENT 5B (OsV5B) in Rice Seedlings
inferred← citeshttps://doi.org/10.1101/2020.01.25.919464openalex-snapshot
Cold tolerance in rice plants is partially controlled by root responses
inferred← citeshttps://doi.org/10.1101/2024.07.02.601777openalex-snapshot
Optimizing Multi-Environment Trials in The US Rice Belt via Smart-Climate-Soil Prediction Based-Models and Economic Importance
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/10.1101/651000openalex-snapshot
PhenoGeneRanker: A Tool for Gene Prioritization Using Complete Multiplex Heterogeneous Networks
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.12629openalex-snapshot
An experimental study on the effects of intermittent chilling at different growth stages on rice yield in Northeast China
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/nph.14482openalex-snapshot
TSV , a putative plastidic oxidoreductase, protects rice chloroplasts from cold stress during development by interacting with plastidic thioredoxin Z
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/pbi.12704openalex-snapshot
A novel functional gene associated with cold tolerance at the 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/pce.12916openalex-snapshot
Rice calcium‐dependent protein kinase OsCPK17 targets plasma membrane intrinsic protein and sucrose‐phosphate synthase and is required for a proper cold stress response
inferred← citeshttps://doi.org/10.1111/pce.13811openalex-snapshot
Natural variation of photosynthetic efficiency in Arabidopsis thaliana accessions under low temperature conditions
inferred← citeshttps://doi.org/10.1111/pce.14868openalex-snapshot
Harnessing weedy rice as functional food and source of novel traits for crop improvement
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/plb.12427openalex-snapshot
A consortium of rhizobacterial strains and biochemical growth elicitors improve cold and drought stress tolerance in rice ( Oryza sativa L.)
inferred← citeshttps://doi.org/10.1111/ppl.12291openalex-snapshot
Global transcriptional profiling of a cold‐tolerant rice variety under moderate cold stress reveals different cold stress response mechanisms
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/10.1126/sciadv.abq5506openalex-snapshot
Natural variation of codon repeats in COLD11 endows rice with chilling resilience
inferred← citeshttps://doi.org/10.1139/cjps-2015-0067openalex-snapshot
Identification and physiological characterization of two sister lines of indica rice (Oryza sativa L.) with contrasting levels of cold tolerance
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/s12284-020-00414-3openalex-snapshot
Multiple Cold Tolerance Trait Phenotyping Reveals Shared Quantitative Trait Loci in Oryza sativa
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/10.1264/jsme2.me19111openalex-snapshot
Diversity of Methylobacterium spp. in the Rice of the Vietnamese Mekong Delta
inferred← citeshttps://doi.org/10.1264/jsme2.me21035openalex-snapshot
Leaf Bleaching in Rice: A New Disease in Vietnam Caused by Methylobacterium indicum, Its Genomic Characterization and the Development of a Suitable Detection Technique
inferred← citeshttps://doi.org/10.1371/journal.pone.0131391openalex-snapshot
Comparative Transcriptome Analysis of Shoots and Roots of TNG67 and TCN1 Rice Seedlings under Cold Stress and Following Subsequent Recovery: Insights into Metabolic Pathways, Phytohormones, and Transcription Factors
inferred← citeshttps://doi.org/10.1371/journal.pone.0338290openalex-snapshot
Stage-specific screening reveals differential resilience response to cold stress in rice
inferred← citeshttps://doi.org/10.15835/nbha49212306openalex-snapshot
Temperature-mediated shifts in chlorophyll biosynthesis in leaves of chlorophyll b-lacking rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1590/0034-737x201663020007openalex-snapshot
Seletividade de herbicidas sobre arroz irrigado em resposta à época de semeadura e redução da luminosidade em fases do desenvolvimento
inferred← citeshttps://doi.org/10.1590/1519-6984.282495openalex-snapshot
Selection of rice breeding lines for resistance to biotic and abiotic stresses
inferred← citeshttps://doi.org/10.1590/1678-4685-gmb-2016-0093openalex-snapshot
A walk on the wild side: Oryza species as source for rice abiotic stress tolerance
inferred← citeshttps://doi.org/10.17221/98/2017-cjgpbopenalex-snapshot
Detection of QTLs for cold tolerance at the booting stage in near-isogenic lines derived from rice landrace Lijiangxintuanheigu
inferred← citeshttps://doi.org/10.18869/acadpub.jcpp.6.20.1openalex-snapshot
Study of Chilling Tolerance in Rice Cultivars at Seedling Stage Using Morphological and Physiological Characteristics
inferred← citeshttps://doi.org/10.20546/ijcmas.2017.612.468openalex-snapshot
Screening of Cold Tolerant Rice Genotypes for Seedling Traits under Low Temperature Regimes
inferred← citeshttps://doi.org/10.20546/ijcmas.2018.701.133openalex-snapshot
Cold Tolerance at Germination and Seedling Stages of Rice: Methods of Evaluation and Characterization of Thirty Rice Genotypes under Stress Conditions
inferred← citeshttps://doi.org/10.21203/rs.3.rs-101299/v1openalex-snapshot
Mapping Quantitative Trait Loci for Cold Tolerance in Rice under Germination Stage by Whole Genome Resequencing and Analysis of Candidate Genes
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1936276/v1openalex-snapshot
QTL detection and fine mapping of qCTB1 for cold tolerance at the early seedling and booting stages in rice
inferred← citeshttps://doi.org/10.21203/rs.3.rs-4090867/v1openalex-snapshot
Genome-wide analysis of Rice OsDHSRP gene family and their Expression profiles under different Abiotic Stresses
inferred← citeshttps://doi.org/10.21203/rs.3.rs-4220217/v1openalex-snapshot
Effects of low-temperature stress during heading stage on carbon and nitrogen allocation in paddy eco-system of northeastern China
inferred← citeshttps://doi.org/10.2135/cropsci2016.11.0941openalex-snapshot
Application of Salicylic Acid Improves Filling of Inferior Grains of Rice during Late Maturity under Mild Cold Stress
inferred← citeshttps://doi.org/10.2174/9789815179699124010010openalex-snapshot
Inoculation of Plant Growth-Promoting Bacteria Aiming to Improve Rice Tolerance to Abiotic Stressful Conditions
inferred← citeshttps://doi.org/10.22271/tpi.2021.v10.i3j.5859openalex-snapshot
Cold stress and the role of signalling hormones: A preliminary study on cold-tolerant high-altitude Himalayan rice genotypes
inferred← citeshttps://doi.org/10.31235/osf.io/bq8geopenalex-snapshot
The Origin and Evolution of Chinese Lineages
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Molecular Genetics of Cold Tolerance at Germination and Seedling Stages in Rice
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Silicon In the Growth of Rice Seedlings Pretreated with Dietholate and Subjected to Cold Stress
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Potentiality of Different Seed Priming Agents to Mitigate Cold Stress of Winter Rice Seedling
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Seed Priming Improves Chilling Stress Tolerance in Rice (Oryza sativa L.) Seedlings
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Cold Injury and Flash Flood Damage in Boro Rice Cultivation in Bangladesh: A Review
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Using Agumented design for screening of cold tolerant rice genotypes for seedling traits under low temperature condition [Oryza sativa (L.)]
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Temperature stress and redox homeostasis in agricultural crops
inferred← citeshttps://doi.org/10.3389/fgene.2020.00022openalex-snapshot
Genome-Wide Association Mapping to Identify Genetic Loci for Cold Tolerance and Cold Recovery During Germination in Rice
inferred← citeshttps://doi.org/10.3389/fgene.2021.789645openalex-snapshot
NILs of Cold Tolerant Japonica Cultivar Exhibited New QTLs for Mineral Elements in Rice
inferred← citeshttps://doi.org/10.3389/fpls.2014.00386openalex-snapshot
Establishment of the chloroplast genetic system in rice during early leaf development and at low temperatures
inferred← citeshttps://doi.org/10.3389/fpls.2017.00957openalex-snapshot
Assessment of Five Chilling Tolerance Traits and GWAS Mapping in Rice Using the USDA Mini-Core Collection
inferred← citeshttps://doi.org/10.3389/fpls.2018.00886openalex-snapshot
Wild Relatives of Maize, Rice, Cotton, and Soybean: Treasure Troves for Tolerance to Biotic and Abiotic Stresses
inferred← citeshttps://doi.org/10.3389/fpls.2020.00329openalex-snapshot
Adaptation of Rice to the Nordic Climate Yields Potential for Rice Cultivation at Most Northerly Site and the Organic Production of Low-Arsenic and High-Protein Rice
inferred← citeshttps://doi.org/10.3389/fpls.2020.569437openalex-snapshot
Cold Stress Response: An Overview in Chlamydomonas
inferred← citeshttps://doi.org/10.3389/fpls.2021.640193openalex-snapshot
Modulation of Abiotic Stress Responses in Rice by E3-Ubiquitin Ligases: A Promising Way to Develop Stress-Tolerant Crops
inferred← citeshttps://doi.org/10.3389/fpls.2023.1303651openalex-snapshot
Navigating rice seedling cold resilience: QTL mapping in two inbred line populations and the search for genes
inferred← citeshttps://doi.org/10.3389/fpls.2023.1310459openalex-snapshot
Freezing stress response of wild and cultivated chickpeas
inferred← citeshttps://doi.org/10.3389/fpls.2024.1458701openalex-snapshot
Optimizing multi-environment trials in the Southern US Rice belt via smart-climate-soil prediction-based models and economic importance
inferred← citeshttps://doi.org/10.3389/fpls.2025.1484734openalex-snapshot
Effects of low-temperature stress during rice heading stage on carbon and nitrogen allocation in paddy eco-system of northeastern China
inferred← citeshttps://doi.org/10.3389/fpls.2025.1729934openalex-snapshot
Cold stress in rice (Oryza sativa L.): Molecular mechanisms of sensing, signaling, transcriptional regulation, membrane lipid remodeling, and hormonal modulation
inferred← citeshttps://doi.org/10.3389/fpls.2026.1845537openalex-snapshot
Genetic architecture of seedling stage chilling tolerance in United States rice germplasm
inferred← citeshttps://doi.org/10.3390/agriculture11060564openalex-snapshot
Pigment Production under Cold Stress in the Green Microalga Chlamydomonas reinhardtii
inferred← citeshttps://doi.org/10.3390/agriculture14091456openalex-snapshot
Effect of Climate Change on Identification of Delayed Chilling Damage of Rice in China’s Cold Region
inferred← citeshttps://doi.org/10.3390/agronomy11010112openalex-snapshot
Morpho-Physiological Characterization of Diverse Rice Genotypes for Seedling Stage High- and Low-Temperature Tolerance
inferred← citeshttps://doi.org/10.3390/agronomy11112125openalex-snapshot
Breeding for Low Temperature Germinability in Temperate Japonica Rice Varieties: Analysis of Candidate Genes in Associated QTLs
inferred← citeshttps://doi.org/10.3390/agronomy12081894openalex-snapshot
Assessing the Genetic Improvement in Inbred Late Rice against Chilling Stress: Consequences for Spikelet Fertility, Pollen Viability and Anther Characteristics
inferred← citeshttps://doi.org/10.3390/agronomy15102265openalex-snapshot
Integrated Approach of Using Biostimulants for Improving Growth, Physiological Traits, and Tolerance to Abiotic Stressors in Rice and Soybean
inferred← citeshttps://doi.org/10.3390/atmos13010103openalex-snapshot
Long-Term Dynamic of Cold Stress during Heading and Flowering Stage and Its Effects on Rice Growth in China
inferred← citeshttps://doi.org/10.3390/genes12101638openalex-snapshot
Transcriptome Profiling of Maize (Zea mays L.) Leaves Reveals Key Cold-Responsive Genes, Transcription Factors, and Metabolic Pathways Regulating Cold Stress Tolerance at the Seedling Stage
inferred← citeshttps://doi.org/10.3390/ijerph19159690openalex-snapshot
Change of Rice Paddy and Its Impact on Human Well-Being from the Perspective of Land Surface Temperature in the Northeastern Sanjiang Plain of China
inferred← citeshttps://doi.org/10.3390/ijms21176155openalex-snapshot
Environmental Signal-Dependent Regulation of Flowering Time in Rice
inferred← citeshttps://doi.org/10.3390/ijms21186872openalex-snapshot
Systematic Analysis of Cold Stress Response and Diurnal Rhythm Using Transcriptome Data in Rice Reveals the Molecular Networks Related to Various Biological Processes
inferred← citeshttps://doi.org/10.3390/ijms241914441openalex-snapshot
AP2/EREBP Pathway Plays an Important Role in Chaling Wild Rice Tolerance to Cold Stress
inferred← citeshttps://doi.org/10.3390/ijms25094991openalex-snapshot
Influence of Cold Stress on Physiological and Phytochemical Characteristics and Secondary Metabolite Accumulation in Microclones of Juglans regia L.
inferred← citeshttps://doi.org/10.3390/microorganisms14030632openalex-snapshot
Low Temperature Impacts Root Physiological Characteristics and Related Microbial Community Diversity in the Rhizosphere of Japonica 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/plants12233948openalex-snapshot
Abiotic Stress in Rice: Visiting the Physiological Response and Its Tolerance Mechanisms
inferred← citeshttps://doi.org/10.3390/plants14060961openalex-snapshot
Nitrogen Supply Mitigates Temperature Stress Effects on Rice Photosynthetic Nitrogen Use Efficiency and Water Relations
inferred← citeshttps://doi.org/10.3390/plants14111683openalex-snapshot
Effect of Priming Treatment on Improving Germination and Seedling Performance of Aged and Iron-Coated Rice Seeds Aiming for Direct Sowing
inferred← citeshttps://doi.org/10.3390/su14148447openalex-snapshot
Screening Technique Based on Seed and Early Seedling Parameters for Cold Tolerance of Selected F2-Derived F3 Rice Genotypes under Controlled Conditions
inferred← citeshttps://doi.org/10.3390/su152416873openalex-snapshot
Cold-Tolerant and Short-Duration Rice (Oryza sativa L.) for Sustainable Food Security of the Flash Flood-Prone Haor Wetlands of Bangladesh
inferred← citeshttps://doi.org/10.34116/nti.2019.aa.80openalex-snapshot
Evaluation of cold damage in a Hungarian rice variety collection
inferred← citeshttps://doi.org/10.35709/ory.2020.57.1.5openalex-snapshot
Evaluation of rice (Oryza sativa L.) genotypes for cold tolerance at seedling stage
inferred← citeshttps://doi.org/10.3724/sp.j.1006.2020.92066openalex-snapshot
Detection of QTLs controlling cold tolerance at bud bursting stage by using a high-density SNP linkage map in japonica rice
inferred← citeshttps://doi.org/10.3724/sp.j.1258.2014.00093openalex-snapshot
Comprehensive evaluation of low-temperature tolerance in soybean cultivars of different eco-types at seedling stage in Shanxi Province
inferred← citeshttps://doi.org/10.3923/ajps.2022.677.684openalex-snapshot
Screening Rice Lines Tolerant to Low Temperature at the Germination Stage Using Thermogradient bar
inferred← citeshttps://doi.org/10.4067/s0717-66432015000100001openalex-snapshot
Cold tolerance evaluation of temperate rice (Oryza sativa L. ssp. japonica) genotypes at seedling stage
inferred← citeshttps://doi.org/10.4172/2375-4338.1000e108openalex-snapshot
Cold Tolerance in Rice Plants: Why, How and When?
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