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Positive regulation of AMS by TDF1 and the formation of a TDF1–AMS complex are required for anther development in Arabidopsis thaliana

https://doi.org/10.1111/nph.14790
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What this work says

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

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AN INTERPRETATION OF THE HYDRODYNAMICS OF POLLEN
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EMS-induced genic male sterility in Arabidopsis thaliana: A model selection experiment
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Ultrastructure of microsporogenesis and microgametogenesis inArabidopsis thaliana (L.) Heynh. ecotype Wassilewskija (Brassicaceae)
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Programmed-cell-death events during tapetum development of angiosperms
inferredcites →https://doi.org/10.1007/s004970050158openalex-snapshot
Anther developmental defects in Arabidopsis thaliana male-sterile mutants
inferredcites →https://doi.org/10.1007/s11427-010-4060-yopenalex-snapshot
AtMYB103 is a crucial regulator of several pathways affecting Arabidopsis anther development
inferredcites →https://doi.org/10.1007/s11434-015-0810-3openalex-snapshot
The functional analysis of OsTDF1 reveals a conserved genetic pathway for tapetal development between rice and Arabidopsis
inferredcites →https://doi.org/10.1016/0012-1606(77)90356-6openalex-snapshot
Role of β-1,3-glucanase in postmeiotic microspore release
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The myb-homologous P gene controls phlobaphene pigmentation in maize floral organs by directly activating a flavonoid biosynthetic gene subset
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Death of a tapetum: A programme of developmental altruism
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Expansins: ever-expanding numbers and functions
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Programmed cell death in plant reproduction
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Protoceras, the New Artiodactyle
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Loosening of plant cell walls by expansins
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The tapetal AHL family protein TEK determines nexine formation in the pollen wall
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Network motifs in the transcriptional regulation network of Escherichia coli
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Network motifs: theory and experimental approaches
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DNA fragmentation is regulated by ethylene during carpel senescence in Pisum sativum
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The Arabidopsis MALE STERILITY1 (MS1) gene is a transcriptional regulator of male gametogenesis, with homology to the PHD‐finger family of transcription factors
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01644.xopenalex-snapshot
The Arabidopsis ABORTED MICROSPORES ( AMS ) gene encodes a MYC class transcription factor
inferredcites →https://doi.org/10.1074/jbc.m207570200openalex-snapshot
Cell Cycle-regulated Gene Expression inArabidopsis
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Water Uptake by Growing Cells: An Assessment of the Controlling Roles of Wall Relaxation, Solute Uptake, and Hydraulic Conductance
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Molecular and Physiological Characterization of the Arabidopsis thaliana Oxidation-Related Zinc Finger 2, a Plasma Membrane Protein Involved in ABA and Salt Stress Response Through the ABI2-Mediated Signaling Pathway
inferredcites →https://doi.org/10.1093/pcp/pct175openalex-snapshot
The Arabidopsis Tandem Zinc Finger 9 Protein Binds RNA and Mediates Pathogen-Associated Molecular Pattern-Triggered Immune Responses
inferredcites →https://doi.org/10.1093/pcp/pcu074openalex-snapshot
Tandem CCCH Zinc Finger Proteins in Plant Growth, Development and Stress Response
inferredcites →https://doi.org/10.1104/pp.109.144469openalex-snapshot
CYP704B1 Is a Long-Chain Fatty Acidω-Hydroxylase Essential for Sporopollenin Synthesis in Pollen of Arabidopsis
inferredcites →https://doi.org/10.1104/pp.109.145656openalex-snapshot
The Arabidopsis Tandem Zinc Finger Protein AtTZF1 Traffics between the Nucleus and Cytoplasmic Foci and Binds Both DNA and RNA
inferredcites →https://doi.org/10.1104/pp.110.157446openalex-snapshot
LAP5 and LAP6 Encode Anther-Specific Proteins with Similarity to Chalcone Synthase Essential for Pollen Exine Development in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.113.214940openalex-snapshot
AUXIN RESPONSE FACTOR17 Is Essential for Pollen Wall Pattern Formation in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.114.253807openalex-snapshot
FlowerNet: A Gene Expression Correlation Network for Anther and Pollen Development
inferredcites →https://doi.org/10.1105/tpc.006130openalex-snapshot
Arabidopsis AtMYC2 (bHLH) and AtMYB2 (MYB) Function as Transcriptional Activators in Abscisic Acid Signaling
inferredcites →https://doi.org/10.1105/tpc.107.054536openalex-snapshot
Arabidopsis MALE STERILITY1 Encodes a PHD-Type Transcription Factor and Regulates Pollen and Tapetum Development
inferredcites →https://doi.org/10.1105/tpc.107.054981openalex-snapshot
MALE STERILITY1 Is Required for Tapetal Development and Pollen Wall Biosynthesis
inferredcites →https://doi.org/10.1105/tpc.109.071803openalex-snapshot
The ABORTED MICROSPORES Regulatory Network Is Required for Postmeiotic Male Reproductive Development in Arabidopsis thaliana
inferredcites →https://doi.org/10.1105/tpc.110.080788openalex-snapshot
The Arabidopsis bHLH Transcription Factors MYC3 and MYC4 Are Targets of JAZ Repressors and Act Additively with MYC2 in the Activation of Jasmonate Responses
inferredcites →https://doi.org/10.1105/tpc.110.082651openalex-snapshot
The MYB80 Transcription Factor Is Required for Pollen Development and the Regulation of Tapetal Programmed Cell Death inArabidopsis thaliana
inferredcites →https://doi.org/10.1105/tpc.114.122986openalex-snapshot
ABORTED MICROSPORESActs as a Master Regulator of Pollen Wall Formation inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.15.00116openalex-snapshot
Regulation of Jasmonate-Mediated Stamen Development and Seed Production by a bHLH-MYB Complex in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.15.00986openalex-snapshot
Feedback Regulation of DYT1 by Interactions with Downstream bHLH Factors Promotes DYT1 Nuclear Localization and Anther Development
inferredcites →https://doi.org/10.1105/tpc.4.8.879openalex-snapshot
The remarkable biology of pollen.
inferredcites →https://doi.org/10.1105/tpc.5.10.1265openalex-snapshot
Male Gametophyte Development
inferredcites →https://doi.org/10.1105/tpc.9.4.611openalex-snapshot
Evidence for direct activation of an anthocyanin promoter by the maize C1 protein and comparison of DNA binding by related Myb domain proteins.
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mapman : a user‐driven tool to display genomics data sets onto diagrams of metabolic pathways and other biological processes
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Chromatin techniques for plant cells
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Differential gene expression in Arabidopsis wild‐type and mutant anthers: insights into anther cell differentiation and regulatory networks
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03254.xopenalex-snapshot
Transcription factor AtMYB103 is required for anther development by regulating tapetum development, callose dissolution and exine formation in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03500.xopenalex-snapshot
Defective in Tapetal Development and Function 1 is essential for anther development and tapetal function for microspore maturation in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2012.05104.xopenalex-snapshot
Regulation of the Arabidopsis anther transcriptome by DYT1 for pollen development
inferredcites →https://doi.org/10.1111/j.1469-8137.2007.02060.xopenalex-snapshot
Pollen wall development in flowering plants
inferredcites →https://doi.org/10.1111/j.1744-7909.2011.01078.xopenalex-snapshot
A Genetic Pathway for Tapetum Development and Function in Arabidopsis
inferredcites →https://doi.org/10.1111/nph.14200openalex-snapshot
Biphasic regulation of the transcription factor ABORTED MICROSPORES ( AMS ) is essential for tapetum and pollen development in Arabidopsis
inferredcites →https://doi.org/10.1111/nph.14207openalex-snapshot
An auxin maximum in the middle layer controls stamen development and pollen maturation in Arabidopsis
inferredcites →https://doi.org/10.1111/pce.12084openalex-snapshot
The A rabidopsis tandem CCCH zinc finger proteins AtTZF4 , 5 and 6 are involved in light‐, abscisic acid‐ and gibberellic acid‐mediated regulation of seed germination
inferredcites →https://doi.org/10.1111/tpj.12694openalex-snapshot
DYT 1 directly regulates the expression of TDF 1 for tapetum development and pollen wall formation in A rabidopsis
inferredcites →https://doi.org/10.1111/tpj.12942openalex-snapshot
The DYT 1‐interacting proteins b HLH 010, b HLH 089 and b HLH 091 are redundantly required for A rabidopsis anther development and transcriptome
inferredcites →https://doi.org/10.1111/tpj.13054openalex-snapshot
Magnesium Transporter 5 plays an important role in Mg transport for male gametophyte development in Arabidopsis
inferredcites →https://doi.org/10.1111/tpj.13284openalex-snapshot
The transcription factors MS 188 and AMS form a complex to activate the expression of CYP 703A2 for sporopollenin biosynthesis in Arabidopsis thaliana
inferredcites →https://doi.org/10.1126/science.1086391openalex-snapshot
Genome-Wide Insertional Mutagenesis of Arabidopsis thaliana
inferredcites →https://doi.org/10.1126/science.298.5594.824openalex-snapshot
Network Motifs: Simple Building Blocks of Complex Networks
inferredcites →https://doi.org/10.1146/annurev-arplant-042809-112312openalex-snapshot
Genetic Regulation of Sporopollenin Synthesis and Pollen Exine Development
inferredcites →https://doi.org/10.1146/annurev.arplant.47.1.445openalex-snapshot
STRUCTURE AND BIOGENESIS OF THE CELL WALLS OF GRASSES
inferredcites →https://doi.org/10.1146/annurev.cellbio.042308.113417openalex-snapshot
Small RNAs and Their Roles in Plant Development
inferredcites →https://doi.org/10.1186/1471-2229-12-23openalex-snapshot
AMS-dependent and independent regulation of anther transcriptome and comparison with those affected by other Arabidopsis anther genes
inferredcites →https://doi.org/10.1186/s12870-014-0401-5openalex-snapshot
Genome-wide identification and comparative analysis of the heat shock transcription factor family in Chinese white pear (Pyrus bretschneideri) and five other Rosaceae species
inferredcites →https://doi.org/10.1242/dev.02463openalex-snapshot
Regulation of Arabidopsis tapetum development and function by DYSFUNCTIONAL TAPETUM1 ( DYT1 ) encoding a putative bHLH transcription factor
inferredcites →https://doi.org/10.1242/jcs.50.1.419openalex-snapshot
Studies on heteromorphic selfincompatibility systems: The cytochemistry and ultrastructure of the tapetum of Primula obconica
inferredcites →https://doi.org/10.3389/fpls.2013.00013openalex-snapshot
Differential Contribution of Transcription Factors to Arabidopsis thaliana Defense Against Spodoptera littoralis

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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inferred← citeshttps://doi.org/10.1007/978-981-95-7033-1_9openalex-snapshot
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Decades’ progress and prospects on maize functional genomics and molecular breeding
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Targeted Overexpression of CBF1 Using a Pollen-specific Promoter Enhances Fertility in Heat-stressed Arabidopsis
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inferred← citeshttps://doi.org/10.1016/j.bbrc.2025.151607openalex-snapshot
OsMADS22 interacts with OsMADS50 to regulate floral transition in rice
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Identification of a locus associated with genic male sterility in maize via EMS mutagenesis and bulked-segregant RNA-seq
inferred← citeshttps://doi.org/10.1016/j.cj.2021.03.016openalex-snapshot
Genome-wide analyses on transcription factors and their potential microRNA regulators involved in maize male fertility
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Male sterility in crops: Application of human intelligence to natural variation
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inferred← citeshttps://doi.org/10.1016/j.jplph.2023.154058openalex-snapshot
SPOTLIGHT: Ascorbate triggers the switch between cell division and cell differentiation in the Arabidopsis tapetum
inferred← citeshttps://doi.org/10.1016/j.jprot.2021.104241openalex-snapshot
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TMT-based comparative proteomic analysis of the male-sterile mutant ms01 sheds light on sporopollenin production and pollen development in wucai (Brassica campestris L.)
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Maize Genic Male-Sterility Genes and Their Applications in Hybrid Breeding: Progress and Perspectives
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inferred← citeshttps://doi.org/10.1016/j.molp.2023.07.010openalex-snapshot
ZmMS1/ZmLBD30-orchestrated transcriptional regulatory networks precisely control pollen exine development
inferred← citeshttps://doi.org/10.1016/j.molp.2024.12.012openalex-snapshot
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TALE protein mediated overexpression of embryogenesis related marker genes in wheat microspores
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inferred← citeshttps://doi.org/10.1016/j.scienta.2023.112465openalex-snapshot
Ectopic expression of PmGRF7 isolated from Japanese apricot in tomato leads to seed sterility
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inferred← citeshttps://doi.org/10.1038/s41477-020-0622-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41477-023-01413-0openalex-snapshot
Biosynthesis and transport of pollen coat precursors in angiosperms
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Full-length transcriptome analysis provides new insights into the early bolting occurrence in medicinal Angelica sinensis
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Genic male and female sterility in vegetable crops
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MS1, a direct target of MS188, regulates the expression of key sporophytic pollen coat protein genes in Arabidopsis
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The WUSCHEL-related homeobox1 gene of cucumber regulates reproductive organ development
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Cold Influences Male Reproductive Development in Plants: A Hazard to Fertility, but a Window for Evolution
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Ascorbic acid-mediated reactive oxygen species homeostasis modulates the switch from tapetal cell division to cell differentiation in Arabidopsis
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Stop vitamins: Low levels of ascorbic acid regulate the transition from cell proliferation to differentiation in Arabidopsis tapetum
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A PP2A phosphatase-defined transcriptional activity window safeguards male fertility
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Abnormal tapetum development in hermaphrodites of an androdioecious tree, Tapiscia sinensis
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TaEXPB5 is responsible for male fertility in thermo-sensitive male-sterility wheat with Aegilops kotschyi cytoplasm
inferred← citeshttps://doi.org/10.1101/2023.02.03.527076openalex-snapshot
Syntaxin of plants 32 regulates pollen wall development and pollen tube cell wall integrity via controlling secretory pathway
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FKF1b controls reproductive transition associated with adaptation to geographical distribution in maize
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The AMS/DYT1–MYB module interacts with the MED25–MYC–MYB complexes to inhibit jasmonate‐regulated floral defense in Arabidopsis
inferred← citeshttps://doi.org/10.1111/nph.17939openalex-snapshot
The GA–DELLA–OsMS188 module controls male reproductive development in rice
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Barley TAPETAL DEVELOPMENT and FUNCTION1 (HvTDF1) gene reveals conserved and unique roles in controlling anther tapetum development in dicot and monocot plants
inferred← citeshttps://doi.org/10.1111/nph.19978openalex-snapshot
Ultraviolet attenuates centromere‐mediated meiotic genome stability and alters gametophytic ploidy consistency in flowering plants
inferred← citeshttps://doi.org/10.1111/nph.20435openalex-snapshot
TIP2 ‐ UDT1 ‐ OsUPEX1 /2 module regulates tapetum development and function in rice
inferred← citeshttps://doi.org/10.1111/pbi.13590openalex-snapshot
CRISPR/Cas9‐based discovery of maize transcription factors regulating male sterility and their functional conservation in plants
inferred← citeshttps://doi.org/10.1111/pbi.13886openalex-snapshot
Mutation of glucose‐methanol‐choline oxidoreductase leads to thermosensitive genic male sterility in rice and Arabidopsis
inferred← citeshttps://doi.org/10.1111/pbi.70512openalex-snapshot
TaRIP2 Positively Regulates Wheat Pollen Wall Formation Through MYB80 ‐Controlled Lipid Metabolism
inferred← citeshttps://doi.org/10.1111/ppl.13501openalex-snapshot
Sesame β‐ketoacyl‐acyl carrier protein synthase I regulates pollen development by interacting with an adenosine triphosphate‐binding cassette transporter in transgenic Arabidopsis
inferred← citeshttps://doi.org/10.1111/ppl.14331openalex-snapshot
GhTKPR1_8 functions to inhibit anther dehiscence and reduce pollen viability in cotton
inferred← citeshttps://doi.org/10.1111/ppl.70182openalex-snapshot
Male sterility‐induced parthenocarpy arose during tomato domestication
inferred← citeshttps://doi.org/10.1111/tpj.14672openalex-snapshot
Brassinosteroid‐mediated reactive oxygen species are essential for tapetum degradation and pollen fertility in tomato
inferred← citeshttps://doi.org/10.1111/tpj.15070openalex-snapshot
An integral insight into pollen wall development: involvement of physical processes in exine ontogeny inCalycanthus floridusL., with an experimental approach
inferred← citeshttps://doi.org/10.1111/tpj.15438openalex-snapshot
Iron insufficiency in floral buds impairs pollen development by disrupting tapetum function
inferred← citeshttps://doi.org/10.1111/tpj.16089openalex-snapshot
The full‐length Auxin Response Factor 8 isoform ARF8 .1 controls pollen cell wall formation and directly regulates TDF1 , AMS and MS188 expression
inferred← citeshttps://doi.org/10.1111/tpj.70126openalex-snapshot
Anther‐specific expression of MsMYB35 transcription factor in alfalfa ( Medicago sativa L.) and its crucial role in pollen development
inferred← citeshttps://doi.org/10.1111/tpj.70164openalex-snapshot
OsMYB103 targets and interacts with AMD1 to form a feed‐forward loop for pollen development in rice
inferred← citeshttps://doi.org/10.1186/s12864-022-08549-xopenalex-snapshot
Gene silencing, knockout and over-expression of a transcription factor ABORTED MICROSPORES (SlAMS) strongly affects pollen viability in tomato (Solanum lycopersicum)
inferred← citeshttps://doi.org/10.1186/s12870-019-2169-0openalex-snapshot
Differential gene expression among three sex types reveals a MALE STERILITY 1 (CpMS1) for sex differentiation in papaya
inferred← citeshttps://doi.org/10.1186/s12870-024-05916-6openalex-snapshot
Single-cell transcriptomic and cell‑type‑specific regulatory networks in Polima temperature-sensitive cytoplasmic male sterility of Brassica napus L.
inferred← citeshttps://doi.org/10.1186/s12870-025-06242-1openalex-snapshot
The dynamic regulatory network of stamens and pistils in papaya
inferred← citeshttps://doi.org/10.1186/s12870-025-06542-6openalex-snapshot
Genome-wide identification of the Medicago sativa L. MYB family and its transcriptional dynamics during pollen development
inferred← citeshttps://doi.org/10.1360/ssv-2024-0051openalex-snapshot
Advance in the anther tapetum development and their regulatory mechanisms
inferred← citeshttps://doi.org/10.1360/tb-2023-0822openalex-snapshot
A newly discovered “brake molecule” gene precisely controls pollen exine development
inferred← citeshttps://doi.org/10.1360/tb-2025-0091openalex-snapshot
Plant genic male sterility genes and their molecular regulatory mechanisms
inferred← citeshttps://doi.org/10.1590/1678-4685-gmb-2023-0171openalex-snapshot
bHLH-regulated routes in anther development in rice and Arabidopsis
inferred← citeshttps://doi.org/10.21203/rs.3.rs-10523110/v1openalex-snapshot
Synergistic regulation of defective meiotic DNA repair, premature tapetal degeneration, and hormone signaling underlies pollen abortion in Arundo donax
inferred← citeshttps://doi.org/10.21203/rs.3.rs-10551119/v1openalex-snapshot
Sexual evolution in plants: genetic network co-option and reproductive innovation
inferred← citeshttps://doi.org/10.2139/ssrn.6874855openalex-snapshot
The function of aborted microspores (SlAMS) in regulating tomato male sterility
inferred← citeshttps://doi.org/10.2139/ssrn.6967802openalex-snapshot
GhEXPA4 Interacts with MYB and GhRDL1 to Regulate Cotton Fiber Development and Secondary Cell Wall Biosynthesis
inferred← citeshttps://doi.org/10.3389/fpls.2019.01667openalex-snapshot
Tapetum-Dependent Male Meiosis Progression in Plants: Increasing Evidence Emerges
inferred← citeshttps://doi.org/10.3389/fpls.2021.768584openalex-snapshot
Pollen Number and Ribosome Gene Expression Altered in a Genome-Editing Mutant of REDUCED POLLEN NUMBER1 Gene
inferred← citeshttps://doi.org/10.3389/fpls.2021.770311openalex-snapshot
Tapetal 3-Ketoacyl-Coenzyme A Synthases Are Involved in Pollen Coat Lipid Accumulation for Pollen-Stigma Interaction in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2022.935413openalex-snapshot
Hydroxyproline-O-Galactosyltransferases Synthesizing Type II Arabinogalactans Are Essential for Male Gametophytic Development in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2023.1044581openalex-snapshot
Integrated transcriptomics and metabolomics analysis provide insight into anthocyanin biosynthesis for sepal color formation in Heptacodium miconioides
inferred← citeshttps://doi.org/10.3389/fpls.2024.1354418openalex-snapshot
The transcription factors and pathways underpinning male reproductive development in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2025.1695628openalex-snapshot
Integrating transcriptomic and proteomic analyses reveals impaired carbohydrate metabolism in tobacco cytoplasmic male sterility
inferred← citeshttps://doi.org/10.3389/fsufs.2023.1333544openalex-snapshot
Male gametogenesis in flowering plants
inferred← citeshttps://doi.org/10.3390/agronomy10050653openalex-snapshot
Transcriptome Analysis Reveals Important Transcription Factor Families and Reproductive Biological Processes of Flower Development in Celery (Apium graveolens L.)
inferred← citeshttps://doi.org/10.3390/agronomy15020312openalex-snapshot
Cytological Characterization of vrnp 1, a Pollen-Free Male Sterile Mutant in Mung Bean (Vigna radiata)
inferred← citeshttps://doi.org/10.3390/agronomy15092058openalex-snapshot
Expression and Functional Analysis of the ABORTED MICROSPORES (AMS) Gene in Marigold (Tagetes erecta L.)
inferred← citeshttps://doi.org/10.3390/cells11111753openalex-snapshot
Genetic Structure and Molecular Mechanisms Underlying the Formation of Tassel, Anther, and Pollen in the Male Inflorescence of Maize (Zea mays L.)
inferred← citeshttps://doi.org/10.3390/cells12020247openalex-snapshot
Comprehensive Insight into Tapetum-Mediated Pollen Development in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3390/cells14070470openalex-snapshot
Identification of Nuclear Localization Sequence (NLS) Sites in R2R3-MYB Transcription Factor Involved in Anther Development
inferred← citeshttps://doi.org/10.3390/f13040531openalex-snapshot
Genome-Wide Identification and Expression Analysis of MYC Transcription Factor Family Genes in Rubber Tree (Hevea brasiliensis Muell. Arg.)
inferred← citeshttps://doi.org/10.3390/genes12020249openalex-snapshot
Two Expansin Genes, AtEXPA4 and AtEXPB5, Are Redundantly Required for Pollen Tube Growth and AtEXPA4 Is Involved in Primary Root Elongation in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3390/horticulturae10121322openalex-snapshot
Fine-Mapping of Tomato male sterile-24 Locus and Marker Development for ms-24 and Its Alleles, ms-10, ms-35, and ms-36
inferred← citeshttps://doi.org/10.3390/horticulturae11040398openalex-snapshot
The Transcription Factor LoTDF1 Plays a Role in Early Anther Development in Lily (Lilium Oriental Hybrids)
inferred← citeshttps://doi.org/10.3390/horticulturae8111056openalex-snapshot
Abnormal Programmed Cell Death of Tapetum Leads to the Pollen Abortion of Lycium barbarum Linnaeus
inferred← citeshttps://doi.org/10.3390/ijms20071789openalex-snapshot
Complementary Transcriptomic and Proteomic Analysis Reveals a Complex Network Regulating Pollen Abortion in GMS (msc-1) Pepper (Capsicum annuum L.)
inferred← citeshttps://doi.org/10.3390/ijms21103424openalex-snapshot
Complex Molecular Evolution and Expression of Expansin Gene Families in Three Basic Diploid Species of Brassica
inferred← citeshttps://doi.org/10.3390/ijms23073563openalex-snapshot
MYB2 Is Important for Tapetal PCD and Pollen Development by Directly Activating Protease Expression in Arabidopsis
inferred← citeshttps://doi.org/10.3390/ijms23147996openalex-snapshot
The Transcription Factors TaTDRL and TaMYB103 Synergistically Activate the Expression of TAA1a in Wheat, Which Positively Regulates the Development of Microspore in Arabidopsis
inferred← citeshttps://doi.org/10.3390/ijms231810420openalex-snapshot
Epigenetic Dynamics and Regulation of Plant Male Reproduction
inferred← citeshttps://doi.org/10.3390/ijms26157036openalex-snapshot
Insights into the Molecular Basis of Pollen Coat Development and Its Role in Male Sterility
inferred← citeshttps://doi.org/10.3390/plants11121556openalex-snapshot
Transcriptome Profiling Identifies Candidate Genes Contributing to Male and Female Gamete Development in Synthetic Brassica Allohexaploids
inferred← citeshttps://doi.org/10.3390/plants14050749openalex-snapshot
Identity Transitions of Tapetum Phases: Insights into Vesicular Dynamics and in Mortem Support During Pollen Maturation
inferred← citeshttps://doi.org/10.48130/seedbio-2022-0005openalex-snapshot
The contributions of sporophytic tapetum to pollen formation
inferred← citeshttps://doi.org/10.6084/m9.figshare.19720169openalex-snapshot
Additional file 10 of Gene silencing, knockout and over-expression of a transcription factor ABORTED MICROSPORES (SlAMS) strongly affects pollen viability in tomato (Solanum lycopersicum)
inferred← citeshttps://doi.org/10.6084/m9.figshare.19720172openalex-snapshot
Additional file 11 of Gene silencing, knockout and over-expression of a transcription factor ABORTED MICROSPORES (SlAMS) strongly affects pollen viability in tomato (Solanum lycopersicum)
inferred← citeshttps://doi.org/10.6084/m9.figshare.19720175openalex-snapshot
Additional file 12 of Gene silencing, knockout and over-expression of a transcription factor ABORTED MICROSPORES (SlAMS) strongly affects pollen viability in tomato (Solanum lycopersicum)
inferred← citeshttps://doi.org/10.6084/m9.figshare.19720178openalex-snapshot
Additional file 13 of Gene silencing, knockout and over-expression of a transcription factor ABORTED MICROSPORES (SlAMS) strongly affects pollen viability in tomato (Solanum lycopersicum)
inferred← citeshttps://doi.org/10.6084/m9.figshare.19720181openalex-snapshot
Additional file 14 of Gene silencing, knockout and over-expression of a transcription factor ABORTED MICROSPORES (SlAMS) strongly affects pollen viability in tomato (Solanum lycopersicum)
inferred← citeshttps://doi.org/10.6084/m9.figshare.19720184openalex-snapshot
Additional file 15 of Gene silencing, knockout and over-expression of a transcription factor ABORTED MICROSPORES (SlAMS) strongly affects pollen viability in tomato (Solanum lycopersicum)
inferred← citeshttps://doi.org/10.6084/m9.figshare.19720187openalex-snapshot
Additional file 16 of Gene silencing, knockout and over-expression of a transcription factor ABORTED MICROSPORES (SlAMS) strongly affects pollen viability in tomato (Solanum lycopersicum)
inferred← citeshttps://doi.org/10.6084/m9.figshare.19720190openalex-snapshot
Additional file 1 of Gene silencing, knockout and over-expression of a transcription factor ABORTED MICROSPORES (SlAMS) strongly affects pollen viability in tomato (Solanum lycopersicum)
inferred← citeshttps://doi.org/10.6084/m9.figshare.19720193openalex-snapshot
Additional file 2 of Gene silencing, knockout and over-expression of a transcription factor ABORTED MICROSPORES (SlAMS) strongly affects pollen viability in tomato (Solanum lycopersicum)
inferred← citeshttps://doi.org/10.6084/m9.figshare.19720196openalex-snapshot
Additional file 3 of Gene silencing, knockout and over-expression of a transcription factor ABORTED MICROSPORES (SlAMS) strongly affects pollen viability in tomato (Solanum lycopersicum)
inferred← citeshttps://doi.org/10.6084/m9.figshare.19720199openalex-snapshot
Additional file 4 of Gene silencing, knockout and over-expression of a transcription factor ABORTED MICROSPORES (SlAMS) strongly affects pollen viability in tomato (Solanum lycopersicum)
inferred← citeshttps://doi.org/10.6084/m9.figshare.19720202openalex-snapshot
Additional file 5 of Gene silencing, knockout and over-expression of a transcription factor ABORTED MICROSPORES (SlAMS) strongly affects pollen viability in tomato (Solanum lycopersicum)
inferred← citeshttps://doi.org/10.6084/m9.figshare.19720205openalex-snapshot
Additional file 6 of Gene silencing, knockout and over-expression of a transcription factor ABORTED MICROSPORES (SlAMS) strongly affects pollen viability in tomato (Solanum lycopersicum)
inferred← citeshttps://doi.org/10.6084/m9.figshare.19720208openalex-snapshot
Additional file 7 of Gene silencing, knockout and over-expression of a transcription factor ABORTED MICROSPORES (SlAMS) strongly affects pollen viability in tomato (Solanum lycopersicum)
inferred← citeshttps://doi.org/10.6084/m9.figshare.19720211openalex-snapshot
Additional file 8 of Gene silencing, knockout and over-expression of a transcription factor ABORTED MICROSPORES (SlAMS) strongly affects pollen viability in tomato (Solanum lycopersicum)
inferred← citeshttps://doi.org/10.6084/m9.figshare.19720214openalex-snapshot
Additional file 9 of Gene silencing, knockout and over-expression of a transcription factor ABORTED MICROSPORES (SlAMS) strongly affects pollen viability in tomato (Solanum lycopersicum)
inferred← citeshttps://doi.org/10.7287/peerj.13981v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Genome-wide identification and transcriptional profiling of the basic helix-loop-helix gene family in tung tree (Vernicia fordii) (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.13981v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Genome-wide identification and transcriptional profiling of the basic helix-loop-helix gene family in tung tree (Vernicia fordii) (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.13981v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Genome-wide identification and transcriptional profiling of the basic helix-loop-helix gene family in tung tree (Vernicia fordii) (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.13981v0.2/reviews/2openalex-snapshot
Peer Review #2 of "Genome-wide identification and transcriptional profiling of the basic helix-loop-helix gene family in tung tree (Vernicia fordii) (v0.2)"
inferred← citeshttps://doi.org/10.7717/peerj.13981openalex-snapshot
Genome-wide identification and transcriptional profiling of the basic helix-loop-helix gene family in tung tree ( Vernicia fordii )
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.