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Pollen-specific gene expression in transgenic plants: coordinate regulation of two different tomato gene promoters during microsporogenesis
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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New cloning vehicles for transformation of higher plants
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GUS fusions: beta‐glucuronidase as a sensitive and versatile gene fusion marker in higher plants.
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Cis‐acting regions sufficient for spermatocyte‐specific transcriptional and spermatid‐specific translational control of the Drosophila melanogaster gene mst(3)gl‐9.
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Gene fusions to lacZ reveal new expression patterns of chimeric genes in transgenic plants.
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The CaMV 35S enhancer contains at least two domains which can confer different developmental and tissue‐specific expression patterns
inferredcites →https://doi.org/10.1007/978-3-7091-6950-6_6openalex-snapshot
Anther- and Pollen-Expressed Genes
inferredcites →https://doi.org/10.1007/bf00015651openalex-snapshot
Molecular and genetic characterization of two pollen-expressed genes that have sequence similarity to pectate lyases of the plant pathogen Erwinia
inferredcites →https://doi.org/10.1007/bf00265600openalex-snapshot
An analysis of the quantity and diversity of messenger RNAs from pollen and shoots of Zea mays
inferredcites →https://doi.org/10.1007/bf00269239openalex-snapshot
Leaf disc transformation of cultivated tomato (L. esculentum) using Agrobacterium tumefaciens
inferredcites →https://doi.org/10.1007/bf00334371openalex-snapshot
β-Glucuronidase activity during development of the male gametophyte from transgenic and non-transgenic plants
inferredcites →https://doi.org/10.1007/bf02464887openalex-snapshot
Isolation and expression of an anther-specific gene from tomato
inferredcites →https://doi.org/10.1007/bf02918566openalex-snapshot
Oxford surveys of plant molecular and cell biology
inferredcites →https://doi.org/10.1016/0014-4827(72)90125-5openalex-snapshot
Isolation of vegetative and generative nuclei from pollen tubes
inferredcites →https://doi.org/10.1016/0168-9452(89)90008-3openalex-snapshot
Polygalacturonase in pollen from corn and other grasses
inferredcites →https://doi.org/10.1016/s0074-7696(08)61072-4openalex-snapshot
Pollen Germination and Pollen-Tube Growth
inferredcites →https://doi.org/10.1016/s0074-7696(08)61076-1openalex-snapshot
Ultrastructural Aspects of Pollen Dimorphism
inferredcites →https://doi.org/10.1073/pnas.83.22.8447openalex-snapshot
beta-Glucuronidase from Escherichia coli as a gene-fusion marker.
inferredcites →https://doi.org/10.1073/pnas.84.15.5316openalex-snapshot
Spermatid-specific expression of protamine 1 in transgenic mice.
inferredcites →https://doi.org/10.1073/pnas.85.15.5536openalex-snapshot
Agrobacterium tumefaciens -mediated transformation of Arabidopsis thaliana root explants by using kanamycin selection
inferredcites →https://doi.org/10.1093/nar/12.22.8711openalex-snapshot
Binary Agrobacterium vectors for plant transformation
inferredcites →https://doi.org/10.1101/gad.3.6.793openalex-snapshot
Protamine 3'-untranslated sequences regulate temporal translational control and subcellular localization of growth hormone in spermatids of transgenic mice.
inferredcites →https://doi.org/10.1104/pp.75.3.865openalex-snapshot
Analysis of the Complexity and Diversity of mRNAs from Pollen and Shoots of Tradescantia
inferredcites →https://doi.org/10.1104/pp.83.2.442openalex-snapshot
Genes Expressed in the Male Gametophyte of Flowering Plants and Their Isolation
inferredcites →https://doi.org/10.1104/pp.91.4.1270openalex-snapshot
Transient Expression of Chimeric Genes Delivered into Pollen by Microprojectile Bombardment
inferredcites →https://doi.org/10.1105/tpc.1.2.169openalex-snapshot
Tracking Down Plant Genes: Paths, Patterns, and Footprints
inferredcites →https://doi.org/10.1105/tpc.1.7.657openalex-snapshot
The Male Gametophyte of Flowering Plants
inferredcites →https://doi.org/10.1105/tpc.1.7.727openalex-snapshot
Gametophytic and sporophytic expression of anther-specific genes in developing tomato anthers.
inferredcites →https://doi.org/10.1105/tpc.2.3.263openalex-snapshot
Characterization of a gene family abundantly expressed in Oenothera organensis pollen that shows sequence similarity to polygalacturonase.
inferredcites →https://doi.org/10.1126/science.227.4691.1229openalex-snapshot
A Simple and General Method for Transferring Genes into Plants
inferredcites →https://doi.org/10.1126/science.234.4778.856openalex-snapshot
Transient and Stable Expression of the Firefly Luciferase Gene in Plant Cells and Transgenic Plants
inferredcites →https://doi.org/10.3109/10520298509113905openalex-snapshot
Applications of Fluorochromes to Pollen Biology. I. Mithramycin and 4′,6-Diamidino-2-Phenylindole (Dapi) as Vital Stains and for Quantitation of Nuclear Dna
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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The Dynamic Shift in Mitochondria from Mature Pollen Grains
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Assessment and Detection of Gene Flow
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The Developmental Biology of Pollen
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Bee species visiting Medicago sativa differ in pollen deposition curves with consequences for gene flow
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An efficient and rapid transgenic pollen screening and detection method using flow cytometry
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Characterization of a Rice Pollen-Specific Gene and Its Expression
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Pollen Expressed Genes and Their Regulation
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RNA Interference of Plant MAPK Cascades for Functional Studies
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Visual Markers for Detecting Gene Conversion Directly in the Gametes of Arabidopsis thaliana
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Isolation and Analysis of mRNAs from Specific Cell Types of Plants by Ribosome Immunopurification
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Levels and Stability of Expression of Transgenes
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Plant Biotechnology: Transgenic Crops for the Third Millennium
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Mechanisms of Microspore Polarity and Differential Cell Fate Determination in Developing Pollen
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Genetic Control of Pollen Development and Function
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Function of Genetic Material: Activity of Genes in Transgenic Plants
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Gene Expression During Pollen Development
inferred← citeshttps://doi.org/10.1007/978-3-642-79133-8_24openalex-snapshot
Structure, Regulation and Function of the Osmotin Gene
inferred← citeshttps://doi.org/10.1007/978-94-009-0103-2_17openalex-snapshot
Transformation of tomato with Agrobacterium tumefaciens
inferred← citeshttps://doi.org/10.1007/978-94-009-0103-2_35openalex-snapshot
Transformation of pollen by particle bombardment
inferred← citeshttps://doi.org/10.1007/978-94-017-1669-7_17openalex-snapshot
Molecular and functional analysis of pollen-active genes
inferred← citeshttps://doi.org/10.1007/978-94-017-1669-7_19openalex-snapshot
Genetic and molecular dissection of male-fertility in higher plants
inferred← citeshttps://doi.org/10.1007/bf00022525openalex-snapshot
Molecular biology of male gametogenesis
inferred← citeshttps://doi.org/10.1007/bf00034950openalex-snapshot
Dissection of a pollen-specific promoter from maize by transient transformation assays
inferred← citeshttps://doi.org/10.1007/bf00228944openalex-snapshot
Deletion analysis of a tobacco pollen-specific polygalacturonase promoter
inferred← citeshttps://doi.org/10.1007/bf00230575openalex-snapshot
Abundance patterns of lily pollen cDNAs: characterization of three pollen-preferential cDNA clones
inferred← citeshttps://doi.org/10.1007/bf00230892openalex-snapshot
The expression of a potato (Solanum tuberosum) S-RNase gene in Nicotiana tabacum pollen
inferred← citeshttps://doi.org/10.1007/bf00231898openalex-snapshot
Activation and developmental regulation of an Arabidopsis anther-specific promoter in microspores and pollen of Nicotiana tabacum
inferred← citeshttps://doi.org/10.1007/bf00538697openalex-snapshot
Brassica anther-specific genes: characterization and in situ localization of expression
inferred← citeshttps://doi.org/10.1007/bf01280243openalex-snapshot
Diphtheria toxin-mediated cell ablation in developing pollen: Vegetative cell ablation blocks generative cell migration
inferred← citeshttps://doi.org/10.1007/bf01969115openalex-snapshot
Pollen viability and transgene expression following storage in honey
inferred← citeshttps://doi.org/10.1007/bf01977679openalex-snapshot
Tagging genomic sequences that direct transgene expression by activation of a promoter trap in plants
inferred← citeshttps://doi.org/10.1007/bf02152705openalex-snapshot
Unilateral incongruity in crosses involving Lycopersicon pennellii and L. esculentum is distinct from self-incompatibility in expression, timing and location
inferred← citeshttps://doi.org/10.1007/bf02522538openalex-snapshot
Pollen-specific expression of theArabidopsis thaliana α1-tubulin promoter assayed by β-glucuronidase, chloramphenicol acetyltransferase and diphtheria toxin reporter genespromoter assayed by β-glucuronidase, chloramphenicol acetyltransferase and diphtheria toxin reporter genes
inferred← citeshttps://doi.org/10.1007/bf02632056openalex-snapshot
Deletion analysis of pollen-expressed promoters
inferred← citeshttps://doi.org/10.1007/pl00009838openalex-snapshot
The MADS box gene ZmMADS2 is specifically expressed in maize pollen and during maize pollen tube growth
inferred← citeshttps://doi.org/10.1007/s00299-002-0487-3openalex-snapshot
Comparative study of promoter activity of three anther-specific genes encoding lipid transfer protein, xyloglucan endotransglucosylase/hydrolase and polygalacturonase in transgenic Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00299-005-0077-2openalex-snapshot
Molecular characterization of mature pollen-specific genes encoding novel small cysteine-rich proteins in rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1007/s00299-010-0839-3openalex-snapshot
Several cis-elements including a palindrome involved in pollen-specific activity of SBgLR promoter
inferred← citeshttps://doi.org/10.1007/s00299-011-1073-3openalex-snapshot
Isolation of a citrus promoter specific for reproductive organs and its functional analysis in isolated juice sacs and tomato
inferred← citeshttps://doi.org/10.1007/s00299-018-2256-yopenalex-snapshot
In silico identification and experimental validation of amino acid motifs required for the Rho-of-plants GTPase-mediated activation of receptor-like cytoplasmic kinases
inferred← citeshttps://doi.org/10.1007/s00299-019-02379-0openalex-snapshot
CRISPR/Cas-mediated gene targeting in plants: finally a turn for the better for homologous recombination
inferred← citeshttps://doi.org/10.1007/s00299-025-03508-8openalex-snapshot
A method for maintaining the release of co-suppression and maximally restoring the RDR6 expression
inferred← citeshttps://doi.org/10.1007/s00425-005-0131-xopenalex-snapshot
Silencing of the tobacco pollen pectin methylesterase NtPPME1 results in retarded in vivo pollen tube growth
inferred← citeshttps://doi.org/10.1007/s00425-007-0625-9openalex-snapshot
Functional characterization of the pollen-specific SBgLR promoter from potato (Solanum tuberosum L.)
inferred← citeshttps://doi.org/10.1007/s00497-006-0021-9openalex-snapshot
Imaging the actin cytoskeleton in growing pollen tubes
inferred← citeshttps://doi.org/10.1007/s00497-009-0114-3openalex-snapshot
Ectopic expression of S-RNase of Petunia inflata in pollen results in its sequestration and non-cytotoxic function
inferred← citeshttps://doi.org/10.1007/s00497-013-0211-1openalex-snapshot
Pollen tube entry into the synergid cell of Arabidopsis is observed at a site distinct from the filiform apparatus
inferred← citeshttps://doi.org/10.1007/s00497-013-0220-0openalex-snapshot
PsPMEP, a pollen-specific pectin methylesterase of pea (Pisum sativum L.)
inferred← citeshttps://doi.org/10.1007/s00497-013-0230-yopenalex-snapshot
Maize Male sterile 8 (Ms8), a putative β-1,3-galactosyltransferase, modulates cell division, expansion, and differentiation during early maize anther development
inferred← citeshttps://doi.org/10.1007/s00497-013-0238-3openalex-snapshot
Identification of the self-incompatibility locus F-box protein-containing complex in Petunia inflata
inferred← citeshttps://doi.org/10.1007/s00497-014-0247-xopenalex-snapshot
Brassinosteroids promote Arabidopsis pollen germination and growth
inferred← citeshttps://doi.org/10.1007/s00497-017-0317-yopenalex-snapshot
Calcium dynamics in tomato pollen tubes using the Yellow Cameleon 3.6 sensor
inferred← citeshttps://doi.org/10.1007/s004970000022openalex-snapshot
Regulation of LAT52 promoter activity during pollen tube growth through the pistil of Nicotiana alata .
inferred← citeshttps://doi.org/10.1007/s004970050108openalex-snapshot
Embryo sac development is affected in Petunia inflata plants transformed with an antisense gene encoding the extracellular domain of receptor kinase PRK1
inferred← citeshttps://doi.org/10.1007/s004970050161openalex-snapshot
Characterization of an anther-expressed protein kinase gene in the potato Solanum berthaultii and its antisense inhibition in transgenic plants
inferred← citeshttps://doi.org/10.1007/s004970050175openalex-snapshot
Pollen-expressed S-RNases are not involved in self-incompatibility in Lycopersicon peruvianum
inferred← citeshttps://doi.org/10.1007/s00709-003-0026-2openalex-snapshot
Imaging plant cells by two-photon excitation
inferred← citeshttps://doi.org/10.1007/s10142-012-0274-3openalex-snapshot
Expression dynamics of metabolic and regulatory components across stages of panicle and seed development in indica rice
inferred← citeshttps://doi.org/10.1007/s10529-012-1100-7openalex-snapshot
A 286 bp upstream regulatory region of a rice anther-specific gene, OSIPP3, confers pollen-specific expression in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s10535-012-0258-0openalex-snapshot
GmPOI gene encoding a Pollen_Ole_e_I conserved domain is involved in response of soybean to various stresses
inferred← citeshttps://doi.org/10.1007/s10535-013-0323-3openalex-snapshot
Arabidopsis LIM proteins PLIM2a and PLIM2b regulate actin configuration during pollen tube growth
inferred← citeshttps://doi.org/10.1007/s11033-010-0553-9openalex-snapshot
Functional analysis of a rice late pollen-abundant UDP-glucose pyrophosphorylase (OsUgp2) promoter
inferred← citeshttps://doi.org/10.1007/s11103-005-2859-xopenalex-snapshot
The Oryza sativa no pollen (Osnop) gene plays a role in male gametophyte development and most likely encodes a C2-GRAM domain-containing protein
inferred← citeshttps://doi.org/10.1007/s11103-006-0030-yopenalex-snapshot
Identification and characterization of PiORP1, a Petunia oxysterol-binding-protein related protein involved in receptor-kinase mediated signaling in pollen, and analysis of the ORP gene family in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s11103-010-9672-xopenalex-snapshot
Functional characterization of two chimeric proteins between a Petunia inflata S-locus F-box protein, PiSLF2, and a PiSLF-like protein, PiSLFLb-S2
inferred← citeshttps://doi.org/10.1007/s11103-011-9756-2openalex-snapshot
Transgene excision in pollen using a codon optimized serine resolvase CinH-RS2 site-specific recombination system
inferred← citeshttps://doi.org/10.1007/s11103-017-0678-5openalex-snapshot
Evolvement of transgenic male-sterility and fertility-restoration system in rice for production of hybrid varieties
inferred← citeshttps://doi.org/10.1007/s11105-012-0429-3openalex-snapshot
The OsGEX2 Gene Promoter Confers Sperm Cell Expression in Transgenic Rice
inferred← citeshttps://doi.org/10.1007/s11105-012-0458-yopenalex-snapshot
Characterization of a Novel Pollen-Specific Promoter from Wheat (Triticum Aestivum L.)
inferred← citeshttps://doi.org/10.1007/s11105-016-0977-zopenalex-snapshot
A Novel PhLRR Gene Promoter is Sufficient for Engineering Male Sterility in Petunia
inferred← citeshttps://doi.org/10.1007/s11248-012-9621-3openalex-snapshot
Spatial and temporal activity of upstream regulatory regions of rice anther-specific genes in transgenic rice and Arabidopsis
inferred← citeshttps://doi.org/10.1007/s11540-024-09783-4openalex-snapshot
Functional Studies of the Pollen-Specific Genes, StLAT52s in Potato
inferred← citeshttps://doi.org/10.1007/s11816-015-0365-4openalex-snapshot
Expression analysis of two rice pollen-specific promoters using homologous and heterologous systems
inferred← citeshttps://doi.org/10.1007/s11816-018-0501-zopenalex-snapshot
Identification and characterization of the promoter of a gene expressing mainly in the tapetum tissue of cotton (Gossypium hirsutum L.)
inferred← citeshttps://doi.org/10.1007/s12033-010-9347-5openalex-snapshot
Pollen-Specific Expression of Oryza sativa Indica Pollen Allergen Gene (OSIPA) Promoter in Rice and Arabidopsis Transgenic Systems
inferred← citeshttps://doi.org/10.1016/0168-9452(91)90281-copenalex-snapshot
The molecular biology of anther differentiation
inferred← citeshttps://doi.org/10.1016/0168-9452(94)90108-2openalex-snapshot
Methanol does not specifically inhibit endogenous β-glucuronidase (GUS) activity
inferred← citeshttps://doi.org/10.1016/0168-9452(95)04266-0openalex-snapshot
A novel transient assay system demonstrates that DT-Atsm is a temperature-sensitive toxin in plant tissues
inferred← citeshttps://doi.org/10.1016/0168-9525(91)90312-eopenalex-snapshot
Molecular analysis of male gametogenesis in plants
inferred← citeshttps://doi.org/10.1016/b978-0-12-405882-8.00015-5openalex-snapshot
Using Hyper as a Molecular Probe to Visualize Hydrogen Peroxide in Living Plant Cells
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Using Hyper as a molecular probe to visualize hydrogen peroxide in living plant cells: An updated method
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.112741openalex-snapshot
RLI2 regulates Arabidopsis female gametophyte and embryo development by facilitating the assembly of the translational machinery
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.116766openalex-snapshot
CELL DEATH1 safeguards microspore fate determination by repressing vacuole-executed programmed cell death
inferred← citeshttps://doi.org/10.1016/j.cub.2012.04.041openalex-snapshot
Gamete Fusion Is Required to Block Multiple Pollen Tubes from Entering an Arabidopsis Ovule
inferred← citeshttps://doi.org/10.1016/j.cub.2013.05.021openalex-snapshot
Three MYB Transcription Factors Control Pollen Tube Differentiation Required for Sperm Release
inferred← citeshttps://doi.org/10.1016/j.cub.2022.05.033openalex-snapshot
In vitro experiments and kinetic models of Arabidopsis pollen hydration mechanics show that MSL8 is not a simple tension-gated osmoregulator
inferred← citeshttps://doi.org/10.1016/j.cub.2024.12.037openalex-snapshot
The atypical proteome of mitochondria from mature pollen grains
inferred← citeshttps://doi.org/10.1016/j.devcel.2014.04.008openalex-snapshot
A Calcium Dialog Mediated by the FERONIA Signal Transduction Pathway Controls Plant Sperm Delivery
inferred← citeshttps://doi.org/10.1016/j.devcel.2018.07.014openalex-snapshot
Sequestration of a Transposon-Derived siRNA by a Target Mimic Imprinted Gene Induces Postzygotic Reproductive Isolation in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.devcel.2018.12.025openalex-snapshot
Dynamic Interactions of Plant CNGC Subunits and Calmodulins Drive Oscillatory Ca2+ Channel Activities
inferred← citeshttps://doi.org/10.1016/j.devcel.2021.02.030openalex-snapshot
Membrane receptor-mediated mechano-transduction maintains cell integrity during pollen tube growth within the pistil
inferred← citeshttps://doi.org/10.1016/j.gene.2023.147372openalex-snapshot
Ectopic expression of pigeonpea Orf147 gene imparts partial sterility in Cicer arietinum
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.134640openalex-snapshot
The MYC transcription factor PbrMYC8 negatively regulates PbrMSL5 expression to promote pollen germination in Pyrus
inferred← citeshttps://doi.org/10.1016/j.jgg.2014.02.001openalex-snapshot
Arabidopsis PTD Is Required for Type I Crossover Formation and Affects Recombination Frequency in Two Different Chromosomal Regions
inferred← citeshttps://doi.org/10.1016/j.jplph.2011.11.015openalex-snapshot
Actin bundler PLIM2s are involved in the regulation of pollen development and tube growth in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plantsci.2009.06.016openalex-snapshot
Tissue-specific expression in transgenic rice and Arabidopsis thaliana plants of GUS gene driven by the 5′ regulatory sequences of an anther specific rice gene YY2
inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111187openalex-snapshot
Genome-wide identification and functional characterization of OsLAT52 genes associated with pollen tube growth in rice (Oryza sativa)
inferred← citeshttps://doi.org/10.1016/j.tibtech.2009.09.008openalex-snapshot
Keeping the genie in the bottle: transgene biocontainment by excision in pollen
inferred← citeshttps://doi.org/10.1016/s0074-7696(08)61091-8openalex-snapshot
Pollen Gene Expression: Molecular Evidence
inferred← citeshttps://doi.org/10.1016/s0074-7696(08)61092-xopenalex-snapshot
Identification and in Situ Localization of Pollen-Specific Genes
inferred← citeshttps://doi.org/10.1016/s1016-8478(23)15086-2openalex-snapshot
BAN103, A Pollen-preferential Gene, from Chinese Cabbage and Its Promoter Activity
inferred← citeshttps://doi.org/10.1016/s1016-8478(23)17314-6openalex-snapshot
Subcellular Localization of Actin Depolymerizing Factor in Mature and Germinating Pollen
inferred← citeshttps://doi.org/10.1016/s1671-2927(08)60131-5openalex-snapshot
Effect of the Antisense BcMF12 Driven by the BcA9 Promoter on Gene Silencing in Brassica campestris L. ssp. chinensis
inferred← citeshttps://doi.org/10.1017/s096719940000143xopenalex-snapshot
Ultrastructural changes ofArabidopsis thalianapollen during final maturation and rehydration
inferred← citeshttps://doi.org/10.1023/a:1005812419151openalex-snapshot
Structure and specific expression of a Nicotiana sylvestris putative amino-acid transporter gene in mature and in vitro germinating pollen.
inferred← citeshttps://doi.org/10.1023/a:1005846527674openalex-snapshot
Analysis of microspore-specific promoters in transgenic tobacco
inferred← citeshttps://doi.org/10.1023/a:1005856531693openalex-snapshot
Identification of the tobacco and Arabidopsis homologues of the pollen-expressed LAT59 gene of tomato
inferred← citeshttps://doi.org/10.1023/a:1006095023050openalex-snapshot
Functional architecture of a late pollen promoter: pollen-specific transcription is developmentally regulated by multiple stage-specific and co-dependent activator elements
inferred← citeshttps://doi.org/10.1023/a:1006157603096openalex-snapshot
Isolation and characterization of an anther-specific gene, RA8, from rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1023/a:1008938728051openalex-snapshot
Green fluorescent protein (GFP) as a marker during pollen development
inferred← citeshttps://doi.org/10.1023/a:1009658614579openalex-snapshot
Agrobacterium tumefaciens-mediated transformation of cauliflower, Brassica oleracea var. botrytis
inferred← citeshttps://doi.org/10.1023/a:1010681129557openalex-snapshot
Pollen-specific regulation of vacuolar H+-PPase expression by multiple cis-acting elements
inferred← citeshttps://doi.org/10.1023/a:1010695226241openalex-snapshot
Functional analysis of cis-regulatory elements within the promoter of the tobacco late pollen gene g10
inferred← citeshttps://doi.org/10.1023/a:1013639528858openalex-snapshot
Identification of a S-ribonuclease-binding protein in Petunia hybrida
inferred← citeshttps://doi.org/10.1023/b:plan.0000004309.06973.16openalex-snapshot
Multiple conserved 5′ elements are required for high-level pollen expression of the Arabidopsis reproductive actin ACT1
inferred← citeshttps://doi.org/10.1034/j.1399-3054.1995.930305.xopenalex-snapshot
Analysis of gene regulation in growing pollen tubes of angiosperm and gymnosperm species using microprojectile bombardment
inferred← citeshttps://doi.org/10.1038/hortres.2014.47openalex-snapshot
Temporal and spatial control of gene expression in horticultural crops
inferred← citeshttps://doi.org/10.1038/ncomms5645openalex-snapshot
Male–female communication triggers calcium signatures during fertilization in Arabidopsis
inferred← citeshttps://doi.org/10.1038/nprot.2007.491openalex-snapshot
Fluorescent Arabidopsis tetrads: a visual assay for quickly developing large crossover and crossover interference data sets
inferred← citeshttps://doi.org/10.1038/s41467-021-22661-8openalex-snapshot
Persistent directional growth capability in Arabidopsis thaliana pollen tubes after nuclear elimination from the apex
inferred← citeshttps://doi.org/10.1038/s41477-020-00781-1openalex-snapshot
ARMADILLO REPEAT ONLY proteins confine Rho GTPase signalling to polar growth sites
inferred← citeshttps://doi.org/10.1038/s41477-021-00853-wopenalex-snapshot
Optogenetic control of plant growth by a microbial rhodopsin
inferred← citeshttps://doi.org/10.1038/s43586-022-00136-4openalex-snapshot
Optogenetics for light control of biological systems
inferred← citeshttps://doi.org/10.1038/s43586-022-00149-zopenalex-snapshot
Optogenetics for light control of biological systems
inferred← citeshttps://doi.org/10.1038/srep40279openalex-snapshot
Exocyst subunit SEC3A marks the germination site and is essential for pollen germination in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1038/srep42535openalex-snapshot
Dynamics of male meiotic recombination frequency during plant development using Fluorescent Tagged Lines in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1046/j.1365-313x.1998.00177.xopenalex-snapshot
Promoters of nuclear‐encoded respiratory chain Complex I genes from Arabidopsis thaliana contain a region essential for anther/pollen‐specific expression
inferred← citeshttps://doi.org/10.1046/j.1365-313x.1998.00304.xopenalex-snapshot
A GFP‐mouse talin fusion protein labels plant actin filamentsin vivoand visualizes the actin cytoskeleton in growing pollen tubes
inferred← citeshttps://doi.org/10.1046/j.1365-313x.2001.00939.xopenalex-snapshot
The MuDR transposon terminal inverted repeat contains a complex plant promoter directing distinct somatic and germinal programs
inferred← citeshttps://doi.org/10.1046/j.1420-9101.1995.8030265.xopenalex-snapshot
Multiple mating, sperm competition and meiotic drive
inferred← citeshttps://doi.org/10.1073/pnas.0608936104openalex-snapshot
Pollen tetrad-based visual assay for meiotic recombination in Arabidopsis
inferred← citeshttps://doi.org/10.1073/pnas.0705874104openalex-snapshot
A distinct mechanism regulating a pollen-specific guanine nucleotide exchange factor for the small GTPase Rop in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1073/pnas.1510854112openalex-snapshot
Intercellular communication in Arabidopsis thaliana pollen discovered via AHG3 transcript movement from the vegetative cell to sperm
inferred← citeshttps://doi.org/10.1073/pnas.92.26.12165openalex-snapshot
Pollen selection: a transgenic reconstruction approach.
inferred← citeshttps://doi.org/10.1073/pnas.92.6.2106openalex-snapshot
Bcp1, a gene required for male fertility in Arabidopsis.
inferred← citeshttps://doi.org/10.1073/pnas.93.21.11763openalex-snapshot
A cytoplasmic male sterility-associated mitochondrial protein causes pollen disruption in transgenic tobacco.
inferred← citeshttps://doi.org/10.1079/ivp2003477openalex-snapshot
Targeting transgene expression in research, agricultural, and environmental applications: Promoters used in plant transformation
inferred← citeshttps://doi.org/10.1080/07352689.2012.664986openalex-snapshot
Anthology of Anther/Pollen-Specific Promoters and Transcription Factors
inferred← citeshttps://doi.org/10.1080/15592324.2015.1075684openalex-snapshot
F-actin forms mobile and unwinding ring-shaped structures in germinatingArabidopsispollen expressing Lifeact
inferred← citeshttps://doi.org/10.1093/aobpla/plr016openalex-snapshot
The amino terminal F-box domain of Petunia inflata S-locus F-box protein is involved in the S-RNase-based self-incompatibility mechanism
inferred← citeshttps://doi.org/10.1093/hr/uhac048openalex-snapshot
Mitogen-activated protein kinase 4 is obligatory for late pollen and early fruit development in tomato
inferred← citeshttps://doi.org/10.1093/jexbot/49.326.1481openalex-snapshot
Antisense-mediated suppression of transgene expression targeted specifically to pollen
inferred← citeshttps://doi.org/10.1093/jexbot/50.338.1471openalex-snapshot
Gametophytic expression of GUS activity controlled by the potato Lhca3.St.1 promoter in tobacco pollen
inferred← citeshttps://doi.org/10.1093/jxb/48.2.265openalex-snapshot
Activities of CaMV 35S andnospromoters in pollen: implications for field release of transgenic plants
inferred← citeshttps://doi.org/10.1093/jxb/eraa367openalex-snapshot
The nuclear envelope protein KAKU4 determines the migration order of the vegetative nucleus and sperm cells in pollen tubes
inferred← citeshttps://doi.org/10.1093/jxb/erab419openalex-snapshot
Arabidopsis annexin 5 is involved in maintenance of pollen membrane integrity and permeability
inferred← citeshttps://doi.org/10.1093/jxb/erab525openalex-snapshot
Interactions between a mechanosensitive channel and cell wall integrity signaling influence pollen germination in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1093/jxb/erg044openalex-snapshot
Regulation of pollen tube growth by Rac-like GTPases
inferred← citeshttps://doi.org/10.1093/jxb/erg065openalex-snapshot
Cloning and characterization of two ripening-related strawberry (Fragariaxananassa cv. Chandler) pectate lyase genes
inferred← citeshttps://doi.org/10.1093/jxb/erp143openalex-snapshot
Overexpression of PwTUA1, a pollen-specific tubulin gene, increases pollen tube elongation by altering the distribution of -tubulin and promoting vesicle transport
inferred← citeshttps://doi.org/10.1093/jxb/err120openalex-snapshot
PwHAP5, a CCAAT-binding transcription factor, interacts with PwFKBP12 and plays a role in pollen tube growth orientation in Picea wilsonii
inferred← citeshttps://doi.org/10.1093/jxb/ert323openalex-snapshot
The juxtamembrane and carboxy-terminal domains of Arabidopsis PRK2 are critical for ROP-induced growth in pollen tubes
inferred← citeshttps://doi.org/10.1093/jxb/erv425openalex-snapshot
SUN anchors pollen WIP–WIT complexes at the vegetative nuclear envelope and is necessary for pollen tube targeting and fertility
inferred← citeshttps://doi.org/10.1093/mp/ssn026openalex-snapshot
The Dynamic Pollen Tube Cytoskeleton: Live Cell Studies Using Actin-Binding and Microtubule-Binding Reporter Proteins
inferred← citeshttps://doi.org/10.1093/mp/ssn032openalex-snapshot
Biochemical Models for S-RNase-Based Self-Incompatibility
inferred← citeshttps://doi.org/10.1093/mp/sst099openalex-snapshot
Microtubule Depolymerization Affects Endocytosis and Exocytosis in the Tip and Influences Endosome Movement in Tobacco Pollen Tubes
inferred← citeshttps://doi.org/10.1093/mp/sst155openalex-snapshot
Four Previously Identified Petunia inflata S-Locus F-Box Genes Are Involved in Pollen Specificity in Self-Incompatibility
inferred← citeshttps://doi.org/10.1093/mp/sst171openalex-snapshot
Annexin5 Is Essential for Pollen Development in Arabidopsis
inferred← citeshttps://doi.org/10.1093/pcp/41.6.757openalex-snapshot
Expression of Bra r 1 Gene in Transgenic Tobacco and Bra r 1 Promoter Activity in Pollen of Various Plant Species
inferred← citeshttps://doi.org/10.1093/pcp/pci075openalex-snapshot
Transcriptional Activity of Male Gamete-specific Histone gcH3 Promoter in Sperm Cells of Lilium longiflorum
inferred← citeshttps://doi.org/10.1093/pcp/pcn084openalex-snapshot
Mitochondrial Dynamics in Plant Male Gametophyte Visualized by Fluorescent Live Imaging
inferred← citeshttps://doi.org/10.1093/pcp/pcp042openalex-snapshot
Visualization of Plastids in Pollen Grains: Involvement of FtsZ1 in Pollen Plastid Division
inferred← citeshttps://doi.org/10.1093/pcp/pcq068openalex-snapshot
The Arabidopsis FLAKY POLLEN1 Gene Encodes a 3-Hydroxy-3-Methylglutaryl-Coenzyme A Synthase Required for Development of Tapetum-Specific Organelles and Fertility of Pollen Grains
inferred← citeshttps://doi.org/10.1093/pcp/pcs166openalex-snapshot
A Cystathionine-β-Synthase Domain-Containing Protein, CBSX2, Regulates Endothecial Secondary Cell Wall Thickening in Anther Development
inferred← citeshttps://doi.org/10.1093/pcp/pcu018openalex-snapshot
Multiple BiP Genes of Arabidopsis thaliana are Required for Male Gametogenesis and Pollen Competitiveness
inferred← citeshttps://doi.org/10.1093/pcp/pcw152openalex-snapshot
Cullin1-P is an Essential Component of Non-Self Recognition System in Self-Incompatibility inPetunia
inferred← citeshttps://doi.org/10.1093/pcp/pcx176openalex-snapshot
Use of Domain-Swapping to Identify Candidate Amino Acids Involved in Differential Interactions between Two Allelic Variants of Type-1 S-Locus F-Box Protein and S3-RNase in Petunia inflata
inferred← citeshttps://doi.org/10.1093/pcp/pcz036openalex-snapshot
Plant AP180 N-Terminal Homolog Proteins Are Involved in Clathrin-Dependent Endocytosis during Pollen Tube Growth in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1093/plcell/koaa035openalex-snapshot
Plasma membrane nano-organization specifies phosphoinositide effects on Rho-GTPases and actin dynamics in tobacco pollen tubes
inferred← citeshttps://doi.org/10.1093/plcell/koac357openalex-snapshot
Analyses of Cullin1 homologs reveal functional redundancy in S-RNase-based self-incompatibility and evolutionary relationships in eudicots
inferred← citeshttps://doi.org/10.1093/plphys/kiae558openalex-snapshot
Plasma membrane and cytoplasmic compartmentalization: A dynamic structural framework required for pollen tube tip growth
inferred← citeshttps://doi.org/10.1093/plphys/kiag198openalex-snapshot
Kinase partner zinc-finger protein modulates pollen tube growth by influencing tip vesicle trafficking
inferred← citeshttps://doi.org/10.1093/plphys/kiag569openalex-snapshot
AcoPMEI acts as a dual-function effector that promotes pollen tube growth and buffers against pistil-derived inhibition in pineapple
inferred← citeshttps://doi.org/10.1101/2021.03.02.433530openalex-snapshot
Arabidopsis annexin 5 controls plasma membrane properties in mature pollen grains
inferred← citeshttps://doi.org/10.1101/2021.10.19.464977openalex-snapshot
In vitro experiments and kinetic models of pollen hydration show that MSL8 is not a simple tension-gated osmoregulator
inferred← citeshttps://doi.org/10.1101/gad.1882810openalex-snapshot
Proper regulation of a sperm-specific cis-nat-siRNA is essential for double fertilization in Arabidopsis
inferred← citeshttps://doi.org/10.1101/gad.5.3.496openalex-snapshot
Promoter analysis of genes that are coordinately expressed during pollen development reveals pollen-specific enhancer sequences and shared regulatory elements.
inferred← citeshttps://doi.org/10.1101/gad.852200openalex-snapshot
Arabidopsis NAC1 transduces auxin signal downstream of TIR1 to promote lateral root development
inferred← citeshttps://doi.org/10.1104/pp.104.054213openalex-snapshot
Green Sperm. Identification of Male Gamete Promoters in Arabidopsis
inferred← citeshttps://doi.org/10.1104/pp.105.059865openalex-snapshot
Pectin Methylesterase, a Regulator of Pollen Tube Growth
inferred← citeshttps://doi.org/10.1104/pp.106.1.25openalex-snapshot
The S-Ribonuclease Gene of Petunia hybrida Is Expressed in Nonstylar Tissue, Including Immature Anthers
inferred← citeshttps://doi.org/10.1104/pp.108.127936openalex-snapshot
A Pollen Protein, NaPCCP, That Binds Pistil Arabinogalactan Proteins Also Binds Phosphatidylinositol 3-Phosphate and Associates with the Pollen Tube Endomembrane System
inferred← citeshttps://doi.org/10.1104/pp.109.1.73openalex-snapshot
Transgenic Analysis of a Hybrid Poplar Wound-Inducible Promoter Reveals Developmental Patterns of Expression Similar to That of Storage Protein Genes
inferred← citeshttps://doi.org/10.1104/pp.112.208611openalex-snapshot
Production of Diploid Male Gametes in Arabidopsis by Cold-Induced Destabilization of Postmeiotic Radial Microtubule Arrays
inferred← citeshttps://doi.org/10.1104/pp.113.231274openalex-snapshot
Two Mitogen-Activated Protein Kinases, MPK3 and MPK6, Are Required for Funicular Guidance of Pollen Tubes in Arabidopsis
inferred← citeshttps://doi.org/10.1104/pp.123.3.895openalex-snapshot
Female Reproductive Tissues Are the Primary Target ofAgrobacterium-Mediated Transformation by the Arabidopsis Floral-Dip Method
inferred← citeshttps://doi.org/10.1104/pp.126.4.1480openalex-snapshot
Isolation and Characterization of Kinase Interacting Protein 1, a Pollen Protein That Interacts with the Kinase Domain of PRK1, a Receptor-Like Kinase of Petunia
inferred← citeshttps://doi.org/10.1104/pp.15.00437openalex-snapshot
Elevation of Pollen Mitochondrial DNA Copy Number by WHIRLY2: Altered Respiration and Pollen Tube Growth in Arabidopsis
inferred← citeshttps://doi.org/10.1104/pp.20.00380openalex-snapshot
Quantitative Structural Organization of Bulk Apical Membrane Traffic in Pollen Tubes
inferred← citeshttps://doi.org/10.1104/pp.20.01081openalex-snapshot
Kinase Partner Protein Plays a Key Role in Controlling the Speed and Shape of Pollen Tube Growth in Tomato
inferred← citeshttps://doi.org/10.1105/tpc.003038openalex-snapshot
The Regulation of Actin Organization by Actin-Depolymerizing Factor in Elongating Pollen Tubes[W]
inferred← citeshttps://doi.org/10.1105/tpc.003103openalex-snapshot
A Cysteine-Rich Extracellular Protein, LAT52, Interacts with the Extracellular Domain of the Pollen Receptor Kinase LePRK2[W]
inferred← citeshttps://doi.org/10.1105/tpc.005702openalex-snapshot
A Tumor Suppressor Homolog, AtPTEN1, Is Essential for Pollen Development in Arabidopsis
inferred← citeshttps://doi.org/10.1105/tpc.007153openalex-snapshot
Actin-Depolymerizing Factor Mediates Rac/Rop GTPase–Regulated Pollen Tube Growth
inferred← citeshttps://doi.org/10.1105/tpc.016550openalex-snapshot
Overexpression of an Arabidopsis Formin Stimulates Supernumerary Actin Cable Formation from Pollen Tube Cell Membrane[W]
inferred← citeshttps://doi.org/10.1105/tpc.10.10.1677openalex-snapshot
The Arabidopsis DIMINUTO/DWARF1 Gene Encodes a Protein Involved in Steroid Synthesis
inferred← citeshttps://doi.org/10.1105/tpc.10.3.319openalex-snapshot
Pollen Tube Localization Implies a Role in Pollen–Pistil Interactions for the Tomato Receptor-like Protein Kinases LePRK1 and LePRK2
inferred← citeshttps://doi.org/10.1105/tpc.105.033183openalex-snapshot
Rab11 GTPase-Regulated Membrane Trafficking Is Crucial for Tip-Focused Pollen Tube Growth in Tobacco
inferred← citeshttps://doi.org/10.1105/tpc.105.037135openalex-snapshot
Calcium-Dependent Protein Kinase Isoforms inPetuniaHave Distinct Functions in Pollen Tube Growth, Including Regulating Polarity
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