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Gametophyte interaction and sexual reproduction: how plants make a zygote
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1097-0169(1997)36:4<323::aid-cm3>3.0.co;2-6openalex-snapshot
Characterization and localization of profilin in pollen grains and tubes ofLilium longiflorum
inferredcites →https://doi.org/10.1002/1521-1878(200101)23:1<86::aid-bies1011>3.0.co;2-dopenalex-snapshot
Cellular oscillations and the regulation of growth: the pollen tube paradigm
inferredcites →https://doi.org/10.1002/1521-1878(200101)23:1<86::aid-bies1011>3.3.co;2-4openalex-snapshot
Cellular oscillations and the regulation of growth: the pollen tube paradigm
inferredcites →https://doi.org/10.1002/j.1460-2075.1994.tb06596.xopenalex-snapshot
Female sterile tobacco plants are produced by stigma‐specific cell ablation.
inferredcites →https://doi.org/10.1002/j.1537-2197.1963.tb06564.xopenalex-snapshot
THE ESSENTIAL ROLE OF CALCIUM ION IN POLLEN GERMINATION AND POLLEN TUBE GROWTH
inferredcites →https://doi.org/10.1002/j.1537-2197.1986.tb09702.xopenalex-snapshot
STIGMA OF NICOTIANA: ULTRASTRUCTURAL AND BIOCHEMICAL STUDIES
inferredcites →https://doi.org/10.1002/j.1537-2197.1987.tb08759.xopenalex-snapshot
INDUCED POLLEN TUBE DIRECTIONALITY
inferredcites →https://doi.org/10.1006/anbo.1999.1031openalex-snapshot
Cysteine-rich Pollen Coat Proteins (PCPs) and their Interactions with StigmaticS (Incompatibility) and S -Related Proteins in Brassica: Putative Roles in SI and Pollination
inferredcites →https://doi.org/10.1006/anbo.1999.1065openalex-snapshot
Signalling and the Cytoskeleton of Pollen Tubes of Papaver rhoeas
inferredcites →https://doi.org/10.1006/anbo.1999.1066openalex-snapshot
Dissecting Arabidopsis Pollen?Stigma Interactions Reveals Novel Mechanisms that Confer Mating Specificity
inferredcites →https://doi.org/10.1006/dbio.1993.1022openalex-snapshot
Promiscuous Germination and Growth of Wildtype Pollen from Arabidopsis and Related Species on the Shoot of the Arabidopsis Mutant, fiddlehead
inferredcites →https://doi.org/10.1006/dbio.1996.0060openalex-snapshot
Tip-Localized Calcium Entry Fluctuates during Pollen Tube Growth
inferredcites →https://doi.org/10.1006/dbio.1997.8671openalex-snapshot
Developmental Regulation of Cell Interactions in theArabidopsis fiddlehead-1Mutant: A Role for the Epidermal Cell Wall and Cuticle
inferredcites →https://doi.org/10.1007/978-1-4612-2958-2_38openalex-snapshot
The Extracellular Matrix in Pollen Tube Growth
inferredcites →https://doi.org/10.1007/978-3-642-69299-4_24openalex-snapshot
Pollen-Pistil Interactions
inferredcites →https://doi.org/10.1007/bf00039616openalex-snapshot
Molecular cloning and characterization of anther-preferential cDNA encoding a putative actin-depolymerizing factor
inferredcites →https://doi.org/10.1007/bf00041387openalex-snapshot
PO149, a new member of pollen pectate lyase-like gene family from alfalfa
inferredcites →https://doi.org/10.1007/bf00043881openalex-snapshot
Characterization of a pollen-expressed gene encoding a putative pectin esterase ofPetunia inflata
inferredcites →https://doi.org/10.1007/bf00047713openalex-snapshot
Characterization of a pollen-specific cDNA clone from Nicotiana tabacum expressed during microgametogenesis and germination
inferredcites →https://doi.org/10.1007/bf00194875openalex-snapshot
Synergid degeneration in Nicotiana: a quantitative, fluorochromatic and chlorotetracycline study
inferredcites →https://doi.org/10.1007/bf00196566openalex-snapshot
Localization of pectins and arabinogalactan-proteins in lily (Lilium longiflorum L.) pollen tube and style, and their possible roles in pollination
inferredcites →https://doi.org/10.1007/bf00201397openalex-snapshot
A 7-kDa pollen coating-borne peptide from Brassica napus interacts with S-locus glycoprotein and S-locus-related glycoprotein
inferredcites →https://doi.org/10.1007/bf00201816openalex-snapshot
Identification and localization of an active cutinase in the pollen of Brassica napus L.
inferredcites →https://doi.org/10.1007/bf00277069openalex-snapshot
Partial characterization of the Nicotiana tabacum actin gene family: Evidence for pollen-specific expression of one of the gene family members
inferredcites →https://doi.org/10.1007/bf00385991openalex-snapshot
Germination and early tube development in vitro of Lycopersicum peruvianum pollen: Ultrastructural features
inferredcites →https://doi.org/10.1007/bf00714557openalex-snapshot
Chemotropic responses by pearl millet pollen tubes
inferredcites →https://doi.org/10.1007/bf01101679openalex-snapshot
Fertilization inNicotiana tabacum: Cytoskeletal modifications in the embryo sac during synergid degeneration
inferredcites →https://doi.org/10.1007/bf01279191openalex-snapshot
Actin microfilaments do not form a dense meshwork inLilium longiflorum pollen tube tips
inferredcites →https://doi.org/10.1007/bf01280244openalex-snapshot
Ion dynamics and its possible role during in vitro pollen germination and tube growth
inferredcites →https://doi.org/10.1007/bf01280289openalex-snapshot
Immunogold localization of arabinogalactan proteins, unesterified and esterified pectins in pollen grains and pollen tubes ofNicotiana tabacum L.
inferredcites →https://doi.org/10.1007/bf01282125openalex-snapshot
The turgor pressure of growing lily pollen tubes
inferredcites →https://doi.org/10.1007/bf01360732openalex-snapshot
Microtubules are involved in maintaining the cellular polarity in pollen tubes ofNicotiana sylvestris
inferredcites →https://doi.org/10.1007/bf01403385openalex-snapshot
Ultrastructure of freeze-substituted pollen tubes ofLilium longiflorum
inferredcites →https://doi.org/10.1007/bf02152699openalex-snapshot
Actin and tubulin expression and isotype pattern during tobacco pollen tube growth
inferredcites →https://doi.org/10.1007/bf02153052openalex-snapshot
Cytoplasmic motors and pollen tube growth
inferredcites →https://doi.org/10.1007/bf02441951openalex-snapshot
The pollen tupe growth pathway: its molecular and biochemical contributions and responses to pollination
inferredcites →https://doi.org/10.1007/bf02441953openalex-snapshot
Pistil strategies controlling pollen tube growth
inferredcites →https://doi.org/10.1007/bf02860839openalex-snapshot
The biochemistry of angiosperm pollen development
inferredcites →https://doi.org/10.1007/pl00000784openalex-snapshot
Arabinogalactan-proteins: structure, expression and function
inferredcites →https://doi.org/10.1007/pl00009837openalex-snapshot
Calcium changes in ovules and embryo sacs of Plumbago zeylanica L.
inferredcites →https://doi.org/10.1007/s00050170openalex-snapshot
Kinetics of double fertilization in Torenia fournieri based on direct observations of the naked embryo sac
inferredcites →https://doi.org/10.1007/s00425-003-1174-5openalex-snapshot
Profilin inhibits pollen tube growth through actin-binding, but not poly-l-proline-binding
inferredcites →https://doi.org/10.1007/s004250000370openalex-snapshot
Peptide growth factor phytosulfokine-α contributes to the pollen population effect
inferredcites →https://doi.org/10.1007/s004250050279openalex-snapshot
Effects of Yariv phenylglycoside on cell wall assembly in the lily pollen tube
inferredcites →https://doi.org/10.1007/s004250050348openalex-snapshot
Genetic control of male fertility in Arabidopsis thaliana : structural analyses of postmeiotic developmental mutants
inferredcites →https://doi.org/10.1007/s004250050421openalex-snapshot
Location of cellulose and callose in pollen tubes and grains of Nicotiana tabacum
inferredcites →https://doi.org/10.1007/s004250050676openalex-snapshot
Late steps of egg cell differentiation are accelerated by pollination in Zea mays L.
inferredcites →https://doi.org/10.1007/s004250100664openalex-snapshot
Detection and localization of pectin methylesterase isoforms in pollen tubes of Nicotiana tabacum L.
inferredcites →https://doi.org/10.1007/s00497-003-0179-3openalex-snapshot
A functional study of stylar hydroxyproline-rich glycoproteins during pollen tube growth
inferredcites →https://doi.org/10.1007/s00497-003-0196-2openalex-snapshot
The PELPIII glycoproteins in Solanaceae: stylar expression and transfer into pollen tube walls
inferredcites →https://doi.org/10.1007/s00497-004-0210-3openalex-snapshot
The local cytomechanical properties of growing pollen tubes correspond to the axial distribution of structural cellular elements
inferredcites →https://doi.org/10.1007/s004970000062openalex-snapshot
Expression of a polygalacturonase enzyme in germinating pollen of Brassica napus
inferredcites →https://doi.org/10.1007/s004970050085openalex-snapshot
Adhesion of lily pollen tubes on an artificial matrix
inferredcites →https://doi.org/10.1007/s004970050091openalex-snapshot
Involvement of SLR1 genes in pollen adhesion to the stigmatic surface in Brassicaceae
inferredcites →https://doi.org/10.1007/s004970050122openalex-snapshot
Biogenesis and function of the lipidic structures of pollen grains
inferredcites →https://doi.org/10.1007/s004970050195openalex-snapshot
The pollen-specific gene Ntp303 encodes a 69-kDa glycoprotein associated with the vegetative membranes and the cell wall
inferredcites →https://doi.org/10.1007/s004970100091openalex-snapshot
Pollen and pistil in the progamic phase
inferredcites →https://doi.org/10.1007/s004970100093openalex-snapshot
Ion dynamics and hydrodynamics in the regulation of pollen tube growth
inferredcites →https://doi.org/10.1007/s00709-003-0026-2openalex-snapshot
Imaging plant cells by two-photon excitation
inferredcites →https://doi.org/10.1007/s007090200009openalex-snapshot
Arabinogalactan proteins, pollen tube growth, and the reversible effects of Yariv phenylglycoside
inferredcites →https://doi.org/10.1016/0012-1606(91)90278-bopenalex-snapshot
A cytoplasmic gradient of Ca2+ is correlated with the growth of lily pollen tubes
inferredcites →https://doi.org/10.1016/0012-1606(92)90088-xopenalex-snapshot
Roles for the extracellular matrix in plant development and pollination: A special case of cell movement in plants
inferredcites →https://doi.org/10.1016/0092-8674(95)90427-1openalex-snapshot
A floral transmitting tissue-specific glycoprotein attracts pollen tubes and stimulates their growth
inferredcites →https://doi.org/10.1016/0092-8674(95)90428-xopenalex-snapshot
A pollen tube growth stimulatory glycoprotein is deglycosylated by pollen tubes and displays a glycosylation gradient in the flower
inferredcites →https://doi.org/10.1016/0168-9452(94)90184-8openalex-snapshot
In vitro pollination and fertilisation in maize (Zea mays L.): technical procedures and prospects for the dissection of the double fertilisation process
inferredcites →https://doi.org/10.1016/0168-9525(92)90166-2openalex-snapshot
The S locus of flowering plants: when self-rejection is self-interest
inferredcites →https://doi.org/10.1016/0168-9525(92)90299-jopenalex-snapshot
The S locus of flowering plants: when self-rejection is self-interest
inferredcites →https://doi.org/10.1016/1369-5266(88)80007-4openalex-snapshot
Maternal control of embryogenesis by MEDEA, a polycomb group gene in Arabidopsis,
inferredcites →https://doi.org/10.1016/s0022-5320(80)90105-7openalex-snapshot
Cytological zonation of Prunus avium L. pollen tubes in Vivo
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)61094-3openalex-snapshot
Cytoskeleton and Cytoplasmic Organization of Pollen and Pollen Tubes
inferredcites →https://doi.org/10.1016/s0074-7696(08)61610-1openalex-snapshot
Functional Interactions among Cytoskeleton, Membranes, and Cell Wall in the Pollen Tube of Flowering Plants
inferredcites →https://doi.org/10.1016/s0092-8674(02)00807-3openalex-snapshot
DEMETER, a DNA Glycosylase Domain Protein, Is Required for Endosperm Gene Imprinting and Seed Viability in Arabidopsis
inferredcites →https://doi.org/10.1016/s0092-8674(03)00479-3openalex-snapshot
Pollen Tube Growth and Guidance Is Regulated by POP2, an Arabidopsis Gene that Controls GABA Levels
inferredcites →https://doi.org/10.1016/s0764-4469(01)01326-9openalex-snapshot
Developmental and evolutionary hypotheses for the origin of double fertilization and endosperm
inferredcites →https://doi.org/10.1016/s0960-9822(03)00093-9openalex-snapshot
Female Control of Male Gamete Delivery during Fertilization in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/s1360-1385(00)01654-xopenalex-snapshot
The Rop GTPase switch turns on polar growth in pollen
inferredcites →https://doi.org/10.1016/s1360-1385(01)02148-3openalex-snapshot
Peptide signals and their receptors in higher plants
inferredcites →https://doi.org/10.1016/s1360-1385(01)02194-xopenalex-snapshot
Peptides: new signalling molecules in plants
inferredcites →https://doi.org/10.1016/s1360-1385(96)80028-8openalex-snapshot
Pollen—pistil interactions during pollen-tube growth
inferredcites →https://doi.org/10.1016/s1360-1385(98)01353-3openalex-snapshot
Epidermal cell interactions: a case for local talk
inferredcites →https://doi.org/10.1016/s1360-1385(99)01473-9openalex-snapshot
Whither chemotropism and pollen tube guidance?
inferredcites →https://doi.org/10.1016/s1369-5266(00)80002-3openalex-snapshot
The male determinant of self-incompatibility in Brassica
inferredcites →https://doi.org/10.1016/s1369-5266(02)00010-9openalex-snapshot
Pollen-tube guidance: beacons from the female gametophyte
inferredcites →https://doi.org/10.1016/s1369-5266(99)00017-5openalex-snapshot
Signaling in pollination
inferredcites →https://doi.org/10.1017/s0967199400001404openalex-snapshot
Cytoskeletal organisation and modification during pollen tube arrival, gamete delivery and fertilisation inPlumbago zeylanica
inferredcites →https://doi.org/10.1023/a:1005741514764openalex-snapshot
The Arabidopsis ACT11 actin gene is strongly expressed in tissues of the emerging inflorescence, pollen, and developing ovules
inferredcites →https://doi.org/10.1023/a:1005828325425openalex-snapshot
Expression in anthers of two genes encoding Brassica oleracea transmembrane channel proteins
inferredcites →https://doi.org/10.1023/a:1006428007826openalex-snapshot
The Brassica MIP-MOD gene encodes a functional water channel that is expressed in the stigma epidermis
inferredcites →https://doi.org/10.1023/a:1010659425399openalex-snapshot
A leucine-rich repeat region is conserved in pollen extensin-like (Pex) proteins in monocots and dicots
inferredcites →https://doi.org/10.1023/a:1016050018779openalex-snapshot
An F-box gene linked to the self-incompatibility (S) locus of Antirrhinum is expressed specifically in pollen and tapetum
inferredcites →https://doi.org/10.1023/a:1016077014583openalex-snapshot
New pollen-specific receptor kinases identified in tomato, maize and Arabidopsis: the tomato kinases show overlapping but distinct localization patterns on pollen tubes
inferredcites →https://doi.org/10.1023/a:1021139502947openalex-snapshot
Expression studies of SCA in lily and confirmation of its role in pollen tube adhesion
inferredcites →https://doi.org/10.1023/a:1021236307508openalex-snapshot
The plant cytoskeleton: recent advances in the study of the plant microtubule-associated proteins MAP-65, MAP-190 and the Xenopus MAP215-like protein, MOR1
inferredcites →https://doi.org/10.1023/b:plan.0000009269.97773.70openalex-snapshot
A novel male-sterile mutant of Arabidopsis thaliana, faceless pollen-1, produces pollen with a smooth surface and an acetolysis-sensitive exine
inferredcites →https://doi.org/10.1038/33929openalex-snapshot
Lipids are required for directional pollen-tube growth
inferredcites →https://doi.org/10.1038/35036623openalex-snapshot
S-RNase uptake by compatible pollen tubes in gametophytic self-incompatibility
inferredcites →https://doi.org/10.1038/35097104openalex-snapshot
Direct ligand–receptor complex interaction controls Brassica self-incompatibility
inferredcites →https://doi.org/10.1038/nature02523openalex-snapshot
Identification of the pollen determinant of S-RNase-mediated self-incompatibility
inferredcites →https://doi.org/10.1038/ncb1201-1120openalex-snapshot
Differential contribution of cytoplasmic Ca2+ and Ca2+ influx to gamete fusion and egg activation in maize
inferredcites →https://doi.org/10.1046/j.0016-8025.2001.00791.xopenalex-snapshot
Plant aquaporins: multifunctional water and solute channels with expanding roles
inferredcites →https://doi.org/10.1046/j.0028-646x.2001.00229.xopenalex-snapshot
The molecular and genetic basis of pollen–pistil interactions
inferredcites →https://doi.org/10.1046/j.1365-2443.2003.00626.xopenalex-snapshot
Comparative analysis of the self‐incompatibility (S‐) locus region of Prunus mume: identification of a pollen‐expressed F‐box gene with allelic diversity
inferredcites →https://doi.org/10.1046/j.1365-3040.2002.00827.xopenalex-snapshot
Water‐conducting properties of lipids during pollen hydration
inferredcites →https://doi.org/10.1046/j.1365-313x.1993.04040631.xopenalex-snapshot
The profilin multigene family of maize: differential expression of three isoforms
inferredcites →https://doi.org/10.1046/j.1365-313x.1995.08050703.xopenalex-snapshot
Identification of genes required for pollen‐stigma recognition in Arabidopsis thaliana
inferredcites →https://doi.org/10.1046/j.1365-313x.1996.10010107.xopenalex-snapshot
Strong, constitutive expression of the Arabidopsis ACT2/ACT8 actin subclass in vegetative tissues
inferredcites →https://doi.org/10.1046/j.1365-313x.1996.10020189.xopenalex-snapshot
The Arabidopsis thaliana ACT4/ACT12 actin gene subclass is strongly expressed throughout pollen development
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00054.xopenalex-snapshot
Re‐evaluation of the role of a transmitting tract‐specific glycoprotein on pollen tube growth
inferredcites →https://doi.org/10.1046/j.1365-313x.1999.00487.xopenalex-snapshot
The late pollen‐specific actins in angiosperms
inferredcites →https://doi.org/10.1046/j.1365-313x.2000.00731.xopenalex-snapshot
A pollen tube growth‐promoting arabinogalactan protein from Nicotiana alata is similar to the tobacco TTS protein
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.00954.xopenalex-snapshot
Interaction of pollen-specific actin-depolymerizing factor with actin
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01219.xopenalex-snapshot
Involvement of extracellular calcium influx in the self‐incompatibility response of Papaver rhoeas
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01305.xopenalex-snapshot
Fertilization in Arabidopsis thaliana wild type: Developmental stages and time course
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01692.xopenalex-snapshot
Double fertilization in maize: the two male gametes from a pollen grain have the ability to fuse with egg cells
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01933.xopenalex-snapshot
KINKY POLLEN encodes a SABRE‐like protein required for tip growth in Arabidopsis and conserved among eukaryotes
inferredcites →https://doi.org/10.1046/j.1469-8137.2003.00846.xopenalex-snapshot
Some reflections on double fertilization, from its discovery to the present
inferredcites →https://doi.org/10.1046/j.1469-8137.2003.00847.xopenalex-snapshot
Control of pollen tube growth: role of ion gradients and fluxes
inferredcites →https://doi.org/10.1073/pnas.0305448101openalex-snapshot
Comparisons of pollen coat genes across Brassicaceae species reveal rapid evolution by repeat expansion and diversification
inferredcites →https://doi.org/10.1073/pnas.0401542101openalex-snapshot
A plant plasma membrane Ca 2+ pump is required for normal pollen tube growth and fertilization
inferredcites →https://doi.org/10.1073/pnas.040580797openalex-snapshot
Isolation and characterization of pollen coat proteins of Brassica campestris that interact with S locus-related glycoprotein 1 involved in pollen-stigma adhesion
inferredcites →https://doi.org/10.1073/pnas.0631728100openalex-snapshot
The receptor kinases LePRK1 and LePRK2 associate in pollen and when expressed in yeast, but dissociate in the presence of style extract
inferredcites →https://doi.org/10.1073/pnas.180243697openalex-snapshot
A calcium influx is triggered and propagates in the zygote as a wavefront during in vitro fertilization of flowering plants
inferredcites →https://doi.org/10.1073/pnas.2533800100openalex-snapshot
Chemocyanin, a small basic protein from the lily stigma, induces pollen tube chemotropism
inferredcites →https://doi.org/10.1073/pnas.82.18.6129openalex-snapshot
Preferential fertilization in Plumbago : Ultrastructural evidence for gamete-level recognition in an angiosperm
inferredcites →https://doi.org/10.1073/pnas.90.2.467openalex-snapshot
Interaction between a coating-borne peptide of the Brassica pollen grain and stigmatic S (self-incompatibility)-locus-specific glycoproteins.
inferredcites →https://doi.org/10.1073/pnas.92.8.3086openalex-snapshot
Pex1, a pollen-specific gene with an extensin-like domain.
inferredcites →https://doi.org/10.1073/pnas.92.9.3913openalex-snapshot
Organismal duplication, inclusive fitness theory, and altruism: understanding the evolution of endosperm and the angiosperm reproductive syndrome.
inferredcites →https://doi.org/10.1073/pnas.93.11.5319openalex-snapshot
A mutation that allows endosperm development without fertilization.
inferredcites →https://doi.org/10.1073/pnas.93.14.7415openalex-snapshot
Pollen specific expression of maize genes encoding actin depolymerizing factor-like proteins.
inferredcites →https://doi.org/10.1073/pnas.93.22.12059openalex-snapshot
How flowering plants discriminate between self and non-self pollen to prevent inbreeding.
inferredcites →https://doi.org/10.1073/pnas.94.12.6559openalex-snapshot
Group I allergens of grass pollen as cell wall-loosening agents
inferredcites →https://doi.org/10.1073/pnas.94.8.4223openalex-snapshot
Fertilization-independent seed development in Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.96.1.296openalex-snapshot
Genes controlling fertilization-independent seed development in Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.96.7.4186openalex-snapshot
Control of fertilization-independent endosperm development by the MEDEA polycomb gene in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.97.3.1311openalex-snapshot
FIDDLEHEAD , a gene required to suppress epidermal cell interactions in Arabidopsis , encodes a putative lipid biosynthetic enzyme
inferredcites →https://doi.org/10.1083/jcb.144.3.483openalex-snapshot
Growing Pollen Tubes Possess a Constitutive Alkaline Band in the Clear Zone and a Growth-dependent Acidic Tip
inferredcites →https://doi.org/10.1083/jcb.145.2.317openalex-snapshot
Rac Homologues and Compartmentalized Phosphatidylinositol 4, 5-Bisphosphate Act in a Common Pathway to Regulate Polar Pollen Tube Growth
inferredcites →https://doi.org/10.1083/jcb.152.5.1019openalex-snapshot
ROP Gtpase–Dependent Dynamics of Tip-Localized F-Actin Controls Tip Growth in Pollen Tubes
inferredcites →https://doi.org/10.1091/mbc.12.8.2534openalex-snapshot
Actin Polymerization Is Essential for Pollen Tube Growth
inferredcites →https://doi.org/10.1093/genetics/145.4.1109openalex-snapshot
Interactions Among Genes Regulating Ovule Development in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/genetics/149.2.607openalex-snapshot
Genetic Analysis of Organ Fusion in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/genetics/158.4.1773openalex-snapshot
Five Gametophytic Mutations Affecting Pollen Development and Pollen Tube Growth in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/genetics/159.1.329openalex-snapshot
Rejection of S-Heteroallelic Pollen by a Dual-Specific S-RNase in Solanum chacoense Predicts a Multimeric SI Pollen Component
inferredcites →https://doi.org/10.1093/jxb/41.11.1461openalex-snapshot
Structure and Behaviour of Organelles in Living Pollen Tubes ofLilium longiflorum
inferredcites →https://doi.org/10.1093/jxb/54.380.149openalex-snapshot
Molecular mechanism of self-recognition in Brassica self-incompatibility
inferredcites →https://doi.org/10.1093/jxb/54.380.47openalex-snapshot
Adhesion and guidance in compatible pollination
inferredcites →https://doi.org/10.1093/jxb/54.380.65openalex-snapshot
Effect of extracellular calcium, pH and borate on growth oscillations in Lilium formosanum pollen tubes
inferredcites →https://doi.org/10.1093/jxb/54.380.73openalex-snapshot
Regulation of pollen tube growth by Rac-like GTPases
inferredcites →https://doi.org/10.1093/jxb/54.380.83openalex-snapshot
Endo/exocytosis in the pollen tube apex is differentially regulated by Ca2+ and GTPases
inferredcites →https://doi.org/10.1093/jxb/54.380.93openalex-snapshot
ROP GTPase regulation of pollen tube growth through the dynamics of tip-localized F-actin
inferredcites →https://doi.org/10.1093/jxb/erg002openalex-snapshot
Characterization and localization of the transmitting tissue-specific PELPIII proteins of Nicotiana tabacum
inferredcites →https://doi.org/10.1093/jxb/erg004openalex-snapshot
Effect of extracellular calcium, pH and borate on growth oscillations in Lilium formosanum pollen tubes
inferredcites →https://doi.org/10.1093/jxb/erg007openalex-snapshot
Molecular mechanism of self-recognition in Brassica self-incompatibility
inferredcites →https://doi.org/10.1093/jxb/erg015openalex-snapshot
Adhesion and guidance in compatible pollination
inferredcites →https://doi.org/10.1093/jxb/erg035openalex-snapshot
ROP GTPase regulation of pollen tube growth through the dynamics of tip-localized F-actin
inferredcites →https://doi.org/10.1093/jxb/erg044openalex-snapshot
Regulation of pollen tube growth by Rac-like GTPases
inferredcites →https://doi.org/10.1093/jxb/erg045openalex-snapshot
S-RNase complexes and pollen rejection
inferredcites →https://doi.org/10.1093/oxfordjournals.aob.a085414openalex-snapshot
The Receptive Surface of the Angiosperm Stigma
inferredcites →https://doi.org/10.1093/pcp/pch049openalex-snapshot
Molecular Cloning of Two Exo-β-glucanases and Their in vivo Substrates in the Cell Walls of Lily Pollen Tubes
inferredcites →https://doi.org/10.1098/rstb.2002.1086openalex-snapshot
Actin–binding proteins in the Arabidopsis genome database: properties of functionally distinct plant actin–depolymerizing factors/cofilins
inferredcites →https://doi.org/10.1098/rstb.2003.1287openalex-snapshot
The different mechanisms of gametophytic self–incompatibility
inferredcites →https://doi.org/10.1098/rstb.2003.1288openalex-snapshot
Investigating mechanisms involved in the self–incompatibility response in Papaver rhoeas
inferredcites →https://doi.org/10.1101/gad.13.22.2971openalex-snapshot
Maintenance of genomic imprinting at the Arabidopsis medea locus requires zygotic DDM1 activity
inferredcites →https://doi.org/10.1101/gad.213902openalex-snapshot
Pollen tube development and competitive ability are impaired by disruption of a Shaker K+ channel in Arabidopsis
inferredcites →https://doi.org/10.1101/gad.7.6.974openalex-snapshot
A conditional sterile mutation eliminates surface components from Arabidopsis pollen and disrupts cell signaling during fertilization.
inferredcites →https://doi.org/10.1104/pp.010517openalex-snapshot
DEX1, a Novel Plant Protein, Is Required for Exine Pattern Formation during Pollen Development in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.103.037747openalex-snapshot
The Putative Arabidopsis Homolog of Yeast Vps52p Is Required for Pollen Tube Elongation, Localizes to Golgi, and Might Be Involved in Vesicle Trafficking
inferredcites →https://doi.org/10.1104/pp.104.041483openalex-snapshot
Identification and Characterization of Stretch-Activated Ion Channels in Pollen Protoplasts
inferredcites →https://doi.org/10.1104/pp.115.3.1221openalex-snapshot
Pollen-Stigma Adhesion in Kale Is Not Dependent on the Self-(In)Compatibility Genotype
inferredcites →https://doi.org/10.1104/pp.118.3.733openalex-snapshot
Directional Guidance of Nicotiana alataPollen Tubes in Vitro and on the Stigma
inferredcites →https://doi.org/10.1104/pp.122.1.11openalex-snapshot
Explosive Discharge of Pollen Tube Contents inTorenia fournieri ,
inferredcites →https://doi.org/10.1104/pp.125.4.2040openalex-snapshot
Pollen Tubes of Nicotiana alata Express Two Genes from Different β-Glucan Synthase Families
inferredcites →https://doi.org/10.1104/pp.125.4.2095openalex-snapshot
A Pollen Coat Protein, SP11/SCR, Determines the PollenS-Specificity in the Self-Incompatibility ofBrassica Species
inferredcites →https://doi.org/10.1104/pp.125.4.2180openalex-snapshot
Class III Pistil-Specific Extensin-Like Proteins from Tobacco Have Characteristics of Arabinogalactan Proteins
inferredcites →https://doi.org/10.1104/pp.126.2.685openalex-snapshot
Pollen Germinates Precociously in the Anthers of raring-to-go, an Arabidopsis Gametophytic Mutant
inferredcites →https://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
inferredcites →https://doi.org/10.1105/tpc.000836openalex-snapshot
Rab2 GTPase Regulates Vesicle Trafficking between the Endoplasmic Reticulum and the Golgi Bodies and Is Important to Pollen Tube Growth[W]
inferredcites →https://doi.org/10.1105/tpc.002170openalex-snapshot
Mitochondrial GFA2 Is Required for Synergid Cell Death in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.003038openalex-snapshot
The Regulation of Actin Organization by Actin-Depolymerizing Factor in Elongating Pollen Tubes[W]
inferredcites →https://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]
inferredcites →https://doi.org/10.1105/tpc.003830openalex-snapshot
Oscillatory Chloride Efflux at the Pollen Tube Apex Has a Role in Growth and Cell Volume Regulation and Is Targeted by Inositol 3,4,5,6-Tetrakisphosphate
inferredcites →https://doi.org/10.1105/tpc.005363openalex-snapshot
Regulation of the Pollen-Specific Actin-Depolymerizing Factor LlADF1
inferredcites →https://doi.org/10.1105/tpc.007153openalex-snapshot
Actin-Depolymerizing Factor Mediates Rac/Rop GTPase–Regulated Pollen Tube Growth
inferredcites →https://doi.org/10.1105/tpc.009290openalex-snapshot
Structural and Transcriptional Analysis of the Self-Incompatibility Locus of Almond: Identification of a Pollen-Expressed F-Box Gene with Haplotype-Specific Polymorphism
inferredcites →https://doi.org/10.1105/tpc.010218openalex-snapshot
A Genome-Wide Analysis of Arabidopsis Rop-Interactive CRIB Motif–Containing Proteins That Act as Rop GTPase Targets
inferredcites →https://doi.org/10.1105/tpc.014407openalex-snapshot
SETH1 and SETH2 , Two Components of the Glycosylphosphatidylinositol Anchor Biosynthetic Pathway, Are Required for Pollen Germination and Tube Growth in Arabidopsis [W]
inferredcites →https://doi.org/10.1105/tpc.015800openalex-snapshot
Pollen and Stigma Structure and Function: The Role of Diversity in Pollination
inferredcites →https://doi.org/10.1105/tpc.016154openalex-snapshot
The Molecular and Genetic Bases of S-RNase-Based Self-Incompatibility
inferredcites →https://doi.org/10.1105/tpc.016550openalex-snapshot
Overexpression of an Arabidopsis Formin Stimulates Supernumerary Actin Cable Formation from Pollen Tube Cell Membrane[W]
inferredcites →https://doi.org/10.1105/tpc.016659openalex-snapshot
Control of Male Gametophyte Development
inferredcites →https://doi.org/10.1105/tpc.017277openalex-snapshot
Developmental Evolution of the Sexual Process in Ancient Flowering Plant Lineages
inferredcites →https://doi.org/10.1105/tpc.017673openalex-snapshot
The F-Box Protein AhSLF-S2 Physically Interacts with S-RNases That May Be Inhibited by the Ubiquitin/26S Proteasome Pathway of Protein Degradation during Compatible Pollination in Antirrhinum
inferredcites →https://doi.org/10.1105/tpc.10.12.2019openalex-snapshot
Guidance in Vitro of the Pollen Tube to the Naked Embryo Sac of Torenia fournieri
inferredcites →https://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
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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