| scholarly article | Q13442814 |
| P2093 | author name string | Ren H | |
| Staiger CJ | |||
| Gibbon BC | |||
| P2860 | cites work | Profilins purified from higher plants bind to actin from cardiac muscle and to actin from a green alga | Q72786383 |
| Actin Purified from Maize Pollen Functions in Living Plant Cells | Q74801419 | ||
| Profilin as a potential mediator of membrane-cytoskeleton communication | Q75293121 | ||
| Bni1p, a yeast formin linking cdc42p and the actin cytoskeleton during polarized morphogenesis | Q24310527 | ||
| Distinct biochemical characteristics of the two human profilin isoforms | Q24318777 | ||
| The proline-rich focal adhesion and microfilament protein VASP is a ligand for profilins | Q24568320 | ||
| The molecular basis for allergen cross-reactivity: crystal structure and IgE-epitope mapping of birch pollen profilin | Q27734686 | ||
| The crystal structure of a major allergen from plants | Q27734729 | ||
| Actin polymerizability is influenced by profilin, a low molecular weight protein in non-muscle cells | Q28254284 | ||
| Mena, a relative of VASP and Drosophila Enabled, is implicated in the control of microfilament dynamics | Q28590972 | ||
| The regulation of rabbit skeletal muscle contraction. I. Biochemical studies of the interaction of the tropomyosin-troponin complex with actin and the proteolytic fragments of myosin | Q29547591 | ||
| Dictyostelium discoideum contains two profilin isoforms that differ in structure and function | Q33270436 | ||
| Identification of Profilin as a Novel Pollen Allergen; IgE Autoreactivity in Sensitized Individuals | Q33346760 | ||
| The mammalian profilin isoforms display complementary affinities for PIP2 and proline-rich sequences | Q33886049 | ||
| How profilin promotes actin filament assembly in the presence of thymosin beta 4. | Q34345724 | ||
| Dynamic actin structures stabilized by profilin. | Q35055080 | ||
| The profilin multigene family of maize: differential expression of three isoforms | Q36757062 | ||
| Plant and animal profilins are functionally equivalent and stabilize microfilaments in living animal cells. | Q36822936 | ||
| Divergence and differential expression of actin gene families in higher plants | Q37717537 | ||
| Actin monomer binding proteins | Q40529157 | ||
| The affinities of human platelet and Acanthamoeba profilin isoforms for polyphosphoinositides account for their relative abilities to inhibit phospholipase C. | Q40647369 | ||
| Effects of profilin and profilactin on actin structure and function in living cells | Q41871048 | ||
| Yeast actin is relatively well behaved | Q43840564 | ||
| Arabidopsis profilins are functionally similar to yeast profilins: identification of a vascular bundle-specific profilin and a pollen-specific profilin. | Q48061677 | ||
| Profilin is required for posterior patterning of the Drosophila oocyte. | Q48062808 | ||
| Plant profilins rescue the aberrant phenotype of profilin-deficient Dictyostelium cells. | Q52203555 | ||
| Dictyostelium amoebae that lack G-actin-sequestering profilins show defects in F-actin content, cytokinesis, and development. | Q52512437 | ||
| Interaction of plant profilin with mammalian actin. | Q54622587 | ||
| Affinity chromatography-based purification of profilin:actin | Q67916459 | ||
| Polyproline affinity method for purification of platelet profilin and modification with pyrene-maleimide | Q70157475 | ||
| Actin | Q70865830 | ||
| Role of nucleotide exchange and hydrolysis in the function of profilin in action assembly | Q71119828 | ||
| Identification of a factor in conventional muscle actin preparations which inhibits actin filament self-association | Q71851196 | ||
| Structural requirements and thermodynamics of the interaction of proline peptides with profilin | Q71955434 | ||
| Localization of a Binding Site for Phosphatidylinositol 4,5-Bisphosphate on Human Profilin | Q72054874 | ||
| Interaction of profilin with G-actin and poly(L-proline) | Q72061945 | ||
| Purification, characterization and crystallization of human platelet profilin expressed in Escherichia coli | Q72138086 | ||
| Rabbit skeletal muscle actin behaves differently than Acanthamoeba actin when added to soluble extracts of Acanthamoeba castellanii | Q72607612 | ||
| Microinjected profilin affects cytoplasmic streaming in plant cells by rapidly depolymerizing actin microfilaments | Q72707894 | ||
| Profilin: at the crossroads of signal transduction and the actin cytoskeleton | Q72767074 | ||
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | maize | Q11575 |
| pollen | Q79932 | ||
| P1104 | number of pages | 7 | |
| P304 | page(s) | 909-915 | |
| P577 | publication date | 1997-11-01 | |
| P1433 | published in | Biochemical Journal | Q864221 |
| P1476 | title | Characterization of maize (Zea mays) pollen profilin function in vitro and in live cells | |
| P478 | volume | 327 ( Pt 3) |
| Q47949251 | A potential signaling role for profilin in pollen of Papaver rhoeas |
| Q42624358 | ACTIN BINDING PROTEIN 29 from Lilium pollen plays an important role in dynamic actin remodeling |
| Q33944118 | Actin polymerization is essential for pollen tube growth |
| Q57512011 | Airborne Poaceae pollen in Porto (Portugal) and allergenic profiles of several grass pollen types |
| Q43214459 | Arabidopsis formin3 directs the formation of actin cables and polarized growth in pollen tubes |
| Q42611621 | Arabidopsis profilin isoforms, PRF1 and PRF2 show distinctive binding activities and subcellular distributions |
| Q33928669 | AtFim1 is an actin filament crosslinking protein from Arabidopsis thaliana |
| Q51607599 | BENT UPPERMOST INTERNODE1 encodes the class II formin FH5 crucial for actin organization and rice development. |
| Q41735725 | Characterization of Ricinus communis phloem profilin, RcPRO1. |
| Q34359867 | Gravisensing in plants and fungi |
| Q24544306 | Isovariant dynamics expand and buffer the responses of complex systems: the diverse plant actin gene family |
| Q52537258 | Latrunculin B has different effects on pollen germination and tube growth. |
| Q47870275 | Maize profilin isoforms are functionally distinct |
| Q33336478 | Mastoparan alters subcellular distribution of profilin and remodels F-actin cytoskeleton in cells of maize root apices |
| Q33367770 | Olive pollen profilin (Ole e 2 allergen) co-localizes with highly active areas of the actin cytoskeleton and is released to the culture medium during in vitro pollen germination |
| Q45853062 | Oryza sativa actin-interacting protein 1 is required for rice growth by promoting actin turnover. |
| Q87423033 | Overexpression of profilin 3 affects cell elongation and F-actin organization in Arabidopsis thaliana |
| Q74480856 | Plant profilin induces actin polymerization from actin : beta-thymosin complexes and competes directly with beta-thymosins and with negative co-operativity with DNase I for binding to actin |
| Q47949241 | Pollen profilin function depends on interaction with proline-rich motifs |
| Q44719818 | Profilin inhibits pollen tube growth through actin-binding, but not poly-L-proline-binding |
| Q52179906 | Profilin is associated with the plasma membrane in microspores and pollen. |
| Q73294999 | Profilin plays a role in cell elongation, cell shape maintenance, and flowering in Arabidopsis |
| Q30988786 | Small changes in the regulation of one Arabidopsis profilin isovariant, PRF1, alter seedling development |
| Q35625496 | The Arabidopsis cytoskeletal genome |
| Q28345198 | The characterization of ligand-specific maize (Zea mays) profilin mutants |
| Q47712278 | The evolution of new structures: clues from plant cytoskeletal genes |
| Q46581093 | The formin homology 1 domain modulates the actin nucleation and bundling activity of Arabidopsis FORMIN1. |
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