about
Guidelines for the use and interpretation of assays for monitoring autophagyA novel role for the nuclear membrane protein emerin in association of the centrosome to the outer nuclear membraneA thermodynamic model of microtubule assembly and disassemblyA maize pectin methylesterase-like gene, ZmC5, specifically expressed in pollen.A compartmental model analysis of integrative and self-regulatory ion dynamics in pollen tube growthThe plant microtubule-associated protein AtMAP65-3/PLE is essential for cytokinetic phragmoplast function.A nucleotide phosphatase activity in the nucleotide binding domain of an orphan resistance protein from rice.Prieurianin/endosidin 1 is an actin-stabilizing small molecule identified from a chemical genetic screen for circadian clock effectors in Arabidopsis thaliana.Microtubule-associated proteins in plants--why we need a MAP.The origin of phragmoplast asymmetry.Arabidopsis CAP1 - a key regulator of actin organisation and development.Actin-binding proteins in the Arabidopsis genome database: properties of functionally distinct plant actin-depolymerizing factors/cofilins.Arp2/3 and SCAR: plants move to the fore.F-actin and G-actin binding are uncoupled by mutation of conserved tyrosine residues in maize actin depolymerizing factor (ZmADF)Pollen specific expression of maize genes encoding actin depolymerizing factor-like proteinsModelling dynamic plant cells.Strategies of actin reorganisation in plant cells.Clathrin is involved in organization of mitotic spindle and phragmoplast as well as in endocytosis in tobacco cell cultures.Re-organisation of the cytoskeleton during developmental programmed cell death in Picea abies embryos.Towards the creation of a systems tip growth model for a pollen tube.ACTIN BINDING PROTEIN 29 from Lilium pollen plays an important role in dynamic actin remodeling.BODIPY probes to study peroxisome dynamics in vivo.MOR1/GEM1 has an essential role in the plant-specific cytokinetic phragmoplast.The plant formin AtFH4 interacts with both actin and microtubules, and contains a newly identified microtubule-binding domain.Tudor staphylococcal nuclease is an evolutionarily conserved component of the programmed cell death degradome.Phosphorylation of plant actin-depolymerising factor by calmodulin-like domain protein kinase.The caspase-related protease separase (extra spindle poles) regulates cell polarity and cytokinesis in Arabidopsis.The Arabidopsis microtubule-associated protein AtMAP65-1: molecular analysis of its microtubule bundling activity.Green fluorescent protein-mTalin causes defects in actin organization and cell expansion in Arabidopsis and inhibits actin depolymerizing factor's actin depolymerizing activity in vitro.The actin-interacting protein AIP1 is essential for actin organization and plant development.Alpha-tubulin gene family of maize (Zea mays L.). Evidence for two ancient alpha-tubulin genes in plants.Arabidopsis homologues of the autophagy protein Atg8 are a novel family of microtubule binding proteins.Ser6 in the maize actin-depolymerizing factor, ZmADF3, is phosphorylated by a calcium-stimulated protein kinase and is essential for the control of functional activity.A new class of microtubule-associated proteins in plants.Pollen profilin function depends on interaction with proline-rich motifs.Herbicide resistance caused by spontaneous mutation of the cytoskeletal protein tubulin.The POLARIS peptide of Arabidopsis regulates auxin transport and root growth via effects on ethylene signaling.A divergent cellular role for the FUSED kinase family in the plant-specific cytokinetic phragmoplast.Arabidopsis NAP1 is essential for Arp2/3-dependent trichome morphogenesis.The beta-tubulin gene family in Zea mays: two differentially expressed beta-tubulin genes.
P50
Q21996341-772B74B1-C824-4483-927F-24E6D1424C28Q24292716-1A801E0E-4500-49B6-B491-B347E225C1ECQ27345761-59338906-A48C-481A-909E-7D24D478A8F2Q32061578-E762E471-17B0-4C7C-97EA-6F6FF7381397Q33719558-58D43BB0-450A-4E63-AE49-8B5754FA7C36Q33842288-3A82A78D-1B2E-444C-A2C8-F9BF2BDC4058Q34096384-A1D8C5E4-C69A-4F63-ACCD-E711A815EB8DQ34191772-426E25DE-67E5-42E4-A110-E04ED64BAABFQ34286361-DE9F8077-4BAC-4BC9-9275-80717E06827FQ34633655-DDB92FA4-763B-445F-BE99-98F0461DD382Q34652308-5E502474-C279-491E-93CA-412DD3D83F27Q34701656-4986EF0D-6399-46AB-831D-49A0BDB9E2E2Q36337958-3ADAF536-8263-418F-9A14-5A170B940510Q36581879-719FB6EC-EA26-45D4-8F45-E4F7CF0DE853Q37507912-B2CE506B-8194-4BE2-8B58-5CDCAB4F3BA0Q37808853-E5A4B27D-AF8A-425B-AF8B-495BA6EF3FE6Q39668941-58A0C37A-E5C9-4480-A454-87D3E1246B67Q40160631-89C60B44-EF83-48FB-98A0-F0DBF5847445Q40667770-7BD979E1-A23D-4D04-A0D5-73BEF046058FQ42573119-3ADCF073-D37D-4905-A840-D79AD3FECF27Q42624358-F564AF44-EC5E-4AE7-8C01-0AFB856F229BQ42829945-94C78802-490E-4FD1-88E9-D1A158E7A65AQ42949963-F127AC03-9B65-4827-B8EA-CDF00AEB8661Q43120773-05D7843C-A856-405D-80DE-1F8486597AF4Q43263626-47CB9614-4A0D-405C-8FDD-45B033C0D9D2Q43647819-5AB49842-FC2A-4299-97AE-131A16B1BBE7Q44668918-6A5C761A-6135-41A5-BE13-1871682E16CDQ44992507-1945B738-FD1A-42D4-B6C3-82CE865A3E83Q45162645-0057C9CE-B2DB-401A-A725-DC2545ECB80BQ47248521-2D52BB07-6DF6-42C3-B6E2-4E87DAD1683DQ47283682-B20D8D6A-2817-49B7-9EF6-14958BB9B5EDQ47393394-47914177-18DA-4829-B21A-E766E17311FEQ47820265-132EBBDA-9357-4D8F-9D1F-5396636270A1Q47823275-561C3D67-B848-4FD1-8D68-E69D74091B94Q47949241-0F66439F-1E1E-4F98-ABB9-D61FF268B5FBQ48024464-CABE3138-50C9-4E83-A1C3-BB62E780299BQ48083163-9DD5F270-FB72-4D0D-B5AF-C9954E2F48E3Q48110021-81711AE2-68EA-4070-959B-3363A9B45F9FQ48178691-1470FFC0-EB30-4E2F-B5AF-3922D0A61C25Q48246548-B9F7AC44-29B8-43FA-9E59-D74547348C6E
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Patrick J Hussey
@nl
Patrick J Hussey
@sl
Patrick J. Hussey
@en
Patrick J. Hussey
@es
type
label
Patrick J Hussey
@nl
Patrick J Hussey
@sl
Patrick J. Hussey
@en
Patrick J. Hussey
@es
prefLabel
Patrick J Hussey
@nl
Patrick J Hussey
@sl
Patrick J. Hussey
@en
Patrick J. Hussey
@es
P106
P1153
7007150704
P21
P31
P496
0000-0002-7349-8722