about
Histochemical Staining of β-Glucuronidase and Its Spatial QuantificationEmergence of tissue polarization from synergy of intracellular and extracellular auxin signaling.Cell wall constrains lateral diffusion of plant plasma-membrane proteins.Plasma membrane-bound AGC3 kinases phosphorylate PIN auxin carriers at TPRXS(N/S) motifs to direct apical PIN recycling.GOLVEN secretory peptides regulate auxin carrier turnover during plant gravitropic responses.Epidermal patterning genes impose non-cell autonomous cell size determination and have additional roles in root meristem size control.Actin-dependent vacuolar occupancy of the cell determines auxin-induced growth repressionRecycling, clustering, and endocytosis jointly maintain PIN auxin carrier polarity at the plasma membrane.Gravity-induced PIN transcytosis for polarization of auxin fluxes in gravity-sensing root cells.Single-cell-based system to monitor carrier driven cellular auxin homeostasis.2,4-D and IAA Amino Acid Conjugates Show Distinct Metabolism in Arabidopsis.Cell polarity, auxin transport, and cytoskeleton-mediated division planes: who comes first?Sequential induction of auxin efflux and influx carriers regulates lateral root emergenceBEX1/ARF1A1C is required for BFA-sensitive recycling of PIN auxin transporters and auxin-mediated development in Arabidopsis.Feedback models for polarized auxin transport: an emerging trend.Cellular auxin homeostasis: gatekeeping is housekeeping.Divide Et Impera--cellular auxin compartmentalization.Differential growth regulation in plants--the acid growth balloon theory.Light triggers PILS-dependent reduction in nuclear auxin signalling for growth transition.Probing plant membranes with FM dyes: tracking, dragging or blocking?Tricho- and atrichoblast cell files show distinct PIN2 auxin efflux carrier exploitations and are jointly required for defined auxin-dependent root organ growth.Auxin regulates SNARE-dependent vacuolar morphology restricting cell size.PPP1, a plant-specific regulator of transcription controls Arabidopsis development and PIN expression.The AP-3 adaptor complex is required for vacuolar function in Arabidopsis.Evolution and Structural Diversification of PILS Putative Auxin Carriers in Plants.Cellular and molecular requirements for polar PIN targeting and transcytosis in plants.PIN auxin efflux carrier polarity is regulated by PINOID kinase-mediated recruitment into GNOM-independent trafficking in Arabidopsis.Trafficking to the outer polar domain defines the root-soil interface.Inositol trisphosphate-induced Ca2+ signaling modulates auxin transport and PIN polarity.Subcellular trafficking of the Arabidopsis auxin influx carrier AUX1 uses a novel pathway distinct from PIN1.ARF GEF-dependent transcytosis and polar delivery of PIN auxin carriers in Arabidopsis.SCF(TIR1/AFB)-auxin signalling regulates PIN vacuolar trafficking and auxin fluxes during root gravitropism.Halotropism: turning down the salty date.The clathrin adaptor complex AP-2 mediates endocytosis of brassinosteroid insensitive1 in Arabidopsis.An auxin transport mechanism restricts positive orthogravitropism in lateral roots.Prototype cell-to-cell auxin transport mechanism by intracellular auxin compartmentalization.Auxin and Cellular Elongation.Vacuolar staining methods in plant cells.A novel putative auxin carrier family regulates intracellular auxin homeostasis in plants.Cytokinin modulates endocytic trafficking of PIN1 auxin efflux carrier to control plant organogenesis.
P50
Q28364831-CD126BEE-12D4-4564-97BC-2ADDF6264474Q30497851-BDF73A90-4F14-4949-B6D0-6E07E989643BQ30523979-39556BC8-90E4-411E-A5CE-3759D403B0E5Q33349734-0DE44762-9AA2-4B51-835F-BB4257AAC3A2Q33353206-281C59C5-8096-41A1-B77F-4897E57BBA28Q33356354-3FE1FBD2-796C-476A-8CA3-99D63C1A3A7EQ33362205-B62A8F5F-4A5E-41D0-A8A9-DA69D0A899E6Q34227444-D13A675A-CF3E-4EDB-A1A3-AAEFEC74543AQ34438381-3559527F-287F-47E5-9CBE-33A5C180A9DAQ34573688-54FC8E48-103D-4FC8-975E-BC4D1BB0A7C8Q36081740-ADB2BDC0-5D7C-4E83-9D91-5A9009761D8CQ36289001-62466BE1-30E2-4B9A-8DCB-622A03A3DCA1Q37279476-D6B8EB59-2AF3-4FE7-A94A-14F93B9E310BQ37695393-305D8F4D-0968-4F82-A244-2164B67660B5Q37887532-B79C57A9-3929-4198-8C15-D9773C95BF20Q37971371-E1331C43-D70C-494F-82F0-DB603AE25617Q38064074-421F8210-C1B1-4984-A409-D5F3A93974A1Q38603830-4714ED4C-9B71-4838-A94B-7927DDDFECDFQ38675871-0CE722B4-C7AD-4EC8-B13E-E43A32A5B118Q39764795-B8A4B5FE-448C-46B5-9714-3DEE6A4554C2Q40871544-8106E989-1C58-4D23-A2A8-7CC9437FF0D6Q41288931-19F3A709-A5D7-408D-92BE-1290F03882BDQ41328083-4D26FE2F-5628-43E8-9695-F64CFC6CD1C2Q41860078-A93F7765-F301-4873-AE77-4A3C357C9455Q42428122-9858620C-4EE8-4377-995E-48CE54A1EC15Q42461294-5A7C7D70-A32D-45CD-AEC6-21E5C21DD850Q42465090-E1F6DDFF-027D-4111-8516-81896E24E798Q42471142-80B23A1A-0CD4-42DE-B4BC-1518CCDC7A9CQ42489816-169CE25C-47B5-4442-8004-EB0B8AC77390Q42504350-9153AA9D-867C-4074-BC62-18C1A7516DC1Q42526493-127910C7-87F2-440A-BB24-F8052675439EQ42947064-ADC7C7C3-BE90-4CE0-9A36-36D494CE50DFQ44153155-E28DF89C-6F9D-4955-9E26-781D7E6726A0Q44301417-CB8EE80A-F425-4588-938F-66C3487A6D8CQ45830102-CC6759DF-040C-40ED-913A-0B172BCD02AEQ47290769-0811D702-95F7-473D-8424-419FA3A54409Q48258873-E7E4CF9C-176F-459A-A44F-51182C68CF16Q48697167-C8BD1377-154A-4A96-99F0-762F0CF076F9Q49027196-6AB0DBC5-FDA4-4642-9F57-EC898C3B7034Q49169491-2FE348CD-BB03-458D-BE4C-A89AB525F387
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
ricercatore
@it
հետազոտող
@hy
name
Jürgen Kleine-Vehn
@ast
Jürgen Kleine-Vehn
@en
Jürgen Kleine-Vehn
@es
Jürgen Kleine-Vehn
@nl
Jürgen Kleine-Vehn
@sl
type
label
Jürgen Kleine-Vehn
@ast
Jürgen Kleine-Vehn
@en
Jürgen Kleine-Vehn
@es
Jürgen Kleine-Vehn
@nl
Jürgen Kleine-Vehn
@sl
prefLabel
Jürgen Kleine-Vehn
@ast
Jürgen Kleine-Vehn
@en
Jürgen Kleine-Vehn
@es
Jürgen Kleine-Vehn
@nl
Jürgen Kleine-Vehn
@sl
P1053
C-8984-2014
P106
P1960
cpo9rKcAAAAJ
P21
P214
274148704303936932128
P31
P3829
P463
P496
0000-0002-4354-3756
P735
P7859
lccn-n2017181151