about
Disturbed local auxin homeostasis enhances cellular anisotropy and reveals alternative wiring of auxin-ethylene crosstalk in Brachypodium distachyon seminal rootsEthylene upregulates auxin biosynthesis in Arabidopsis seedlings to enhance inhibition of root cell elongationRapid Synthesis of Auxin via a New Tryptophan-Dependent Pathway Is Required for Shade Avoidance in PlantsDevelopmental regulation of indole-3-acetic acid turnover in Scots pine seedlingsLocalization of the auxin permease AUX1 suggests two functionally distinct hormone transport pathways operate in the Arabidopsis root apexADP1 affects plant architecture by regulating local auxin biosynthesisThree ancient hormonal cues co-ordinate shoot branching in a mosscis-Cinnamic Acid Is a Novel, Natural Auxin Efflux Inhibitor That Promotes Lateral Root FormationControl of axillary bud initiation and shoot architecture in Arabidopsis through the SUPERSHOOT gene.AtPIN4 mediates sink-driven auxin gradients and root patterning in Arabidopsis.FLOOZY of petunia is a flavin mono-oxygenase-like protein required for the specification of leaf and flower architecture.A PINOID-dependent binary switch in apical-basal PIN polar targeting directs auxin efflux.Sites and regulation of auxin biosynthesis in Arabidopsis roots.Computer simulations reveal properties of the cell-cell signaling network at the shoot apex in Arabidopsis.Ubiquitin lysine 63 chain forming ligases regulate apical dominance in Arabidopsis.Ethylene regulates root growth through effects on auxin biosynthesis and transport-dependent auxin distribution.Inhibited polar auxin transport results in aberrant embryo development in Norway spruce.Requirement of B2-type cyclin-dependent kinases for meristem integrity in Arabidopsis thaliana.The AUXIN BINDING PROTEIN 1 is required for differential auxin responses mediating root growthControl of bud activation by an auxin transport switch.Hormonal control of the shoot stem-cell niche.Short-Root regulates primary, lateral, and adventitious root development in Arabidopsis.Subterranean space exploration: the development of root system architecture.Strigolactone signaling is required for auxin-dependent stimulation of secondary growth in plantsRoot gravitropism and root hair development constitute coupled developmental responses regulated by auxin homeostasis in the Arabidopsis root apex.Spatial coordination between stem cell activity and cell differentiation in the root meristem.Cell-Type-Specific Cytokinin Distribution within the Arabidopsis Primary Root Apex.The Arabidopsis bZIP11 transcription factor links low-energy signalling to auxin-mediated control of primary root growth.Regulating plant physiology with organic electronics.Light intensity modulates the regulatory network of the shade avoidance response in ArabidopsisA gradient of auxin and auxin-dependent transcription precedes tropic growth responses.Cotyledon-Generated Auxin Is Required for Shade-Induced Hypocotyl Growth in Brassica rapa.Cryptochromes Interact Directly with PIFs to Control Plant Growth in Limiting Blue Light.The AFB4 auxin receptor is a negative regulator of auxin signaling in seedlingsA regulated auxin minimum is required for seed dispersal in Arabidopsis.Auxin-induced K+ channel expression represents an essential step in coleoptile growth and gravitropism.Root gravitropism is regulated by a transient lateral auxin gradient controlled by a tipping-point mechanism.The SUR2 gene of Arabidopsis thaliana encodes the cytochrome P450 CYP83B1, a modulator of auxin homeostasisLinking photoreceptor excitation to changes in plant architectureConnective Auxin Transport in the Shoot Facilitates Communication between Shoot Apices
P50
Q21144891-486725AB-B07F-4D50-889F-7D0BEA3BCCEDQ24673462-8AE55037-7830-4660-A3F2-C3B0A0CFD4E7Q27650264-C200D543-7980-466D-BDC8-5AFBD613B9DEQ28345757-2A822365-2DD3-46C0-87BF-B56BB989C119Q28362209-1F09C85A-6E44-471E-9680-9EED2EA350A8Q28538237-DED11431-4D28-44C8-8B8C-B122C5CC235EQ28649925-3B53DCE6-CDCD-4F34-9E5C-42BE5F10E5EEQ28818080-71F179F4-B016-48AD-AAA4-40C964B94252Q33335689-90FD1846-BACB-4FC7-8AFB-CB7A733A6C5DQ33336995-E8E754B4-0DBC-4F85-9A43-9455C74F4BDFQ33337042-97CFCB53-BFED-4237-8B3B-51B95977171FQ33340560-B225174B-333C-4C67-A75B-391908F16098Q33340986-EA614E81-BB0A-4FE5-94CD-BFF1222473BCQ33342050-141FF20A-0EEC-4BF3-A4BD-9779A1E95BBBQ33344184-9CBD9C6B-0577-47E7-8D46-011775FEDDE1Q33344273-CEE213B7-5991-4FB5-891F-23CC9212C95EQ33344888-BE9C5CAC-E108-438C-A656-71A5BD4DE9E4Q33345127-F593EB82-B0B6-4C83-9058-9C448CE5B144Q33347898-B935D5F8-21E2-4287-AAAC-D919EF3F0A1FQ33347950-56E31C54-3B69-49ED-9746-F8FCA3B475CDQ33349308-12B9EBF8-28D5-4422-8B47-E6FF4708D318Q33350021-1BCC0082-17CB-4314-BFF5-EC7AE6B249F2Q33352402-FCA39D45-121D-496A-8E25-CE715D1FF1E0Q33352618-F42B8B03-6E2B-4443-ABCC-52F144241F5BQ33354910-D1FF0173-470E-4582-BA33-971524D5BFC8Q33356440-5754D91D-0E12-4564-ACE5-835FB31C2919Q33361092-DBFD2AF6-96A0-467A-BC0B-C0A6B9DEB345Q33364700-1A7935CA-C990-419C-9EEA-B9A9D88E8957Q33650940-0F2D1339-8396-4D45-9394-7EAABD2E8DDEQ33674430-03BAF86E-0017-443E-B816-C12D620D9AD2Q34248235-1E7BB1BD-0FBA-4F20-B71D-46AADC99DFD8Q34422650-ADD0B844-7155-4CCB-B76B-96E8CDFC613AQ34507212-A5EE37DB-872F-406C-960C-F81A6DADA6E1Q34973708-7630A816-B82C-4BD7-8E9E-86CF34C385C6Q34983671-5306E072-F9D0-47AF-A23D-25D637EF6633Q35737050-7C3C263C-9D14-4135-8F9B-3968A41BA6D3Q35849787-4A72EEBF-7A11-4F00-A581-02FCF346D9FCQ35857471-6CD8D816-3CA8-4896-94CB-60D465865387Q35914902-763B40C0-FD95-4A48-801B-2B51A88BE004Q36000681-BC79A091-EBF6-41DD-9A7F-94D9EE0931AF
P50
description
Zweeds onderzoekster
@nl
hulumtuese
@sq
researcher
@en
taighdeoir
@ga
հետազոտող
@hy
name
Karin Ljung
@ast
Karin Ljung
@en
Karin Ljung
@es
Karin Ljung
@ga
Karin Ljung
@nl
Karin Ljung
@sl
Karin Ljung
@sq
type
label
Karin Ljung
@ast
Karin Ljung
@en
Karin Ljung
@es
Karin Ljung
@ga
Karin Ljung
@nl
Karin Ljung
@sl
Karin Ljung
@sq
prefLabel
Karin Ljung
@ast
Karin Ljung
@en
Karin Ljung
@es
Karin Ljung
@ga
Karin Ljung
@nl
Karin Ljung
@sl
Karin Ljung
@sq
P1053
C-8971-2017
P106
P21
P27
P31
P496
0000-0003-2901-189X