about
The MAP kinase MPK4 is required for cytokinesis in Arabidopsis thalianaThe Naming of Names: Guidelines for Gene Nomenclature in MarchantiaModulation of plant growth in vivo and identification of kinase substrates using an analog-sensitive variant of CYCLIN-DEPENDENT KINASE A;1MASCP Gator: an aggregation portal for the visualization of Arabidopsis proteomics dataChanges in PUB22 Ubiquitination Modes Triggered by MITOGEN-ACTIVATED PROTEIN KINASE3 Dampen the Immune Response.Plant GSK3 proteins regulate xylem cell differentiation downstream of TDIF-TDR signalling.TDM1 Regulation Determines the Number of Meiotic Divisions.Quantitative Circadian Phosphoproteomic Analysis of Arabidopsis Reveals Extensive Clock Control of Key Components in Physiological, Metabolic, and Signaling Pathways.Circadian Profiling of the Arabidopsis Proteome Using 2D-DIGEThe Arabidopsis CERK1-associated kinase PBL27 connects chitin perception to MAPK activation.Shotguns in the front line: phosphoproteomics in plants.Analysis of differential expression patterns of mRNA and protein during cold-acclimation and de-acclimation in Arabidopsis.Large-scale phosphorylation mapping reveals the extent of tyrosine phosphorylation in Arabidopsis.Regulation of sugar transporter activity for antibacterial defense in Arabidopsis.Phosphorylation of retinoblastoma-related protein by the cyclin D/cyclin-dependent kinase complex is activated at the G1/S-phase transition in tobacco.Chitin Nanofiber Elucidates the Elicitor Activity of Polymeric Chitin in Plants.Isolation and characterization of the E2F-like gene in plants.OMTK1, a novel MAPKKK, channels oxidative stress signaling through direct MAPK interaction.The membrane-anchored BOTRYTIS-INDUCED KINASE1 plays distinct roles in Arabidopsis resistance to necrotrophic and biotrophic pathogens.Insights into Land Plant Evolution Garnered from the Marchantia polymorpha Genome.A Mitogen-activated protein kinase kinase kinase mediates reactive oxygen species homeostasis in Arabidopsis.Large-scale comparative phosphoproteomics identifies conserved phosphorylation sites in plants.The GYF domain protein PSIG1 dampens the induction of cell death during plant-pathogen interactions.An atypical tubulin kinase mediates stress-induced microtubule depolymerization in Arabidopsis.Plasma membrane localization is essential for Oryza sativa Pto-interacting protein 1a-mediated negative regulation of immune signaling in rice.Blue-light excited LOV1 and LOV2 domains cooperatively regulate the kinase activity of full-length phototropin2 from Arabidopsis.Two distinct families of protein kinases are required for plant growth under high external Mg2+ concentrations in Arabidopsis.Stable accumulation of photosystem II requires ONE-HELIX PROTEIN1 (OHP1) of the light harvesting-like family.Comparative analysis of plant isochorismate synthases reveals structural mechanisms underlying their distinct biochemical properties.Heavy metal stress. Activation of distinct mitogen-activated protein kinase pathways by copper and cadmiumSWITCH 1/DYAD is a WINGS APART-LIKE antagonist that maintains sister chromatid cohesion in meiosisTrojan horse strategy in Agrobacterium transformation: abusing MAPK defense signalingEmerging MAP kinase pathways in plant stress signallingStageTip-based HAMMOC, an efficient and inexpensive phosphopeptide enrichment method for plant shotgun phosphoproteomicsThe Arabidopsis Cdk1/Cdk2 homolog CDKA;1 controls chromosome axis assembly during plant meiosisA Golgi-Released Subpopulation of the Trans-Golgi Network Mediates Protein Secretion in ArabidopsisCyanidioschyzon merolae aurora kinase phosphorylates evolutionarily conserved sites on its target to regulate mitochondrial divisionMultidimensional gene regulatory landscape of a bacterial pathogen in plants
P50
Q24605714-93BF45BD-74CA-4853-9A7F-186EA62A3E65Q26773759-63324CEC-B691-4061-9C5F-87D26C09FF7CQ28828893-CC8D5A94-63DD-47D7-A3AC-D7B758382ECEQ30000953-25B212BE-431B-45FC-B767-B66CD2CF2D26Q30313353-78AD67AF-313B-4AB9-83DE-B361DC5D4146Q33358105-4B7ACB57-F4C6-4BE4-9156-BF11047CDEBEQ35922040-F0CBC1AD-48B7-46C6-8237-EB1F015752A2Q35926212-56259D4C-5AC2-4C6A-8D48-94C23C333233Q37083936-C05252AF-6F43-4537-80B0-8E580868AB00Q37414039-450F2CC8-4149-423F-8BC5-947716A24481Q37950986-C2D25DC5-E8EB-45DE-95BA-E6CB76A11293Q38471925-5735ADDA-837F-4609-A9A4-8EB295A80810Q39045929-724AB738-7A45-4CD3-A234-551BCF1CED04Q40436667-F962A482-569A-43B3-9666-5DB296747D66Q40711490-DCB2FE5A-5879-4172-A298-15591C9E646FQ40860009-AEAD850F-3CC3-42C3-8E7A-F079D2E99B0EQ40916511-C408A7A4-EF56-4318-88BC-DA45096E4FECQ42458912-38690AFE-1B03-4847-8879-8E3297184C19Q42487716-DCC77B82-B76C-4842-A4DD-E38C5AE4E68BQ42516441-13D1011F-797C-4F3D-989D-B6DA57E4B594Q42600749-A28D72F1-9E2D-4E05-A8D9-B3C654E371DAQ43064151-E58A3A46-CFC7-4871-ADDD-651947447C26Q46274157-9DD33BEB-2377-489B-A655-FDF715C3632FQ46521288-2566ADD0-71A5-4498-B923-AEE6D30B45F0Q46875293-078A5344-CF1F-4555-9BAB-D91A82B2D099Q47340124-69D44C62-5D88-445B-B9C0-FF0C5298CFC3Q48232751-2B5FA9E7-C672-4BD0-90BB-80EF8DC403E3Q50042738-F92C76C6-6A94-46D4-9490-08FAB2DDB3CBQ50048295-54BC385C-EC07-4ECE-8906-C40CF8362589Q60376311-ED857C46-0AB1-40A2-8AC1-EDAEC476DA22Q64114499-A31860CE-E68B-454D-9007-09BEE60584E3Q81464126-D3126B26-635B-4D93-ACE3-19E639BEF466Q81845056-7F87087A-93F1-42EA-AF2E-9A93E047AA25Q86548869-2119A982-99D2-46BB-B142-2B495EE1B0AFQ90300212-C7CAED85-C7B7-4084-A8EA-5E372AD33411Q90462813-388857C8-25FD-4AF6-8245-6A03C0B62C68Q92315092-5F0C16CB-0F7A-40A2-A6A7-E1B5CCA174F9Q96431856-031D458D-343F-4AD7-B979-E56C5FFFFA79
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Hirofumi Nakagami
@ast
Hirofumi Nakagami
@en
Hirofumi Nakagami
@es
Hirofumi Nakagami
@nl
Hirofumi Nakagami
@sl
type
label
Hirofumi Nakagami
@ast
Hirofumi Nakagami
@en
Hirofumi Nakagami
@es
Hirofumi Nakagami
@nl
Hirofumi Nakagami
@sl
altLabel
Hiro Nakagami
@en
prefLabel
Hirofumi Nakagami
@ast
Hirofumi Nakagami
@en
Hirofumi Nakagami
@es
Hirofumi Nakagami
@nl
Hirofumi Nakagami
@sl
P1053
A-4122-2011
P106
P21
P31
P3829
P496
0000-0003-2569-7062
P569
2000-01-01T00:00:00Z