about
Quantitative trait loci mapping and transcriptome analysis reveal candidate genes regulating the response to ozone in Arabidopsis thaliana.Natural Variation in Arabidopsis Cvi-0 Accession Reveals an Important Role of MPK12 in Guard Cell CO2 Signaling.More than the sum of its parts--how to achieve a specific transcriptional response to abiotic stress.Specificity in ROS signaling and transcript signatures.RCD1-DREB2A interaction in leaf senescence and stress responses in Arabidopsis thaliana.Ligand-binding domain determines endoplasmic reticulum exit of AMPA receptorsMultifactorial biological modulation of warm ischemia reperfusion injury in liver transplantation from non-heart-beating donors eliminates primary nonfunction and reduces bile salt toxicity.Comparison of bleomycin-detectable iron and labile plasma iron assays.Roles of Defense Hormones in the Regulation of Ozone-Induced Changes in Gene Expression and Cell Death.Addition of a water-soluble propofol formulation to preservation solution in experimental kidney transplantation.Cyclodextrin curcumin formulation improves outcome in a preclinical pig model of marginal kidney transplantation.Curcumin as Treatment for Bladder Cancer: A Preclinical Study of Cyclodextrin-Curcumin Complex and BCG as Intravesical Treatment in an Orthotopic Bladder Cancer Rat Model.Cell wall integrity modulates cell cycle gene expression in a cytokinin- and nitrate reductase-dependent mannerThe plant cell wall integrity maintenance and immune signaling systems cooperate to control stress responses inArabidopsis thalianaCell wall integrity maintenance during plant development and interaction with the environmentMitogen-activated protein kinases MPK4 and MPK12 are key components mediating CO2 -induced stomatal movements
P50
Q35510689-43884484-F026-4A1F-AC2B-EEA60C2D02D3Q36214174-4F2E3DCA-B000-4D9A-AD3B-1321FF153A41Q37855289-B1FE451C-1ED3-4C64-85D3-F63210EC85E9Q39322696-57B349F9-10E8-4EAB-BD9B-D5904346024EQ39545489-579EDC25-BB8A-435C-AE0B-90E1D70A274AQ42087907-0E4C519A-5011-4BF9-AE97-4B12E9481ABCQ43262133-5ED101F2-C5F3-4019-AD8E-59C178797FE5Q45165095-EE1B214A-152E-4435-A2DA-B4892041EE6EQ46672949-07D674D1-CD7E-4FFE-822D-F0AAB6F5E71BQ48251936-F2D39B42-3497-4738-A8AF-050A4E9D7BC2Q50711738-55D659DF-9AC0-4E77-A6C6-E467DD2B5973Q55500236-48D8D7B0-847D-4177-861C-ED1B32E17CBBQ57045776-C4A3627B-64D8-4655-89F2-BCA3EF528C0DQ58379584-B79BC51C-8AB2-4E12-B138-D697A0F1D19CQ90045863-DAAB9578-274C-468D-BB1B-2B7446DECA65Q91379765-EA0F32BC-C060-4684-860F-3A86CBDB4D25
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Lauri Vaahtera
@ast
Lauri Vaahtera
@en
Lauri Vaahtera
@es
Lauri Vaahtera
@nl
Lauri Vaahtera
@sl
type
label
Lauri Vaahtera
@ast
Lauri Vaahtera
@en
Lauri Vaahtera
@es
Lauri Vaahtera
@nl
Lauri Vaahtera
@sl
prefLabel
Lauri Vaahtera
@ast
Lauri Vaahtera
@en
Lauri Vaahtera
@es
Lauri Vaahtera
@nl
Lauri Vaahtera
@sl
P106
P21
P31
P496
0000-0003-4733-4430
P569
2000-01-01T00:00:00Z