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Current understanding of grapevine defense mechanisms against the biotrophic fungus (Erysiphe necator), the causal agent of powdery mildew diseaseCommandeering Channel Voltage Sensors for Secretion, Cell Turgor, and Volume ControlArabidopsis R-SNARE proteins VAMP721 and VAMP722 are required for cell plate formationHow membranes shape plant symbioses: signaling and transport in nodulation and arbuscular mycorrhizaActivation of defense against Phytophthora infestans in potato by down-regulation of syntaxin gene expression.MoVam7, a conserved SNARE involved in vacuole assembly, is required for growth, endocytosis, ROS accumulation, and pathogenesis of Magnaporthe oryzaeMapping the Arabidopsis organelle proteomeVinyl sulfone silica: application of an open preactivated support to the study of transnitrosylation of plant proteins by S-nitrosoglutathione.A physical map of the heterozygous grapevine 'Cabernet Sauvignon' allows mapping candidate genes for disease resistanceSNAREs: cogs and coordinators in signaling and development.Transcriptome Analysis of Chilling-Imbibed Embryo Revealed Membrane Recovery Related Genes in Maize.Arabidopsis Qc-SNARE gene AtSFT12 is involved in salt and osmotic stress responses and Na(+) accumulation in vacuoles.Interactomics of Qa-SNARE in Arabidopsis thaliana.Arabidopsis Sec1/Munc18 protein SEC11 is a competitive and dynamic modulator of SNARE binding and SYP121-dependent vesicle traffic.Selective mobility and sensitivity to SNAREs is exhibited by the Arabidopsis KAT1 K+ channel at the plasma membrane.Binding of SEC11 indicates its role in SNARE recycling after vesicle fusion and identifies two pathways for vesicular traffic to the plasma membrane.SNARE protein FgVam7 controls growth, asexual and sexual development, and plant infection in Fusarium graminearum.A novel di-acidic motif facilitates ER export of the syntaxin SYP31.Selective regulation of maize plasma membrane aquaporin trafficking and activity by the SNARE SYP121.Mutations in the Arabidopsis phosphoinositide phosphatase gene SAC9 lead to overaccumulation of PtdIns(4,5)P2 and constitutive expression of the stress-response pathway.Arabidopsis SNAREs SYP61 and SYP121 coordinate the trafficking of plasma membrane aquaporin PIP2;7 to modulate the cell membrane water permeability.Participation of endomembrane cation/H+ exchanger AtCHX20 in osmoregulation of guard cells.Overexpression of the Arabidopsis syntaxin PEP12/SYP21 inhibits transport from the prevacuolar compartment to the lytic vacuole in vivo.Functional characterization of ice plant SKD1, an AAA-type ATPase associated with the endoplasmic reticulum-Golgi network, and its role in adaptation to salt stress.Novel targeting signals mediate the sorting of different isoforms of the tail-anchored membrane protein cytochrome b5 to either endoplasmic reticulum or mitochondria.The Arabidopsis R-SNARE VAMP721 Interacts with KAT1 and KC1 K+ Channels to Moderate K+ Current at the Plasma Membrane.VAMP711 Is Required for Abscisic Acid-Mediated Inhibition of Plasma Membrane H-ATPase Activity
P2860
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P2860
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
A new catch in the SNARE.
@ast
A new catch in the SNARE.
@en
type
label
A new catch in the SNARE.
@ast
A new catch in the SNARE.
@en
prefLabel
A new catch in the SNARE.
@ast
A new catch in the SNARE.
@en
P1476
A new catch in the SNARE
@en
P2093
Jens-Uwe Sutter
Réjane Pratelli
P304
P356
10.1016/J.TPLANTS.2004.02.007
P577
2004-04-01T00:00:00Z