scholarly article | Q13442814 |
P2093 | author name string | Marty F | |
P2860 | cites work | Vegetative and Seed-Specific Forms of Tonoplast Intrinsic Protein in the Vacuolar Membrane of Arabidopsis thaliana | Q46510037 |
Getting through the Golgi complex | Q47721647 | ||
Sorting of phaseolin to the vacuole is saturable and requires a short C-terminal peptide. | Q47949203 | ||
Molecular cloning and further characterization of a probable plant vacuolar sorting receptor. | Q48043811 | ||
Cloning and subcellular location of an Arabidopsis receptor-like protein that shares common features with protein-sorting receptors of eukaryotic cells | Q48050460 | ||
Expression of protein disulfide isomerase is elevated in the endosperm of the maize floury-2 mutant | Q48065939 | ||
The plant Golgi apparatus | Q48567126 | ||
Protein storage vacuoles form de novo during pea cotyledon development. | Q49165710 | ||
The tobacco luminal binding protein is encoded by a multigene family | Q49169599 | ||
Determination of the functional elements within the vacuolar targeting signal of barley lectin | Q52518064 | ||
Increased Expression of Vacuolar Aquaporin and H+-ATPase Related to Motor Cell Function in Mimosa pudica L | Q56688782 | ||
The barley lectin carboxyl-terminal propeptide is a vacuolar protein sorting determinant in plants | Q67895029 | ||
Different legumin protein domains act as vacuolar targeting signals | Q67908765 | ||
Changes in the zein composition of protein bodies during maize endosperm development | Q69366516 | ||
Uptake and apparent digestion of cytoplasmic organelles by protein bodies (protein storage vacuoles) in mung bean cotyledons | Q70940377 | ||
Plant cells contain two functionally distinct vacuolar compartments | Q71129259 | ||
Transport of storage proteins to the vacuole is mediated by vesicles without a clathrin coat | Q71787567 | ||
The maize gamma-zein sequesters alpha-zein and stabilizes its accumulation in protein bodies of transgenic tobacco endosperm | Q71959832 | ||
Expression of alpha-amylases, carbohydrate metabolism, and autophagy in cultured rice cells is coordinately regulated by sugar nutrient | Q71986285 | ||
Mutation analysis of the C-terminal vacuolar targeting peptide of tobacco chitinase: low specificity of the sorting system, and gradual transition between intracellular retention and secretion into the extracellular space | Q72299038 | ||
A carboxy-terminal plant vacuolar targeting signal is not recognized by yeast | Q72703229 | ||
The syntaxin homolog AtPEP12p resides on a late post-Golgi compartment in plants | Q73326949 | ||
Coexpression of the maize delta-zein and beta-zein genes results in stable accumulation of delta-zein in endoplasmic reticulum-derived protein bodies formed by beta-zein | Q73808104 | ||
Protein quality control along the route to the plant vacuole | Q73877650 | ||
A Vacuolar-Type H+-ATPase in a Nonvacuolar Organelle Is Required for the Sorting of Soluble Vacuolar Protein Precursors in Tobacco Cells | Q74801347 | ||
Two Structural Domains Mediate Two Sequential Events in [gamma]-Zein Targeting: Protein Endoplasmic Reticulum Retention and Protein Body Formation | Q74817410 | ||
The molecular characterization of transport vesicles | Q77304417 | ||
Deposition of storage proteins | Q77304424 | ||
Sorting of proteins to vacuoles in plant cells | Q77304438 | ||
What do proteins need to reach different vacuoles? | Q77735910 | ||
Novel Regulation of Vegetative Storage Protein Genes | Q78299710 | ||
Protein storage bodies and vacuoles | Q95297204 | ||
The endoplasmic reticulum-gateway of the secretory pathway | Q95297208 | ||
Exocytosis and endocytosis | Q95297219 | ||
Energization of plant cell membranes by H+-pumping ATPases. Regulation and biosynthesis | Q95297226 | ||
Transport of Storage Proteins to Protein Storage Vacuoles Is Mediated by Large Precursor-Accumulating Vesicles | Q95433061 | ||
Autophagy in Tobacco Suspension-Cultured Cells in Response to Sucrose Starvation | Q24673602 | ||
Seed storage proteins: structures and biosynthesis | Q24674134 | ||
Mechanisms of intracellular protein transport | Q28131681 | ||
VPS27 controls vacuolar and endocytic traffic through a prevacuolar compartment in Saccharomyces cerevisiae | Q29620184 | ||
Cell-Mediated Crystallization of Calcium Oxalate in Plants | Q30040079 | ||
Tonoplast intrinsic proteins from cauliflower ( Brassica oleracea L. var. botrytis ): immunological analysis, cDNA cloning and evidence for expression in meristematic tissues | Q32073680 | ||
The Expression Pattern of the Tonoplast Intrinsic Protein gamma-TIP in Arabidopsis thaliana Is Correlated with Cell Enlargement | Q33342382 | ||
Targeting and release of phytohemagglutinin from the roots of bean seedlings | Q33366744 | ||
Antibodies to the tonoplast from the storage parenchyma cells of beetroot recognize a major intrinsic protein related to TIPs | Q33366966 | ||
The specificity of vesicle trafficking: coat proteins and SNAREs | Q33600192 | ||
Proteins for transport of water and mineral nutrients across the membranes of plant cells | Q33600198 | ||
Cytochemical studies on GERL, provacuoles, and vacuoles in root meristematic cells of Euphorbia | Q33962240 | ||
Barley aleurone cells contain two types of vacuoles. Characterization Of lytic organelles by use of fluorescent probes | Q34468782 | ||
Purification and initial characterization of a potential plant vacuolar targeting receptor | Q35173574 | ||
Vacuolar H(+)-translocating ATPases from plants: structure, function, and isoforms | Q35384391 | ||
FROM VACUOLAR GS-X PUMPS TO MULTISPECIFIC ABC TRANSPORTERS. | Q35687194 | ||
PHYSIOLOGY OF ION TRANSPORT ACROSS THE TONOPLAST OF HIGHER PLANTS. | Q35687252 | ||
COMPARTMENTATION OF PROTEINS IN THE ENDOMEMBRANE SYSTEM OF PLANT CELLS. | Q35687276 | ||
Different sensitivity to wortmannin of two vacuolar sorting signals indicates the presence of distinct sorting machineries in tobacco cells. | Q36236046 | ||
Ultrastructural and biochemical characterization of autophagy in higher plant cells subjected to carbon deprivation: control by the supply of mitochondria with respiratory substrates | Q36237121 | ||
Integral membrane protein sorting to vacuoles in plant cells: evidence for two pathways. | Q36256386 | ||
A putative vacuolar cargo receptor partially colocalizes with AtPEP12p on a prevacuolar compartment in Arabidopsis roots | Q36280368 | ||
delta-Tonoplast intrinsic protein defines unique plant vacuole functions. | Q36633862 | ||
Short peptide domains target proteins to plant vacuoles | Q36776293 | ||
AQUAPORINS AND WATER PERMEABILITY OF PLANT MEMBRANES. | Q40891410 | ||
Evidence for secretion of vacuolar α-mannosidase, class I chitinase, and class I β-1,3-glucanase in suspension cultures of tobacco cells | Q41040455 | ||
Evidence for a novel route of wheat storage proteins to vacuoles | Q42028404 | ||
Proaleurain vacuolar targeting is mediated by short contiguous peptide interactions | Q43460307 | ||
Protein sorting to the vacuolar membrane | Q44553422 | ||
Increased expression of the maize immunoglobulin binding protein homolog b-70 in three zein regulatory mutants | Q44816325 | ||
A short domain of the plant vacuolar protein phytohemagglutinin targets invertase to the yeast vacuole | Q46080275 | ||
Tonoplast and Soluble Vacuolar Proteins Are Targeted by Different Mechanisms | Q46198488 | ||
P433 | issue | 4 | |
P921 | main subject | vacuole | Q127702 |
P304 | page(s) | 587-600 | |
P577 | publication date | 1999-04-01 | |
P1433 | published in | The Plant Cell | Q3988745 |
P1476 | title | Plant vacuoles | |
P478 | volume | 11 |
Q35019863 | 3-D analysis of dictyosomes and multivesicular bodies in the green alga Micrasterias denticulata by FIB/SEM tomography |
Q35943858 | A Novel Antifouling Defense Strategy from Red Seaweed: Exocytosis and Deposition of Fatty Acid Derivatives at the Cell Wall Surface |
Q93155166 | A Review of Plant Vacuoles: Formation, Located Proteins, and Functions |
Q58480519 | A complex and mobile structure forms a distinct subregion within the continuous vacuolar membrane in young cotyledons ofArabidopsis |
Q36632710 | A general framework of persistence strategies for biological systems helps explain domains of life |
Q44709144 | A gibberellin-induced nuclease is localized in the nucleus of wheat aleurone cells undergoing programmed cell death |
Q42650629 | A kiss of death--proteasome-mediated membrane fusion and programmed cell death in plant defense against bacterial infection |
Q38574289 | A proteomics dissection of Arabidopsis thaliana vacuoles isolated from cell culture |
Q36883354 | A single cytosine deletion in the OsPLS1 gene encoding vacuolar-type H+-ATPase subunit A1 leads to premature leaf senescence and seed dormancy in rice |
Q53645248 | A unique pattern of F-actin organization supports cytokinesis in vacuolated cells of Macrocystis pyrifera (Phaeophyceae) gametophytes |
Q28350955 | A vacuolar sorting domain may also influence the way in which proteins leave the endoplasmic reticulum |
Q90596661 | A whole-cell electron tomography model of vacuole biogenesis in Arabidopsis root cells |
Q50629372 | AGL61 interacts with AGL80 and is required for central cell development in Arabidopsis |
Q39910829 | Acceleration of vacuolar regeneration and cell growth by overexpression of an aquaporin NtTIP1;1 in tobacco BY-2 cells |
Q36833680 | Accumulation of TIP2;2 Aquaporin during Dark Adaptation Is Partially PhyA Dependent in Roots of Arabidopsis Seedlings |
Q37510793 | Actin bundling in plants. |
Q40284208 | Actin microfilaments regulate vacuolar structures and dynamics: dual observation of actin microfilaments and vacuolar membrane in living tobacco BY-2 Cells |
Q50687633 | Actin-filament-dependent remodeling of the vacuole in cultured mesophyll protoplasts |
Q99635667 | Activities of leaf and spike carbohydrate-metabolic and antioxidant enzymes are linked with yield performance in three spring wheat genotypes grown under well-watered and drought conditions |
Q37848977 | Advances in qualitative and quantitative plant membrane proteomics |
Q33875376 | Ageratum enation virus Infection Induces Programmed Cell Death and Alters Metabolite Biosynthesis in Papaver somniferum |
Q42124435 | Amorphous areas in the cytoplasm of Dendrobium tepal cells: production through organelle degradation and destruction through macroautophagy? |
Q51572923 | An efficient chromatin immunoprecipitation (ChIP) protocol for studying histone modifications in Arabidopsis plants |
Q44171472 | Analysis of the Ca2+ domain in the Arabidopsis H+/Ca2+ antiporters CAX1 and CAX3. |
Q35564752 | Analyzing serial cDNA libraries revealed reactive oxygen species and gibberellins signaling pathways in the salt response of Upland cotton (Gossypium hirsutum L.). |
Q33624905 | Annexins as Overlooked Regulators of Membrane Trafficking in Plant Cells |
Q50699829 | Arabidopsis KAM2/GRV2 is required for proper endosome formation and functions in vacuolar sorting and determination of the embryo growth axis. |
Q47354799 | Arabidopsis VPS38 is required for vacuolar trafficking but dispensable for autophagy |
Q44251369 | Arabidopsis protein disulfide isomerase-5 inhibits cysteine proteases during trafficking to vacuoles before programmed cell death of the endothelium in developing seeds |
Q33359748 | Arabidopsis ribosomal proteins control vacuole trafficking and developmental programs through the regulation of lipid metabolism |
Q64955593 | Arabidopsis tonoplast intrinsic protein and vacuolar H+-adenosinetriphosphatase reflect vacuole dynamics during development of syncytia induced by the beet cyst nematode Heterodera schachtii. |
Q53885767 | Assembly, secretion, and vacuolar delivery of a hybrid immunoglobulin in plants |
Q33343368 | AtATG genes, homologs of yeast autophagy genes, are involved in constitutive autophagy in Arabidopsis root tip cells |
Q53530525 | AtCCX3 is an Arabidopsis endomembrane H+ -dependent K+ transporter |
Q48665199 | AtPTR4 and AtPTR6 are differentially expressed, tonoplast-localized members of the peptide transporter/nitrate transporter 1 (PTR/NRT1) family. |
Q41288931 | Auxin regulates SNARE-dependent vacuolar morphology restricting cell size |
Q46172548 | Biochemical and molecular characterization of senescence-related cysteine protease-cystatin complex from spinach leaf |
Q40738642 | Bud development in corydalis (Corydalis bracteata) requires low temperature: a study of developmental and carbohydrate changes. |
Q27340454 | Cadmium stress disrupts the endomembrane organelles and endocytosis during Picea wilsonii pollen germination and tube growth |
Q48357441 | Calcium controls the formation of vacuoles from mitochondria to regulate microspore development in wheat. |
Q61812968 | Calcium: A Critical Factor in Pollen Germination and Tube Elongation |
Q39139901 | Cell Structural Changes in the Needles of Norway Spruce Exposed to Long-term Ozone and Drought |
Q33341576 | Cell cycle-dependent changes in Golgi stacks, vacuoles, clathrin-coated vesicles and multivesicular bodies in meristematic cells of Arabidopsis thaliana: a quantitative and spatial analysis. |
Q104453571 | Ceropsylla pouteriae Burckhardt sp. nov. (Hemiptera: Psylloidea: Triozidae), a new species of jumping plant-louse inducing galls on the leaves of Pouteria ramiflora (Mart.) Radlk. (Sapotaceae): taxonomy, gall structure and histochemistry |
Q46108877 | Chalk5 encodes a vacuolar H(+)-translocating pyrophosphatase influencing grain chalkiness in rice |
Q37600450 | Chapter 3. New insights into plant vacuolar structure and dynamics |
Q30963252 | Characterization of CAX-like genes in plants: implications for functional diversity |
Q31048375 | Characterization of CAX4, an Arabidopsis H(+)/cation antiporter. |
Q30495595 | Characterization of a novel organelle in Toxoplasma gondii with similar composition and function to the plant vacuole |
Q43125482 | Characterization of anthocyanic vacuolar inclusions in Vitis vinifera L. cell suspension cultures |
Q37903549 | Classes of programmed cell death in plants, compared to those in animals |
Q33356796 | Classical macroautophagy in Lobivia rauschii (Cactaceae) and possible plastidial autophagy in Tillandsia albida (Bromeliaceae) tapetum cells |
Q41730148 | Clathrin-dependent and independent endocytic pathways in tobacco protoplasts revealed by labelling with charged nanogold |
Q24655001 | Cloning of chlorophyllase, the key enzyme in chlorophyll degradation: finding of a lipase motif and the induction by methyl jasmonate |
Q53457291 | Co-occurrence of tannin and tannin-less vacuoles in sensitive plants |
Q84834924 | Comparative spatiotemporal analysis of root aerenchyma formation processes in maize due to sulphate, nitrate or phosphate deprivation |
Q58480248 | Compartmentation of proteins in the protein storage vacuole: A compound organelle in plant cells |
Q33907963 | Contribution of chitinase A's C-terminal vacuolar sorting determinant to the study of soluble protein compartmentation |
Q38086417 | Current Progress in Tonoplast Proteomics Reveals Insights into the Function of the Large Central Vacuole |
Q26743410 | Cytoplasmic vacuolization in cell death and survival |
Q33749127 | Dealing with iron metabolism in rice: from breeding for stress tolerance to biofortification |
Q42136484 | Detecting autophagy in Arabidopsis roots by membrane-permeable cysteine protease inhibitor E-64d and endocytosis tracer FM4–64 |
Q73409547 | Detection and characterization of a 36-kDa peptide in C-terminal region of a 24-kDa vacuolar protein (VP24) precursor in anthocyanin-producing sweet potato cells in suspension culture |
Q41129166 | Different heavy metals have various effects on Picea wilsonii pollen germination and tube growth |
Q36153510 | Dimerization of the Vacuolar Receptors AtRMR1 and -2 from Arabidopsis thaliana Contributes to Their Localization in the trans-Golgi Network |
Q44603584 | Discovery of an extended bundle sheath in Ricinus communis L. and its role as a temporal storage compartment for the iron chelator nicotianamine. |
Q44177299 | Distinct N-terminal regulatory domains of Ca(2+)/H(+) antiporters |
Q42649357 | Do mitochondria in Dendrobium petal mesophyll cells form vacuole-like vesicles? |
Q37853472 | Dynamic intracellular reorganization of cytoskeletons and the vacuole in defense responses and hypersensitive cell death in plants. |
Q44887717 | Dynamic localization of rop GTPases to the tonoplast during vacuole development |
Q37552224 | ER and vacuoles: never been closer. |
Q46556988 | Effect of photosynthetically elevated pH on performance of surface flow-constructed wetland planted with Phragmites australis |
Q33801771 | Endomembranes and vesicle trafficking |
Q38159680 | Endoreduplication and fruit growth in tomato: evidence in favour of the karyoplasmic ratio theory. |
Q95297226 | Energization of plant cell membranes by H+-pumping ATPases. Regulation and biosynthesis |
Q54532807 | Equilibrium dialysis measurements of the Ca2+-binding properties of recombinant radish vacuolar Ca2+-binding protein expressed in Escherichia coli |
Q58788053 | Evidence for preservation of vacuolar compartments during foehn-induced chalky ring formation of Oryza sativa L |
Q52844821 | Evidence for sequential action of Rab5 and Rab7 GTPases in prevacuolar organelle partitioning |
Q87204168 | Expression and functional analysis of putative vacuolar Ca2+-transporters (CAXs and ACAs) in roots of salt tolerant and sensitive rice cultivars |
Q73176608 | Expression of Arabidopsis CAX1 in tobacco: altered calcium homeostasis and increased stress sensitivity |
Q47448098 | Expression of a cauliflower tonoplast aquaporin tagged with GFP in tobacco suspension cells correlates with an increase in cell size |
Q35679063 | Expression of a rice glutaredoxin in aleurone layers of developing and mature seeds: subcellular localization and possible functions in antioxidant defense |
Q45894432 | Expression profiles of aquaporin homologues and petal movement during petal development in Tulipagesneriana |
Q42177089 | Fluorescence imaging-based forward genetic screens to identify trafficking regulators in plants |
Q46756193 | Four-dimensional imaging of transvacuolar strand dynamics in tobacco BY-2 cells |
Q28255106 | Function and evolution of the vacuolar compartment in green algae and land plants (Viridiplantae) |
Q52042884 | Functional association of Arabidopsis CAX1 and CAX3 is required for normal growth and ion homeostasis |
Q33553435 | Functional studies of split Arabidopsis Ca2+/H+ exchangers |
Q37801563 | Gene networks in the synthesis and deposition of protein polymers during grain development of wheat |
Q37461833 | Genes for plant autophagy: functions and interactions |
Q42323519 | Heat stress induces ferroptosis-like cell death in plants. |
Q39174481 | Heterologous expression of the TsVP gene improves the drought resistance of maize |
Q40446201 | Heterologous expression of the plant cysteine protease bromelain and its inhibitor in Pichia pastoris. |
Q38756014 | How do secretory products cross the plant cell wall to be released? A new hypothesis involving cyclic mechanical actions of the protoplast |
Q37643873 | Identification and Functional Characterization of a Tonoplast Dicarboxylate Transporter in Tomato (Solanum lycopersicum). |
Q51109355 | Identification and characterization of two rice autophagy associated genes, OsAtg8 and OsAtg4. |
Q50691280 | Identification and mitotic partitioning strategies of vacuoles in the unicellular red alga Cyanidioschyzon merolae |
Q40292836 | Identification of a nuclear-localized nuclease from wheat cells undergoing programmed cell death that is able to trigger DNA fragmentation and apoptotic morphology on nuclei from human cells |
Q36768265 | Identification of plant vacuolar transporters mediating phosphate storage |
Q44733135 | Identification of the protein storage vacuole and protein targeting to the vacuole in leaf cells of three plant species |
Q34662426 | Immunity in plants and animals: common ends through different means using similar tools. |
Q73907224 | Immunolocalization of a cysteine protease in vacuoles, vesicles, and symbiosomes of pea nodule cells |
Q77485487 | Impacts of elevated CO2 and/or O3 on leaf ultrastructure of aspen (Populus tremuloides) and birch (Betula papyrifera) in the Aspen FACE experiment |
Q38011381 | In and out of the plant storage vacuole |
Q38208310 | Involvement of autophagy in the direct ER to vacuole protein trafficking route in plants |
Q48082158 | Isolation and functional characterization of PgTIP1, a hormone-autotrophic cells-specific tonoplast aquaporin in ginseng |
Q51404478 | Isolation of Vacuoles and the Tonoplast |
Q33361956 | Job Sharing in the Endomembrane System: Vacuolar Acidification Requires the Combined Activity of V-ATPase and V-PPase. |
Q48293886 | Leaf senescence and starvation-induced chlorosis are accelerated by the disruption of an Arabidopsis autophagy gene |
Q24813531 | Light-induced morphological alteration in anthocyanin-accumulating vacuoles of maize cells |
Q38860921 | Lysosomal and vacuolar sorting: not so different after all! |
Q33365474 | Macroautophagy occurs in distal TMV-uninfected root tip tissue of tomato taking place systemic PCD. |
Q54798759 | Manganese specificity determinants in the Arabidopsis metal/H+ antiporter CAX2. |
Q48093830 | MdMYB1 Regulates Anthocyanin and Malate Accumulation by Directly Facilitating Their Transport into Vacuoles in Apples |
Q38976072 | MdVHA-A encodes an apple subunit A of vacuolar H+-ATPase and enhances drought tolerance in transgenic tobacco seedlings |
Q38976076 | MdVHP1 encodes an apple vacuolar H+-PPase and enhances stress tolerance in transgenic apple callus and tomato |
Q38008636 | Mechanisms and concepts paving the way towards a complete transport cycle of plant vacuolar sorting receptors. |
Q39799995 | Membrane Traffic and Fusion at Post-Golgi Compartments |
Q42229614 | Membrane trafficking in guard cells during stomatal movement: Application of an image processing technique |
Q46913531 | Metabolic efficiency underpins performance trade-offs in growth of Arabidopsis thaliana |
Q46836271 | Methods for analysis of autophagy in plants |
Q58090579 | Microtubules play a role in trafficking prevacuolar compartments to vacuoles in tobacco pollen tubes |
Q34207876 | Mobile factories: Golgi dynamics in plant cells. |
Q38953837 | Morphological changes in senescing petal cells and the regulatory mechanism of petal senescence |
Q37865383 | Morphological classification of plant cell deaths. |
Q24806666 | Multi site polyadenylation and transcriptional response to stress of a vacuolar type H+-ATPase subunit A gene in Arabidopsis thaliana |
Q48051310 | Multiple Domains in MtENOD8 Protein Including the Signal Peptide Target It to The Symbiosome |
Q44664125 | Mutations in the Ca2+/H+ transporter CAX1 increase CBF/DREB1 expression and the cold-acclimation response in Arabidopsis. |
Q28363935 | Native and artificial reticuloplasmins co-accumulate in distinct domains of the endoplasmic reticulum and in post-endoplasmic reticulum compartments |
Q38875842 | Network-Guided GWAS Improves Identification of Genes Affecting Free Amino Acids |
Q33235636 | Neutral red as a probe for confocal laser scanning microscopy studies of plant roots. |
Q35099380 | New insights into globoids of protein storage vacuoles in wheat aleurone using synchrotron soft X-ray microscopy |
Q24815592 | New insights into the tonoplast architecture of plant vacuoles and vacuolar dynamics during osmotic stress |
Q33344771 | Newly formed vacuoles in root meristems of barley and pea seedlings have characteristics of both protein storage and lytic vacuoles |
Q50672400 | Novel regulation of aquaporins during osmotic stress. |
Q33344307 | Novel tonoplast transporters identified using a proteomic approach with vacuoles isolated from cauliflower buds |
Q86603168 | Ontogenesis of the collapsed layer during haustorium development in the root hemi‐parasite Santalum album Linn |
Q50528158 | Origin and function of the stalk-cell vacuole in Dictyostelium |
Q39348073 | Overexpression of a Panax ginseng tonoplast aquaporin alters salt tolerance, drought tolerance and cold acclimation ability in transgenic Arabidopsis plants |
Q38863068 | Overexpression of the potassium channel TPKb in small vacuoles confers osmotic and drought tolerance to rice |
Q33362001 | Phenotypic Changes in Transgenic Tobacco Plants Overexpressing Vacuole-Targeted Thermotoga maritima BglB Related to Elevated Levels of Liberated Hormones |
Q74136092 | Phenotypic changes in Arabidopsis caused by expression of a yeast vacuolar Ca2+/H+ antiporter |
Q43351232 | Photodegradation of naproxen and its photoproducts in aqueous solution at 254 nm: a kinetic investigation. |
Q38959787 | Physiological Roles of Plant Post-Golgi Transport Pathways in Membrane Trafficking |
Q64068245 | Physiological and Transcriptome Analyses of Early Leaf Senescence for Mutant Rice ( L.) during the Grain-Filling Stage |
Q37805395 | Plant organelle proteomics: collaborating for optimal cell function. |
Q34245919 | Plants on the move: Towards common mechanisms governing mechanically-induced plant movements |
Q84561470 | Pollen tube reuses intracellular components of nucellar cells undergoing programmed cell death in Pinus densiflora |
Q37894596 | Pollen vacuoles and their significance. |
Q48354873 | Pollen-specific regulation of vacuolar H+-PPase expression by multiple cis-acting elements. |
Q37152888 | Preventing unintended proteolysis in plant protein biofactories |
Q28345754 | Primary structure and expression of a 24-kD vacuolar protein (VP24) precursor in anthocyanin-producing cells of sweet potato in suspension culture |
Q50788960 | Processing of ATG8s, ubiquitin-like proteins, and their deconjugation by ATG4s are essential for plant autophagy |
Q43148865 | Production of the Main Celiac Disease Autoantigen by Transient Expression in Nicotiana benthamiana |
Q42291124 | Protein Delivery into Plant Cells: Toward In vivo Structural Biology |
Q88102206 | Protein Storage Vacuoles Originate from Remodeled Preexisting Vacuoles in Arabidopsis thaliana |
Q47924628 | Protein dynamics, activity and cellular localization of soybean lipoxygenases indicate distinct functional roles for individual isoforms. |
Q47676810 | Protein secretion in plants: conventional and unconventional pathways and new techniques |
Q95297204 | Protein storage bodies and vacuoles |
Q33350551 | Protein storage vacuoles are transformed into lytic vacuoles in root meristematic cells of germinating seedlings by multiple, cell type-specific mechanisms. |
Q33600198 | Proteins for transport of water and mineral nutrients across the membranes of plant cells |
Q61807759 | Proteomic dissection of the rice-Fusarium fujikuroi interaction and the correlation between the proteome and transcriptome under disease stress |
Q37524674 | RETRACTED: Overexpression of VP, a vacuolar H+-pyrophosphatase gene in wheat (Triticum aestivum L.), improves tobacco plant growth under Pi and N deprivation, high salinity, and drought |
Q36801483 | Recent progress in living cell imaging of plant cytoskeleton and vacuole using fluorescent-protein transgenic lines and three-dimensional imaging |
Q77591339 | Reevaluation of the effects of brefeldin A on plant cells using tobacco Bright Yellow 2 cells expressing Golgi-targeted green fluorescent protein and COPI antisera |
Q64985890 | Regulation of lipid peroxidation and ferroptosis in diverse species. |
Q41916920 | Reprogramming cells to study vacuolar development |
Q43687221 | Rice two-pore K+ channels are expressed in different types of vacuoles |
Q37832883 | Role of magnesium in alleviation of aluminium toxicity in plants |
Q38771707 | Role of vacuoles in phosphorus storage and remobilization |
Q38291821 | Roles of phosphatidylinositol 3-kinase in root hair growth |
Q46779068 | Routes to the Tonoplast: The Sorting of Tonoplast Transporters in Arabidopsis Mesophyll Protoplasts |
Q33983759 | Scaling properties of cell and organelle size |
Q31013474 | Secretory acid ribonucleases from tomato, Lycopersicon esculentum Mill |
Q34080598 | Sorting of soluble proteins in the secretory pathway of plants |
Q33229459 | Starvation-induced expression of autophagy-related genes in Arabidopsis |
Q38039296 | Structure and function of endosomes in plant cells |
Q39645048 | Sucrose transporter NtSUT4 from tobacco BY-2 involved in plant cell shape during miniprotoplast culture |
Q48058617 | TNO1 Is Involved in Salt Tolerance and Vacuolar Trafficking in Arabidopsis |
Q50729583 | Targeting of the plant vacuolar sorting receptor BP80 is dependent on multiple sorting signals in the cytosolic tail |
Q37325875 | Techniques to study autophagy in plants |
Q92511429 | Tethering of Multi-Vesicular Bodies and the Tonoplast to the Plasma Membrane in Plants |
Q41860078 | The AP-3 adaptor complex is required for vacuolar function in Arabidopsis |
Q49171252 | The AP-3 β adaptin mediates the biogenesis and function of lytic vacuoles in Arabidopsis |
Q59465305 | The Arabidopsis Vacuolar Sorting Receptor1 is required for osmotic stress-induced abscisic acid biosynthesis |
Q78882856 | The Arabidopsis cax1 mutant exhibits impaired ion homeostasis, development, and hormonal responses and reveals interplay among vacuolar transporters |
Q46925211 | The Arabidopsis cax3 mutants display altered salt tolerance, pH sensitivity and reduced plasma membrane H+-ATPase activity. |
Q45529599 | The Arabidopsis central vacuole as an expression system for intracellular transporters: functional characterization of the Cl-/H+ exchanger CLC-7. |
Q28603098 | The Arabidopsis tonoplast is almost devoid of glycoproteins with complex N-glycans, unlike the rat lysosomal membrane |
Q61821921 | The Dual Function of Sugar Carriers: Transport and Sugar Sensing |
Q44102671 | The Role of auxin, pH, and stress in the activation of embryogenic cell division in leaf protoplast-derived cells of alfalfa. |
Q35890900 | The calcium conundrum. Both versatile nutrient and specific signal |
Q37918148 | The cell cycle, including the mitotic cycle and organelle division cycles, as revealed by cytological observations |
Q43028505 | The coiled-coil protein VIG1 is essential for tethering vacuoles to mitochondria during vacuole inheritance of Cyanidioschyzon merolae |
Q83857688 | The effects of various parameters during processing for cryopreservation on the ultrastructure and viability of recalcitrant zygotic embryos of Amaryllis belladonna |
Q47676453 | The endoplasmic reticulum is a hub to sort proteins toward unconventional traffic pathways and endosymbiotic organelles |
Q33356485 | The endoplasmic reticulum is the main membrane source for biogenesis of the lytic vacuole in Arabidopsis. |
Q95297208 | The endoplasmic reticulum-gateway of the secretory pathway |
Q33596356 | The formation of Anthocyanic Vacuolar Inclusions in Arabidopsis thaliana and implications for the sequestration of anthocyanin pigments. |
Q50519300 | The occurrence of 'bulbs', a complex configuration of the vacuolar membrane, is affected by mutations of vacuolar SNARE and phospholipase in Arabidopsis. |
Q36328331 | The plant vacuolar sorting receptor AtELP is involved in transport of NH(2)-terminal propeptide-containing vacuolar proteins in Arabidopsis thaliana. |
Q42574320 | The proteolytic landscape of the yeast vacuole |
Q44101694 | The reorganization of actin filaments is required for vacuolar fusion of guard cells during stomatal opening in Arabidopsis |
Q33881826 | The role of aquaporins in cellular and whole plant water balance |
Q35045498 | The role of vacuolar processing enzymes in plant immunity |
Q33600192 | The specificity of vesicle trafficking: coat proteins and SNAREs |
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