scholarly article | Q13442814 |
P50 | author | Jesus Aguirre | Q61448505 |
Olivia Santana | Q92094013 | ||
Kazuyuki Kuchitsu | Q57560846 | ||
P2093 | author name string | Luis Cárdenas | |
Kenji Hashimoto | |||
Saul Jimenez-Jimenez | |||
P2860 | cites work | Multivesicular compartments proliferate in susceptible and resistant MLA12-barley leaves in response to infection by the biotrophic powdery mildew fungus | Q59382773 |
Multivesicular bodies participate in a cell wall-associated defence response in barley leaves attacked by the pathogenic powdery mildew fungus | Q59382774 | ||
Endocytosis, intracellular sorting, and processing of exosomes by dendritic cells | Q80396444 | ||
The tetraspanin gene ClPLS1 is essential for appressorium-mediated penetration of the fungal pathogen Colletotrichum lindemuthianum | Q81480934 | ||
Exosomes and extracellular vesicles: the path forward | Q88683923 | ||
Plants send small RNAs in extracellular vesicles to fungal pathogen to silence virulence genes | Q88721113 | ||
Exosomal NADPH Oxidase: Delivering Redox Signaling for Healing | Q89061795 | ||
Tyrosine cross-linking of extracellular matrix is catalyzed by Duox, a multidomain oxidase/peroxidase with homology to the phagocyte oxidase subunit gp91phox | Q24291589 | ||
Role of adaptor complex AP-3 in targeting wild-type and mutated CD63 to lysosomes | Q24548353 | ||
Structural organization and interactions of transmembrane domains in tetraspanin proteins | Q24815599 | ||
Exosomes and Other Extracellular Vesicles: The New Communicators in Parasite Infections | Q26782503 | ||
The cuticle and plant defense to pathogens | Q26851416 | ||
Role of tetraspanin CD9 molecule in fertilization of mammals | Q26997100 | ||
The NADPH oxidase complexes in Botrytis cinerea: evidence for a close association with the ER and the tetraspanin Pls1 | Q27315959 | ||
Functional Analysis of the Arabidopsis TETRASPANIN Gene Family in Plant Growth and Development | Q27320154 | ||
Tetraspanin is required for generation of reactive oxygen species by the dual oxidase system in Caenorhabditis elegans | Q27331504 | ||
Tetraspanins in viral infections: a fundamental role in viral biology? | Q27470936 | ||
Reactive oxygen species produced by NADPH oxidase regulate plant cell growth | Q28186765 | ||
Tetraspanin functions and associated microdomains | Q28284176 | ||
The tetraspanin CD63 enhances the internalization of the H,K-ATPase beta-subunit | Q28581216 | ||
Exosomes: extracellular organelles important in intercellular communication | Q29620346 | ||
Strategies for targeting tetraspanin proteins: potential therapeutic applications in microbial infections. | Q30382341 | ||
Crystal Structure of a Full-Length Human Tetraspanin Reveals a Cholesterol-Binding Pocket | Q30395581 | ||
Syntenin-1 is a new component of tetraspanin-enriched microdomains: mechanisms and consequences of the interaction of syntenin-1 with CD63. | Q30445386 | ||
Single-molecule analysis of CD9 dynamics and partitioning reveals multiple modes of interaction in the tetraspanin web. | Q30483143 | ||
Endosomal compartmentalization in three dimensions: Implications for membrane fusion | Q30485900 | ||
A new class of tetraspanins in fungi. | Q30737223 | ||
Fungi have three tetraspanin families with distinct functions | Q31145110 | ||
Tornado1 and tornado2 are required for the specification of radial and circumferential pattern in the Arabidopsis root. | Q33334738 | ||
The TORNADO1 and TORNADO2 genes function in several patterning processes during early leaf development in Arabidopsis thaliana. | Q33342191 | ||
Arabidopsis WIH1 and WIH2 genes act in the transition from somatic to reproductive cell fate | Q33351505 | ||
The tetraspanin superfamily: molecular facilitators | Q33368144 | ||
Clathrin- and caveolin-independent entry of human papillomavirus type 16--involvement of tetraspanin-enriched microdomains (TEMs) | Q33374009 | ||
TETRASPANINs in Plants | Q33571469 | ||
Fungal small RNAs suppress plant immunity by hijacking host RNA interference pathways. | Q33894403 | ||
A permeable cuticle is associated with the release of reactive oxygen species and induction of innate immunity | Q33987429 | ||
Arabidopsis NDR1 is an integrin-like protein with a role in fluid loss and plasma membrane-cell wall adhesion. | Q34170328 | ||
Co-occurrence of tetraspanin and ROS generators: Conservation in protein cross-linking and other developmental processes | Q42846203 | ||
The protein interaction network of extracellular vesicles derived from human colorectal cancer cells | Q43457137 | ||
Molecular characterization of the NADPH oxidase complex in the ergot fungus Claviceps purpurea: CpNox2 and CpPls1 are important for a balanced host-pathogen interaction | Q44044970 | ||
Origin of the tetraspanin uroplakins and their co-evolution with associated proteins: implications for uroplakin structure and function. | Q44266065 | ||
Arabidopsis tetraspanins are confined to discrete expression domains and cell types in reproductive tissues and form homo- and heterodimers when expressed in yeast | Q45245364 | ||
A new panel of epitope mapped monoclonal antibodies recognising the prototypical tetraspanin CD81. | Q46453274 | ||
A mechanism for localized lignin deposition in the endodermis. | Q46705936 | ||
Tetraspanin protein (TSP-15) is required for epidermal integrity in Caenorhabditis elegans. | Q47069533 | ||
Plant extracellular vesicles are incorporated by a fungal pathogen and inhibit its growth. | Q47395352 | ||
The tetraspanin BcPls1 is required for appressorium-mediated penetration of Botrytis cinerea into host plant leaves. | Q48209908 | ||
Fatty acids in arbuscular mycorrhizal fungi are synthesized by the host plant. | Q48304440 | ||
Characterization of exosomes derived from Toxoplasma gondii and their functions in modulating immune responses. | Q48502915 | ||
The Cuticle Mutant eca2 Modifies Plant Defense Responses to Biotrophic and Necrotrophic Pathogens and Herbivory Insects. | Q50052670 | ||
Reactive oxygen species regulate axonal regeneration through the release of exosomal NADPH oxidase 2 complexes into injured axons. | Q50055070 | ||
Understanding the Arbuscule at the Heart of Endomycorrhizal Symbioses in Plants. | Q50131685 | ||
The ekeko mutant demonstrates a role for tetraspanin-like protein in plant development | Q52099107 | ||
Exosomes as emerging players in cancer biology. | Q52350019 | ||
Exosomes derived from Toxoplasma gondii stimulate an inflammatory response through JNK signaling pathway. | Q52654638 | ||
Exosomes in Pathogen Infections: A Bridge to Deliver Molecules and Link Functions. | Q52684228 | ||
Independent genetic mechanisms mediate turgor generation and penetration peg formation during plant infection in the rice blast fungus. | Q53635213 | ||
Exosomes in melanoma: a role in tumor progression, metastasis and impaired immune system activity. | Q54966511 | ||
Appearance of new tetraspanin genes during vertebrate evolution. | Q55048780 | ||
Critical role of exosomes in sperm-egg fusion and virus-induced cell-cell fusion. | Q55262668 | ||
Exosomes: a novel therapeutic target for Alzheimer's disease? | Q55416682 | ||
Engineered exosomes: A new promise for the management of musculoskeletal diseases | Q56335488 | ||
MRP-1/CD9 gene transduction regulates the actin cytoskeleton through the downregulation of WAVE2 | Q57369991 | ||
Mechanism of Structural Tuning of the Hepatitis C Virus Human Cellular Receptor CD81 Large Extracellular Loop | Q58038920 | ||
Dominant point mutation in a tetraspanin gene associated with field-evolved resistance of cotton bollworm to transgenic Bt cotton | Q58091457 | ||
A membrane trafficking pathway regulated by the plant-specific RAB GTPase ARA6 | Q58480443 | ||
EWI-2 and EWI-F link the tetraspanin web to the actin cytoskeleton through their direct association with ezrin-radixin-moesin proteins | Q34524664 | ||
Molecular interactions shaping the tetraspanin web. | Q34557947 | ||
Exosomes secreted by nematode parasites transfer small RNAs to mammalian cells and modulate innate immunity | Q34677714 | ||
Local positive feedback regulation determines cell shape in root hair cells | Q34756725 | ||
Exosome function: from tumor immunology to pathogen biology | Q34760438 | ||
Functional domains in tetraspanin proteins | Q35063179 | ||
Exosomes Secreted from Human Cancer Cell Lines Contain Inhibitors of Apoptosis (IAP). | Q35975247 | ||
Protein-protein interactions in the tetraspanin web. | Q36197803 | ||
Translocation of sickle cell erythrocyte microRNAs into Plasmodium falciparum inhibits parasite translation and contributes to malaria resistance | Q36233996 | ||
An injury-response mechanism conserved across kingdoms determines entry of the fungus Trichoderma atroviride into development | Q36236270 | ||
PLS1, a gene encoding a tetraspanin-like protein, is required for penetration of rice leaf by the fungal pathogen Magnaporthe grisea | Q36244621 | ||
Characterization of integrin-tetraspanin adhesion complexes: role of tetraspanins in integrin signaling | Q36301561 | ||
Fungal Pls1 tetraspanins as key factors of penetration into host plants: a role in re-establishing polarized growth in the appressorium? | Q36405600 | ||
The molecular players of sperm-egg fusion in mammals | Q36436127 | ||
Tetraspanins as regulators of protein trafficking | Q36689336 | ||
Itinerant exosomes: emerging roles in cell and tissue polarity | Q37125856 | ||
Bidirectional cross-kingdom RNAi and fungal uptake of external RNAs confer plant protection. | Q37293060 | ||
Trafficking and function of the tetraspanin CD63. | Q37302224 | ||
Tetraspanins: push and pull in suppressing and promoting metastasis | Q37349647 | ||
Tetraspanin 6: a pivotal protein of the multiple vesicular body determining exosome release and lysosomal degradation of amyloid precursor protein fragments | Q37692628 | ||
Tetraspanins Function as Regulators of Cellular Signaling. | Q37739091 | ||
Intercellular communication: diverse structures for exchange of genetic information | Q38003288 | ||
Tetraspanin genes in plants | Q38011379 | ||
A novel widespread interkingdom signaling circuit | Q38054347 | ||
Extracellular vesicles as emerging intercellular communicasomes | Q38238011 | ||
Tetraspanins at a glance. | Q38240344 | ||
Extracellular vesicles including exosomes are mediators of signal transduction: are they protective or pathogenic? | Q38259278 | ||
Small RNAs--the secret agents in the plant-pathogen interactions. | Q38540282 | ||
Tetraspanin microdomains control localized protein kinase C signaling in B cells | Q38795253 | ||
The tetraspanin web revisited by super-resolution microscopy | Q38852168 | ||
The Multiple Roles of Exosomes in Metastasis | Q39061503 | ||
Molecular cloning, expression pattern, and phylogenetic analysis of a tetraspanin CD82-like molecule in lamprey Lampetra japonica | Q39953189 | ||
Botrytis small RNA Bc-siR37 suppresses plant defense genes by cross-kingdom RNAi. | Q40305383 | ||
Extracellular Vesicles Isolated from the Leaf Apoplast Carry Stress-Response Proteins. | Q40455072 | ||
Multiple levels of interactions within the tetraspanin web. | Q40653750 | ||
Differential stability of tetraspanin/tetraspanin interactions: role of palmitoylation | Q40737579 | ||
Do plant cells secrete exosomes derived from multivesicular bodies? | Q41762411 | ||
Resistance to Botrytis cinerea induced in Arabidopsis by elicitors is independent of salicylic acid, ethylene, or jasmonate signaling but requires PHYTOALEXIN DEFICIENT3. | Q42510135 | ||
P433 | issue | 4 | |
P304 | page(s) | e1581559 | |
P577 | publication date | 2019-03-04 | |
P1433 | published in | Plant Signaling and Behavior | Q15757476 |
P1476 | title | Emerging roles of tetraspanins in plant inter-cellular and inter-kingdom communication | |
P478 | volume | 14 |
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