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  • Search Condition : Filter (MeSH = Caenorhabditis elegans / ultrastructure)
Species Resource
C.elegans tm9602 Pathogenetic basis of Takenouchi-Kosaki syndrome: Electron microscopy study using platelets in patients and functional studies in a Caenorhabditis elegans model.
C.elegans SFT-4/Surf4 control ER export of soluble cargo proteins and participate in ER exit site organization.
C.elegans tm3489 , tm5755 , tm2423 , tm847 , tm2253 Autophagy mediates phosphatidylserine exposure and phagosome degradation during apoptosis through specific functions of GABARAP/LGG-1 and LC3/LGG-2.
C.elegans tm1944 Genome-wide surveys reveal polarity and cytoskeletal regulators mediate LKB1-associated germline stem cell quiescence.
C.elegans tm2214 , tm2423 EFF-1 fusogen promotes phagosome sealing during cell process clearance in Caenorhabditis elegans.
C.elegans tm2702 Modulation of caveolae by insulin/IGF-1 signaling regulates aging of Caenorhabditis elegans.
C.elegans An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes.
C.elegans tm1906 , tm2939 , tm2739 , tm5375 PIGN prevents protein aggregation in the endoplasmic reticulum independently of its function in the GPI synthesis.
C.elegans tm3659 , tm6600 The lysosomal membrane protein SCAV-3 maintains lysosome integrity and adult longevity.
C.elegans tm597 WAVE regulates Cadherin junction assembly and turnover during epithelial polarization.
C.elegans tm6221 Novel functions for the RNA-binding protein ETR-1 in Caenorhabditis elegans reproduction and engulfment of germline apoptotic cell corpses.
C.elegans tm2452 , tm3067 , tm3433 , tm3951 , tm4927 , tm925 Centrioles initiate cilia assembly but are dispensable for maturation and maintenance in C. elegans.
C.elegans tm5755 Monitoring Autophagic Responses in Caenorhabditis elegans.
C.elegans tm999 , tm504 , tm1425 Apicobasal domain identities of expanding tubular membranes depend on glycosphingolipid biosynthesis.
C.elegans tm611 Dynein-dependent processive chromosome motions promote homologous pairing in C. elegans meiosis.
C.elegans tm1711 , tm2426 , tm3686 UNC-41/stonin functions with AP2 to recycle synaptic vesicles in Caenorhabditis elegans.
C.elegans tm299 Cell architecture: surrounding muscle cells shape gland cell morphology in the Caenorhabditis elegans pharynx.
C.elegans tm4275 The Caenorhabditis elegans GARP complex contains the conserved Vps51 subunit and is required to maintain lysosomal morphology.
C.elegans tm1108 A molecular switch that governs mitochondrial fusion and fission mediated by the BCL2-like protein CED-9 of Caenorhabditis elegans.
C.elegans tm2452 , tm3100 , tm2547 , tm925 TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone.