A dynamin GTPase mutation causes a rapid and reversible temperature-inducible locomotion defect in C. elegans. - Wikidata - awgldk - TriplyDB

A dynamin GTPase mutation causes a rapid and reversible temperature-inducible locomotion defect in C. elegans.

A dynamin GTPase mutation causes a rapid and reversible temperature-inducible locomotion defect in C. elegans.

http://www.wikidata.org/entity/Q36587400

about

Evidence that dynamin-2 functions as a signal-transducing GTPase Phagosome maturation during the removal of apoptotic cells: receptors lead the way Collapse of proteostasis represents an early molecular event in Caenorhabditis elegans aging A human dynamin-related protein controls the distribution of mitochondria Defective membrane remodeling in neuromuscular diseases: insights from animal models The C. elegans Opa1 homologue EAT-3 is essential for resistance to free radicals A missense mutation in a highly conserved alternate exon of dynamin-1 causes epilepsy in fitful mice A conserved role for SNX9-family members in the regulation of phagosome maturation during engulfment of apoptotic cells Crystal structure of a dynamin GTPase domain in both nucleotide-free and GDP-bound forms A monoclonal antibody toolkit for C. elegans Nicotine modulates expression of dynamin 1 in rat brain and SH-SY5Y cells.A pathway for phagosome maturation during engulfment of apoptotic cells Cell- and stimulus-dependent heterogeneity of synaptic vesicle endocytic recycling mechanisms revealed by studies of dynamin 1-null neurons.Live-cell imaging in Caenorhabditis elegans reveals the distinct roles of dynamin self-assembly and guanosine triphosphate hydrolysis in the removal of apoptotic cells.The large GTPase dynamin associates with the spindle midzone and is required for cytokinesis.Cellular uptake and infection by canine parvovirus involves rapid dynamin-regulated clathrin-mediated endocytosis, followed by slower intracellular trafficking The advantage of channeling nucleotides for very processive functions Using Caenorhabditis elegans as a model system to study protein homeostasis in a multicellular organism.Smed-dynA-1 is a planarian nervous system specific dynamin 1 homolog required for normal locomotion Neuronal serotonin release triggers the heat shock response in C. elegans in the absence of temperature increase.An overview of C. Elegans trafficking mutants.Genetic analysis of endocytosis in Caenorhabditis elegans: coelomocyte uptake defective mutants Mechanics of dynamin-mediated membrane fission.Synaptic tetraspan vesicle membrane proteins are conserved but not needed for synaptogenesis and neuronal function in Caenorhabditis elegans.Polarity mediates asymmetric trafficking of the Gbeta heterotrimeric G-protein subunit GPB-1 in C. elegans embryos Calpain dysregulation in Alzheimer's disease β-Amyloid carrying the Dutch mutation has diverse effects on calpain-mediated toxicity in hippocampal neurons.Proteomic analysis uncovers a metabolic phenotype in C. elegans after nhr-40 reduction of function Caenorhabditis elegans intersectin: a synaptic protein regulating neurotransmission.Redundant and distinct functions for dynamin-1 and dynamin-2 isoforms.Dynamin and cytokinesis.Dynamin, a membrane-remodelling GTPase.RAB-5- and DYNAMIN-1-Mediated Endocytosis of EFF-1 Fusogen Controls Cell-Cell Fusion.Contribution of the GTPase domain to the subcellular localization of dynamin in the nematode Caenorhabditis elegans Ubiquitously expressed dynamin-II has a higher intrinsic GTPase activity and a greater propensity for self-assembly than neuronal dynamin-I Receptor-mediated endocytosis in the Caenorhabditis elegans oocyte.Clathrin adaptor AP-1 complex excludes multiple postsynaptic receptors from axons in C. elegans In vivo synaptic recovery following optogenetic hyperstimulation Decreased function of survival motor neuron protein impairs endocytic pathways.Ultrafast endocytosis at Caenorhabditis elegans neuromuscular junctions.

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P2860

A dynamin GTPase mutation causes a rapid and reversible temperature-inducible locomotion defect in C. elegans.

http://www.wikidata.org/entity/Q36587400

description

1997 nî lūn-bûn

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A dynamin GTPase mutation caus ...... comotion defect in C. elegans.

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A dynamin GTPase mutation caus ...... comotion defect in C. elegans.

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A dynamin GTPase mutation caus ...... comotion defect in C. elegans.

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A dynamin GTPase mutation caus ...... comotion defect in C. elegans.

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A dynamin GTPase mutation caus ...... comotion defect in C. elegans.

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A dynamin GTPase mutation caus ...... comotion defect in C. elegans.

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Proceedings of the National Academy of Sciences of the United States of America

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A dynamin GTPase mutation caus ...... comotion defect in C. elegans.

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P2093

A M van der Bliek

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C I Bargmann

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D L Shurland

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E M Meyerowitz

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P2860

The genetics of Caenorhabditis elegans

Mutations in human dynamin block an intermediate stage in coated vesicle formation

Efficient gene transfer in C.elegans: extrachromosomal maintenance and integration of transforming sequences

Mitochondrial DNA maintenance in yeast requires a protein containing a region related to the GTP-binding domain of dynamin.

Dynamin self-assembles into rings suggesting a mechanism for coated vesicle budding

The GTPase dynamin binds to and is activated by a subset of SH3 domains

Tubular membrane invaginations coated by dynamin rings are induced by GTP-gamma S in nerve terminals

Genetic analysis of the cha-1-unc-17 gene complex in Caenorhabditis.

Suppression and function of X-linked lethal and sterile mutations in Caenorhabditis elegans.

Differential expression and regulation of multiple dynamins.

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Caenorhabditis elegans

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23381

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