Pages that link to "Q24322595"
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The following pages link to A class of dynamin-like GTPases involved in the generation of the tubular ER network (Q24322595):
Displayed 50 items.
- Reticulon 4 (Q21106505) (← links)
- Atlastin GTPase 3 (Q21116755) (← links)
- Atlastin GTPase 2 (Q21116756) (← links)
- Atlastin GTPase 1 (Q21116759) (← links)
- Receptor expression-enhancing protein 5 (Q21979852) (← links)
- Reticulon 3 (Q21991605) (← links)
- Rab18 and a Rab18 GEF complex are required for normal ER structure (Q24298701) (← links)
- Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12 (Q24301516) (← links)
- Hereditary spastic paraplegia proteins REEP1, spastin, and atlastin-1 coordinate microtubule interactions with the tubular ER network (Q24301595) (← links)
- The cargo-selective retromer complex is a recruiting hub for protein complexes that regulate endosomal tubule dynamics (Q24301952) (← links)
- Rab10 GTPase regulates ER dynamics and morphology (Q24306806) (← links)
- Structural basis for conformational switching and GTP loading of the large G protein atlastin (Q24310183) (← links)
- Protrudin binds atlastins and endoplasmic reticulum-shaping proteins and regulates network formation (Q24318948) (← links)
- Mutation in CPT1C Associated With Pure Autosomal Dominant Spastic Paraplegia (Q24321657) (← links)
- Protein N-myristoylation plays a critical role in the endoplasmic reticulum morphological change induced by overexpression of protein Lunapark, an integral membrane protein of the endoplasmic reticulum (Q24339575) (← links)
- An intimate liaison: spatial organization of the endoplasmic reticulum-mitochondria relationship (Q24630079) (← links)
- Lipid-anchored SNAREs lacking transmembrane regions fully support membrane fusion during neurotransmitter release (Q26269847) (← links)
- Endoplasmic Reticulum: The Favorite Intracellular Niche for Viral Replication and Assembly (Q26747459) (← links)
- The endoplasmic reticulum: structure, function and response to cellular signaling (Q26782462) (← links)
- Membrane-shaping disorders: a common pathway in axon degeneration (Q26852808) (← links)
- Building a nuclear envelope at the end of mitosis: coordinating membrane reorganization, nuclear pore complex assembly, and chromatin de-condensation (Q27025232) (← links)
- The ER-Membrane Transport System Is Critical for Intercellular Trafficking of the NSm Movement Protein and Tomato Spotted Wilt Tospovirus (Q27315865) (← links)
- Phosphorylation of the C Terminus of RHD3 Has a Critical Role in Homotypic ER Membrane Fusion in Arabidopsis (Q27320208) (← links)
- Assembly and release of infectious hepatitis C virus involving unusual organization of the secretory pathway (Q27468952) (← links)
- Yop1p YPR028W (Q27548201) (← links)
- Rtn1p YDR233C (Q27549623) (← links)
- Dynamin-like GTPase SEY1 YOR165W (Q27549844) (← links)
- Structural basis for the nucleotide-dependent dimerization of the large G protein atlastin-1/SPG3A (Q27666539) (← links)
- Structures of the atlastin GTPase provide insight into homotypic fusion of endoplasmic reticulum membranes (Q27667148) (← links)
- Hereditary spastic paraplegia SPG4: what is known and not known about the disease (Q27690406) (← links)
- Peroxins Pex30 and Pex29 Dynamically Associate with Reticulons to Regulate Peroxisome Biogenesis from the Endoplasmic Reticulum (Q27929790) (← links)
- ER network formation requires a balance of the dynamin-like GTPase Sey1p and the Lunapark family member Lnp1p (Q27930779) (← links)
- The dynamin-like GTPase Sey1p mediates homotypic ER fusion in S. cerevisiae (Q27934843) (← links)
- Reticulons Regulate the ER Inheritance Block during ER Stress. (Q27935606) (← links)
- Invited review: Mechanisms of GTP hydrolysis and conformational transitions in the dynamin superfamily (Q28079024) (← links)
- Membrane fission by dynamin: what we know and what we need to know (Q28080135) (← links)
- Protrudin serves as an adaptor molecule that connects KIF5 and its cargoes in vesicular transport during process formation (Q28115614) (← links)
- Arl6IP1 has the ability to shape the mammalian ER membrane in a reticulon-like fashion (Q28116124) (← links)
- Protrudin regulates endoplasmic reticulum morphology and function associated with the pathogenesis of hereditary spastic paraplegia (Q28118650) (← links)
- Transmembrane protein TMEM170A is a newly discovered regulator of ER and nuclear envelope morphogenesis in human cells (Q28118857) (← links)
- Characterization of the chromosome 4 genes that affect fluconazole-induced disomy formation in Cryptococcus neoformans (Q28481426) (← links)
- Atlastin GTPase 1 (Q28562955) (← links)
- A model for the generation and interconversion of ER morphologies (Q28596563) (← links)
- Differentiation of mesenchymal stem cells derived from pancreatic islets and bone marrow into islet-like cell phenotype (Q28741267) (← links)
- Identification of endoplasmic reticulum-shaping proteins in Plasmodium parasites (Q30043108) (← links)
- Transmembrane and coiled-coil domain family 1 is a novel protein of the endoplasmic reticulum (Q30179417) (← links)
- Endoplasmic reticulum-mediated signalling in cellular microdomains (Q30277155) (← links)
- Membrane fission by protein crowding (Q30400661) (← links)
- ADP Ribosylation Factors 1 and 4 and Group VIA Phospholipase A2Regulate Morphology and Intraorganellar Traffic in the Endoplasmic Reticulum–Golgi Intermediate Compartment (Q30497505) (← links)
- Inhibition of TFG function causes hereditary axon degeneration by impairing endoplasmic reticulum structure (Q30538198) (← links)