| scholarly article | Q13442814 |
| P50 | author | Phyllis I Hanson | Q94142273 |
| Teresa V Naismith | Q124153599 | ||
| Abigail B Vander Heyden | Q124153618 | ||
| Erik Lee Snapp | Q57192502 | ||
| P2860 | cites work | Targeting proteins to the lumen of endoplasmic reticulum using N-terminal domains of 11beta-hydroxysteroid dehydrogenase and the 50-kDa esterase | Q22009536 |
| Appropriate function of 11beta-hydroxysteroid dehydrogenase type 1 in the endoplasmic reticulum lumen is dependent on its N-terminal region sharing similar topological determinants with 50-kDa esterase | Q24293608 | ||
| TorsinA in PC12 cells: localization in the endoplasmic reticulum and response to stress | Q24299130 | ||
| Biosynthesis of the dystonia-associated AAA+ ATPase torsinA at the endoplasmic reticulum | Q24306755 | ||
| LULL1 retargets TorsinA to the nuclear envelope revealing an activity that is impaired by the DYT1 dystonia mutation | Q24311570 | ||
| TorsinA binds the KASH domain of nesprins and participates in linkage between nuclear envelope and cytoskeleton | Q24317502 | ||
| Membrane lipids: where they are and how they behave | Q24653084 | ||
| The AAA+ protein torsinA interacts with a conserved domain present in LAP1 and a novel ER protein | Q24678547 | ||
| Malectin: A Novel Carbohydrate-binding Protein of the Endoplasmic Reticulum and a Candidate Player in the Early Steps of Protein N-Glycosylation | Q27650749 | ||
| The X-ray crystal structure of the membrane protein prostaglandin H2 synthase-1 | Q27731226 | ||
| The ERD2 gene determines the specificity of the luminal ER protein retention system | Q27938328 | ||
| A class of membrane proteins shaping the tubular endoplasmic reticulum | Q27940194 | ||
| The N-terminal anchor sequences of 11beta-hydroxysteroid dehydrogenases determine their orientation in the endoplasmic reticulum membrane | Q28144963 | ||
| Prostaglandin H synthase-1: evaluation of C-terminus function | Q28307526 | ||
| Loss of the dystonia-associated protein torsinA selectively disrupts the neuronal nuclear envelope | Q28589351 | ||
| Dynamics of transitional endoplasmic reticulum sites in vertebrate cells | Q28645796 | ||
| ER-to-Golgi transport visualized in living cells | Q29547526 | ||
| Phase separation of integral membrane proteins in Triton X-114 solution | Q29547600 | ||
| Membrane curvature and mechanisms of dynamic cell membrane remodelling | Q29617321 | ||
| AAA+ proteins: have engine, will work | Q29617410 | ||
| How proteins produce cellular membrane curvature | Q29618016 | ||
| Sec16A defines the site for vesicle budding from the endoplasmic reticulum on exit from mitosis | Q30497404 | ||
| Structure of UDP-glucuronosyltransferases in membranes | Q30805786 | ||
| Measuring protein mobility by photobleaching GFP chimeras in living cells | Q33316966 | ||
| MPEx: a tool for exploring membrane proteins | Q33507121 | ||
| Malectin participates in a backup glycoprotein quality control pathway in the mammalian ER. | Q33813564 | ||
| Helix insertion into bilayers and the evolution of membrane proteins | Q33822760 | ||
| The length of and nonhydrophobic residues in the transmembrane domain of dengue virus envelope protein are critical for its retention and assembly in the endoplasmic reticulum | Q33826597 | ||
| Torsin A and its torsion dystonia-associated mutant forms are lumenal glycoproteins that exhibit distinct subcellular localizations | Q33907326 | ||
| A comprehensive comparison of transmembrane domains reveals organelle-specific properties | Q34083658 | ||
| TorsinA: movement at many levels | Q34332541 | ||
| TorsinA in the nuclear envelope | Q34336308 | ||
| Topogenesis of membrane proteins: determinants and dynamics. | Q34353219 | ||
| Mechanisms determining the morphology of the peripheral ER | Q34432619 | ||
| Morphological analysis of the transfer of VSV ts-045 G glycoprotein from the endoplasmic reticulum to the intermediate compartment in vero cells | Q71591238 | ||
| C-terminal Ser/Pro-Thr-Glu-Leu tetrapeptides of prostaglandin endoperoxide H synthases-1 and -2 target the enzymes to the endoplasmic reticulum | Q71607321 | ||
| The transmembrane domain of a carboxyl-terminal anchored protein determines localization to the endoplasmic reticulum | Q71985086 | ||
| An internal signal sequence mediates the targeting and retention of the human UDP-glucuronosyltransferase 1A6 to the endoplasmic reticulum | Q73107093 | ||
| Stop-transfer function of pseudo-random amino acid segments during translocation across prokaryotic and eukaryotic membranes | Q74267941 | ||
| The transitional ER defines a boundary for quality control in the secretion of tsO45 VSV glycoprotein | Q78383188 | ||
| Quantitative proteomics analysis of the secretory pathway | Q79438532 | ||
| The human FK506-binding proteins: characterization of human FKBP19 | Q83095284 | ||
| The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein | Q34438326 | ||
| Distinct roles for the AAA ATPases NSF and p97 in the secretory pathway | Q35799558 | ||
| The organization of endoplasmic reticulum export complexes | Q36237498 | ||
| The torsin-family AAA+ protein OOC-5 contains a critical disulfide adjacent to Sensor-II that couples redox state to nucleotide binding | Q36796834 | ||
| TorsinA protein degradation and autophagy in DYT1 dystonia | Q37023190 | ||
| The pathophysiological basis of dystonias. | Q37088920 | ||
| Interaction of torsinA with its major binding partners is impaired by the dystonia-associated DeltaGAG deletion | Q37459854 | ||
| Mechanisms shaping the membranes of cellular organelles | Q37540213 | ||
| Protein folding in membranes. | Q37681352 | ||
| Protein sorting receptors in the early secretory pathway | Q37763713 | ||
| Molecular pathways in dystonia | Q37816579 | ||
| The membrane association sequences of the prostaglandin endoperoxide synthases-1 and -2 isozymes | Q38331928 | ||
| Low temperature-induced transport blocks as tools to manipulate membrane traffic. | Q38751280 | ||
| Concept and classification of dystonia | Q39512463 | ||
| Rer1p, a retrieval receptor for ER membrane proteins, recognizes transmembrane domains in multiple modes. | Q39897193 | ||
| Consequences of the DYT1 mutation on torsinA oligomerization and degradation | Q39926996 | ||
| Transmembrane domain-dependent partitioning of membrane proteins within the endoplasmic reticulum | Q39994820 | ||
| Phosphatidylinositol 4-phosphate formation at ER exit sites regulates ER export | Q40212158 | ||
| siRNA knock-down of mutant torsinA restores processing through secretory pathway in DYT1 dystonia cells | Q40260791 | ||
| Recognition of transmembrane helices by the endoplasmic reticulum translocon. | Q40464906 | ||
| Characterization of human torsinA and its dystonia-associated mutant form | Q40643431 | ||
| Cholesterol and the Golgi apparatus | Q40840990 | ||
| Hepatitis C virus glycoprotein complex localization in the endoplasmic reticulum involves a determinant for retention and not retrieval. | Q40993767 | ||
| Localization of prostaglandin endoperoxide synthase-1 to the endoplasmic reticulum and nuclear envelope is independent of its C-terminal tetrapeptide-PTEL. | Q41360565 | ||
| Temperature and energy dependence of secretory protein transport in the exocrine pancreas. | Q41860697 | ||
| Transmembrane domain-dependent sorting of proteins to the ER and plasma membrane in yeast | Q42128889 | ||
| A novel transmembrane domain mediating retention of a highly motile herpesvirus glycoprotein in the endoplasmic reticulum | Q42648710 | ||
| Generation and characterization of Dyt1 DeltaGAG knock-in mouse as a model for early-onset dystonia | Q42671584 | ||
| SDS micelles as a membrane-mimetic environment for transmembrane segments | Q43239665 | ||
| Bulk flow revisited: transport of a soluble protein in the secretory pathway | Q43496672 | ||
| Transmembrane domain modulates sorting of membrane proteins in Toxoplasma gondii | Q44824212 | ||
| Conformational flexibility in crystal structures of human 11beta-hydroxysteroid dehydrogenase type I provide insights into glucocorticoid interconversion and enzyme regulation | Q45129829 | ||
| A comparative study of the COX-1 and COX-2 isozymes bound to lipid membranes | Q46304025 | ||
| Molecular code for transmembrane-helix recognition by the Sec61 translocon | Q46853934 | ||
| Determinants of UDP glucuronosyltransferase membrane association and residency in the endoplasmic reticulum | Q47774865 | ||
| Evolutionary biology. Pelvic problems for mammals | Q47778685 | ||
| Protein folding stability can determine the efficiency of escape from endoplasmic reticulum quality control | Q47792459 | ||
| Colocalization of fluorescent markers in confocal microscope images of plant cells. | Q50639755 | ||
| Recapture after exocytosis causes differential retention of protein in granules of bovine chromaffin cells. | Q50796308 | ||
| Anchoring of a monotopic membrane protein: the binding of prostaglandin H2 synthase-1 to the surface of a phospholipid bilayer. | Q52071525 | ||
| RGS4 binds to membranes through an amphipathic alpha -helix. | Q52538794 | ||
| Distinct influences of carboxyl terminal segment structure on function in the two isoforms of prostaglandin H synthase. | Q52543050 | ||
| Interaction of monotopic membrane enzymes with a lipid bilayer: a coarse-grained MD simulation study. | Q53518474 | ||
| ATP-Dependent Formation of Phosphatidylserine-Rich Vesicles from the Endoplasmic Reticulum of Leek Cells | Q57374030 | ||
| Tolcapone: COMT inhibition for the treatment of Parkinson's disease | Q64891739 | ||
| P433 | issue | 16 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | endoplasmic reticulum | Q79927 |
| membrane protein | Q423042 | ||
| P304 | page(s) | 3217-3231 | |
| P577 | publication date | 2011-07-22 | |
| P1433 | published in | The EMBO Journal | Q1278554 |
| P1476 | title | Static retention of the lumenal monotopic membrane protein torsinA in the endoplasmic reticulum | |
| P478 | volume | 30 |
| Q34755811 | A novel carboxyl-terminal heptapeptide initiates the regulated secretion of LH from unique sub-domains of the ER. |
| Q24337565 | A unique C-terminal domain allows retention of matrix metalloproteinase-27 in the endoplasmic reticulum |
| Q35968774 | Access of torsinA to the inner nuclear membrane is activity dependent and regulated in the endoplasmic reticulum |
| Q24310079 | Arresting a Torsin ATPase reshapes the endoplasmic reticulum |
| Q34052884 | Biochemical and cellular analysis of human variants of the DYT1 dystonia protein, TorsinA/TOR1A |
| Q34245374 | Current Gaps in the Understanding of the Subcellular Distribution of Exogenous and Endogenous Protein TorsinA. |
| Q28587463 | ERdj4 protein is a soluble endoplasmic reticulum (ER) DnaJ family protein that interacts with ER-associated degradation machinery |
| Q38646083 | Early-onset torsion dystonia: a novel high-throughput yeast genetic screen for factors modifying protein levels of torsinAΔE. |
| Q28066509 | Getting membrane proteins on and off the shuttle bus between the endoplasmic reticulum and the Golgi complex |
| Q35173159 | How lamina-associated polypeptide 1 (LAP1) activates Torsin. |
| Q35059239 | Intracellular complexes of the early-onset torsion dystonia-associated AAA+ ATPase TorsinA. |
| Q41785405 | LINCing defective nuclear-cytoskeletal coupling and DYT1 dystonia |
| Q39026993 | Membrane defects and genetic redundancy: Are we at a turning point for DYT1 dystonia? |
| Q26825411 | Molecular mechanisms of the localization of membrane proteins in the yeast Golgi compartments |
| Q38976723 | Nuclear envelope breakdown induced by herpes simplex virus type 1 involves the activity of viral fusion proteins. |
| Q86176639 | Putting a finger in the ring |
| Q38697490 | Quantitative Brightness Analysis of Protein Oligomerization in the Nuclear Envelope. |
| Q24338125 | Regulation of Torsin ATPases by LAP1 and LULL1 |
| Q36849988 | Site-specific Proteolysis Mobilizes TorsinA from the Membrane of the Endoplasmic Reticulum (ER) in Response to ER Stress and B Cell Stimulation |
| Q92092210 | The AAA + ATPase TorsinA polymerizes into hollow helical tubes with 8.5 subunits per turn |
| Q33556224 | The BiP molecular chaperone plays multiple roles during the biogenesis of torsinA, an AAA+ ATPase associated with the neurological disease early-onset torsion dystonia |
| Q36934972 | The genetics of dystonias |
| Q38054482 | The oxidative protein folding machinery in plant cells |
| Q36331007 | The ubiquitin ligase F-box/G-domain protein 1 promotes the degradation of the disease-linked protein torsinA through the ubiquitin-proteasome pathway and macroautophagy. |
| Q39095656 | Topology and membrane anchoring of the lysosomal storage disease-related protein CLN5. |
| Q37318355 | Topology of the yeast Ras converting enzyme as inferred from cysteine accessibility studies |
| Q38714582 | TorsinA controls TAN line assembly and the retrograde flow of dorsal perinuclear actin cables during rearward nuclear movement. |
| Q28087663 | Torsins: not your typical AAA+ ATPases |
| Q33887717 | Two membrane-associated regions within the Nodamura virus RNA-dependent RNA polymerase are critical for both mitochondrial localization and RNA replication |
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