| scholarly article | Q13442814 |
| P50 | author | Enrico Schleiff | Q30190796 |
| Martina Königer | Q63364031 | ||
| P2093 | author name string | Maik S Sommer | |
| Benjamin L Weis | |||
| Anu B Machettira | |||
| Lucia E Groß | |||
| Bodo Tillmann | |||
| Gisela Englich | |||
| P2860 | cites work | In vivo analysis of interactions between GFP-labeled microfilaments and plastid stromules | Q21261977 |
| Functional characterization of sequence motifs in the transit peptide of Arabidopsis small subunit of rubisco | Q24537590 | ||
| Membrane lipids: where they are and how they behave | Q24653084 | ||
| UGO1 encodes an outer membrane protein required for mitochondrial fusion | Q27937632 | ||
| Exchange of protein molecules through connections between higher plant plastids | Q28241867 | ||
| Stromules: a characteristic cell-specific feature of plastid morphology | Q28306401 | ||
| The mitochondrial isovaleryl-coenzyme a dehydrogenase of arabidopsis oxidizes intermediates of leucine and valine catabolism | Q28366653 | ||
| Chloroplast Omp85 proteins change orientation during evolution. | Q30155498 | ||
| Antimicrobial peptides temporins B and L induce formation of tubular lipid protrusions from supported phospholipid bilayers | Q30478852 | ||
| Non-invasive quantitative detection and applications of non-toxic, S65T-type green fluorescent protein in living plants | Q30734147 | ||
| Mitochondria-targeted GFP highlights the heterogeneity of mitochondrial shape, size and movement within living plant cells | Q30906029 | ||
| MitoTracker Green labeling of mitochondrial proteins and their subsequent analysis by capillary electrophoresis with laser-induced fluorescence detection | Q31150745 | ||
| Random GFP::cDNA fusions enable visualization of subcellular structures in cells of Arabidopsis at a high frequency | Q33180061 | ||
| Temperature-sensitive formation of chloroplast protrusions and stromules in mesophyll cells of Arabidopsis thaliana. | Q33277849 | ||
| A post genomic characterization of Arabidopsis ferredoxins | Q34284953 | ||
| Lipid-protein interactions in biological membranes: a structural perspective | Q35120901 | ||
| GFP technology for live cell imaging | Q35581454 | ||
| Studies of the minimum hydrophobicity of alpha-helical peptides required to maintain a stable transmembrane association with phospholipid bilayer membranes | Q35635918 | ||
| Stromules and the dynamic nature of plastid morphology. | Q35752957 | ||
| Three-dimensional electron microscopic imaging of membrane invaginations in Escherichia coli overproducing the chemotaxis receptor Tsr | Q35893775 | ||
| How lipids affect the activities of integral membrane proteins | Q35935383 | ||
| Increased amounts of HMG-CoA reductase induce "karmellae": a proliferation of stacked membrane pairs surrounding the yeast nucleus | Q36219042 | ||
| Plant mitochondrial dynamics | Q36424412 | ||
| Z-membranes: artificial organelles for overexpressing recombinant integral membrane proteins. | Q36807122 | ||
| Dynamic morphology of plastids and stromules in angiosperm plants | Q37035349 | ||
| Protein modulation of lipids, and vice-versa, in membranes | Q37092582 | ||
| Mechanisms of lipid transport involved in organelle biogenesis in plant cells | Q37538761 | ||
| Links between lipid homeostasis, organelle morphodynamics and protein trafficking in eukaryotic and plant secretory pathways | Q37814211 | ||
| The regulation of mitochondrial morphology: intricate mechanisms and dynamic machinery | Q37891347 | ||
| In the complex family of heat stress transcription factors, HsfA1 has a unique role as master regulator of thermotolerance in tomato | Q38287858 | ||
| The Arabidopsis Dynamin-Like Proteins ADL1C and ADL1E Play a Critical Role in Mitochondrial Morphogenesis | Q38349692 | ||
| Correlated behavior implicates stromules in increasing the interactive surface between plastids and ER tubules | Q38411163 | ||
| Lipid composition of outer leaflet of chloroplast outer envelope determines topology of OEP7. | Q39250697 | ||
| Regulation of leucoplast morphology in roots: interorganellar signaling from mitochondria? | Q41600746 | ||
| Dynamic Remodeling of the Plastid Envelope Membranes - A Tool for Chloroplast Envelope in vivo Localizations | Q42174846 | ||
| Cellular and subcellular localization of phototropin 1. | Q42524695 | ||
| A high-conductance solute channel in the chloroplastic outer envelope from Pea. | Q42681061 | ||
| Visualisation of stromules in transgenic wheat expressing a plastid-targeted yellow fluorescent protein | Q43509471 | ||
| GFP-labelled Rubisco and aspartate aminotransferase are present in plastid stromules and traffic between plastids | Q44750394 | ||
| A role for SENSITIVE TO FREEZING2 in protecting chloroplasts against freeze-induced damage in Arabidopsis | Q45339863 | ||
| Chloroplast import signals: the length requirement for translocation in vitro and in vivo | Q45362257 | ||
| Calcium depletion and calmodulin inhibition affect the import of nuclear-encoded proteins into plant mitochondria | Q46142832 | ||
| Plant mitochondrial rhomboid, AtRBL12, has different substrate specificity from its yeast counterpart. | Q46548852 | ||
| Identification and characterization of Cor413im proteins as novel components of the chloroplast inner envelope | Q46669483 | ||
| Two DEAD-box proteins may be part of RNA-dependent high-molecular-mass protein complexes in Arabidopsis mitochondria | Q46939137 | ||
| BIGYIN, an orthologue of human and yeast FIS1 genes functions in the control of mitochondrial size and number in Arabidopsis thaliana | Q47347611 | ||
| Light-dependent intracellular positioning of mitochondria in Arabidopsis thaliana mesophyll cells | Q47977903 | ||
| Molecular basis of the functional specificities of phototropin 1 and 2. | Q50457851 | ||
| The chloroplast outer membrane protein CHUP1 interacts with actin and profilin | Q50461682 | ||
| Exploring the function-location nexus: using multiple lines of evidence in defining the subcellular location of plant proteins. | Q50589996 | ||
| Approaches to defining dual-targeted proteins in Arabidopsis. | Q50611421 | ||
| Arabidopsis ELONGATED MITOCHONDRIA1 is required for localization of DYNAMIN-RELATED PROTEIN3A to mitochondrial fission sites. | Q50631203 | ||
| Molecular and genetic analyses of Tic20 homologues in Arabidopsis thaliana chloroplasts. | Q51886833 | ||
| Unifying description of the effect of membrane proteins on lipid order. Verification for the melittin/dimyristoylphosphatidylcholine system. | Q52712464 | ||
| Five Arabidopsis reticulon isoforms share endoplasmic reticulum location, topology, and membrane-shaping properties. | Q55052860 | ||
| Convergent Evolution of Receptors for Protein Import into Mitochondria | Q55113469 | ||
| The localization of Tic20 proteins in Arabidopsis thaliana is not restricted to the inner envelope membrane of chloroplasts | Q55113597 | ||
| Does the membrane's physical state control the expression of heat shock and other genes? | Q57364266 | ||
| Stromules: recent insights into a long neglected feature of plastid morphology and function | Q61558877 | ||
| Analysis of short-term changes in the Arabidopsis thaliana glycerolipidome in response to temperature and light | Q61875798 | ||
| Characterisation of new intracellular membranes in Escherichia coli accompanying large scale over-production of the b subunit of F(1)F(o) ATP synthase | Q73055713 | ||
| Cold Acclimation of Arabidopsis thaliana (Effect on Plasma Membrane Lipid Composition and Freeze-Induced Lesions) | Q74781790 | ||
| Changes in chloroplast ultrastructure in some high-alpine plants: adaptation to metabolic demands and climate? | Q80551888 | ||
| Plastid stromules: video microscopy of their outgrowth, retraction, tensioning, anchoring, branching, bridging, and tip-shedding | Q81709481 | ||
| Arabidopsis Tic40 expression in tobacco chloroplasts results in massive proliferation of the inner envelope membrane and upregulation of associated proteins | Q82855357 | ||
| P304 | page(s) | 118 | |
| P577 | publication date | 2011-01-01 | |
| P1433 | published in | Frontiers in Plant Science | Q27723840 |
| P1476 | title | Protein-induced modulation of chloroplast membrane morphology | |
| P478 | volume | 2 |
| Q30152766 | Characterization of the targeting signal in mitochondrial β-barrel proteins |
| Q42373151 | Chloroplast protrusions in leaves of Ranunculus glacialis L. respond significantly to different ambient conditions, but are not related to temperature stress. |
| Q42318264 | Co-expression with the Type 3 Secretion Chaperone CesT from Enterohemorrhagic E. coli Increases Accumulation of Recombinant Tir in Plant Chloroplasts |
| Q51550790 | DNA-binding and repressor function are prerequisites for the turnover of the tomato heat stress transcription factor HsfB1. |
| Q42174846 | Dynamic Remodeling of the Plastid Envelope Membranes - A Tool for Chloroplast Envelope in vivo Localizations |
| Q39381256 | Functional identification of oleate 12-desaturase and ω-3 fatty acid desaturase genes from Perilla frutescens var. frutescens |
| Q92997990 | Maize defective kernel5 is a bacterial TamB homologue required for chloroplast envelope biogenesis |
| Q59127941 | New Insights Into Sunflower ( L.) FatA and FatB Thioesterases, Their Regulation, Structure and Distribution |
| Q55392785 | Plastid Envelope-Localized Proteins Exhibit a Stochastic Spatiotemporal Relationship to Stromules. |
| Q45013568 | Quantitative analysis of the mitochondrial and plastid proteomes of the moss Physcomitrella patens reveals protein macrocompartmentation and microcompartmentation |
| Q47676861 | Sorting of SEC translocase SCY components to different membranes in chloroplasts. |
| Q48373529 | Stromules: Probing Formation and Function. |
| Q27332267 | The Formation of Stromules In Vitro from Chloroplasts Isolated from Nicotiana benthamiana |
| Q40501108 | The Sec2 translocase of the chloroplast inner envelope contains a unique and dedicated SECE2 component. |
| Q48245034 | The plastid outer membrane localized LPTD1 is important for glycerolipid remodelling under phosphate starvation |
| Q92743763 | Toc75-V/OEP80 is processed during translocation into chloroplasts, and the membrane-embedded form exposes its POTRA domain to the intermembrane space |
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