scholarly article | Q13442814 |
P50 | author | Christa Schleper | Q21256844 |
Sonja-Verena Albers | Q21264709 | ||
Egbert J. Boekema | Q114082224 | ||
Behnam Zolghadr | Q114449125 | ||
Mihaela Folea | Q123171762 | ||
Daniela Teichmann | Q125293262 | ||
Malgorzata Ajon | Q125293263 | ||
Sabrina Fröls | Q125293459 | ||
P2093 | author name string | Michaela Wagner | |
Arnold J. M. Driessen | |||
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Gene transfer occurs with enhanced efficiency in biofilms and induces enhanced stabilisation of the biofilm structure | Q34212571 | ||
Active-site residues in the type IV prepilin peptidase homologue PibD from the archaeon Sulfolobus solfataricus. | Q34354030 | ||
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Occurrence and characterization of mercury resistance in the hyperthermophilic archaeon Sulfolobus solfataricus by use of gene disruption | Q34674956 | ||
Type II protein secretion and its relationship to bacterial type IV pili and archaeal flagella | Q35576644 | ||
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Identification of diverse archaeal proteins with class III signal peptides cleaved by distinct archaeal prepilin peptidases. | Q35634559 | ||
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Identification of a system required for the functional surface localization of sugar binding proteins with class III signal peptides in Sulfolobus solfataricus. | Q38302318 | ||
Flagella of Pyrococcus furiosus: multifunctional organelles, made for swimming, adhesion to various surfaces, and cell-cell contacts | Q38503993 | ||
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High spontaneous mutation rate in the hyperthermophilic archaeon Sulfolobus solfataricus is mediated by transposable elements | Q39587443 | ||
Archaeal homolog of bacterial type IV prepilin signal peptidases with broad substrate specificity. | Q39775185 | ||
Pilus formation and protein secretion by the same machinery in Escherichia coli | Q40749053 | ||
Signal Processing and Flagellar Motor Switching During Phototaxis of Halobacterium salinarum | Q40830292 | ||
The flagellar filament structure of the extreme acidothermophile Sulfolobus shibatae B12 suggests that archaeabacterial flagella have a unique and common symmetry and design | Q41623624 | ||
The unique structure of archaeal 'hami', highly complex cell appendages with nano-grappling hooks | Q41627393 | ||
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Conditions for gene disruption by homologous recombination of exogenous DNA into the Sulfolobus solfataricus genome. | Q41829564 | ||
An insertion element of the extremely thermophilic archaeon Sulfolobus solfataricus transposes into the endogenous beta-galactosidase gene | Q42606311 | ||
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Production of recombinant and tagged proteins in the hyperthermophilic archaeon Sulfolobus solfataricus. | Q43019254 | ||
Ca(2+)-dependent cell aggregation of halophilic archaeon, Halobacterium salinarum | Q43019566 | ||
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Structure and assembly of the pseudopilin PulG | Q64449381 | ||
The composition, structure and stability of a group II chaperonin are temperature regulated in a hyperthermophilic archaeon | Q73173102 | ||
Wavelength dependence of ultraviolet-induced DNA damage distribution: involvement of direct or indirect mechanisms and possible artefacts | Q77870753 | ||
An archaeal bi-species biofilm formed by Pyrococcus furiosus and Methanopyrus kandleri | Q81157750 | ||
P433 | issue | 4 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Sulfolobus solfataricus | Q3503466 |
P304 | page(s) | 938-952 | |
P577 | publication date | 2008-10-09 | |
P1433 | published in | Molecular Microbiology | Q6895967 |
P1476 | title | UV-inducible cellular aggregation of the hyperthermophilic archaeon Sulfolobus solfataricus is mediated by pili formation | |
P478 | volume | 70 |
Q35600011 | 40 Years of archaeal virology: Expanding viral diversity |
Q98465470 | A Unique B-Family DNA Polymerase Facilitating Error-Prone DNA Damage Tolerance in Crenarchaeota |
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Q64914374 | An Orc1/Cdc6 ortholog functions as a key regulator in the DNA damage response in Archaea. |
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Q64448582 | Archaeal cell surface biogenesis |
Q35212015 | Archaeal type IV pili and their involvement in biofilm formation |
Q26771992 | Assessing the Ecophysiology of Methanogens in the Context of Recent Astrobiological and Planetological Studies |
Q37123660 | Augmenting the genetic toolbox for Sulfolobus islandicus with a stringent positive selectable marker for agmatine prototrophy |
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Q95695195 | Editorial |
Q64448565 | Effect of UV irradiation on Sulfolobus acidocaldarius and involvement of the general transcription factor TFB3 in the early UV response |
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Q35080773 | Identification of an additional minor pilin essential for piliation in the archaeon Methanococcus maripaludis |
Q64388770 | Increase of positive supercoiling in a hyperthermophilic archaeon after UV irradiation |
Q50508304 | Influence of cell surface structures on crenarchaeal biofilm formation using a thermostable green fluorescent protein |
Q64093463 | Limited Cross-Complementation Between PilB1-C1 and PilB3-C3 Paralogs |
Q37662320 | Lrs14 transcriptional regulators influence biofilm formation and cell motility of Crenarchaea. |
Q42582867 | Mass spectrometry unmasks mystery Methanococcus pilin |
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Q37832278 | Model organisms for genetics in the domain Archaea: methanogens, halophiles, Thermococcales and Sulfolobales |
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Q47119780 | Surface modifications for phase change cooling applications via crenarchaeon Sulfolobus solfataricus P2 bio-coatings. |
Q43031549 | Survival of thermophilic and hyperthermophilic microorganisms after exposure to UV-C, ionizing radiation and desiccation |
Q34223513 | Swapping genes to survive - a new role for archaeal type IV pili |
Q34487668 | Tackling the minority: sulfate-reducing bacteria in an archaea-dominated subsurface biofilm |
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Q36658877 | The archaeal Ced system imports DNA. |
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Q34443421 | The genome of the ammonia-oxidizing Candidatus Nitrososphaera gargensis: insights into metabolic versatility and environmental adaptations. |
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Q46250170 | Versatile cell surface structures of archaea. |
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