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Статті в журналах з теми "Flagellati"
Schuhmacher, Jan S., Florian Rossmann, Felix Dempwolff, Carina Knauer, Florian Altegoer, Wieland Steinchen, Anja K. Dörrich, et al. "MinD-like ATPase FlhG effects location and number of bacterial flagella during C-ring assembly." Proceedings of the National Academy of Sciences 112, no. 10 (March 2, 2015): 3092–97. http://dx.doi.org/10.1073/pnas.1419388112.
Повний текст джерелаJensen, C., G. A. Schaub, and D. H. Molyneux. "The effect of Blastocrithidia triatomae (Trypanosomatidae) on the midgut of the reduviid bug Triatoma infestans." Parasitology 100, no. 1 (February 1990): 1–9. http://dx.doi.org/10.1017/s0031182000060054.
Повний текст джерелаNielsen, Lasse Tor, and Thomas Kiørboe. "Foraging trade-offs, flagellar arrangements, and flow architecture of planktonic protists." Proceedings of the National Academy of Sciences 118, no. 3 (January 11, 2021): e2009930118. http://dx.doi.org/10.1073/pnas.2009930118.
Повний текст джерелаMoestrup, Øjvind, and Jahn Throndsen. "Light and electron microscopical studies on Pseudoscourfieldia marina, a primitive scaly green flagellate (Prasinophyceae) with posterior flagella." Canadian Journal of Botany 66, no. 7 (July 1, 1988): 1415–34. http://dx.doi.org/10.1139/b88-197.
Повний текст джерелаWei, Xueming, and Wolfgang D. Bauer. "Starvation-Induced Changes in Motility, Chemotaxis, and Flagellation of Rhizobium meliloti." Applied and Environmental Microbiology 64, no. 5 (May 1, 1998): 1708–14. http://dx.doi.org/10.1128/aem.64.5.1708-1714.1998.
Повний текст джерелаLowenthal, Andrew C., Marla Hill, Laura K. Sycuro, Khalid Mehmood, Nina R. Salama, and Karen M. Ottemann. "Functional Analysis of the Helicobacter pylori Flagellar Switch Proteins." Journal of Bacteriology 191, no. 23 (September 18, 2009): 7147–56. http://dx.doi.org/10.1128/jb.00749-09.
Повний текст джерелаMurat, Dorothée, Marion Hérisse, Leon Espinosa, Alicia Bossa, François Alberto, and Long-Fei Wu. "Opposite and Coordinated Rotation of Amphitrichous Flagella Governs Oriented Swimming and Reversals in a Magnetotactic Spirillum." Journal of Bacteriology 197, no. 20 (August 3, 2015): 3275–82. http://dx.doi.org/10.1128/jb.00172-15.
Повний текст джерелаGray, Victoria L., Michael O'Reilly, Carsten T. Müller, Ian D. Watkins, and David Lloyd. "Low tyrosine content of growth media yields aflagellate Salmonella enterica serovar Typhimurium." Microbiology 152, no. 1 (January 1, 2006): 23–28. http://dx.doi.org/10.1099/mic.0.28442-0.
Повний текст джерелаALLEN-VERCOE, E., A. R. SAYERS, and M. J. WOODWARD. "Virulence of Salmonella enterica serotype Enteritidis aflagellate and afimbriate mutants in a day-old chick model." Epidemiology and Infection 122, no. 3 (June 1999): 395–402. http://dx.doi.org/10.1017/s0950268899002460.
Повний текст джерелаBouteiller, Mathilde, Charly Dupont, Yvann Bourigault, Xavier Latour, Corinne Barbey, Yoan Konto-Ghiorghi, and Annabelle Merieau. "Pseudomonas Flagella: Generalities and Specificities." International Journal of Molecular Sciences 22, no. 7 (March 24, 2021): 3337. http://dx.doi.org/10.3390/ijms22073337.
Повний текст джерелаДисертації з теми "Flagellati"
Antonioli, Marta. "Effects of natural drivers on marine prokaryotic community structure." Doctoral thesis, Università degli studi di Trieste, 2014. http://hdl.handle.net/10077/10136.
Повний текст джерелаHeterotrophic nanoflagellate (HNF) grazing is one of the major source of prokaryotic mortality in marine ecosystems, acting as a strong selection pressure on communities. Protozoans may thus affect prokaryotic abundance and alter the diversity and the taxonomic composition of the prey community, as individual prokaryotes can develop distinct grazing-resistant mechanisms. Moreover, the microbial loop is well known to regulate carbon fluxes in surface marine environments but few studies have quantified the impact of HNF predation on prokaryotes in the dark ocean. The present work was aimed to: (1) quantify the impact of HNF predation on the deep prokaryotes biomass; (2) investigate if and how prey diversity varies in response to different predation pressure; (3) define taxonomic community composition in studied areas and identify most affected prokaryotic phylotypes by HNF grazing (4) evaluate the effects of small HNF (<3 µm), which are known to dominate nano-sized compartment and represent the main bacterivores in aquatic ecosystems, being an important link between bacteria and larger protists; (5) evidence differences in community sensitivity to grazing between surface and mesopelagic ecosystems (6) identify the main environmental drivers shaping microbial community diversity. Predation experiments were performed with surface and mesopelagic water samples collected from the Southern Adriatic and Northern Ionian basins. An additional predation experiment was set up in the North-eastern Adriatic Sea. We coupled the traditional ‘dilution method’ with high-throughput molecular analysis (ARISA and Ion Torrent/454 sequencing) to provide a quantitatively and qualitatively evaluation of the grazing process occurring in marine microbial communities. The present work is structured by four manuscripts in preparation and one manuscript already submitted. 1. Heterotrophic nanoflagellate grazing on picoplankton in deep waters (manuscript in preparation) 2. Effects of heterotrophic flagellate predation on bacterial community diversity (manuscript in preparation) 3. HNF grazing impact on taxonomic composition of marine prokaryotic community (manuscript in preparation) 4. Environmental drivers structuring surface and deep bacterial communities in Adriatic and Ionian Seas (manuscript in preparation) 5. Biodiversity changes of bacterial community under predation pressure analyzed by 16S rRNA pyrosequencing (manuscript submitted) My PhD research led to important progresses in the comprehension of microbial dynamics regulating carbon cycles and bacterial diversity in the Adriatic and Ionian basins. Prokaryotic abundance and biomass were one order of magnitude higher in the photic than in the aphotic layers of Southern Adriatic and Ionian Seas (surface biomass 1.68 ± 1.76 µC L-1, deep biomass 9.00 ± 2.11 µC L-1). The Northern Adriatic community presented the highest biomass value (57.46 µC L-1), according to its richer trophic status. All in situ communities displayed the same evenness, being dominated by rare phylotypes. Rare taxa were confirmed to represent the major contributors of microbial communities, with only a few phylotypes dominant. Mesopelagic bacterial communities were as rich and variable as surface assemblages, despite the significant biomass decrease along the water column. Natural archaeal assemblages were characterized by very low richness as we recovered only two genera (Cenarchaeum and Nitrosopumilus), while in situ bacterial communities were composed by the six major marine phyla (Proteobacteria, Cyanobacteria, Bacteroidetes, Actinobacteria, Firmicutes and Deinococcus-Thermus), whose contribution varied according to sampling depth. Flagellates were demonstrated to efficiently control their preys (ingestion rates: 7.86-22.26 µg C L-1 in surface experiments, 0.53-10.61 µg C L-1 in deep experiments), causing important losses in the potentially produced prokaryotic biomass. Despite picoplankton and HNF abundance reduction with depth contrasts with the hypothesis that at least 108 picoplanktonic cells L-1 are necessary to sustain HNF community, our data confirm that also in mesopelagic waters prey and predator concentrations are sufficient to sustain efficient microbial food webs. HNF grazing modified bacterial community diversity in both surface and deep marine systems but with different strength. Mesopelagic communities were more sensitive to grazing impact, evidencing a bell-shaped response to the increasing ingestion rates. Moderate-high top-down control preserved or enhanced bacterial diversity, that fell at low predation. In upper communities grazing did not induce wide variations of bacterial richness and evenness, revealing to be more stable. Small HNF (<3 µm) were the dominant size fraction within flagellate communities and likely constituted the main bacterivores. After the removal of large HNF, a higher fraction of prokaryotic phylotypes was affected. Larger protists partially reduced small flagellate impact on their preys. Larger HNF had a more important role in photic systems compared to mesopelagic waters. The fraction of bacterial taxa favored or affected by predation when small HNF were the only predators more markedly varied in surface experiments, while few phylotypes changes their behavior between the two size treatments in deep experiments. Some taxa were consumed mainly by larger HNF (3-10 µm), while others were grazed by smaller ones (<3 µm). Over 50% of the predated phylotypes belonged to the rare biosphere, mainly in the surface experiments. Rare bacteria are thus not only a dormant ‘seed bank’ but constitute a fundamental component of microbial food webs and actively vector the carbon transfer toward higher trophic levels, being as important as dominant organisms. Although general patterns applicable to all communities were not found, trends of selectivity over different phylotypes were highlighted within sampling layer along the water column and between different systems. While the majority of predator-prey interactions were characteristic to specific environments, some can be considered common to different systems (e.g. Burkholderiaceae and Pseudomonadaceae were exclusively selected in all mesopelagic sites, Bacterivoracaceae were subjected to small HNF predation independently from sampling site or depth). The Southern Adriatic and Ionian basins were significantly distinguished by both the physicochemical water characteristics and the prokaryotes and protists abundance distributions. Cluster analysis based on Jaccard and Bray-Curtis metrics evidenced that depth and geographical location of sampling sites influenced bacterial community similarity. The Southern Adriatic Sea was clearly distinguished from the Ionian Sea. The Northern Adriatic samples were always separated from the others, coherently with different biotic and abiotic characteristics of the sub-basin. Additionally, temperature, chl a and O2 concentration represented important environmental drivers shaping biodiversity of bacterial communities that inhabit Adriatic and Ionian basins. In conclusion, we evidenced that heterotrophic flagellates control bacterial biomass and select certain taxa among all possible preys, grazing also on the rare ones. HNF predation thus shapes bacterial community structures, which in turn influence the ecosystem functioning. Despite the cell abundance decrease of both predators and preys reduces encounter probabilities, the dark ocean hosts complex microbial food webs, structured around three trophic levels (i.e. prokaryotes, small and large heterotrophic flagellates).
I nanoflagellati eterotrofi (HNF) costituiscono una delle principali cause di mortalità dei procarioti in ambiente marino, esercitando una forte selezione sulle comunità predate. Possono modificarne l’abbondanza cellulare e alterarne la diversità e la composizione tassonomica, in quanto le diverse specie procariotiche possono sviluppare distintivi meccanismi di resistenza alla predazione. Mentre l’impatto degli HNF sui procarioti degli acque marine superficiali è ben noto, pochi studi si sono focalizzati sullo studio degli ambienti profondi. Il presenta lavoro di dottorato è stato finalizzato a: (1) quantificare l’impatto della predazione da parte degli HNF sulla biomassa procariotica profonda; (2) capire se e come la biodiversità della comunità predata vari in risposta alla diversa pressione di predazione; (3) definire la composizione tassonomica delle comunità presenti nell’area di studio e identificare i filotipi maggiormente colpiti dalla predazione da parte degli HNF; (4) valutare il contributo dei piccolo flagellati (<3 µm), i quali costituiscono la più abbondante frazione nanoplanctonica e rappresentano i principali organismi batterivori negli ambienti acquatici; (5) evidenziare possibili differenze nella risposta alla predazione tra comunità procariotiche che vivono in acque superficiali e profonde; (6) identificare i principali fattori ambientali che modulano la diversità delle comunità microbiche. Esperimenti di predazione sono stati condotti su campioni di acqua superficiale e mesopelagica raccolti nel Mar Adriatico meridionale e nel Mar Ionio settentrionale. Un ulteriore esperimento è stato condotto nel Mar Adriatico nord-orientale. Il tradizionale metodo delle diluizioni è stato abbinato ad analisi molecolari quali elettroforesi capillare (ARISA) e sequenziamento (Ion Torrent e 454) per consentire una valutazione quali-quantitativa degli effetti della predazione sulle comunità microbiche marine. La presente tesi è costituita da quattro articoli in preparazione e un articolo già sottomesso: 1. Heterotrophic nanoflagellate grazing on picoplankton in deep waters (articolo in preparazione) 2. Effects of heterotrophic flagellate predation on bacterial community diversity (articolo in preparazione) 3. HNF grazing impact on taxonomic composition of marine prokaryotic community (articolo in preparazione) 4. Environmental drivers structuring surface and deep bacterial communities in Adriatic and Ionian Seas (articolo in preparazione) 5. Biodiversity changes of bacterial community under predation pressure analyzed by 16S rRNA pyrosequencing (articolo sottomesso) La ricerca condotta durante il mio dottorato ha portato a interessanti progressi nella comprensione delle dinamiche microbiche che regolano i cicli del carbonio e la diversità batterica nei bacini adriatico e ionico. L’abbondanza e la biomassa delle comunità procariotiche superficiali è risultata un ordine di grandezza superiore rispetto alle comunità profonde in Mar Adriatico meridionale e Mar Ionio (biomassa superficiale 9.00 ± 2.11 µC L-1, biomassa profonda 1.68 ± 1.76 µC L-1). La comunità descritta nel Mar Adriatico settentrionale è caratterizzata dai valori più elevati di biomassa (57.46 µC L-1), coerentemente con l’eutrofia del bacino. I flagellati eterotrofi hanno causando perdite significative nella biomassa procariotica in tutti gli esperimenti condotti, con tassi di ingestione pari a 7.86-22.26 µgC L-1 negli esperimenti superficiali e 0.53-10.61 µgC L-1 negli esperimenti profondi. Un’abbondanza picoplanctonica di 108 cellule L-1 è stata ipotizzata come necessaria per sostenere la comunità degli flagellati. Nonostante l’aumento della profondità comporti una riduzione dell’abbondanza del picoplancton tale da non raggiungere questa soglia, i nostri dati confermano che anche negli ambienti profondi si instaurano interazione preda-predatore sufficienti a sostenere le reti trofiche microbiche. Tutte le comunità in situ hanno mostrato la medesima distribuzione, con prevalenza di filotipi rari e pochi gruppi dominanti. Le comunità mesopelagiche presentano diversità e variabilità analoghe a quelle superficiali, nonostante il decremento in biomassa lungo la colonna d’acqua. Una bassa diversità è stata osservata nelle comunità naturali di Archea, dove sono stati rilevati due soli generi (Cenarchaeum e Nitrosopumilus), mentre le comunità batteriche sono composte dai sei principali phyla marini (Proteobacteria, Cyanobacteria, Bacteroidetes, Actinobacteria, Firmicutes e Deinococcus-Thermus), la cui frequenza varia in base alla profondità di campionamento. La predazione esercitata dagli HNF ha modificato la diversità delle comunità sia superficiali che profonde ma con diversi effetti. Le comunità profonde si sono dimostrate più suscettibili alla diversa intensità della predazione. Un controllo top-down medio-alto ha preservato o incrementato la diversità batterica, che invece è risultata fortemente ridotta con bassa pressione di predazione. Al contrario, le comunità superficiali hanno subito solo leggere variazioni nella biodiversità batterica in risposta ai diversi tassi di ingestione, dimostrandosi più stabili. I piccoli flagellati (<3 µm) costituiscono la frazione dominante delle comunità nanoplanctoniche. In seguito alla rimozione dei predatori >3 µm, variazione significative dell’abbondanza sono state riscontrate in una maggiore percentuale di filotipi procariotici. Flagellati di maggiori dimensioni possono quindi mitigare l’impatto dei piccoli predatori sulle prede, con una maggior influenza nei sistemi fotici. Alcuni taxa batterici sono stati consumati prevalentemente dal grandi HNF (3-10 µm), mentre altri sono stati selezionati dai piccoli flagellati (<3 µm). Oltre il 50% dei filotipi predati apparteneva alla biosfera rara, soprattutto negli esperimenti condotti in superficie. I batteri rari (0.1-1% dell’abbondanza totale) non rappresentano quindi una frazione ‘dormiente’ il cui contributo varia in seguito a cambiamenti delle condizioni ambientali, come inizialmente ipotizzato. Costituiscono invece una componente fondamentale delle reti trofiche microbiche e contribuiscono attivamente al trasferimento di carbonio verso i livelli trofici superiori, così come gli organismi dominanti. Nonostante ciascuna comunità risponda in maniera distintiva alla predazione, in funzione della composizione tassonomica delle comunità stesse e dello stato trofico del sistema, alcuni indizi di selettività sono stati individuati. Alcune interazioni preda-predatore si sono rivelate tipiche delle comunità profonde o superficiali, mentre altre erano comuni ad entrambi i sistemi (es. Burkholderiaceae e Pseudomonadaceae sono stati selezionati sono in ambiente pelagico, Bacterivoracaceae sono stati sottoposti a predazione da parte di piccolo flagellati in tutti gli esperimenti, indipendentemente dalla profondità e dal sito di campionamento). I bacini Adriatico meridionale e Ionio settentrionale sono significativamente distinti sia per le caratteristiche chimico-fisiche della colonna d’acqua, sia per l’abbondanza di pico- e nanoplancton. La cluster analisi basata sugli indici di Jaccard e Bray-Curtis ha evidenziato che profondità di campionamento e localizzazione geografica sono i principali fattori che determinano la similarità tra le comunità batteriche. Il Mar Adriatico settentrionale è risultato sempre separato dagli altri campioni, coerentemente con le diverse caratteristiche biotiche e abiotiche del bacino. Oltre a profondità e sito geografico, temperatura, concentrazione di chl a e ossigeno contribuiscono a determinare la biodiversità batterica adriatica e ionica. In conclusione, il presente lavoro ha evidenziato come i flagellati eterotrofi controllino la biomassa procariotica e mostrino preferenza per determinati taxa, selezionando anche quelli rari. La predazione influenza la struttura delle comunità e di conseguenza il funzionamento degli ecosistemi. Anche gli ambienti marini profondi ospitano complesse reti trofiche, strutturate attorno a tre livelli principali (procarioti, piccoli e grandi flagellati eterotrofi) così come le acque superficiali.
XXVI Ciclo
1986
Weatherby, Kate Michelle. "The flagellated form of Chromera velia." Thesis, The University of Sydney, 2015. http://hdl.handle.net/2123/14982.
Повний текст джерелаO'Malley, Stephen. "Bi-flagellate swimming dynamics." Thesis, University of Glasgow, 2011. http://theses.gla.ac.uk/2706/.
Повний текст джерелаBiallas, Sandra. "Zur Bedeutung von Endoparasiten bei Chamäleons (Sauria: Chamaeleonidae) aus Wildfängen und Nachzuchten." Doctoral thesis, Universitätsbibliothek Leipzig, 2014. http://nbn-resolving.de/urn:nbn:de:bsz:15-qucosa-133462.
Повний текст джерелаIn the present study 212 chameleon fecal samples were examined for parasite stages and 75 carcasses were examined histopathologically and pathologically in a proven case of a parasite infestation. The basis of this study was to describe the occurrence and harmful effects of internal parasites considering the origin, age and sex of the chameleons. Of the 212 fecal samples 55.2% showed stages of endoparasites. Parasites were detected at 54.7% of 64 evaluated and dissected animals. The proportion of positive samples shows no significant difference between offspring (55.5%) and wild specimens (54.1%). In wild specimens common internal parasites could be determined with an indirect life cycle, however offspring harbored more parasites with a direct life cycle. In the studied chameleons coccidia as the genus Isospora and Oxyurids were regularly detected. In the coprological study Cestodes could not be found, while in the pathological examination they could be diagnosed sporadically in the intestine. Based on the total number of investigated chameleons the frequency of detection of parasite stages are presented as follows: Protozoa were found in 30.4%, 21.7% of the animals were infected with coccidia (of which 78,3% Isospora spp, 13,0% Choleoeimeria spp., 6.5% Eimeria spp., 2.2% polyinfections between Isospora spp./ Choleoeimeria spp.) and 8.5% with flagellates or ciliates. At 83.3% of the animals with gastrointestinal symptoms coccidia of the genus Isospora were detected. In 38.7% of the fecal examination nematodes were determined (65.9% Oxyurids, 19.5% Ascarids/ Heterakis, 1.4% Rhabdias sp., 2.8% Strongyloides sp., 0.5% Spirurida, Heterakids/ Filariae, Oxyurids/ Strongyloides sp.) and Trematodes in 2.8% (Digenea) were found. The anamnesis showed that clinical symptoms could be observed in 35.8% of all of the animals, whereas endoparasite infestation could be detected inn 88.2% of the affected animals. Overall, 64.1% of the dissected chameleons were infested with parasites, of which 68.3% harbored mono- and 31.7% polyinfections. In 31.3% of the dissected chameleons nematode infestations were found and 55.0% of these cases were classified as severe. Prevalences were registered: 25.0% for Strongyloides spp., 23.4% for Ascarids/ Heterakids, 15.0% for Filaria, 5.0% for Rhabdias sp., 9.4% for Cestodes, 10.9% for Digenea. In 11.3% of the cases mixed infections were reported. Thus, endoparasite infestation is common among chameleons and can lead to diseases. Exposure differs from wild-specimens and captive-bred due to the different environmental conditions. Also, 27.8% of clinically healthy animals were also infested with parasites, which means that clinical symptoms are not necessarily the result of a parasitic infestation. Overall, chameleon endoparasites deserve the attention of veterinarians and pet owners and should be treated promptly when there is a high likelihood of infection or hygiene is of concern
Birchall, Christopher. "Coupling flagellar gene expression to flagellar assembly in Caulobacter crescentus." Thesis, University of Newcastle upon Tyne, 2012. http://hdl.handle.net/10443/1617.
Повний текст джерелаWoods, Richard David. "Functionalised Flagellar Nanotubes." Thesis, University of Nottingham, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.489968.
Повний текст джерелаTetley, Laurence. "Ultrastructural studies on parasitic flagellates." Thesis, University of Glasgow, 1986. http://theses.gla.ac.uk/1566/.
Повний текст джерелаKim, Min Jun. "Bacterial flows : mixing and pumping in microfluidic systems using flagellated bacteria /." View online version; access limited to Brown University users, 2005. http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&res_dat=xri:pqdiss&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&rft_dat=xri:pqdiss:3174627.
Повний текст джерелаTiesen, K. L. "Studies on monogenetic kinetoplastid flagellates of hemiptera." Thesis, University of Salford, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.376881.
Повний текст джерелаFraser-Pitt, Douglas. "Microbial and cellular interactions of flagellate pathogen Salmonella enterica serovar enteritidis and flagellate intestinal resident Roseburia sp with intestinal epithelial cells." Thesis, University of Aberdeen, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.446222.
Повний текст джерелаКниги з теми "Flagellati"
T͡Svetaeva, Marina. Les flagellantes: Édition bilingue. Paris: Clémence Hiver, 1988.
Знайти повний текст джерела1932-, Louis-Combet Claude, ed. Histoire des flagellants: Le bon et le mauvais usage de la flagellation parmi les chrétiens, 1701. Montbonnot-St-Martin [France]: J. Millon, 1986.
Знайти повний текст джерелаInternational, Wendlandian Symposium :. Five Decades of Basic Research on Cilia/Flagella and Ciliates/Flagellates (2012 Lüchow Lower Saxony Germany). Cilia and flagella, ciliates and flagellates: Ultrastructure and cell biology, function and systematics, symbiosis and biodiversity. Stuttgart: Schweizerbart Science Publishers, 2014.
Знайти повний текст джерелаFlagellanty: [roman]. Moskva: Vagrius, 2006.
Знайти повний текст джерелаPolite, Carlene Hatcher. The flagellants. Boston: Beacon Press, 1987.
Знайти повний текст джерелаFlagellant on horseback. Lewisville, Tex: Accelerated Christian Education, 1994.
Знайти повний текст джерелаRondeau, Jennifer Fisk. Lay piety and spirituality in the late Middle Ages: The confraternities of North-Central Italy, ca. 1250 to 1348. Ann Arbor, MI: University Microfilms International, 1990.
Знайти повний текст джерелаRondeau, Jennifer Fisk. Lay piety and spirituality in the late Middle Ages [microform]: The confraternities of North-Central Italy, ca. 1250-1348. Ann Arbor, MI: University Microfilms International, 1988.
Знайти повний текст джерелаThe history of the rod: Flagellation and the flagellants in all countries, from the earliest period to the present time. London: Kegan Paul, 2002.
Знайти повний текст джерелаJones, Roger I., and Veijo Ilmavirta, eds. Flagellates in Freshwater Ecosystems. Dordrecht: Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-009-3097-1.
Повний текст джерелаЧастини книг з теми "Flagellati"
Minamino, Tohru, and Shin-Ichi Aizawa. "Biogenesis of Flagella: Export of Flagellar Proteins via the Flagellar Machine." In Protein Secretion Pathways in Bacteria, 249–70. Dordrecht: Springer Netherlands, 2003. http://dx.doi.org/10.1007/978-94-010-0095-6_13.
Повний текст джерелаPiekarski, Gerhard. "Flagellates." In Medical Parasitology, 7–46. Berlin, Heidelberg: Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-72948-5_2.
Повний текст джерелаPeakman, Julie. "Flagellation." In Mighty Lewd Books, 161–86. London: Palgrave Macmillan UK, 2003. http://dx.doi.org/10.1057/9780230512573_8.
Повний текст джерелаBrugerolle, G. "Flagellar and cytoskeletal systems in amitochondrial flagellates: Archamoeba, Metamonada and Parabasala." In The Cytoskeleton of Flagellate and Ciliate Protists, 70–90. Vienna: Springer Vienna, 1991. http://dx.doi.org/10.1007/978-3-7091-6714-4_8.
Повний текст джерелаMehlhorn, Heinz. "Flagella." In Encyclopedia of Parasitology, 1–3. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-642-27769-6_1203-2.
Повний текст джерелаMehlhorn, Heinz. "Flagella." In Encyclopedia of Parasitology, 1024–25. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-43978-4_1203.
Повний текст джерелаLamps, Laura W. "Intestinal Flagellates." In Surgical Pathology of the Gastrointestinal System: Bacterial, Fungal, Viral, and Parasitic Infections, 177–82. New York, NY: Springer US, 2009. http://dx.doi.org/10.1007/978-1-4419-0861-2_29.
Повний текст джерелаHammel, Gavin. "Revolutionary Flagellants? Clerical Perceptions of Flagellant Brotherhoods in Late Medieval Flanders and Italy." In Europa Sacra, 303–30. Turnhout: Brepols Publishers, 2012. http://dx.doi.org/10.1484/m.es-eb.4.00038.
Повний текст джерелаMehlhorn, Heinz. "Flagellar Pocket." In Encyclopedia of Parasitology, 1. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-642-27769-6_1204-2.
Повний текст джерелаMehlhorn, Heinz. "Flagellar Pocket." In Encyclopedia of Parasitology, 1026. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-43978-4_1204.
Повний текст джерелаТези доповідей конференцій з теми "Flagellati"
Okamoto, R. J., J. Ying, B. L. Lewis, E. C. Ranz, J. Y. Shao, S. K. Dutcher, and P. V. Bayly. "Flexural Rigidity of Intact Chlamydomonas Flagella Measured With an Optical Trap." In ASME 2011 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2011. http://dx.doi.org/10.1115/sbc2011-53615.
Повний текст джерелаCheang, U. Kei, Jun Hee Lee, Paul Kim, and Min Jun Kim. "Magnetic Control of Biologically Inspired Robotic Microswimmers." In ASME-JSME-KSME 2011 Joint Fluids Engineering Conference. ASMEDC, 2011. http://dx.doi.org/10.1115/ajk2011-19014.
Повний текст джерелаHesse, William R., Matthew Federici, David M. Casale, Peter Fink, Basil Milton, and Min Jun Kim. "Biologically Inspired Robotic Microswimmers." In ASME 2009 International Mechanical Engineering Congress and Exposition. ASMEDC, 2009. http://dx.doi.org/10.1115/imece2009-10565.
Повний текст джерелаMori, N., K. Kuribayashi, and S. Takeuchi. "“Artificial flagellates” selective attachment of flagella as a bioactuator of micro-object." In TRANSDUCERS 2009 - 2009 International Solid-State Sensors, Actuators and Microsystems Conference. IEEE, 2009. http://dx.doi.org/10.1109/sensor.2009.5285806.
Повний текст джерелаAsadzadeh, Saeed Sayed, Emily Riley, Lasse Tor Nielsen, Thomas Kiørboe, Anders Andersen, and Jens Honore Walther. "Poster: Flagellate Flow." In 71th Annual Meeting of the APS Division of Fluid Dynamics. American Physical Society, 2018. http://dx.doi.org/10.1103/aps.dfd.2018.gfm.p0034.
Повний текст джерелаWong, Denise, Edward B. Steager, and Vijay Kumar. "Near-Wall Dynamics and Photoresponse of Swimming Microbiorobots." In ASME 2012 International Design Engineering Technical Conferences and Computers and Information in Engineering Conference. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/detc2012-71033.
Повний текст джерелаPooran, Ryan, Jin-Woo Kim, Steve Tung, Ajay P. Malshe, and Chuen Cheak Lee. "A Cellular Motor Based Micro Pump: Integration of Cellular Motors With Micro Channels." In ASME 2003 International Mechanical Engineering Congress and Exposition. ASMEDC, 2003. http://dx.doi.org/10.1115/imece2003-41545.
Повний текст джерелаTaheri, Arash, and Meysam Mohammadi-Amin. "Towards a Multi-Flagella Architecture for E.coli Inspired Swimming Microrobot Propulsion." In ASME 2008 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2008. http://dx.doi.org/10.1115/sbc2008-192525.
Повний текст джерелаMulero, Rafael, Alejandro Moraga, and Min Jun Kim. "High Resolution Detection and Configuration of Bacteria Using Microscale Pores." In ASME 2007 International Mechanical Engineering Congress and Exposition. ASMEDC, 2007. http://dx.doi.org/10.1115/imece2007-41199.
Повний текст джерелаPooran, Ryan, Mohamed Al-Fandi, Steve Tung, Jin-Woo Kim, Nalini Kotagi, and Ju Seok Lee. "Bacterial Flagellar Motors as Microfluidic Actuators." In ASME 2004 International Mechanical Engineering Congress and Exposition. ASMEDC, 2004. http://dx.doi.org/10.1115/imece2004-61224.
Повний текст джерелаЗвіти організацій з теми "Flagellati"
Blaser, Martin J., Janet A. Hopkins, Guillermo I. Perez-Perez, Henry J. Cody, and Diane G. Newell. Antigenicity of Campylobacter Jejuni Flagella. Fort Belvoir, VA: Defense Technical Information Center, March 1986. http://dx.doi.org/10.21236/ada265460.
Повний текст джерелаMontie, Thomas C. Mechanism of Flagellar Vaccine Protection Related to Pseudomonas Pathogenesis in Trauma Burns. Fort Belvoir, VA: Defense Technical Information Center, January 1989. http://dx.doi.org/10.21236/ada203539.
Повний текст джерелаQiu, D., Q. Tu, Zhili He, and Jizhong Zhou. Comparative Genomics Analysis and Phenotypic Characterization of Shewanella putrefaciens W3-18-1: Anaerobic Respiration, Bacterial Microcompartments, and Lateral Flagella. Office of Scientific and Technical Information (OSTI), May 2010. http://dx.doi.org/10.2172/986497.
Повний текст джерелаMao, Chuanbin, Penghe Qiu, Lin Wang, Songyuan Yao, Xuewei Qu, and Ningyun Zhou. Controlled synthesis and ordered assembly of Co<sub>3</sub>O<sub>4</sub> nanowires using genetically engineered bacterial flagella as biotemplates (Final Technical Report). Office of Scientific and Technical Information (OSTI), March 2021. http://dx.doi.org/10.2172/1772896.
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