Results 251 to 260 of about 50,736 (296)
Development of flow cytometry assay to quantify packaging of C. jejuni by Tetrahymena species. [PDF]
Schacter M +6 more
europepmc +1 more source
Multi-Task Cascade Forest Framework for Predicting Acute Toxicity across Species. [PDF]
Liu K +7 more
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CABI Compendium, 2022
This datasheet on Tetrahymena pyriformis covers Identity, Distribution, Hosts/Species Affected.
Jerome S. Perlish
semanticscholar +1 more source
This datasheet on Tetrahymena pyriformis covers Identity, Distribution, Hosts/Species Affected.
Jerome S. Perlish
semanticscholar +1 more source
European Journal of Protistology, 1990
Chemotaxis - that is oriented locomotion of single cells - was shown by motion analysis of Tetrahymena thermophila. An electronic registration of swimming tracks was carried out in gradients of chemoattractant established in a modified Zigmond chamber. The attractants used were proteose peptone, platelet extract and fibroblast growth factor.
P, Hellung-Larsen +3 more
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Chemotaxis - that is oriented locomotion of single cells - was shown by motion analysis of Tetrahymena thermophila. An electronic registration of swimming tracks was carried out in gradients of chemoattractant established in a modified Zigmond chamber. The attractants used were proteose peptone, platelet extract and fibroblast growth factor.
P, Hellung-Larsen +3 more
openaire +2 more sources
The Journal of Protozoology, 1977
SYNOPSIS. The source of force generation of beating cilia and flagella is an interaction between the doublet microtubules mediated by the dynein‐1 arms which cause the doublets to slide relative to one another. Previously, we demonstrated direct sliding of Tetrahymena ciliary axonemes by dark field light microscopy.
P, Satir, W S, Sale
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SYNOPSIS. The source of force generation of beating cilia and flagella is an interaction between the doublet microtubules mediated by the dynein‐1 arms which cause the doublets to slide relative to one another. Previously, we demonstrated direct sliding of Tetrahymena ciliary axonemes by dark field light microscopy.
P, Satir, W S, Sale
openaire +2 more sources
Cadmium-thionein in Tetrahymena thermophila and Tetrahymena pyriformis
European Journal of Protistology, 1990The treatment of Tetrahymena thermophila with cadmium causes a reduction in growth rate according to dose; almost all the metal is accumulated in the cytosol where the Zn content is also increased threefold. Bio-Gel and Water 160 (HPLC) column chromatography show that Cd and Zn are bound to a protein with an ultraviolet (UV) spectrum that appears to be
PICCINNI, ESTER +2 more
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2020
Tetrahymena pyriformis (Ehrenberg, 1830) Record as endobiont in Ostracods: This species was recorded in Tonnacypris lutaria (Koch, 1838) found between carapace lamellae and inside limb from Melenci—Bašaid, Danube basin in Serbia (Nikolić & Karan-Žnidaršič 2005).
Chatterjee, Tapas +3 more
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Tetrahymena pyriformis (Ehrenberg, 1830) Record as endobiont in Ostracods: This species was recorded in Tonnacypris lutaria (Koch, 1838) found between carapace lamellae and inside limb from Melenci—Bašaid, Danube basin in Serbia (Nikolić & Karan-Žnidaršič 2005).
Chatterjee, Tapas +3 more
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Tracking Mercury in Individual Tetrahymena Using Capillary Single-cell ICP-MS Online System.
Analytical Chemistry, 2019As a kind of unicellular eukaryotic protozoa, Tetrahymena is located at the bottom of the aquatic food webs and plays an essential role in the bioaccumulation of mercury (Hg).
Jianbo Shi +7 more
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Glutamate dehydrogenase of Tetrahymena
Biochimica et Biophysica Acta (BBA) - Enzymology, 1974Abstract Glutamate dehydrogenase [ l -glutamate: NAD(P) oxidoreductase (deaminating), EC 1.4.1.3] located in the mitochondria and able to utilize NAD, NADP, NADH or NADPH as substrate, has been purified 67-fold from Tetrahymena pyriformis . The activity with the four pyridine nucleotide substrates was catalyzed by a single enzyme as indicated by the
A B, Hooper, K R, Terry, K D, Kemp
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