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• W2300514967 abstract "Previous articleNext article No AccessPhotographic Technique for Quantitative Physiological Studies of Paramecia and Other Motile CellsMarion L. FergusonMarion L. Ferguson Search for more articles by this author PDFPDF PLUS Add to favoritesDownload CitationTrack CitationsPermissionsReprints Share onFacebookTwitterLinkedInRedditEmail SectionsMoreDetailsFiguresReferencesCited by Volume 30, Number 3Jul., 1957 Article DOIhttps://doi.org/10.1086/physzool.30.3.30160922 Views: 1Total views on this site Citations: 22Citations are reported from Crossref Journal History This article was published in Physiological Zoology (1928-1998), which is continued by Physiological and Biochemical Zoology (1999-present). PDF download Crossref reports the following articles citing this article:Cezary Bregier, Lucja KrzemieŃ-Ojak, Dorota WŁOga, Maria Jerka-Dziadosz, Ewa Joachimiak, Katarzyna Batko, Iwona Filipiuk, Urszula ŚMietanka, Jacek Gaertig, StanisŁAw Fabczak, Hanna Fabczak PHLP2 is essential and plays a role in ciliogenesis and microtubule assembly in Tetrahymena thermophila, Journal of Cellular Physiology 228, no.1111 (Jul 2013): 2175–2189.https://doi.org/10.1002/jcp.24384Katarzyna Sobierajska, Ewa Joachimiak, Cezary Bregier, Stanisław Fabczak, Hanna Fabczak Effect of phosducin silencing on the photokinetic motile response of Blepharisma japonicum, Photochem. Photobiol. Sci. 10, no.11 (Jan 2011): 19–24.https://doi.org/10.1039/C0PP00221FKatarzyna Sobierajska, Ewa Joachimiak, Cezary Bregier, Stanisław Fabczak, Hanna Fabczak Effect of phosducin silencing on the photokinetic motile response of Blepharisma japonicum, Photochem. Photobiol. Sci. 10, no.11 (Jan 2011): 19–24.https://doi.org/10.1039/C0PP00221FMiroslawa Walerczyk, Hanna Fabczak, Stanislaw Fabczak A Videomicroscopic Study of the Effect of l-cis-Diltiazem on the Photobehavior of Stentor coeruleus¶, Photochemistry and Photobiology 77, no.33 (May 2007): 339–342.https://doi.org/10.1562/0031-8655(2003)0770339AVSOTE2.0.CO2Miroslawa Walerczyk, Hanna Fabczak, Stanislaw Fabczak , Photochemistry and Photobiology 77, no.33 ( 2003): 339.https://doi.org/10.1562/0031-8655(2003)077<0339:AVSOTE>2.0.CO;2Hanna Fabczak Contribution of phosphoinositide-dependent signalling to photomotility of Blepharisma ciliate, Journal of Photochemistry and Photobiology B: Biology 55, no.2-32-3 (May 2000): 120–127.https://doi.org/10.1016/S1011-1344(00)00031-2Judith Van Houten, Robin R. Preston Chemokinesis, (Jan 1998): 282–300.https://doi.org/10.1007/978-3-642-73086-3_18Rainer Uhl, Peter Hegemann Adaptation ofChlamydomonas phototaxis: I. A light-scattering apparatus for measuring the phototactic rate of microorganisms with high time resolution, Cell Motility and the Cytoskeleton 15, no.44 (Jan 1990): 230–244.https://doi.org/10.1002/cm.970150406MICHAEL J. DOUGHTY Effect of Extracellular pH on Motility and K + -Induced Ciliary Reversal in Paramecium caudatum1, The Journal of Protozoology 33, no.33 (Apr 2007): 435–441.https://doi.org/10.1111/j.1550-7408.1986.tb05635.xManfred Kraml, Wolfgang Marwan PHOTOMOVEMENT RESPONSES OF THE HETEROTRICHOUS CILIATE Blepharisma Japonicum, Photochemistry and Photobiology 37, no.33 (Mar 1983): 313–319.https://doi.org/10.1111/j.1751-1097.1983.tb04479.xEilo Hildebrand, Stanis?aw Dryl Dependence of ciliary reversal inParamecium on extracellular Ca2+ concentration, Journal of Comparative Physiology ? A 152, no.33 (Jan 1983): 385–394.https://doi.org/10.1007/BF00606243Norma M. Allewell, Janice Oles, J. Wolfe A physicochemical analysis of conjugation in Tetrahymena pyriformis, Experimental Cell Research 97, no.22 (Feb 1976): 394–405.https://doi.org/10.1016/0014-4827(76)90631-5STEPHEN M. GITTLESON, MICHAEL ROGERS Effect of Viscosity on Formation and Sedimentation of Polytomella agilis Vertical Aggregates*, The Journal of Protozoology 19, no.44 (Apr 2007): 630–632.https://doi.org/10.1111/j.1550-7408.1972.tb03545.xUdo Halbach Zum Adaptivwert der zyklomorphen Dornenbildung von Brachionus calyciflorus Pallas (Rotatoria), Oecologia 6, no.33 (Jan 1971): 267–288.https://doi.org/10.1007/BF00344919T.M. Sonneborn Chapter 12 Methods in Paramecium Research, (Jan 1970): 241–339.https://doi.org/10.1016/S0091-679X(08)61758-6 S. M. Gittleson , and T. L. Jahn Pattern Swimming by Polytomella agilis, The American Naturalist 102, no.927927 (Oct 2015): 413–425.https://doi.org/10.1086/282555S.M. Gittleson, T.L. Jahn Vertical aggregations of Polytomella agilis, Experimental Cell Research 51, no.2-32-3 (Jul 1968): 579–586.https://doi.org/10.1016/0014-4827(68)90145-6S. Dryl, A. Grębecki Progress in the study of excitation and response in ciliates, Protoplasma 62, no.2-32-3 (Jun 1966): 255–284.https://doi.org/10.1007/BF01248088D. F. SEARS, S. M. GITTLESON Cellular Narcosis of Paramecium multimicronucleatum by Xenon and Other Chemically Inert Gases*, The Journal of Protozoology 11, no.44 (Apr 2007): 538–546.https://doi.org/10.1111/j.1550-7408.1964.tb01795.xSTEPHEN M. GITTLESON, D. F. SEARS Effects of CO 2 on Paramecium multimicronucleatum *, The Journal of Protozoology 11, no.22 (Apr 2007): 191–199.https://doi.org/10.1111/j.1550-7408.1964.tb01740.xS. Dryl Contributions to mechanism of chemotactic response in Paramecium caudatum, Animal Behaviour 11, no.2-32-3 (Apr 1963): 393–396.https://doi.org/10.1016/S0003-3472(63)80130-XPar E. Faure-Fremiet CILS VIBRATILES ET FLAGELLES, Biological Reviews 36, no.44 (Nov 1961): 464–533.https://doi.org/10.1111/j.1469-185X.1961.tb01598.x" @default.
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