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Cilia and Mucus: From Development to Respiratory Defense by Matthias Salathe

By Matthias Salathe

This booklet information advances in study relating to cilia, mucus, and mucociliary clearance, studying adjustments in mucus expression and goblet mobilephone metaplasia, and assessing the power of the mucociliary process to reply to abnormalities. acknowledges that cilia and dynein palms play pivotal roles in constructing mammalian embryos!Examines the function of genetics in basic and irregular ciliary function!Discussing clinical basics, present diagnostic ideas, and clinically established remedies, Cilia and Mucus analyzes the legislation of ciliary waves on the mobile point considers irregularities of higher and decrease airlines and cilia in platforms of the physique explores strength modulators of airway mucin secretion proposes a singular remedy for airway hypersecretion as a result epidermal development issue cascade clarifies gamma digicam imaging to degree mucociliary clearance describes the impression of purinergic receptors and dry powder mannitol on airway passages and extra! With contributions from over a hundred foreign researchers and clinicians, and containing over 1300 references, drawings, images, tables, and equations, Cilia and Mucus is a distinct single-source reference for pulmonologists, physiologists, immunologists, allergists, otolaryngologists, pediatricians, microbiologists, uncomplicated scientists, and graduate and scientific institution scholars in those disciplines.

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Develop Growth Differ 22:373–384, 1980. 43. MM Pratt. The identification of a dynein ATPase in unfertilized sea urchin eggs. Dev Biol 74:364–378, 1980. 44. JM Scholey, B Neighbors, JR McIntosh, ED Salmon. Isolation of microtubules and a dynein-like MgATPase from unfertilized sea urchin eggs. J Biol Chem 259:6516– 6525, 1984. 16 Asai 45. PJ Hollenbeck, F Suprynowicz, WZ Cande. Cytoplasmic dynein-like ATPase crosslinks microtubules in an ATP-sensitive manner. J Cell Biol 99:1251–1258, 1984. 46. DJ Asai, L Wilson.

Y Tanaka, Z Zhang, N Hirokawa. Identification and molecular evolution of new dynein-like protein sequences in rat brain. J Cell Sci 108:1883–1893, 1995. 59. EA Vaisberg, PM Grissom, JR McIntosh. Mammalian cells express three distinct dynein heavy chains that are localized to different cytoplasmic organelles. J Cell Biol 133:831–842, 1996. 60. A Harada, Y Takei, Y Kanai, Y Tanaka, S Nonaka, N Hirokawa. Golgi vesiculation and lysosome dispersion in cells lacking cytoplasmic dynein. J Cell Biol 141:51– 59, 1998.

DJ Asai. Multi-dynein hypothesis. Cell Motil Cytoskel 32:129–132, 1995. 29. DJ Asai. Functional and molecular diversity of dynein heavy chains. Sems Cell Devel Biol 7:311–320, 1996. 30. D Mazia, RR Chaffee, RM Iverson. Adenosine triphosphatase in the mitotic apparatus. Proc Natl Acad Sci USA 47:788–790, 1961. 31. R Weisenberg, EW Taylor. Studies on ATPase activity of sea urchin eggs and the isolated mitotic apparatus. Exp Cell Res 53:372–384, 1968. 32. T Miki. The ATPase activity of the mitotic apparatus of the sea urchin egg.

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