By Wallace F. Marshall (Eds.)
This new quantity of Methods in Enzymology keeps the legacy of this finest serial with caliber chapters authored by way of leaders within the box. This quantity covers cilia and comprises chapters on such subject matters as equipment for learning ciliary polarity in Xenopus, research of signaling pathways in mammalian spermatozoa, and biochemical and physiological research of axonemal dyneins.
- Continues the legacy of this most appropriate serial with caliber chapters authored through leaders within the box
- Covers cilia
- Contains chapters on such themes as equipment for learning ciliary polarity in Xenopus,
analysis of signaling pathways in mammalian spermatozoa, and biochemical and physiological research of axonemal dyneins
Read Online or Download Cilia, Part B PDF
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Additional resources for Cilia, Part B
A. Each cell type has a specific ciliary length, which reflects their optimal fluid-shear stress. b. 1 to 50 dyne/cm2. 2). 10. Depending on the shape of the chamber, shear stress can be calculated using the following formula. a. Cylindrical shape: tw ¼ 4Q pr 3 b. 1428 r ¼ radius of cylinder in cm a ¼ height of the chamber or thickness of gasket in cm b ¼ width of the chamber or gasket in cm. c. 0076 dyne s/cm2. d. Flow-induced cilium activation is accomplished by a step change in fluid flow rate from a static condition to the designated shear stress.
LOCKSHIN, AND MAURO PIACENTINI Methods in Enzymology li VOLUME 447. RNA Turnover in Bacteria, Archaea and Organelles Edited by LYNNE E. MAQUAT AND CECILIA M. ARRAIANO VOLUME 448. RNA Turnover in Eukaryotes: Nucleases, Pathways and Analysis of mRNA Decay Edited by LYNNE E. MAQUAT AND MEGERDITCH KILEDJIAN VOLUME 449. RNA Turnover in Eukaryotes: Analysis of Specialized and Quality Control RNA Decay Pathways Edited by LYNNE E. MAQUAT AND MEGERDITCH KILEDJIAN VOLUME 450. Fluorescence Spectroscopy Edited by LUDWIG BRAND AND MICHAEL L.
Polycystin-1, STAT6, and P100 function in a pathway that transduces ciliary mechanosensation and is activated in polycystic kidney disease. Developmental Cell, 10(1), 57–69. , Ward, C. , et al. (2001). Comparison of Pkd1-targeted mutants reveals that loss of polycystin-1 causes cystogenesis and bone defects. Human Molecular Genetics, 10(21), 2385–2396.
Cilia, Part B by Wallace F. Marshall (Eds.)