By Kornelia Neveling, Anneke I. den Hollander, Frans P. M. Cremers, Rob W. J. Collin (auth.), Bernhard H.F. Weber, THOMAS LANGMANN (eds.)
ISBN-10: 1627030794
ISBN-13: 9781627030793
ISBN-10: 1627030808
ISBN-13: 9781627030809
Over the earlier many years, wisdom concerning the mobile and molecular foundation underlying the visible technique has remarkably elevated. In Retinal Degeneration: equipment and Protocols, specialist researchers within the box supply a advisor of suitable and cutting-edge equipment for learning retinal homeostasis and sickness. those contain tools and methods for addressing telephone tradition platforms and animal types of affliction, their iteration, their phenotypic and molecular characterization in addition to their use in healing methods to the retina. Written within the hugely winning Methods in Molecular Biology™ sequence layout, chapters comprise introductions to their respective themes, lists of the required fabrics and reagents, step by step, conveniently reproducible laboratory protocols, and key pointers on troubleshooting and fending off identified pitfalls.
Authoritative and functional, Retinal Degeneration: equipment and Protocols aids scientists in carrying on with to review the state of the art thoughts of retinal mobilephone biology in health and wellbeing and disease.
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Extra info for Retinal Degeneration: Methods and Protocols
Example text
If F1 mice are not affected but ~25% of F2 mice are affected, the pedigree is designated as a recessive mutation. Once heritability of the observed retinal phenotype is established, retinal mutants are bred and maintained for further characterization leading to gene identification (23, 24). 4. Notes 1. Mouse fundus examination is a very powerful, noninvasive, and high-throughput method for evaluating mouse retinal appearances. It is also very effective in screening for mouse models of human retinal degeneration and diseases, as there are many examples of mouse models of retinal degeneration that were discovered by fundus examination (see refs.
4. SPECTRALIS ® HRA + OCT The principal function of the SPECTRALIS® HRA + OCT (Heidelberg Engineering, Dossenheim, Germany) is based on the confocal scanning laser ophthalmoscopy. Briefly, the retina is illuminated by a focussed laser beam, and the reflected light is captured by a photodetector after passing through a pinhole. The pinhole blocks the light that is not reflected or emitted by the area of interest and in this way blocks scattered light. The intensity of the reflected light or of the emitted fluorescent light at each point is measured by a light-sensitive detector.
Ozgul RK, Siemiatkowska AM, Yucel D, Myers CA, Collin RWJ, Zonneveld MN et al (2011) Exome sequencing and cis-regulatory mapping identify mutations in MAK, a gene encoding a regulator of ciliary length, as a cause of retinitis pigmentosa. Am J Hum Genet 89:253–264 72. Thompson DA, Janecke AR, Lange J, Feathers KL, Hubner CA, McHenry CL et al (2005) Retinal degeneration associated with RDH12 mutations results from decreased 11-cis retinal synthesis due to disruption of the visual cycle. Hum Mol Genet 14:3865–3875 73.
Retinal Degeneration: Methods and Protocols by Kornelia Neveling, Anneke I. den Hollander, Frans P. M. Cremers, Rob W. J. Collin (auth.), Bernhard H.F. Weber, THOMAS LANGMANN (eds.)
by Donald
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