Desmin and Vimentin Expression during Embryonic Development of Tensor Veli Palatini Muscle in Mice

Fumiaki Kobayashi; Masahito Yamamoto; Kei Kitamura; Kishi Asuka; Hideaki Kinoshita; Satoru Matsunaga; Shin-ichi Abe

doi:10.2485/jhtb.24.134

Desmin and Vimentin Expression during Embryonic Development of Tensor Veli Palatini Muscle in Mice

Journal of Hard Tissue Biology ◽

10.2485/jhtb.24.134 ◽

2015 ◽

Vol 24 (2) ◽

pp. 134-142 ◽

Cited By ~ 3

Author(s):

Fumiaki Kobayashi ◽

Masahito Yamamoto ◽

Kei Kitamura ◽

Kishi Asuka ◽

Hideaki Kinoshita ◽

...

Keyword(s):

Embryonic Development ◽

Vimentin Expression ◽

Tensor Veli Palatini Muscle

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Transient vimentin expression during the embryonic development of the chicken cerebellum

International Journal of Developmental Neuroscience ◽

10.1016/j.ijdevneu.2017.10.003 ◽

2017 ◽

Vol 65 (1) ◽

pp. 11-20 ◽

Cited By ~ 1

Author(s):

Vasiliki Kommata ◽

Catherine R. Dermon

Keyword(s):

Embryonic Development ◽

Vimentin Expression

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Live Confocal Analysis of Fertilization and Early Development

Microscopy and Microanalysis ◽

10.1017/s1431927600031135 ◽

2001 ◽

Vol 7 (S2) ◽

pp. 1012-1013

Author(s):

Uyen Tram ◽

William Sullivan

Keyword(s):

Drosophila Melanogaster ◽

Embryonic Development ◽

Real Time ◽

Early Development ◽

Fluorescent Probes ◽

Primary Defect ◽

Fluorescent Analysis ◽

Dynamic Event ◽

Enormous Amount ◽

Fluorescent Studies

Embryonic development is a dynamic event and is best studied in live animals in real time. Much of our knowledge of the early events of embryogenesis, however, comes from immunofluourescent analysis of fixed embryos. While these studies provide an enormous amount of information about the organization of different structures during development, they can give only a static glimpse of a very dynamic event. More recently real-time fluorescent studies of living embryos have become much more routine and have given new insights to how different structures and organelles (chromosomes, centrosomes, cytoskeleton, etc.) are coordinately regulated. This is in large part due to the development of commercially available fluorescent probes, GFP technology, and newly developed sensitive fluorescent microscopes. For example, live confocal fluorescent analysis proved essential in determining the primary defect in mutations that disrupt early nuclear divisions in Drosophila melanogaster. For organisms in which GPF transgenics is not available, fluorescent probes that label DNA, microtubules, and actin are available for microinjection.

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