Results 131 to 140 of about 869 (158)
Some of the next articles are maybe not open access.
Cell Motility, 1989
AbstractImmunofluorescence and phase‐contrast microscopic studies of goldfish xanthophores with aggregated or dispersed pigment show two unusual features. First, immunofluorescence studies with anti‐actin show punctate structures instead of filaments. These punctate structures are unique for the xanthophores and are absent from both goldfish dermal no ...
G R, Walker, J D, Taylor, T T, Tchen
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AbstractImmunofluorescence and phase‐contrast microscopic studies of goldfish xanthophores with aggregated or dispersed pigment show two unusual features. First, immunofluorescence studies with anti‐actin show punctate structures instead of filaments. These punctate structures are unique for the xanthophores and are absent from both goldfish dermal no ...
G R, Walker, J D, Taylor, T T, Tchen
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Light‐Induced Pigment Aggregation in Xanthophores of the Medaka, Oryzias latipes
Pigment Cell Research, 1998The response mechanism of medaka xanthophores to light was examined at the cellular level. Innervated and denervated xanthophores of adult medakas responded to light (9,000 lux) within 30 sec by pigment aggregation, and this aggregation was not mediated through α‐adrenoceptors on the cell membrane. Maximum sensitivity to light was at wavelengths of 410–
N, Oshima +3 more
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[5] Translocation of carotenoid droplets in goldfish xanthophores
1993Publisher Summary This chapter describes the isolation and maintenance of xanthophores, the preparation of a permeabilized system capable of carotenoid droplet dispersion, and the identification of carotenoid droplet protein p57/pp57 and a cytosolic protein anterogin as important determinants for carotenoid droplet dispersion. Two radically different
T.T. Tchen, John D. Taylor
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Microscopy Research and Technique, 2002
AbstractPigmentary organelle translocations within fish chromatophores undergo physiological color changes when exposed to external signals. Chromatophores can be isolated in high yields, and their pigmentary organelles can be tracked readily by microscopy.
Victoria A, Kimler, John D, Taylor
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AbstractPigmentary organelle translocations within fish chromatophores undergo physiological color changes when exposed to external signals. Chromatophores can be isolated in high yields, and their pigmentary organelles can be tracked readily by microscopy.
Victoria A, Kimler, John D, Taylor
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Wilhelm Roux's Archives of Developmental Biology, 1982
The subepidermal distribution of xanthophores and melanophores is investigated in embryos ofTriturus alpestris with a uniform (stage 28+) and a banded melanophore pattern (stage 35/36). In ultrathin head and trunk sections from stage 35/36 embryos which externally show longitudinal dorsal and lateral melanophore bands in the trunk and less compact ...
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The subepidermal distribution of xanthophores and melanophores is investigated in embryos ofTriturus alpestris with a uniform (stage 28+) and a banded melanophore pattern (stage 35/36). In ultrathin head and trunk sections from stage 35/36 embryos which externally show longitudinal dorsal and lateral melanophore bands in the trunk and less compact ...
exaly +3 more sources
Wilhelm Roux's Archives of Developmental Biology, 1984
The barred pigment pattern (Lehman 1957) of the axolotl larva is best observed from stage 41 onwards, where it already consists of alternating transverse bands of melanophores and xanthophores along the dorsal side of the trunk. The present study investigateswhen the two populations of neural crest derived chromatophores, melanophores and xanthophores ...
Jan Löfberg
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The barred pigment pattern (Lehman 1957) of the axolotl larva is best observed from stage 41 onwards, where it already consists of alternating transverse bands of melanophores and xanthophores along the dorsal side of the trunk. The present study investigateswhen the two populations of neural crest derived chromatophores, melanophores and xanthophores ...
Jan Löfberg
exaly +3 more sources
The Non-Identity of the Neurohumors for the Melanophores and the Xanthophores of Fundulus
The American Naturalist, 1936IT has been shown that the reactions of the xanthophores (yellow pigment cells) in Fundulus heteroclitus are independent of the responses of the melanophoresblack pigment cells (Connolly, 1925; Fries, 1931). For example, both the xanthophores and the melanlophores are contracted in a fish which has been kept for some time in an illuminated white vessel,
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Pigment dispersion by prolactin in cultured xanthophores and erythrophores of some fish species
The Journal of Experimental Zoology, 1996The direct effects of a pair of tilapia prolactins (tPRL177 and tPRL188) and of ovine prolactin (oPRL) on cultured xanthophores and erythrophores isolated from some fish species were examined. Cultured xanthophores of the Nile tilapia, paradise goby, and medaka responded to tPRL177 and oPRL at concentrations of less than 100 nM by pigment dispersion ...
Noriko Oshima, Shawichi Iwamuro
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ACTH-induced internalization of plasma membrane in xanthophores of the goldfish, Carassiusauratus L
Biochemical and Biophysical Research Communications, 1979Abstract The ACTH-induced pigment dispersion in primary cultures and in suspensions of xanthophores of the goldfish, Carassius auratus L., has been shown to include the formation of rosette-like membranous structures and plasma membrane invaginations (pits).
S J, Lo, T T, Tchen, J D, Taylor
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Pigment Cell Research, 2002
We have identified two simple methods to analyse xanthophore and pterinosome biogenesis in zebrafish. The first uses methylene blue (methylthionium chloride), a redox dye which specifically labels xanthophores and pterinosomes, while the second uses autofluorescence to detect pteridine levels; these methods may be used to detect the number, location ...
Sylvie, Le Guyader, Suresh, Jesuthasan
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We have identified two simple methods to analyse xanthophore and pterinosome biogenesis in zebrafish. The first uses methylene blue (methylthionium chloride), a redox dye which specifically labels xanthophores and pterinosomes, while the second uses autofluorescence to detect pteridine levels; these methods may be used to detect the number, location ...
Sylvie, Le Guyader, Suresh, Jesuthasan
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