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Light-induced alterations in cell shape and pigment displacement in chromatophores of the sea urchin Centrostephanus longispinus
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ange.19730850315openalex-snapshot
Mechanismen der Erregung von Lichtsinneszellen
inferredcites →https://doi.org/10.1002/jez.1401910312openalex-snapshot
The changes in cell shape during pigment migration in melanophores of a teleost, Oryzias latipes
inferredcites →https://doi.org/10.1007/bf00224270openalex-snapshot
Light-sensitivity of isolated pigment cells of the sea urchin Centrostephanus longispinus
inferredcites →https://doi.org/10.1007/bf00306604openalex-snapshot
Pigment movements in fish melanophores: Morphological and physiological studies
inferredcites →https://doi.org/10.1007/bf00307069openalex-snapshot
Am�boid bewegliche Pigmentzellen im Epithel des Seeigels Centrostephanus longispinus
inferredcites →https://doi.org/10.1007/bf00340434openalex-snapshot
Die Reaktion der Chromatophoren des Seeigels Centrostephanus longispinus auf Licht
inferredcites →https://doi.org/10.1016/0012-1606(76)90111-1openalex-snapshot
The induction of filopodia in the cellular slime mold Dictyostelium discoideum by cyclic adenosine monophosphate: Mechanism of aggregation
inferredcites →https://doi.org/10.1016/0016-6480(61)90041-7openalex-snapshot
Sodium dependence of intermedin action on melanophores in tissue culture
inferredcites →https://doi.org/10.1016/0016-6480(73)90072-5openalex-snapshot
Effects of ACTH on melanophores and iridophores isolated from bullfrog tadpoles
inferredcites →https://doi.org/10.1016/s0022-5320(69)80045-6openalex-snapshot
Ultrastructure of amphibian melanophores after light-dark adaptation and hormonal treatment
inferredcites →https://doi.org/10.1016/s0074-7696(08)60339-3openalex-snapshot
Polarized Intracellular Particle Transport: Saltatory Movements and Cytoplasmic Streaming
inferredcites →https://doi.org/10.1038/244093a0openalex-snapshot
Model for Membrane Movements in the Neural Growth Cone
inferredcites →https://doi.org/10.1083/jcb.66.1.145openalex-snapshot
Motility in Echinosphaerium nucleofilum. I. An analysis of particle motions in the axopodia and a direct test of the involvement of the axoneme.
inferredcites →https://doi.org/10.1083/jcb.69.2.275openalex-snapshot
Filopodia of spreading 3T3 cells. Do they have a substrate-exploring function?
inferredcites →https://doi.org/10.1242/jcs.11.3.875openalex-snapshot
Patterns of Particle Movement in Nerve Fibres In Vitro-An Analysis by Photokymography and Microscopy
inferredcites →https://doi.org/10.1242/jcs.14.2.319openalex-snapshot
Limpet haemocytes: II. The role of spikes in locomotion and spreading
inferredcites →https://doi.org/10.1242/jcs.15.3.513openalex-snapshot
Contractile filopodia and in vivo cell movement in the tunic of the ascidian, Botryllus schlosseri
inferredcites →https://doi.org/10.1242/jeb.34.3.394openalex-snapshot
The Spectral Sensitivity of the Echinoid Diadema Antillarum Philippi
inferredcites →https://doi.org/10.2183/pjab1912.20.484openalex-snapshot
103. Movement of Granules in Fish Melanophores
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/zootaxa.4639.1zenodo-depositor-declared
The Echinoderm Fauna of the Azores (NE Atlantic Ocean)
inferred← citeshttps://doi.org/10.1002/jez.1402360310openalex-snapshot
Light response of cultured melanophores of a teleost adult fish, Oryzias latipes
inferred← citeshttps://doi.org/10.1007/978-1-4684-4592-3_1openalex-snapshot
Mechanisms of Intracellular Organelle Transport
inferred← citeshttps://doi.org/10.1007/bf00233604openalex-snapshot
Ultrastructural observations on changes in cell shape in chromatophores of the sea urchin Centrostephanus longispinus
inferred← citeshttps://doi.org/10.1007/bf00312172openalex-snapshot
Fine structure of the dorsal arm plate of Ophiocoma wendti: Evidence for a photoreceptor system (Echinodermata, Ophiuroidea)
inferred← citeshttps://doi.org/10.1007/bf00363933openalex-snapshot
Ultrastructure of the chromatophore system on the tracheal bladders of the phantom larva of Chaoborus crystallinus (Insecta, Diptera)
inferred← citeshttps://doi.org/10.1007/bf00392885openalex-snapshot
A chromatophore system in the hermatypic, deep-water coral Leptoseris fragilis (Anthozoa: Hexacorallia)
inferred← citeshttps://doi.org/10.1016/0022-0981(79)90045-5openalex-snapshot
Ultrastructure of the chromatophores of Palaemon affinis Heilprin (Crustacea, Decapoda). Modifications in the shape of hindgut chromatophores associated with pigment movements
inferred← citeshttps://doi.org/10.1016/0300-9629(83)90327-4openalex-snapshot
Spectral light sensitivity of isolated chromatophores of the sea urchin, Centrostephanus longispinus
inferred← citeshttps://doi.org/10.1016/b978-0-12-106409-9.50017-8openalex-snapshot
Pigmentary Effectors
inferred← citeshttps://doi.org/10.1016/j.jembe.2012.05.014openalex-snapshot
Ecological physiology of the circadian pigmentation rhythm in the fiddler crab Uca panacea
inferred← citeshttps://doi.org/10.1016/s0074-7696(08)61544-2openalex-snapshot
The Chemical Basis of Diatom Morphogenesis
inferred← citeshttps://doi.org/10.1016/s0167-9309(07)80074-3openalex-snapshot
Chapter 10 Ecology of Centrostephanus
inferred← citeshttps://doi.org/10.1071/mf9940233openalex-snapshot
Colour variation in southern Tasmania populations of Heliocidaris erythrogramma (Echinometridae: Echinoidea)
inferred← citeshttps://doi.org/10.1080/17451000.2018.1529414openalex-snapshot
Rediscovery of the poorly known sea urchinCentrostephanus longispinus rubicingulus(H.L. Clark, 1921) (Echinodermata, Echinoidea, Diadematidae) on the continental shelf of Brazil, with notes on its morphology and synonymy
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2009.04506.xopenalex-snapshot
Genetic divergence and assortative mating between colour morphs of the sea urchinParacentrotus gaimardi
inferred← citeshttps://doi.org/10.1111/j.1440-169x.1979.00129.xopenalex-snapshot
SOME ASPECTS ON PIGMENT CELL DISTRIBUTION AND FUNCTION IN THE DEVELOPING ECHINOPLUTEUS OF PSAMMECHINUS MILIARIS
inferred← citeshttps://doi.org/10.1111/j.1744-7410.2012.00272.xopenalex-snapshot
Morphology and gametic compatibility of color morphs of P aracentrotus gaimardi ( E chinodermata: E chinoidea)
inferred← citeshttps://doi.org/10.11369/jji1950.27.72openalex-snapshot
Leucosome Dispersion under Light in Medaka Leucophores
inferred← citeshttps://doi.org/10.11646/zootaxa.4639.1.1openalex-snapshot
The Echinoderm Fauna of the Azores (NE Atlantic Ocean)
inferred← citeshttps://doi.org/10.1242/dev.00647openalex-snapshot
Isolation of pigment cell specific genes in the sea urchin embryo by differential macroarray screening
inferred← citeshttps://doi.org/10.1242/jcs.41.1.65openalex-snapshot
Light-induced pigment aggregation in cultured fish melanophores: spectral sensitivity and inhibitory effects of theophylline and cyclic adenosine-3′,5′-monophosphate
inferred← citeshttps://doi.org/10.1247/csf.14.113openalex-snapshot
Light response of cultured melanophores of a freshwater teleost, Zacco temmincki.
inferred← citeshttps://doi.org/10.2108/zsj.18.807openalex-snapshot
Spectacular Fluorescence Emission in Sea Urchin Larvae
inferred← citeshttps://doi.org/10.3390/d17110758openalex-snapshot
Improving the Knowledge on the Distribution and Ecology of the Protected Echinoid Centrostephanus longispinus (Philippi, 1845) in the Alboran Sea
inferred← citeshttps://doi.org/10.3856/vol44-issue1-fulltext-5openalex-snapshot
Genetic variation in color morphs of the endangered species, Paracentrotus gaimardi (Echinoidea: Echinidae)
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