On the public citation graph

Formation of pterinosomes and carotenoid granules in xanthophores of the teleost Oryzias latipes as revealed by the rapid-freezing and freeze-substitution method

0 signed · 44 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/aja.1001570110openalex-snapshot
The ultrastructure of rapid‐frozen, substitution fixed parotid gland acinar cells of the mongolian gerbil (Meriones meridianus)
inferredcites →https://doi.org/10.1002/cm.970100119openalex-snapshot
Regulation of the distribution of carotenoid droplets in goldfish xanthophores and possible implication to secretory processes
inferredcites →https://doi.org/10.1002/jez.1402270309openalex-snapshot
The blockade of pigment displacement in swordtail erythrophores by microinjection of antiactin antibody
inferredcites →https://doi.org/10.1007/bf00219075openalex-snapshot
The fine structure of sublingual gland acinar cells of the Mongolian gerbil, Meriones unguiculatus, processed by rapid freezing followed by freeze-substitution fixation
inferredcites →https://doi.org/10.1007/bf00219203openalex-snapshot
Growth and maturation of melanosomes in the melanophores of a teleost, Oryzias latipes
inferredcites →https://doi.org/10.1007/bf00219555openalex-snapshot
Ultrastructural demonstration of hormone-induced movement of carotenoid droplets and endoplasmic reticulum in xanthophores of the goldfish, Carassius auratus L.
inferredcites →https://doi.org/10.1016/0045-6039(87)90430-1openalex-snapshot
Induction of xanthophores from non-pigmented dermal cells of xanthic goldfish in vitro
inferredcites →https://doi.org/10.1016/0092-8674(88)90176-6openalex-snapshot
The microtubule-dependent formation of a tubulovesicular network with characteristics of the ER from cultured cell extracts
inferredcites →https://doi.org/10.1016/s0022-5320(71)80058-8openalex-snapshot
Structural change of pterinosome (pteridine pigment granule) during the xanthophore differentiation of Oryzias fish
inferredcites →https://doi.org/10.1016/s0022-5320(75)80004-9openalex-snapshot
Melanosome formation in the goldfish: the role of multivesicular bodies
inferredcites →https://doi.org/10.1083/jcb.39.2.233openalex-snapshot
MORPHOLOGICAL AND BIOCHEMICAL CHARACTERIZATION OF GOLDFISH ERYTHROPHORES AND THEIR PTERINOSOMES
inferredcites →https://doi.org/10.1083/jcb.75.2.541openalex-snapshot
Transformations in the structure of the cytoplasmic ground substance in erythrophores during pigment aggregation and dispersion. I. A study using whole-cell preparations in stereo high voltage electron microscopy.
inferredcites →https://doi.org/10.1083/jcb.81.2.275openalex-snapshot
Synaptic vesicle exocytosis captured by quick freezing and correlated with quantal transmitter release.
inferredcites →https://doi.org/10.1093/oxfordjournals.jmicro.a050382openalex-snapshot
High Resolution Analysis of Three-Dimensional Structure of the Golgi Apparatus in Rapid-Frozen, Substitution Fixed Gerbil Sublingual Gland Acinar Cells
inferredcites →https://doi.org/10.1093/oxfordjournals.jmicro.a050786openalex-snapshot
A Simple Apparatus and Technique for the Rapid-Freeze and Freeze-Substitution of Single-Cell Algae
inferredcites →https://doi.org/10.1111/j.1600-0749.1992.tb00001.xopenalex-snapshot
Does the Introduction of a New Player, the Endoplasmic Reticulum, Create More or Less Confusion in Understanding the Mechanism(s) of Pigmentary Organelle Translocations?
inferredcites →https://doi.org/10.15027/357openalex-snapshot
Electron-microscopic Observation on the Dermal Chromatophores of Normal Frogs and Three Kinds of Color Variants in Rhacophorus schlegelii

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4767229openalex-extracted
Transcriptome and Metabolome Provide Insight into the Formation Mechanism of Skin Pigmentation Diversity in Chinese Soft-Shelled Turtle (Pelodiscus Sinensis)
inferred← citeshttps://doi.org/10.1002/(sici)1096-9861(19990419)406:4<425::aid-cne1>3.0.co;2-1openalex-snapshot
Immunochemical localization of calretinin in the retina of the turbot (Psetta maxima) during development
inferred← citeshttps://doi.org/10.1002/ijch.202100069openalex-snapshot
Functional Molecular Crystals in Biology
inferred← citeshttps://doi.org/10.1007/978-981-16-1490-3_7openalex-snapshot
Pigment Cell Development in Teleosts
inferred← citeshttps://doi.org/10.1007/s00239-011-9431-xopenalex-snapshot
Identification and Characterization of Gene Expression Involved in the Coloration of Cichlid Fish Using Microarray and qRT-PCR Approaches
inferred← citeshttps://doi.org/10.1016/bs.ircmb.2015.09.005openalex-snapshot
Fish Chromatophores—From Molecular Motors to Animal Behavior
inferred← citeshttps://doi.org/10.1016/j.aqrep.2025.102883openalex-snapshot
Effects of light intensity on erythrophore number and astaxanthin amount in the skin of coral trout Plectropomus leopardus
inferred← citeshttps://doi.org/10.1016/j.ydbio.2004.09.029openalex-snapshot
Esrom, an ortholog of PAM (protein associated with c-myc), regulates pteridine synthesis in the zebrafish
inferred← citeshttps://doi.org/10.1034/j.1600-0749.2002.01085.xopenalex-snapshot
An Ultrastructural and Carotenoid Analysis of the Red Ventrum of the Japanese Newt, Cynops pyrrhogaster
inferred← citeshttps://doi.org/10.1034/j.1600-0749.2003.00079.xopenalex-snapshot
Localization of Sepiapterin Reductase in Pigment Cells of Oryzias latipes
inferred← citeshttps://doi.org/10.1073/pnas.2215193120openalex-snapshot
Lizards exploit the changing optics of developing chromatophore cells to switch defensive colors during ontogeny
inferred← citeshttps://doi.org/10.1098/rsbl.2021.0221openalex-snapshot
Pterin-based pigmentation in animals
inferred← citeshttps://doi.org/10.1098/rsos.190319openalex-snapshot
Body coloration and mechanisms of colour production in Archelosauria: the case of deirocheline turtles
inferred← citeshttps://doi.org/10.1101/2022.01.12.475993openalex-snapshot
Ontogenetic Color Switching in Lizards as a by-Product of Guanine Cell Development
inferred← citeshttps://doi.org/10.1111/j.1600-0749.1993.tb00624.xopenalex-snapshot
Cytoskeletal Architecture of Dermal Chromatophores of the Freshwater Teleost Oryzias latipes
inferred← citeshttps://doi.org/10.1111/j.1600-0749.2005.00216.xopenalex-snapshot
Pigment pattern formation in the medaka embryo
inferred← citeshttps://doi.org/10.1111/jfb.15718openalex-snapshot
Structural and ultrastructural aspects of the skin of large yellow croaker Larimichthys crocea
inferred← citeshttps://doi.org/10.1111/joa.12373openalex-snapshot
Comparison of pigment cell ultrastructure and organisation in the dermis of marble trout and brown trout, and first description of erythrophore ultrastructure in salmonids
inferred← citeshttps://doi.org/10.1111/jwas.12010openalex-snapshot
Dietary Esterified Astaxanthin Concentration Effect on Dermal Coloration and Chromatophore Physiology in Spinecheek Anemonefish, Premnas biaculeatus
inferred← citeshttps://doi.org/10.1242/dev.123.1.391openalex-snapshot
Mutations affecting xanthophore pigmentation in the zebrafish, Danio rerio
inferred← citeshttps://doi.org/10.1371/journal.pone.0085647openalex-snapshot
Multiple Pigment Cell Types Contribute to the Black, Blue, and Orange Ornaments of Male Guppies (Poecilia reticulata)
inferred← citeshttps://doi.org/10.14670/hh-14.383openalex-snapshot
Ultrastructural and biochemical analysis of epidermal xanthophores and dermal chromatophores of the teleost Sparus aurata.
inferred← citeshttps://doi.org/10.1560/ijee_52_3-4_405openalex-snapshot
Regressive Evolution of Pigmentation in the Cavefish Astyanax
inferred← citeshttps://doi.org/10.3410/f.735847584.793583903openalex-snapshot
Faculty Opinions recommendation of Thyroid hormone regulates distinct paths to maturation in pigment cell lineages.
inferred← citeshttps://doi.org/10.46989/001c.20620openalex-snapshot
Ultrastructure of Erythrophores and Xanthophores of the Siamese Fighting Fish, Betta splendens
inferred← citeshttps://doi.org/10.46989/001c.20672openalex-snapshot
Cellular Basis of Metallic Iridescence in the Siamese Fighting Fish, Betta splendens
inferred← citeshttps://doi.org/10.7554/elife.45181openalex-snapshot
Thyroid hormone regulates distinct paths to maturation in pigment cell lineages
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.