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Caleb H. Slater

Researcher at Oregon State University

Publications -  5
Citations -  464

Caleb H. Slater is an academic researcher from Oregon State University. The author has contributed to research in topics: Receptor & Testosterone. The author has an hindex of 5, co-authored 5 publications receiving 450 citations.

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Journal ArticleDOI

Testosterone Alters the Immune Response of Chinook Salmon, Oncorhynchus tshawytscha

TL;DR: The magnitude of the steroid-induced immunosuppression was reduced during winter and increased again in spring, and Testosterone and cortisol administered together had a significantly greater effect than did either administered alone.
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Plasma profiles of the sex steroids and gonadotropins in maturing female spring chinook salmon (Oncorhynchus tshawytscha)

TL;DR: Plasma testosterone concentrations were low through the spring and early summer, concentrations began rising in late July and reached maximum levels by ovulation in September, and plasma gonadotropin I concentrations paralleled those of estradiol and exceeded gonadotropic levels prior to ovulation.
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Characterization of an Androgen Receptor in Salmonid Lymphocytes: Possible Link to Androgen-Induced Immunosuppression

TL;DR: The data strongly suggest that androgen receptors exists in salmonid leukocytes and support the hypothesis that these receptors play a role in androgen induced immunosuppression.
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Immune and endocrine responses of adult chinook salmon during freshwater immigration and sexual maturation

TL;DR: The fact that in both years all endocrine and immune variables that correlated with each other also correlated with the date of sample, raises the question as to whether or not these are cause-and-effect relations.
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Physiological levels of testosterone kill salmonid leukocytes in vitro.

TL;DR: It is concluded that testosterone may exert its immunosuppressive effects by direct action on salmonid leukocytes, through the androgen receptor described, and that this action leads to the death of a significant number of these leuk cells.