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Featured researches published by V. L. Miller.


Toxicology and Applied Pharmacology | 1960

Absorption, distribution and excretion of phenylmercuric acetate.

V. L. Miller; P.A. Klavano; Elizabeth Csonka

Abstract Phenylmercuric acetate was given intravenously, intramuscularly, or per os to chicks, rats, and dogs. The compound is apparently absorbed unchanged. Metabolism in the body was fairly rapid, detectable amounts of phenylmercuric acetate occurring for only approximately 96 hours. Small amounts were excreted in the urine.


Toxicology and Applied Pharmacology | 1961

Absorption, distribution, and excretion of ethylmercuric chloride

V. L. Miller; P.A. Klavano; A.C. Jerstad; Elizabeth Csonka

Abstract Ethylmercuric chloride was given to chicks and rats intramuscularly and orally. The compound is apparently absorbed unchanged. Metabolism of ethylmercury is much slower than of phenylmercury. Intact ethylmercury is detectable in the liver and kidneys for 21 days after dosing. The ethylmercury is present to a much greater extent in the chick liver than in the kidney, whereas in the rat, the ethylmercury is predominantly in the kidney and blood.


Toxicology and Applied Pharmacology | 1968

Mercury retention in two strains of mice.

V. L. Miller; Elizabeth Csonka

Abstract Two strains of mice were given 3.0 mg of mercury as mercuric chloride, phenylmercuric acetate, or methyl- mercuric chloride. The type A mice tended to retain more mercury in the liver and kidneys from injections of all three mercurials over an 8-day test period than did type C57 mice. Mercury from mercuric chloride was retained primarily in the kidneys of both strains and from phenylmercuric acetate by the A strain. Mercury from methylmercuric chloride was retained in about equal amounts by the liver and kidneys of both strains and by the C57 strain from phenylmercuric acetate.


Experimental Biology and Medicine | 1959

Strain Differences in Mercury Retention by Chicks.

V. L. Miller; Gordon E. Bearse; Yoshikiyo Kimura; Elizabeth Csonka

Summary Studies made with 3 strains of chicks showed one strain to be significantly different in retention of mercury in liver and kidneys, following intramuscular injections of phenylmercury acetate or mercuric chloride. Differences following injection of equivalent amounts of mercury as ethylmercury chloride or Salyrgan were much less. Mercury retention was greater in the strain selected for resistance to lymphomatosis than in the 2 susceptible strains which showed little difference.


Toxicology and Applied Pharmacology | 1963

Differences in copper retention in two strains of chickens.

Donna V. Lillis; V. L. Miller; Gordon E. Bearse; C. M. Hamilton

Abstract Cupric acetate was injected intramuscularly in two strains of chickens developed by selection for a difference in susceptibility to the avian leukosis complex. When given a dose of 9.1 mg copper per kilogram of body weight as cupric acetate, one strain retained significantly more copper in the liver than the other strain. However, when injected with a dose of 0.91 mg copper per kilogram of body weight as cupric acetate no differences were observed.


Analytical Chemistry | 1958

Microestimation of Intact Phenylmercury Compounds in Animal Tissue

V. L. Miller; Donna. Lillis; Elizabeth. Csonka


Journal of Agricultural and Food Chemistry | 1973

Metal coordination compounds of thiabendazole

V. L. Miller; Charles J. Gould; Elizabeth. Csonka; Roy L. Jensen


Journal of Agricultural and Food Chemistry | 1974

Estimation of thiabendazole in the milligram and submilligram ranges.

V. L. Miller; Charles J. Gould; Elizabeth. Csonka


Journal of Agricultural and Food Chemistry | 1974

Estimation of benomyl in the milligram range.

V. L. Miller; Charles J. Gould; Elizabeth. Csonka


Poultry Science | 1970

Mercury Retention in Several Strains and Strain Crosses of Chickens

V. L. Miller; Gordon E. Bearse; Elizabeth Csonka

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Gordon E. Bearse

Washington State University

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Elizabeth Csonka

Washington State University

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T. S. Russell

Washington State University

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J. A. McIntyre

Washington State University

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P.A. Klavano

Washington State University

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A.C. Jerstad

Washington State University

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C. F. McClary

Washington State University

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C. M. Hamilton

Washington State University

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Donna V. Lillis

Washington State University

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H.L. Van Nice

Washington State University

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