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Dive into the research topics where William G. Kelly is active.

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Featured researches published by William G. Kelly.


Journal of Clinical Investigation | 1960

Aldosterone secretion and primary and malignant hypertension.

John H. Laragh; Stanley Ulick; Vlodzimierz Januszewicz; Quentin B. Deming; William G. Kelly; Seymour Lieberman

After the synthesis of desoxycorticosterone (DOC), it became apparent that this corticosteroid, the physiological effects of which are concerned primarily with sodium and potassium metabolism, can produce a state of hypertension both in animals and in man (1, 2). The induced hypertension is dependent upon the administration of adequate amounts of dietary sodium, whereas the hypertensive state, produced by administration of glucocorticoids such as cortisone, differs in that it is independent of the dietary sodium content (3). More recently, following the chemical and biological characterization of the mineralocorticoid hormone, aldosterone (4), a disease state associated with primary hypersecretion of this hormone has been described in man (5). Aldosterone produces effects on sodium and potassium metabolism similar to those of desoxycorticosterone, and the clinical syndrome of primary aldosteronism resembles the disease state produced by chronic administration of DOCto dogs (6). Arterial hypertension has been a consistent finding in patients with primary hyperaldosteronism. A number of other observations have suggested a relationship between the dietary sodium intake and the blood pressure level of patients with primary (benign essential) hypertension. The beneficial effects of sodium deprivation, and of various natriuretic agents in certain patients with hypertension, is well known. In addition, other studies have suggested that abnormalities of intracellular sodium and potassium content may occur in patients with arterial hypertension (7). Genest, Koiw, Nowaczynski and Lebouef (8) have re-


Annals of Internal Medicine | 1960

Electrolyte metabolism and aldosterone secretion in benign and malignant hypertension.

John H. Laragh; Stanley Ulick; Vlodzimierz Januszewicz; William G. Kelly; Seymour Lieberman

Excerpt The fundamental relationship between intravascular pressure and electrolyte metabolism is poorly understood. The hormones of the adrenal cortex which act to regulate sodium and potassium ba...


JAMA | 1960

Hypotensive Agents and Pressor Substances: The Effect of Epinephrine, Norepinephrine, Angiotensin II, and Others on the Secretory Rate of Aldosterone in Man

John H. Laragh; Marielena Angers; William G. Kelly; Seymour Lieberman


Biochemistry | 1977

Aromatization of delta4-androstene-3,17-dione, 19-hydroxy-delta4-androstene-3,17-dione, and 19-oxo-delta4-androstene-3,17-dione at a common catalytic site in human placental microsomes.

William G. Kelly; Dianne Judd; Ann Stolee


Biochemistry | 1962

Isolation and characterization of aldosterone metabolites from human urine; two metabolites bearing a bicyclic acetal structure.

William G. Kelly; Lajos Bandi; James N. Shoolery; Seymour Lieberman


Biochemistry | 1969

Partial purification and preliminary characterization of estrogen-binding globulins from human plasma.

William Rosner; Nicholas P. Christy; William G. Kelly


Biochemistry | 1962

Isolation and Characterization of Human Urinary Metabolites of Aldosterone. III. Three Isomeric Tetrahydro Metabolites

William G. Kelly; Lajos Bandi; Seymour Lieberman


Biochemistry | 1963

ISOLATION AND CHARACTERIZATION OF HUMAN URINARY METABOLITES OF ALDOSTERONE. V. DIHYDROALDOSTERONE AND 21-DEOXYTETRAHYDROALDOSTERONE.

William G. Kelly; Lajos Bandi; Seymour Lieberman


The Journal of Clinical Endocrinology and Metabolism | 1974

Estriol Conjugates in Amniotic Fluid of Normal and Rh-Isoimmunized Patients1

Bruce K. Young; Helmut Jirku; Andrew J. Slyper; Mortimer Levitz; William G. Kelly; Sidney Yaverbaum


Advances in metabolic disorders | 1964

Aldosterone: Its Biochemistry and Physiology‡

John H. Laragh; William G. Kelly

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Ann Stolee

University of Minnesota

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