Biomedical subjects
L SOKOLOFF
Publications and source records attributed to L SOKOLOFF.
MOVEMENT AND COMPOSITION OF INTERSTITIAL FLUID OF CARTILAGE.
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STUDIES ON THE MECHANISM OF METHYLCHOLANTHRENE INDUCTION OF ENZYME ACTIVITIES OF RAT LIVER. I. AMINO ACID INCORPORATION IN RAT-LIVER HOMOGENATES.
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INFECTIOUS ARTHRITIS COMPLICATING NEOPLASTIC DISEASE.
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THE LITERATURE ANALYSIS PROJECT OF THE AMERICAN RHEUMATISM ASSOCIATION.
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IN MEMORIAM: JOSEPH JAY BUNIM.
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THYROXINE STIMULATION OF AMINO ACID INCORPORATION INTO PROTEIN INDEPENDENT OF ANY ACTION ON MESSENGER RNA SYNTHESIS.
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MITOCHONDRIAL DIFFERENCES IN MATURE AND IMMATURE BRAIN; INFLUENCE ON RATE OF AMINO ACID INCORPORATION INTO PROTEIN AND RESPONSES TO THYROXINE.
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EFFECTS OF L-THYROXINE ON AMINO ACID INCORPORATION INTO PROTEIN IN MATURE AND IMMATURE RAT BRAIN.
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COMPARATIVE EFFECTS OF VARIOUS ANALOGUES OF THYROXINE ON AMINO ACID INCORPORATION INTO PROTEIN.
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CLINICAL, PATHOLOGIC, AND SEROLOGIC STUDIES IN SJOEGREN'S SYNDROME; COMBINED CLINICAL STAFF CONFERENCE AT THE NATIONAL INSTITUTES OF HEALTH.
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CARDIAC INVOLVEMENT IN RHEUMATOID ARTHRITIS AND ALLIED DISORDERS: CURRENT CONCEPTS.
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THYROXINE STIMULATION OF AMINO ACID INCORPORATION INTO RIBOSOMAL PROTEIN.
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ELASTICITY OF ARTICULAR CARTILAGE: EFFECT OF IONS AND VISCOUS SOLUTIONS.
The deformability of articular cartilage is increased by cations, more so by polyvalent than monovalent ones. Trivalent cations also depress elastic recovery. Failure of viscous solutions to alter the elastic behavior suggests ultra-filtration by cartilage as a possible mechanism in synovial lubrication.
Thyroxine: effects on amino acid incorporation into protein in vivo.
Treatment of rats with L-thyroxine increases the incorporation in vivo of radioactive amino acids into protein of liver, kidney, and heart, but not of spleen, testis, or brain. The distribution of the effect among the organs is the same as that observed in thyroxine stimulation of oxidative metabolism. Thus, stimulation of protein synthesis seems to be a physiological action of the thyroid hormone.
Reversal of thyroxine-induced hypermetabolism by puromycin.
Previous studies have demonstrated that in addition to its effects on metabolic rate, thyroxine stimulates protein biosynthesis. The administration of puromycin, a drug which blocks protein synthesis and, therefore, the thyroxine effect on protein synthesis, acutely reverses the hypermetabolism induced in rats by prior administration of thyroxine and restores the oxygen consumption of the thyrotoxic rats to the euthyroid level. The results suggest that a larger fraction of the total body basal oxygen consumption in hyperthyroidism is related to the process of protein synthesis than in the euthyroid state and that the calorigenic effect of thyroxine is secondary to its effect on protein synthesis.
RELATION OF EEG TO CEREBRAL BLOOD FLOW AND METABOLISM IN OLD AGE.
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THE BIOLOGY OF DEGENERATIVE JOINT DISEASE.
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