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br-j13 | For example , arrow 17 in Figure 3 portrays the proximal radial epiphysis for boy 34 , whereas the same epiphysis for girl 2 is portrayed by arrow 18 in Figure 4 . | <NONE> | <NONE> | [
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br-j13 | We have attempted to simplify the extensive task of analyzing onset ages and completion ages of each child - more than 1700 values for the entire group - by constructing figures for each of the 21 centers so that the data for all 34 boys and 34 of the girls will appear together for each growth center . | <NONE> | <NONE> | [
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br-j13 | Figures 5 and 6 are examples of our method of analyzing the results for each growth center . | <NONE> | <NONE> | [
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br-j13 | Forty other figures similar to 5 and 6 and the original data used in the construction of all figures and tables in this monograph have been included in the Appendix . | <NONE> | <NONE> | [
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br-j13 | The principles used in making each arrow for Figures 3 and 4 were applied to the construction of Figures 5 and 6 as well as all figures in the Appendix . | <NONE> | <NONE> | [
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br-j13 | One growth center in a short bone - distal phalanx of the second finger - was chosen as an example for discussion here , primarily because epiphyseal diaphyseal fusion , the maturity indicator for Completion in long and short bones , occurs in this center for girls near the menarche and for boys near their comparable pubescent stage . | <NONE> | <NONE> | [
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br-j13 | The following summary , based on Figures 5 and 6 , is an example of one way of interpreting the 42 figures constructed from onset ages and completion ages of individual children with respect to the appropriate mean age for each growth center . | <NONE> | <NONE> | [
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br-j13 | Accordingly , girls 31 , 29 , 33 , 21 , 26 , 13 , 3 , 4 , 14 , 32 , 24 , 25 , 34 , 23 , 6 , 15 , 22 , and 16 may be said to have the `` same schedule '' at Onset and Completion . | <NONE> | <NONE> | [
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br-j14 | Interestingly enough , the effect of the digitalis glycosides is inhibited by a high concentration of potassium in the incubation medium and is enhanced by the absence of potassium (Wolff , 1960). | <NONE> | <NONE> | [
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br-j14 | The mechanism of this coupling has been studied in some detail with non-enzymatic systems in vitro and can be simulated by certain di-iodotyrosine analogues (Pitt-Rivers and James , 1958). | <NONE> | <NONE> | [
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br-j14 | Little is known of the synthetic mechanisms for formation of thyroglobulin . | <NONE> | <NONE> | [
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br-j14 | Its synthesis has not been demonstrated in cell-free systems , nor has its synthesis by systems with intact thyroid cells in vitro been unequivocally proven . | <NONE> | <NONE> | [
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br-j14 | There is some reason to think that thyroglobulin synthesis may proceed independently of iodination , for in certain transplantable tumours of the rat thyroid containing essentially no iodinated thyroglobulin , a protein that appears to be thyroglobulin has been observed in ultracentrifuge experiments (Wolff , Robbins and Rall , 1959). | <NONE> | <NONE> | [
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br-j14 | Similar findings have been noted in a patient with congenital absence of the organification enzymes , whose thyroid tissue could only concentrate iodide . | <NONE> | <NONE> | [
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br-j14 | A microsomal de-iodinase with a pH optimum of around 8 , and requiring reduced triphosphopyridine nucleotide for activity , has been identified in the thyroid (Stanbury , 1957). | <NONE> | <NONE> | [
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br-j14 | This de-iodinating enzyme is effective against mono - and di-iodotyrosine , but does not de-iodinate thyroxine or tri-iodothyronine . | <NONE> | <NONE> | [
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br-j14 | It is assumed that the iodine released from the iodotyrosines remains in the iodide pool of the thyroid , where it is oxidised and re-incorporated into thyroglobulin . | <NONE> | <NONE> | [
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br-j14 | The thyroxine and tri-iodothyronine released by proteolysis and so escaping de-iodination presumably diffuse into the blood stream . | <NONE> | <NONE> | [
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br-j14 | It has been shown that thyroglobulin binds thyroxine , but the binding does not appear to be particularly strong . | <NONE> | <NONE> | [
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br-j14 | It has been suggested that the plasma thyroxine binding proteins , which have an extremely high affinity for thyroxine , compete with thyroglobulin for thyroxine (Ingbar and Freinkel , 1957). | <NONE> | <NONE> | [
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br-j14 | Antithyroid drugs are of two general types . | <NONE> | <NONE> | [
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br-j14 | Besides those of the thiouracil and resorcinol types , certain antithyroid drugs have been found in naturally occurring foods . | <NONE> | <NONE> | [
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br-j14 | The most conclusively identified is L - 5 - vinyl - 2 - thio oxazolidone , which was isolated from rutabaga (Greer , 1950). | <NONE> | <NONE> | [
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br-j14 | There is some evidence that naturally occurring goitrogens may play a role in the development of goitre , particularly in Tasmania and Australia (Clements and Wishart , 1956). | <NONE> | <NONE> | [
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br-j14 | Here we shall restrict discussion to those methods that appear sufficiently sensitive and precise for determining the concentration of TSH in blood . | <NONE> | <NONE> | [
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br-j14 | As long ago as 1851 it was pointed out by Niepce (1851) that there is a connection between the pituitary and the thyroid . | <NONE> | <NONE> | [
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br-j14 | The first attempts to isolate TSH came a decade later , when Janssen and Loeser (1931) used trichloroacetic acid to separate the soluble TSH from insoluble impurities . | <NONE> | <NONE> | [
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br-j14 | After their work other investigators applied salt fractionation techniques to the problem , as well as fractionation with organic solvents , such as acetone . | <NONE> | <NONE> | [
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br-j14 | Albert (1949) has concluded that the most active preparations of TSH made during this period , from 1931 to 1945 , were probably about 100 to 300 times as potent as the starting material . | <NONE> | <NONE> | [
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