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10,001,400 | The concentration of metallothionein (MT) in the liver of the perinatal rat is relatively high at term and 7 days after birth and then decreases to barely detectable levels by day 28. The developmental pattern MT-zinc parallels that of MT. When challenged with a single injection of cadmium chloride, the 26-day-old rat responds with a dose-related increase in hepatic MT which sequesters both cadmium and zinc. When the 5-day-old rat is similarly challenged, induction of MT occurs only at the highest dose tested (6 mg Cd/kg); however, due to the pre-existence of MT in these younger rats, cadmium administered at the lower doses still binds to the MT in a dose-related manner. Despite the induction of MT seen in both age groups following the 6.0 mg/kg dose, exposure to that level of the metal produced death in 30% of the younger animals but in only 4% of the older animals. When cadmium was administered to pregnant rats on day 19 of gestation, it was found to produce a dose-related induction of maternal hepatic MT over the following 48 hr. In contrast, maternal exposure to the metal led to a significant depression of fetal hepatic MT over the same time interval. | [
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10,001,401 | Estrogen in high doses inhibits perphenazine-induced prolactin release. | [
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10,001,402 | We investigated the effects of high doses of estrogen on the basal and stimulated secretion of PRL. Daily administration of 0.1 micrograms estradiol benzoate to female mice for 4 weeks significantly increased the amplitude of PRL release induced by perphenazine. A dose of 1.0 micrograms had no stimulatory effect, while doses of 10, 20, and 50 micrograms completely prevented the release of PRL in response to perphenazine. The rise in basal serum PRL concentrations seen at lower doses of estradiol benzoate was also minimized with 20- and 50-micrigrams doses. At the same time, PRL concentrations within the pituitary gland as well as pituitary weight consistently increased in response to all high doses of estradiol benzoate tested, although the increment at the highest dose (50 micrograms) was somewhat smaller. These results suggest that prolonged administration of estrogen in large amounts may be detrimental to the natural, acute release of PRL. We postulate that this effect may account, in part, for the observed mammostatic and antigalactic effects of high doses of estrogen. | [
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10,001,403 | Vasopressin-related peptides increase the hippocampal corticosterone receptor capacity of diabetes insipidus (Brattleboro) rats. | [
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10,001,404 | The binding of [3H]corticosterone to receptors in cytosol of several brain regions and of [3H]dexamethasone to receptors in pituitary cytosol was measured after chronic treatment of homozygous diabetes insipidus rats (Ho-Di) with various neuropeptides. All rats were adrenalectomized 24 h before sacrifice for depletion of endogenous adrenal hormones and at that time administration of the peptides was discontinued. At sacrifice the rats were perfused with saline to remove plasma transcortin from the tissues. The apparent maximal binding capacity for corticosterone and dexamethasone was significantly lower in hippocampus and anterior pituitary (36.8% and 39.2%, respectively) of Ho-Di rats than of homozygous nondiabetic rats (Ho-No) of the same strain. In contrast, the neurointermediate pituitary lobe of Ho-Di rats had more than twice as many (211%) binding sites, whereas neither receptor capacity in hypothalamus and septum nor plasma transcortin in these rats were significantly different from those in Ho-No rats. Treatment of Ho-Di rats with arginine-vasopressin, des-glycinamide arginine vasopressin, or 1-desamino-8-D-arginine-vasopressin daily for 1 week resulted in an elevation of receptor capacity in hippocampus and anterior pituitary near the level observed in nondiabetic controls. No effects on the other brain regions, the neurointermediate pituitary lobe, and on plasma transcortin were observed with these peptide treatments. Administration of oxytocin and ACTH-(4-10) did not affect receptor binding. It is concluded that in the Ho-Di Brattleboro rat the glucocorticoid receptor system in the hippocampus and in the anterior pituitary is selectively affected by neuropeptides related to vasopressin. | [
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10,001,405 | Endogenous inhibition of prolactin secretion in pregnant lactating rats. | [
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10,001,406 | The purpose of the present study was to test whether rat placental lactogen, proposed to be inhibitory for endogenous rhythmic PRL secretion during pregnancy, is also inhibitory for a neurally mediated PRL response to exogenous stimulation, i.e. suckling. Pregnant lactating rats were used as the model in this study. Blood samples for PRL were taken via a chronic atrial cannula before and after 30 min of suckling stimulation in the following groups of females: 1) bearing conceptuses of different degrees of development; 2) after removal of conceptuses; and 3) after injection of placental extract immediately before exposure to suckling stimulation. It was found that 1) the PRL response to suckling diminished in conjunction with placental development and the known concomitant rise in rat placental lactogen; 2) removal of the conceptuses permits elevation of PRL after suckling stimulation; and 3) injection of placental extract obtained on days 11-12 of pregnancy failed to block the elevation of PRL in response to suckling. It was concluded that 1) lactation can be maintained even in the presence of very low levels of PRL, provided developed placentae are present, and 2) the developed placentae are capable of inhibiting the acute PRL release in response to exogenous stimulation as well as endogenous rhythmic PRL secretion. | [
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10,001,407 | Structure-activity relationships of inhibition of hepatic monodeiodination of thyroxine to 3,5,3'-triiodothyronine by thiouracil and related compounds. | [
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10,001,408 | The effects of gonadectomy and testosterone treatment on luteinizing hormone secretion in fetal rhesus monkeys. | [
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10,001,409 | Preferential inhibition of thyroxine and 3,5,3'-triiodothyronine formation by propylthiouracil and methylmercaptoimidazole in thyroid peroxidase-catalyzed iodination of thyroglobulin. | [
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10,001,410 | The present study was undertaken to determine whether the thioureylene antithyroid drugs propylthiouracil [6-propyl-2-thiouracil (PTU)] and methylmercaptoimidazole [1-methyl-2-mercaptoimidazole (MMI)] have a specific inhibitory effect on the thyroid peroxidase (TPO)-catalyzed conversion of diiodotyrosine to T4 (coupling reaction) independent of their well known inhibitory effect on peroxidase-catalyzed iodination. We have employed model incubation systems containing highly purified TPO to examine this question. Most experiments were performed with a model iodination system containing TPO, low iodine thyroglobulin, [131]iodide, and glucose-glucose oxidase. Both PTU and MMI are effective inhibitors of iodination of this system at physiological concentrations, and the system is well suited for studying the simultaneous action of these drugs on iodination and coupling. The addition of graded doses of the drugs to the iodination system demonstrated a relatively greater inhibitory effect on iodothyronine than on iodotyrosine formation. However, this observation in itself does not establish a specific inhibitory effect on coupling, since the formation of T4 involves a reaction between two molecules of 3,5-diiodotyrosine (DIT). The rate of this reaction, therefore, is second order with respect to DIT concentration, and the inhibition of DIT formation by thioureylene drugs would be expected to result in a disproportionately greater reduction in T4 formation even id there were no selective inhibitory effect of the drugs on the coupling reaction. Under certain conditions of incubation, however, it was possible to demonstrate a significant inhibitory effect on T4 and T3 formation without any decrease (in fact, a slight increase) in diiodotyrosine formation. These observations indicate that, at least under some conditions, PTU and MMI can exert a specific inhibitory effect on the coupling reaction. In the case of PTU, a specific inhibitory effect on coupling was also demonstrated with an incubation system in which TPO-catalyzed coupling was measured in the absence of iodination. | [
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10,001,411 | Comprehensive kinetics of triiodothyronine production, distribution, and metabolism in blood and tissue pools of the rat using optimized blood-sampling protocols. | [
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10,001,412 | We have determined estimates for 24 physiological parameters of production, interpool transport, distribution, and metabolism of T3 in the major T3 pools of the unanesthetized male Sprague-Dawley rat, from blood-borne data and a comprehensive model and analysis of this system. Most of these indices have previously been unavailable. Whereas only 3% (2 ng/100 g BW) of the total body T3 pool (74 ng/100 g BW) is in plasma, the composite of slowly equilibrating (slow) tissue pools (e.g. muscle, skin, and brain) appears to contain most of the T3, 76% (57 ng/100 g BW) of the total. The composite of rapidly equilibrating (fast) tissue pools (e.g. liver and kidney) contains the remaining 19% (16 ng/100 g BW). The total body T3 production rate is 0.12 ng/100 g BW . min, and we estimate that about half of this emanates directly from T4 in the slow pools, whereas the remainder is derived from both thyroidal secretion and T4 to T3 conversion in the fast pools. Our results also indicate that T3 molecules spend an average of only 0.5 min in transit each time through plasma, whereas the single pass mean transit times in fast and slow tissue pools (the times available for hormone action) are 10 times and 200 times greater. In contrast, the mean residence time for T3 in the entire system is greater than 12 h despite the extremely rapid early disappearance of injected T3 from plasma. To obtain the required accuracy, we used a novel optimization approach for choosing blood-sampling schedules (1, 4, 44, 202, and 600 min), a remarkably small number of sample times, and each was adjustable by about +/- 20% without effect on optimized parameter accuracies. | [
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10,001,413 | The antiandrogenic effects of delta 1-testolactone (Teslac) in vivo in rats and in vitro in human cultured fibroblasts, rat mammary carcinoma cells, and rat prostate cytosol. | [
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] |
10,001,414 | The antiandrogenic properties of delta 1-testolactone (17 alpha-oxa-D-homo-1,4-androstane-3,17-dione; Teslac) were investigated in vivo and in vitro. Teslac (75 mg/day for 7 days) inhibited the rise in ventral prostate weight induced by testosterone (T) (P less than 0.001), dihydrotestosterone (DHT) (P less than 0.05), and a combination of T plus 17 beta-estradiol (E2) (P less than 0.01) in immature castrate rats. Similar effects were seen on the seminal vesicles after T and T plus E2 (P less than 0.001). Teslac also decreased prostate and seminal vesicle weights in intact immature rats. The effects of Teslac were dose and time dependent. Teslac did not change the concentration of serum T or DHT. However, Teslac inhibited DHT binding to the androgen receptor (Ki = 2.5 +/- 0.8 X 10(-7) M) in cytosol of the rat prostate. Teslac also inhibited DHT binding to the androgen receptor in cultured human prepuce fibroblasts and cultured rat mammary tumor cells (Ki = 1.9 +/- 0.3 X 10(-5) M). The results indicate that Teslac, in addition to its antiaromatase activity, is an antiandrogen by virtue of its interaction with the androgen receptor. | [
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10,001,415 | Effect of sulfhydryl reagents on the conversion of thyroxine to 3,5,3'-triiodothyronine: direct action on thyroxine molecules. | [
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10,001,416 | Sulfhydryl reagents are good stimulators of the enzymatic conversion of T4 to T3. Previous studies have suggested that the underlying mechanism for this property is that these reagents may serve as a cofactor in the reaction, or they maintain the enzyme in its active reduced form. We examined another possibility, namely that sulfhydryl reagents affect T4 itself and hence increase T3 generation by the enzyme. The substrate T4 and sulfhydryl reagents dithiothreitol, mercaptoethanol, and reduced glutathione were incubated at 37 C for 1 h and then combined with rat liver homogenate and incubated for additional 15 min to permit the enzymatic formation of T3. For control, substrate T4 was not preincubated with reagents, and those reagents were added just before the incubation. Preincubation of T4 with these reagents markedly enhanced subsequent T3 generation by the homogenate. Without preincubation, however, reduced glutathione and mercaptoethanol did not enhance T3 generation by simultaneous incubation with the homogenate. Dithiothreitol increased T3 generation when introduced into the incubation medium simultaneously with the homogenate and incubated only 15 min. However, the magnitude of stimulation was far less than that obtained from T4 preincubated with this reagent. These procedures did not alter the nonenzymatic generation of T3 significantly. These results suggest that sulfhydryl reagents can affect T4 itself and make it more susceptible to enzymatic outer ring monodeiodination. | [
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10,001,417 | Differential stimulation by 17 beta-estradiol and synthetic estrogens of progesterone-receptor and of translocation of estrogen-receptor in rat pituitary and uterus. | [
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10,001,418 | Central and peripheral actions of physiological and synthetic estrogens with elevated biological potencies were investigated. The synthetic estrogens were 1,3-diacetoxy-17 alpha-ethinyl-7 alpha-methyl-1,3,5(10)-estratrien-17 beta-ol (DM-EE2) and 1,3-dibenzoyloxy-17 alpha-ethinyl-7 alpha-methyl-1,3,5(10)-estratrien-17 beta-ol (DB-EE2). More prolonged nuclear retention of the estrogen-receptor was found after application of DM-EE2 and DB-EE2, than in the pituitary and uterus after injection of the same dose of 17 beta-estradiol (E2). Longer nuclear retention of the estrogen-receptor was observed in the pituitary after DB-EE2 application and in the uterus after DM-EE2 than in E2-treated rats. Pituitary progesterone-receptor was raised to 706% of controls by treatment with E2 and 1187% and 2308% after injection of DM-EE2 and DB-EE2, respectively. On the other hand, only 208% and 225% stimulation, respectively, of progesterone-receptor was observed in the uterus after treatment with the synthetic estrogens DM-EE2 and DB-EE2. In vitro cytosol receptor binding assays revealed low relative binding affinities of the synthetic estrogens compared to E2. The results may be explained by the hypothesis that differences in biological activity of estrogens may be caused by different metabolic and/or cellular events localized in distinct target organs or by altered affinity of the nuclear estrogen receptor complex to chromatin receptor sites due to a change in receptor conformation. | [
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10,001,419 | Estradiol inhibits prolactin induced alpha-lactalbumin production in normal primate mammary tissue in vitro. | [
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10,001,420 | The effect of estradiol on prolactin induced alpha-lactalbumin production in normal primate mammary tissue was studied by maintaining tissues in organ culture with or without various combinations of oPRL and 17 beta-estradiol. As expected alpha-lactalbumin was increased byoPRL. 17 Beta-estradiol was found to have a significant inhibitory effect on oPRL-induced alpha-lactalbumin production. By 9 days in culture estradiol (10(-11) M) caused a mean 31% inhibition of prolactin-induced alpha-lactalbumin; with estradiol (10(-8) M) the inhibition was 40%. In the absence of oPRL, estradiol did not inhibit alpha-lactalbumin production. Thus it appears that estradiol directly antagonizes the lactogenic effect of prolactin on the normal primate mammary gland. | [
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10,001,421 | The possible involvement of intestinal bacteria in steroidal hypertension. | [
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10,001,422 | The bacterial flora of rats ws modified, using antibiotics, in order to interrupt the enterohepatic circulation of steroids excreted in bile. Antibiotic treatment was contined while corticosterone was administered to these animals, and over five days corticosterone raised blood pressures by an average of 9.2 mmHg compared with 24.6 mmHg in rats given steroid alone. These findings are consistent with the possibility that in normal rats bacterial metabolites of steroids, when reabsorbed in the enterohepatic circulation, contribute to the physiological response to exogenous steroids. | [
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10,001,423 | Inhibition of the enzymatic degradation of Met-enkephalin by catecholamines. | [
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10,001,424 | The influence of the catecholamine hormones and some of their metabolites on the enzymatic degradation of met-enkephalin by rat brain homogenates has been evaluated. The enzyme activity was determined by the release of [125I]-tyrosine from radioiodinated met-enkephalin following Porapak Q column chromatography. Each of the biologically active catecholamines inhibited the measured enzyme activity, and dose-response curves indicated that dopamine was most effective and epinephrine least effective. At 5 x 10(-5)M the O-methylated metabolite of each hormone failed to inhibit the enzyme activity. An enzyme activity similar to that found in brain was also found in adrenal and ileal homogenates. This enzyme activity was strongly inhibited by dopamine as well as by puromycin. | [
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10,001,425 | Parathyroid hormone stimulates mammalian renal 25-hydroxyvitamin D3-1 alpha-hydroxylase in vitro. | [
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10,001,426 | We have shown that parathyroid hormone (PTH) stimulates 25-hydroxyvitamin D2-1 alpha-hydroxylase activity in mitochondrial preparations of guinea pig kidney in vitro.1,25-[3H]dihydroxyvitamin D3 produced from 25-[3H]hydroxyvitamin D3 was identified by both normal phase and reversed-phase high pressure liquid chromatography. Enzyme stimulation by PTH was dose-dependent, peaked after 15 minutes of incubation with hormone and was maximal at concentrations of approximately 10(-10) M PTH-(1-84) and PTH-(1-34). This guinea pig renal model therefore permits direct examination of hormonal regulation of the mammalian enzyme in vitro. | [
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10,001,427 | Rat placenta is an active site of inner ring deiodination of thyroxine and 3,3',5-triiodothyronine. | [
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10,001,428 | Inner ring deiodination of L-T4 and L-T3 by rat placental homogenates resulted in the generation of rT3 from T4 and 3,3'-diiodothyronine and 3'-monoiodothyronine from T3. Dithiothreitol is required in the incubation medium. There was little or no detectable outer ring deiodination of T4 and T3. These findings suggest that placenta enzymatic inner ring monodeiodination of T4 and T3 could prevent the transplacental passage of T4 and T3 from dam to fetus. They also provide an explanation for our previous observations that fetal serum rT3 is partially dependent on maternal thyroid function. | [
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10,001,429 | Salivary gland weight and nerve growth factor in the genetically obese (ob/ob) mouse. | [
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10,001,430 | The salivary glands of genetically obese male mice are significantly smaller than those of lean male mice, but the salivary glands of female mice do not differ in weight. The increases in weight of salivary glands in male mice after treatment with T3 at 50, 150, or 500 ng/day or with several doses of isoproterenol were comparable on a percentage basis, but the weights in the ob/ob mice were always smaller than any of those in the lean mice. Measurements of nerve growth factor (NGF) in several tissues showed a significantly lower concentration in the salivary glands of obese female mice than in same tissue from female lean mice. There were no differences in NGF levels in brown fat or in the cortex, cerebellum, or brain stem. The concentration of epidermal growth factor, in contrast to that of NGF, was not lower in the salivary glands of obese mice. Testosterone increased the weight of the salivary glands, spleen, and kidney in obese female mice, but the weight of the salivary glands in lean animals remained significantly higher than that in the obese mice both with and without treatment. Testosterone significantly increased the NGF concentration in salivary glands, but the values in treated male mice were only one tenth those in the treated lean animals. | [
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10,001,431 | Degradation of rat and human lipoproteins by cultured rat ovary granulosa cells. | [
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10,001,432 | We have investigated the degradation of 125I-labeled rat and human lipoproteins by rat ovary granulosa cells cultured in serum-free medium. The granulosa cells degrade rat [125I]iodo high density lipoprotein (HDL) to acid-soluble products, mainly monoiodotyrosine. The degradation of 125I-labeled rat HDL is a specific, saturable, high affinity (Km = 21 micrograms protein/ml) process. In studies of rat [125I]iodo-HDL degradation and progestin (progesterone plus 20 alpha-dihydroprogesterone) production by the same granulosa cell cultures, the cholesterol potentially made available to the cells by degradation can account for the majority of the substrate necessary for the increased progestin production. Granulosa cells degrade human [125I]iodo-HDL by a specific, saturable, high affinity (Km = 20 micrograms protein/ml) process. The degradation of human [125I]iodo-HDL can account for only 20% of the cholesterol substrate necessary for increased progestin production. The degradation of human [125I]iodo-low density lipoprotein (LDL) is saturable and a high affinity (Km = 8 micrograms protein/ml) process, but can be inhibited significantly by a 10-fold excess of unlabeled human HDL. In contrast to both rat [125I]iodo-HDL and human [125I]iodo-HDL, the degradation of human [125I]iodo-LDL can potentially provide twice the cholesterol necessary for increased progestin production. Pronase treatment of the granulosa cells inhibits human [125I]iodo-LDL degradation but stimulates rat [125I]iodo-HDL degradation, indicating that the mechanisms of degradation are separate. The data demonstrate that cultured rat ovary granulosa cells degrade rat HDL, human HDL, and human LDL, and this process has the potential for providing cholesterol for cellular steroid hormone synthesis. | [
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10,001,433 | Relationship of estradiol to luteal function in the cycling baboon. | [
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10,001,434 | Since exogenous 17 beta-estradiol (E2) is luteolytic in some primates, it is reasonable to conclude that endogenous E2 is the naturally occurring luteolytic substance. However, a link between endogenous E2 and spontaneous luteolysis has not been demonstrated. In an attempt to understand the function of E2 in spontaneous luteolysis, we employed the antiestrogen clomiphene. We administered E2, clomiphene, or E2 plus clomiphene to baboons during the luteal phase and measured systemic levels of estrone, E2, progesterone (P), and LH, E2 alone depressed the concentrations of P and bioassayable LH prematurely. The length of the luteal phase was significantly shortened (12.8 +/- 0.9 vs. 15.8 +/- 0.4 days for sham controls; P less than 0.01). Clomiphene blocked the luteolytic effect of exogenous E2, resulting in P levels which were not significantly different (P greater than 0.01) from control and a luteal phase of normal length (15.0 +/- 1.0 days). Treatment with E2 alone caused serum LH concentrations to decrease. The administration of clomiphene alone maintained circulating LH at early to midluteal phase levels but did not alter luteal phase P concentrations or prolong the length of the luteal phase (15.6 +/- 0.4 days). The results suggest that E2-induced luteolysis is a result of the withdrawal of luteotropic support from the (corpus) luteum, while spontaneous luteolysis is a result of some other mechanism which may not involve endogenous E2. | [
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10,001,435 | Role of the pituitary in restitution of blood volume after hemorrhage. | [
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10,001,436 | Characteristics of inner ring (3 or 5) monodeiodination of 3,5-diiodothyronine in rat liver: evidence suggesting marked similarities of inner and outer ring deiodinases for iodothyronines. | [
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10,001,437 | Xerophthalmia: a review of hospital out-patient records. | [
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10,001,438 | Management of bronchial asthma in Ethiopian children. | [
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10,001,439 | Glomerulonephritis: A preliminary clinico-pathological report on 29 patients. | [
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10,001,440 | Dental health conditions of students in Ethiopia: findings from the Development Through Cooperation Campaign, 1976-77. | [
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10,001,442 | Autosomal mutations that interfere with sex determination in somatic cells of Drosophila have no direct effect on the germline. | [
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10,001,443 | The segregation and early migration of cranial neural crest cells in the avian embryo. | [
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10,001,445 | Neural crest cell behavior in white and dark embryos of Ambystoma mexicanum: epidermal inhibition of pigment cell migration in the white axolotl. | [
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10,001,446 | Isolation of sea urchin embryo histone H2A and immunological identification of other stage-specific H2A proteins. | [
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10,001,447 | The development of the conduction system in the mouse embryo heart. | [
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10,001,448 | The effect of experimentally induced triploidy on the lethal expression of the t(12) mutation in mouse embryos. | [
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10,001,449 | Nuclear morphology of ichthyosis mutant mice as a cell marker in chimeric brain. | [
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10,001,450 | The relationship between cumulus cell-oocyte coupling, oocyte meiotic maturation, and cumulus expansion. | [
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10,001,451 | Persistence of attention to a novel conspecific: some developmental variables in laboratory rats. | [
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10,001,452 | Persistence of social attention by male and female laboratory rats was examined following exposure to novel conspecifics. In experiment I we compared performance of castrate female controls. Testosterone significantly prolonged mean social investigation time. Castrate females treated with a 10-day regimen of testosterone propionate to that of intact males and castrate females treated with a relatively high dosage of testosterone failed to differ from intact males. In Experiment II we compared neonatally androgenized female castrates with castrate male and castrate female controls. Postnatal exposure to testosterone increased sensitivity of females to exogenous testosterone in maturity as measured by persistence of social investigation. In Experiment III we compared investigation time of intact and castrate males and females at 10-day intervals from 40 to 80 days of age. Intact males investigated novel conspecifics significantly longer than other groups, with longest investigation times at 60 and 70 days of age. In Experiment IV we compared investigation times of 30-day, 60-day, and 200-day-old males. Sixty-day-old males investigated significantly longer than 30-day-old or 200-day-old groups, which failed to differ from each other. The combined results demonstrate a gender and age-related effect of testosterone on persistence of social investigation. | [
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10,001,453 | Motor asymmetries in preterm infants: effects of prematurity and illness. | [
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10,001,454 | Two types of motor asymmetry, postural asymmetry and lateral head turning, were assessed in 3 groups of preterm infants, one of which had experienced respiratory distress syndrome (RDS) in the postnatal period. Results reveal that maintenance of a right postural asymmetry is present as early as 34 weeks conceptional age and is not disrupted by postnatal illness. Lateral head turning after midline placement was evident as early as 36 weeks conceptional age but was disrupted by physiologic condition. Infants who had experienced RDS had poor muscle tonus and did not assume the head right position even at 39 weeks conceptional age. These data argue that lateral responding may be affected by illness and that studies of preterm populations must evaluate postnatal medical condition when assessing both the short- and long-term outcomes of lateral asymmetries. | [
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10,001,455 | A quantitative analysis of the feeding behavior of suckling rabbits. | [
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10,001,456 | Three experiments are reported on the feeding behavior of suckling rabbits ("kittens"). In the 1st the latency with which the kittens attached to the nipple, and then left the nipple, was determined. Attachment was very rapid and wholly reliable: on the 80 tests the nipple was seized in every case in under 9 sec, and on 67 of these in less than 3 sec. The kittens also invariably left the nipple within the next minute. If the kittens were 5 or 10 days old speed of attachment was unaffected by the presence or absence of saliva on the nipple, but 15- and 20-day-old kittens seized the sucked nipples more rapidly than the unsucked nipples. In a 2nd experiment with 12-day-old kittens, washing the nipple with solvents did not affect speed of attachment; nor did saliva. The results show that suckling rabbits, in contrast to rat pups, are not heavily dependent on saliva cues. In the 3rd experiment both attachment latency and milk intake were shown to be affected by an internal stimulus, a gastric load of.9% saline, 5 g/25 g body weight: attachment latency was significantly increased and milk intake reduced by 75%. | [
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10,001,457 | Ontogeny of hoarding in the golden hamster: the development of motor patterns and their sequential coordination. | [
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10,001,458 | The hoarding behavior of 4 litters of Golden hamster pups (n = 3) was observed every 2nd day between the age of 13 and 47 days (2 litters) or 13 and 55 (2 litters). Each litter lived with the mother until Day 30; then the pups were put in social isolation. Immature forms of pouch filling and emptying, which were not integrated into coherent behavior sequences, appeared from the beginning of the observation period. Coordinated hoarding trips were shown from Day 21 onwards, once the motor patterns of inserting and extracting food had gained their definitive form. The development of hoarding was correlated with the animal's body weight and therefore with maturational factors. Mature hoarding behavior was greatly enhanced by the subject's separation from its family unit. | [
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10,001,459 | Maturation and d-amphetamine-induced changes in web building. | [
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10,001,460 | Webs of Araneus diadematus Cl. were obtained under drugged (dextroamphetamine) and control conditions at three age-periods in the development of the spider from juvenility to sexual maturity. Although certain features of construction are affected in all periods and some exhibit differential effects with age, it was not possible to separate the latter from changes in body mass between periods. | [
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] |
10,001,461 | Effect of cross-rearing on species identification in zebra fish and pearl danios. | [
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10,001,462 | Zebra fish and pearl danios were either cross-reared or raised with conspecifics and tested as adults for species preference over 4 days. Subjects were then placed with conspecifics by group for 30 days and retested over 2 days. Initial testing showed less preference (species identification) for conspecifics by cross-reared subjects and less conspecific preference by pearls than zebras. At retesting pearls showed a great increase in preference for conspecifics whereas zebras showed little change. | [
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10,001,463 | Effects of early social experience on activity and object investigation in the ferret. | [
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10,001,464 | Earlier experiments have shown that many of the effects of early social isolation in the rat may be due to deprivation of social play. The isolated ferret, like the isolated rat, is hyperactive; furthermore, its hyperactivity appears to be related to deprivation of social play. However, the relationship between object investigation and social rearing is more complex in the ferret than it is in the rat. | [
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10,001,465 | Effect of brain growth stages on T-maze acquisition in mice. | [
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10,001,466 | Recently, it has been shown that brain growth is characterized by periods of especially large increases in growth, with "plateaus" in growth between these "spurt" periods. In humans, these spurts in brain growth are correlated with spurts in mind growth, collectively termed phrenoblysis. Brain growth spurts in rodents occur at 0-6, 8-12, and 17-23 days of age with plateaus in-between. We examined two questions. First, are there differences in learning ability associated with spurts and plateaus in brain growth? Second, can learning during these stages be altered through genetic and environmental manipulations? We employed the high and low lines of the Fuller brain weight selection mice, which are known to have different developmental patterns, and early handling procedures, known to alter growth rates. The results showed that animals tested during a proposed brain growth spurt were superior to animals tested during a brain growth plateau in learning a shock-escape T-maze. | [
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10,001,467 | Age and brightness discrimination learning by c57BL/6J mice. | [
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10,001,468 | hyperprolactinemia of portal hypertension in rats. | [
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10,001,469 | Plasma prolactin levels are often raised in patients with liver cirrhosis and portal hypertension. To obtain more insight into the underlying mechanisms we examined the synthesis and release of prolactin in male rats with partially ligated portal veins. Portal hypertension led to an increase in pituitary prolactin, plasma prolactin, and plasma 17 beta-estradiol, and a decrease in hypophyseal stalk dopamine levels. Castration decreased plasma prolactin levels and prevented the induction of hyperprolactinemia by portal hypertension. Administration of dihydrotestosterone to castrated animals did not affect prolactin levels in the pituitary gland or in the plasma. Plasma tryptophan and tyrosine concentrations did not change in portal hypertension. A low protein diet caused a decrease in plasma tryptophan and an increase in plasma tyrosine levels without affecting prolactin levels in either controls or portal hypertensive rats. The hyperprolactinemia of portal hypertension is probably caused by elevated estrogen levels which interfere with hypothalamic dopamine release. Changes in plasma amino acid levels are of little importance in the regulation of prolactin release in portal hypertensive rats.U | [
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10,001,470 | Effects of lactulose and neomycin on urea metabolism in cirrhotic subjects. | [
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10,001,471 | In our previous studies of cirrhotic subjects lactulose caused a 25% decrease in the urea production rate associated with a decrease in urinary urea excretion and an increase in stool nitrogen. The decrease in the rate of urea production was an indirect measure of reduction in gut ammonia production. The present study was designed to determined if the poorly adsorbed antibiotic neomycin had an additive effect in reducing ammonia production when administered in combination with lactulose. Six stable cirrhotic subjects received isonitrogenous diets during separate lactulose and lactulose + neomycin treatment periods. The addition of neomycin to a lactulose regimen caused a 17% reduction in the urea production rate that was quantitatively accounted for by a 70% reduction in the urea degradation rate. The intestinal urea clearance rate demonstrated a parallel reduction, indicating an inhibition of bacterial ureolysis. There was no evidence that neomycin altered the effects of lactulose since urinary urea excretion did not rise, fecal nitrogen remained high, and stools remained acidic. These results demonstrate that neomycin inhibited bacterial ureolysis when administered with lactulose while lactulose itself was metabolized and its individual effect on nitrogen metabolism persisted. Lactulose and neomycin, when administered together, had an additive effect in reducing gut ammonia production in cirrhotic subjects. | [
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10,001,472 | S-adenosyl-L-methionine antagonizes ethynylestradiol-induced bile cholesterol supersaturation in humans without modifying the estrogen plasma kinetics. | [
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10,001,473 | Previous investigations have shown that S-adenosyl-L-methionine antagonizes both cholestasis and bile lipid alterations induced by ethynylestradiol in the rat. Since it is still unknown whether S-adenosyl-L-methionine prevents ethynylestradiol-induced cholesterol supersaturation of bile in humans also and how methynation interferes with plasma ethynylestradiol disappearance, the present study has been carried out. On different days, 5 nonobese subjects with indwelling biliary drainage and reestablished enterohepatic bile circulation received 200 micrograms of intravenous ethynylestradiol or ethynylestradiol plus 200 mg of S-adenosyl-L-methionine intramuscularly. S-adenosyl-L-methionine administration prevented any ethynylestradiol-induced changes in hepatic bile saturation index. Moreover, S-adenosyl-L-methionine did not affect ethylnylestradiol pharmacokinetics which was evaluated in a group of 6 nonobese women receiving 100 micrograms of intravenous ethynylestradiol or ethynylestradiol plus 100 mg of S-adenosyl-L-methionine intramuscularly. These findings indicate that S-adenosyl-L-methionine prevents ethynylestradiol-induced bile lipid changes without interfering with ethynylestradiol kinetics in humans. | [
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10,001,474 | Prospective evaluation of biopsy number in the diagnosis of esophageal and gastric carcinoma. | [
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10,001,475 | A prospective trial was performed in which biopsy and cytology specimens were obtained on 202 consecutive patients including 47 with esophageal or gastric carcinomas. The first biopsy specimen yielded a correct diagnosis in the majority of instances: 70% of gastric carcinomas and 93% of esophageal carcinomas. Three additional biopsy specimens increased the yield to greater than 95%, a total of seven biopsy specimens yielded greater than 98%. Seven biopsy and cytology specimens yielded the correct diagnosis in all patients. Seventeen percent of all lesions subsequently proven to be malignant were thought to be benign, endoscopically. This reinforces the belief that all lesions seen at endoscopy should have biopsies performed and at least seven specimens should be obtained. | [
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10,001,476 | Cell renewal and migration in lymphoid follicles of Peyer's patches and cecum--an autoradiographic study in mice. | [
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10,001,477 | Peyer's patch lymphoid follicles are characterized by a cuboidal epithelium, which has low numbers of mucus-secreting goblet cells, infiltration with clusters of lymphoid cells, and unique antigen-transporting M cells. M cells have short, irregular microvilli similar to undifferentiated crypt epithelial cells, which suggested that M-cell renewal might occur over follicle surfaces. By autoradiography we found that epithelial renewal over follicles only occurs by proliferation in multiple adjacent crypts with cell migration onto follicle surfaces. Nuclear labeling of M cells was observed after 72 h among fully differentiated cuboidal cells from which M cells appear to develop. Goblet-cell flow from surrounding crypts supplied large numbers of goblet cells to adjacent villi, but it was remarkably restricted onto the Peyer's patch follicle surfaces, creating a breach in the mucus barrier that may facilitate antigen sampling. | [
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10,001,478 | Histamine synthesis by intact mast cells from canine fundic mucosa and liver. | [
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10,001,479 | The synthesis and degradation of histamine by dog fundic mucosa was studied by using cells dispersed by enzymatic digestion and separated sequentially by velocity sedimentation in an elutriator rotor, and by density gradient. Histidine decarboxylase activity was found in appreciable amounts in fractions highly enriched in mast cells when these cells were studied intact, whereas only trace activity was detected in homogenates of these mucosal mast cells or of whole mucosa. Unlike the rat gastric mucosal histamine cell, dihydroxyphenylalanine decarboxylase activity was not present in the canine fundic mast cell. Serotonin, which is found in the rat peritoneal mast cell, was not detectable in the canine mast cell. The histamine-degrading enzyme, histamine methyltransferase, was also present in gastric mucosal cells, but not diamine oxidase. This methyltransferase activity was primarily associated with parietal cells and was not found in the mast cell-enriched functions. For comparison, fractions containing 60%-80% mast cells were enriched by elutriation from enzyme-dispersed cells of canine liver. As with the gastric mast cells, histidine decarboxylase activity was found in intact cell, but it was lost upon cell disruption. | [
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10,001,480 | Gastric mucosal prostaglandin E levels in patients with gastric ulcer disease and carcinoma. | [
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10,001,481 | Prostaglandin E was measured by radioimmunoassay in endoscopic biopsy specimens obtained from 7 normal healthy volunteers, 28 patients with a benign gastric ulcer, and 10 with a malignant gastric ulcer. Biopsy specimens were taken from the antral and body mucosa and from the ulcer edge in patients. The median value in normal antrum specimens was 5.15 (4.44-8.40) ng PGE/mg protein which was more than the body with 3.50 (1.86-9.28), p less than 0.05. In the 28 patients with benign gastric ulcer the ulcer edge contained 2.33 (0.48-7.67) ng PGE/mg protein which was more than the antrum with 1.06 (0.30-4.17) or the body with 0.97 (0.20-7.67), p less than 0.01 respectively. The antral and body levels in patients with gastric ulcers were lower than those found in the normal volunteers, p less than 0.01. There was no difference between the levels found in patients with malignant as opposed to benign gastric ulcer. In patients with gastric ulcer lower levels of PGE were found in body mucosa with atrophic gastritis 0.83 (0.53-2.66) ng PGE/mg protein as compared with histologically normal body mucosa 2.55 (0.63-7.67), p less than 0.05. These results suggest that mucosal PGE levels are reduced in patients with gastric ulcer disease and that this may be due to the presence of atrophic gastritis. | [
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10,001,482 | Luminal lymphoid cells in the rabbit intestine. | [
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10,001,483 | In normal rabbits, lymphocytes have been identified in large numbers on the luminal epithelial aspects of both Peyer's patches and the appendix by scanning and transmission electron microscopy. Luminal cells shared an intimate relationship with intestinal microorganisms. Irrigation of the appendiceal lumen has proved a useful technique for collecting 8.5 x 10(6) (mean) viable lymphocytes (73%) and macrophages (22%). Functional characteristics (mitogen responsiveness, T-cell numbers and cells with positive cytoplasmic immunoglobulin A fluorescence) were similar to isolated intestinal mucosal cell preparations. In vivo cytokinetic studies indicated that 50% of luminal appendiceal lymphocytes were recently divided (within 5 h). The passage of lymphoid cells into the the appendix lumen was antigen responsive, as was the size of the appendiceal lymphoid mass. This evidence suggests that migration of lymphoid cells into the lumen of the intestine in healthy animals occurs normally probably from the gut-associated lymphoid tissue--a phenomenon similar to that observed in the bronchial tract. Both mucosal surfaces may, therefore, be important sites of lymphocyte and macrophage traffic. | [
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10,001,484 | Inflammatory and structural changes in the opossum esophagus after resection of the cardia. | [
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10,001,485 | Transmembrane voltage of opossum esophageal smooth muscle and its response to electrical stimulation of intrinsic nerves. | [
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10,001,486 | Effects of experimental chronic hypercalcemia on feline exocrine pancreatic secretion. | [
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] |
10,001,487 | Regression of biliary cirrhosis following choledochal cyst drainage. | [
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10,001,488 | Invasive enterocolitis caused by Edwardsiella tarda. | [
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10,001,489 | Lymphoreticular malignancy presenting as fulminant hepatic disease. | [
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10,001,490 | Four cases of fulminant hepatic disease caused by lymphoreticular infiltration are described. All 4 patients died within a few weeks and clinical diagnoses included viral hepatitis, alcoholic hepatitis, and drug hepatitis. A diagnosis of malignancy was made prior to autopsy in only 1 of the 4 patients. Autopsies revealed typical malignant histiocytosis in 3 patients and the fourth had a primitive lymphoreticular malignancy with malignant histiocytosis the favored diagnosis. The extent of the liver infiltrate as judged histologically was mild compared with the severe clinical illness. Randomly scattered foci of necrosis associated with the malignant infiltrate were seen in the 2 patients who had marked elevations of serum glutamic oxaloacetic transaminase. | [
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10,001,491 | Tissue diagnosis in ulcer gastrointestinal malignancy. | [
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10,001,492 | Gastric acid secretion, smoke and duodenal ulcer healing. | [
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] |
10,001,493 | Radioimmunoassay for HBcAg. | [
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10,001,494 | Tuberculosis after cimetidine therapy: an adverse clinical immune effect? | [
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] |
10,001,495 | Diabetic control and gastrointestinal function. | [
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10,001,496 | The intestinal phase of pancreatic polypeptide release. | [
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10,001,497 | Patient acceptance and effectiveness of a balanced lavage solution (Golytely) versus the standard preparation for colonoscopy. | [
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] |
10,001,498 | An oral electrolyte solution containing 125 mM/L sodium, 10 mM/L potassium, 80 mM/L sulfate, 20 mM/L bicarbonate, and 80 mM/L of polyethylene glycol, and associated with little water or electrolyte absorption from the gut was recently described in this journal. To determine the efficacy of this solution (Golytely) for colonoscopy, 20 consecutive patients were randomized to either a standard colonoscopy prep or Golytely. Both preps resulted in a feces-free colon, allowing colonoscopy to the cecum in most cases. Although Golytely produced mild cramps (3 of 12) and transient fullness (6 of 12 vs. 0 of 8 with standard prep, p less than 0.02), 11 of 12 were willing to repeat Golytely vs. 3 of 8 with the standard prep (p less than 0.02). It is concluded that Golytely is an effective prep for colonoscopy and well tolerated by patients. It is especially useful for those requiring repeated examinations because of patient acceptance and efficacy. | [
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10,001,499 | Contact electrode method in hydrogen gas clearance technique: a new method for determination of regional gastric mucosal blood flow in animals and humans. | [
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