[Radiobiological studies of the protein synthetic activity of isolated calf liver].
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Biomedical subjects
Publications and source records attributed to G Corte.
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Immunofluorescent and "in vitro" biosynthetic techniques have been used to study the connections between the maturation process of human lymphocytes that leads to the appearance of actively secreting cells and a possible switchover from IgD to IgM production, both in homogeneous CLL cell populations and in heterogeneous cell suspensions from tonsils. The results obtained are compatible with the hypothesis that the switchover from IgD to IgM productions can be a clonal maturation phenomenon.
The volatility of two fungicidal seed dressings, Panogen 15 B liquid and Panogen PX powder, containing methyl mercuric dicyandiamide in equivalent amounts at the dosage used, was compared with that of triple distilled mercury. Tests were made in the absence and presence of cleaned Manitou wheat of 12.0% and 17.1% moisture content. The Panogen formulations were compared at the recommended and twice the recommended rate at different dosages, storage periods and storage temperatures. The Hg content of air samples was determined by the Corte-Monkman method, capable of determining 0.4 ng of Hg, which in a 1-L air sample is equivalent to 0.049 ppb (v/v). The volatility of the interstitial air expressed as mug of Hg vapor/m3 air depended on temperature, wheat moisture content and storage duration and ranged from 150 to 2,240 for metallic Hg, 21 to 350 for Panogen 15 B, and 31 to 380 for PX. In the absence of wheat the volatility of 15 B was greatest (395) at -17.5 degees C and least (75) at 4.5 degrees C, but increased rapidly thereafter with increased temperature. Volatility of metallic Hg after application to wheat of 12.0% and 17.1% moisture content was not significantly reduced after four days storage, but that of Panogen 15 B and PX was reduced considerably, particularly at the higher moisture level. Thus, volatility of mercurial seed dressings cannot be predicted from Hg content alone. Reduction of volatility through possible irreversible chemical bonding of Hg with seed components is suggested for more detailed investigation.
Airborne mercury from dental offices was selectively trapped by silber gauze elements in borosilicate glass obsorbers, followed by heat-desorption and spectrophotometric measurement at 2537A. As little as 0.4 ng of Hg could be accurately determined, which is equivalent to 49 ppt in a wone-L air sample on a v/v basis. Over 860 air samples were taken over a range of locations and working conditions at 88 different dental offices, and at the Dental Training Clinic of the University of Manitoba. The Hg vapor concentrations at the dental facilities ranged from 0.45 to 742 mug/m3 of air, 29% of the samples were within 0.45 to 5 mug; 37.8 were within 5.1 to 25mug;and 33.2% were above 25 mug. Mercury concentrations varied during the working day, depending on the time of sampling, the number of amalgams placed, and the interval between placements. The lowest concentrations were obtained in the morning. Disturbance of residual mercury droplets on floors or working areas by sweeping or dusting, or immediately after attempted clean-up of a mercury spill, sharply increased the amount of airborne mercury.
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Differences in ethanol pharmacokinetics within the menstrual cycle have previously been reported and attributed to variations in body composition, hormonal influences and gastric emptying. To establish the role of the menstrual cycle in ethanol pharmacokinetics associated with changes in body composition, ethanol blood concentrations were measured in nine healthy women during the midfollicular (P1, days 8-10) and midluteal (P2, days 22-24) phases of the menstrual cycle after a postprandial oral ethanol dose (0.3 g kg(-1)). Total body water was assessed by dual-energy x-ray densitometry (DEXA) on both occasions. Median total body water did not vary during either phase of the menstrual cycle (P1 = 54.54%, P2 = 54.66%; P = 0.9296). Median area under the ethanol concentration-time curve (AUC) was lower during P1 (215.33 mg.h dl(-1)) than during P2 (231.33 mg.h dl(-1))(P = 0.8253). No significant differences were found on ethanol pharmacokinetics in either phase of the menstrual cycle.
Adult stem cells are self-renewing, pluripotent, and able to repopulate the tissue in which they reside. Cells endowed with these properties have been isolated from several tissues and an increasing number of reports provide evidence of their ability, following transplantation, to engraft host tissues other than those of their origin. In this setting, interest in the well-documented capacity of bone marrow stromal cells to undergo multilineage differentiation is growing. Neural and cardiomyogenic lineages have recently been proposed as additional differentiative pathways of these cells. However, culture conditions and inductive molecules can alter the behavior of bone marrow stromal cells and the microenvironment is critical for proper in vivo delivery. The maintenance of their stem properties and the possibility of reprogramming their commitment is a field of primary interest given the potential use of these cells in regenerative medicine. We discuss here how the microenvironmental cues, and the growth factors that physiologically govern commitment and subsequent differentiation, influence the properties of bone marrow stromal cells and modulate their engraftment into host tissues.
Familial hypercholesterolemia is a metabolic disorder inherited as an autosomal dominant trait characterized by an increased plasma low density lipoprotein (LDL) level. It has been demonstrated that the disease is caused by several different mutations in the LDL receptor gene. Although early identification of individuals carrying the defective gene could be useful in reducing the risk of atherosclerosis and myocardial infarction, the available techniques for determining the number of the functional LDL receptor molecules are not sufficiently accurate. The recent isolation of the LDL receptor gene now makes it possible to use restriction fragment length polymorphisms to study the inheritance of the defective allele in families with familial hypercholesterolemia. In the present study, we report the use of a Pvu II restriction fragment length polymorphism to follow the inheritance of familial hypercholesterolemia in a total of 79 patients from 37 different families. This restriction fragment length polymorphism allowed unequivocal diagnosis in 32.5% of the cases. Furthermore, in the Italians studied, the absence of a polymorphic Pvu II cutting site (P1 allele) was found to be strongly associated with familial hypercholesterolemia.
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The process of Immunoglobulin secretion has been extensively studied but the cellular mechanisms underlying assembly and transport of these molecules are still poorly understood. Evicence is presented in this paper for the presence, in the secretory pathway of mouse myeloma cells, of an energy requiring step, as indicated by the strong inhibition of Immunoglobulin secretion by a variety of respiratory chain inhibitors and of oxidative phosphorylation uncouplers.
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Two different methods, immunofluorescence and lactoperoxidase-catalysed radioiodination, were used to investigate mIg on two different myeloma cell lines. The data indicate that, even though both techniques are highly sensitive, different results can be obtained in the same cell line depending on the technique employed.
UNLABELLED: Our objective was to evaluate prospectively, objectively and in a systematic way the evaluation of patients with Ulcerative Colitis (UC) with moderate activity. We studied 14 outpatients, who were evaluated for an experimental therapeutic protocol. The activity of the disease was established using clinical, endoscopic and histologic parameters. The Kappa Index (K) was used for statistical analysis. The average number of bowel movements was 4/day; rectal bleeding and urgency were found in 100%, diarrhea in 78% and abdominal pain in 64%. The severity of rectal bleeding and urgency was graded II or III in 92% and 78% respectively. The correlation between endoscopy and histology (K = 0.55), and between clinical and endoscopy (K = 0.45) was moderate. There was no correlation between clinical and histological parameters. IN CONCLUSION: the variability of symptoms impairs the clinical evaluation as the unique method to determine the activity of UC and to take therapeutical decisions is necessary to perform a endoscopic/histology correlation.
Recently it has been described in the literature a subpopulation of PBC patients with negative AMA that might represent patients with ANA positive autoimmune cholangitis. We review 25 cases of PBC (23 females) with AMA negative. Our aim was to determine the frequency of ANA(+) in this group. We studied serum transaminases, total bilirubin, AMA and ANA by indirect immunofluorescence considering positive dilutions of 1:40. All patients had elevated alkaline phosphatase (641 +/- 389 U/l). Total bilirubin was below 2.5 in 59%. Thirteen patients had esophageal varices. The histologic stage was I-II in eleven and III-IV in 14 cases. Fourteen patients (56%) has ANA(+) (dilution 1:40), 44% had lower dilutions. We confirm the presence of a subpopulation of PBC AMA negative, ANA positive patients and the observations of different and diverse immune alterations in PBC patients.