Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0027819 (neuroblastoma)
 27,800 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

A method of digestion by using a mixture of hydrochloric, nitric, and sulfuric acids has been developed for the determination of total mercury in a wide range of food samples. Good recoveries of mercury were obtained from NBS (National Bureau of Standards) Albacore Tuna and from food samples spiked with inorganic mercury. A detection limit of 0.01 microgram mercury/g can be obtained.
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PMID:Digestion of food samples for total mercury determination. 299 10

An improved two-step clean up procedure involving alumina-silica column chromatography and gel permeation chromatography (GPC) of air particulate matter (NBS SRM 1648) and river sediment extracts and a GPC clean up procedure for marine biota samples are described for the determination of polycyclic aromatic hydrocarbons with two to five rings and selected polychlorinated biphenyl congeners, respectively. Bio-Beads SX-12 and SX-3 were used as packing materials. The recoveries obtained varied from 52 to 78% depending on the compound. Quantitative data for NBS SRM 1648 were comparable with those described previously for this sample.
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PMID:Selective enrichment procedures for the determination of polychlorinated biphenyls and polycyclic aromatic hydrocarbons in environmental samples by gel permeation chromatography. 314 50

This improved isotope-dilution gas chromatographic/mass spectrometric (GC/MS) method, in which [13C]glucose is the internal standard, meets the requirements of a Definitive Method. In a first study with five reconstituted lyophilized sera, a nested analysis of variance of GC/MS values indicated considerable among-vial variation. The CV for 32 measurements per serum ranged from 0.5 to 0.9%. However, concentration and uncertainty values (mmol/L per gram of serum) assigned to one serum by the NBS Definitive Method (7.56 +/- 0.28) were practically identical to those obtained with the proposed method (7.57 +/- 0.20). In the second study, we used twice more [13C]glucose diluent to assay four serum pools and two lyophilized sera. The CV ranged from 0.26 to 0.5% for the serum pools and from 0.28 to 0.59% for the lyophilized sera. In comparison, results by the hexokinase/glucose-6-phosphate dehydrogenase reference method agreed within acceptable limits with those by the Definitive Method but tended to be slightly higher (up to 3%) for lyophilized serum samples or slightly lower (up to 2.5%) for serum pools.
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PMID:Precision of glucose measurements in control sera by isotope dilution/mass spectrometry: proposed definitive method compared with a reference method. 330 Oct 68

A detailed derivation is presented of the formulas required to determine Ngas and Dmed in the AAPM TG-21 dosimetry protocol. This protocol specifies how to determine the absorbed dose in an electron or photon beam when using exposure or absorbed dose calibrated ion chambers. It is shown that the expression given in TG-21's recent letter of clarification is incorrect. Accounting for humidity correctly increases, by 0.4%, all absorbed dose determinations using an exposure calibrated ion chamber. Taking into account other correction factors in the equation for exposure could also have varying, but significant effects (possibly over 1%). These are the stem scatter correction, the axial nonuniformity correction and the electrode correction for electrodes made of different materials from the wall. Attention is drawn to differences in the definitions of the exposure and absorbed dose calibration factors, Nx and ND, respectively, as supplied by the NBS and the NRCC.
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PMID:The role of humidity and other correction factors in the AAPM TG-21 dosimetry protocol. 335 50

A new fast, accurate and simple quantification method for C, N and O in biomedical samples by external-beam proton-induced gamma-ray emission analysis is presented. Concentration values for C, N and O in commercial standards of NBS bovine liver 1577a, IAEA animal muscle H-4 and IAEA horse kidney H-8 were determined using the new method. The concentrations of C, N, O, Na, Mg and P were determined from placental samples of 13 alcoholic mothers and from 16 abstinent controls. The values obtained for C, N, O, Mg and P were the first values ever obtained for human placentas.
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PMID:A rapid method for the quantification of C, N and O in biomedical samples by proton-induced gamma-ray emission analysis applied to human placental samples. 335 53

The measurement of total calcium (CaT) in biological fluids by flame atomic absorption spectroscopy (FAAS) is one of the more accurate yet practical methods available today. With attention to details at every analytical step, the imprecision of FAAS outlined above can be as low as +/- 0.01 mmol/liter at the 2.65 mmol/liter upper reference level of CaT found in the serum of healthy young adults (a CV of 0.4%). The accuracy of FAAS as judged by measurements of NBS/SRM #909, a lyophilized serum material carrying CaT values assigned by isotope dilution mass spectrometry, can be within +/- 1% (recovery of 99-101%) or less in skilled hands. As our brief section on application suggests, FAAS methods for CaT can be adopted to provide rapid and accurate results in many different biological fluids and tissues.
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PMID:Measurement of total calcium in biological fluids: flame atomic absorption spectrometry. 337 81

Dihydrotestosterone (DHT) is essential for sperm maturation within the epididymis, but the roles of estradiol-17 beta (E2) and progesterone (P) in epididymal function are unknown. To identify sites of potential action of these hormones, and any effect of season on their concentrations, specific binding of steroids to receptors in extracts of ram epididymal tissue was quantified in two studies. Tissue was taken from three broad regions of the epididymis (caput, corpus, and cauda; Study 1) or from seven discrete regions of the epididymis (Study 2) in February to May (nonbreeding season; NBS) or late August to October (breeding season; BS). Specific binding of P was not detected. Saturable high-affinity binding sites specific for DHT (Ka = 2.6 x 10(8).M-1) and E2 (Ka = 5.4 x 10(8).M-1) were detected. Binding was not to androgen-binding protein, testosterone-estradiol-binding globulin, or sperm nuclei. There was no regional or seasonal difference in affinity of DHT or E2 binding. In both studies, concentration of DHT-binding sites (fmol/mg protein for low- plus high-salt extracts) was higher (p less than 0.05) in the BS than NBS. In Study 1, mean concentration of DHT-binding sites was higher (p less than 0.05) in the caput than in the corpus and cauda. The more definitive localization possible in Study 2 revealed that concentration of DHT-binding sites was highest in the distal caput, lowest in the proximal cauda (p less than 0.05), and intermediate in other regions. For E2, however, concentration of binding sites was higher (p less than 0.05) in the BS than NBS only in Study 1, and was higher (p less than 0.05) in the cauda or corpus than in the caput epididymidis. In Study 2, the season by region interaction was significant (p less than 0.05); concentration of E2-binding sites was higher in the distal cauda during the NBS. These data support the concept that the central caput through proximal corpus epididymidis are most dependent on androgenic stimulation, whereas distal regions may respond to estrogenic stimulation.
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PMID:Regional and seasonal differences in concentrations of androgen and estrogen receptors in ram epididymal tissue. 340 73

A screening method for determination of cadmium, lead, and copper in foods was developed. The sample (1-3 g) is digested with HNO3-H2SO4-HClO4 in a centrifuge tube attached to a straight glass tube that prevents loss of HNO3 by volatilization. After digestion, potassium iodide, H2SO4, and MIBK (4-methyl 2-pentanone) are added, and the metals are extracted with MIBK as metal iodides. The MIBK solution is injected and the metals are determined by flame polarized Zeeman atomic absorption spectrometry using a discrete nebulization technique. Recoveries of metals from fortified milk powder, unpolished rice, fish, beef, peanut butter, apple, and cabbage were satisfactory. The analytical results for NBS Oyster Tissue and NIES Pepperbush, Chlorella, and Mussel agreed with certified or reference values except lead in Pepperbush. The limits of quantitation for cadmium, lead, and copper were 0.01, 0.09, and 0.02 ppm, respectively. This method is simple and safe for routine analysis of high levels of cadmium, lead, and copper in foods.
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PMID:Screening method for determination of high levels of cadmium, lead, and copper in foods by polarized Zeeman atomic absorption spectrometry using discrete nebulization technique. 341 11

Trp-155 in bovine DNase A (EC 3.1.4.5) appeared to be unessential for the enzymatic activity for the following reasons: (1) A unique peptide which suggests the environmental difference of Trp-155 was obtained from porcine pancreatic DNase A. (2) Inactivation of the porcine DNase A by NBS modification was fairly paralleled with a decrease in the CD signal, which is characteristic of the "buried" tryptophan in the hydrophobic region (trp-191 in bovine DNase) but not of tryptophans in the hydrophilic portion. Binding of DNase to the poly I: poly C double helix confirmed the important role of this tryptophan.
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PMID:Functional evaluation of tryptophanyl residues of bovine and porcine pancreatic deoxyribonucleases. 345 85

In some small-scale tests of combustion-product toxicity, perfluorinated polymers (FP) have been shown to be much more toxic than other common materials. These studies were conducted to determine the conditions under which highly toxic decomposition products of FP are formed. A modification of the National Bureau of Standards exposure system (Levin et al. National Bureau of Standards 1982, NBS IR 82-2532) was used, in which materials could be heated either in a cup furnace or above a small methane flame. At 700 degrees C, the approximate lethal concentrations (ALCs) of the products formed from polytetrafluoroethylene (pTFE) and from hexafluoropropylene/tetrafluoroethylene copolymer (FEP) in the CH4 flame (applied for 1 min) are approximately 850 times higher than the ALCs of the products formed in the cup furnace. Analytically, the major products formed initially from pTFE at 700 degrees C under either condition (flame or cup furnace) are similar but they disappear rapidly in the presence of continuous heat. When the cup furnace is removed 1 min after pTFE is added (a procedure temporally similar to the use of the flame) the toxicity of the products is again low. However, when heat from either the cup furnace or from a small secondary flame is applied continuously (for up to 30 min) to the initial products formed from pTFE in the flame, high toxicity is observed. These observations are supported by pathological evaluation of the respiratory tracts of exposed rats. Thus, the inhalation toxicity of FP thermal decomposition products is related to a heat- and time-dependent atmospheric reaction. Such mechanisms should be considered in estimating the fire hazard of these materials in use.
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PMID:Formation of acute pulmonary toxicants following thermal degradation of perfluorinated polymers: evidence for a critical atmospheric reaction. 355 41


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