Biomedical subjects
H Smith
Publications and source records attributed to H Smith.
The chemistry of fungi. L. Rosenonolactone.
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Total synthesis of derivatives of (+)-oxa and aza-estrone.
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Blood types of the Cherokee Indians.
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The determination of haptoglobins in normal human serum.
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SERUM HAPTOGLOBINS IN HAEMOLYTIC STATES.
Serum haptoglobin levels have been studied in patients with a number of haemolytic disorders. In general, serum haptoglobins were low in patients with increased haemolysis. Values were reduced irrespective of whether haemolysis occurred intravascularly or extravascularly. The reduction was related to the amount of haemoglobin destroyed per day. Serum haptoglobins may be raised in certain neoplasms and infections and during adrenocortical steroid hormone therapy. A rise in haptoglobins due to one of these factors may mask a fall due to haemolysis. Thus a normal or raised serum haptoglobin does not necessarily exclude a haemolytic process.
The virulence-enhancing factor of mucins. 1. A biological assay of virulence-enhancing activity.
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The virulence-enhancing factor of mucins. 2. Fractionation studies on hog gastric mucin.
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Rate of regeneration of peripheral nerves in man.
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Acetylcholine receptor antibodies in myasthenia gravis.
A multivariate statistical analysis of levels of serum acetylcholine receptor antibody (AChR Ab) obtained from 197 patients with various clinical forms of myasthenia gravis (MG) was performed. Elevated AChR Ab levels are specific for MG, but normal AChR Ab levels do not rule out MG. Patients in remission or with purely ocular MG had the lowest incidence of elevation of serum AChR Ab levels, while patients with generalized, severe MG, particularly in the presence of thymoma, tended to have the greatest antibody elevations. Corticosteroids depressed AChR Ab levels, but thymectomy did not exert a consistent effect on antibody levels within a 24- to 30-month postoperative period. The relatively low 55% positivity of antibody elevations in all 197 patients probably reflects the use of heterologous (rat) AChR.
Selection of high-affinity and high-specificity monoclonal antibodies for 1 alpha,25-dihydroxyvitamin D.
The preparation of high-affinity and high-specificity monoclonal antibodies to 1 alpha,25-dihydroxyvitamin D is described. Monoclonal antibodies were derived from Balb-c mice immunised with either 1 alpha-hydroxy-25,26,27-trinor-24-cholecalcioic acid or with 1 alpha-hydroxy-26,27-dinor-cholecalciferol-25-oxime, and spleen cells were hybridised with mouse myeloma cells. From six fusions nine monoclonal antibodies (MAb's) were selected from 676 antibody-secreting hybrids. Antibodies varied widely in their ability to bind 1 alpha,25-dihydroxyvitamin D3 (50% displacement of radioligand ranged from 25 - 900 pg); two had particularly useful characteristics for 1 alpha,25-dihydroxyvitamin D assay. MAb 5F2 has high affinity (Ka = 1.39 X 10(10) M-1) and does not discriminate between 1 alpha,25-dihydroxyvitamin D2 and D3, thus enabling the two forms to be measured together. MAb 1G7 is highly specific, having no cross-reactivity with 25-hydroxy-, 24,25-dihydroxy- or 25,26-dihydroxyvitamin D at concentrations found in normal human serum; this MAb has the potential to eliminate the lengthy extraction procedures involved in currently available assays for 1 alpha,25-dihydroxyvitamin D.
Effects of a nutrition intervention program during pregnancy. Maternal data phases 1 and 2.
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The detection, identification and measurement of indole, tryptamine and 2-phenethylamine in putrefying human tissue.
Indole, tryptamine and 2-phenethylamine are putrefactive products which may be found in decaying human tissue. They may be identified by the data given found in decaying human tissue. They may be identified by the data given for infrared and ultraviolet spectrometry, fluorometry, thin layer and gas chromatography and mass spectrometry. Quantitative studies may be made using the gas chromatography method described. The rate of formation is affected by temperature and preservatives and may be prevented if necessary by the use of sodium fluoride. No relationship between the production of these materials (and alcohol) and time since the post-mortem examination could be established. The post-mortem examinations took place within 24 hours of death.
A suicide by thiopentone injection.
Post-mortem tissues from a thiopentone suicide were analysed by ultraviolet spectrometry and gas chromatography. The thiopentone concentrations found (0.6 mg/100 ml of blood and 2 6 mg/100 g of tissue) are consistent with those reported for 'anaesthetic' deaths where only thiopentone and other anaesthetic agents were present. The gas chromatographic method gave more accurate result with the tissues.
A suicide by ingestion of a mixture of copper, chromium and arsenic compounds.
A suicide resulting from the ingestion of copper, chromium and arsenic is reported. Death was delayed for 36 hours, during which time copper was rapidly eliminated from the body but chromium and arsenic remained in substantial quantities. The different metabolism of these elements is discussed and the tissue levels discovered are compared with the normal levels.
The measurement and interpretation of morphine in blood.
A method for the determination of morphine is post-mortem blood by HPLC with electrochemical detection is described. Blood morphine levels in post-mortem cases are reported and the importance of these in causing death is discussed. These post-mortem levels are compared further with morphine levels in the blood of patients receiving morphine as an analgesic.
Radioreceptor assay and radioimmunoassay of triazolam in urine samples from racing greyhounds.
Two complimentary assay techniques were used to determine triazolam levels in greyhound urine samples following a single oral dose. The results from the trials were statistically compared. The relative non-specificity of the benzodiazepine antibody used in radioimmunoassay caused a significant difference in teh two sets of results. This was independent of hydrolysis.