scholarly journals PHENYLPYRUVIC OLIGOPHRENIA. REPORT OF A CASE IN AN INFANT WITH QUANTITATIVE CHEMICAL STUDIES OF THE URINE

1943 ◽  
Vol 22 (1) ◽  
pp. 87-93 ◽  
Author(s):  
Margaret Dann ◽  
Eleanor Marples ◽  
Samuel Z. Levine
1942 ◽  
Vol 75 (3) ◽  
pp. 285-295 ◽  
Author(s):  
Michael Heidelberger ◽  
Manfred Mayer

1. A modified method is given for the titration of human complement so that C'1 titers are measured, as in guinea pig serum, instead of the C'2 titers yielded by the usual titration. 2. The measurement of complement combining component or components in weight units, instead of relative terms, is carried out as in guinea pig serum and leads to similar values, 0.03 to 0.05 mg. of C' N per ml. of human serum. 3. Other similarities in human and guinea pig complements are noted and discussed.


1941 ◽  
Vol 73 (6) ◽  
pp. 681-694 ◽  
Author(s):  
Michael Heidelberger

1. A quantitative micro method, conforming to the criteria of analytical chemistry, is proposed for the estimation of complement, or its combining component or components, in milligrams per milliliter instead of in the customary relative and variable volume units. 2. Data are given showing the range of accuracy and reproducibility of the new method.


1916 ◽  
Vol 14 (2) ◽  
pp. 26-27 ◽  
Author(s):  
R. L. Kahn ◽  
J. B. Neal

1941 ◽  
Vol 73 (6) ◽  
pp. 695-709 ◽  
Author(s):  
Michael Heidelberger ◽  
Alfred J. Weil ◽  
Henry P. Treffers

1. The molecular quantities of hemolysin and complement combining component or components (C'1) involved in hemolysis have been calculated on the basis of new, quantitative, absolute methods of analysis. 2. Molecular combining ratios between antigen, antibody, and C'1 have been established. 3. The data are shown to be in accord with the theory of combination of multivalent antigen with multivalent antibody. 4. The fixation of complement by antigen-antibody combination is qualitatively and quantitatively accounted for on this basis.


1941 ◽  
Vol 74 (4) ◽  
pp. 359-367 ◽  
Author(s):  
Michael Heidelberger ◽  
M. Rocha e Silva ◽  
Manfred Mayer

1. Quantitative data are given on the effect of variations in the time of contact and the proportions of the reactants on the quantity of complement combining component nitrogen (C'1 N) found in active guinea pig serum. 2. C'1 N was the same when determined with precipitates containing excess antibody or excess antigen. 3. Finely divided specific precipitates took up the complement combining component (C'1) from subsequently added guinea pig serum almost as well as specific precipitates formed in the presence of complement.


1942 ◽  
Vol 25 (4) ◽  
pp. 523-531 ◽  
Author(s):  
Michael Heidelberger ◽  
Henry P. Treffers

1. Total antibody in hemolysins may be estimated from the nitrogen added to sheep stromata suspensions. 2. The method is applied to a number of hemolysins and a correlation, valid to within 20 per cent, established between hemolytic titer and total antibody. 3. When stromata combine with antibody in the presence of guinea pig complement they may take up at least 80 per cent of their weight of complement combining component(s).


1969 ◽  
Vol 17 (3) ◽  
pp. 139-155 ◽  
Author(s):  
EZIO GIACOBINI

Remarkable methodologic advances in recent years make it possible to study with high precision, sensitivity and accuracy the activities of most enzymes and the levels of most substrates and metabolites in individual cells. The limits and the value of quantitative chemical studies in individual nerve cells are critically evaluated and discussed.


Author(s):  
J.R. Mcintosh

The mitotic apparatus is a structure of obvious biological and medical interest, but it has proved to be a difficult cellular machine to understand. The chemical composition of the spindle is only slightly elucidated, largely because of the difficulties in preparing useful isolates of the structure. Chemical studies of the mitotic spindle have been reviewed elsewhere (Mcintosh, 1977), and will not be discussed further here. One would think that structural studies on the mitotic apparatus (MA) in situ would be straightforward, but even with this approach there is some disagreement in the results obtained with various methods and by different investigators. In this paper I will review briefly the approaches which have been used in structural studies of the MA, pointing out the strengths and problems of each approach. I will summarize the principal findings of the different methods, and identify what seem to be fruitful avenues for further work.


Author(s):  
K.A. Carson ◽  
C.B. Nemeroff ◽  
M.S. Rone ◽  
J.S. Kizer ◽  
J.S. Hanker

Biochemical, physiological, pharmacological, and more recently enzyme histo- chemical data have indicated that cholinergic circuits exist in the hypothalamus. Ultrastructural correlates of these pathways such as acetylcholinesterase (AchE) positive neurons in the arcuate nucleus (ARC) and stained terminals in the median eminence (ME) have yet to be described. Initial studies in our laboratories utilizing chemical lesioning and microdissection techniques coupled with microchemical and light microscopic enzyme histo- chemical studies suggested the existence of cholinergic neurons in the ARC which project to the ME (1). Furthermore, in adult male rats with Halasz deafferentations (hypothalamic islands composed primarily of the isolated ARC and the ME) choline acetyltransferase (ChAc) activity, a good marker for cholinergic neurons, was not significantly reduced in the ME and was only somewhat reduced in the ARC (2). Treatment of neonatal rats with high doses of monosodium 1-glutamate (MSG) results in a lesion largely restricted to the neurons of the ARC.


Author(s):  
Xudong Weng ◽  
Peter Rez

In electron energy loss spectroscopy, quantitative chemical microanalysis is performed by comparison of the intensity under a specific inner shell edge with the corresponding partial cross section. There are two commonly used models for calculations of atomic partial cross sections, the hydrogenic model and the Hartree-Slater model. Partial cross sections could also be measured from standards of known compositions. These partial cross sections are complicated by variations in the edge shapes, such as the near edge structure (ELNES) and extended fine structures (ELEXFS). The role of these solid state effects in the partial cross sections, and the transferability of the partial cross sections from material to material, has yet to be fully explored. In this work, we consider the oxygen K edge in several oxides as oxygen is present in many materials. Since the energy window of interest is in the range of 20-100 eV, we limit ourselves to the near edge structures.


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