Folic acid metabolism. VII. Transformation of one-carbon compounds and of folic acid in germinating plants

1962 ◽  
Vol 27 (6) ◽  
pp. 1470-1475 ◽  
Author(s):  
J. Shejbal ◽  
K. Slavík ◽  
J. Souček
1959 ◽  
Vol 7 (3) ◽  
pp. 302-310
Author(s):  
A. V. TRUFANOV

2018 ◽  
Vol 309 ◽  
pp. 14-22 ◽  
Author(s):  
Nafisa M. Jadavji ◽  
Joshua T. Emmerson ◽  
Ushananthini Shanmugalingam ◽  
Amanda J. MacFarlane ◽  
William G. Willmore ◽  
...  

1969 ◽  
Vol 104 (5) ◽  
pp. 745-747 ◽  
Author(s):  
Frederick W. McLean ◽  
M.Wayne Heine ◽  
Berel Held ◽  
Richard R. Streiff

1967 ◽  
Vol 47 (1) ◽  
pp. 83-116 ◽  
Author(s):  
E L Stokstad ◽  
J Koch

The Lancet ◽  
1964 ◽  
Vol 284 (7372) ◽  
pp. 1295
Author(s):  
J.E. Maciver ◽  
W.H.C. Walker ◽  
E.J. Watson-Williams

Blood ◽  
1959 ◽  
Vol 14 (12) ◽  
pp. 1269-1279 ◽  
Author(s):  
MIGUEL LAYRISSE ◽  
NORMA BLUMENFELD ◽  
IRIS DUGARTE ◽  
MARCEL ROCHE

Abstract Studies on the metabolism of B12 and folic acid were performed in patients with heavy hookworm infection and severe iron deficiency anemia, and in patients with light infection, noninfected patients and normal subjects. Patients with heavy hookworm infection showed a marked decrease of the serum B12 as compared with normal subjects. Eight of 21 cases studied showed values of serum B12 below 100 µµg./ml. Twelve of 13 patients with severe hookworm infection showed impairment of the pteroylglutamic acid intestinal absorption; however, none of them exhibited megaloblastic proliferation in the bone marrow. They all recovered with iron therapy alone. The patients with light infection and the noninfected patients with iron deficiency anemia did not demonstrate significant differences from the normal subjects studied.


Brain ◽  
1968 ◽  
Vol 91 (2) ◽  
pp. 197-214 ◽  
Author(s):  
E. H. REYNOLDS

1974 ◽  
Vol 142 (1) ◽  
pp. 105-117 ◽  
Author(s):  
Richard M. Smith ◽  
William S. Osborne-White ◽  
Jeffrey M. Gawthorne

1. The effects of injected l-methionine (2g every second day for 28 days) on liver folates and other constituents of liver associated with folate metabolism were studied in vitamin B12-deficient ewes and their pair-fed controls receiving vitamin B12. The dose rate of methionine used was sufficient to restore almost to normal the elevated excretion in the urine of formiminoglutamate in the deficient animals. 2. Liver folates active for Lactobacillus casei, Streptococcus faecalis R and Pediococcus cerevisiae were severely depressed in deficient livers and were partly restored by methionine. Analysis of the folates after ion-exchange chromatography showed that the major effect of methionine was to increase the concentrations of tetrahydrofolates and formyltetrahydrofolates. Methyltetrahydrofolates were also increased, but there was no effect of methionine on the small amounts of incompletely reduced folates present in deficient livers. The folates present were predominantly penta-, hexa- and hepta-glutamates whether or not animals received vitamin B12 or methionine. 3. Concentrations of ATP, NAD+, NADH and NADPH were lower in freeze-clamped liver from vitamin B12-deficient sheep than in liver from pair-fed, vitamin B12-treated sheep. These changes were not affected by methionine which was also without effect on the elevated K+/Na+ ratios found in deficient livers. 4. The livers of vitamin B12-deficient animals contained lower concentrations of choline and higher concentrations of lipid than their pair-fed controls. These effects were reversed by methionine.


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