Hereditary disorders of erythrocyte metabolism : proceedings of the symposium held February 13-15, 1967, at the City of Hope Medical Center, Duarte, California / edited by Ernest Beutler.

Date:
[1968]
Catalogue details

Licence: Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)

Credit: Hereditary disorders of erythrocyte metabolism : proceedings of the symposium held February 13-15, 1967, at the City of Hope Medical Center, Duarte, California / edited by Ernest Beutler. Source: Wellcome Collection.

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    INDEX 343 glucose-6-phosphate dehydrogenase, 128- 129, 132-133, 143ff. Thêta waves, encephalograms, 191 Thioalcohol, reduction of thioketone, 101 Thioketone, reduction to thioalcohol, 101 Thiol groups. See Sulfhydryl groups Thrombopenia, glucose reductase deficiency, 185 a-Tocopherol, 93 Townes, P. L., 183, 259, 261 Toxoflavin, 93 Transaminases, activity in white cells of acatalasemics, 44 Transesterase, role in cholesterol depletion, 220 Transhydrogenases, 90 Tricarboxylic acid, effect on isoenzyme mo¬ bility, 5 Tricarboxylic cycle, 273 Triethanolamine, electrophoretic buffer, hu¬ man pyruvate kinase, 260 Triosephosphate isomerase, 255, 293 activity in tissues, 271 deficiency, 230 association with sickle cell trait and glucose-6-phosphate dehydrogenase deficiency, 270 carbohydrate metabolism, 273ff. cellular damage, 278 clinical and genetic aspects, 265ff. enzyme activity, erythrocytes, 277 erythrocyte enzymes, 273ff. genetics, 268, 269, 270 glycolytic intermediates in erythrocytes, 274-275 hematology, 266 neuromuscular symptoms, 265, 270 substrate specificity, 279 Triphosphopyridine nucleotide complementation with glucose-6-phos- phate dehydrogenase, 142 dehydrogenase, 104 diaphorase deficiency, 106 in galactosemia screening, 67 Km glucose-6-phosphate dehydrogenase, ]26ff., 153 Km for glutathione reductase, 197, 199 reduced, 87ff. Tryptic peptide, of glucose-6-phosphate de¬ hydrogenase, 155ff. pattern of partially-purified pyruvate kinase isoenzymes, 253 Tumors, origin of malignant, 117ff. Twins, dizygous and monozygous in hetero- zygotic glucose-6-phosphate dehydro¬ genase deficiency, 313 United States, frequency of acatalasia, 58 Urine, excretion of coproporpyrin and bili¬ rubin in acatalasemia, 28 screening for galactosemia, 72 Uterine fibroma, expression of X-chromo- some, 117, 121 Valentine, W. N., 174, 175, 180, 206, 229, 245, 246, 265, 288, 301 Vascular stasis, spleen glucose levels, 218ff. Vicia faba. See Fava bean Vitamin C, generation of H-O- combined with oxyhemoglobin, 166 Waller, H. D., 108, 109, 175. 176, 205, 206, 208 Ways, P., 225, 227, 279 Weinstein, I. M., 273 White cells. See Leucocytes Williams, K. O., 246 X-chromosome, derepression, 120 gene inactivation, 114ff., 312 glucose-6-phosphate dehydrogenase defi¬ ciency, 114flf. Xg locus, linkage, 315 X-irradiation, Heinz body formation in rabbits, 175 life span RBC, 180 osmotic resistance of RBC, 180 protection of RBC, 169 sensitivity, acatalasemic RBC, 47, 181 Yeast, glucose-6-phosphate dehydrogenase molecular weight, 152 Yoshida, A., 146, 163, 164 Zürcher, е., 165, 280