Hostname: page-component-cd9895bd7-hc48f Total loading time: 0 Render date: 2024-12-25T03:11:19.450Z Has data issue: false hasContentIssue false
  • English
  • Français

Erythrocyte Galactose-1-Phosphate Uridyltransferase and Galactokinase Levels in Twins

Published online by Cambridge University Press:  01 August 2014

P. Cholnoky ,
F.C. Sitzmann ,
I. Teubl  and
H. Kaloud
P. Cholnoky*
Affiliation:
County Hospital, Department of Paediatrics, Szombathely, Hungary
F.C. Sitzmann
Affiliation:
Children's Department of the Medical School of the University of Erlangen-Nürnberg, GFR
I. Teubl
Affiliation:
Department of Blood Transfusion and Blood Serology of the Surgical Clinic, Graz, Austria
H. Kaloud
Affiliation:
Children's Department of the University of Graz, Austria
*
Pf. 143, 9701 Szombathely, Hungary

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

The levels of the two enzymes, GAL-1-PUT and GAL-KIN, have been examined in a sample of 35 MZ and 45 DZ twin pairs of both sexes. The activities of these enzymes do not appear to be influenced by sex. The role of genetic factors appears to be rather limited in the case of GAL-1-PUT, but much higher in the case of GAL-KIN.

Type
Short Notes
Information
Acta geneticae medicae et gemellologiae: twin research , Volume 24 , Issue 3-4 , 07-10 1975 , pp. 325 - 328
Copyright
Copyright © The International Society for Twin Studies 1975

References

REFERENCES

Arfors, K.E., Beckmann, L., Lundin, L.G. 1963. Genetic variations of human serum phosphatases. Acta Genet. (Basel), 13: 89–94.Google Scholar
Beckmann, L. Wetterberg, L. 1967. Genetic and drug induced variations in serum naphthylamidase isoenzymes. Acta Genet. (Basel), 17: 314–320.Google Scholar
Beiguelman, B., Colli-Inglez, G., Bonder-Ilskan, S., Saldanha, P.H. 1970. Glucose-6-phosphate dehydrogenase activity among Caucasoid twins. Hum. Hered., 20: 535–539.CrossRefGoogle ScholarPubMed
Beutler, E., Baluda, M.C. 1966. Improved method for measurement of galactose-1-phosphate uridyl-transferase activity of erythrocytes. Clin. Chim. Acta, 13: 369–376.CrossRefGoogle Scholar
Beutler, E., Mitchell, M. 1968. New rapid method for the estimation of red cell galactose-1-phosphate uridyltransferase activity. J. Lab. Clin. Med., 72: 527–532.Google Scholar
Beutler, E., Paniker, V., Trinidad, F. 1971. The assay of red cell galactokinase. Biochem. Med., 5: 325–332.Google Scholar
Brewer, G.J., Gall, J.C., Honeyman, M., Gershowitz, H., Schreffler, D.C., Dern, R.J., Hames, C. 1967. Inheritance of quantitative expression of erythrocyte glucose-6-phosphate dehydrogenase activity in the Negro. A twin study. Biochem. Genet., 1: 41–53.Google Scholar
Gedda, L., Poggi, D. 1960. Sulla regolazione genetica del colesterolo ematico. (Uno studio su 50 coppie gemellari MZ e 50 coppie DZ). Acta Genet. Med. Gemellol. (Roma), 9: 135–154.Google Scholar
Gedda, L., Casa, D., Brenci, G. 1968. Hereditary influences on the hematic level of adenosinetriphosphate. A twin study. Acta Genet. Med. Gemellol. (Roma), 17: 381–384.CrossRefGoogle ScholarPubMed
Gedda, L., Tatarelli, R. 1970. Il controllo genetico della glutationemia. Studio gemellare. Acta Genet. Med. Gemellol. (Roma), 19: 117–121.Google Scholar
Hosenfeld, D., Drossier, E. 1970. Three serum enzymes in twins. Acta Genet. Med. Gemellol. (Roma), 19: 122–126.CrossRefGoogle ScholarPubMed
Inouye, T.H., Nadler, H.L., Hsia, D.Y. 1968. Galactose-1-phosphate uridyltransferase in red blood cells. Clin. Chim. Acta, 19: 169–174.Google Scholar
Kaloud, H., Sitzmann, F.C. 1971 a. Ergebnisse klinischer und biochemischer Untersuchungen bei einer Sippe mit Erkrankungen an Galaktosämie. Arch. Kinderheilkd., Beiheft 64.Google Scholar
Kaloud, H., Sitzmann, F.C. 1971 b. Die Aktivität der Galaktose-1-phosphat-Uridyltransferase in den Erythrozyten bei Heterozygoten der Galaktosämie in verschiedenen Alterstufen. Paediatr. Paedol., 6: 268–273.Google Scholar
Kaloud, H., Sitzmann, F.C. 1974. Vergleichende Genfrequenzuntersuchungen für den Galaktokinasedefekt in der Steiermark und in Franken. Z. Kinderheilkd., 116: 185–191.Google Scholar
Kaloud, H., Sitzmann, F.C., Mayer, R., Patlauf, F. 1973. Klinische und biochemische Befunde bei einem Kleinkind mit hereditärem Galaktokinase-Defekt. Klin. Paediatr., 185: 18–22.Google Scholar
Kamaryt, J., Laxova, R., Zahalkova, M. 1970. Hladiny aktivit izoamylaz krevniho séra u monozygotnich a dizygotnich dvojcat. Cesk. Pediatr., 25: 82–85.Google Scholar
Kulonen, E. 1967. Experience with clinical chemical data of Finnish twins. Ann. Med. Exp. Biol. Fenn, 45: 178–181.Google Scholar
Simpson, N.E., Kalow, W. 1963. Serum Cholinesterase levels in families and twins. Am. J. Hum. Genet., 15: 280–287.Google Scholar
Sitzmann, F.C., Kaloud, H., Teubl, J., Müller, H.E. 1973. Die Aktivität des Enzyms Galaktokinase in den Erythrozyten gesunder Kinder und Erwachsener. Klin. Paediatr., 185: 444–448.Google Scholar
Thompson, A., Horne, C.H.W., Steele, H., Goudie, R.B. 1969. Concentrations of serum alpha-2-macroglobulin in twins. Nature (Lond.), 221: 289–290.Google Scholar