|
11. |
C3 Allotypes in Pregnancy Hypertension and Eclampsia |
|
Human Heredity,
Volume 38,
Issue 1,
1988,
Page 52-55
D.W. Cooper,
E.M. Deane,
P. Marshall,
E.D.M. Gallery,
Preview
|
PDF (543KB)
|
|
摘要:
C3 allotyping has been performed on 424 Australian women, 203 with normotensive pregnancies, 161 with hypertensive noneclamptic pregnancies and 60 eclamptic women. The frequency of women heterozygous for ‘rare’ C3 alleles was 1 % in the normotensive women and 3.7% in the hypertensive group. Three out of 25 (12%) of the women with proteinuric hypertension in pregnancy carried ‘rare’ C3 alleles. This suggested the hypothesis that pre-eclampsia/eclampsia is associated with a higher frequency of rare alleles. The sample of 60 eclamptic women collected to test the hypothesis had no rare alleles, refuting the hypothesis. The frequency of the common (C3F, C3S) alleles did not differ significantly between the three groups. We conclude that there is no evidence for any association between susceptibility to eclampsia and allotypes of the C3 complement co
ISSN:0001-5652
DOI:10.1159/000153755
出版商:S. Karger AG
年代:1988
数据来源: Karger
|
12. |
Transferrin C2 and Radiation-Induced Chromosomal Damage |
|
Human Heredity,
Volume 38,
Issue 1,
1988,
Page 56-58
L. Beckman,
I. Nordenson,
Preview
|
PDF (341KB)
|
|
摘要:
Radiation-induced chromosomal damage (after exposure to 1 Gy) in lymphocytes was studied in relation to transferrin C subtype (C1 vs. C2). In 72-hour lymphocyte cultures a significantly increased frequency of cells with radiation induced aberrations was observed in individuals with the transferrin type C2. Thus the results lend some support to the hypothesis that transferrin C2 may act as an enhancer of chromosomal damage.
ISSN:0001-5652
DOI:10.1159/000153756
出版商:S. Karger AG
年代:1988
数据来源: Karger
|
13. |
Esterase D Polymorphism in Serbia (Yugoslavia) |
|
Human Heredity,
Volume 38,
Issue 1,
1988,
Page 59-61
Zorica Lemić,
Vesna Kalimanovska,
Zorana Jelić-Ivanović,
Nada Majkić-Singh,
Preview
|
PDF (324KB)
|
|
摘要:
Phenotypes of human red cell esterase D (EsD) were determined in 351 unrelated adults from Serbia (Yugoslavia). The calculated allele frequencies were 0.911 for EsD1 and 0.089 for EsD2.The phenotype distribution was in good agreement with the Hardy-Weinberg equilibrium.
ISSN:0001-5652
DOI:10.1159/000153757
出版商:S. Karger AG
年代:1988
数据来源: Karger
|
14. |
Glyoxalase I Polymorphism in Catalonia (Spain) |
|
Human Heredity,
Volume 38,
Issue 1,
1988,
Page 62-63
G. Ribó,
J. Más,
P. Moreno,
Preview
|
PDF (227KB)
|
|
摘要:
Blood samples from two Catalonian populations (North-East of Spain) were analysed for glyoxalase (GLO) I polymorphism. Gene frequencies of GLO1 (0.46 and 0.41) are comparable to those reported for Central-European Caucasoid populations.
ISSN:0001-5652
DOI:10.1159/000153758
出版商:S. Karger AG
年代:1988
数据来源: Karger
|
15. |
Announcement |
|
Human Heredity,
Volume 38,
Issue 1,
1988,
Page 64-64
Preview
|
PDF (52KB)
|
|
ISSN:0001-5652
DOI:10.1159/000153759
出版商:S. Karger AG
年代:1988
数据来源: Karger
|
|