Pathogenesis and genetics of pre-eclampsia

Lancet

Volumn 357, Issue 9249, 2001, Pages 53-56

  Roberts, J M ^a   Cooper, D W ^b  

^a UNIVERSITY OF PITTSBURGH   (United States)

^b MACQUARIE UNIVERSITY   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; ECLAMPSIA; FEMALE; FETOPLACENTAL UNIT; GENE MAPPING; GENETIC SUSCEPTIBILITY; GENOTYPE; HUMAN; OXIDATIVE STRESS; PATHOGENESIS; PREECLAMPSIA; PRIORITY JOURNAL; VASCULAR ENDOTHELIUM;

EID: 0035814640     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(00)03577-7     Document Type: Review

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30. Absence of close linkage between maternal genes for susceptibility to pre-eclampsia/eclampsia and the HLA DRB
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32. HLA-G deletion polymorphism and pre-eclamptic/eclampsia
33. Is angiotensinogen gene polymorphism associated with hypertension in pregnancy?
34. The L10F mutation of angiotesinogen is rare in pre-eclampsia
35. Angiotensin-converting enzyme insertion-deletion polymorphism in normotensive and pre-eclamptic pregnancies
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37. Association of pre-eclampsia with common coding sequence variations in the lipoprotein lipase gene
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40. Apolipoprotein E polymorphism in pre-eclampsia
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42. A genome-wide scan reveals a maternal susceptibility locus for pre-eclampsia on chromosome 2p13
43. Genetic susceptibility to preeclampsia and chromosome 7q36
44. Evidence for a familial pregnancy-induced hypertension locus in the eNOS-c region
45. Failure to detect linkage of preeclampsia to the region of the NOS3 locus on chromosome 7q
46. The eNOS gene: A candidate for the preeclampsia susceptibility locus?
47. A genome scan in Australian and New Zealand families confirms the presence of a maternal susceptibility locus for pre-eclampsia on chromosome 2