Genetic analysis in human hypertension

Hypertension Research

Volumn 25, Issue 3, 2002, Pages 319-327

  Kato, Norihiro ^a  

^a NATIONAL CENTER FOR GLOBAL HEALTH AND MEDICINE   (Japan)

Author keywords

Association; Genetics; Linkage; Polymorphism; Quantitative trait loci

Indexed keywords

BIOINFORMATICS; CONTROLLED STUDY; DEMOGRAPHY; DISEASE ASSOCIATION; ENVIRONMENTAL FACTOR; ESSENTIAL HYPERTENSION; ETHNIC DIFFERENCE; FOLLOW UP; GENE FUNCTION; GENE IDENTIFICATION; GENE MUTATION; GENETIC ANALYSIS; GENETIC VARIABILITY; GENOTYPE; HEREDITY; HUMAN; NUCLEIC ACID BASE SUBSTITUTION; PHENOTYPE; POPULATION RESEARCH; REVIEW; SCREENING; SEX DIFFERENCE; SINGLE NUCLEOTIDE POLYMORPHISM; STATISTICAL ANALYSIS; ANIMAL; CHROMOSOME 17; CHROMOSOME 5; GENETIC LINKAGE; GENETICS; HYPERTENSION; RAT;

ANGIOTENSINOGEN; ANIMAL; CHROMOSOMES, HUMAN, PAIR 17; CHROMOSOMES, HUMAN, PAIR 5; HUMAN; HYPERTENSION; LINKAGE (GENETICS); PEPTIDYL-DIPEPTIDASE A; RATS; RECEPTORS, ADRENERGIC, BETA-3; ANIMALS; HUMANS;

ANGIOTENSINOGEN; BETA 3 ADRENERGIC RECEPTOR; DIPEPTIDYL CARBOXYPEPTIDASE;

EID: 0035991087     PISSN: 09169636     EISSN: None     Source Type: Journal    
DOI: 10.1291/hypres.25.319     Document Type: Review

References (49)

1. Molecular genetics of human blood pressure variation
2. A chimaeric 11 beta-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension
3. Liddle's syndrome: Heritable human hypertension caused by mutations in the beta subunit of the epithelial sodium channel
4. Hypertension caused by a truncated epithelial sodium channel gamma subunit: Genetic heterogeneity of Liddle syndrome
5. Human hypertension caused by mutations in the kidney isozyme of 11 beta-hydroxysteroid dehydrogenase
6. Activating mineralocorticoid receptor mutation in hypertension exacerbated by pregnancy
7. Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21
8. Seven lessons from two candidate genes in human essential hypertension: Angiotensinogen and epithelial sodium channel
9. Genomewide scans of complex human diseases: True linkage is hard to find
10. Genetically complex cardiovascular traits: Origins, problems, and potential solutions
11. Heredity and blood pressure
12. The TDT and other family-based tests for linkage disequilibrium and association
13. Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
14. Linkage strategies for genetically complex traits: II. the power of affected relative pairs
15. Multiple loci for multiple sclerosis
16. The future of genetic studies of complex human diseases
17. Association of hypertension with T594M mutation in beta subunit of epithelial sodium channels in black people resident in London
18. Genetic variants in the epithelial sodium channel in relation to aldosterone and potassium excretion and risk for hypertension
19. Evaluation of selected polymorphisms of the Mendelian hypertensive disease genes in the Japanese population
20. Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type I
21. Molecular basis of human hypertension: Role of angiotensinogen
22. Genetic control of blood pressure and the angiotensinogen locus
23. A nucleotide substitution in the promoter of human angiotensinogen is associated with essential hypertension and affects basal transcription in vitro
24. Association between the angiotensinogen 235T-variant and essential hypertension in whites: A systematic review and methodological appraisal
25. M235T angiotensinogen gene polymorphisms and cardiovascular renal risk
26. Angiotensinogen polymorphisms and elevated blood pressure in the general population: The Copenhagen City Heart Study
27. Hypertension: Genes and environment
28. Evidence, from combined segregation and linkage analysis, that a variant of the angiotensin I-converting enzyme (ACE) gene controls plasma ACE levels
29. The deletion/insertion polymorphism of the angiotensin converting enzyme gene and cardiovascular-renal risk
30. Lack of sex-specific effects on the association between angiotensin-converting enzyme gene polymorphism and hypertension in Japanese
31. Evidence for association and genetic linkage of the angiotensin-converting enzyme locus with hypertension and blood pressure in men but not women in the Framingham Heart Study
32. Variation in the region of the angiotensin-converting enzyme gene influences interindividual differences in blood pressure levels in young white males
33. Deletion allele of angiotensin-converting enzyme gene increases risk of essential hypertension in Japanese men: The Suita Study
34. Context-dependent associations of the ACE I/D polymorphism with blood pressure
35. Genetic susceptibility for human familial essential hypertension in a region of homology with blood pressure linkage on rat chromosome 10
36. Evidence for linkage between essential hypertension and a putative locus on human chromosome 17
37. Enhanced G protein activation in immortalized lymphoblasts from patients with essential hypertension
38. Membrane sodium-proton exchange and primary hypertension
39. Association of a human G-protein β subunit variant with hypertension
40. G protein beta 3 subunit variant and essential hypertension in Japanese
41. G-Protein beta 3 subunit C825T variant and ambulatory blood pressure in essential hypertension
42. Two point mutations within the adducin genes are involved in blood pressure variation
43. Polymorphisms of alpha-adducin and salt sensitivity in patients with essential hypertension
44. New target regions for human hypertension via comparative genomics
45. Genome-wide scan of predisposing loci for increased diastolic blood pressure in Finnish siblings
46. Genome-wide linkage analyses of systolic blood pressure using highly discordant siblings
47. Quantitative trait locus mapping of human blood pressure to a genetic region at or near the lipoprotein lipase gene locus on chromosome 8p22
48. Linkage and association of adrenergic and dopamine receptor genes in the distal portion of the long arm of chromosome 5 with systolic blood pressure variation
49. Association studies in cardiovascular medicine