Chromosome 11-linked coronary heart disease susceptibility gene CHD1
US6225451A · kind A · utility
Assignee
Inventors
Key dates
| Filing date | Mar 4, 1999 |
| Grant date | May 1, 2001 |
| Priority date | — |
| Expiry date | Mar 4, 2019 |
Classification
- Technology area (CPC G)Physics
- CPC primaryG01N2800/324
- WIPO fieldPharmaceuticals
- WIPO sectorChemistry
Abstract
Human coronary heart disease susceptibility gene (CHD1), some alleles of which are related to susceptibility to coronary heart disease. Germline mutations in the CHD1 gene and their use in the diagnosis of predisposition to coronary heart disease and to metabolic disorders, including hypoalphalipoproteinemia, familial combined hyperlipidemia, insulin resistant syndrome X or multiple metabolic disorder, obesity, diabetes and dyslipidemic hypertension. Presymptomatic therapy of individuals who carry deleterious alleles of the CHD1 gene (including gene therapy, protein replacement therapy, and administration of protein mimetics and inhibitors). The screening of drugs for dyslipidemic therapy.
Source: USPTO / EPO open patent data. Objective bibliographic and citation counts.