(CA/CT) dinucleotid repeat polymorphism in ET-1 gene in essential hypertension

VAŠKŮ, Anna, Viera KUHROVÁ, Svatava TSCHÖPLOVÁ, Lydie HOLLÁ and Vladimír ZNOJIL. (CA/CT) dinucleotid repeat polymorphism in ET-1 gene in essential hypertension ((CA/CT) dinucleotid repeat polymorphism in ET-1 gene in essential hypertension). In Physiol Research, Suppl 1. Praha: Institute of Physiology, Academy of Sciences of the Czech Republic, 1999, p. 134. ISBN 0862-8408.

Basic information

• Original name: (CA/CT) dinucleotid repeat polymorphism in ET-1 gene in essential hypertension
• Authors: VAŠKŮ, Anna (203 Czech Republic, guarantor), Viera KUHROVÁ (203 Czech Republic), Svatava TSCHÖPLOVÁ (203 Czech Republic), Lydie HOLLÁ (203 Czech Republic) and Vladimír ZNOJIL (203 Czech Republic).
• Edition: Praha, Physiol Research, Suppl 1, p. 134-134, 1999.
• Publisher: Institute of Physiology, Academy of Sciences of the Czech Republic

Other information

• Original language: English
• Type of outcome: Proceedings paper
• Field of Study: 30201 Cardiac and Cardiovascular systems
• Country of publisher: Czech Republic
• Confidentiality degree: is not subject to a state or trade secret
• RIV identification code: RIV/00216224:14110/99:00001094
• Organization unit: Faculty of Medicine
• ISBN: 0862-8408
• Keywords in English: CA/CT dinucleotide repeat polymorphism; endothelin-1; essential hypertension
• Tags: CA/CT dinucleotide repeat polymorphism, Endothelin-1, essential hypertension

Abstract

Lengths of CA/CT dinucleotide repeat polymorphhism in the gene coding for endothelin-1 were associated with essential hypertension. Significant increase of the length of allelic variants of the polymorphism in essential hypertensives was found (P=0.03).

Links

• GA306/96/0099, research and development project: Name: Polymorfismus genu pro endotelin - 1 (EDN 1) u esenciální hypertense

Investor: Czech Science Foundation, Polymorphism of endothelin - 1 gene (EDN 1) in essential hypertension

• MSM 141100002, plan (intention): Name: Molekulární patofyziologie multigenních chorob

Investor: Ministry of Education, Youth and Sports of the CR, Molecular pathophysiology of multigene diseases

• VS96097, research and development project: Name: Molekulární patofyziologie vybraných "civilizačních", multigenně podmíněných chorob

Investor: Ministry of Education, Youth and Sports of the CR, Molecular pathophysiology of selected multigenic related to civilization diseases