D 1999

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

VAŠKŮ, Anna, Viera KUHROVÁ, Svatava TSCHÖPLOVÁ, Lydie HOLLÁ, Vladimír ZNOJIL et. al.

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

Language

English

Type of outcome

Stať ve sborníku

Field of Study

30201 Cardiac and Cardiovascular systems

Country of publisher

Czech Republic

Confidentiality degree

není předmětem státního či obchodního tajemství

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
Změněno: 24/4/2003 10:53, prof. MUDr. Anna Vašků, CSc.

Abstract

V originále

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