FREIBERGER, Tomáš, Martina VYSKOČILOVÁ, Lenka KOLÁŘOVÁ, Pavel KUKLÍNEK, Olga KRYŠTŮFKOVÁ, Marie LAHODNÁ, Jana HANZLÍKOVÁ and Jiří LITZMAN. Exon 1 polymorphism of the B2BKR gene does not influence the clinical status of patients with hereditary angioedema. Hum Immunol. Elsevier, 2002, vol. 63, No 6, p. 492-494. ISSN 0198-8859.
Other formats:   BibTeX LaTeX RIS
Basic information
Original name Exon 1 polymorphism of the B2BKR gene does not influence the clinical status of patients with hereditary angioedema.
Name in Czech Polymorfismy genu B2BKR nemají vliv na klinický stav pacientů s HAE
Authors FREIBERGER, Tomáš (203 Czech Republic, guarantor), Martina VYSKOČILOVÁ (203 Czech Republic), Lenka KOLÁŘOVÁ (203 Czech Republic), Pavel KUKLÍNEK (203 Czech Republic), Olga KRYŠTŮFKOVÁ (203 Czech Republic), Marie LAHODNÁ (203 Czech Republic), Jana HANZLÍKOVÁ (203 Czech Republic) and Jiří LITZMAN (203 Czech Republic).
Edition Hum Immunol, Elsevier, 2002, 0198-8859.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30102 Immunology
Country of publisher United Kingdom of Great Britain and Northern Ireland
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 2.573
RIV identification code RIV/00216224:14110/02:00007516
Organization unit Faculty of Medicine
UT WoS 000176152800008
Keywords in English B2 bradykinin receptor; polymorphism; hereditary angioedema
Tags B2 bradykinin receptor, hereditary angioedema, polymorphism
Changed by Changed by: prof. MUDr. Tomáš Freiberger, Ph.D., učo 24036. Changed: 27/6/2009 07:38.
Abstract
Polymorphic variants of B2 receptors for bradykinin (B2BKR) have been postulated to influence a clinical manifestation of hereditary angioedema. In this study, exon 1 nonanucleotide deletion polymorphism in the B2BKR gene was examined in 37 patients with hereditary angioedema. The patients were grouped according to disease severity or the age of the first clinical manifestation of disease. No significant differences in allelic frequencies were found between particular subgroups of patients. Therefore, we concluded that this polymorphism does not seem to have any significant effect on the course and severity of hereditary angioedema in Caucasians.
Links
NI5558, research and development projectName: Molekulárně genetická analýza u pacientů s hereditárním angioedémem
Investor: Ministry of Health of the CR, Molecular Genetic Analysis in Patients with Hereditary Angioedema
PrintDisplayed: 30/4/2024 22:52