Zobrazeno 1 - 10
of 22
pro vyhledávání: '"K. E. Berge"'
Publikováno v:
The Open Inflammation Journal. 1:1-6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::335c64124289104142855764292d6459
https://doi.org/10.2174/1875041900801010001
https://doi.org/10.2174/1875041900801010001
Autor:
Kristian Berg, K. E. Berge
Publikováno v:
Clinical Genetics. 41:90-95
Endothelin is a peptide reported to be one of the most potent vasoconstrictors known. Presumably, endothelin could play a role in the physiological regulation of blood pressure in healthy or hypertensive people. We have studied a normal restriction f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d8d663789ad372191ff2981d0b6ad33
https://doi.org/10.1111/j.1399-0004.1992.tb03640.x
https://doi.org/10.1111/j.1399-0004.1992.tb03640.x
Publikováno v:
Clinical Genetics. 52:86-95
The kallikrein-kinin system is involved in the maintenance of blood pressure (BP), and studies have shown an inverse correlation between BP and urinary kallikrein levels. These and other effects, make the human tissue kallikrein (hKLK1) gene a candid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8cf5a5a247a79c9aa07c16ba391b0fcf
https://doi.org/10.1111/j.1399-0004.1997.tb02524.x
https://doi.org/10.1111/j.1399-0004.1997.tb02524.x
Autor:
Kristian Berg, K. E. Berge
Publikováno v:
Clinical Genetics. 53:214-219
The M235T polymorphism at the angiotensinogen (AGT) locus and the A1166C polymorphism at the angiotensin II type 1 receptor (AT1R) locus have been reported to be associated with hypertension in several populations. We examined these polymorphisms in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c7529add9e3300f89d548d6ed582300
https://doi.org/10.1111/j.1399-0004.1998.tb02680.x
https://doi.org/10.1111/j.1399-0004.1998.tb02680.x
Publikováno v:
Europe PubMed Central
The reason(s) for the atherogenic properties of Lp(a) lipoprotein is still unclear, and several mechanisms have been studied. Alterations in gene expression in endothelial cells (ECs) could be important with respect to risk for coronary heart disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b9a4a100fccdb424139336f67dbb416
https://doi.org/10.1111/j.1399-0004.1997.tb04349.x
https://doi.org/10.1111/j.1399-0004.1997.tb04349.x
Autor:
E. Kongsgård, Nina Øyen, Gottfried Greve, O.‐G. Anfinsen, T. P. Leren, K. E. Berge, Kristina H. Haugaa, Knut Gjesdal, A. Früh, A. Carlsson, Geir Siem, Torleiv O. Rognum, J. P. Amlie, M. Hallerud
Publikováno v:
Scandinavian Journal of Clinical and Laboratory Investigation. 68:362-368
Mutations in the KCNQ1, HERG, SCN5A, minK and MiRP1 genes cause long QT syndrome (LQTS), of which there are two forms: the Romano Ward syndrome and the Jervell and Lange-Nielsen syndrome. We have performed DNA sequencing of the LQTS-associated genes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18b44558be8ed5185b5fe30a95234e6f
https://doi.org/10.1080/00365510701765643
https://doi.org/10.1080/00365510701765643
Publikováno v:
Alcohol and Alcoholism. 40:102-105
Aims: Epidemiological studies have shown that moderate consumption of alcohol is associated with a decreased risk of developing cardiovascular disease, but the causal mechanisms are only partly understood. As inflammation is an important process in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1dc8347a595ce0bc02a901b2b9d1e54
https://doi.org/10.1093/alcalc/agh132
https://doi.org/10.1093/alcalc/agh132
Autor:
Kristian Berg, K. E. Berge
Publikováno v:
Clinical Genetics. 46:436-438
We have studied a normal restriction fragment length polymorphism at the renin locus, detected with the restriction enzyme BglI in healthy Norwegians. No association with blood pressure level or variability was found. Thus, the normal genes detected
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a305e0b45a1463ef5241766a86adb421
https://doi.org/10.1111/j.1399-0004.1994.tb04413.x
https://doi.org/10.1111/j.1399-0004.1994.tb04413.x
Autor:
K E, Berge, T P, Leren
Publikováno v:
Clinical genetics. 86(4)
Genetic testing for hypertrophic cardiomyopathy (HCM) became available in Norway in 2003. Here, we describe the results of this testing in probands with HCM referred until the end of 2012. The translated exons of MYBPC3, MYH7, TNNI3, TNNT2, MYL2 and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cc3191f21d4b54cd0db018d9c9c746a0
https://pubmed.ncbi.nlm.nih.gov/24111713
https://pubmed.ncbi.nlm.nih.gov/24111713
Publikováno v:
APMIS. 104:523-530
In this study we demonstrate that human endothelial cells (EC) synthesize mRNA for vitronectin by using techniques based on reverse transcriptase (RT) reaction and polymerase chain reaction (PCR). The identification of vitronectin mRNA, shown by sequ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de4e1cd529c40fd7f8bbe26d1f509a56
https://doi.org/10.1111/j.1699-0463.1996.tb04907.x
https://doi.org/10.1111/j.1699-0463.1996.tb04907.x