131 related articles for article (PubMed ID: 17143181)
1. The functional variant of the CLC-Kb channel T481S is not associated with blood pressure or hypertension in Swedes.
Fava C; Montagnana M; Almgren P; Rosberg L; Guidi GC; Berglund G; Melander O
J Hypertens; 2007 Jan; 25(1):111-6. PubMed ID: 17143181
[TBL] [Abstract][Full Text] [Related]
2. Association between adducin-1 G460W variant and blood pressure in Swedes is dependent on interaction with body mass index and gender.
Fava C; Montagnana M; Almgren P; Rosberg L; Guidi GC; Berglund G; Melander O
Am J Hypertens; 2007 Sep; 20(9):981-9. PubMed ID: 17765140
[TBL] [Abstract][Full Text] [Related]
3. Activating mutation of the renal epithelial chloride channel ClC-Kb predisposing to hypertension.
Jeck N; Waldegger S; Lampert A; Boehmer C; Waldegger P; Lang PA; Wissinger B; Friedrich B; Risler T; Moehle R; Lang UE; Zill P; Bondy B; Schaeffeler E; Asante-Poku S; Seyberth H; Schwab M; Lang F
Hypertension; 2004 Jun; 43(6):1175-81. PubMed ID: 15148291
[TBL] [Abstract][Full Text] [Related]
4. CLCNKB-T481S and essential hypertension in a Ghanaian population.
Sile S; Velez DR; Gillani NB; Narsia T; Moore JH; George AL; Vanoye CG; Williams SM
J Hypertens; 2009 Feb; 27(2):298-304. PubMed ID: 19226700
[TBL] [Abstract][Full Text] [Related]
5. Influence of gain of function epithelial chloride channel ClC-Kb mutation on hearing thresholds.
Frey A; Lampert A; Waldegger S; Jeck N; Waldegger P; Artunc F; Seebohm G; Lang UE; Kupka S; Pfister M; Hoppe J; Gerloff C; Schaeffeler E; Schwab M; Lang F
Hear Res; 2006 Apr; 214(1-2):68-75. PubMed ID: 16549283
[TBL] [Abstract][Full Text] [Related]
6. Lack of association of variants of the renal salt reabsorption-related genes SLC12A3 and ClC-Kb and hypertension in Mongolian and Han populations in Inner Mongolia.
Chang PY; Zhang XG; Su XL
Genet Mol Res; 2011 May; 10(2):948-54. PubMed ID: 21644212
[TBL] [Abstract][Full Text] [Related]
7. Genetic variance of SGK-1 is associated with blood pressure, blood pressure change over time and strength of the insulin-diastolic blood pressure relationship.
von Wowern F; Berglund G; Carlson J; Månsson H; Hedblad B; Melander O
Kidney Int; 2005 Nov; 68(5):2164-72. PubMed ID: 16221215
[TBL] [Abstract][Full Text] [Related]
8. No association with hypertension of CLCNKB and TNFRSF1B polymorphisms at a hypertension locus on chromosome 1p36.
Speirs HJ; Wang WY; Benjafield AV; Morris BJ
J Hypertens; 2005 Aug; 23(8):1491-6. PubMed ID: 16003175
[TBL] [Abstract][Full Text] [Related]
9. Vanin-1 T26I polymorphism, hypertension and cardiovascular events in two large urban-based prospective studies in Swedes.
Fava C; Montagnana M; Danese E; Sjögren M; Almgren P; Engström G; Hedblad B; Guidi GC; Minuz P; Melander O
Nutr Metab Cardiovasc Dis; 2013 Jan; 23(1):53-60. PubMed ID: 21550219
[TBL] [Abstract][Full Text] [Related]
10. Prediction of blood pressure changes over time and incidence of hypertension by a genetic risk score in Swedes.
Fava C; Sjögren M; Montagnana M; Danese E; Almgren P; Engström G; Nilsson P; Hedblad B; Guidi GC; Minuz P; Melander O
Hypertension; 2013 Feb; 61(2):319-26. PubMed ID: 23232644
[TBL] [Abstract][Full Text] [Related]
11. Genetic architecture of ambulatory blood pressure in the general population: insights from cardiovascular gene-centric array.
Tomaszewski M; Debiec R; Braund PS; Nelson CP; Hardwick R; Christofidou P; Denniff M; Codd V; Rafelt S; van der Harst P; Waterworth D; Song K; Vollenweider P; Waeber G; Zukowska-Szczechowska E; Burton PR; Mooser V; Charchar FJ; Thompson JR; Tobin MD; Samani NJ
Hypertension; 2010 Dec; 56(6):1069-76. PubMed ID: 21060006
[TBL] [Abstract][Full Text] [Related]
12. A common sequence variation of the CLCNKB gene strongly activates ClC-Kb chloride channel activity.
Jeck N; Waldegger P; Doroszewicz J; Seyberth H; Waldegger S
Kidney Int; 2004 Jan; 65(1):190-7. PubMed ID: 14675050
[TBL] [Abstract][Full Text] [Related]
13. The common functional polymorphism -50G>T of the CYP2J2 gene is not associated with ischemic coronary and cerebrovascular events in an urban-based sample of Swedes.
Fava C; Montagnana M; Almgren P; Hedblad B; Engström G; Berglund G; Minuz P; Melander O
J Hypertens; 2010 Feb; 28(2):294-9. PubMed ID: 19851119
[TBL] [Abstract][Full Text] [Related]
14. The V433M variant of the CYP4F2 is associated with ischemic stroke in male Swedes beyond its effect on blood pressure.
Fava C; Montagnana M; Almgren P; Rosberg L; Lippi G; Hedblad B; Engström G; Berglund G; Minuz P; Melander O
Hypertension; 2008 Aug; 52(2):373-80. PubMed ID: 18574070
[TBL] [Abstract][Full Text] [Related]
15. HindIII(+/-) polymorphism of the Y chromosome, blood pressure, and serum lipids: no evidence of association in three white populations.
Russo P; Venezia A; Lauria F; Strazzullo P; Cappuccio FP; Iacoviello L; Barba G; Siani A
Am J Hypertens; 2006 Apr; 19(4):331-8. PubMed ID: 16580565
[TBL] [Abstract][Full Text] [Related]
16. Causal Effect of Adiposity Measures on Blood Pressure Traits in 2 Urban Swedish Cohorts: A Mendelian Randomization Study.
Giontella A; Lotta LA; Overton JD; Baras A; ; Minuz P; Melander O; Gill D; Fava C
J Am Heart Assoc; 2021 Jul; 10(13):e020405. PubMed ID: 34120448
[TBL] [Abstract][Full Text] [Related]
17. FURIN variant associations with postexercise hypotension are intensity and race dependent.
Cilhoroz BT; Schifano ED; Panza GA; Ash GI; Corso L; Chen MH; Deshpande V; Zaleski A; Farinatti P; Santos LP; Taylor BA; O'Neill RJ; Thompson PD; Pescatello LS
Physiol Rep; 2019 Feb; 7(3):e13952. PubMed ID: 30706700
[TBL] [Abstract][Full Text] [Related]
18. Effects of angiotensinogen and angiotensin II type I receptor genes on blood pressure and left ventricular mass trajectories in multiethnic youth.
Wang X; Zhu H; Dong Y; Treiber FA; Snieder H
Twin Res Hum Genet; 2006 Jun; 9(3):393-402. PubMed ID: 16790149
[TBL] [Abstract][Full Text] [Related]
19. Association analysis between hypertension and CYBA, CLCNKB, and KCNMB1 functional polymorphisms in the Japanese population--the Suita Study.
Kokubo Y; Iwai N; Tago N; Inamoto N; Okayama A; Yamawaki H; Naraba H; Tomoike H
Circ J; 2005 Feb; 69(2):138-42. PubMed ID: 15671602
[TBL] [Abstract][Full Text] [Related]
20. Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension Risk.
Yu B; Pulit SL; Hwang SJ; Brody JA; Amin N; Auer PL; Bis JC; Boerwinkle E; Burke GL; Chakravarti A; Correa A; Dreisbach AW; Franco OH; Ehret GB; Franceschini N; Hofman A; Lin DY; Metcalf GA; Musani SK; Muzny D; Palmas W; Raffel L; Reiner A; Rice K; Rotter JI; Veeraraghavan N; Fox E; Guo X; North KE; Gibbs RA; van Duijn CM; Psaty BM; Levy D; Newton-Cheh C; Morrison AC;
Circ Cardiovasc Genet; 2016 Feb; 9(1):64-70. PubMed ID: 26658788
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
