Melien O - Search Results

1

Single nucleotide polymorphisms in G protein signaling pathway genes in preeclampsia.

Kvehaugen AS, Melien O, Holmen OL, Laivuori H, Oian P, Andersgaard AB, Dechend R, Staff AC. Kvehaugen AS, et al. Among authors: melien o. Hypertension. 2013 Mar;61(3):655-61. doi: 10.1161/HYPERTENSIONAHA.111.00331. Epub 2013 Jan 21. Hypertension. 2013. PMID: 23339167

2

Hypertension after preeclampsia and relation to the C1114G polymorphism (rs4606) in RGS2: data from the Norwegian HUNT2 study.

Kvehaugen AS, Melien Ø, Holmen OL, Laivuori H, Dechend R, Staff AC. Kvehaugen AS, et al. Among authors: melien o. BMC Med Genet. 2014 Mar 5;15:28. doi: 10.1186/1471-2350-15-28. BMC Med Genet. 2014. PMID: 24593135 Free PMC article.

3

Association between the G protein β3 subunit C825T polymorphism and the occurrence of cardiovascular disease in hypertensives: The Nord-Trøndelag Health Study (HUNT).

Holmen OL, Romundstad S, Melien O. Holmen OL, et al. Among authors: melien o. Am J Hypertens. 2010 Oct;23(10):1121-7. doi: 10.1038/ajh.2010.121. Epub 2010 Jun 10. Am J Hypertens. 2010. PMID: 20539277

4

PP084. Hypertension after preeclampsia in women with C1114G polymorphism in rgs2 (the regulator of g protein signaling 2).

Kvehaugen AS, Melien Ø, Holmen OL, Laivuori H, Dechend R, Staff AC. Kvehaugen AS, et al. Among authors: melien o. Pregnancy Hypertens. 2013 Apr;3(2):98. doi: 10.1016/j.preghy.2013.04.109. Epub 2013 Jun 6. Pregnancy Hypertens. 2013. PMID: 26105937

5

The G protein β3 subunit C825T polymorphism is associated with microalbuminuria in hypertensive women and cardiovascular disease in hypertensive men.

Romundstad S, Melien O, Holmen J. Romundstad S, et al. Among authors: melien o. Am J Hypertens. 2010 Oct;23(10):1114-20. doi: 10.1038/ajh.2010.131. Epub 2010 Jun 24. Am J Hypertens. 2010. PMID: 20577224

6

The G protein beta3 subunit 825C allele is associated with sudden infant death due to infection.

Hauge Opdal S, Melien Ø, Rootwelt H, Vege A, Arnestad M, Ole Rognum T. Hauge Opdal S, et al. Among authors: melien o. Acta Paediatr. 2006 Sep;95(9):1129-32. doi: 10.1080/08035250600580529. Acta Paediatr. 2006. PMID: 16938762

7

G protein beta3 subunit C825T polymorphism modifies the presentation of temporal lobe epilepsy.

Osberg S, Melien O, Taubøll E, Gjerstad L; Norwegian GenEpA Group. Osberg S, et al. Among authors: melien o. Acta Neurol Scand Suppl. 2008;188:62-6. doi: 10.1111/j.1600-0404.2008.01034.x. Acta Neurol Scand Suppl. 2008. PMID: 18439224

8

The brain-derived neutrophic factor val66met polymorphism and sudden unexpected infant death.

Opdal SH, Melien O, Hynnekleiv T, Rognum TO. Opdal SH, et al. Among authors: melien o. Acta Paediatr. 2011 Jan;100(1):86-9. doi: 10.1111/j.1651-2227.2010.01960.x. Acta Paediatr. 2011. PMID: 20653606

9

Heterotrimeric G proteins and disease.

Melien O. Melien O. Methods Mol Biol. 2007;361:119-44. doi: 10.1385/1-59745-208-4:119. Methods Mol Biol. 2007. PMID: 17172709 Review.

10

Role of diacylglycerol (DAG) in hormonal induction of S phase in hepatocytes: the DAG-dependent protein kinase C pathway is not activated by epidermal growth factor (EGF), but is involved in mediating the enhancement of responsiveness to EGF by vasopressin, angiotensin II, and norepinephrine.

Dajani OF, Sandnes D, Melien O, Rezvani F, Nilssen LS, Thoresen GH, Christoffersen T. Dajani OF, et al. Among authors: melien o. J Cell Physiol. 1999 Aug;180(2):203-14. doi: 10.1002/(SICI)1097-4652(199908)180:2<203::AID-JCP8>3.0.CO;2-T. J Cell Physiol. 1999. PMID: 10395290

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