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Results: 1 to 20 of 29

PubMed for Gene (Select 6296)

1.

Left ventricular structure in relation to the human SAH gene in the European Project on Genes in Hypertension.

Jin Y, Kuznetsova T, Tikhonoff V, Thijs L, Hasenkamp S, Bäumer V, Stolarz-Skrzypek K, Ryabikov A, Richart T, Malyutina S, Nikitin Y, Casiglia E, Kawecka-Jaszcz K, Olszanecka A, Brand-Herrmann SM, Brand E, Fagard R, Staessen JA; European Project on Genes in Hypertension (EPOGH) Investigators.

Hypertens Res. 2009 Feb;32(2):145-51. doi: 10.1038/hr.2008.30. Epub 2009 Jan 16. Erratum in: Hypertens Res. 2011 Aug;34(8):980.

PMID:
19262474
2.

Human SA gene polymorphisms are associated with non-high-density lipoprotein cholesterol in postmenopausal women: a pilot study.

Lin MW, Hwu CM, Liou TL, Hsiao LC, Ho LT.

Maturitas. 2009 Jan 20;62(1):66-71. doi: 10.1016/j.maturitas.2008.11.002. Epub 2008 Dec 23.

PMID:
19108963
3.

Segmental renal sodium handling in relation to the human SAH gene.

Jin Y, Kuznetsova T, Tikhonoff V, Maillard M, Bochud M, Burnier M, Hasenkamp S, Brand E, Brand-Herrmann SM, Richart T, Staessen JA.

Hypertension. 2008 Aug;52(2):e12-3. doi: 10.1161/HYPERTENSIONAHA.108.115642. Epub 2008 Jun 2. No abstract available.

4.

SAH gene variants revisited in the European Project On Genes in Hypertension.

Tikhonoff V, Staessen JA, Kuznetsova T, Thijs L, Hasenkamp S, Bäumer V, Stolarz K, Seidlerová J, Filipovský J, Nikitin Y, Peleska J, Kawecka-Jaszcz K, Casiglia E, Brand-Herrmann SM, Brand E; European Project On Genes in Hypertension (EPOGH) investigators.

J Hypertens. 2008 Feb;26(2):244-50. doi: 10.1097/HJH.0b013e3282f2d36f.

PMID:
18192838
5.

SAH gene variants are associated with obesity-related hypertension in Caucasians: the PEGASE Study.

Telgmann R, Brand E, Nicaud V, Hagedorn C, Beining K, Schönfelder J, Brink-Spalink V, Schmidt-Petersen K, Matanis T, Vischer P, Nofer JR, Hasenkamp S, Plouin PF, Drouet L, Cambien F, Paul M, Tiret L, Brand-Herrmann SM.

J Hypertens. 2007 Mar;25(3):557-64.

PMID:
17278971
6.

[Relationship between SA gene Pst1 polymorphism and predisposition to H-gestosis].

Nałogowska-Głośnicka K, Łacka B, Zychma M, Grzeszczak W, Zukowska-Szczechowska E, Michalski B, Poreba R, Kniazewski B, Rzempołuch J.

Pol Arch Med Wewn. 2002 Jan;107(1):7-11. Polish.

PMID:
12046348
7.

Association between SAH, an acyl-CoA synthetase gene, and hypertriglyceridemia, obesity, and hypertension.

Iwai N, Katsuya T, Mannami T, Higaki J, Ogihara T, Kokame K, Ogata J, Baba S.

Circulation. 2002 Jan 1;105(1):41-7.

8.

Human SA gene Pst1 polymorphism and chronic renal failure: results of the family-based study.

Gumprecht J, Zychma MJ, Grzeszczak W, Zukowska-Szczechowska E; End-stage Renal Disease Study Group.

Nephrol Dial Transplant. 2001 Feb;16(2):387-90.

9.

Chromosomal assignment of the human SA gene to 16p13.11 and demonstration of its expression in the kidney.

Samani NJ, Whitmore SA, Kaiser MA, Harris J, See CG, Callen DF, Lodwick D.

Biochem Biophys Res Commun. 1994 Mar 15;199(2):862-8.

PMID:
8135833
10.

Human SA gene locus as a candidate locus for essential hypertension.

Iwai N, Ohmichi N, Hanai K, Nakamura Y, Kinoshita M.

Hypertension. 1994 Mar;23(3):375-80.

11.

Evaluation of the SA locus in human hypertension.

Nabika T, Bonnardeaux A, James M, Julier C, Jeunemaitre X, Corvol P, Lathrop M, Soubrier F.

Hypertension. 1995 Jan;25(1):6-13.

12.
13.

Overweight, but not hypertension, is associated with SAH polymorphisms in Caucasians with essential hypertension.

Benjafield AV, Iwai N, Ishikawa K, Wang WY, Morris BJ.

Hypertens Res. 2003 Aug;26(8):591-5.

14.

Role of genetic polymorphism in the SA gene on the blood pressure and prognosis of renal function in patients with immunoglobulin A nephropathy.

Narita I, Saito N, Goto S, Shirasaki A, Morioka Y, Jin S, Omori K, Sakatsume M, Arakawa M, Gejyo F.

Hypertens Res. 2002 Nov;25(6):831-6.

15.

Impaired butyrate oxidation in ulcerative colitis is due to decreased butyrate uptake and a defect in the oxidation pathway.

De Preter V, Arijs I, Windey K, Vanhove W, Vermeire S, Schuit F, Rutgeerts P, Verbeke K.

Inflamm Bowel Dis. 2012 Jun;18(6):1127-36. doi: 10.1002/ibd.21894. Epub 2011 Oct 10.

PMID:
21987487
16.

Assessment of the genetic component of hypertension.

Yamada Y, Matsuo H, Segawa T, Watanabe S, Kato K, Hibino T, Yokoi K, Ichihara S, Metoki N, Yoshida H, Satoh K, Nozawa Y.

Am J Hypertens. 2006 Nov;19(11):1158-65.

PMID:
17070428
17.

Molecular identification and characterization of two medium-chain acyl-CoA synthetases, MACS1 and the Sa gene product.

Fujino T, Takei YA, Sone H, Ioka RX, Kamataki A, Magoori K, Takahashi S, Sakai J, Yamamoto TT.

J Biol Chem. 2001 Sep 21;276(38):35961-6. Epub 2001 Jul 24.

18.

Structural biology of human H3K9 methyltransferases.

Wu H, Min J, Lunin VV, Antoshenko T, Dombrovski L, Zeng H, Allali-Hassani A, Campagna-Slater V, Vedadi M, Arrowsmith CH, Plotnikov AN, Schapira M.

PLoS One. 2010 Jan 11;5(1):e8570. doi: 10.1371/journal.pone.0008570.

19.

Pharmacogenetic analysis of lipid responses to rosuvastatin in Chinese patients.

Hu M, Lui SS, Mak VW, Chu TT, Lee VW, Poon EW, Tsui TK, Ko GT, Baum L, Tam LS, Li EK, Tomlinson B.

Pharmacogenet Genomics. 2010 Oct;20(10):634-7. doi: 10.1097/FPC.0b013e32833de489.

PMID:
20679960
20.

Genome duplications and other features in 12 Mb of DNA sequence from human chromosome 16p and 16q.

Loftus BJ, Kim UJ, Sneddon VP, Kalush F, Brandon R, Fuhrmann J, Mason T, Crosby ML, Barnstead M, Cronin L, Deslattes Mays A, Cao Y, Xu RX, Kang HL, Mitchell S, Eichler EE, Harris PC, Venter JC, Adams MD.

Genomics. 1999 Sep 15;60(3):295-308.

PMID:
10493829
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