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    ACSM3 acyl-CoA synthetase medium chain family member 3 [ Homo sapiens (human) ]

    Gene ID: 6296, updated on 27-Nov-2024

    GeneRIFs: Gene References Into Functions

    GeneRIFPubMed TitleDate
    Acyl-CoA Medium-Chain Synthetase-3 (ACSM3) Is Regulated by Insulin Like Growth Factor 2 mRNA Binding Protein 3 (IGF2BP3) and Inhibits Proliferation, Motility and Stem Cell Properties of Breast Invasive Carcinoma.

    Acyl-CoA Medium-Chain Synthetase-3 (ACSM3) Is Regulated by Insulin Like Growth Factor 2 mRNA Binding Protein 3 (IGF2BP3) and Inhibits Proliferation, Motility and Stem Cell Properties of Breast Invasive Carcinoma.
    Zhu W, Wei X, Fang M.

    08/30/2023
    ACSM3 suppresses the pathogenesis of high-grade serous ovarian carcinoma via promoting AMPK activity.

    ACSM3 suppresses the pathogenesis of high-grade serous ovarian carcinoma via promoting AMPK activity.
    Yang X, Wu G, Zhang Q, Chen X, Li J, Han Q, Yang L, Wang C, Huang M, Li Y, Chen J, LiLi, Wang H, Liu K.

    04/2/2022
    Our data provide evidence for a differential expression and regulation of the ACSM3 gene in hepatocellular carcinoma

    Integrative transcriptome analysis of liver cancer profiles identifies upstream regulators and clinical significance of ACSM3 gene expression.
    Gopal R, Selvarasu K, Pandian PP, Ganesan K.

    08/11/2018
    Reduced ACSM3 is associated with impaired butyrate oxidation in ulcerative colitis.

    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.

    10/27/2012
    Observational study of gene-disease association, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator)

    Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.
    Bailey SD, Xie C, Do R, Montpetit A, Diaz R, Mohan V, Keavney B, Yusuf S, Gerstein HC, Engert JC, Anand S, DREAM investigators., Free PMC Article

    09/15/2010
    Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator)

    Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.
    Rose JE, Behm FM, Drgon T, Johnson C, Uhl GR., Free PMC Article

    06/30/2010
    left ventricular mass index and mean wall thickness , two phenotypes that are jointly influenced by blood pressure and obesity, might be related to variation in the human SAH gene

    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, 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.

    01/21/2010
    Observational study of gene-disease association and gene-environment interaction. (HuGE Navigator)

    Association of genetic variants with chronic kidney disease in individuals with different lipid profiles.
    Yoshida T, Kato K, Yokoi K, Oguri M, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nishigaki Y, Nozawa Y, Yamada Y.

    09/20/2009
    SA hypertension-associated homolog(SAH) gene polymorphisms are associated with non-high-density lipoprotein cholesterol in postmenopausal women

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

    01/21/2010
    We conclude that, in spite of its renal expression,1-3 the human SAH gene is unlikely to have an important role in renal sodium handling.

    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.

    01/21/2010
    family-based analyses of SA hypertension-associated homolog (SAH) gene variants did not reveal population stratification supporting an association of hypertension and gene variants

    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.

    01/21/2010
    Observational study of gene-disease association and gene-gene interaction. (HuGE Navigator)

    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.

    03/13/2008
    Observational study of gene-disease association. (HuGE Navigator)See all PubMed (13) articles

    Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression.
    Hendrickson SL, Lautenberger JA, Chinn LW, Malasky M, Sezgin E, Kingsley LA, Goedert JJ, Kirk GD, Gomperts ED, Buchbinder SP, Troyer JL, O'Brien SJ.

    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.

    Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.
    Talmud PJ, Drenos F, Shah S, Shah T, Palmen J, Verzilli C, Gaunt TR, Pallas J, Lovering R, Li K, Casas JP, Sofat R, Kumari M, Rodriguez S, Johnson T, Newhouse SJ, Dominiczak A, Samani NJ, Caulfield M, Sever P, Stanton A, Shields DC, Padmanabhan S, Melander O, Hastie C, Delles C, Ebrahim S, Marmot MG, Smith GD, Lawlor DA, Munroe PB, Day IN, Kivimaki M, Whittaker J, Humphries SE, Hingorani AD, ASCOT investigators, NORDIL investigators, BRIGHT Consortium.

    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, 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.

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

    Multiple genetic variants along candidate pathways influence plasma high-density lipoprotein cholesterol concentrations.
    Lu Y, Dollé ME, Imholz S, van 't Slot R, Verschuren WM, Wijmenga C, Feskens EJ, Boer JM.

    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, 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.

    Two medium-chain acyl-coenzyme A synthetase genes, SAH and MACS1, are associated with plasma high-density lipoprotein cholesterol levels, but they are not associated with essential hypertension.
    Haketa A, Soma M, Nakayama T, Sato M, Kosuge K, Aoi N, Matsumoto K.

    Overweight, but not hypertension, is associated with SAH polymorphisms in Caucasians with essential hypertension.
    Benjafield AV, Iwai N, Ishikawa K, Wang WY, Morris BJ, Benjafield AV, Iwai N, Ishikawa K, Wang WY, Morris BJ.

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

    [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.

    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.

    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.

    03/13/2008
    confirms recent evidence that the SAH locus is associated with obesity-related hypertension

    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, 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.

    01/21/2010
    variation in SAH has a role in predisposition to overweight in hypertensives.

    Overweight, but not hypertension, is associated with SAH polymorphisms in Caucasians with essential hypertension.
    Benjafield AV, Iwai N, Ishikawa K, Wang WY, Morris BJ, Benjafield AV, Iwai N, Ishikawa K, Wang WY, Morris BJ.

    01/21/2010
    SA gene polymorphism may be associated with the renal prognosis of immunoglobulin A nephropathy through its effect on blood pressure. Sensitivity to this gene polymorphism increases in patients with renal injury.

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

    01/21/2010
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