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Items: 1 to 20 of 105

1.

Allelic expression imbalance at high-density lipoprotein cholesterol locus MMAB-MVK.

Fogarty MP, Xiao R, Prokunina-Olsson L, Scott LJ, Mohlke KL.

Hum Mol Genet. 2010 May 15;19(10):1921-9. doi: 10.1093/hmg/ddq067. Epub 2010 Feb 16.

2.

Novel variants at KCTD10, MVK, and MMAB genes interact with dietary carbohydrates to modulate HDL-cholesterol concentrations in the Genetics of Lipid Lowering Drugs and Diet Network Study.

Junyent M, Parnell LD, Lai CQ, Lee YC, Smith CE, Arnett DK, Tsai MY, Kabagambe EK, Straka RJ, Province M, An P, Borecki I, Ordovás JM.

Am J Clin Nutr. 2009 Sep;90(3):686-94. doi: 10.3945/ajcn.2009.27738. Epub 2009 Jul 15.

3.

Association of KCTD10, MVK, and MMAB polymorphisms with dyslipidemia and coronary heart disease in Han Chinese population.

Sun J, Qian Y, Jiang Y, Chen J, Dai J, Jin G, Wang J, Hu Z, Liu S, Shen C, Shen H.

Lipids Health Dis. 2016 Oct 4;15(1):171.

4.

Allelic expression imbalance screening of genes in chromosome 1q21-24 region to identify functional variants for Type 2 diabetes susceptibility.

Mondal AK, Sharma NK, Elbein SC, Das SK.

Physiol Genomics. 2013 Jul 2;45(13):509-20. doi: 10.1152/physiolgenomics.00048.2013. Epub 2013 May 14.

5.

Association of GWAS-based candidate genes with HDL-cholesterol levels before and after bariatric surgery in the Swedish obese subjects study.

Sarzynski MA, Jacobson P, Rankinen T, Carlsson B, Sjöström L, Carlsson LM, Bouchard C.

J Clin Endocrinol Metab. 2011 Jun;96(6):E953-7. doi: 10.1210/jc.2010-2227. Epub 2011 Mar 23.

PMID:
21430028
6.

Next-generation DNA sequencing-based assay for measuring allelic expression imbalance (AEI) of candidate neuropsychiatric disorder genes in human brain.

Xu X, Wang H, Zhu M, Sun Y, Tao Y, He Q, Wang J, Chen L, Saffen D.

BMC Genomics. 2011 Oct 20;12:518. doi: 10.1186/1471-2164-12-518.

7.

Tryptophan hydroxylase 2 (TPH2) haplotypes predict levels of TPH2 mRNA expression in human pons.

Lim JE, Pinsonneault J, Sadee W, Saffen D.

Mol Psychiatry. 2007 May;12(5):491-501. Epub 2006 Dec 12.

PMID:
17453063
8.

The effect of MVK-MMAB variants, their haplotypes and G×E interactions on serum lipid levels and the risk of coronary heart disease and ischemic stroke.

Miao L, Yin RX, Huang F, Chen WX, Cao XL, Wu JZ.

Oncotarget. 2017 Aug 18;8(42):72801-72817. doi: 10.18632/oncotarget.20349. eCollection 2017 Sep 22.

9.

Allelic expression imbalance of the schizophrenia susceptibility gene CHI3L1: evidence of cis-acting variation and tissue specific regulation.

Hill MJ, Kenny E, Roche S, Morris DW, Corvin A, Hawi Z, Gill M, Anney RJ.

Psychiatr Genet. 2011 Dec;21(6):281-6. doi: 10.1097/YPG.0b013e328348045b.

PMID:
21642896
10.

An intronic PICALM polymorphism, rs588076, is associated with allelic expression of a PICALM isoform.

Parikh I, Medway C, Younkin S, Fardo DW, Estus S.

Mol Neurodegener. 2014 Aug 29;9:32. doi: 10.1186/1750-1326-9-32.

11.

Targeted allelic expression profiling in human islets identifies cis-regulatory effects for multiple variants identified by type 2 diabetes genome-wide association studies.

Locke JM, Hysenaj G, Wood AR, Weedon MN, Harries LW.

Diabetes. 2015 Apr;64(4):1484-91. doi: 10.2337/db14-0957. Epub 2014 Nov 12.

12.

Association between the MVK and MMAB polymorphisms and serum lipid levels.

Miao L, Yin RX, Pan SL, Yang S, Yang DZ, Lin WX.

Oncotarget. 2017 Jul 31;8(41):70378-70393. doi: 10.18632/oncotarget.19707. eCollection 2017 Sep 19.

13.

Polymorphisms affecting gene transcription and mRNA processing in pharmacogenetic candidate genes: detection through allelic expression imbalance in human target tissues.

Johnson AD, Zhang Y, Papp AC, Pinsonneault JK, Lim JE, Saffen D, Dai Z, Wang D, Sadée W.

Pharmacogenet Genomics. 2008 Sep;18(9):781-91. doi: 10.1097/FPC.0b013e3283050107.

14.

Genome-wide association analysis of total cholesterol and high-density lipoprotein cholesterol levels using the Framingham heart study data.

Ma L, Yang J, Runesha HB, Tanaka T, Ferrucci L, Bandinelli S, Da Y.

BMC Med Genet. 2010 Apr 6;11:55. doi: 10.1186/1471-2350-11-55.

15.

Allelic mRNA expression imbalance in C-type lectins reveals a frequent regulatory SNP in the human surfactant protein A (SP-A) gene.

Azad AK, Curtis A, Papp A, Webb A, Knoell D, Sadee W, Schlesinger LS.

Genes Immun. 2013 Mar;14(2):99-106. doi: 10.1038/gene.2012.61. Epub 2013 Jan 17.

16.

Multiple Hepatic Regulatory Variants at the GALNT2 GWAS Locus Associated with High-Density Lipoprotein Cholesterol.

Roman TS, Marvelle AF, Fogarty MP, Vadlamudi S, Gonzalez AJ, Buchkovich ML, Huyghe JR, Fuchsberger C, Jackson AU, Wu Y, Civelek M, Lusis AJ, Gaulton KJ, Sethupathy P, Kangas AJ, Soininen P, Ala-Korpela M, Kuusisto J, Collins FS, Laakso M, Boehnke M, Mohlke KL.

Am J Hum Genet. 2015 Dec 3;97(6):801-15. doi: 10.1016/j.ajhg.2015.10.016.

17.

Allelic expression analysis of the osteoarthritis susceptibility gene COL11A1 in human joint tissues.

Raine EV, Dodd AW, Reynard LN, Loughlin J.

BMC Musculoskelet Disord. 2013 Mar 8;14:85. doi: 10.1186/1471-2474-14-85.

19.

Analyzing allele specific RNA expression using mixture models.

Lu R, Smith RM, Seweryn M, Wang D, Hartmann K, Webb A, Sadee W, Rempala GA.

BMC Genomics. 2015 Aug 1;16:566. doi: 10.1186/s12864-015-1749-0.

20.

The rs1024611 regulatory region polymorphism is associated with CCL2 allelic expression imbalance.

Pham MH, Bonello GB, Castiblanco J, Le T, Sigala J, He W, Mummidi S.

PLoS One. 2012;7(11):e49498. doi: 10.1371/journal.pone.0049498. Epub 2012 Nov 16.

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