Human Genome Epidemiology Literature Finder
|
Records 1 - 13 (of 13 Records) |
| Query Trace: Disease and NR1H3[original query] |
|---|
| Liver X receptor a gene polymorphisms and variable cardiovascular outcomes in patients treated with antihypertensive therapy: results from the INVEST-GENES study. Pharmacogenetics and genomics 2011 Jun 21 (6): 333-40. Price Elvin Tyrone, Pacanowski Michael A, Martin Michael A, Cooper-DeHoff Rhonda M, Pepine Carl J, Zineh Issam, Johnson Julie |
| A common polymorphism in NR1H2 (LXRbeta) is associated with preeclampsia. BMC medical genetics 2011 12 (1): 145. Mouzat Kevin, Mercier Eric, Polge Anne, Evrard Alexandre, Baron Silvère, Balducchi Jean-Pierre, Brouillet Jean-Paul, Lumbroso Serge, Gris Jean-Christop |
| Genetic analysis of genes involved in amyloid-ß degradation and clearance in Alzheimer's disease. Journal of Alzheimer's disease : JAD 2012 28 (3): 553-9. Natunen Teemu, Helisalmi Seppo, Vepsäläinen Saila, Sarajärvi Timo, Antikainen Leila, Mäkinen Petra, Herukka Sanna-Kaisa, Koivisto Anne Maria, Haapasalo Annakaisa, Soininen Hilkka, Hiltunen Mik |
| Effects of NR1H3 genetic variation on the expression of liver X receptor a and the progression of Alzheimer's disease. PloS one 2013 8 (11): e80700. Natunen Teemu, Martiskainen Henna, Sarajärvi Timo, Helisalmi Seppo, Pursiheimo Juha-Pekka, Viswanathan Jayashree, Laitinen Marjo, Mäkinen Petra, Kauppinen Tarja, Rauramaa Tuomas, Leinonen Ville, Alafuzoff Irina, Haapasalo Annakaisa, Soininen Hilkka, Hiltunen Mik |
| Liver X receptors alpha gene (NR1H3) promoter polymorphisms are associated with systemic lupus erythematosus in Koreans. Arthritis research & therapy 2014 16 (3): R112. Jeon Ja-Young, Nam Jin-Young, Kim Hyoun-Ah, Park Yong-Beom, Bae Sang-Cheol, Suh Chang-H |
| Nuclear Receptor NR1H3 in Familial Multiple Sclerosis. Neuron 2016 Jun 90 (5): 948-54. Wang Zhe, Sadovnick A Dessa, Traboulsee Anthony L, Ross Jay P, Bernales Cecily Q, Encarnacion Mary, Yee Irene M, de Lemos Madonna, Greenwood Talitha, Lee Joshua D, Wright Galen, Ross Colin J, Zhang Si, Song Weihong, Vilariño-Güell Carl |
| Variants with large effects on blood lipids and the role of cholesterol and triglycerides in coronary disease. Nature genetics 2016 May . Helgadottir Anna, Gretarsdottir Solveig, Thorleifsson Gudmar, Hjartarson Eirikur, Sigurdsson Asgeir, Magnusdottir Audur, Jonasdottir Aslaug, Kristjansson Helgi, Sulem Patrick, Oddsson Asmundur, Sveinbjornsson Gardar, Steinthorsdottir Valgerdur, Rafnar Thorunn, Masson Gisli, Jonsdottir Ingileif, Olafsson Isleifur, Eyjolfsson Gudmundur I, Sigurdardottir Olof, Daneshpour Maryam S, Khalili Davood, Azizi Fereidoun, Swinkels Dorine W, Kiemeney Lambertus, Quyyumi Arshed A, Levey Allan I, Patel Riyaz S, Hayek Salim S, Gudmundsdottir Ingibjorg J, Thorgeirsson Gudmundur, Thorsteinsdottir Unnur, Gudbjartsson Daniel F, Holm Hilma, Stefansson Ka |
| Publicly Available Data Provide Evidence against NR1H3 R415Q Causing Multiple Sclerosis. Neuron 2016 Oct 92 (2): 336-338. Minikel Eric Vallabh, MacArthur Daniel |
| NR1H3 p.Arg415Gln Is Not Associated to Multiple Sclerosis Risk. Neuron 2016 Oct 92 (2): 333-335. , |
| Abruptio placentae risk and genetic variations in mitochondrial biogenesis and oxidative phosphorylation: replication of a candidate gene association study. American journal of obstetrics and gynecology 2018 Sep . Workalemahu Tsegaselassie, Enquobahrie Daniel A, Gelaye Bizu, Thornton Timothy A, Tekola-Ayele Fasil, Sanchez Sixto E, Garcia Pedro J, Palomino Henry G, Hajat Anjum, Romero Roberto, Ananth Cande V, Williams Michelle |
| GWAS-Top Polymorphisms Associated With Late-Onset Alzheimer Disease in Brazil: Pointing Out Possible New Culprits Among Non-Coding RNAs. Frontiers in molecular biosciences 2021 8 632314. Kretzschmar Gabriela Canalli, Alencar Nina Moura, da Silva Saritha Suellen Lopes, Sulzbach Carla Daniela, Meissner Caroline Grisbach, Petzl-Erler Maria Luiza, Souza Ricardo Lehtonen R, Boldt Angelica Beate Wint |
| Association of insulin signaling pathway-related gene polymorphisms and gene-gene interactions with MAFLD in obese children. Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences 2023 6 48 (4): 516-525. Xiang Xiao, Junxia Yan, Ning'an Xu, Rutong Kang, Jiayou Luo, Yan Zho |
| Contributions of NR1H3 genetic polymorphisms to susceptibility and effects of narrowband UVB phototherapy to nonsegmental vitiligo. Scientific reports 2023 2 13 (1): 3384. Xu Meifeng, Xu Qiuyu, Liu Yan, Li Xiaoli, Wang Mei, Dong Wei, Song Yuning, Xiao Shengxia |
- Page last reviewed:Feb 1, 2024
- Content source: