Human Genome Epidemiology Literature Finder
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Records 1 - 21 (of 21 Records) |
| Query Trace: Disease and FOS[original query] |
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| Common variants in the gene encoding ATP-binding cassette transporter 1 in men with low HDL cholesterol levels and coronary heart disease. Atherosclerosis 2001 Feb 154 (3): 607-11. Brousseau M E, Bodzioch M, Schaefer E J, Goldkamp A L, Kielar D, Probst M, Ordovas J M, Aslanidis C, Lackner K J, Bloomfield Rubins H, Collins D, Robins S J, Wilson P W, Schmitz |
| Cholesteryl ester transfer protein TaqI B2B2 genotype is associated with higher HDL cholesterol levels and lower risk of coronary heart disease end points in men with HDL deficiency: Veterans Affairs HDL Cholesterol Intervention Trial. Arteriosclerosis, thrombosis, and vascular biology 2002 Jul 22 (7): 1148-54. Brousseau Margaret E, O'Connor John J, Ordovas Jose M, Collins Dorothea, Otvos James D, Massov Tatyana, McNamara Judith R, Rubins Hanna B, Robins Sander J, Schaefer Ernst |
| Polymorphisms in the gene encoding lipoprotein lipase in men with low HDL-C and coronary heart disease: the Veterans Affairs HDL Intervention Trial. Journal of lipid research 2004 Oct 45 (10): 1885-91. Brousseau Margaret E, Goldkamp Allison L, Collins Dorothea, Demissie Serkalem, Connolly Allison C, Cupples L Adrienne, Ordovas Jose M, Bloomfield Hanna E, Robins Sander J, Schaefer Ernst |
| [Abnormal expression of c-myc, p53, p16 protein and GNAS1 gene mutation in fibrous dysplasia]. Zhonghua bing li xue za zhi Chinese journal of pathology 2009 May 38 (5): 292-7. Tang Juan, Zhao Hong-ye, Zheng Li, Zhang Hui-zhen, Jiang Zhi-mi |
| Common genetic variation in multiple metabolic pathways influences susceptibility to low HDL-cholesterol and coronary heart disease. Journal of lipid research 2010 Dec 51 (12): 3524-32. Peloso Gina M, Demissie Serkalem, Collins Dorothea, Mirel Daniel B, Gabriel Stacey B, Cupples L Adrienne, Robins Sander J, Schaefer Ernst J, Brousseau Margaret |
| Genetic susceptibility to refractive error: association of vasoactive intestinal peptide receptor 2 (VIPR2) with high myopia in Chinese. PloS one 2013 8 (4): e61805. Yiu Wai Chi, Yap Maurice K H, Fung Wai Yan, Ng Po Wah, Yip Shea Pi |
Genome-wide association study of ulcerative colitis in Koreans suggests extensive overlapping of genetic susceptibility with Caucasians.
Inflammatory bowel diseases 2013 Apr 19 (5): 954-66. Yang Suk-Kyun, Hong Myunghee, Zhao Wanting, Jung Yusun, Tayebi Naeimeh, Ye Byong Duk, Kim Kyung-Jo, Park Sang Hyoung, Lee Inchul, Shin Hyoung Doo, Cheong Hyun Sub, Kim Lyoung Hyo, Kim Hyo-Jong, Jung Sung-Ae, Kang Daehee, Youn Hee-Shang, Liu Jianjun, Song Kyuyou |
| Association of FOS-like antigen 1 promoter polymorphism with podocyte foot process effacement in immunoglobulin A nephropathy patients. Journal of clinical laboratory analysis 2014 Sep 28 (5): 391-7. Park Hae Jeong, Kim Jong Woo, Cho Byoung-Soo, Chung Joo- |
| Ocular signs correlate well with disease severity and genotype in Fabry disease. PloS one 2015 10 (3): e0120814. Pitz Susanne, Kalkum Gisela, Arash Laila, Karabul Nesrin, Sodi Andrea, Larroque Sylvain, Beck Michael, Gal Andre |
| Age at First Cardiac Symptoms in Fabry Disease: Association with a Chinese Hotspot Fabry Mutation (IVS4+919G>A), Classical Fabry Mutations, and Sex in a Taiwanese Population from the Fabry Outcome Survey (FOS). JIMD reports 2015 22 107-13. Liu Hao-Chuan, Perrin Amandine, Hsu Ting-Rong, Yang Chia-Feng, Lin Hsiang-Yu, Yu Wen-Chung, Niu Dau-Mi |
| Relation of fish oil supplementation to markers of atherothrombotic risk in patients with cardiovascular disease not receiving lipid-lowering therapy. The American journal of cardiology 2015 May 115 (9): 1204-11. Franzese Christopher J, Bliden Kevin P, Gesheff Martin G, Pandya Shachi, Guyer Kirk E, Singla Anand, Tantry Udaya S, Toth Peter P, Gurbel Paul |
| The Hypertension Risk Variant Rs820430 Functions as an Enhancer of SLC4A7. American journal of hypertension 2016 Oct . Wang Laiyuan, Li Hongfan, Yang Bin, Guo Liwei, Han Xikun, Li Lin, Li Mengting, Huang Jianfeng, Gu Dongfe |
| Multiple functional SNPs in differentially expressed genes modify risk and survival of non-small cell lung cancer in Chinese female non-smokers. Oncotarget 2017 Jan . Fang Xue, Yin Zhihua, Li Xuelian, Xia Lingzi, Quan Xiaowei, Zhao Yuxia, Zhou Baos |
| Hydrogen Sulfide Ameliorates Homocysteine-Induced Cardiac Remodeling and Dysfunction. Frontiers in physiology 2019 10 598. Kar Sumit, Shahshahan Hamid R, Kambis Tyler N, Yadav Santosh K, Li Zhen, Lefer David J, Mishra Paras |
| Rare non-coding Desmoglein-2 variant contributes to Arrhythmogenic right ventricular cardiomyopathy. Journal of molecular and cellular cardiology 2019 5 131 164-170. Christensen Alex Hørby, Andersen Claus B, Wassilew Katharina, Svendsen Jesper Hastrup, Bundgaard Henning, Brand Stefan-Martin, Schmitz Bor |
| A functional variant alters binding of activating protein 1 regulating expression of FGF7 gene associated with chronic obstructive pulmonary disease. BMC medical genetics 2019 Feb 20 (1): 33. Zhang Xiaomei, Guo Yongxin, Yang Jing, Niu Jianlou, Du Lina, Li Haiyan, Li Xiaok |
| A rare variant in EZH2 is associated with prostate cancer risk. International journal of cancer 2021 Apr . Raspin Kelsie, FitzGerald Liesel M, Marthick James R, Field Matt A, Malley Roslyn C, Banks Annette, Donovan Shaun, Thomson Russell J, Foley Georgea R, Stanford Janet L, Dickinson Joanne |
| Multimodal single-cell/nucleus RNA sequencing data analysis uncovers molecular networks between disease-associated microglia and astrocytes with implications for drug repurposing in Alzheimer's disease. Genome research 2021 2 31 (10): 1900-1912. Xu Jielin, Zhang Pengyue, Huang Yin, Zhou Yadi, Hou Yuan, Bekris Lynn M, Lathia Justin, Chiang Chien-Wei, Li Lang, Pieper Andrew A, Leverenz James B, Cummings Jeffrey, Cheng Feixio |
| The relationship between FOSB and SOCS3 gene polymorphisms and the susceptibility to periodontitis and osteopenia in the Chinese population. Odontology 2022 Jun . Liu Liuhui, Zhang Limin, Li Yinghua, Wang Yanhua, He Liu, Song Liang, Shi Xiaoj |
| The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia. Nature communications 2022 6 13 (1): 3690. Nehme Ralda, Pietiläinen Olli, Artomov Mykyta, Tegtmeyer Matthew, Valakh Vera, Lehtonen Leevi, Bell Christina, Singh Tarjinder, Trehan Aditi, Sherwood John, Manning Danielle, Peirent Emily, Malik Rhea, Guss Ellen J, Hawes Derek, Beccard Amanda, Bara Anne M, Hazelbaker Dane Z, Zuccaro Emanuela, Genovese Giulio, Loboda Alexander A, Neumann Anna, Lilliehook Christina, Kuismin Outi, Hamalainen Eija, Kurki Mitja, Hultman Christina M, Kähler Anna K, Paulo Joao A, Ganna Andrea, Madison Jon, Cohen Bruce, McPhie Donna, Adolfsson Rolf, Perlis Roy, Dolmetsch Ricardo, Farhi Samouil, McCarroll Steven, Hyman Steven, Neale Ben, Barrett Lindy E, Harper Wade, Palotie Aarno, Daly Mark, Eggan Kev |
| Interleukin-1? activated c-FOS transcription factor binds preferentially to a specific allele of the matrix metalloproteinase-13 promoter and increases susceptibility to endometriosis. Journal of cellular physiology 2022 May . Pandit Anuradha, Das Mahapatra Pramathes, Saha Priyanka, Srivastava Amit Kumar, Swarnakar Snehasik |
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