Human Genome Epidemiology Literature Finder
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Records 1 - 26 (of 26 Records) |
| Query Trace: Disease and RXRA[original query] |
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| RXRA gene variations influence Alzheimer's disease risk and cholesterol metabolism. Journal of cellular and molecular medicine 2009 Mar 13 (3): 589-98. Kölsch Heike, Lütjohann Dieter, Jessen Frank, Popp Julius, Hentschel Frank, Kelemen Peter, Friedrichs Silvia, Maier T A Wolfgang, Heun Reinha |
| 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 |
| Two novel mutations of the IRX4 gene in patients with congenital heart disease. Human genetics 2011 May . Cheng Z, Wang J, Su D, Pan H, Huang G, Li X, Li Z, Shen A, Xie X, Wang B, Ma X |
| Using gene-network landscape to dissect genotype effects of TCF7L2 genetic variant on diabetes and cardiovascular risk. Physiological genomics 2012 Oct 44 (19): 903-14. Vaquero Andre R, Ferreira Noely E, Omae Samantha V, Rodrigues Mariliza V, Teixeira Samantha K, Krieger Jose E, Pereira Alexandre |
| Vitamin D-related genetic variation, plasma vitamin D, and risk of lethal prostate cancer: a prospective nested case-control study. Journal of the National Cancer Institute 2012 May 104 (9): 690-9. Shui Irene M, Mucci Lorelei A, Kraft Peter, Tamimi Rulla M, Lindstrom Sara, Penney Kathryn L, Nimptsch Katharina, Hollis Bruce W, Dupre Natalie, Platz Elizabeth A, Stampfer Meir J, Giovannucci Edwa |
| Genetic variants in the vitamin D pathway and breast cancer disease-free survival. Carcinogenesis 2012 Nov . Pande M, Thompson PA, Do KA, Sahin AA, Amos CI, Frazier ML, Bondy ML, Brewster AM |
| PPARA, RXRA, NR1I2 and NR1I3 gene polymorphisms and lipid and lipoprotein levels in a Southern Brazilian population. Molecular biology reports 2012 Oct . Lima LO, Almeida S, Hutz MH, Fiegenbaum M |
| Genetic variants in vitamin d pathway genes and risk of pancreas cancer; results from a population-based case-control study in ontario, Canada. PloS one 2013 8 (6): e66768. Anderson Laura N, Cotterchio Michelle, Knight Julia A, Borgida Ayelet, Gallinger Steven, Cleary Sean |
Multidimensional prognostic risk assessment identifies association between IL12B variation and surgery in Crohn's disease.
Inflammatory bowel diseases 2013 Jul 19 (8): 1662-70. Dubinsky Marla C, Kugathasan Subra, Kwon Soonil, Haritunians Talin, Wrobel Iwona, Wahbeh Ghassan, Quiros Antonio, Bahar Ron, Silber Gary, Farrior Sharmayne, Stephens Michael, Teleten Nick, Panikkath Deepa, Ippoliti Andrew, Vasiliauskas Eric, Fleshner Phillip, Williams Chadwick, Landers Carol, Rotter Jerome I, Targan Stephan R, Taylor Kent D, McGovern Dermot P |
| Single nucleotide polymorphisms of vitamin D binding protein, vitamin D receptor and retinoid X receptor alpha genes and response to hepatitis B vaccination in renal replacement therapy patients. Expert review of vaccines 2014 Nov 13 (11): 1395-403. Grzegorzewska Alicja E, Jod?owska El?bieta, Mostowska Adrianna, Sowi?ska Anna, Jagodzi?ski Pawe? |
| Case-control association between CCT-associated variants and keratoconus in a Saudi Arabian population. Journal of negative results in biomedicine 2015 14 10. Abu-Amero Khaled K, Helwa Inas, Al-Muammar Abdulrahman, Strickland Shelby, Hauser Michael A, Allingham R Rand, Liu Yut |
| T helper cell-related cytokine gene polymorphisms and vitamin D pathway gene polymorphisms as predictors of survival probability in patients on renal replacement therapy. Polskie Archiwum Medycyny Wewn?trznej 2015 Aug 125 (7-8): 511-20. ?widerska Monika, Mostowska Adrianna, Grzegorzewska Alicja |
| Genetic variants in the vitamin D pathway genes VDBP and RXRA modulate cutaneous melanoma disease-specific survival. Pigment cell & melanoma research 2015 Nov . Yin Jieyun, Liu Hongliang, Yi Xiaohua, Wu Wenting, Amos Christopher I, Fang Shenying, Lee Jeffrey E, Han Jiali, Wei Qing |
| T-cell cytokine gene polymorphisms and vitamin D pathway gene polymorphisms in end-stage renal disease due to type 2 diabetes mellitus nephropathy: comparisons with health status and other main causes of end-stage renal disease. Journal of diabetes research 2014 2014 120317. Grzegorzewska Alicja E, Ostromecki Grzegorz, Zieli?ska Paulina, Mostowska Adrianna, Jagodzi?ski Pawe? |
| Genetic associations for keratoconus: a systematic review and meta-analysis. Scientific reports 2017 Jul 7 (1): 4620. Rong Shi Song, Ma Sarah Tsz Ue, Yu Xin Ting, Ma Li, Chu Wai Kit, Chan Tommy Chung Yan, Wang Yu Meng, Young Alvin L, Pang Chi Pui, Jhanji Vishal, Chen Li J |
| Prevalence, determinants and clinical correlates of vitamin D deficiency in patients with Chronic Obstructive Pulmonary Disease in London, UK. The Journal of steroid biochemistry and molecular biology 2018 01 175 138-145. Jolliffe David A, James Wai Yee, Hooper Richard L, Barnes Neil C, Greiller Claire L, Islam Kamrul, Bhowmik Angshu, Timms Peter M, Rajakulasingam Raj K, Choudhury Aklak B, Simcock David E, Hyppönen Elina, Walton Robert T, Corrigan Christopher J, Griffiths Christopher J, Martineau Adrian |
| SNP rs11185644 of RXRA gene is identified for dose-response variability to vitamin D3 supplementation: a randomized clinical trial. Scientific reports 2017 Jan 7 40593. Zhang Mingzhi, Zhao Lan-Juan, Zhou Yu, Badr Rhamee, Watson Patrice, Ye An, Zhou Boting, Zhang Jigang, Deng Hong-Wen, Recker Robert R, Lappe Joan |
| ENHO, RXRA, and LXRA polymorphisms and dyslipidaemia, related comorbidities and survival in haemodialysis patients. BMC medical genetics 2018 Nov 19 (1): 194. Grzegorzewska Alicja E, Niepolski Leszek, ?widerska Monika K, Mostowska Adrianna, Stolarek Ireneusz, Warcho? Wojciech, Figlerowicz Marek, Jagodzi?ski Pawe? |
| Smoking and Parkinson disease: Evidence for gene-by-smoking interactions. Neurology 2018 Jan . Lee Pei-Chen, Ahmed Ismaïl, Loriot Marie-Anne, Mulot Claire, Paul Kimberly C, Bronstein Jeff M, Ritz Beate, Elbaz Alex |
| Epigenomic signatures in liver and blood of Wilson disease patients include hypermethylation of liver-specific enhancers. Epigenetics & chromatin 2019 02 12 (1): 10. Mordaunt Charles E, Kieffer Dorothy A, Shibata Noreene M, Cz?onkowska Anna, Litwin Tomasz, Weiss Karl-Heinz, Zhu Yihui, Bowlus Christopher L, Sarkar Souvik, Cooper Stewart, Wan Yu-Jui Yvonne, Ali Mohamed R, LaSalle Janine M, Medici Valenti |
| Association of VDBP rs4701 Variant, but not VDR/RXR-? Over-Expression with Bone Mineral Density in Pediatric Well-Chelated ?-Thalassemia Patients. Mediterranean journal of hematology and infectious diseases 2020 7 12 (1): e2020037. Sahmoud Shaimaa, Ibrahim Mostafa S, Toraih Eman A, Kamel Noha, Fawzy Manal S, Elfiky Sam |
| Assessment of prognostic implication of a panel of oncogenes in bladder cancer and identification of a 3-gene signature associated with recurrence and progression risk in non-muscle-invasive bladder cancer. Scientific reports 2020 10 10 (1): 16641. Le Goux Constance, Vacher Sophie, Schnitzler Anne, Barry Delongchamps Nicolas, Zerbib Marc, Peyromaure Michael, Sibony Mathilde, Allory Yves, Bieche Ivan, Damotte Diane, Pignot Geraldi |
| Multi-omics integration identifies key upstream regulators of pathomechanisms in hypertrophic cardiomyopathy due to truncating MYBPC3 mutations. Clinical epigenetics 2021 3 13 (1): 61. Pei J, Schuldt M, Nagyova E, Gu Z, El Bouhaddani S, Yiangou L, Jansen M, Calis J J A, Dorsch L M, Blok C Snijders, van den Dungen N A M, Lansu N, Boukens B J, Efimov I R, Michels M, Verhaar M C, de Weger R, Vink A, van Steenbeek F G, Baas A F, Davis R P, Uh H W, Kuster D W D, Cheng C, Mokry M, van der Velden J, Asselbergs F W, Harakalova |
| A Non-coding HES1 Variant Predisposes Children to Congenital Heart Disease in Chinese Population. Frontiers in cell and developmental biology 2021 2 9 631942. Song Yangliu, Chen Weicheng, Huang Zitong, Tian Guixiang, Li Mengru, Zhao Zhengshan, Feng Zhiyu, Wu Feizhen, Qian Maoxiang, Ma Xiaojing, Sheng Wei, Huang Guoyi |
| SNP rs11185644 in RXRA gene and SNP rs2235544 in DIO1 gene predict dosage requirements in a cross-sectional sample of hypothyroid patients. BMC endocrine disorders 2023 8 23 (1): 167. Rowan AlEjielat, Anas Khaleel, Yazan S Batarseh, Luay Abu-Qatouseh, Suzan Al-Wawi, Toleen AlSun |
| Association of Novel Loci With Keratoconus Susceptibility in a Chinese Genome-Wide Association Study. Investigative ophthalmology & visual science 2024 5 65 (5): 29. Liyan Xu, Xiaodong Zheng, Shanshan Yin, Kaili Yang, Qi Fan, Yuwei Gu, Yi Yuan, Chenchen Yin, Yonghao Zang, Chenjiu Pang, Liangdan Sun, Shengwei R |
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