Human Genome Epidemiology Literature Finder
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Records 1 - 27 (of 27 Records) |
| Query Trace: Syndrome and ABCA1[original query] |
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| Genetic variation in ABC transporter A1 contributes to HDL cholesterol in the general population. The Journal of clinical investigation 2004 Nov 114 (9): 1343-53. Frikke-Schmidt Ruth, Nordestgaard Børge G, Jensen Gorm B, Tybjaerg-Hansen An |
| [Significance of -191G/C single nucleotide polymorphisms in the promoter region of ATP-binding cassette transporter gene in coronary artery disease]. Di 1 jun yi da xue xue bao = Academic journal of the first medical college of PLA 2005 Jun 25 (6): 660-2, 666. Liu Ling, Guo Zhi-gang, Wang Qi-guang, Liu Sheng-lin, Lai Wen-yan, Tu Y |
| Mutation in ABCA1 predicted risk of ischemic heart disease in the Copenhagen City Heart Study Population. Journal of the American College of Cardiology 2005 Oct 46 (8): 1516-20. Frikke-Schmidt Ruth, Nordestgaard Børge G, Schnohr Peter, Steffensen Rolf, Tybjaerg-Hansen An |
| ABCA1 single nucleotide polymorphisms on high-density lipoprotein-cholesterol and overweight: the D.E.S.I.R. study. Obesity (Silver Spring, Md.) 2006 Nov 14 (11): 1874-9. Porchay Isabelle, Péan Franck, Bellili Naïma, Royer Bernard, Cogneau Joël, Chesnier Marie-Claude, Caradec Ariane, Tichet Jean, Balkau Beverley, Marre Michel, Fumeron Frédér |
| Association of the ATP-binding cassette transporter A1 R230C variant with early-onset type 2 diabetes in a Mexican population. Diabetes 2008 Feb 57 (2): 509-13. Villarreal-Molina M Teresa, Flores-Dorantes M Teresa, Arellano-Campos Olimpia, Villalobos-Comparan Marisela, Rodríguez-Cruz Maricela, Miliar-García Angel, Huertas-Vazquez Adriana, Menjivar Marta, Romero-Hidalgo Sandra, Wacher Niels H, Tusie-Luna M Teresa, Cruz Miguel, Aguilar-Salinas Carlos A, Canizales-Quinteros Samuel, |
| Association of a polymorphism of the apolipoprotein E gene with chronic kidney disease in Japanese individuals with metabolic syndrome. Genomics 2009 Mar 93 (3): 221-6. Yoshida Tetsuro, Kato Kimihiko, Fujimaki Tetsuo, Yokoi Kiyoshi, Oguri Mitsutoshi, Watanabe Sachiro, Metoki Norifumi, Yoshida Hidemi, Satoh Kei, Aoyagi Yukitoshi, Nishigaki Yutaka, Tanaka Masashi, Nozawa Yoshinori, Yamada Yoshi |
| Association between liver X receptor alpha gene polymorphisms and risk of metabolic syndrome in French populations. International journal of obesity (2005) 2008 Mar 32 (3): 421-8. Legry V, Cottel D, Ferrières J, Chinetti G, Deroide T, Staels B, Amouyel P, Meirhaeghe |
| Is dyslipidemia sustained during remission of nephrotic syndrome genetically determined? Evaluation of genetic polymorphisms of proteins involved in lipoprotein metabolism in children and adolescents with nephrotic syndrome. Polskie Archiwum Medycyny Wewn?trznej 0 119 (1-2): 11-6. Ksiazek Joanna, Ciechanowicz Andrzej, Wierzbicka Aldona, Syczewska Ma?gorzata, Grenda Rysza |
| A dietary pattern including nopal, chia seed, soy protein, and oat reduces serum triglycerides and glucose intolerance in patients with metabolic syndrome. The Journal of nutrition 2012 Jan 142 (1): 64-9. Guevara-Cruz Martha, Tovar Armando R, Aguilar-Salinas Carlos A, Medina-Vera Isabel, Gil-Zenteno Lidia, Hernández-Viveros Isaac, López-Romero Patricia, Ordaz-Nava Guillermo, Canizales-Quinteros Samuel, Guillen Pineda Luz E, Torres Nim |
| Effect Of G2706A and G1051A polymorphisms of the ABCA1 gene on the lipid, oxidative stress and homocystein levels in Turkish patients with polycystic ovary syndrome. Lipids in health and disease 2011 10 (1): 193. Karadeniz Muammer, Erdo?an Mehmet, Ayhan Zengi, Yalcin Murat, Olukman Murat, Cetinkalp Sevki, Alper Gulinnaz E, Eroglu Zuhal, Tetik Asli, Cetintas Vildan, Ozgen Ahmet G, Saygili Fusun, Yilmaz Candeg |
| Maternal ABCA1 genotype is associated with severity of Smith-Lemli-Opitz syndrome and with viability of patients homozygous for null mutations. European journal of human genetics : EJHG 2012 Aug . Lanthaler B, Steichen-Gersdorf E, Kollerits B, Zschocke J, Witsch-Baumgartner M |
| Omental adipose tissue gene expression, gene variants, branched-chain amino acids, and their relationship with metabolic syndrome and insulin resistance in humans. Genes & nutrition 2014 Nov 9 (6): 431. Serralde-Zúñiga Aurora E, Guevara-Cruz Martha, Tovar Armando R, Herrera-Hernández Miguel F, Noriega Lilia G, Granados Omar, Torres Nim |
| Negative results in screening for possible new sequence variations on ATP-binding cassette transporter A1 gene in Turkish adults with metabolic syndrome. Türk Kardiyoloji Derne?i ar?ivi : Türk Kardiyoloji Derne?inin yay?n organ?d?r 2014 Sep 42 (6): 524-30. Çoban Neslihan, Onat Altan, Geyik Filiz, Erginel Ünaltuna Nih |
| Novel association of the R230C variant of the ABCA1 gene with high triglyceride levels and low high-density lipoprotein cholesterol levels in Mexican school-age children with high prevalence of obesity. Archives of medical research 2015 Aug 46 (6): 495-501. Gamboa-Meléndez Marco Alberto, Galindo-Gómez Carlos, Juárez-Martínez Liliana, Gómez F Enrique, Diaz-Diaz Eulises, Ávila-Arcos Marco Antonio, Ávila-Curiel Abelar |
| Association between the ABCA1-565C/T gene promoter polymorphism and coronary heart disease severity and cholesterol efflux in the Chinese Han population. Genetic testing and molecular biomarkers 2015 Jul 19 (7): 347-52. Qi Li-Ping, Chen Lian-Feng, Dang Ai-Min, Li Li-Yun, Fang Quan, Yan Xiao-W |
| MicroRNA-33a regulates cholesterol synthesis and cholesterol efflux-related genes in osteoarthritic chondrocytes. Arthritis research & therapy 2015 17 42. Kostopoulou Fotini, Malizos Konstantinos N, Papathanasiou Ioanna, Tsezou Aspas |
| Accelerated Atherogenicity in Tangier Disease. Journal of atherosclerosis and thrombosis 2018 3 25 (10): 1076-1085. Muratsu Jun, Koseki Masahiro, Masuda Daisaku, Yasuga Yuji, Tomoyama Satoki, Ataka Keiji, Yagi Yoshiki, Nakagawa Atsushi, Hamada Hidehumi, Fujita Shigeki, Hattori Hiroaki, Ohama Tohru, Nishida Makoto, Hiraoka Hisatoyo, Matsuzawa Yuji, Yamashita Shizu |
| Multiple Gene Polymorphisms Associated with Exfoliation Syndrome in the Uygur Population. Journal of ophthalmology 2019 2019 9687823. Ma Yi-Nu, Xie Ting-Yu, Chen Xue- |
| Contribution of genetic, biochemical and environmental factors on insulin resistance and obesity in Mexican young adults. Obesity research & clinical practice 2019 Nov . Flores-Viveros Karla Lucero, Aguilar-Galarza Beatriz Adriana, Ordóñez-Sánchez María Luisa, Anaya-Loyola Miriam Aracely, Moreno-Celis Ulisses, Vázquez-Cárdenas Paola, García-Gasca Tere |
| ABCA1 gene R1587K polymorphism could be associated with metabolic syndrome and increased plasma triglyceride concentration in adults from northern Mexico. Nutricion hospitalaria 2020 Jul . Porchas Quijada Mildren, Reyes Castillo Zyanya, Román Pellegrini Oney, Artalejo Ochoa Elizabeth, Moya Camarena Silvia Yolanda, Montalvo Corral Maricela, Ballesteros Vásquez Martha Nyd |
| HDL-Mediated Cholesterol Efflux and Plasma Loading Capacities Are Altered in Subjects with Metabolically- but Not Genetically Driven Non-Alcoholic Fatty Liver Disease (NAFLD). Biomedicines 2020 12 8 (12): . Di Costanzo Alessia, Ronca Annalisa, D'Erasmo Laura, Manfredini Matteo, Baratta Francesco, Pastori Daniele, Di Martino Michele, Ceci Fabrizio, Angelico Francesco, Del Ben Maria, Pavanello Chiara, Turri Marta, Calabresi Laura, Favari Elda, Arca Marcel |
| Association of FTO, ABCA1, ADRB3, and PPARG variants with obesity, type 2 diabetes, and metabolic syndrome in a Northwest Mexican adult population. Journal of diabetes and its complications 2021 Aug 108025. Velazquez-Roman Jorge, Angulo-Zamudio Uriel A, León-Sicairos Nidia, Medina-Serrano Julio, DeLira-Bustillos Nora, Villamil-Ramírez Hugo, Canizales-Quinteros Samuel, Macías-Kauffer Luis, Campos-Romero Abraham, Alcántar-Fernández Jonathan, Canizalez-Roman Adri |
| Epigenomic Profiles of African-American Transthyretin Val122Ile Carriers Reveals Putatively Dysregulated Amyloid Mechanisms. Circulation. Genomic and precision medicine 2021 1 14 (1): e003011. Pathak Gita A, Wendt Frank R, De Lillo Antonella, Nunez Yaira Z, Goswami Aranyak, De Angelis Flavio, Fuciarelli Maria, Kranzler Henry R, Gelernter Joel, Polimanti Rena |
| Identification of genetic variants related to metabolic syndrome by next-generation sequencing. Diabetology & metabolic syndrome 2022 Aug 14 (1): 119. Lee Sanghoo, Kim Seol-A, Hong Jeonghoon, Kim Yejin, Hong Gayeon, Baik SaeYun, Choi Kyeonghwan, Lee Mi-Kyeong, Lee Kyoung-Ry |
Potential role of regulatory DNA variants in modifying the risk of severe cutaneous reactions induced by aromatic anti-seizure medications.
Epilepsia 2022 Feb . Mullan Kerry A, Anderson Alison, Shi Yi-Wu, Ding Jia-Hong, Ng Ching-Ching, Chen Zhibin, Baum Larry, Cherny Stacey, Petrovski Slave, Sham Pak C, Lim Kheng-Seang, Liao Wei-Ping, Kwan Patri |
| Targeted next-generation sequencing panel to investigate antiplatelet adverse reactions in acute coronary syndrome patients undergoing percutaneous coronary intervention with stenting. Thrombosis research 2024 6 240 109060. Alba Antúnez-Rodríguez, Sonia García-Rodríguez, Ana Pozo-Agundo, Jesús Gabriel Sánchez-Ramos, Eduardo Moreno-Escobar, José Matías Triviño-Juárez, Luis Javier Martínez-González, Cristina Lucía Dávila-Fajar |
| ABCA1 variant rs9282541 is associated with metabolic syndrome in Maya children. Annals of human genetics 2024 1 . Barbara I Peña-Espinoza, Emmanuel Torre-Horta, María G Ortiz-López, Marta Menjiv |
- Page last reviewed:Feb 1, 2024
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