Human Genome Epidemiology Literature Finder
Records 1 - 17 (of 17 Records) |
Query Trace: Tangier Disease and ABCA1[original query] |
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Novel polymorphisms in promoter region of atp binding cassette transporter gene and plasma lipids, severity, progression, and regression of coronary atherosclerosis and response to therapy. Circulation research 2001 May 88 (9): 969-73. Lutucuta S, Ballantyne C M, Elghannam H, Gotto A M, Marian A |
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 |
R219K polymorphism of the ABCA1 gene and its modulation of the variations in serum high-density lipoprotein cholesterol and triglycerides related to age and adiposity in white versus black young adults. The Bogalusa heart study. Metabolism: clinical and experimental 2003 Jul 52 (7): 930-4. Srinivasan Sathanur R, Li Shengxu, Chen Wei, Boerwinkle Eric, Berenson Gerald |
ABCA1 gene polymorphisms and their associations with coronary artery disease and plasma lipids in males from three ethnic populations in Singapore. Human genetics 2003 Jul 113 (2): 106-17. Tan Jenny Hui-Hui, Low Poh-Sim, Tan Yong-Seng, Tong Ming-Chuan, Saha Nilmani, Yang Hongyuan, Heng Chew-Ki |
A common variant in the ABCA1 gene is associated with a lower risk for premature coronary heart disease in familial hypercholesterolaemia. Journal of medical genetics 2003 Mar 40 (3): 163-8. Cenarro A, Artieda M, Castillo S, Mozas P, Reyes G, Tejedor D, Alonso R, Mata P, Pocoví M, Civeira F, |
ATP-binding cassette transporter A1 locus is not a major determinant of HDL-C levels in a population at high risk for coronary heart disease. Atherosclerosis 2003 Feb 166 (2): 285-90. Kakko Sakari, Kelloniemi Jani, von Rohr Peter, Hoeschele Ina, Tamminen Minna, Brousseau Margaret E, Kesäniemi Y Antero, Savolainen Markku |
Screening for functional sequence variations and mutations in ABCA1. Atherosclerosis 2004 Aug 175 (2): 269-79. Probst Mario C O, Thumann Harald, Aslanidis Charalampos, Langmann Thomas, Buechler Christa, Patsch Wolfgang, Baralle Francisco E, Dallinga-Thie Geesje M, Geisel Jürgen, Keller Christiane, Menys Valentine C, Schmitz Ge |
Genotypic effect of the -565C>T polymorphism in the ABCA1 gene promoter on ABCA1 expression and severity of atherosclerosis. Arteriosclerosis, thrombosis, and vascular biology 2005 Feb 25 (2): 418-23. Kyriakou Theodosios, Hodgkinson Conrad, Pontefract David E, Iyengar Srikanth, Howell W Martin, Wong Yuk-ki, Eriksson Per, Ye S |
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 |
ABCA1 polymorphisms and prognosis after myocardial infarction in young patients. International journal of cardiology 2006 Jun 110 (2): 267-8. Martín María, González Pelayo, Reguero J J R, Batalla Alberto, García Castro Mónica, Coto Eliecer, Morís Cés |
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 |
Functional polymorphism in ABCA1 influences age of symptom onset in coronary artery disease patients. Human molecular genetics 2007 Jun 16 (12): 1412-22. Kyriakou Theodosios, Pontefract David E, Viturro Enrique, Hodgkinson Conrad P, Laxton Ross C, Bogari Neda, Cooper George, Davies Michael, Giblett Joel, Day Ian N M, Simpson Iain A, Albrecht Christiane, Ye S |
Common ABCA1 variants, HDL levels, and cellular cholesterol efflux in subjects with familial low HDL. Journal of lipid research 2007 Jun 48 (6): 1409-16. Soro-Paavonen Aino, Naukkarinen Jussi, Lee-Rueckert Miriam, Watanabe Hiroshi, Rantala Elina, Soderlund Sanni, Hiukka Anne, Kovanen Petri T, Jauhiainen Matti, Peltonen Leena, Taskinen Marja-Riit |
R219K polymorphism of ATP binding cassette transporter A1 related with low HDL in overweight/obese Thai males. Archives of medical research 2007 Nov 38 (8): 834-8. Kitjaroentham Anong, Hananantachai Hathairad, Tungtrongchitr Anchalee, Pooudong Somchai, Tungtrongchitr Rungsu |
Whole exome sequencing combined with integrated variant annotation prediction identifies asymptomatic Tangier disease with compound heterozygous mutations in ABCA1 gene. Atherosclerosis 2015 Jun 240 (2): 324-9. Tada Hayato, Kawashiri Masa-Aki, Nohara Atsushi, Saito Reina, Tanaka Yoshihiro, Nomura Akihiro, Konno Tetsuo, Sakata Kenji, Fujino Noboru, Takamura Toshinari, Inazu Akihiro, Mabuchi Hiroshi, Yamagishi Masakazu, Hayashi Kens |
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 |
A case of premature and recurrent myocardial infarction associated with ABCA.1 gene mutation. Journal of postgraduate medicine 2020 Dec . Subramaniam K, Babu L A, Shah |
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- Page last updated:May 06, 2024
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