Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 53 Records) |
Query Trace: LCAT[original query] |
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LCAT, HDL cholesterol and ischemic cardiovascular disease: a Mendelian randomization study of HDL cholesterol in 54,500 individuals. The Journal of clinical endocrinology and metabolism 2012 Feb 97 (2): E248-56. Haase Christiane L, Tybjærg-Hansen Anne, Qayyum Abbas Ali, Schou Jesper, Nordestgaard Børge G, Frikke-Schmidt Ru |
Segregation of LIPG, CETP, and GALNT2 mutations in Caucasian families with extremely high HDL cholesterol. PloS one 2012 7 (8): e37437. Tietjen Ian, Hovingh G Kees, Singaraja Roshni R, Radomski Chris, Barhdadi Amina, McEwen Jason, Chan Elden, Mattice Maryanne, Legendre Annick, Franchini Patrick L, Dubé Marie-Pierre, Kastelein John J P, Hayden Michael |
Patients with low HDL-cholesterol caused by mutations in LCAT have increased arterial stiffness. Atherosclerosis 2012 Sep . van den Bogaard B, Holleboom AG, Duivenvoorden R, Hutten BA, Kastelein JJ, Hovingh GK, Kuivenhoven JA, Stroes ES, van den Born BJ |
Lipid oxidation in carriers of lecithin:cholesterol acyltransferase gene mutations. Arteriosclerosis, thrombosis, and vascular biology 2012 Dec 32 (12): 3066-75. Holleboom Adriaan G, Daniil Georgios, Fu Xiaoming, Zhang Renliang, Hovingh G Kees, Schimmel Alinda W, Kastelein John J P, Stroes Erik S G, Witztum Joseph L, Hutten Barbara A, Tsimikas Sotirios, Hazen Stanley L, Chroni Angeliki, Kuivenhoven Jan Albe |
Common Variants in 6 Lipid-Related Genes Discovered by High-Resolution DNA Melting Analysis and Their Association with Plasma Lipids. Journal of clinical & experimental cardiology 2011 Jul 2 (138): 138. Carlquist John F, McKinney Jason T, Horne Benjamin D, Camp Nicola J, Cannon-Albright Lisa, Muhlestein Joseph B, Hopkins Paul, Clarke Jessica L, Mower Chrissa P, Park James J, Nicholas Zachary P, Huntinghouse John A, Anderson Jeffrey |
Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained. PLoS genetics 2013 Mar 9 (3): e1003379. Wu Ying, Waite Lindsay L, Jackson Anne U, Sheu Wayne H-H, Buyske Steven, Absher Devin, Arnett Donna K, Boerwinkle Eric, Bonnycastle Lori L, Carty Cara L, Cheng Iona, Cochran Barbara, Croteau-Chonka Damien C, Dumitrescu Logan, Eaton Charles B, Franceschini Nora, Guo Xiuqing, Henderson Brian E, Hindorff Lucia A, Kim Eric, Kinnunen Leena, Komulainen Pirjo, Lee Wen-Jane, Le Marchand Loic, Lin Yi, Lindström Jaana, Lingaas-Holmen Oddgeir, Mitchell Sabrina L, Narisu Narisu, Robinson Jennifer G, Schumacher Fred, Stan?áková Alena, Sundvall Jouko, Sung Yun-Ju, Swift Amy J, Wang Wen-Chang, Wilkens Lynne, Wilsgaard Tom, Young Alicia M, Adair Linda S, Ballantyne Christie M, B?žková Petra, Chakravarti Aravinda, Collins Francis S, Duggan David, Feranil Alan B, Ho Low-Tone, Hung Yi-Jen, Hunt Steven C, Hveem Kristian, Juang Jyh-Ming J, Kesäniemi Antero Y, Kuusisto Johanna, Laakso Markku, Lakka Timo A, Lee I-Te, Leppert Mark F, Matise Tara C, Moilanen Leena, Njølstad Inger, Peters Ulrike, Quertermous Thomas, Rauramaa Rainer, Rotter Jerome I, Saramies Jouko, Tuomilehto Jaakko, Uusitupa Matti, Wang Tzung-Dau, Boehnke Michael, Haiman Christopher A, Chen Yii-Der I, Kooperberg Charles, Assimes Themistocles L, Crawford Dana C, Hsiung Chao A, North Kari E, Mohlke Karen |
Evaluation of links between high-density lipoprotein genetics, functionality, and aortic valve stenosis risk in humans. Arteriosclerosis, thrombosis, and vascular biology 2014 Feb 34 (2): 457-62. Arsenault Benoit J, Dubé Marie-Pierre, Brodeur Mathieu R, de Oliveira Moraes Adriana Benjamin, Lavoie Véronique, Kernaleguen Anne-Elen, Guauque-Olarte Sandra, Mathieu Patrick, Pibarot Philippe, Messika-Zeitoun David, Bossé Yohan, Rhainds David, Rhéaume Eric, Tardif Jean-Clau |
Increased risk of premature coronary artery disease in Egyptians with ABCA1 (R219K), CETP (TaqIB), and LCAT (4886C/T) genes polymorphism. Journal of clinical lipidology 0 8 (4): 381-9. Abd El-Aziz Tarek A, Mohamed Rasha H, Hagrass Hoda |
Identification of four novel genes contributing to familial elevated plasma HDL cholesterol in humans. Journal of lipid research 2014 Jun 55 (8): 1693-1701. Singaraja Roshni R, Tietjen Ian, Hovingh G Kees, Franchini Patrick L, Radomski Chris, Wong Kenny, vanHeek Margaret, Stylianou Ioannis M, Lin Linus, Wang Liangsu, Mitnaul Lyndon, Hubbard Brian, Winther Michael, Mattice Maryanne, Legendre Annick, Sherrington Robin, Kastelein John J, Akinsanya Karen, Plump Andrew, Hayden Michael |
Identification of genetic variants of lecithin cholesterol acyltransferase in individuals with high HDL-C levels. Molecular medicine reports 2014 Jul 10 (1): 496-502. Naseri Mohsen, Hedayati Mehdi, Daneshpour Maryam Sadat, Bandarian Fatemeh, Azizi Fereido |
Adrenal Function in females with low plasma HDL-C due to mutations in ABCA1 and LCAT. PloS one 2014 9 (5): e90967. Bochem Andrea E, Holleboom Adriaan G, Romijn Johannes A, Hoekstra Menno, Dallinga Geesje M, Motazacker Mahdi M, Hovingh G Kees, Kuivenhoven Jan A, Stroes Erik S |
Gene-based sequencing identifies lipid-influencing variants with ethnicity-specific effects in African Americans. PLoS genetics 2014 Mar 10 (3): e1004190. Bentley Amy R, Chen Guanjie, Shriner Daniel, Doumatey Ayo P, Zhou Jie, Huang Hanxia, Mullikin James C, Blakesley Robert W, Hansen Nancy F, Bouffard Gerard G, Cherukuri Praveen F, Maskeri Baishali, Young Alice C, Adeyemo Adebowale, Rotimi Charles |
Association of Lecithin Cholesterol Acyltransferase rs5923 Polymorphism in Iranian Individuals with Extremely Low High-Density Lipoprotein Cholesterol: Tehran Lipid and Glucose Study. Iranian biomedical journal 2015 19 (3): 172-6. Naseri Mohsen, Hedayati Mehdi, Daneshpour Maryam Sadat, Bandarian Fatemeh, Azizi Fereido |
The effect of weight loss on HDL subfractions and LCAT activity in two genotypes of APOA-II -265T>C polymorphism. Nutrition journal 2017 May 16 (1): 34. Moradi Masoumeh, Mahmoudi Maryam, Saedisomeolia Ahmad, Zahirihashemi Roxana, Koohdani Fari |
Plasma levels of Apolipoprotein A1 and Lecithin:Cholesterol Acyltransferase in type 2 diabetes mellitus: Correlations with haptoglobin phenotypes. Diabetes & metabolic syndrome 2017 Apr . Awadallah Samir, Madkour Mohammed, Hamidi Reem Al, Alwafa Esraa Abo, Hattab Maram, Zakkour Buhour, Al-Matroushi Amna, Ahmed Eslah, Al-Kitbi Mari |
Polymorphisms of lipid metabolism enzyme-coding genes in patients with diabetic dyslipidemia. Anatolian journal of cardiology 2017 Mar . Tetik Vardarl? Asl?, Harman Ece, Bozok Çetinta? Vildan, Kay?kç?o?lu Meral, Vardarl? Egemen, Zengi Ayhan, Küçükaslan Ali ?ahin, Ero?lu Zuh |
The Effect of apoM Polymorphism Associated with HDL Metabolism on Obese Korean Adults. Journal of nutrigenetics and nutrigenomics 2017 Mar 9 (5-6): 306-317. Lee Myoungsook, Kim Jung-Im, Choi Seojin, Jang Yangsoo, Sorn Sungbin Richa |
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
PLoS genetics 2017 Oct 13 (10): e1007079. Davis James P, Huyghe Jeroen R, Locke Adam E, Jackson Anne U, Sim Xueling, Stringham Heather M, Teslovich Tanya M, Welch Ryan P, Fuchsberger Christian, Narisu Narisu, Chines Peter S, Kangas Antti J, Soininen Pasi, Ala-Korpela Mika, Kuusisto Johanna, Collins Francis S, Laakso Markku, Boehnke Michael, Mohlke Karen |
Large-scale deletions of the ABCA1 gene in patients with hypoalphalipoproteinemia. Journal of lipid research 2018 6 59 (8): 1529-1535. Dron Jacqueline S, Wang Jian, Berberich Amanda J, Iacocca Michael A, Cao Henian, Yang Ping, Knoll Joan, Tremblay Karine, Brisson Diane, Netzer Christian, Gouni-Berthold Ioanna, Gaudet Daniel, Hegele Robert |
Plasma PCSK9 levels and lipoprotein distribution are preserved in carriers of genetic HDL disorders. Biochimica et biophysica acta. Molecular and cell biology of lipids 2018 6 1863 (9): 991-997. Ruscica Massimiliano, Simonelli Sara, Botta Margherita, Ossoli Alice, Lupo Maria Giovanna, Magni Paolo, Corsini Alberto, Arca Marcello, Pisciotta Livia, Veglia Fabrizio, Franceschini Guido, Ferri Nicola, Calabresi Lau |
Interactions among genes involved in reverse cholesterol transport and in the response to environmental factors in dyslipidemia in subjects from the Xinjiang rural area. PloS one 2018 13 (5): e0196042. Wang Xinping, Guo Heng, Li Yu, Wang Haixia, He Jia, Mu Lati, Hu Yunhua, Ma Jiaolong, Yan Yizhong, Li Shugang, Ding Yusong, Zhang Mei, Niu Qiang, Liu Jiaming, Zhang Jingyu, Ma Rulin, Guo Shux |
CETP and LCAT Gene Polymorphisms Are Associated with High-Density Lipoprotein Subclasses and Acute Coronary Syndrome. Lipids 2018 Feb 53 (2): 157-166. Vargas-Alarcon Gilberto, Perez-Mendez Oscar, Herrera-Maya Gabriel, Garcia-Sanchez Cynthia, Martinez-Rios Marco Antonio, Peña-Duque Marco Antonio, Posadas-Sanchez Rosalinda, Posadas-Romero Carlos, Escobedo Galileo, Fragoso Jose Manu |
Identification and functional analysis of missense mutations in the lecithin cholesterol acyltransferase gene in a Chilean patient with hypoalphalipoproteinemia. Lipids in health and disease 2019 6 18 (1): 132. Tobar Hugo E, Cataldo Luis R, González Trinidad, Rodríguez Ricardo, Serrano Valentina, Arteaga Antonio, Álvarez-Mercado Ana, Lagos Carlos F, Vicuña Lucas, Miranda José P, Pereira Ana, Bravo Carolina, Aguilera Concepción M, Eyheramendy Susana, Uauy Ricardo, Martínez Álvaro, Gil Ángel, Francone Omar, Rigotti Attilio, Santos José |
Structure-function analysis of naturally occurring apolipoprotein A-I L144R, A164S and L178P mutants provides insight on their role on HDL levels and cardiovascular risk. Cellular and molecular life sciences : CMLS 2020 7 78 (4): 1523-1544. Gkolfinopoulou Christina, Soukou Faye, Dafnis Ioannis, Kellici Tahsin F, Sanoudou Despina, Mavromoustakos Thomas, Stratikos Efstratios, Chroni Angeli |
Candidate Gene Analysis Reveals Strong Association of CETP Variants With High Density Lipoprotein Cholesterol and PCSK9 Variants With Low Density Lipoprotein Cholesterol in Ghanaian Adults: An AWI-Gen Sub-Study. Frontiers in genetics 2020 11 456661. Agongo Godfred, Amenga-Etego Lucas, Nonterah Engelbert A, Debpuur Cornelius, Choudhury Ananyo, Bentley Amy R, Oduro Abraham R, Rotimi Charles N, Crowther Nigel J, Ramsay Michèle, , H Afric |
Single nucleotide polymorphisms in LCAT may contribute to dyslipidaemia in HIV-infected individuals on HAART in a Ghanaian population. Scientific reports 2020 11 10 (1): 19419. Bani Simon Bannison, Danquah Kwabena Owusu, Obirikorang Christian, Owiredu William K B A, Quaye Lawrence, Muonir Der Edmund, Acheampong Emmanuel, Adams Yussif, Dapare Peter Paul M, Banyeh Moses, Anto Enoch Odame, Sakyi Samuel Asamo |
Plasma FA composition in familial LCAT deficiency indicates SOAT2-derived cholesteryl ester formation in humans. Journal of lipid research 2022 5 63 (7): 100232. Pavanello Chiara, Ossoli Alice, Strazzella Arianna, Risè Patrizia, Veglia Fabrizio, Lhomme Marie, Parini Paolo, Calabresi Lau |
Familial lecithin-cholesterol acyltransferase deficiency: If so rare, why so frequent in the state of Piauí, northeastern Brazil? Molecular genetics and metabolism reports 2022 3 30 100840. de Serpa Brandão Rafael Melo Santos, Britto Fábio Barros, do Monte Neto José Tiburcio, Lima Marcelo Cunha, do Monte Semiramis Jamil Hadad, de Sousa Lima Antonio Vanildo, Pereira Ester Miranda, da Silva Higo José Neri, Oliveira Deylane Menezes Teles E, Coelho Antonio Gilberto Borges, da Silva Adalberto Socor |
Apolipoprotein E isoforms differentially affect LCAT-dependent cholesterol esterification. Atherosclerosis 2023 9 382 117266. Cecilia Vitali, Chiara Pavanello, Marta Turri, Sissel Lund-Katz, Michael C Phillips, Alberico Luigi Catapano, Andrea Baragetti, Giuseppe Danilo Norata, Fabrizio Veglia, Laura Calabre |
Association of metallothionein 2A rs10636 with low mean corpuscular volume (MCV), low mean corpuscular haemoglobin (MCH) in healthy Taiwanese. Scientific reports 2023 1 13 (1): 1292. Chen Rong-Fu, Chen Po-Ming, Pan Chau-Shiung, Huang Chieh-Cheng, Chiang En-Pei Isab |
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- Page last updated:Apr 29, 2024
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