Human Genome Epidemiology Literature Finder
Records 1 - 16 (of 16 Records) |
Query Trace: PCSK7[original query] |
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Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels.
Human molecular genetics 2011 Mar 20 (5): 1042-7. Oexle Konrad, Ried Janina S, Hicks Andrew A, Tanaka Toshiko, Hayward Caroline, Bruegel Mathias, Gögele Martin, Lichtner Peter, Müller-Myhsok Bertram, Döring Angela, Illig Thomas, Schwienbacher Christine, Minelli Cosetta, Pichler Irene, Fiedler G Martin, Thiery Joachim, Rudan Igor, Wright Alan F, Campbell Harry, Ferrucci Luigi, Bandinelli Stefania, Pramstaller Peter P, Wichmann H-Erich, Gieger Christian, Winkelmann Juliane, Meitinger Thom |
Evaluation of genome-wide loci of iron metabolism in hereditary hemochromatosis identifies PCSK7 as a host risk factor of liver cirrhosis. Human molecular genetics 2014 Jul 23 (14): 3883-90. Stickel Felix, Buch Stephan, Zoller Heinz, Hultcrantz Rolf, Gallati Sabina, Österreicher Christoph, Finkenstedt Armin, Stadlmayr Andreas, Aigner Elmar, Sahinbegovic Enijad, Sarrazin Christoph, Schafmayer Clemens, Braun Felix, Erhart Wiebke, Nothnagel Michael, Lerch Markus M, Mayerle Julia, Völzke Henry, Schaller André, Kratzer Wolfgang, Boehm Bernhard O, Sipos Bence, D'Amato Mauro, Torkvist Leif, Stal Per, Arlt Alexander, Franke Andre, Becker Thomas, Krawczak Michael, Zwerina Jochen, Berg Thomas, Hinrichsen Holger, Krones Elisabeth, Dejaco Christian, Strasser Michael, Datz Christian, Hampe Joch |
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks.
American journal of human genetics 2014 Feb 94 (2): 223-32. Peloso Gina M, Auer Paul L, Bis Joshua C, Voorman Arend, Morrison Alanna C, Stitziel Nathan O, Brody Jennifer A, Khetarpal Sumeet A, Crosby Jacy R, Fornage Myriam, Isaacs Aaron, Jakobsdottir Johanna, Feitosa Mary F, Davies Gail, Huffman Jennifer E, Manichaikul Ani, Davis Brian, Lohman Kurt, Joon Aron Y, Smith Albert V, Grove Megan L, Zanoni Paolo, Redon Valeska, Demissie Serkalem, Lawson Kim, Peters Ulrike, Carlson Christopher, Jackson Rebecca D, Ryckman Kelli K, Mackey Rachel H, Robinson Jennifer G, Siscovick David S, Schreiner Pamela J, Mychaleckyj Josyf C, Pankow James S, Hofman Albert, Uitterlinden Andre G, Harris Tamara B, Taylor Kent D, Stafford Jeanette M, Reynolds Lindsay M, Marioni Riccardo E, Dehghan Abbas, Franco Oscar H, Patel Aniruddh P, Lu Yingchang, Hindy George, Gottesman Omri, Bottinger Erwin P, Melander Olle, Orho-Melander Marju, Loos Ruth J F, Duga Stefano, Merlini Piera Angelica, Farrall Martin, Goel Anuj, Asselta Rosanna, Girelli Domenico, Martinelli Nicola, Shah Svati H, Kraus William E, Li Mingyao, Rader Daniel J, Reilly Muredach P, McPherson Ruth, Watkins Hugh, Ardissino Diego, , Zhang Qunyuan, Wang Judy, Tsai Michael Y, Taylor Herman A, Correa Adolfo, Griswold Michael E, Lange Leslie A, Starr John M, Rudan Igor, Eiriksdottir Gudny, Launer Lenore J, Ordovas Jose M, Levy Daniel, Chen Y-D Ida, Reiner Alexander P, Hayward Caroline, Polasek Ozren, Deary Ian J, Borecki Ingrid B, Liu Yongmei, Gudnason Vilmundur, Wilson James G, van Duijn Cornelia M, Kooperberg Charles, Rich Stephen S, Psaty Bruce M, Rotter Jerome I, O'Donnell Christopher J, Rice Kenneth, Boerwinkle Eric, Kathiresan Sekar, Cupples L Adrien |
PCSK7 genotype modifies effect of a weight-loss diet on 2-year changes of insulin resistance: the POUNDS LOST trial. Diabetes care 2015 Mar 38 (3): 439-44. Huang Tao, Huang Jinyan, Qi Qibin, Li Yanping, Bray George A, Rood Jennifer, Sacks Frank M, Qi |
Multiple susceptibility loci at chromosome 11q23.3 are associated with plasma triglyceride in East Asians. Journal of lipid research 2015 Dec . Gombojav Bayasgalan, Lee Soo Ji, Kho Minjung, Song Yun-Mi, Lee Kayoung, Sung Jooh |
Proprotein convertase 7 rs236918 associated with liver fibrosis in Italian patients with HFE-related hemochromatosis. Journal of gastroenterology and hepatology 2016 Feb . Pelucchi Sara, Galimberti Stefania, Greni Federico, Rametta Raffaela, Mariani Raffaella, Pelloni Irene, Girelli Domenico, Busti Fabiana, Ravasi Giulia, Valsecchi Maria Grazia, Valenti Luca, Piperno Alber |
Genome-wide association study of serum lipids confirms previously reported associations as well as new associations of common SNPs within PCSK7 gene with triglyceride.
Journal of human genetics 2016 Jan . Kurano Makoto, Tsukamoto Kazuhisa, Kamitsuji Shigeo, Kamatani Naoyuki, Hara Masumi, Ishikawa Toshio, Kim Bong-Jo, Moon Sanghoon, Jin Kim Young, Teramoto Tam |
A single-nucleotide polymorphism in transferrin is associated with soluble transferrin receptor in Chinese adolescents. Asia Pacific journal of clinical nutrition 2017 26 (6): 1170-1178. Piao Wei, Wang Li, Zhang Ting, Wang Zhen, Shangguan Shaofang, Sun Jing, Huo Junshe |
PNPLA3 and RNF7 Gene Variants are Associated with the Risk of Developing Liver Fibrosis and Cirrhosis in an Eastern European Population. Journal of gastrointestinal and liver diseases : JGLD 2017 Mar 26 (1): 37-43. Kupcinskas Juozas, Valantiene Irena, Varkalaite Greta, Steponaitiene Ruta, Skieceviciene Jurgita, Sumskiene Jolanta, Petrenkiene Vitalija, Kondrackiene Jurate, Kiudelis Gediminas, Lammert Frank, Kupcinskas Lim |
Rare Copy Number Variants Identify Novel Genes in Sporadic Total Anomalous Pulmonary Vein Connection. Frontiers in genetics 2018 9 559. Shi Xin, Cheng Liangping, Jiao XianTing, Chen Bo, Li Zixiong, Liang Yulai, Liu Wei, Wang Jing, Liu Gang, Xu Yuejuan, Sun Jing, Fu Qihua, Lu Yanan, Chen S |
PCSK7 gene variation bridges atherogenic dyslipidemia with hepatic inflammation in NAFLD patients. Journal of lipid research 2019 Mar . Dongiovanni Paola, Meroni Marica, Baselli Guido, Mancina Rosellina M, Ruscica Massimiliano, Longo Miriam, Rametta Raffaela, Cespiati Annalisa, Pelusi Serena, Ferri Nicola, Ranzani Valeria, Nobili Valerio, Pihlajamaki Jussi, Fracanzani Anna Ludovica, Badiali Sara, Petta Salvatore, Fargion Silvia, Romeo Stefano, Kozlitina Julia, Valenti Lu |
Proprotein convertase 7 (PCSK7) reduces apoA-V levels. The FEBS journal 2020 Jan . Ashraf Yahya, Duval Stéphanie, Sachan Vatsal, Essalmani Rachid, Susan-Resiga Delia, Roubtsova Anna, Hamelin Josée, Gerhardy Stefan, Kirchhofer Daniel, Tagliabracci Vincent S, Prat Annik, Kiss Robert Scott, Seidah Nabil |
The rs508487, rs236911, and rs236918 Genetic Variants of the Proprotein Convertase Subtilisin-Kexin Type 7 (PCSK7) Gene Are Associated with Acute Coronary Syndrome and with Plasma Concentrations of HDL-Cholesterol and Triglycerides. Cells 2021 Jun 10 (6): . Vargas-Alarcón Gilberto, Pérez-Méndez Oscar, González-Pacheco Héctor, Ramírez-Bello Julián, Posadas-Sánchez Rosalinda, Escobedo Galileo, Fragoso José Manu |
Variants in PCSK7, PNPLA3 and TM6SF2 are risk factors for the development of cirrhosis in hereditary haemochromatosis. Alimentary pharmacology & therapeutics 2021 Feb . Buch Stephan, Sharma Aneesh, Ryan Eleanor, Datz Christian, Griffiths William J H, Way Michael, Buckley Thomas W M, Ryan John D, Stewart Stephen, Wright Callum, Dongiovanni Paola, Fracanzani Anna, Zwerina Jochen, Merle Uta, Weiss Karl Heinz, Aigner Elmar, Krones Elisabeth, Dejaco Christian, Fischer Janett, Berg Thomas, Valenti Luca, Zoller Heinz, McQuillin Andrew, Hampe Jochen, Stickel Felix, Morgan Marsha |
Variations in TM6SF2, PCSK9 and PCSK7 genes and risk of hepatic steatosis after liver transplantation: a cross-sectional study. BMC gastroenterology 2021 12 21 (1): 458. Eshraghian Ahad, Moasser Elham, Azarpira Negar, Fattahi Mohammad Reza, Nikeghbalian Saman, Malek-Hosseini Seyed Ali, Geramizadeh Bi |
Identification of novel non-HFE mutations in Chinese patients with hereditary hemochromatosis. Orphanet journal of rare diseases 2022 6 17 (1): 216. Zhang Wei, Li Yanmeng, Xu Anjian, Ouyang Qin, Wu Liyan, Zhou Donghu, Wu Lina, Zhang Bei, Zhao Xinyan, Wang Yu, Wang Xiaoming, Duan Weijia, Wang Qianyi, You Hong, Huang Jian, Ou Xiaojuan, Jia Jidong, |
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