HuGE Literature Finder
Records 1-16
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ACE2, TMPRSS2, and Furin variants and SARS-CoV-2 infection in Madrid, Spain.
Journal of medical virology 2020 Jul . Torre-Fuentes Laura, Matías-Guiu Jorge, Hernández-Lorenzo Laura, Montero-Escribano Paloma, Pytel Vanesa, Porta-Etessam Jesús, Gómez-Pinedo Ulises, Matías-Guiu Jordi |
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Influence of a Coronary Artery Disease-Associated Genetic Variant on FURIN Expression and Effect of Furin on Macrophage Behavior.
Arteriosclerosis, thrombosis, and vascular biology 2018 Jul . Zhao Guojun, Yang Wei, Wu Jingchun, Chen Bairu, Yang Xu, Chen Junhui, McVey David G, Andreadi Catherine, Gong Peng, Webb Tom R, Samani Nilesh J, Ye S |
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Frequency, impact and a preclinical study of novel
Therapeutic advances in medical oncology 2018 10 1758835918778297. Elster Naomi, Toomey Sinead, Fan Yue, Cremona Mattia, Morgan Clare, Weiner Gorzel Karolina, Bhreathnach Una, Milewska Malgorzata, Murphy Madeline, Madden Stephen, Naidoo Jarushka, Fay Joanna, Kay Elaine, Carr Aoife, Kennedy Sean, Furney Simon, Mezynski Janusz, Breathhnach Oscar, Morris Patrick, Grogan Liam, Hill Arnold, Kennedy Susan, Crown John, Gallagher William, Hennessy Bryan, Eustace Al |
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Association of Rs2071410 on Furin with Transient Ischemic Attack Susceptibility and Prognosis in a Chinese Population.
Medical science monitor : international medical journal of experimental and clinical research 2016 Oct 22 3828-3834. Sun Qin-Xiang, Zhou Hai-Mei, Du Qing-W |
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Gene expression elucidates functional impact of polygenic risk for schizophrenia.
Nature neuroscience 2016 Sep . Fromer Menachem, Roussos Panos, Sieberts Solveig K, Johnson Jessica S, Kavanagh David H, Perumal Thanneer M, Ruderfer Douglas M, Oh Edwin C, Topol Aaron, Shah Hardik R, Klei Lambertus L, Kramer Robin, Pinto Dalila, Gümü? Zeynep H, Cicek A Ercument, Dang Kristen K, Browne Andrew, Lu Cong, Xie Lu, Readhead Ben, Stahl Eli A, Xiao Jianqiu, Parvizi Mahsa, Hamamsy Tymor, Fullard John F, Wang Ying-Chih, Mahajan Milind C, Derry Jonathan M J, Dudley Joel T, Hemby Scott E, Logsdon Benjamin A, Talbot Konrad, Raj Towfique, Bennett David A, De Jager Philip L, Zhu Jun, Zhang Bin, Sullivan Patrick F, Chess Andrew, Purcell Shaun M, Shinobu Leslie A, Mangravite Lara M, Toyoshiba Hiroyoshi, Gur Raquel E, Hahn Chang-Gyu, Lewis David A, Haroutunian Vahram, Peters Mette A, Lipska Barbara K, Buxbaum Joseph D, Schadt Eric E, Hirai Keisuke, Roeder Kathryn, Brennand Kristen J, Katsanis Nicholas, Domenici Enrico, Devlin Bernie, Sklar Pame |
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Association of genetic variants with dyslipidemia.
Molecular medicine reports 2015 Oct 12 (4): 5429-36. Abe Shintaro, Tokoro Fumitaka, Matsuoka Reiko, Arai Masazumi, Noda Toshiyuki, Watanabe Sachiro, Horibe Hideki, Fujimaki Tetsuo, Oguri Mitsutoshi, Kato Kimihiko, Minatoguchi Shinya, Yamada Yoshi |
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Diagnostic utility of BNP, corin and furin as biomarkers for cardiovascular complications in type 2 diabetes mellitus patients.
Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals 2015 Oct 1-10. Fathy Shadia A, Abdel Hamid Fatma F, Zabut Baker M, Jamee Amal F, Ali Mohamed A M, Abu Mustafa Ayman |
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Single Nucleotide Polymorphism (rs4932178) in the P1 Promoter of FURIN Is Not Prognostic to Colon Cancer.
BioMed research international 2015 2015 321276. Declercq Jeroen, Jacobs Bart, Biesmans Bart, Roth Arnaud, Klingbiel Dirk, Tejpar Sabine, Creemers John |
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[Relationship between genetic variation of furin gene and hypercholesterolemia and hyper-low-density lipoprotein cholesterolemia in Kazakh general population].
Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae 2014 Apr 36 (2): 168-75. Wang Hong-mei, Li Nan-fang, Hong Jing, Luo Wen-li, Yan Zhi-tao, Wang Xin-ling, Zhu Yi, Shen Y |
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[Association between sequence variation of Furin gene and obesity in ethnic Kazakh from Xinjiang].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2013 Apr 30 (2): 227-32. Wang Hong-mei, Shen Yan, Hong Jing, Zhou Ling, Luo Wen-li, Wang Xin-ling, Zhu Yi, Li Nan-fa |
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Loci influencing blood pressure identified using a cardiovascular gene-centric array.
Human molecular genetics 2013 Apr 22 (8): 1663-78. Ganesh Santhi K, Tragante Vinicius, Guo Wei, Guo Yiran, Lanktree Matthew B, Smith Erin N, Johnson Toby, Castillo Berta Almoguera, Barnard John, Baumert Jens, Chang Yen-Pei Christy, Elbers Clara C, Farrall Martin, Fischer Mary E, Franceschini Nora, Gaunt Tom R, Gho Johannes M I H, Gieger Christian, Gong Yan, Isaacs Aaron, Kleber Marcus E, Mateo Leach Irene, McDonough Caitrin W, Meijs Matthijs F L, Mellander Olle, Molony Cliona M, Nolte Ilja M, Padmanabhan Sandosh, Price Tom S, Rajagopalan Ramakrishnan, Shaffer Jonathan, Shah Sonia, Shen Haiqing, Soranzo Nicole, van der Most Peter J, Van Iperen Erik P A, Van Setten Jessica, Van Setten Jessic A, Vonk Judith M, Zhang Li, Beitelshees Amber L, Berenson Gerald S, Bhatt Deepak L, Boer Jolanda M A, Boerwinkle Eric, Burkley Ben, Burt Amber, Chakravarti Aravinda, Chen Wei, Cooper-Dehoff Rhonda M, Curtis Sean P, Dreisbach Albert, Duggan David, Ehret Georg B, Fabsitz Richard R, Fornage Myriam, Fox Ervin, Furlong Clement E, Gansevoort Ron T, Hofker Marten H, Hovingh G Kees, Kirkland Susan A, Kottke-Marchant Kandice, Kutlar Abdullah, Lacroix Andrea Z, Langaee Taimour Y, Li Yun R, Lin Honghuang, Liu Kiang, Maiwald Steffi, Malik Rainer, , Murugesan Gurunathan, Newton-Cheh Christopher, O'Connell Jeffery R, Onland-Moret N Charlotte, Ouwehand Willem H, Palmas Walter, Penninx Brenda W, Pepine Carl J, Pettinger Mary, Polak Joseph F, Ramachandran Vasan S, Ranchalis Jane, Redline Susan, Ridker Paul M, Rose Lynda M, Scharnag Hubert, Schork Nicholas J, Shimbo Daichi, Shuldiner Alan R, Srinivasan Sathanur R, Stolk Ronald P, Taylor Herman A, Thorand Barbara, Trip Mieke D, van Duijn Cornelia M, Verschuren W Monique, Wijmenga Cisca, Winkelmann Bernhard R, Wyatt Sharon, Young J Hunter, Boehm Bernhard O, Caulfield Mark J, Chasman Daniel I, Davidson Karina W, Doevendans Pieter A, Fitzgerald Garret A, Gums John G, Hakonarson Hakon, Hillege Hans L, Illig Thomas, Jarvik Gail P, Johnson Julie A, Kastelein John J P, Koenig Wolfgang, , März Winfried, Mitchell Braxton D, Murray Sarah S, Oldehinkel Albertine J, Rader Daniel J, Reilly Muredach P, Reiner Alex P, Schadt Eric E, Silverstein Roy L, Snieder Harold, Stanton Alice V, Uitterlinden André G, van der Harst Pim, van der Schouw Yvonne T, Samani Nilesh J, Johnson Andrew D, Munroe Patricia B, de Bakker Paul I W, Zhu Xiaofeng, Levy Daniel, Keating Brendan J, Asselbergs Folkert |
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
Nature 2011 Oct 478 (7367): 7367. Ehret GB, Munroe PB, Rice KM, Bochud M, Johnson AD, Chasman DI, Smith AV, Tobin MD, Verwoert GC, Hwang SJ, Pihur V, Vollenweider P, O'Reilly PF, Amin N, Bragg-Gresham JL, Teumer A, Glazer NL, Launer L, Zhao JH, Aulchenko Y, Heath S, Sõber S, Parsa A, Luan J, Arora P, Dehghan A, Zhang F, Lucas G, Hicks AA, Jackson AU, Peden JF, Tanaka T, Wild SH, Rudan I, Igl W, Milaneschi Y, Parker AN, Fava C, Chambers JC, Fox ER, Kumari M, Go MJ, van der Harst P, Kao WH, Sjögren M, Vinay DG, Alexander M, Tabara Y, Shaw-Hawkins S, Whincup PH, Liu Y, Shi G, Kuusisto J, Tayo B, Seielstad M, Sim X, Nguyen KD, Lehtimäki T, Matullo G, Wu Y, Gaunt TR, Onland-Moret NC, Cooper MN, Platou CG, Org E, Hardy R, Dahgam S, Palmen J, Vitart V, Braund PS, Kuznetsova T, Uiterwaal CS, Adeyemo A, Palmas W, Campbell H, Ludwig B, Tomaszewski M, Tzoulaki I, Palmer ND, Aspelund T, Garcia M, Chang YP, O'Connell JR, Steinle NI, Grobbee DE, Arking DE, Kardia SL, Morrison AC, Hernandez D, Najjar S, McArdle WL, Hadley D, Brown MJ, Connell JM, Hingorani AD, Day IN, Lawlor DA, Beilby JP, Lawrence RW, Clarke R, Hopewell JC, Ongen H, Dreisbach AW, Li Y, Young JH, Bis JC, Kähönen M, Viikari J, Adair LS, Lee NR, Chen MH, Olden M, Pattaro C, Bolton JA, Köttgen A, Bergmann S, Mooser V, Chaturvedi N, Frayling TM, Islam M, Jafar TH, Erdmann J, Kulkarni SR, Bornstein SR, Grässler J, Groop L, Voight BF, Kettunen J, Howard P, Taylor A, Guarrera S, Ricceri F, Emilsson V, Plump A, Barroso I, Khaw KT, Weder AB, Hunt SC, Sun YV, Bergman RN, Collins FS, Bonnycastle LL, Scott LJ, Stringham HM, Peltonen L, Perola M, Vartiainen E, Brand SM, Staessen JA, Wang TJ, Burton PR, Soler Artigas M, Dong Y, Snieder H, Wang X, Zhu H, Lohman KK, Rudock ME, Heckbert SR, Smith NL, Wiggins KL, Doumatey A, Shriner D, Veldre G, Viigimaa M, Kinra S, Prabhakaran D, Tripathy V, Langefeld CD, Rosengren A, Thelle DS, Corsi AM, Singleton A, Forrester T, Hilton G, McKenzie CA, Salako T, Iwai N, Kita Y, Ogihara T, Ohkubo T, Okamura T, Ueshima H, Umemura S, Eyheramendy S, Meitinger T, Wichmann HE, Cho YS, Kim HL, Lee JY, Scott J, Sehmi JS, Zhang W, Hedblad B, Nilsson P, Smith GD, Wong A, Narisu N, Stan?áková A, Raffel LJ, Yao J, Kathiresan S, O'Donnell CJ, Schwartz SM, Ikram MA, Longstreth WT, Mosley TH, Seshadri S, Shrine NR, Wain LV, Morken MA, Swift AJ, Laitinen J, Prokopenko I, Zitting P, Cooper JA, Humphries SE, Danesh J, Rasheed A, Goel A, Hamsten A, Watkins H, Bakker SJ, van Gilst WH, Janipalli CS, Mani KR, Yajnik CS, Hofman A, Mattace-Raso FU, Oostra BA, Demirkan A, Isaacs A, Rivadeneira F, Lakatta EG, Orru M, Scuteri A, Ala-Korpela M, Kangas AJ, Lyytikäinen LP, Soininen P, Tukiainen T, Würtz P, Ong RT, Dörr M, Kroemer HK, Völker U, Völzke H, Galan P, Hercberg S, Lathrop M, Zelenika D, Deloukas P, Mangino M, Spector TD, Zhai G, Meschia JF, Nalls MA, Sharma P, Terzic J, Kumar MV, Denniff M, Zukowska-Szczechowska E, Wagenknecht LE, Fowkes FG, Charchar FJ, Schwarz PE, Hayward C, Guo X, Rotimi C, Bots ML, Brand E, Samani NJ, Polasek O, Talmud PJ, Nyberg F, Kuh D, Laan M, Hveem K, Palmer LJ, van der Schouw YT, Casas JP, Mohlke KL, Vineis P, Raitakari O, Ganesh SK, Wong TY, Tai ES, Cooper RS, Laakso M, Rao DC, Harris TB, Morris RW, Dominiczak AF, Kivimaki M, Marmot MG, Miki T, Saleheen D, Chandak GR, Coresh J, Navis G, Salomaa V, Han BG, Zhu X, Kooner JS, Melander O, Ridker PM, Bandinelli S, Gyllensten UB, Wright AF, Wilson JF, Ferrucci L, Farrall M, Tuomilehto J, Pramstaller PP, Elosua R, Soranzo N, Sijbrands EJ, Altshuler D, Loos RJ, Shuldiner AR, Gieger C, Meneton P, Uitterlinden AG, Wareham NJ, Gudnason V, Rotter JI, Rettig R, Uda M, Strachan DP, Witteman JC, Hartikainen AL, Beckmann JS, Boerwinkle E, Vasan RS, Boehnke M, Larson MG, Järvelin MR, Psaty BM, Abecasis GR, Chakravarti A, Elliott P, van Duijn CM, Newton-Cheh C, Levy D, Caulfield MJ, Johnson T |
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Polymorphisms in the transforming growth factor beta 1 pathway in relation to colorectal cancer progression.
Genes, chromosomes & cancer 2010 Mar 49 (3): 270-81. Försti Asta, Li Xuchen, Wagner Kerstin, Tavelin Björn, Enquist Kerstin, Palmqvist Richard, Altieri Andrea, Hallmans Göran, Hemminki Kari, Lenner P |
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Associations between genetic variations in the FURIN gene and hypertension.
BMC medical genetics 2010 11 (1): 124. Li Nanfang, Luo Wenli, Juhong Zhang, Yang Jin, Wang Hongmei, Zhou Ling, Chang Jianha |
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Influence of a single nucleotide polymorphism in the P1 promoter of the furin gene on transcription activity and hepatitis B virus infection.
Hepatology (Baltimore, Md.) 2009 Sep 50 (3): 763-71. Lei Rui Xiang, Shi Hong, Peng Xiao Mou, Zhu Yin Hong, Cheng Jie, Chen Gui H |
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Mutation analysis of hepcidin and ferroportin genes in Italian prospective blood donors with iron overload.
American journal of hematology 2009 Sep 84 (9): 592-3. Duca Lorena, Delbini Paola, Nava Isabella, Vaja Valentina, Fiorelli Gemino, Cappellini Maria Domeni |
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- Page last updated:Jan 19, 2021
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