Human Genome Epidemiology Literature Finder
Records 1 - 26 (of 26 Records) |
Query Trace: ACTA2[original query] |
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Mutation of ACTA2 gene as an important cause of familial and nonfamilial nonsyndromatic thoracic aortic aneurysm and/or dissection (TAAD). Human mutation 2009 Oct 30 (10): 1406-11. Morisaki Hiroko, Akutsu Koichi, Ogino Hitoshi, Kondo Norihiro, Yamanaka Itaru, Tsutsumi Yoshiaki, Yoshimuta Tsuyoshi, Okajima Toshiya, Matsuda Hitoshi, Minatoya Kenji, Sasaki Hiroaki, Tanaka Hiroshi, Ishibashi-Ueda Hatsue, Morisaki Takayu |
Risk of dissection in thoracic aneurysms associated with mutations of smooth muscle alpha-actin 2 (ACTA2). Heart (British Cardiac Society) 2011 Feb 97 (4): 321-6. Disabella Eliana, Grasso Maurizia, Gambarin Fabiana Isabella, Narula Nupoor, Dore Roberto, Favalli Valentina, Serio Alessandra, Antoniazzi Elena, Mosconi Mario, Pasotti Michele, Odero Attilio, Arbustini Eloi |
TGFßRIIb mutations trigger aortic aneurysm pathogenesis by altering transforming growth factor ß2 signal transduction. Circulation. Cardiovascular genetics 2012 Dec 5 (6): 621-9. Bee Katharine J, Wilkes David C, Devereux Richard B, Basson Craig T, Hatcher Cathy |
Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia.
Nature genetics 2013 Aug 45 (8): 868-76. Berndt Sonja I, Skibola Christine F, Joseph Vijai, Camp Nicola J, Nieters Alexandra, Wang Zhaoming, Cozen Wendy, Monnereau Alain, Wang Sophia S, Kelly Rachel S, Lan Qing, Teras Lauren R, Chatterjee Nilanjan, Chung Charles C, Yeager Meredith, Brooks-Wilson Angela R, Hartge Patricia, Purdue Mark P, Birmann Brenda M, Armstrong Bruce K, Cocco Pierluigi, Zhang Yawei, Severi Gianluca, Zeleniuch-Jacquotte Anne, Lawrence Charles, Burdette Laurie, Yuenger Jeffrey, Hutchinson Amy, Jacobs Kevin B, Call Timothy G, Shanafelt Tait D, Novak Anne J, Kay Neil E, Liebow Mark, Wang Alice H, Smedby Karin E, Adami Hans-Olov, Melbye Mads, Glimelius Bengt, Chang Ellen T, Glenn Martha, Curtin Karen, Cannon-Albright Lisa A, Jones Brandt, Diver W Ryan, Link Brian K, Weiner George J, Conde Lucia, Bracci Paige M, Riby Jacques, Holly Elizabeth A, Smith Martyn T, Jackson Rebecca D, Tinker Lesley F, Benavente Yolanda, Becker Nikolaus, Boffetta Paolo, Brennan Paul, Foretova Lenka, Maynadie Marc, McKay James, Staines Anthony, Rabe Kari G, Achenbach Sara J, Vachon Celine M, Goldin Lynn R, Strom Sara S, Lanasa Mark C, Spector Logan G, Leis Jose F, Cunningham Julie M, Weinberg J Brice, Morrison Vicki A, Caporaso Neil E, Norman Aaron D, Linet Martha S, De Roos Anneclaire J, Morton Lindsay M, Severson Richard K, Riboli Elio, Vineis Paolo, Kaaks Rudolph, Trichopoulos Dimitrios, Masala Giovanna, Weiderpass Elisabete, Chirlaque María-Dolores, Vermeulen Roel C H, Travis Ruth C, Giles Graham G, Albanes Demetrius, Virtamo Jarmo, Weinstein Stephanie, Clavel Jacqueline, Zheng Tongzhang, Holford Theodore R, Offit Kenneth, Zelenetz Andrew, Klein Robert J, Spinelli John J, Bertrand Kimberly A, Laden Francine, Giovannucci Edward, Kraft Peter, Kricker Anne, Turner Jenny, Vajdic Claire M, Ennas Maria Grazia, Ferri Giovanni M, Miligi Lucia, Liang Liming, Sampson Joshua, Crouch Simon, Park Ju-Hyun, North Kari E, Cox Angela, Snowden John A, Wright Josh, Carracedo Angel, Lopez-Otin Carlos, Bea Silvia, Salaverria Itziar, Martin-Garcia David, Campo Elias, Fraumeni Joseph F, de Sanjose Silvia, Hjalgrim Henrik, Cerhan James R, Chanock Stephen J, Rothman Nathaniel, Slager Susan |
Acute aortic dissections with pregnancy in women with ACTA2 mutations. American journal of medical genetics. Part A 2014 Jan 164A (1): 106-12. Regalado Ellen S, Guo Dong-chuan, Estrera Anthony L, Buja L Maximilian, Milewicz Dianna |
Correlation between single nucleotide polymorphisms of the ACTA2 gene and coronary artery stenosis in patients with type 2 diabetes mellitus. Experimental and therapeutic medicine 2014 Apr 7 (4): 970-976. Fang Hui, Luo Xiaoli, Wang Yan, Liu Nian, Fu Chunjiang, Wang Hongyong, Fang Yuqiang, Shi Weibin, Zhang Ye, Zeng Chunyu, Wang Xuk |
First genetic analysis of aneurysm genes in familial and sporadic abdominal aortic aneurysm. Human genetics 2015 Aug 134 (8): 881-93. van de Luijtgaarden Koen M, Heijsman Daphne, Maugeri Alessandra, Weiss Marjan M, Verhagen Hence J M, IJpma Arne, Brüggenwirth Hennie T, Majoor-Krakauer Daniel |
Polymorphisms in C-reactive protein and Glypican-5 are associated with lung cancer risk and Gartrokine-1 influences Cisplatin-based chemotherapy response in a Chinese Han population. Disease markers 2015 2015 824304. Zhang Shuo, Thakur Asmitananda, Liang Yiqian, Wang Ting, Gao Lei, Yang Tian, Li Yang, Geng Tingting, Jin Tianbo, Chen Tianjun, Liu Johnson J, Chen Mingw |
Mutation genotypes of RNF213 gene from moyamoya patients in Taiwan. Journal of the neurological sciences 2015 Jun 353 (1-2): 161-5. Lee Ming-Jen, Chen Ya-Fang, Fan Pi-Chuan, Wang Kuo-Chuan, Wang Kai, Wang Jinyuan, Kuo Meng-F |
Congenital heart defects are rarely caused by mutations in cardiac and smooth muscle actin genes. BioMed research international 2015 2015 127807. Khodyuchenko Tatiana, Zlotina Anna, Pervunina Tatiana, Zverev Dmitry, Malashicheva Anna, Kostareva An |
Alpha-actin-2 mutations in Chinese patients with a non-syndromatic thoracic aortic aneurysm. BMC medical genetics 2016 17 (1): 45. Ke Tie, Han Meng, Zhao Miao, Wang Qing Kenneth, Zhang Huazhi, Zhao Yuanyuan, Ruan Xinlong, Li Hui, Xu Chengqi, Sun Tuche |
Tobacco smoking and methylation of genes related to lung cancer development. Oncotarget 2016 Jun . Gao Xu, Zhang Yan, Breitling Lutz Philipp, Brenner Herma |
RNF213 as the major susceptibility gene for Chinese patients with moyamoya disease and its clinical relevance. Journal of neurosurgery 2017 Apr 126 (4): 1106-1113. Zhang Qian, Liu Yaping, Zhang Dong, Wang Rong, Zhang Yan, Wang Shuo, Yu Lanbing, Lu Chaoxia, Liu Fang, Zhou Jian, Zhang Xue, Zhao Jizo |
Genetic Bases of Bicuspid Aortic Valve: The Contribution of Traditional and High-Throughput Sequencing Approaches on Research and Diagnosis. Frontiers in physiology 2017 8 612. Giusti Betti, Sticchi Elena, De Cario Rosina, Magi Alberto, Nistri Stefano, Pepe Guglielmi |
Genome-Wide Interactions with Dairy Intake for Body Mass Index in Adults of European Descent. Molecular nutrition & food research 2017 Sep . Smith Caren E, Follis Jack L, Dashti Hassan S, Tanaka Toshiko, Graff Mariaelisa, Fretts Amanda M, Kilpeläinen Tuomas O, Wojczynski Mary K, Richardson Kris, Nalls Mike A, Schulz Christina-Alexandra, Liu Yongmei, Frazier-Wood Alexis C, van Eekelen Esther, Wang Carol, de Vries Paul S, Mikkilä Vera, Rohde Rebecca, Psaty Bruce M, Hansen Torben, Feitosa Mary F, Lai Chao-Qiang, Houston Denise K, Ferruci Luigi, Ericson Ulrika, Wang Zhe, de Mutsert Renée, Oddy Wendy H, de Jonge Ester A L, Seppälä Ilkka, Justice Anne E, Lemaitre Rozenn N, Sørensen Thorkild I A, Province Michael A, Parnell Laurence D, Garcia Melissa E, Bandinelli Stefania, Orho-Melander Marju, Rich Stephen S, Rosendaal Frits R, Pennell Craig E, Kiefte-de Jong Jessica C, Kähönen Mika, Young Kristin L, Pedersen Oluf, Aslibekyan Stella, Rotter Jerome I, Mook-Kanamori Dennis O, Zillikens M Carola, Raitakari Olli T, North Kari E, Overvad Kim, Arnett Donna K, Hofman Albert, Lehtimäki Terho, Tjønneland Anne, Uitterlinden André G, Rivadeneira Fernando, Franco Oscar H, German J Bruce, Siscovick David S, Cupples L Adrienne, Ordovás José |
Search for genetic factors in bicuspid aortic valve disease: ACTA2 mutations do not play a major role. Interactive cardiovascular and thoracic surgery 2017 Nov 25 (5): 813-817. Tortora Giada, Wischmeijer Anita, Berretta Paolo, Alfonsi Jacopo, Di Marco Luca, Barbieri Andrea, Marconi Caterina, Isidori Federica, Rossi Cesare, Leone Ornella, Di Bartolomeo Roberto, Seri Marco, Pacini Davi |
Genetic diagnosis of acute aortic dissection in South China Han population using next-generation sequencing. International journal of legal medicine 2018 7 132 (5): 1273-1280. Zheng Jinxiang, Guo Jian, Huang Lei, Wu Qiuping, Yin Kun, Wang Lin, Zhang Tongda, Quan Li, Zhao Qianhao, Cheng Jiandi |
Genetic basis of hereditary thoracic aortic aneurysms and dissections. Journal of cardiology 2019 4 74 (2): 136-143. Takeda Norifumi, Komuro Iss |
Acute Stanford type B aortic dissection-who benefits from genetic testing? Journal of thoracic disease 2020 12 12 (11): 6806-6812. Erhart Philipp, Gieldon Laura, Ante Marius, Körfer Daniel, Strom Tim, Grond-Ginsbach Caspar, Böckler Dittm |
Cerebrovascular Disease Progression in Patients With ACTA2 Arg179 Pathogenic Variants. Neurology 2020 11 96 (4): e538-e552. Lauer Arne, Speroni Samantha L, Patel Jay B, Regalado Ellen, Choi Myoung, Smith Edward, Kalpathy-Kramer Jayashree, Caruso Paul, Milewicz Dianna M, Musolino Patricia |
99-Case Study of Sporadic Aortic Dissection by Whole Exome Sequencing Indicated Novel Disease-Associated Genes and Variants in Chinese Population. BioMed research international 2020 2020 7857043. Wang Zanxin, Zhuang Xianmian, Chen Bailang, Wen Junmin, Peng Fang, Liu Xiling, Wei Minx |
First Report: Rare RNF213 Variant Associated with Familial Moyamoya Disease in an African American Family. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2021 10 30 (12): 106123. Sunmonu N Abimbola, Ambati Naveen Kumar, Thomas Matthew J, Ulep Robin D, Worrall Bradfo |
Comparative Risks of Initial Aortic Events Associated With Genetic Thoracic Aortic Disease. Journal of the American College of Cardiology 2022 Aug 80 (9): 857-869. Regalado Ellen S, Morris Shaine A, Braverman Alan C, Hostetler Ellen M, De Backer Julie, Li Ruosha, Pyeritz Reed E, Yetman Anji T, Cervi Elena, Shalhub Sherene, Jeremy Richmond, LeMaire Scott, Ouzounian Maral, Evangelista Arturo, Boileau Catherine, Jondeau Guillaume, Milewicz Dianna |
A highly penetrant ACTA2 mutation of thoracic aortic disease. Journal of cardiothoracic surgery 2023 12 18 (1): 352. Christopher M Bobba, Ryan Azarrafiy, John R Spratt, Jill Hendrickson, Tomas D Martin, George J Arnaoutakis, Eric I Jeng, Thomas M Beav |
Markers of extracellular matrix remodeling and systemic inflammation in patients with heritable thoracic aortic diseases. Frontiers in cardiovascular medicine 2023 1 9 1073069. Seim Bjørn Edvard, Holt Margrethe Flesvig, Ratajska Aleksandra, Michelsen Annika, Ringseth Monica Myklebust, Halvorsen Bente Evy, Skjelland Mona, Kvitting John-Peder Escobar, Lundblad Runar, Krohg-Sørensen Kirsten, Osnes Liv T N, Aukrust Pål, Paus Benedicte, Ueland Th |
The proprotein convertase FURIN is a novel aneurysm predisposition gene impairing TGF-? signaling. Cardiovascular research 2024 4 . Zongsheng He, Arne S IJpma, Dianne Vreeken, Daphne Heijsman, Karen Rosier, Hence J M Verhagen, Jorg de Bruin, Hennie T Brüggenwirth, Jolien W Roos-Hesselink, Jos A Bekkers, Danny Huylebroeck, Heleen van Beusekom, John W M Creemers, Danielle Majoor-Krakau |
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