Human Genome Epidemiology Literature Finder
Records 1 - 28 (of 28 Records) |
Query Trace: MYLK[original query] |
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Novel polymorphisms in the myosin light chain kinase gene confer risk for acute lung injury. American journal of respiratory cell and molecular biology 2006 Apr 34 (4): 487-95. Gao Li, Grant Audrey, Halder Indrani, Brower Roy, Sevransky Jonathan, Maloney James P, Moss Marc, Shanholtz Carl, Yates Charles R, Meduri Gianfranco Umberto, Shriver Mark D, Ingersoll Roxann, Scott Alan F, Beaty Terri H, Moitra Jaideep, Ma Shwu Fan, Ye Shui Q, Barnes Kathleen C, Garcia Joe G |
Polymorphisms in the myosin light chain kinase gene that confer risk of severe sepsis are associated with a lower risk of asthma. The Journal of allergy and clinical immunology 2007 May 119 (5): 1111-8. Gao Li, Grant Audrey V, Rafaels Nicholas, Stockton-Porter Maria, Watkins Tonya, Gao Peisong, Chi Peter, Muñoz Melba, Watson Harold, Dunston Georgia, Togias Alkis, Hansel Nadia, Sevransky Jonathan, Maloney James P, Moss Marc, Shanholtz Carl, Brower Roy, Garcia Joe G N, Grigoryev Dmitry N, Cheadle Christopher, Beaty Terri H, Mathias Rasika A, Barnes Kathleen |
A variant of the myosin light chain kinase gene is associated with severe asthma in African Americans. Genetic epidemiology 2007 May 31 (4): 296-305. Flores Carlos, Ma Shwu-Fan, Maresso Karen, Ober Carole, Garcia Joe G |
A common cortactin gene variation confers differential susceptibility to severe asthma. Genetic epidemiology 2008 Jun . Ma SF, Flores C, Wade MS, Dudek SM, Nicolae DL, Ober C, Garcia JG |
Interactions among genetic variants from contractile pathway of vascular smooth muscle cell in essential hypertension susceptibility of Chinese Han population. Pharmacogenetics and genomics 2008 Jun 18 (6): 459-66. Zhao Qi, Wang Laiyuan, Yang Wei, Chen Shufeng, Huang Jianfeng, Fan Zhongjie, Li Hongfan, Lu Xiangfeng, Gu Dongfe |
Variation in the myosin light chain kinase gene is associated with development of acute lung injury after major trauma. Critical care medicine 2008 Oct 36 (10): 2794-800. Christie Jason D, Ma Shwu-Fan, Aplenc Richard, Li Mingyao, Lanken Paul N, Shah Chirag V, Fuchs Barry, Albelda Steven M, Flores Carlos, Garcia Joe G |
Validation study of genetic associations with coronary artery disease on chromosome 3q13-21 and potential effect modification by smoking. Annals of human genetics 2009 Nov 73 (Pt 6): 551-8. Horne Benjamin D, Hauser Elizabeth R, Wang Liyong, Muhlestein Joseph B, Anderson Jeffrey L, Carlquist John F, Shah Svati H, Kraus William |
MYLK polymorphism associated with blood eosinophil level among asthmatic patients in a Korean population. Molecules and cells 2009 Feb 27 (2): 175-81. Lee Soo Ok, Cheong Hyun Sub, Park Byung Lae, Bae Joon Seol, Sim Won Chul, Chun Ji-Yong, Isbat Mohammad, Uh Soo-Taek, Kim Yong Hooun, Jang An-Soo, Park Choon-Sik, Shin Hyoung D |
Genetic variation in MYLK and lung injury in children and adults with community-acquired pneumonia. Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies 2010 Nov 11 (6): 731-6. Russell Rebecca, Quasney Michael W, Halligan Nadine, Li Shun-Hwa, Simpson Pippa, Waterer Grant, Wunderink Richard G, Dahmer Mary |
Heterozygote genotypes at rs2222823 and rs2811712 SNP loci are associated with cerebral small vessel disease in Han Chinese population. CNS neuroscience & therapeutics 2012 Jul 18 (7): 558-65. Li Wei, Hu Bo, Li Gui-Lin, Zhao Xing-Quan, Xin Bao-Zhong, Lin Jin-Xi, Shen Yuan, Liang Xian-Hong, Liu Gai-Fen, Gao Han-Qing, Liao Xiao-Ling, Liang Zhi-Gang, Wang Yong-J |
Genetic polymorphisms associated with exertional rhabdomyolysis. European journal of applied physiology 2013 Aug 113 (8): 1997-2004. Deuster Patricia A, Contreras-Sesvold Carmen L, O'Connor Francis G, Campbell William W, Kenney Kimbra, Capacchione John F, Landau Mark E, Muldoon Sheila M, Rushing Elisabeth J, Heled Yuv |
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 |
Epigenetic contribution of the myosin light chain kinase gene to the risk for acute respiratory distress syndrome. Translational research : the journal of laboratory and clinical medicine 2016 Aug . Szilágyi Keely L, Liu Cong, Zhang Xu, Wang Ting, Fortman Jeffrey D, Zhang Wei, Garcia Joe G |
Clinically relevant variants identified in thoracic aortic aneurysm patients by research exome sequencing. American journal of medical genetics. Part A 2016 Feb . Schubert Jeffrey A, Landis Benjamin J, Shikany Amy R, Hinton Robert B, Ware Stephanie |
Single nucleotide polymorphisms in the MYLKP1 pseudogene are associated with increased colon cancer risk in African Americans. PloS one 2018 13 (8): e0200916. Lynn Heather, Sun Xiaoguang, Ayshiev Djanybek, Siegler Jessica H, Rizzo Alicia N, Karnes Jason H, Gonzales Garay Manuel, Wang Ting, Casanova Nancy, Camp Sara M, Ellis Nathan A, Garcia Joe G |
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 |
Myosin light chain kinase ( MYLK) coding polymorphisms modulate human lung endothelial cell barrier responses via altered tyrosine phosphorylation, spatial localization, and lamellipodial protrusions. Pulmonary circulation 2018 2 8 (2): 2045894018764171. Wang Ting, Brown Mary E, Kelly Gabriel T, Camp Sara M, Mascarenhas Joseph B, Sun Xiaoguang, Dudek Steven M, Garcia Joe G |
Genetic basis of hereditary thoracic aortic aneurysms and dissections. Journal of cardiology 2019 4 74 (2): 136-143. Takeda Norifumi, Komuro Iss |
High polygenic burden is associated with blood DNA methylation changes in individuals with suicidal behavior. Journal of psychiatric research 2020 Jan 123 62-71. Cabrera-Mendoza Brenda, Martínez-Magaña José Jaime, Genis-Mendoza Alma Delia, Sarmiento Emmanuel, Ruíz-Ramos David, Tovilla-Zárate Carlos Alfonso, González-Castro Thelma Beatriz, Juárez-Rojop Isela Esther, García-de la Cruz Dulce Dajheanne, López-Armenta Mauro, Real Fernanda, García-Dolores Fernando, Flores Gonzalo, Vázquez-Roque Rubén Antonio, Lanzagorta Nuria, Escamilla Michael, Saucedo-Uribe Erasmo, Rodríguez-Mayoral Oscar, Jiménez-Genchi Janet, Castañeda-González Carlos, Roche-Bergua Andrés, Nicolini Humber |
Spontaneous Coronary Artery Dissection: Insights on Rare Genetic Variation From Genome Sequencing. Circulation. Genomic and precision medicine 2020 10 13 (6): e003030. Carss Keren J, Baranowska Anna A, Armisen Javier, Webb Tom R, Hamby Stephen E, Premawardhana Diluka, Al-Hussaini Abtehale, Wood Alice, Wang Quanli, Deevi Sri V V, Vitsios Dimitrios, Lewis Samuel H, Kotecha Deevia, Bouatia-Naji Nabila, Hesselson Stephanie, Iismaa Siiri E, Tarr Ingrid, McGrath-Cadell Lucy, Muller David W, Dunwoodie Sally L, Fatkin Diane, Graham Robert M, Giannoulatou Eleni, Samani Nilesh J, Petrovski Slavé, Haefliger Carolina, Adlam Dav |
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 |
Recurrent germline mutations as genetic markers for aortic root dilatation in bicuspid aortic valve patients. Heart and vessels 2020 Oct . Wu Boting, Li Jun, Wang Yongshi, Cheng Yunfeng, Wang Chunsheng, Shu Xianho |
Analysis of the contribution of 129 candidate genes to thoracic aortic aneurysm or dissection of a mixed cohort of sporadic and familial cases in South China. American journal of translational research 2021 6 13 (5): 4281-4295. Li Ying, Fang Miaoxian, Yang Jue, Yu Changjiang, Kuang Juntao, Sun Tucheng, Fan Ruix |
The genetic association with injury risk in male academy soccer players depends on maturity status. Scandinavian journal of medicine & science in sports 2021 Oct . Hall Elliott C R, Baumert Philipp, Larruskain Jon, Gil Susana M, Lekue Josean A, Rienzi Edgardo, Moreno Sacha, Tannure Marcio, Murtagh Conall F, Ade Jack D, Squires Paul, Orme Patrick, Anderson Liam, Brownlee Thomas E, Whitworth-Turner Craig M, Morton James P, Drust Barry, Williams Alun G, Erskine Robert |
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 |
The Identification by Exome Sequencing of Candidate Genes in BRCA-Negative Tunisian Patients at a High Risk of Hereditary Breast/Ovarian Cancer. Genes 2022 7 13 (8): . BenAyed-Guerfali Dorra, Kifagi Chamseddine, BenKridis-Rejeb Wala, Ammous-Boukhris Nihel, Ayedi Wajdi, Khanfir Afef, Daoud Jamel, Mokdad-Gargouri Ra |
Genetic architecture of thoracic aortic dissection in the female population. Gene 2023 8 887 147727. Yanghui Chen, Linlin Wang, Xin Xu, Ke Li, Yang Sun, Yan Wang, Dao Wen Wa |
A novel cuproptosis-related LncRNA signature: Prognostic and therapeutic value for low grade glioma. Frontiers in oncology 2023 2 12 1087762. Wen Jun, Zhao Wenting, Shu Xiaol |
- Page last reviewed:Feb 1, 2024
- Page last updated:May 13, 2024
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