HuGE Literature Finder
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| The clinical and molecular characteristics of progressive hypothalamic/optic pathway pilocytic astrocytoma. Neuro-oncology 2022 10 . Li Xiaoyu, Moreira Daniel C, Bag Asim K, Qaddoumi Ibrahim, Acharya Sahaja, Chiang Jas |
| Association of NFKB1, NKX2-5, GATA4 and RANKL Gene Polymorphisms with Sporadic Congenital Heart Disease in Greek Patients. Balkan journal of medical genetics : BJMG 2021 8 24 (1): 15-20. Aidinidou L, Chatzikyriakidou A, Giannopoulos A, Karpa V, Tzimou I, Aidinidou E, Fidani |
| ISL1 loss-of-function variation causes familial atrial fibrillation. European journal of medical genetics 2020 8 63 (11): 104029. Wu Shao-Hui, Wang Xin-Hua, Xu Ying-Jia, Gu Jia-Ning, Yang Chen-Xi, Qiao Qi, Guo Xiao-Juan, Guo Yu-Han, Qiu Xing-Biao, Jiang Wei-Feng, Yang Yi-Qi |
| Novel Genetic Associations Between Lung Cancer and Indoor Radon Exposure. Journal of cancer prevention 2018 1 22 (4): 234-240. Choi Jung Ran, Koh Sang-Baek, Park Seong Yong, Kim Hye Run, Lee Hyojin, Kang Dae Ryo |
| Variants in NKX2-5 and FLNC Cause Dilated Cardiomyopathy and Sudden Cardiac Death. Circulation. Genomic and precision medicine 2018 08 11 (8): e002151. Sveinbjornsson Gardar, Olafsdottir Eva F, Thorolfsdottir Rosa B, Davidsson Olafur B, Helgadottir Anna, Jonasdottir Adalbjorg, Jonasdottir Aslaug, Bjornsson Eythor, Jensson Brynjar O, Arnadottir Gudny A, Kristinsdottir Hallfridur, Stephensen Sigurdur S, Oskarsson Gylfi, Gudbjartsson Tomas, Sigurdsson Emil L, Andersen Karl, Danielsen Ragnar, Arnar David O, Jonsdottir Ingileif, Thorsteinsdottir Unnur, Sulem Patrick, Thorgeirsson Gudmundur, Gudbjartsson Daniel F, Holm Hilma, Stefansson Ka |
| A novel NKX2.6 mutation associated with congenital ventricular septal defect. Pediatric cardiology 2015 Mar 36 (3): 646-56. Wang Juan, Mao Jian-Hui, Ding Ke-Ke, Xu Wei-Jun, Liu Xing-Yuan, Qiu Xing-Biao, Li Ruo-Gu, Qu Xin-Kai, Xu Ying-Jia, Huang Ri-Tai, Xue Song, Yang Yi-Qi |
| NKX2-5 mutations in an inbred consanguineous population: genetic and phenotypic diversity. Scientific reports 2015 5 8848. Abou Hassan Ossama K, Fahed Akl C, Batrawi Manal, Arabi Mariam, Refaat Marwan M, DePalma Steven R, Seidman J G, Seidman Christine E, Bitar Fadi F, Nemer Georges |
| Prevalence and spectrum of Nkx2.6 mutations in patients with congenital heart disease. European journal of medical genetics 2014 Oct 57 (10): 579-86. Zhao Lan, Ni Shi-Hong, Liu Xing-Yuan, Wei Dong, Yuan Fang, Xu Lei, Xin-Li , Li Ruo-Gu, Qu Xin-Kai, Xu Ying-Jia, Fang Wei-Yi, Yang Yi-Qing, Qiu Xing-Bi |
| A de novo mutation in NKX2.5 associated with atrial septal defects, ventricular noncompaction, syncope and sudden death. Clinica chimica acta; international journal of clinical chemistry 2011 Jan 412 (1-2): 170-5. Ouyang Ping, Saarel Elizabeth, Bai Ying, Luo Chunyan, Lv Qiulun, Xu Yan, Wang Fan, Fan Chun, Younoszai Adel, Chen Qiuyun, Tu Xin, Wang Qing |
| Single-nucleotide polymorphisms of NKX2.5 found in congenital heart disease patients of Mysore, South India. Genetic testing and molecular biomarkers 2010 Dec 14 (6): 873-9. Dinesh S M, Kusuma L, Smitha R, Savitha M R, Krishnamurthy B, Narayanappa D, Ramachandra Nallur |
| Age-related DNA methylation changes in normal human prostate tissues. Clinical cancer research : an official journal of the American Association for Cancer Research 2007 7 13 (13): 3796-802. Kwabi-Addo Bernard, Chung Woonbok, Shen Lanlan, Ittmann Michael, Wheeler Thomas, Jelinek Jaroslav, Issa Jean-Pierre |
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