Human Genome Epidemiology Literature Finder
Records 1 - 23 (of 23 Records) |
Query Trace: GRHL2[original query] |
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The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairment. Human molecular genetics 2008 Jan 17 (2): 159-69. Van Laer Lut, Van Eyken Els, Fransen Erik, Huyghe Jeroen R, Topsakal Vedat, Hendrickx Jan-Jaap, Hannula Samuli, Mäki-Torkko Elina, Jensen Mona, Demeester Kelly, Baur Manuela, Bonaconsa Amanda, Mazzoli Manuela, Espeso Angeles, Verbruggen Katia, Huyghe Joke, Huygen Patrick, Kunst Sylvia, Manninen Minna, Konings Annelies, Diaz-Lacava Amalia N, Steffens Michael, Wienker Thomas F, Pyykkö Ilmari, Cremers Cor W R J, Kremer Hannie, Dhooge Ingeborg, Stephens Dafydd, Orzan Eva, Pfister Markus, Bille Michael, Parving Agnete, Sorri Martti, Van de Heyning Paul H, Van Camp G |
The grainyhead-like 2 gene (GRHL2) single nucleotide polymorphism is not associated with age-related hearing impairment in Han Chinese. The Laryngoscope 2011 Jun 121 (6): 1303-7. Lin Yan-Han, Wu Chen-Chi, Hsu Chuan-Jen, Hwang Juen-Haur, Liu Tien-Ch |
Association between genetic variations in GRHL2 and noise-induced hearing loss in Chinese high intensity noise exposed workers: a case-control analysis. Industrial health 2013 51 (6): 612-21. Li Xin, Huo Xinying, Liu Kai, Li Xiuting, Wang Meilin, Chu Haiyan, Hu Feifei, Sheng Huanxi, Zhang Zhengdong, Zhu Bao |
Associations of genetic variations in EYA4, GRHL2 and DFNA5 with noise-induced hearing loss in Chinese population: a case- control study. Environmental health : a global access science source 2015 14 (1): 77. Zhang Xuhui, Liu Yi, Zhang Lei, Yang Zhangping, Yang Luoxian, Wang Xuchu, Jiang CaiXia, Wang Qiang, Xia Yuyong, Chen Yanjuan, Wu Ou, Zhu Yim |
Evaluation of the contribution of the EYA4 and GRHL2 genes in Korean patients with autosomal dominant non-syndromic hearing loss. PloS one 2015 10 (3): e0119443. Kim Ye-Ri, Kim Min-A, Sagong Borum, Bae Seung-Hyun, Lee Hyo-Jeong, Kim Hyung-Jong, Choi Jae Young, Lee Kyu-Yup, Kim Un-Kyu |
Marked overlap of four genetic syndromes with dyskeratosis congenita confounds clinical diagnosis. Haematologica 2016 Sep . Walne Amanda J, Collopy Laura, Cardoso Shirleny, Ellison Alicia, Plagnol Vincent, Albayrak Canan, Albayrak Davut, Kilic Sara Sebnem, Patiroglu Turkan, Akar Haluk, Godfrey Keith, Carter Tina, Marafie Makia, Vora Ajay, Sundin Mikael, Vulliamy Thomas, Tummala Hemanth, Dokal Inderje |
Genetic Variation in POU4F3 and GRHL2 Associated with Noise-Induced Hearing Loss in Chinese Population: A Case-Control Study. International journal of environmental research and public health 2016 Jun 13 (6): . Xu Xiangrong, Yang Qiuyue, Jiao Jie, He Lihua, Yu Shanfa, Wang Jingjing, Gu Guizhen, Chen Guoshun, Zhou Wenhui, Wu Hui, Li Yanhong, Zhang Huanli |
[Association between grainyhead-like 2 gene polymorphisms and noise-induced hearing loss]. Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2016 Jun 48 (3): 409-13. Yang Q Y, Xu X R, Jiao J, He L H, Yu S F, Gu G Z, Chen G S, Zhou W H, Wu H, Li Y |
GRHL2 genetic polymorphisms may confer a protective effect against sudden sensorineural hearing loss. Molecular medicine reports 2016 Feb . Lin Xiaojiang, Teng Yaoshu, Lan Jinshan, He Benjun, Sun Huijuan, Xu Fengl |
Potential protective role of Grainyhead-like genes in the development of clear cell renal cell carcinoma. Molecular carcinogenesis 2017 Nov 56 (11): 2414-2423. Pawlak Magdalena, Kikulska Agnieszka, Wrzesinski Tomasz, Rausch Tobias, Kwias Zbigniew, Wilczynski Bartek, Benes Vladimir, Wesoly Joanna, Wilanowski Toma |
A microdeletion in the GRHL2 Gene in two unrelated patients with congenital fibrosis of the extra ocular muscles. BMC research notes 2017 Nov 10 (1): 562. Abu-Amero Khaled K, Kondkar Altaf A, Khan Arif |
Somatic mutations in early onset luminal breast cancer. Oncotarget 2018 Apr 9 (32): 22460-22479. Encinas Giselly, Sabelnykova Veronica Y, de Lyra Eduardo Carneiro, Hirata Katayama Maria Lucia, Maistro Simone, de Vasconcellos Valle Pedro Wilson Mompean, de Lima Pereira Gláucia Fernanda, Rodrigues Lívia Munhoz, de Menezes Pacheco Serio Pedro Adolpho, de Gouvêa Ana Carolina Ribeiro Chaves, Geyer Felipe Correa, Basso Ricardo Alves, Pasini Fátima Solange, Del Pilar Esteves Diz Maria, Brentani Maria Mitzi, Guedes Sampaio Góes João Carlos, Chammas Roger, Boutros Paul C, Koike Folgueira Maria Aparecida Azeve |
Age-Related Hearing Impairment Associated NAT2, GRM7, GRHL2 Susceptibility Gene Polymorphisms and Haplotypes in Roma and Hungarian Populations. Pathology oncology research : POR 2018 Feb . Matyas Petra, Postyeni Etelka, Komlosi Katalin, Szalai Renata, Bene Judit, Magyari Lili, Melegh Bela, Hadzsiev Kin |
Association of polymorphisms in grainyhead-like-2 gene with the susceptibility to age-related hearing loss: A systematic review and meta-analysis. Medicine 2019 Jun 98 (25): e16128. Han Baoai, Yang Xiuping, Li Yongqin, Hosseini Davood K, Tu Yaqin, Dong Yaodong, He Zuhong, Yuan Jie, Cai Hua, Zhang Kai, Zhang Xiujuan, Zhou Tao, Sun Haiyi |
Polymorphism in GRHL2 gene may contribute to noise-induced hearing loss susceptibility: a meta-analysis. Brazilian journal of otorhinolaryngology 2019 Feb . Li Xin, Zhu Zhengping, Li Wei, Wei Li, Zhao Baocheng, Hao Zhe |
Mutation screening in non-syndromic hearing loss patients with cochlear implantation by massive parallel sequencing in Taiwan. PloS one 2019 1 14 (1): e0211261. Liu Wei-Hsiu, Chang Pi-Yueh, Chang Shih-Cheng, Lu Jang-Jih, Wu Che-Mi |
Clinical and genetic evaluation of six children with diffuse capillary malformation and undergrowth. Pediatric dermatology 2020 7 37 (5): 833-838. Cubiró Xavier, Rozas-Muñoz Eduardo, Castel Pau, Roé Crespo Esther, Garcia-Melendo Cristina, Puig Lluis, Baselga Eulal |
Phenogenon: Gene to phenotype associations for rare genetic diseases. PloS one 2020 4 15 (4): e0230587. Pontikos Nikolas, Murphy Cian, Moghul Ismail, Arno Gavin, Fujinami Kaoru, Fujinami Yu, Sumodhee Dayyanah, Downes Susan, Webster Andrew, Yu Jing, |
Transcription factors Krüppel-like factor 4 and paired box 5 regulate the expression of the Grainyhead-like genes. PloS one 2021 9 16 (9): e0257977. Kotarba Grzegorz, Taracha-Wisniewska Agnieszka, Miller Michal, Dabrowski Michal, Wilanowski Toma |
Novel GRHL2 Gene Variant Associated with Hearing Loss: A Case Report and Review of the Literature. Genes 2021 4 12 (4): . Trebusak Podkrajsek Katarina, Tesovnik Tine, Bozanic Urbancic Nina, Battelino Sa |
Genome-wide association study identifies new loci associated with risk of HBV infection and disease progression.
BMC medical genomics 2021 Mar 14 (1): 84. Zeng Zheng, Liu Hankui, Xu Huifang, Lu Haiying, Yu Yanyan, Xu Xiaoyuan, Yu Min, Zhang Tao, Tian Xiulan, Xi Hongli, Guan Liping, Zhang Jianguo, O'Brien Stephen J, |
Posterior corneal vesicles are not associated with the genetic variants that cause posterior polymorphous corneal dystrophy. Acta ophthalmologica 2022 2 100 (7): e1426-e1430. Liskova Petra, Hafford-Tear Nathaniel J, Skalicka Pavlina, Malinka Frantisek, Jedlickova Jana, ?u?áková ?ubica, Pontikos Nikolas, Davidson Alice E, Tuft Steph |
Polymorphisms and NIHL: a systematic review and meta-analyses. Frontiers in cellular neuroscience 2023 7 17 1175427. Lu Wang, HanYu Wang, Feng Xiang, YuLu Xiang, Feng Xiong, QinXiu Zha |
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