Human Genome Epidemiology Literature Finder
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Records 1 - 22 (of 22 Records) |
| Query Trace: Disease and EDNRB[original query] |
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| Association study of PHOX2B as a candidate gene for Hirschsprung's disease. Gut 2003 Apr 52 (4): 563-7. Garcia-Barceló M, Sham M H, Lui V C H, Chen B L S, Ott J, Tam P K |
| Significance of novel endothelin-B receptor gene polymorphisms in Hirschsprung's disease: predominance of a novel variant (561C/T) in patients with co-existing Down's syndrome. Molecular and cellular probes 2003 Feb 17 (1): 49-54. Zaahl M G, du Plessis L, Warnich L, Kotze M J, Moore S |
| Association between endothelin receptor B nonsynonymous variants and melanoma risk. Journal of the National Cancer Institute 2005 Sep 97 (17): 1297-301. Soufir Nadem, Meziani Roubila, Lacapère Jean-Jacques, Bertrand Guylene, Fumeron Frederic, Bourillon Agnes, Gérard Bénédicte, Descamps Vincent, Crickx Béatrice, Ollivaud Laurence, Archimbaud Alain, Lebbe Céleste, Basset-Seguin Nicole, Saiag Philippe, Grandchamp Bernard, |
| Mutations and polymorphisms of Hirschsprung disease candidate genes in Thai patients. Journal of human genetics 2006 51 (12): 1126-32. Sangkhathat Surasak, Kusafuka Takeshi, Chengkriwate Piyawan, Patrapinyokul Sakda, Sangthong Burapat, Fukuzawa Masahi |
| New variations of the EDNRB gene and its association with sporadic Hirschsprung's disease in Korea. Journal of pediatric surgery 2006 Oct 41 (10): 1708-12. Kim Jeong-Hyun, Yoon Kyong-Oh, Kim Hyungtae, Kim Jeong-Kook, Kim Jong-Won, Lee Suk-Koo, Seo Jeong-Me |
| Mutation analysis of endothelin-B receptor gene in patients with Hirschsprung disease in Taiwan. Journal of pediatric gastroenterology and nutrition 2008 Jan 46 (1): 36-40. Lin Yu-Cheng, Lai Hong-Shiee, Hsu Wen-Ming, Lee Ping-Ing, Chen Huey-Ling, Chang Mei-Hw |
| A novel point variant in NTRK3, R645C, suggests a role of this gene in the pathogenesis of Hirschsprung disease. Annals of human genetics 2009 Jan 73 (1): 19-25. Fernández R M, Sánchez-Mejías A, Mena M D, Ruiz-Ferrer M, López-Alonso M, Antiñolo G, Borrego |
| EDNRA variants associate with smooth muscle mRNA levels, cell proliferation rates, and cystic fibrosis pulmonary disease severity. Physiological genomics 2010 Mar 41 (1): 71-7. Darrah Rebecca, McKone Edward, O'Connor Clare, Rodgers Christine, Genatossio Alan, McNamara Sharon, Gibson Ronald, Stuart Elborn J, Ennis Madeleine, Gallagher Charles G, Kalsheker Noor, Aitken Moira, Wiese Dawn, Dunn John, Smith Paul, Pace Rhonda, Londono Douglas, Goddard Katrina A B, Knowles Michael R, Drumm Mitchell |
| New roles of EDNRB and EDN3 in the pathogenesis of Hirschsprung disease. Genetics in medicine : official journal of the American College of Medical Genetics 2010 Jan 12 (1): 39-43. Sánchez-Mejías Avencia, Fernández Raquel Maria, López-Alonso Manuel, Antiñolo Guillermo, Borrego Sal |
| Clinical and genetic differences in total colonic aganglionosis in Hirschsprung's disease. Journal of pediatric surgery 2009 Oct 44 (10): 1899-903. Moore Samuel W, Zaahl Moniq |
| The correlation of genetic markers with anatomoclinical and histopathological forms in Hirschsprung's disease. Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie 2010 51 (2): 283-8. Broasc? V, Ciobotaru Camelia, Dimofte Iuliana, A?chie Mariana, Prun? A, Severin Beatri |
| Novel classification and pathogenetic analysis of hypoganglionosis and adult-onset Hirschsprung's disease. Digestive diseases and sciences 2011 Jun 56 (6): 1818-27. Do Mi Young, Myung Seung-Jae, Park Hyo-Jin, Chung Jun-Won, Kim In-Wha, Lee Sun Mi, Yu Chang Sik, Lee Hye Kyung, Lee Jong-Keuk, Park Young Soo, Jang Se Jin, Kim Hye Jin, Ye Byong Duk, Byeon Jeong-Sik, Yang Suk-Kyun, Kim Jin- |
| Genetic variance in nitric oxide synthase and endothelin genes among children with and without endothelial dysfunction. Journal of translational medicine 2013 11 227. Chatsuriyawong Siriporn, Gozal David, Kheirandish-Gozal Leila, Bhattacharjee Rakesh, Khalyfa Ahamed A, Wang Yang, Hakonarson Hakon, Keating Brendan, Sukhumsirichart Wasana, Khalyfa Abdelna |
| RET and EDNRB mutation screening in patients with Hirschsprung disease: Functional studies and its implications for genetic counseling. European journal of human genetics : EJHG 2015 Sep . Widowati Titis, Melhem Shamiram, Patria Suryono Y, de Graaf Bianca M, Sinke Richard J, Viel Martijn, Dijkhuis Jos, Sadewa Ahmad H, Purwohardjono Rochadi, Soenarto Yati, Hofstra Robert Mw, Sribudiani Yun |
| Genetic variation in the GDNF promoter affects its expression and modifies the severity of Hirschsprung's disease (HSCR) in rats carrying Ednrb(sl) mutations. Gene 2015 Aug . Huang Jieping, Dang Ruihua, Torigoe Daisuke, Li Anqi, Lei Chuzhao, Sasaki Nobuya, Wang Jinxi, Agui Takas |
| Identification of genetic loci affecting the severity of symptoms of Hirschsprung disease in rats carrying Ednrbsl mutations by quantitative trait locus analysis. PloS one 2015 10 (3): e0122068. Huang Jieping, Dang Ruihua, Torigoe Daisuke, Lei Chuzhao, Lan Xianyong, Chen Hong, Sasaki Nobuya, Wang Jinxi, Agui Takas |
| Clinical and genetic correlations of familial Hirschsprung's disease. Journal of pediatric surgery 2015 Feb 50 (2): 285-8. Moore Sam W, Zaahl Moniq |
| Genetic determinants of essential hypertension in the population of Tatars from Russia. Journal of hypertension 2017 05 35 Suppl 1 S16-S23. Timasheva Yanina, Nasibullin Timur, Imaeva Elvira, Erdman Vera, Tuktarova Ilsiyar, Mustafina Ol |
| Genetic analysis of a Chinese family with members affected with Usher syndrome type II and Waardenburg syndrome type IV. International journal of pediatric otorhinolaryngology 2017 11 102 114-118. Wang Xueling, Lin Xiao-Jiang, Tang Xiangrong, Chai Yong-Chuan, Yu De-Hong, Chen Dong-Ye, Wu H |
| The heterozygous EDNRB mutation in a Chinese family with Waardenburg syndrome type I. International journal of ophthalmology 2019 9 12 (9): 1507-1509. Cheng Huan-Huan, Ling Shi-Qi, Zhao Pei-Zhen, Li Wei-Li, Deng Ju |
| Significant Association of rs2147555 Genetic Polymorphism in the EDNRB Gene with Hirschsprung Disease in Southern Chinese Children. BioMed research international 2020 11 2020 5956412. Zheng Yi, Lan ChaoTing, Wang Ning, Xu Xiaogang, Hu Tuqun, Wu Qi, Xie Xiaoli, Wang Zhe, Zhang Yan, Li Co |
| High incidence of EDNRB gene mutation in seven southern Chinese familial cases with Hirschsprung's disease. Pediatric surgery international 2024 1 40 (1): 38. Hui-Yang Ding, Wen Lei, Shang-Jie Xiao, Hua Deng, Li-Ke Yuan, Lu Xu, Jia-Liang Zhou, Rong Huang, Yuan-Long Fang, Qing-Yuan Wang, Ying Zhang, Liang Zhang, Xiao-Chun Z |
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