Human Genome Epidemiology Literature Finder

---

Filtered By: Select to fine-tune your search Disease Gene Year Journal Country Study Design

Previous

Records 1 - 7 (of 7 Records)

Query Trace: Hirschsprung Disease and EDNRB[original query]
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, Similar articles in PubMed
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 Similar articles in PubMed
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 Similar articles in PubMed
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 Similar articles in PubMed
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 Similar articles in PubMed
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 Similar articles in PubMed
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 Similar articles in PubMed