Human Genome Epidemiology Literature Finder
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Records 1 - 8 (of 8 Records) |
| Query Trace: Disease and EDN3[original query] |
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| 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 |
| 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 |
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
Nature 2011 Oct 478 (7367): 7367. Ehret GB, Munroe PB, Rice KM, Bochud M, Johnson AD, Chasman DI, Smith AV, Tobin MD, Verwoert GC, Hwang SJ, Pihur V, Vollenweider P, O'Reilly PF, Amin N, Bragg-Gresham JL, Teumer A, Glazer NL, Launer L, Zhao JH, Aulchenko Y, Heath S, Sõber S, Parsa A, Luan J, Arora P, Dehghan A, Zhang F, Lucas G, Hicks AA, Jackson AU, Peden JF, Tanaka T, Wild SH, Rudan I, Igl W, Milaneschi Y, Parker AN, Fava C, Chambers JC, Fox ER, Kumari M, Go MJ, van der Harst P, Kao WH, Sjögren M, Vinay DG, Alexander M, Tabara Y, Shaw-Hawkins S, Whincup PH, Liu Y, Shi G, Kuusisto J, Tayo B, Seielstad M, Sim X, Nguyen KD, Lehtimäki T, Matullo G, Wu Y, Gaunt TR, Onland-Moret NC, Cooper MN, Platou CG, Org E, Hardy R, Dahgam S, Palmen J, Vitart V, Braund PS, Kuznetsova T, Uiterwaal CS, Adeyemo A, Palmas W, Campbell H, Ludwig B, Tomaszewski M, Tzoulaki I, Palmer ND, Aspelund T, Garcia M, Chang YP, O'Connell JR, Steinle NI, Grobbee DE, Arking DE, Kardia SL, Morrison AC, Hernandez D, Najjar S, McArdle WL, Hadley D, Brown MJ, Connell JM, Hingorani AD, Day IN, Lawlor DA, Beilby JP, Lawrence RW, Clarke R, Hopewell JC, Ongen H, Dreisbach AW, Li Y, Young JH, Bis JC, Kähönen M, Viikari J, Adair LS, Lee NR, Chen MH, Olden M, Pattaro C, Bolton JA, Köttgen A, Bergmann S, Mooser V, Chaturvedi N, Frayling TM, Islam M, Jafar TH, Erdmann J, Kulkarni SR, Bornstein SR, Grässler J, Groop L, Voight BF, Kettunen J, Howard P, Taylor A, Guarrera S, Ricceri F, Emilsson V, Plump A, Barroso I, Khaw KT, Weder AB, Hunt SC, Sun YV, Bergman RN, Collins FS, Bonnycastle LL, Scott LJ, Stringham HM, Peltonen L, Perola M, Vartiainen E, Brand SM, Staessen JA, Wang TJ, Burton PR, Soler Artigas M, Dong Y, Snieder H, Wang X, Zhu H, Lohman KK, Rudock ME, Heckbert SR, Smith NL, Wiggins KL, Doumatey A, Shriner D, Veldre G, Viigimaa M, Kinra S, Prabhakaran D, Tripathy V, Langefeld CD, Rosengren A, Thelle DS, Corsi AM, Singleton A, Forrester T, Hilton G, McKenzie CA, Salako T, Iwai N, Kita Y, Ogihara T, Ohkubo T, Okamura T, Ueshima H, Umemura S, Eyheramendy S, Meitinger T, Wichmann HE, Cho YS, Kim HL, Lee JY, Scott J, Sehmi JS, Zhang W, Hedblad B, Nilsson P, Smith GD, Wong A, Narisu N, Stan?áková A, Raffel LJ, Yao J, Kathiresan S, O'Donnell CJ, Schwartz SM, Ikram MA, Longstreth WT, Mosley TH, Seshadri S, Shrine NR, Wain LV, Morken MA, Swift AJ, Laitinen J, Prokopenko I, Zitting P, Cooper JA, Humphries SE, Danesh J, Rasheed A, Goel A, Hamsten A, Watkins H, Bakker SJ, van Gilst WH, Janipalli CS, Mani KR, Yajnik CS, Hofman A, Mattace-Raso FU, Oostra BA, Demirkan A, Isaacs A, Rivadeneira F, Lakatta EG, Orru M, Scuteri A, Ala-Korpela M, Kangas AJ, Lyytikäinen LP, Soininen P, Tukiainen T, Würtz P, Ong RT, Dörr M, Kroemer HK, Völker U, Völzke H, Galan P, Hercberg S, Lathrop M, Zelenika D, Deloukas P, Mangino M, Spector TD, Zhai G, Meschia JF, Nalls MA, Sharma P, Terzic J, Kumar MV, Denniff M, Zukowska-Szczechowska E, Wagenknecht LE, Fowkes FG, Charchar FJ, Schwarz PE, Hayward C, Guo X, Rotimi C, Bots ML, Brand E, Samani NJ, Polasek O, Talmud PJ, Nyberg F, Kuh D, Laan M, Hveem K, Palmer LJ, van der Schouw YT, Casas JP, Mohlke KL, Vineis P, Raitakari O, Ganesh SK, Wong TY, Tai ES, Cooper RS, Laakso M, Rao DC, Harris TB, Morris RW, Dominiczak AF, Kivimaki M, Marmot MG, Miki T, Saleheen D, Chandak GR, Coresh J, Navis G, Salomaa V, Han BG, Zhu X, Kooner JS, Melander O, Ridker PM, Bandinelli S, Gyllensten UB, Wright AF, Wilson JF, Ferrucci L, Farrall M, Tuomilehto J, Pramstaller PP, Elosua R, Soranzo N, Sijbrands EJ, Altshuler D, Loos RJ, Shuldiner AR, Gieger C, Meneton P, Uitterlinden AG, Wareham NJ, Gudnason V, Rotter JI, Rettig R, Uda M, Strachan DP, Witteman JC, Hartikainen AL, Beckmann JS, Boerwinkle E, Vasan RS, Boehnke M, Larson MG, Järvelin MR, Psaty BM, Abecasis GR, Chakravarti A, Elliott P, van Duijn CM, Newton-Cheh C, Levy D, Caulfield MJ, Johnson T |
| 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 |
| Association of endothelin genetic variants and hospitalized infection complications in end-stage renal disease (ESRD) patients. BMC nephrology 2019 Jun 20 (1): 203. Kao Chih-Chin, Cheng Shih-Ying, Wang Yu-Jia, Chien Shu-Chen, Hsu Yu-Wen, Wu Mei-Yi, Lu Hsing-Fang, Nam Sean, Sun Tao, Wu Mai-Szu, Chang Wei-Chi |
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