Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 47 Records) |
| Query Trace: Disease and EDN1[original query] |
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| Analysis of endothelin-1 and endothelin-1 receptor A gene polymorphisms in patients with pulmonary arterial hypertension. Internal and emergency medicine 2012 Oct 7 (5): 425-30. Calabrò Paolo, Limongelli Giuseppe, Maddaloni Valeria, Vizza Carmine Dario, D'Alto Michele, D'Alessandro Raffaella, Poscia Roberto, Argiento Paola, Ziello Brunella, Badagliacca Roberto, Romeo Emanuele, Pacileo Giuseppe, Russo Maria Giovanna, Fedele Francesco, Calabrò Raffae |
| Polymorphisms in the endothelin-1 and endothelin a receptor genes and survival in patients with locoregionally advanced nasopharyngeal carcinoma. Clinical cancer research : an official journal of the American Association for Cancer Research 2011 Apr 17 (8): 2451-8. Wen Yue-Feng, Qi Bin, Liu Huai, Mo Hao-Yuan, Chen Qiu-Yan, Li Juan, Huang Pei-Yu, Ye Yan-Fang, Zhang Ying, Deng Man-Quan, Guo Xiang, Hong Ming-Huang, Cao Ka-Jia, Mai Hai-Qia |
| Epistatic interactions in idiopathic pulmonary arterial hypertension. Indian journal of human genetics 2012 Jan 18 (1): 56-61. Vadapalli Shivani, Satyanarayana M L, Chaitra K L, Rani H Surekh, Sastry B K S, Nallari Pratib |
| Genetic influences on right ventricular systolic pressure (RVSP) in chronic obstructive pulmonary disease (COPD). BMC pulmonary medicine 2012 12 (1): 25. Shaw Janet G, Dent Annette G, Passmore Linda H, Burstow Darryl J, Bowman Rayleen V, Zimmerman Paul V, Fong Kwun M, Yang Ian |
| Multiple single-nucleotide polymorphism-based risk model for clinical outcomes after allogeneic stem-cell transplantation, especially for acute graft-versus-host disease. Transplantation 2012 Nov . Kim DD, Yun J, Won HH, Cheng L, Su J, Xu W, Uhm J, Gupta V, Kuruvilla J, Messner HA, Lipton JH |
| 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 |
| Polymorphisms of endothelin 1 (G5665T and T-1370G) and endothelin receptor type A (C+70G and G-231A) in Graves' disease. International immunopharmacology 2014 Jan 18 (1): 198-202. Ayd?n A Fatih, Develi-?? Seval, Do?ru-Abbaso?lu Semra, Vural Pervin, Ozderya Ay?enur, Karada? Berrin, Uysal Müjd |
| Endothelin 1 gene as a modifier in dilated cardiomyopathy. Gene 2014 Sep 548 (2): 256-62. Matsa Lova Satyanarayna, Sagurthi Someswar Rao, Ananthapur Venkateshwari, Nalla Swapna, Nallari Pratib |
| The evaluation of endothelin 1 (EDN1) and endothelin receptor type A (EDNRA) gene polymorphisms in Hashimoto's thyroiditis. International immunopharmacology 2014 Jul 21 (1): 181-5. Aydin A Fatih, Vural Pervin, Oruç Ço?kun Umut, Do?ru-Abbaso?lu Semra, Özderya Ay?enur, Karada? Berrin, Uysal Müjd |
| Endothelin-1 genetic polymorphism as predictive marker for bevacizumab in metastatic breast cancer. The pharmacogenomics journal 2016 May . Gampenrieder S P, Hufnagl C, Brechelmacher S, Huemer F, Hackl H, Rinnerthaler G, Romeder F, Monzo Fuentes C, Morre P, Hauser-Kronberger C, Mlineritsch B, Greil |
| The paternal polymorphism rs5370 in the EDN1 gene decreases the risk of preeclampsia. Pregnancy hypertension 2016 Oct 6 (4): 327-332. Galaviz-Hernandez Carlos, Arámbula-Meraz Eliakym, Medina-Bastidas Diana, Sosa-Macías Martha, Lazalde-Ramos Blanca P, Ortega-Chávez Margarita, Hernandez-García Lore |
| Associations of genetic variants of endothelin with cardiovascular complications in patients with renal failure. BMC nephrology 2017 Sep 18 (1): 291. Kao Chih-Chin, Cheng Shih-Ying, Wu Mei-Yi, Chien Shu-Chen, Lu Hsing-Fang, Hsu Yu-Wen, Zhang Yan-Feng, Wu Mai-Szu, Chang Wei-Chi |
| Protein Z and Endothelin-1 genetic polymorphisms in pediatric Egyptian sickle cell disease patients. Journal of clinical laboratory analysis 2018 Feb 32 (2): . Khorshied Mervat M, Mohamed Nohair S, Hamza Rania S, Ali Rasha M, El-Ghamrawy Mona |
| Dysregulated aldosterone secretion in persons of African descent with endothelin-1 gene variants. JCI insight 2017 Dec 2 (23): . Tan Jia W, Gupta Tina, Manosroi Worapaka, Yao Tham M, Hopkins Paul N, Williams Jonathan S, Adler Gail K, Romero Jose R, Williams Gordon |
| Genetic Susceptibility to Postdiarrheal Hemolytic-Uremic Syndrome After Shiga Toxin-Producing Escherichia coli Infection: A Centers for Disease Control and Prevention FoodNet Study. The Journal of infectious diseases 2018 03 217 (6): 1000-1010. Kallianpur Asha R, Bradford Yuki, Mody Rajal K, Garman Katie N, Comstock Nicole, Lathrop Sarah L, Lyons Carol, Saupe Amy, Wymore Katie, Canter Jeffrey A, Olson Lana M, Palmer Amanda, Jones Timothy |
| Genetic susceptibility of five tagSNPs in the endothelin-1 (EDN1) gene to coronary artery disease in a Chinese Han population. Bioscience reports 2018 Apr . Liang Li-Li, Chen Lin, Zhou Meng-Yuan, Cai Meng-Yun, Cheng Jie, Chen Yi, You Si-Kun, Chen Lin-Bin, Tang Zi-Bin, Yang Xi-Li, Chen Can, Liu Xinguang, Xiong Xing-Do |
| [The association of LYS198ASN -polymorphism of endothelin-1 gene (EDN1) with development of arterial hypertension in ukrainian population]. Wiadomosci lekarskie (Warsaw, Poland : 1960) 2019 72 (4): 568-574. Smiianova Ylia O, Pristupa Ludmyla N, Harbuzova Viktoriia Yu, Harbuzova Yelizaveta |
| Levels of nitric oxide metabolites, adiponectin and endothelin are associated with SNPs of the adiponectin and endothelin genes. Biomedical reports 2019 Oct 11 (4): 154-164. Gumanova Nadezhda G, Klimushina Marina V, Smetnev Stepan A, Kiseleva Anna V, Skirko Olga P, Meshkov Alexey N, Shanoyan Artem S, Kots Alexander Y, Metelskaya Victoria |
| Association between Lys198Asn polymorphism of endothelin-1 gene and ischemic stroke: A meta-analysis. Brain and behavior 2019 10 9 (10): e01424. Nepal Gaurav, Ojha Rajeev, Dulal Hari Prasad, Yadav Binod Kum |
| Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection. Journal of the American College of Cardiology 2019 1 73 (1): 58-66. Adlam David, Olson Timothy M, Combaret Nicolas, Kovacic Jason C, Iismaa Siiri E, Al-Hussaini Abtehale, O'Byrne Megan M, Bouajila Sara, Georges Adrien, Mishra Ketan, Braund Peter S, d'Escamard Valentina, Huang Siying, Margaritis Marios, Nelson Christopher P, de Andrade Mariza, Kadian-Dodov Daniella, Welch Catherine A, Mazurkiewicz Stephani, Jeunemaitre Xavier, , Wong Claire Mei Yi, Giannoulatou Eleni, Sweeting Michael, Muller David, Wood Alice, McGrath-Cadell Lucy, Fatkin Diane, Dunwoodie Sally L, Harvey Richard, Holloway Cameron, Empana Jean-Philippe, Jouven Xavier, , Olin Jeffrey W, Gulati Rajiv, Tweet Marysia S, Hayes Sharonne N, Samani Nilesh J, Graham Robert M, Motreff Pascal, Bouatia-Naji Nabi |
| [Endothelin-1 rs5370 gene polymorphism in primary nephrotic syndrome: A case-control study]. Anales de pediatria 2020 Dec . Rizk Hoda, Hammad Ayman, El-Said Afaf, Wahba Yah |
| Genetic dysregulation of endothelin-1 is implicated in coronary microvascular dysfunction. European heart journal 2020 Jan . Ford Thomas J, Corcoran David, Padmanabhan Sandosh, Aman Alisha, Rocchiccioli Paul, Good Richard, McEntegart Margaret, Maguire Janet J, Watkins Stuart, Eteiba Hany, Shaukat Aadil, Lindsay Mitchell, Robertson Keith, Hood Stuart, McGeoch Ross, McDade Robert, Yii Eric, Sattar Naveed, Hsu Li-Yueh, Arai Andrew E, Oldroyd Keith G, Touyz Rhian M, Davenport Anthony P, Berry Col |
| Association of Gene Polymorphisms of Some Endothelial Factors with Stent Reendothelization after Elective Coronary Artery Revascularization. Bulletin of experimental biology and medicine 2021 6 171 (2): 194-197. Timizheva K B, Azova M M, Aissa A Ait, Aghajanyan A V, Tskhovrebova L V, Blagonravov M |
| In vivo assessment of a single adenine mutation in 5'UTR of Endothelin-1 gene in paediatric cases with severe pulmonary hypertension: an observational study. BMC research notes 2021 May 14 (1): 194. Kumar Abhishek, Choudhury Minati, Batra Sakshi Dhingra, Sikri Kriti, Gupta Anushr |
| Priapism in sickle cell disease: Associations between NOS3 and EDN1 genetic polymorphisms and laboratory biomarkers. PloS one 2021 16 (2): e0246067. Figueiredo Camylla Vilas Boas, Santiago Rayra Pereira, da Guarda Caroline Conceição, Oliveira Rodrigo Mota, Fiuza Luciana Magalhães, Yahouédéhou Sètondji Cocou Modeste Alexandre, Carvalho Suéllen Pinheiro, Neres Joelma Santana Dos Santos, Oliveira Antonio Mateus de Jesus, Fonseca Cleverson Alves, Nascimento Valma Maria Lopes, Lyra Isa Menezes, Aleluia Milena Magalhães, Goncalves Marilda Sou |
| Endothelin-1 RS5370 gene polymorphism in primary nephrotic syndrome: A case-control study. Anales de pediatria 2021 12 95 (6): 406-412. Rizk Hoda, Hammad Ayman, El-Said Afaf, Wahba Yah |
| Fibromyalgia: A Review of Related Polymorphisms and Clinical Relevance. Anais da Academia Brasileira de Ciencias 2021 11 93 (suppl 4): e20210618. Janssen Luísa P, Medeiros Liciane F, Souza Andressa DE, Silva Juliana |
| Association of PHACTR1 intronic variants with the first myocardial infarction and their effect on PHACTR1 mRNA expression in PBMCs. Gene 2021 Jan 145428. Kuveljic Jovana, Djuric Tamara, Stankovic Goran, Dekleva Milica, Stankovic Aleksandra, Alavantic Dragan, Zivkovic Ma |
| Common Variation in EDN1 Regulatory Regions Highlights the Role of PPAR? as a Key Regulator of Endothelin in vitro. Frontiers in cardiovascular medicine 2022 3 9 823133. Lago-Docampo Mauro, Solarat Carlos, Méndez-Martínez Luis, Baloira Adolfo, Valverde Dia |
| Pharmacogenomics of intravenous immunoglobulin response in Kawasaki disease. Frontiers in immunology 2024 1 14 1287094. Sadeep Shrestha, Howard W Wiener, Hidemi Kajimoto, Vinodh Srinivasasainagendra, Dolena Ledee, Sabrina Chowdhury, Jinhong Cui, Jake Y Chen, Mikayla A Beckley, Luz A Padilla, Nagib Dahdah, Hemant K Tiwari, Michael A Portm |
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