Human Genome Epidemiology Literature Finder
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Records 1 - 23 (of 23 Records) |
| Query Trace: Disease and VUR[original query] |
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| The deletion polymorphism of the ACE gene is not an independent risk factor for renal scarring in children with vesico-ureteric reflux. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2002 Apr 17 (4): 652-4. Dudley Jan, Johnston Allyson, Gardner Anne, McGraw Ma |
| Lack of major involvement of human uroplakin genes in vesicoureteral reflux: implications for disease heterogeneity. Kidney international 2004 Jul 66 (1): 10-9. Jiang Songshan, Gitlin Jordan, Deng Fang-Ming, Liang Feng-Xia, Lee Andy, Atala Anthony, Bauer Stuart B, Ehrlich Garth D, Feather Sally A, Goldberg Judith D, Goodship Judith A, Goodship Timothy H J, Hermanns Monika, Hu Fen Ze, Jones Katrin E, Malcolm Sue, Mendelsohn Cathy, Preston Robert A, Retik Alan B, Schneck Francis X, Wright Victoria, Ye Xiang Y, Woolf Adrian S, Wu Xue-Ru, Ostrer Harry, Shapiro Ellen, Yu Jun, Sun Tung-Ti |
| Significance of the tissue kallikrein promoter and transforming growth factor-beta1 polymorphisms with renal progression in children with vesicoureteral reflux. Kidney international 2004 Apr 65 (4): 1467-72. Lee-Chen GJ, Liu KP, Lai YC, Juang HS, Huang SY, Lin CY |
| Renin-angiotensin system polymorphisms in Taiwanese primary vesicoureteral reflux. Pediatric nephrology (Berlin, Germany) 2004 Jun 19 (6): 594-601. Liu Kuo-Pao, Lin Ching-Yuang, Chen Han-Jou, Wei Chou-Fu, Lee-Chen Guey-J |
| ACE gene insertion/deletion polymorphism and renal scarring in children with urinary tract infections. Pediatric nephrology (Berlin, Germany) 2009 Oct 24 (10): 1975-80. Sekerli Eleni, Katsanidis Dimitrios, Vavatsi Norma, Makedou Areti, Gatzola Magdali |
| Renin-angiotensin system polymorphisms: a risk factor for progression to end-stage renal disease in vesicoureteral reflux patients. Renal failure 2009 31 (3): 196-200. Akman B, Tarhan C, Arat Z, Sezer S, Ozdemir F |
| Functional polymorphisms in transforming growth factor-beta-1 (TGFbeta-1) and vascular endothelial growth factor (VEGF) genes modify risk of renal parenchymal scarring following childhood urinary tract infection. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2010 Mar 25 (3): 779-85. Hussein Almontaser, Askar Eman, Elsaeid Moustafa, Schaefer Fra |
| Genes in the ureteric budding pathway: association study on vesico-ureteral reflux patients. PloS one 2012 7 (4): e31327. van Eerde Albertien M, Duran Karen, van Riel Els, de Kovel Carolien G F, Koeleman Bobby P C, Knoers Nine V A M, Renkema Kirsten Y, van der Horst Henricus J R, Bökenkamp Arend, van Hagen Johanna M, van den Berg Leonard H, Wolffenbuttel Katja P, van den Hoek Joop, Feitz Wouter F, de Jong Tom P V M, Giltay Jacques C, Wijmenga Cis |
| Genetic polymorphisms in Toll-like receptors among pediatric patients with renal parenchymal infections of different clinical severities. PloS one 2013 8 (3): 3. Cheng CH, Lee YS, Chang CJ, Lin TY |
| Study of the association between the BMP4 gene and congenital anomalies of the kidney and urinary tract. Jornal de pediatria 0 90 (1): 58-64. Reis Geisilaine Soares dos, Simões E Silva Ana Cristina, Freitas Izabella Silva, Heilbuth Thiago Ramos, Marco Luiz Armando de, Oliveira Eduardo Araújo, Miranda Débora Marqu |
| The role of genetic polymorphisms of the Renin-Angiotensin System in renal diseases: A meta-analysis. Computational and structural biotechnology journal 2014 Jun 10 (16): 1-7. Braliou Georgia G, Grigoriadou Athina-Maria G, Kontou Panagiota I, Bagos Pantelis |
| Rare variants in tenascin genes in a cohort of children with primary vesicoureteric reflux. Pediatric nephrology (Berlin, Germany) 2015 Sep . Elahi Shan, Homstad Alison, Vaidya Himani, Stout Jennifer, Hall Gentzon, Wu Guanghong, Conlon Peter, Routh Jonathan C, Wiener John S, Ross Sherry S, Nagaraj Shashi, Wigfall Delbert, Foreman John, Adeyemo Adebowale, Gupta Indra R, Brophy Patrick D, Rabinovich C Egla, Gbadegesin Rasheed |
| Association between angiotensin converting enzyme gene insertion/deletion polymorphism and renal scar risk in children vesicoureteral reflex: a reappraise meta-analysis. Scientific reports 2016 08 6 31243. Ai Jin-Wei, Zeng Xian-Tao, Liu Ying, Fu Yu, Liu Tong-Zu, Pei B |
| Analysis of the IL-10, IL-12, and TNF-a Gene Polymorphisms in Patients With Vesicoureteral Reflux Among the Southeast Iranian Population. Nephro-urology monthly 2016 Mar 8 (2): e34061. Kordi Tamandani Dor Mohammad, Naeimi Nasim, Ghasemi Ali, Baranzahi Taybe, Sadeghi-Bojd Sim |
| DNA copy number variations in children with vesicoureteral reflux and urinary tract infections. PloS one 2019 14 (8): e0220617. Liang Dong, McHugh Kirk M, Brophy Pat D, Shaikh Nader, Manak J Robert, Andrews Peter, Hakker Inessa, Wang Zihua, Schwaderer Andrew L, Hains David |
| COL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humans. Human genetics 2019 6 138 (10): 1105-1115. Kitzler Thomas M, Schneider Ronen, Kohl Stefan, Kolvenbach Caroline M, Connaughton Dervla M, Dai Rufeng, Mann Nina, Nakayama Makiko, Majmundar Amar J, Wu Chen-Han W, Kari Jameela A, El Desoky Sherif M, Senguttuvan Prabha, Bogdanovic Radovan, Stajic Natasa, Valivullah Zaheer, Lek Monkol, Mane Shrikant, Lifton Richard P, Tasic Velibor, Shril Shirlee, Hildebrandt Friedhe |
| Association of Genetic Polymorphisms in GSTP1, GSTM1, and GSTT1 Genes with Vesicoureteral Reflux Susceptibility in the Children of Southeast Iran. Iranian journal of public health 2020 Jul 49 (7): 1364-1371. Shahrokhzadeh Sima, Soleimani Azam, Kordi-Tamandani Dor-Mohammad, Sangtarash Mohammad Hossein, Nejati Omid, Taheri Mohs |
| Molecular Screening of PAX2 Gene Polymorphism in Primary Vesicoureteral Reflux Patients in Taif Governorate, KSA. Pakistan journal of biological sciences : PJBS 2021 9 24 (4): 492-499. I El-Hallous Ehab, Alharthi Abdulla A, Gaber Ahmed, M Hassan Moham |
| Evaluation of insertion/deletion (I/D) polymorphisms of ACE gene and circulating levels of angiotensin II in congenital anomalies of the kidney and urinary tract. Molecular biology reports 2022 Feb . Pousa Pedro Antunes, Mendonça Tamires Sara Campos, Fonseca Larissa Marques, Oliveira Eduardo Araújo, Belisário André Rolim, Simões E Silva Ana Cristi |
| Deciphering the mutation spectrum in south Indian children with congenital anomalies of the kidney and urinary tract. BMC nephrology 2022 1 23 (1): 1. Narikot Ambili, Pardeshi Varsha Chhotusing, Shubha A M, Iyengar Arpana, Vasudevan An |
| Early Evidence on Genetic Polymorphisms in Conferring A "Two-Hit" Propensity to Renal Injury in Asian Indian Children. Journal of Indian Association of Pediatric Surgeons 2023 1 27 (6): 741-746. Anand Suramya, Bajpai Minu, Kumar Alok, Kapahtia Siddhar |
| Variable phenotype and genotype of pediatric patients with HNF1B nephropathy. Clinical nephrology 2024 5 . Bora Gülhan, Ozan Ekici, ?smail Dursun, Nilüfer Göknar, Selçuk Yüksel, Demet Alaygut, Zeynep Birsin Özçakar, Hülya Nalçac?o?lu, Beltinge Demircio?lu K?l?ç, O?uz Söylemezo?lu, Ali Duzova, Rezan Topaloglu, Fatih Ozalt |
| Genetic determinants of renal scarring in children with febrile UTI. Pediatric nephrology (Berlin, Germany) 2024 5 . Therese Rosenblad, Magnus Lindén, Ines Ambite, Per Brandström, Sverker Hansson, Gabriela Goda |
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