Human Genome Epidemiology Literature Finder
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Records 1 - 8 (of 8 Records) |
| Query Trace: Proteinuria and MYH9[original query] |
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| MYH9 and APOL1 are both associated with sickle cell disease nephropathy. British journal of haematology 2011 Nov 155 (3): 386-94. Ashley-Koch Allison E, Okocha Emmanuel C, Garrett Melanie E, Soldano Karen, De Castro Laura M, Jonassaint Jude C, Orringer Eugene P, Eckman James R, Telen Marilyn |
| APOL1 variants increase risk for FSGS and HIVAN but not IgA nephropathy. Journal of the American Society of Nephrology : JASN 2011 Nov 22 (11): 1991-6. Papeta Natalia, Kiryluk Krzysztof, Patel Ami, Sterken Roel, Kacak Nilgun, Snyder Holly J, Imus Phil H, Mhatre Anand N, Lawani Anil K, Julian Bruce A, Wyatt Robert J, Novak Jan, Wyatt Christina M, Ross Michael J, Winston Jonathan A, Klotman Mary E, Cohen David J, Appel Gerald B, D'Agati Vivette D, Klotman Paul E, Gharavi Ali |
| Epistatic role of the MYH9/APOL1 region on familial hematuria genes. PloS one 2013 8 (3): e57925. Voskarides Konstantinos, Demosthenous Panayiota, Papazachariou Louiza, Arsali Maria, Athanasiou Yiannis, Zavros Michalis, Stylianou Kostas, Xydakis Dimitris, Daphnis Eugenios, Gale Daniel P, Maxwell Patrick H, Elia Avraam, Pattaro Cristian, Pierides Alkis, Deltas Constantin |
| Association between polymorphism rs2032487 in the non-muscle myosin heavy chain IIA gene (MHY9) and chronic kidney disease secondary to type 2 diabetes mellitus in a population of the Canary Islands. Endocrinologia, diabetes y nutricion 2019 Apr . Boronat Mauro, Tugores Antonio, Saavedra Pedro, Garay Paloma, Bosch Elvira, Lorenzo Dionisio, García-Cantón Cés |
| Effect of donor non-muscle myosin heavy chain (MYH9) gene polymorphisms on clinically relevant kidney allograft dysfunction. BMC nephrology 2020 Sep 21 (1): 380. Pazik Joanna, Oldak Monika, Ozi?b?o Dominika, Materkowska Dominika D?borska, Sadowska Anna, Malejczyk Jacek, Durlik Magdale |
| Association of MYH9-rs3752462 polymorphisms with chronic kidney disease among clinically diagnosed hypertensive patients: a case-control study in a Ghanaian population. Clinical hypertension 2020 26 15. Owiredu William K B A, Appiah Michael, Obirikorang Christian, Adu Evans Asamoah, Boima Vincent, Amos-Abanyie Ernestine Kubi, Akyaw Priscilla Abena, Owiredu Eddie-Williams, Acheampong Emmanu |
| The Potential Impact of MYH9 (rs3752462) and ELMO1 (rs741301) Genetic Variants on the Risk of Nephrotic Syndrome Incidence. Biochemical genetics 2023 8 . Eglal A Hassan, Afaf M Elsaid, M M Abou-Elzahab, Ahmed M El-Refaey, Rehab Elmougy, Magdy M Youss |
| Genetic features and kidney morphological changes in women with X-linked Alport syndrome. Journal of medical genetics 2023 5 . Hongling Di, Qing Wang, Dandan Liang, Jiahui Zhang, Erzhi Gao, Chunxia Zheng, Xiaomin Yu, Zhihong L |
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- Page last updated:Sep 18, 2023
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