Human Genome Epidemiology Literature Finder
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Records 1 - 6 (of 6 Records) |
| Query Trace: Disease and TTC21B[original query] |
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| TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum. Nature genetics 2011 1 43 (3): 189-96. Davis Erica E, Zhang Qi, Liu Qin, Diplas Bill H, Davey Lisa M, Hartley Jane, Stoetzel Corinne, Szymanska Katarzyna, Ramaswami Gokul, Logan Clare V, Muzny Donna M, Young Alice C, Wheeler David A, Cruz Pedro, Morgan Margaret, Lewis Lora R, Cherukuri Praveen, Maskeri Baishali, Hansen Nancy F, Mullikin James C, Blakesley Robert W, Bouffard Gerard G, , Gyapay Gabor, Rieger Susanne, Tönshoff Burkhard, Kern Ilse, Soliman Neveen A, Neuhaus Thomas J, Swoboda Kathryn J, Kayserili Hulya, Gallagher Tomas E, Lewis Richard A, Bergmann Carsten, Otto Edgar A, Saunier Sophie, Scambler Peter J, Beales Philip L, Gleeson Joseph G, Maher Eamonn R, Attié-Bitach Tania, Dollfus Hélène, Johnson Colin A, Green Eric D, Gibbs Richard A, Hildebrandt Friedhelm, Pierce Eric A, Katsanis Nichol |
| Association of kidney structure-related gene variants with type 2 diabetes-attributed end-stage kidney disease in African Americans. Human genetics 2016 Jul . Guan Meijian, Ma Jun, Keaton Jacob M, Dimitrov Latchezar, Mudgal Poorva, Stromberg Mary, Bonomo Jason A, Hicks Pamela J, Freedman Barry I, Bowden Donald W, Ng Maggie C |
| Contribution of the TTC21B gene to glomerular and cystic kidney diseases. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2016 Mar . Bullich Gemma, Vargas Iván, Trujillano Daniel, Mendizábal Santiago, Piñero-Fernández Juan Alberto, Fraga Gloria, García-Solano José, Ballarín José, Estivill Xavier, Torra Roser, Ars Elisab |
| Kidney failure in Bardet-Biedl syndrome. Clinical genetics 2022 2 101 (4): 429-441. Meyer Jennifer R, Krentz Anthony D, Berg Richard L, Richardson Jesse G, Pomeroy Jeremy, Hebbring Scott J, Haws Robert |
| Idiopathic collapsing glomerulopathy is associated with APOL1 high-risk genotypes or Mendelian variants in most affected individuals in a highly admixed population. Kidney international 2023 12 . Precil D Neves, Andreia Watanabe, Elieser H Watanabe, Amanda M Narcizo, Kelly Nunes, Antonio M Lerario, Frederico Moraes Ferreira, Lívia B Cavalcante, Janewit Wongboonsin, Denise M Malheiros, Lectícia B Jorge, Matthew G Sampsom, Irene L Noronha, Luiz F Onuch |
| Genetic exploration of Dravet syndrome: two case report. Journal of medical case reports 2024 4 18 (1): 215. Agung Triono, Elisabeth Siti Herini, Guna |
- Page last reviewed:Feb 1, 2024
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