Human Genome Epidemiology Literature Finder
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Records 1 - 22 (of 22 Records) |
| Query Trace: Disease and TRPC6[original query] |
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| Lack of association between transient receptor potential cation channel 6 polymorphisms and primary membranous glomerulonephritis. Renal failure 2010 Jul 32 (6): 666-72. Chen Wen-Chi, Chen Shih-Yin, Chen Cheng-Hsu, Chen Huey-Yi, Lin Yi-Wen, Ho Tsung-Jung, Huang Yu-Chuen, Shen Jui-Lung, Tsai Fuu-Jen, Chen Yung-Hsia |
| TRPC6 gene variants in Turkish children with steroid-resistant nephrotic syndrome. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2012 Jan 27 (1): 205-9. Mir Sevgi, Yavascan Onder, Berdeli Afig, Sozeri Bet |
| Mutations in the INF2 gene account for a significant proportion of familial but not sporadic focal and segmental glomerulosclerosis. Kidney international 2013 Feb 83 (2): 316-22. Barua Moumita, Brown Elizabeth J, Charoonratana Victoria T, Genovese Giulio, Sun Hua, Pollak Martin |
| TRPC6 gene variants in Czech adult patients with focal segmental glomerulosclerosis and minimal change disease. Folia biologica 2012 58 (4): 173-6. Obeidová L, Reiterová J, Ln?ni?ka P, Štekrová J, Šafránková H, Kohoutová M, Tesa? |
| Mutations in podocyte genes are a rare cause of primary FSGS associated with ESRD in adult patients. Clinical nephrology 2012 Jul 78 (1): 47-53. Büscher Anja K, Konrad Martin, Nagel Mato, Witzke Oliver, Kribben Andreas, Hoyer Peter F, Weber Stefan |
| 254C>G: a TRPC6 promoter variation associated with enhanced transcription and steroid-resistant nephrotic syndrome in Chinese children. Pediatric research 2013 Sep . Kuang XY, Huang WY, Xu H, Shi Y, Zhang XL, Niu XL, Wu Y, Mei CZ, Zha XL, Zhao ZH, Zhang ZG |
| Screening of ACTN4 and TRPC6 mutations in a Chinese cohort of patients with adult-onset familial focal segmental glomerulosclerosis. Contributions to nephrology 2013 181 91-100. Zhang Qianying, Ma Jun, Xie Jingyuan, Wang Zhaohui, Zhu Bin, Hao Xu, Yang Li, Ren Hong, Chen N |
| Genetic screening in adolescents with steroid-resistant nephrotic syndrome. Kidney international 2013 Jul 84 (1): 206-13. Lipska Beata S, Iatropoulos Paraskevas, Maranta Ramona, Caridi Gianluca, Ozaltin Fatih, Anarat Ali, Balat Ayse, Gellermann Jutta, Trautmann Agnes, Erdogan Ozlem, Saeed Bassam, Emre Sevinc, Bogdanovic Radovan, Azocar Marta, Balasz-Chmielewska Irena, Benetti Elisa, Caliskan Salim, Mir Sevgi, Melk Anette, Ertan Pelin, Baskin Esra, Jardim Helena, Davitaia Tinatin, Wasilewska Anna, Drozdz Dorota, Szczepanska Maria, Jankauskiene Augustina, Higuita Lina Maria Serna, Ardissino Gianluigi, Ozkaya Ozan, Kuzma-Mroczkowska Elzbieta, Soylemezoglu Oguz, Ranchin Bruno, Medynska Anna, Tkaczyk Marcin, Peco-Antic Amira, Akil Ipek, Jarmolinski Tomasz, Firszt-Adamczyk Agnieszka, Dusek Jiri, Simonetti Giacomo D, Gok Faysal, Gheissari Alaleh, Emma Francesco, Krmar Rafael T, Fischbach Michel, Printza Nikoleta, Simkova Eva, Mele Caterina, Ghiggeri Gian Marco, Schaefer Franz, |
| TRPC6 single nucleotide polymorphisms and progression of idiopathic membranous nephropathy. PloS one 2014 9 (7): e102065. Hofstra Julia M, Coenen Marieke J H, Schijvenaars Mascha M V A P, Berden Jo H M, van der Vlag Johan, Hoefsloot Lies H, Knoers Nine V A M, Wetzels Jack F M, Nijenhuis T |
| Evaluation of candidate nephropathy susceptibility genes in a genome-wide association study of African American diabetic kidney disease. PloS one 2014 9 (2): e88273. Palmer Nicholette D, Ng Maggie C Y, Hicks Pamela J, Mudgal Poorva, Langefeld Carl D, Freedman Barry I, Bowden Donald |
| Targeted next-generation sequencing in steroid-resistant nephrotic syndrome: mutations in multiple glomerular genes may influence disease severity. European journal of human genetics : EJHG 2015 Sep 23 (9): 1192-9. Bullich Gemma, Trujillano Daniel, Santín Sheila, Ossowski Stephan, Mendizábal Santiago, Fraga Gloria, Madrid Álvaro, Ariceta Gema, Ballarín José, Torra Roser, Estivill Xavier, Ars Elisab |
| TRPC6 gene variants and neuropsychiatric lupus. Journal of neuroimmunology 2015 Nov 288 21-4. Ramirez Giuseppe A, Lanzani Chiara, Bozzolo Enrica P, Citterio Lorena, Zagato Laura, Casamassima Nunzia, Canti Valentina, Sabbadini Maria Grazia, Rovere-Querini Patrizia, Manunta Paolo, Manfredi Angelo |
| Molecular and clinical analysis of TRPC6 and AGTR1 genes in patients with pulmonary arterial hypertension. Orphanet journal of rare diseases 2015 10 (1): 1. Pousada Guillermo, Baloira Adolfo, Valverde Dia |
| Analysis of 24 genes reveals a monogenic cause in 11.1% of cases with steroid-resistant nephrotic syndrome at a single center. Pediatric nephrology (Berlin, Germany) 2017 Sep . Tan Weizhen, Lovric Svjetlana, Ashraf Shazia, Rao Jia, Schapiro David, Airik Merlin, Shril Shirlee, Gee Heon Yung, Baum Michelle, Daouk Ghaleb, Ferguson Michael A, Rodig Nancy, Somers Michael J G, Stein Deborah R, Vivante Asaf, Warejko Jillian K, Widmeier Eugen, Hildebrandt Friedhe |
| Spectrum of mutations in Chinese children with steroid-resistant nephrotic syndrome. Pediatric nephrology (Berlin, Germany) 2017 Feb . Wang Fang, Zhang Yanqin, Mao Jianhua, Yu Zihua, Yi Zhuwen, Yu Li, Sun Jun, Wei Xiuxiu, Ding Fangrui, Zhang Hongwen, Xiao Huijie, Yao Yong, Tan Weizhen, Lovric Svjetlana, Ding Jie, Hildebrandt Friedhe |
| The TRPC6 intronic polymorphism, associated with the risk of neurological disorders in systemic lupus erythematous, influences immune cell function. Journal of neuroimmunology 2018 Dec 325 43-53. Ramirez Giuseppe A, Coletto Lavinia A, Bozzolo Enrica P, Citterio Lorena, Delli Carpini Simona, Zagato Laura, Rovere-Querini Patrizia, Lanzani Chiara, Manunta Paolo, Manfredi Angelo A, Sciorati Cla |
| Identification of genetic factors underlying persistent pulmonary hypertension of newborns in a cohort of Chinese neonates. Respiratory research 2019 Aug 20 (1): 174. Liu Xu, Mei Mei, Chen Xiang, Lu Yulan, Dong Xinran, Hu Liyuan, Hu Xiaojing, Cheng Guoqiang, Cao Yun, Yang Lin, Zhou Wenh |
| A Systematic Analysis of Major Susceptible Genes in Childhood-onset Steroid-resistant Nephrotic Syndrome. Annals of clinical and laboratory science 2019 7 49 (3): 330-337. Li Yongzhen, He Qingnan, Wang Ying, Dang Xiqiang, Wu Xiaochuan, Li Xiaoyan, Shuai Lanjun, Yi Zhuw |
| TRPC6 Mutational Analysis in Iranian Children With Focal Segmental Glomerulosclerosis. Iranian journal of kidney diseases 2019 1 12 (6): 341-349. Gheissari Alaleh, Meamar Rokhsareh, Kheirollahi Majid, Rouigari Maedeh, Dehbashi Moein, Dehghani Leila, Abedini Am |
| Mutational landscape of TRPC6, WT1, LMX1B, APOL1, PTPRO, PMM2, LAMB2 and WT1 genes associated with Steroid resistant nephrotic syndrome. Molecular biology reports 2021 Sep . Thakor Jinal M, Parmar Glory, Mistry Kinnari N, Gang Sishir, Rank Dharamshibhai N, Joshi Chaitanya |
Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy.
JAMA cardiology 2023 6 . Jaakko S Tyrmi, Tea Kaartokallio, A Inkeri Lokki, Tiina Jääskeläinen, Eija Kortelainen, Sanni Ruotsalainen, Juha Karjalainen, Samuli Ripatti, Anna Kivioja, Triin Laisk, Johannes Kettunen, Anneli Pouta, Katja Kivinen, Eero Kajantie, Seppo Heinonen, Juha Kere, Hannele Laivuori, |
| 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 |
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