Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 46 Records) |
Query Trace: TRPC6[original query] |
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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 |
Modeling non-syndromic autism and the impact of TRPC6 disruption in human neurons. Molecular psychiatry 2014 Nov . Griesi-Oliveira K, Acab A, Gupta A R, Sunaga D Y, Chailangkarn T, Nicol X, Nunez Y, Walker M F, Murdoch J D, Sanders S J, Fernandez T V, Ji W, Lifton R P, Vadasz E, Dietrich A, Pradhan D, Song H, Ming G-L, Gu X, Haddad G, Marchetto M C N, Spitzer N, Passos-Bueno M R, State M W, Muotri A |
Genetic Interactions Between TRPC6 and NPHS1 Variants Affect Posttransplant Risk of Recurrent Focal Segmental Glomerulosclerosis. American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons 2015 Jul . Sun Z J, Ng K H, Liao P, Zhang Y, Ng J L, Liu I D, Tan P H, Chong S S C, Chan Y H, Liu J, Davila S, Heng C K, Jordan S C, Soong T W, Yap H |
Role of the transient receptor potential (TRP) channel gene expressions and TRP melastatin (TRPM) channel gene polymorphisms in obesity-related metabolic syndrome. European review for medical and pharmacological sciences 2015 Apr 19 (8): 1388-97. Tabur S, Oztuzcu S, Duzen I V, Eraydin A, Eroglu S, Ozkaya M, Demiryürek A |
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 |
Identification of TRPCs genetic variants that modify risk for lung cancer based on the pathway and two-stage study. Meta gene 2016 Sep 9 191-6. Zhang Zili, Wang Jian, He Jianxing, Zeng Xiansheng, Chen Xindong, Xiong Mingmei, Zhou Qipeng, Guo Meihua, Li Defu, Lu Wen |
Single nucleotide polymorphisms and genotypes of transient receptor potential ion channel and acetylcholine receptor genes from isolated B lymphocytes in myalgic encephalomyelitis/chronic fatigue syndrome patients. The Journal of international medical research 2016 Nov . Marshall-Gradisnik Sonya, Johnston Samantha, Chacko Anu, Nguyen Thao, Smith Peter, Staines Dona |
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 |
Genome-wide association study of cardiotoxicity in the NCCTG N9831 (Alliance) adjuvant trastuzumab trial.
Pharmacogenetics and genomics 2017 Jul . Serie Daniel J, Crook Julia E, Necela Brian M, Dockter Travis J, Wang Xue, Asmann Yan W, Fairweather DeLisa, Bruno Katelyn A, Colon-Otero Gerardo, Perez Edith A, Thompson E Aubrey, Norton Nadi |
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 |
TRPC6 and NPHS2 gene variants in adult patients with steroid-resistant nephrotic syndrome in North-West of Iran. Molecular biology reports 2019 Sep . Zununi Vahed Sepideh, Moghaddas Sani Hakimeh, Haghi Mehdi, Mohajel Shoja Mohammadali, Ardalan Mohammadre |
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 |
-254C>G SNP in the TRPC6 Gene Promoter Influences Its Expression via Interaction with the NF-?B Subunit RELA in Steroid-Resistant Nephrotic Syndrome Children. International journal of genomics 2019 7 2019 2197837. Kuang Xinyu, Zhou Qian, Li Zhuying, Hu Yujie, Kang Yulin, Huang Weny |
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 |
Association of Genetic Variants at TRPC6 With Chemotherapy-Related Heart Failure. Frontiers in cardiovascular medicine 2020 9 7 142. Norton Nadine, Crook Julia E, Wang Liwei, Olson Janet E, Kachergus Jennifer M, Serie Daniel J, Necela Brian M, Borgman Paul G, Advani Pooja P, Ray Jordan C, Landolfo Carolyn, Di Florio Damian N, Hill Anneliese R, Bruno Katelyn A, Fairweather DeLi |
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 determinants of daytime napping and effects on cardiometabolic health.
Nature communications 2021 (1): 900. Dashti Hassan S, Daghlas Iyas, Lane Jacqueline M, Huang Yunru, Udler Miriam S, Wang Heming, Ollila Hanna M, Jones Samuel E, Kim Jaegil, Wood Andrew R, , Weedon Michael N, Aslibekyan Stella, Garaulet Marta, Saxena Ric |
Genome-Wide Association Study and Polygenic Risk Scores of Serum DHEAS Levels in a Chilean Children Cohort.
The Journal of clinical endocrinology and metabolism 2021 Nov . Miranda José Patricio, Lardone María Cecilia, Rodríguez Fernando, Cutler Gordon B, Santos José Luis, Corvalán Camila, Pereira Ana, Mericq Veróni |
Causal and putative pathogenic mutations identified in 39% of children with primary steroid-resistant nephrotic syndrome in South Africa. European journal of pediatrics 2022 Oct 181 (10): 3595-3606. Nandlal Louansha, Winkler Cheryl A, Bhimma Rajendra, Cho Sungkweon, Nelson George W, Haripershad Sudesh, Naicker Thajasvar |
TRPC6 N338S is a gain-of-function mutant identified in patient with doxorubicin-induced cardiotoxicity. Biochimica et biophysica acta. Molecular basis of disease 2022 7 1868 (11): 166505. Lu Tong, Sun Xiaojing, Necela Brian M, Lee Hon-Chi, Norton Nadi |
TRP Family Genes Are Differently Expressed and Correlated with Immune Response in Glioma. Brain sciences 2022 5 12 (5): . Fang Chaoyou, Xu Houshi, Liu Yibo, Huang Chenkai, Wang Xiaoyu, Zhang Zeyu, Xu Yuanzhi, Yuan Ling, Zhang Anke, Shao Anwen, Lou Meiqi |
Tacrolimus in the treatment of childhood nephrotic syndrome: Machine learning detects novel biomarkers and predicts efficacy. Pharmacotherapy 2022 12 43 (1): 43-52. Mo Xiaolan, Chen Xiujuan, Zeng Huasong, Zheng Wei, Ieong Chifong, Li Huixian, Huang Qiongbo, Xu Zichuan, Yang Jinlian, Liang Qianying, Liang Huiying, Gao Xia, Huang Min, Li Jia |
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, |
Replication of genetic associations of chemotherapy-related cardiotoxicity in the adjuvant NSABP B-31 clinical trial. Frontiers in oncology 2023 6 13 1139347. Pooja P Advani, Kathryn J Ruddy, Joerg Herrmann, Jordan C Ray, Emily C Craver, Greg Yothers, Reena S Cecchini, Corey Lipchik, Huichen Feng, Priya Rastogi, Eleftherios P Mamounas, Sandra M Swain, Charles E Geyer, Norman Wolmark, Soonmyung Paik, Katherine L Pogue-Geile, Gerardo Colon-Otero, Edith A Perez, Nadine Nort |
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 |
HER2 and BARD1 Polymorphisms in Early HER2-Positive Breast Cancer Patients: Relationship with Response to Neoadjuvant Anti-HER2 Treatment. Cancers 2023 2 15 (3): . Novillo Apolonia, Gaibar María, Romero-Lorca Alicia, Malón Diego, Antón Beatriz, Moreno Amalia, Fernández-Santander A |
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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- Page last updated:Apr 16, 2024
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