Human Genome Epidemiology Literature Finder
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Records 1 - 13 (of 13 Records) |
| Query Trace: Disease and TGFBR3[original query] |
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| Association of polymorphisms of IGF1R and genes in the transforming growth factor- beta /bone morphogenetic protein pathway with bacteremia in sickle cell anemia. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2006 Sep 43 (5): 593-8. Adewoye Adeboye H, Nolan Vikki G, Ma Qianli, Baldwin Clinton, Wyszynski Diego F, Farrell John J, Farrer Lindsay A, Steinberg Martin |
| Genetic polymorphisms associated with priapism in sickle cell disease. British journal of haematology 2007 May 137 (3): 262-7. Elliott Laine, Ashley-Koch Allison E, De Castro Laura, Jonassaint Jude, Price Jennifer, Ataga Kenneth I, Levesque Marc C, Brice Weinberg J, Eckman James R, Orringer Eugene P, Vance Jeffery M, Telen Marilyn |
| Sequencing of TGF-beta pathway genes in familial cases of intracranial aneurysm. Stroke; a journal of cerebral circulation 2009 May 40 (5): 1604-11. Santiago-Sim Teresa, Mathew-Joseph Sumy, Pannu Hariyadarshi, Milewicz Dianna M, Seidman Christine E, Seidman J G, Kim Dong |
| Transforming growth factor-beta receptor-3 is associated with pulmonary emphysema. American journal of respiratory cell and molecular biology 2009 Sep 41 (3): 324-31. Hersh Craig P, Hansel Nadia N, Barnes Kathleen C, Lomas David A, Pillai Sreekumar G, Coxson Harvey O, Mathias Rasika A, Rafaels Nicholas M, Wise Robert A, Connett John E, Klanderman Barbara J, Jacobson Francine L, Gill Ritu, Litonjua Augusto A, Sparrow David, Reilly John J, Silverman Edwin K, |
| A genome-wide association study of men with symptoms of testicular dysgenesis syndrome and its network biology interpretation. Journal of medical genetics 2012 Jan 49 (1): 58-65. Dalgaard Marlene D, Weinhold Nils, Edsgärd Daniel, Silver Jeremy D, Pers Tune H, Nielsen John E, Jørgensen Niels, Juul Anders, Gerds Thomas A, Giwercman Aleksander, Giwercman Yvonne L, Cohn-Cedermark Gabriella, Virtanen Helena E, Toppari Jorma, Daugaard Gedske, Jensen Thomas S, Brunak Søren, Rajpert-De Meyts Ewa, Skakkebæk Niels E, Leffers Henrik, Gupta Ramne |
| Association analysis of TGFBR3 gene with Vogt-Koyanagi-Harada disease and Behcet's disease in the Chinese Han population. Current eye research 2012 Apr 37 (4): 312-7. Chen Yuanyuan, Yang Peizeng, Li Fuzhen, Hou Shengping, Jiang Zhengxuan, Shu Qinmeng, Kijlstra Ai |
| The genetics of Behçet's disease in a Chinese population. Frontiers of medicine 2012 Nov . Hou S, Kijlstra A, Yang P |
| Surrogate molecular markers for IGHV mutational status in chronic lymphocytic leukemia for predicting time to first treatment. Leukemia research 2015 Aug 39 (8): 840-5. Morabito Fortunato, Cutrona Giovanna, Mosca Laura, D'Anca Marianna, Matis Serena, Gentile Massimo, Vigna Ernesto, Colombo Monica, Recchia Anna Grazia, Bossio Sabrina, De Stefano Laura, Maura Francesco, Manzoni Martina, Ilariucci Fiorella, Consoli Ugo, Vincelli Iolanda, Musolino Caterina, Cortelezzi Agostino, Molica Stefano, Ferrarini Manlio, Neri Antoni |
A common variant near TGFBR3 is associated with primary open angle glaucoma.
Human molecular genetics 2015 Jul 24 (13): 3880-92. Li Zheng, Allingham R Rand, Nakano Masakazu, Jia Liyun, Chen Yuhong, Ikeda Yoko, Mani Baskaran, Chen Li-Jia, Kee Changwon, Garway-Heath David F, Sripriya Sarangapani, Fuse Nobuo, Abu-Amero Khaled K, Huang Chukai, Namburi Prasanthi, Burdon Kathryn, Perera Shamira A, Gharahkhani Puya, Lin Ying, Ueno Morio, Ozaki Mineo, Mizoguchi Takanori, Krishnadas Subbiah Ramasamy, Osman Essam A, Lee Mei Chin, Chan Anita S Y, Tajudin Liza-Sharmini A, Do Tan, Goncalves Aurelien, Reynier Pascal, Zhang Hong, Bourne Rupert, Goh David, Broadway David, Husain Rahat, Negi Anil K, Su Daniel H, Ho Ching-Lin, Blanco Augusto Azuara, Leung Christopher K S, Wong Tina T, Yakub Azhany, Liu Yutao, Nongpiur Monisha E, Han Jong Chul, Hon Do Nhu, Shantha Balekudaru, Zhao Bowen, Sang Jinghong, Zhang NiHong, Sato Ryuichi, Yoshii Kengo, Panda-Jonas Songhomita, Ashley Koch Allison E, Herndon Leon W, Moroi Sayoko E, Challa Pratap, Foo Jia Nee, Bei Jin-Xin, Zeng Yi-Xin, Simmons Cameron P, Bich Chau Tran Nguyen, Sharmila Philomenadin Ferdinamarie, Chew Merwyn, Lim Blanche, Tam Pansy O S, Chua Elaine, Ng Xiao Yu, Yong Victor H K, Chong Yaan Fun, Meah Wee Yang, Vijayan Saravanan, Seongsoo Sohn, Xu Wang, Teo Yik Ying, Cooke Bailey Jessica N, Kang Jae H, Haines Jonathan L, Cheng Ching Yu, Saw Seang-Mei, Tai E-Shyong, , , Richards Julia E, Ritch Robert, Gaasterland Douglas E, Pasquale Louis R, Liu Jianjun, Jonas Jost B, Milea Dan, George Ronnie, Al-Obeidan Saleh A, Mori Kazuhiko, Macgregor Stuart, Hewitt Alex W, Girkin Christopher A, Zhang Mingzhi, Sundaresan Periasamy, Vijaya Lingam, Mackey David A, Wong Tien Yin, Craig Jamie E, Sun Xinghuai, Kinoshita Shigeru, Wiggs Janey L, Khor Chiea-Chuen, Yang Zhenglin, Pang Chi Pui, Wang Ningli, Hauser Michael A, Tashiro Kei, Aung Tin, Vithana Eranga |
| Association analysis of TGFBR3 gene with Behçet's disease and idiopathic intermediate uveitis in a Caucasian population. The British journal of ophthalmology 2015 May 99 (5): 696-9. Barry Robert J, Alsalem Jawaher A, Faassen Juliet, Murray Philip I, Curnow S John, Wallace Graham |
| Clinical and Genetic Predictors of Priapism in Sickle Cell Disease: Results from the Recipient Epidemiology and Donor Evaluation Study III Brazil Cohort Study.
The journal of sexual medicine 2019 Oct . Cintho Ozahata Mina, Page Grier P, Guo Yuelong, Ferreira João Eduardo, Dinardo Carla Luana, Carneiro-Proietti Anna Bárbara F, Loureiro Paula, Mota Rosimere Afonso, Rodrigues Daniela O W, Belisario André Rolim, Maximo Claudia, Flor-Park Miriam V, Custer Brian, Kelly Shannon, Sabino Ester Cerdeira, |
| Transforming Growth Factor Beta Receptor 3 Haplotypes in Sickle Cell Disease Are Associated with Lipid Profile and Clinical Manifestations. Mediators of inflammation 2020 11 2020 3185015. Santiago Rayra P, Figueiredo Camylla V B, Fiuza Luciana M, Yahouédéhou Sètondji C M A, Oliveira Rodrigo M, Aleluia Milena M, Carvalho Suellen P, Fonseca Cleverson A, Nascimento Valma M L, Rocha Larissa C, Guarda Caroline C, Gonçalves Marilda |
| Does TGFBR3 Polymorphism Increase the Risk of Silent Cerebral Infarction in Egyptian Children with Sickle Cell Disease? Indian journal of pediatrics 2022 Jul . Hassab Hoda, Hanafi Marwa, Elbeheiry Ahmed, Hassan Mona, Chazli Yasmine |
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