Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 40 Records) |
| Query Trace: Disease and TGFBR1[original query] |
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| 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 |
| Genetic variations and interactions in anti-inflammatory cytokine pathway genes in the outcome of leprosy: a study conducted on a MassARRAY platform. The Journal of infectious diseases 2011 Oct 204 (8): 1264-73. Aggarwal Shweta, Ali Shafat, Chopra Rupali, Srivastava Amit, Kalaiarasan Ponnusamy, Malhotra Dheeraj, Gochhait Sailesh, Garg Vijay K, Bhattacharya S N, Bamezai Rameshwar N |
| Mutations in TGFBR2 gene cause spontaneous cervical artery dissection. Journal of neurology, neurosurgery, and psychiatry 2011 Dec 82 (12): 1372-4. Pezzini Alessandro, Drera Bruno, Del Zotto Elisabetta, Ritelli Marco, Carletti Monica, Tomelleri Gianpaolo, Bovi Paolo, Giossi Alessia, Volonghi Irene, Costa Paolo, Magoni Mauro, Padovani Alessandro, Barlati Sergio, Colombi Mari |
| Wound healing genes and susceptibility to cutaneous leishmaniasis in Brazil. Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases 2012 Jul 12 (5): 1102-10. Castellucci Léa, Jamieson Sarra E, Almeida Lucas, Oliveira Joyce, Guimarães Luiz Henrique, Lessa Marcus, Fakiola Michaela, Jesus Amélia Ribeiro de, Nancy Miller E, Carvalho Edgar M, Blackwell Jenefer |
| 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 |
| Alpha-actin-2 mutations in Chinese patients with a non-syndromatic thoracic aortic aneurysm. BMC medical genetics 2016 17 (1): 45. Ke Tie, Han Meng, Zhao Miao, Wang Qing Kenneth, Zhang Huazhi, Zhao Yuanyuan, Ruan Xinlong, Li Hui, Xu Chengqi, Sun Tuche |
| Genetic Polymorphisms of TGFB1, TGFBR1, SNAI1 and TWIST1 Are Associated with Endometrial Cancer Susceptibility in Chinese Han Women. PloS one 2016 11 (5): e0155270. Yang Li, Wang Ya-Jun, Zheng Li-Yuan, Jia Yu-Mian, Chen Yi-Lin, Chen Lan, Liu Dong-Ge, Li Xiang-Hong, Guo Hong-Yan, Sun Ying-Li, Tian Xin-Xia, Fang Wei-Ga |
| Negative Correlation Between Hepatitis C Virus (HCV) and Let-7 MicroRNA Family in Transplanted Livers: The Role of rs868 Single-Nucleotide Polymorphism. Annals of transplantation 2017 Oct 22 638-645. Sajjad Emir Ahmed, Radkowski Marek, Perkowska-Ptasi?ska Agnieszka, Pacholczyk Marek, Durlik Magdalena, Fedorowicz Miko?aj, Pietrzak Renata, Ziarkiewicz-Wróblewska Bogna, W?odarski Pawe?, Malejczyk Jac |
| Genome-wide haplotype association study identifies risk genes for non-small cell lung cancer. Journal of theoretical biology 2018 Aug 456 84-90. Teng Yanbo, Ding Yanjun, Zhang Mingming, Chen Xinren, Wang Xizi, Yu Hang, Liu Chonghui, Lv Hongchao, Zhang Ruij |
| Genetic diagnosis of acute aortic dissection in South China Han population using next-generation sequencing. International journal of legal medicine 2018 7 132 (5): 1273-1280. Zheng Jinxiang, Guo Jian, Huang Lei, Wu Qiuping, Yin Kun, Wang Lin, Zhang Tongda, Quan Li, Zhao Qianhao, Cheng Jiandi |
| Integrated bioinformatics analysis reveals that the expression of cathepsin S is associated with lymph node metastasis and poor prognosis in papillary thyroid cancer. Oncology reports 2018 5 40 (1): 111-122. Tan Juan, Qian Xiaoxiao, Song Bin, An Xiumin, Cai Tingting, Zuo Zhihua, Ding Dafa, Lu Yibing, Li Ho |
| Features of multiple self-healing squamous epithelioma and Loeys-Dietz syndrome in a patient with a novel TGFBR1 variant. American journal of medical genetics. Part A 2018 12 176 (12): 2892-2895. Sirisomboonwong Korawan E, Martindale Joanne, Keefe Martin, Goudie David, Poke Gem |
| Rotator Cuff Tear Susceptibility Is Associated With Variants in Genes Involved in Tendon Extracellular Matrix Homeostasis. Journal of orthopaedic research : official publication of the Orthopaedic Research Society 2019 Aug . Figueiredo Eduardo A, Loyola Leonor Casilla, Belangero Paulo S, Campos Ribeiro-Dos-Santos Ândrea Kely, Emanuel Batista Santos Sidney, Cohen Carina, Wajnsztejn Andre, Martins de Oliveira Adrielle, Smith Marília C, Pochini Alberto de Castro, Andreoli Carlos V, Ejnisman Benno, Cohen Moises, Leal Mariana |
| Application of next-generation sequencing to screen for pathogenic mutations in 123 unrelated Chinese patients with Marfan syndrome or a related disease. Science China. Life sciences 2019 5 62 (12): 1630-1637. Li Jiacheng, Lu Chaoxia, Wu Wei, Liu Yaping, Wang Rongrong, Si Nuo, Meng Xiaolu, Zhang Shuyang, Zhang X |
| Targeted next?generation sequencing for research and diagnostics in congenital heart disease, and cleft lip and/or palate. Molecular medicine reports 2019 Mar . Bu Haisong, Liu Lin, Hu Shijun, Tan Zhiping, Zhao Tian |
| Prognostic value of transforming growth factor beta receptor 1 polymorphisms in patients with oral cancer. Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology 2019 Oct . Chen Lin, Chen Fa, Wang Xiaoxia, Chen Qing, Lin Jing, Bao Xiaodan, Wang Rui, Wang Jing, Yan Lingjun, Lin Lisong, Qiu Yu, Pan Lizhen, Shi Bin, Zheng Xiaoyan, Liu Fengqiong, He Baocha |
| Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patients. Genetics in medicine : official journal of the American College of Medical Genetics 2019 Jan . Renner Sina, Schüler Helke, Alawi Malik, Kolbe Verena, Rybczynski Meike, Woitschach Rixa, Sheikhzadeh Sara, Stark Veronika C, Olfe Jakob, Roser Elke, Seggewies Friederike Sophia, Mahlmann Adrian, Hempel Maja, Hartmann Melanie J, Hillebrand Mathias, Wieczorek Dagmar, Volk Alexander Erich, Kloth Katja, Koch-Hogrebe Margarete, Abou Jamra Rami, Mitter Diana, Altmüller Janine, Wey-Fabrizius Alexandra, Petersen Christine, Rau Isabella, Borck Guntram, Kubisch Christian, Mir Thomas S, von Kodolitsch Yskert, Kutsche Kerstin, Rosenberger Geo |
| Genetic variants involved in extracellular matrix homeostasis play a role in the susceptibility to frozen shoulder: A case-control study. Journal of orthopaedic research : official publication of the Orthopaedic Research Society 2019 Jan . Cohen Carina, Leal Mariana Ferreira, Loyola Leonor Casilla, Santos Sidney Emanuel Batista, Ribeiro-Dos-Santos Ândrea Kely Campos, Belangero Paulo Santoro, Figueiredo Eduardo Antônio, Wajnsztejn Andre, de Oliveira Adrielle Martins, Smith Marília Cardoso, Andreoli Carlos Vicente, de Castro Pochini Alberto, Cohen Moises, Ejnisman Benno, Faloppa Fláv |
| Sequence variations of ACVRL1 play a critical role in hepatic vascular malformations in hereditary hemorrhagic telangiectasia. Orphanet journal of rare diseases 2020 9 15 (1): 254. Giraud Sophie, Bardel Claire, Dupuis-Girod Sophie, Carette Marie-France, Gilbert-Dussardier Brigitte, Riviere Sophie, Saurin Jean-Christophe, Eyries Mélanie, Patri Sylvie, Decullier Evelyne, Calender Alain, Lesca Gaët |
| An integrative microenvironment approach for follicular lymphoma: roles of inflammatory cell subsets and immune-response polymorphisms on disease clinical course. Oncotarget 2020 Aug 11 (33): 3153-3173. Assis-Mendonça Guilherme Rossi, Fattori André, Rocha Rafael Malagoli, Lourenço Gustavo Jacob, Delamain Márcia Torresan, Nonogaki Suely, de Lima Vladmir Cláudio Cordeiro, Colleoni Gisele Wally Braga, de Souza Cármino Antonio, Soares Fernando Augusto, Lima Carmen Silvia Passos, Vassallo Jo |
| Statistical methods with exhaustive search in the identification of gene-gene interactions for colorectal cancer. Genetic epidemiology 2020 11 45 (2): 222-234. Kafaie Somayeh, Xu Ling, Hu Ti |
| TRPV4 is a Prognostic Biomarker that Correlates with the Immunosuppressive Microenvironment and Chemoresistance of Anti-Cancer Drugs. Frontiers in molecular biosciences 2021 7 8 690500. Wang Kai, Feng Xingjun, Zheng Lingzhi, Chai Zeying, Yu Junhui, You Xinxin, Li Xiaodan, Cheng Xiaodo |
| Analysis of the contribution of 129 candidate genes to thoracic aortic aneurysm or dissection of a mixed cohort of sporadic and familial cases in South China. American journal of translational research 2021 6 13 (5): 4281-4295. Li Ying, Fang Miaoxian, Yang Jue, Yu Changjiang, Kuang Juntao, Sun Tucheng, Fan Ruix |
| Single nucleotide variants in immune-response genes and the tumor microenvironment composition predict progression of mantle cell lymphoma. BMC cancer 2021 3 21 (1): 209. Assis-Mendonça Guilherme Rossi, Fattori André, Rocha Rafael Malagoli, Lourenço Gustavo Jacob, Delamain Márcia Torresan, Nonogaki Suely, de Lima Vladmir Cláudio Cordeiro, Colleoni Gisele Wally Braga, de Souza Cármino Antonio, Soares Fernando Augusto, Lima Carmen Silvia Passos, Vassallo Jo |
| [Echocardiographic manifestation and analysis of TGFBR1 gene variant in a Chinese patient with Loeys-Dietz syndrome]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2021 11 38 (12): 1220-1223. Wang Yueli, Niu Baorong, Li Rongjuan, Xie Jinjie, Li Xiaoy |
| Common and rare genetic risk variants in age-related macular degeneration and genetic risk score in the Coimbra eye study. Acta ophthalmologica 2022 Aug . Farinha Cláudia, Barreto Patricia, Coimbra Rita, Cachulo Maria Luz, Melo Joana Barbosa, Cunha-Vaz José, Lechanteur Yara, Hoyng Carel B, Silva Rufi |
| Comparative Risks of Initial Aortic Events Associated With Genetic Thoracic Aortic Disease. Journal of the American College of Cardiology 2022 Aug 80 (9): 857-869. Regalado Ellen S, Morris Shaine A, Braverman Alan C, Hostetler Ellen M, De Backer Julie, Li Ruosha, Pyeritz Reed E, Yetman Anji T, Cervi Elena, Shalhub Sherene, Jeremy Richmond, LeMaire Scott, Ouzounian Maral, Evangelista Arturo, Boileau Catherine, Jondeau Guillaume, Milewicz Dianna |
| Cytokines in Abdominal Aortic Aneurysm: Master Regulators With Clinical Application. Biomarker insights 2022 5 17 11772719221095676. Puchenkova Olesya A, Soldatov Vladislav O, Belykh Andrei E, Bushueva OlgaYu, Piavchenko Gennadii A, Venediktov Artem A, Shakhpazyan Nikolay K, Deykin Alexey V, Korokin Mikhail V, Pokrovskiy Mikhail |
| Spontaneous coronary artery dissection is infrequent in individuals with heritable thoracic aortic disease despite partially shared genetic susceptibility. American journal of medical genetics. Part A 2022 Jan . Murad Andrea M, Hill Hannah L, Wang Yu, Ghannam Michael, Yang Min-Lee, Pugh Norma L, Asch Federico M, Hornsby Whitney, Driscoll Anisa, McNamara Jennifer, Willer Cristen J, Regalado Ellen S, , , Milewicz Dianna M, Eagle Kim A, Ganesh Santhi |
| [Clinical and genetic characteristics of 12 cases of Loeys-Dietz syndrome]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2023 8 40 (9): 1093-1099. Jiaqi Fan, Hairui Sun, Xin Wang, Yuduo Wu, Siyao Zhang, Xiaoyan Hao, Jiancheng Han, Xiaoyan Gu, Ye Zhang, Lin Sun, Yihua |
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