Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 137 Records) |
Query Trace: TGFBR1[original query] |
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A polymorphism in the cachexia-associated gene INHBA predicts efficacy of regorafenib in patients with refractory metastatic colorectal cancer. PloS one 2020 9 15 (9): e0239439. Miyamoto Yuji, Schirripa Marta, Suenaga Mitsukuni, Cao Shu, Zhang Wu, Okazaki Satoshi, Berger Martin D, Matsusaka Satoshi, Yang Dongyun, Ning Yan, Baba Hideo, Loupakis Fotios, Lonardi Sara, Pietrantonio Filippo, Borelli Beatrice, Cremolini Chiara, Yamaguchi Toshiharu, Lenz Heinz-Jos |
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 |
Genetic Variability in the microRNA Binding Sites of BMPR1B, TGFBR1, IQGAP1, KRAS, SETD8 and RYR3 and Risk of Breast Cancer in Colombian Women. OncoTargets and therapy 2020 13 12281-12287. Garcia Mesa Karen, Bermejo Justo Lorenzo, Torres Diana, Gilbert Michael, Plass Christoph, Hamann U |
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 |
Optimising the mutation screening strategy in Marfan syndrome and identifying genotypes with more severe aortic involvement. Orphanet journal of rare diseases 2020 Oct 15 (1): 290. Stengl Roland, Bors András, Ágg Bence, Pólos Miklós, Matyas Gabor, Molnár Mária Judit, Fekete Bálint, Csabán Dóra, Andrikovics Hajnalka, Merkely Béla, Radovits Tamás, Szabolcs Zoltán, Benke Kálm |
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 |
Association of Myopia and Genetic Variants of TGFB2-AS1 and TGFBR1 in the TGF-? Signaling Pathway: A Longitudinal Study in Chinese School-Aged Children. Frontiers in cell and developmental biology 2021 5 9 628182. Liu Linjie, He Juan, Lu Xiaoyan, Yuan Yimin, Jiang Dandan, Xiao Haishao, Lin Shudan, Xu Liangde, Chen Yany |
Clinical utility of TGFB1 and its receptors (TGFBR1 and TGFBR2) in thyroid nodules: evaluation based on single nucleotide polymorphisms and mRNA analysis. Archives of endocrinology and metabolism 2021 4 65 (2): 172-184. Peres Karina Colombera, Teodoro Larissa, Amaral Laís Helena Pereira, Teixeira Elisângela Souza, Barreto Icléia Siqueira, de Freitas Leandro Luiz Lopes, Maximo Valdemar, Assumpção Lígia V Montalli, Bufalo Natassia Elena, Ward Laura Steri |
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 |
Comparison of risk allele frequencies of single nucleotide polymorphisms associated with age-related macular degeneration in different ethnic groups. BMC ophthalmology 2021 2 21 (1): 97. Shin Hyun-Tae, Yoon Byung Woo, Seo Je Hy |
Polymorphisms in MicroRNA Target Sites of TGF-? Signaling Pathway Genes and Susceptibility to Allergic Rhinitis. International archives of allergy and immunology 2021 Feb 1-9. Chen Ruo-Xi, Lu Wen-Min, Lu Mei-Ping, Wang Mei-Lin, Zhu Xin-Jie, Wu Zhong-Fei, Tian Hui-Qin, Zhu Lu-Ping, Zhang Zheng-Dong, Cheng L |
Association of gene polymorphisms in MYH11 and TGF-? signaling with the susceptibility and clinical outcomes of DeBakey type III aortic dissection. Mammalian genome : official journal of the International Mammalian Genome Society 2021 Nov . Chang Yafei, Yuan Qinghua, Jiang Peipei, Sun Ling, Ma Yitong, Ma Xia |
[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 |
A Promising Role of TGF-? Pathway in Response to Regorafenib in Metastatic Colorectal Cancer: A Case Report. Medicina (Kaunas, Lithuania) 2021 11 57 (11): . De Summa Simona, Danza Katia, Pilato Brunella, Matera Giuseppina, Fasano Rossella, Calabrese Angela, Lacalamita Rosanna, Silvestris Nicola, Tommasi Stefania, Argentiero Antonella, Brunetti Oron |
Identification of Risk Loci for Radiotoxicity in Prostate Cancer by Comprehensive Genotyping of TGFB1 and TGFBR1. Cancers 2021 11 13 (21): . Guhlich Manuel, Hubert Laura, Mergler Caroline Patricia Nadine, Rave-Fraenk Margret, Dröge Leif Hendrik, Leu Martin, Schmidberger Heinz, Rieken Stefan, Hille Andrea, Schirmer Markus Ant |
Surgical Outcome and Histological Differences between Individuals with TGFBR1 and TGFBR2 Mutations in Loeys-Dietz Syndrome. Annals of thoracic and cardiovascular surgery : official journal of the Association of Thoracic and Cardiovascular Surgeons of Asia 2021 1 27 (1): 56-63. Seike Yoshimasa, Matsuda Hitoshi, Ishibashi-Ueda Hatsue, Morisaki Hiroko, Morisaki Takayuki, Minatoya Kenji, Ogino Hitos |
Genetic Interaction of H19 and TGFBR1 Polymorphisms with Risk of Epilepsy in a Chinese Population. Pharmacogenomics and personalized medicine 2021 14 77-86. Zheng Zhaoshi, Yan Yayun, Guo Qi, Wang Libo, Han Xuemei, Liu Songy |
[Association analysis of seven single nucleotide polymorphisms identified by genome-wide association study with age-related macular degeneration among ethnic Han Chinese population]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2022 Sep 39 (9): 963-968. Huang Guo, Li Huan, Xiao Jialing, Wang Liang, Xu Huijuan, Lei Chuntao, Yu Man, Shuai Ping, Liu Yuping, Gong Bo, Yang Zhengl |
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 |
SHCBP1 Is a Prognostic Biomarker Related to the Tumour Immune Microenvironment in Pan-Cancer. Annals of clinical and laboratory science 2022 12 52 (6): 904-917. Huang Yufan, You Maojin, Wu Qingfeng, Zhu Wei, Guo Fei, Lin Wangch |
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 |
Retraction: Associations of TGFBR1 and TGFBR2 gene polymorphisms with the risk of hypospadias: a case-control study in a Chinese population. Bioscience reports 2022 Aug 42 (8): . Authors are not available |
[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 |
The evaluation of six genes combined value in glioma diagnosis and prognosis. Journal of cancer research and clinical oncology 2023 7 . Ping Lin, Lingyan He, Nan Tian, Xuchen |
Coexistence of Multiple self-healing squamous epithelioma and features of Loeys-Dietz syndrome caused by a pathogenic missense variant in the kinase domain of TGFBR1 gene. Clinical and experimental dermatology 2023 12 . Schaida Schirwani, Bea Suarez, Matthew Sommerlad, Emma Corden, Geeta Belgi, Diana Eccles, Adam Fity |
Prognostic DNA mutation and mRNA expression analysis of perineural invasion in oral squamous cell carcinoma. Scientific reports 2024 1 14 (1): 2427. Su Kyung Kuk, Kitae Kim, Jae Il Lee, KangMi Pa |
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- Page last updated:Apr 22, 2024
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