Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: PTPRB[original query] |
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Association of PTPRB gene polymorphism with drug addiction. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008 Oct 147B (7): 1167-72. Ishiguro Hiroki, Gong Jian-Ping, Hall F Scott, Arinami Tadao, Uhl George |
Recurrent PTPRB and PLCG1 mutations in angiosarcoma. Nature genetics 2014 Apr 46 (4): 376-9. Behjati Sam, Tarpey Patrick S, Sheldon Helen, Martincorena Inigo, Van Loo Peter, Gundem Gunes, Wedge David C, Ramakrishna Manasa, Cooke Susanna L, Pillay Nischalan, Vollan Hans Kristian M, Papaemmanuil Elli, Koss Hans, Bunney Tom D, Hardy Claire, Joseph Olivia R, Martin Sancha, Mudie Laura, Butler Adam, Teague Jon W, Patil Meena, Steers Graham, Cao Yu, Gumbs Curtis, Ingram Davis, Lazar Alexander J, Little Latasha, Mahadeshwar Harshad, Protopopov Alexei, Al Sannaa Ghadah A, Seth Sahil, Song Xingzhi, Tang Jiabin, Zhang Jianhua, Ravi Vinod, Torres Keila E, Khatri Bhavisha, Halai Dina, Roxanis Ioannis, Baumhoer Daniel, Tirabosco Roberto, Amary M Fernanda, Boshoff Chris, McDermott Ultan, Katan Matilda, Stratton Michael R, Futreal P Andrew, Flanagan Adrienne M, Harris Adrian, Campbell Peter |
Clonal architectures and driver mutations in metastatic melanomas. PloS one 2014 9 (11): e111153. Ding Li, Kim Minjung, Kanchi Krishna L, Dees Nathan D, Lu Charles, Griffith Malachi, Fenstermacher David, Sung Hyeran, Miller Christopher A, Goetz Brian, Wendl Michael C, Griffith Obi, Cornelius Lynn A, Linette Gerald P, McMichael Joshua F, Sondak Vernon K, Fields Ryan C, Ley Timothy J, Mulé James J, Wilson Richard K, Weber Jeffrey |
Recurrent CIC Gene Abnormalities in Angiosarcomas: A Molecular Study of 120 Cases With Concurrent Investigation of PLCG1, KDR, MYC, and FLT4 Gene Alterations. The American journal of surgical pathology 2016 Jan . Huang Shih-Chiang, Zhang Lei, Sung Yun-Shao, Chen Chun-Liang, Kao Yu-Chien, Agaram Narasimhan P, Singer Samuel, Tap William D, D'Angelo Sandra, Antonescu Cristina |
Exome sequencing in families with chronic central serous chorioretinopathy. Molecular genetics & genomic medicine 2019 2 7 (4): e00576. Schellevis Rosa L, van Dijk Elon H C, Breukink Myrte B, Keunen Jan E E, Santen Gijs W E, Hoyng Carel B, de Jong Eiko K, Boon Camiel J F, den Hollander Anneke |
Primary mammary angiosarcomas harbor frequent mutations in KDR and PIK3CA and show evidence of distinct pathogenesis. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2020 Mar . Beca Francisco, Krings Gregor, Chen Yunn-Yi, Hosfield Elizabeth M, Vohra Poonam, Sibley Richard K, Troxell Megan L, West Robert B, Allison Kimberly H, Bean Gregory |
Post-radiotherapy vascular lesions of the breast: immunohistochemical and molecular features of 74 cases with long-term follow-up and literature review. Histopathology 2020 2 77 (2): 293-302. Corradini Angelo G, Asioli Sofia, Morandi Luca, Brotto Maurizio, Righi Alberto, Iommi Marica, Agostinelli Claudio, Rucci Paola, Asioli Silvia, Sapino Anna, Viale Giuseppe, Foschini Maria |
Preliminary study of genome-wide association identified novel susceptibility genes for thyroid-related hormones in Chinese population. Genes & genomics 2021 Sep . Huang Liang, Bai Fenghua, Zhang Yutian, Zhang Shanshan, Jin Tianbo, Wei Xingwei, Zhou Xiaoli, Lin Mei, Xie Yufei, He Chanyi, Lin Qi, Xie Tian, Ding Yipe |
Screening of Graves' disease susceptibility genes by whole exome sequencing in a three-generation family. BMC medical genomics 2021 Feb 14 (1): 46. Hu Zhuoqing, Li Wei, Li Miaosheng, Wei Hao, Hu Zhihui, Chen Yanting, Luo Ai, Li Wang |
Case report: Unique FLT4 variants associated with differential response to anlotinib in angiosarcoma. Frontiers in oncology 2022 12 12 1027696. Gu Yuanyuan, Meng Jing, Ju Yongzhi, You Xia, Sun Tingting, Lu Jun, Guan Y |
Whole-exome sequencing study identifies rare variants and genes associated with intraocular pressure and glaucoma.
Nature communications 2022 11 13 (1): 7376. Gao Xiaoyi Raymond, Chiariglione Marion, Arch Alexander |
The variants in PTPRB, TRAF3IP3, and DISC1 genes were associated with Graves' disease in the Chinese population. Medicine 2022 11 101 (45): e31501. Li Wei, Jiang Haidong, Chen Xu, Yang Kevin, Deng Xindan, Tang Zheng, Hu Zhihui, Zhang Xiaodan, Lin Shihan, Zou Yuanlin, Wu H |
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- Page last updated:Apr 22, 2024
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