HuGE Literature Finder
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| Clinicopathologic and survival correlates of embryonal rhabdomyosarcoma driven by RAS/RAF mutations. Genes, chromosomes & cancer 2021 Nov . Agaram Narasimhan P, Huang Shih-Chiang, Tap William D, Wexler Leonard H, Antonescu Cristina |
| Predictive and Prognostic Implications of Mutation Profiling and Microsatellite Instability Status in Patients with Metastatic Colorectal Carcinoma. Gastroenterology research and practice 2018 2018 4585802. Liu Jianhua, Zeng Weiqiang, Huang Chengzhi, Wang Junjiang, Yang Dongyang, Ma Do |
| Epithelial-Myoepithelial Carcinoma: Frequent Morphologic and Molecular Evidence of Preexisting Pleomorphic Adenoma, Common HRAS Mutations in PLAG1-intact and HMGA2-intact Cases, and Occasional TP53, FBXW7, and SMARCB1 Alterations in High-grade Cases. The American journal of surgical pathology 2017 Nov . El Hallani Soufiane, Udager Aaron M, Bell Diana, Fonseca Isabel, Thompson Lester D R, Assaad Adel, Agaimy Abbas, Luvison Alyssa M, Miller Caitlyn, Seethala Raja R, Chiosea Simi |
| Frequent HRAS Mutations in Malignant Ectomesenchymoma: Overlapping Genetic Abnormalities With Embryonal Rhabdomyosarcoma. The American journal of surgical pathology 2016 Feb . Huang Shih-Chiang, Alaggio Rita, Sung Yun-Shao, Chen Chun-Liang, Zhang Lei, Kao Yu-Chien, Agaram Narasimhan P, Wexler Leonard H, Antonescu Cristina |
| Somatic Copy Number Abnormalities and Mutations in PI3K/AKT/mTOR Pathway Have Prognostic Significance for Overall Survival in Platinum Treated Locally Advanced or Metastatic Urothelial Tumors. PloS one 2015 10 (6): e0124711. Bellmunt Joaquim, Werner Lillian, Leow Jeffrey J, Mullane Stephanie A, Fay André P, Riester Markus, Van Hummelen Paul, Taplin Mary-Ellen, Choueiri Toni K, Van Allen Eliezer, Rosenberg Jonath |
| Human gene copy number spectra analysis in congenital heart malformations. Physiological genomics 2012 Feb . Tomita-Mitchell A, Mahnke DK, Struble CA, Tuffnell ME, Stamm KD, Hidestrand M, Harris SE, Goetsch MA, Simpson PM, Bick DP, Broeckel U, Pelech AN, Tweddell JS, Mitchell ME |
| Molecular and clinical analysis of RAF1 in Noonan syndrome and related disorders: dephosphorylation of serine 259 as the essential mechanism for mutant activation. Human mutation 2010 1 31 (3): 284-94. Kobayashi Tomoko, Aoki Yoko, Niihori Tetsuya, Cavé Hélène, Verloes Alain, Okamoto Nobuhiko, Kawame Hiroshi, Fujiwara Ikuma, Takada Fumio, Ohata Takako, Sakazume Satoru, Ando Tatsuya, Nakagawa Noriko, Lapunzina Pablo, Meneses Antonio G, Gillessen-Kaesbach Gabriele, Wieczorek Dagmar, Kurosawa Kenji, Mizuno Seiji, Ohashi Hirofumi, David Albert, Philip Nicole, Guliyeva Afag, Narumi Yoko, Kure Shigeo, Tsuchiya Shigeru, Matsubara Yoic |
| Clinical, Pathologic, and Genetic Features of Wilms Tumors With WTX Gene Mutation. Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society 0 20 (2): 105-111. Alexandrescu Sanda, Akhavanfard Sara, Harris Marian H, Vargas Sara |
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- Page last updated:Feb 03, 2023
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