Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: Abnormalities and MUT[original query] |
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P53 abnormalities and outcomes in colorectal cancer: a systematic review. British journal of cancer 2005 1 92 (3): 434-44. Munro A J, Lain S, Lane D |
Prevalence and prognostic impact of NPM1 mutations in 1485 adult patients with acute myeloid leukemia (AML). Blood 2006 May 107 (10): 4011-20. Thiede Christian, Koch Sina, Creutzig Eva, Steudel Christine, Illmer Thomas, Schaich Markus, Ehninger Gerha |
Clinical and biochemical differences in patients having Parkinson disease with vs without GBA mutations. JAMA neurology 2013 Jul 70 (7): 852-8. Chahine Lama M, Qiang Judy, Ashbridge Emily, Minger James, Yearout Dora, Horn Stacy, Colcher Amy, Hurtig Howard I, Lee Virginia M-Y, Van Deerlin Vivianna M, Leverenz James B, Siderowf Andrew D, Trojanowski John Q, Zabetian Cyrus P, Chen-Plotkin Ali |
High number of additional genetic lesions in acute myeloid leukemia with t(8;21)/RUNX1-RUNX1T1: frequency and impact on clinical outcome. Leukemia 2014 Jul 28 (7): 1449-58. Krauth M-T, Eder C, Alpermann T, Bacher U, Nadarajah N, Kern W, Haferlach C, Haferlach T, Schnittger |
Molecular classification of anaplastic oligodendroglioma using next-generation sequencing: a report of the prospective randomized EORTC Brain Tumor Group 26951 phase III trial. Neuro-oncology 2015 Sep . Dubbink Hendrikus J, Atmodimedjo Peggy N, Kros Johan M, French Pim J, Sanson Marc, Idbaih Ahmed, Wesseling Pieter, Enting Roelien, Spliet Wim, Tijssen Cees, Dinjens Winand N M, Gorlia Thierry, van den Bent Martin |
HNF1B Mutations Are Associated With a Gitelman-like Tubulopathy That Develops During Childhood. Kidney international reports 2019 9 4 (9): 1304-1311. Adalat Shazia, Hayes Wesley N, Bryant William A, Booth John, Woolf Adrian S, Kleta Robert, Subtil Sandra, Clissold Rhian, Colclough Kevin, Ellard Sian, Bockenhauer Detl |
Novel genetic characteristics in low-grade fetal adenocarcinoma of the lung. Thoracic cancer 2021 8 12 (20): 2789-2795. Zhang Shuyang, Yin Huihui, Zhang Jing, Yang Lu, Yang Guangjian, Jia Jia, Jiao Yuchen, Ying Jianming, Wang Y |
A novel mutation in DNAH17 is present in a patient with multiple morphological abnormalities of the flagella. Reproductive biomedicine online 2021 8 43 (3): 532-541. Zheng Rui, Sun Yongkang, Jiang Chuan, Chen Daijuan, Yang Yihong, Shen Yi |
A rare mutation c.1663G?>?A (p.A555T) in the MMUT gene associated with mild clinical and biochemical phenotypes of methylmalonic acidemia in 30 Chinese patients. Orphanet journal of rare diseases 2021 Jan 16 (1): 22. Liang Lili, Shuai Ruixue, Yu Yue, Qiu Wenjuan, Shen Linghua, Wu Shengnan, Wei Haiyan, Chen Yongxing, Yang Chiju, Xu Peng, Chen Xigui, Zou Hui, Feng Jizhen, Niu Tingting, Hu Haili, Ye Jun, Zhang Huiwen, Lu Deyun, Gong Zhuwen, Zhan Xia, Ji Wenjun, Yu Yongguo, Gu Xuefan, Han Lians |
Clinical characteristics and outcomes of EZH2-mutant myelodysplastic syndrome: A large single institution analysis of 1774 patients. Leukemia research 2022 12 124 106999. Ball Somedeb, Aguirre Luis E, Jain Akriti G, Ali Najla Al, Tinsley Sara M, Chan Onyee, Kuykendall Andrew T, Sweet Kendra, Lancet Jeffrey E, Sallman David A, Hussaini Mohammad Omar, Padron Eric, Komrokji Rami |
Establishment and validation of an immune infiltration predictive model for ovarian cancer. BMC medical genomics 2023 9 16 (1): 227. Zhenxia Song, Jingwen Zhang, Yue Sun, Zhongmin Jiang, Xiaoning L |
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- Page last updated:Apr 22, 2024
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