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1	LETTER doi:nature09999 A novel tumour-suppressor function for the Notch pathway in myeloid leukaemia Add to Reading List Source URL: michorlab.dfci.harvard.edu Language: English - Date: 2014-08-06 11:15:16 Biology Cell biology Transcription factors Induced stem cells Signal transduction Tyrosine kinase receptors Developmental biology Notch signaling pathway HES1 Chronic myelomonocytic leukemia Haematopoiesis CEBPA
2	Table 13.1 Classification of acute myeloid leukaemia (AML) according to the WHO classification[removed]modified). Acute myeloid leukaemia with recurrent genetic abnormalities AML with t(8;21)(q22;q22); RUNX1-RUNX1T1 Add to Reading List Source URL: www.essentialhaematology6.com Language: English - Date: 2011-02-25 06:19:27 Acute myeloid leukemia Acute promyelocytic leukemia RUNX1 Myelodysplastic syndrome CEBPA Leukemia Acute panmyelosis with myelofibrosis Auer rod Myeloid sarcoma Myeloid leukemia Medicine Acute leukemia
3	Beneficiary Full Name: ___________________________________________ Sponsor’s SSN: ______-_____-_______ Date of Birth: ____________________________________ Beneficiary State of Residence: _______________ Dear Provide Add to Reading List Source URL: www.hnfs.com Language: English - Date: 2015-01-02 17:18:38 Health TRICARE Medical ethics CEBPA Genetic testing Health Net Acute myeloid leukemia Health Insurance Portability and Accountability Act Medicine Healthcare in the United States United States Department of Defense
4	Wilms’ Tumour gene (WT1) as a potential MRD marker in AML David Grimwade Standardised leukaemia-specific RT-qPCR assays for Add to Reading List Source URL: www.fda.gov Language: English CEBPA WT1 Transcription factors CD135 RUNX1