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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Disease and BLNK[original query]
RUNX1 mutations are associated with poor outcome in younger and older patients with cytogenetically normal acute myeloid leukemia and with distinct gene and MicroRNA expression signatures.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2012 Sep 30 (25): 3109-18.
Mendler Jason H, Maharry Kati, Radmacher Michael D, Mrózek Krzysztof, Becker Heiko, Metzeler Klaus H, Schwind Sebastian, Whitman Susan P, Khalife Jihane, Kohlschmidt Jessica, Nicolet Deedra, Powell Bayard L, Carter Thomas H, Wetzler Meir, Moore Joseph O, Kolitz Jonathan E, Baer Maria R, Carroll Andrew J, Larson Richard A, Caligiuri Michael A, Marcucci Guido, Bloomfield Clara
Novel Alzheimer risk genes determine the microglia response to amyloid-ß but not to TAU pathology.
EMBO molecular medicine 2020 Jan e10606.
Sierksma Annerieke, Lu Ashley, Mancuso Renzo, Fattorelli Nicola, Thrupp Nicola, Salta Evgenia, Zoco Jesus, Blum David, Buée Luc, De Strooper Bart, Fiers Ma
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