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Literature Citations for OriGene clone representing NM_001001890


Platelet Protein Kinase C-{theta} Deficiency With Human RUNX1 Mutation: PRKCQ Is a Transcriptional Target of RUNX1, Gauthami Jalagadugula, Guangfen Mao, Gurpreet Kaur, Danny N. Dhanasekaran, and A. Koneti Rao, Arterioscler Thromb Vasc Biol, Apr 2011; 31: 921 - 927

Regulation of platelet myosin light chain (MYL9) by RUNX1: implications for thrombocytopenia and platelet dysfunction in RUNX1 haplodeficiency, Gauthami Jalagadugula, Guangfen Mao, Gurpreet Kaur, Lawrence E. Goldfinger, Danny N. Dhanasekaran, and A. Koneti Rao, Blood, Dec 2010; 116: 6037 - 6045

Regulation of platelet myosin light chain (MYL9) by RUNX1: implications for thrombocytopenia and platelet dysfunction in RUNX1 haplodeficiency, Gauthami Jalagadugula, Guangfen Mao, Gurpreet Kaur, Lawrence E. Goldfinger, Danny N. Dhanasekaran, and A. Koneti Rao, Blood, Dec 2010; 116: 6037 - 6045

AML1 is overexpressed in patients with myeloproliferative neoplasms and mediates JAK2V617F-independent overexpression of NF-E2, Wei Wang, Sven Schwemmers, Elizabeth O. Hexner, and Heike L. Pahl, Blood, Jul 2010; 116: 254 - 266

RUNX1/core binding factor A2 regulates platelet 12-lipoxygenase gene (ALOX12): studies in human RUNX1 haplodeficiency, Gurpreet Kaur, Gauthami Jalagadugula, Guangfen Mao, and A. Koneti Rao, Blood, Apr 2010; 115: 3128 - 3135