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Journal Abstract Search

151 related items for PubMed ID: 28676520

  • 1. Transcription Factor RUNX1 Regulates Platelet PCTP (Phosphatidylcholine Transfer Protein): Implications for Cardiovascular Events: Differential Effects of RUNX1 Variants.
    Mao G, Songdej N, Voora D, Goldfinger LE, Del Carpio-Cano FE, Myers RA, Rao AK.
    Circulation; 2017 Sep 05; 136(10):927-939. PubMed ID: 28676520
    [Abstract] [Full Text] [Related]

  • 2. Dysregulation of PLDN (pallidin) is a mechanism for platelet dense granule deficiency in RUNX1 haplodeficiency.
    Mao GF, Goldfinger LE, Fan DC, Lambert MP, Jalagadugula G, Freishtat R, Rao AK.
    J Thromb Haemost; 2017 Apr 05; 15(4):792-801. PubMed ID: 28075530
    [Abstract] [Full Text] [Related]

  • 3. RUNX1/core binding factor A2 regulates platelet 12-lipoxygenase gene (ALOX12): studies in human RUNX1 haplodeficiency.
    Kaur G, Jalagadugula G, Mao G, Rao AK.
    Blood; 2010 Apr 15; 115(15):3128-35. PubMed ID: 20181616
    [Abstract] [Full Text] [Related]

  • 4. Platelet protein kinase C-theta deficiency with human RUNX1 mutation: PRKCQ is a transcriptional target of RUNX1.
    Jalagadugula G, Mao G, Kaur G, Dhanasekaran DN, Rao AK.
    Arterioscler Thromb Vasc Biol; 2011 Apr 15; 31(4):921-7. PubMed ID: 21252065
    [Abstract] [Full Text] [Related]

  • 5. Defective RAB1B-related megakaryocytic ER-to-Golgi transport in RUNX1 haplodeficiency: impact on von Willebrand factor.
    Jalagadugula G, Goldfinger LE, Mao G, Lambert MP, Rao AK.
    Blood Adv; 2018 Apr 10; 2(7):797-806. PubMed ID: 29632235
    [Abstract] [Full Text] [Related]

  • 6. Mechanism of platelet factor 4 (PF4) deficiency with RUNX1 haplodeficiency: RUNX1 is a transcriptional regulator of PF4.
    Aneja K, Jalagadugula G, Mao G, Singh A, Rao AK.
    J Thromb Haemost; 2011 Feb 10; 9(2):383-91. PubMed ID: 21129147
    [Abstract] [Full Text] [Related]

  • 7. Identification of a functional genetic variant driving racially dimorphic platelet gene expression of the thrombin receptor regulator, PCTP.
    Kong X, Simon LM, Holinstat M, Shaw CA, Bray PF, Edelstein LC.
    Thromb Haemost; 2017 May 03; 117(5):962-970. PubMed ID: 28251237
    [Abstract] [Full Text] [Related]

  • 8. Systems Pharmacogenomics Finds RUNX1 Is an Aspirin-Responsive Transcription Factor Linked to Cardiovascular Disease and Colon Cancer.
    Voora D, Rao AK, Jalagadugula GS, Myers R, Harris E, Ortel TL, Ginsburg GS.
    EBioMedicine; 2016 Sep 03; 11():157-164. PubMed ID: 27566955
    [Abstract] [Full Text] [Related]

  • 9. Transcriptional Auto-Regulation of RUNX1 P1 Promoter.
    Martinez M, Hinojosa M, Trombly D, Morin V, Stein J, Stein G, Javed A, Gutierrez SE.
    PLoS One; 2016 Sep 03; 11(2):e0149119. PubMed ID: 26901859
    [Abstract] [Full Text] [Related]

  • 10. Regulation of platelet myosin light chain (MYL9) by RUNX1: implications for thrombocytopenia and platelet dysfunction in RUNX1 haplodeficiency.
    Jalagadugula G, Mao G, Kaur G, Goldfinger LE, Dhanasekaran DN, Rao AK.
    Blood; 2010 Dec 23; 116(26):6037-45. PubMed ID: 20876458
    [Abstract] [Full Text] [Related]

  • 11. RUNX1 isoforms regulate RUNX1 and target genes differentially in platelets-megakaryocytes: association with clinical cardiovascular events.
    Guan L, Voora D, Myers R, Del Carpio-Cano F, Rao AK.
    J Thromb Haemost; 2024 Dec 23; 22(12):3581-3598. PubMed ID: 39181539
    [Abstract] [Full Text] [Related]

  • 12. Racial differences in human platelet PAR4 reactivity reflect expression of PCTP and miR-376c.
    Edelstein LC, Simon LM, Montoya RT, Holinstat M, Chen ES, Bergeron A, Kong X, Nagalla S, Mohandas N, Cohen DE, Dong JF, Shaw C, Bray PF.
    Nat Med; 2013 Dec 23; 19(12):1609-16. PubMed ID: 24216752
    [Abstract] [Full Text] [Related]

  • 13. RUNX1 Isoforms Regulate RUNX1 and Target-Genes Differentially in Platelets-Megakaryocytes: Association with Clinical Cardiovascular Events.
    Guan L, Voora D, Myers R, Del Carpio-Cano F, Rao AK.
    bioRxiv; 2024 Jun 21. PubMed ID: 38948740
    [Abstract] [Full Text] [Related]

  • 14. PCTP contributes to human platelet activation by enhancing dense granule secretion.
    Abraham S, Ma L, Kong X, Askari S, Edelstein LC, McKenzie SE.
    Thromb Res; 2021 Jun 21; 202():67-73. PubMed ID: 33770537
    [Abstract] [Full Text] [Related]

  • 15. Developmentally regulated promoter-switch transcriptionally controls Runx1 function during embryonic hematopoiesis.
    Pozner A, Lotem J, Xiao C, Goldenberg D, Brenner O, Negreanu V, Levanon D, Groner Y.
    BMC Dev Biol; 2007 Jul 12; 7():84. PubMed ID: 17626615
    [Abstract] [Full Text] [Related]

  • 16. Downregulation of TREM-like transcript-1 and collagen receptor α2 subunit, two novel RUNX1-targets, contributes to platelet dysfunction in familial platelet disorder with predisposition to acute myelogenous leukemia.
    Glembotsky AC, Sliwa D, Bluteau D, Balayn N, Marin Oyarzún CP, Raimbault A, Bordas M, Droin N, Pirozhkova I, Washington V, Goette NP, Marta RF, Favier R, Raslova H, Heller PG.
    Haematologica; 2019 Jun 12; 104(6):1244-1255. PubMed ID: 30545930
    [Abstract] [Full Text] [Related]

  • 17. Functional characterization of the promoter region of the human EVI1 gene in acute myeloid leukemia: RUNX1 and ELK1 directly regulate its transcription.
    Maicas M, Vázquez I, Vicente C, García-Sánchez MA, Marcotegui N, Urquiza L, Calasanz MJ, Odero MD.
    Oncogene; 2013 Apr 18; 32(16):2069-78. PubMed ID: 22689058
    [Abstract] [Full Text] [Related]

  • 18. Age-related promoter-switch regulates Runx1 expression in adult rat hearts.
    Song J, Zhang X, Lv S, Liu M, Hua X, Yue L, Wang S, He W.
    BMC Cardiovasc Disord; 2023 Nov 07; 23(1):541. PubMed ID: 37936072
    [Abstract] [Full Text] [Related]

  • 19. RUNX1, but not its familial platelet disorder mutants, synergistically activates PF4 gene expression in combination with ETS family proteins.
    Okada Y, Watanabe M, Nakai T, Kamikawa Y, Shimizu M, Fukuhara Y, Yonekura M, Matsuura E, Hoshika Y, Nagai R, Aird WC, Doi T.
    J Thromb Haemost; 2013 Sep 07; 11(9):1742-50. PubMed ID: 23848403
    [Abstract] [Full Text] [Related]

  • 20. Repression of vascular endothelial growth factor expression by the runt-related transcription factor 1 in acute myeloid leukemia.
    Ter Elst A, Ma B, Scherpen FJ, de Jonge HJ, Douwes J, Wierenga AT, Schuringa JJ, Kamps WA, de Bont ES.
    Cancer Res; 2011 Apr 01; 71(7):2761-71. PubMed ID: 21447743
    [Abstract] [Full Text] [Related]

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