190 related articles for article (PubMed ID: 21129147)
1. 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; 9(2):383-91. PubMed ID: 21129147
[TBL] [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; 15(4):792-801. PubMed ID: 28075530
[TBL] [Abstract][Full Text] [Related]
3. 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; 31(4):921-7. PubMed ID: 21252065
[TBL] [Abstract][Full Text] [Related]
4. 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; 2(7):797-806. PubMed ID: 29632235
[TBL] [Abstract][Full Text] [Related]
5. 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; 115(15):3128-35. PubMed ID: 20181616
[TBL] [Abstract][Full Text] [Related]
6. 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; 11(9):1742-50. PubMed ID: 23848403
[TBL] [Abstract][Full Text] [Related]
7. 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; 116(26):6037-45. PubMed ID: 20876458
[TBL] [Abstract][Full Text] [Related]
8. Altered platelet-megakaryocyte endocytosis and trafficking of albumin and fibrinogen in RUNX1 haplodeficiency.
Del Carpio-Cano F; Mao G; Goldfinger LE; Wurtzel J; Guan L; Alam MA; Lee K; Poncz M; Rao AK
Blood Adv; 2024 Apr; 8(7):1699-1714. PubMed ID: 38330198
[TBL] [Abstract][Full Text] [Related]
9. Defective RAB31-mediated megakaryocytic early endosomal trafficking of VWF, EGFR, and M6PR in RUNX1 deficiency.
Jalagadugula G; Mao G; Goldfinger LE; Wurtzel J; Del Carpio-Cano F; Lambert MP; Estevez B; French DL; Poncz M; Rao AK
Blood Adv; 2022 Sep; 6(17):5100-5112. PubMed ID: 35839075
[TBL] [Abstract][Full Text] [Related]
10. Altered Platelet-Megakaryocyte Endocytosis and Trafficking of Albumin and Fibrinogen in
Carpio-Cano FD; Mao G; Goldfinger LE; Wurtzel J; Guan L; Alam AM; Lee K; Poncz ME; Rao AK
medRxiv; 2023 Oct; ():. PubMed ID: 37961544
[TBL] [Abstract][Full Text] [Related]
11. Transcription Factor RUNX1 Regulates Platelet
Mao G; Songdej N; Voora D; Goldfinger LE; Del Carpio-Cano FE; Myers RA; Rao AK
Circulation; 2017 Sep; 136(10):927-939. PubMed ID: 28676520
[TBL] [Abstract][Full Text] [Related]
12. Defective acid hydrolase secretion in RUNX1 haplodeficiency: Evidence for a global platelet secretory defect.
Rao AK; Poncz M
Haemophilia; 2017 Sep; 23(5):784-792. PubMed ID: 28662545
[TBL] [Abstract][Full Text] [Related]
13. Mechanisms underlying platelet function defect in a pedigree with familial platelet disorder with a predisposition to acute myelogenous leukemia: potential role for candidate RUNX1 targets.
Glembotsky AC; Bluteau D; Espasandin YR; Goette NP; Marta RF; Marin Oyarzun CP; Korin L; Lev PR; Laguens RP; Molinas FC; Raslova H; Heller PG
J Thromb Haemost; 2014 May; 12(5):761-72. PubMed ID: 24606315
[TBL] [Abstract][Full Text] [Related]
14. Multiple ETS family proteins regulate PF4 gene expression by binding to the same ETS binding site.
Okada Y; Nobori H; Shimizu M; Watanabe M; Yonekura M; Nakai T; Kamikawa Y; Wakimura A; Funahashi N; Naruse H; Watanabe A; Yamasaki D; Fukada S; Yasui K; Matsumoto K; Sato T; Kitajima K; Nakano T; Aird WC; Doi T
PLoS One; 2011; 6(9):e24837. PubMed ID: 21931859
[TBL] [Abstract][Full Text] [Related]
15. Probing platelet factor 4 alpha-granule targeting.
Briquet-Laugier V; Lavenu-Bombled C; Schmitt A; Leboeuf M; Uzan G; Dubart-Kupperschmitt A; Rosa JP
J Thromb Haemost; 2004 Dec; 2(12):2231-40. PubMed ID: 15613031
[TBL] [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; 104(6):1244-1255. PubMed ID: 30545930
[TBL] [Abstract][Full Text] [Related]
17. Regulation of RUNX1 transcriptional function by GATA-1.
Elagib KE; Goldfarb AN
Crit Rev Eukaryot Gene Expr; 2007; 17(4):271-80. PubMed ID: 17725493
[TBL] [Abstract][Full Text] [Related]
18. Intramedullary megakaryocytes internalize released platelet factor 4 and store it in alpha granules.
Lambert MP; Meng R; Xiao L; Harper DC; Marks MS; Kowalska MA; Poncz M
J Thromb Haemost; 2015 Oct; 13(10):1888-99. PubMed ID: 26256688
[TBL] [Abstract][Full Text] [Related]
19. Runx1 is a co-activator with FOXO3 to mediate transforming growth factor beta (TGFbeta)-induced Bim transcription in hepatic cells.
Wildey GM; Howe PH
J Biol Chem; 2009 Jul; 284(30):20227-39. PubMed ID: 19494111
[TBL] [Abstract][Full Text] [Related]
20. Characterization of the Platelet Phenotype Caused by a Germline RUNX1 Variant in a CRISPR/Cas9-Generated Murine Model.
Marín-Quílez A; García-Tuñón I; Fernández-Infante C; Hernández-Cano L; Palma-Barqueros V; Vuelta E; Sánchez-Martín M; González-Porras JR; Guerrero C; Benito R; Rivera J; Hernández-Rivas JM; Bastida JM
Thromb Haemost; 2021 Sep; 121(9):1193-1205. PubMed ID: 33626581
[No Abstract] [Full Text] [Related]
[Next] [New Search]
