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1.

Hematopoietic transcription factor mutations: important players in inherited platelet defects.

Songdej, Natthapol; Rao, A Koneti.

Blood ; 129(21): 2873-2881, 2017 05 25.

Article in English | MEDLINE | ID: mdl-28416505

2.

Platelet microparticles infiltrating solid tumors transfer miRNAs that suppress tumor growth.

Michael, James V; Wurtzel, Jeremy G T; Mao, Guang Fen; Rao, A Koneti; Kolpakov, Mikhail A; Sabri, Abdelkarim; Hoffman, Nicholas E; Rajan, Sudarsan; Tomar, Dhanendra; Madesh, Muniswamy; Nieman, Marvin T; Yu, Johnny; Edelstein, Leonard C; Rowley, Jesse W; Weyrich, Andrew S; Goldfinger, Lawrence E.

Blood ; 130(5): 567-580, 2017 08 03.

Article in English | MEDLINE | ID: mdl-28500171

3.

Transcription Factor RUNX1 Regulates Platelet PCTP (Phosphatidylcholine Transfer Protein): Implications for Cardiovascular Events: Differential Effects of RUNX1 Variants.

Mao, Guangfen; Songdej, Natthapol; Voora, Deepak; Goldfinger, Lawrence E; Del Carpio-Cano, Fabiola E; Myers, Rachel A; Rao, A Koneti.

Circulation ; 136(10): 927-939, 2017 Sep 05.

Article in English | MEDLINE | ID: mdl-28676520

4.

Gray platelet syndrome: immunity goes awry.

Rao, A Koneti; Rao, Deepak A.

Blood ; 136(17): 1898-1900, 2020 10 22.

Article in English | MEDLINE | ID: mdl-33091137

5.

Inherited thrombocytopenias: the beat goes on.

Rao, A Koneti; Songdej, Natthapol.

Blood ; 125(5): 748-50, 2015 Jan 29.

Article in English | MEDLINE | ID: mdl-25634615

6.

Inherited platelet dysfunction and hematopoietic transcription factor mutations.

Songdej, Natthapol; Rao, A Koneti.

Platelets ; 28(1): 20-26, 2017 Jan.

Article in English | MEDLINE | ID: mdl-27463948

7.

P2Y12 receptor inhibition and LPS-induced coagulation.

Essex, David W; Rao, A Koneti.

Clin Sci (Lond) ; 130(6): 441-2, 2016 Mar.

Article in English | MEDLINE | ID: mdl-26846581

8.

Spotlight on FLI1, RUNX1, and platelet dysfunction.

Rao, A Koneti.

Blood ; 122(25): 4004-6, 2013 Dec 12.

Article in English | MEDLINE | ID: mdl-24335028

9.

Parsing the repertoire of GPIb-IX-V disorders.

Rao, A Koneti; Songdej, Natthapol.

Blood ; 129(4): 403-404, 2017 01 26.

Article in English | MEDLINE | ID: mdl-28126957

10.

Altered platelet-megakaryocyte endocytosis and trafficking of albumin and fibrinogen in RUNX1 haplodeficiency.

Del Carpio-Cano, Fabiola; Mao, Guangfen; Goldfinger, Lawrence E; Wurtzel, Jeremy; Guan, Liying; Alam, Mohammad Afaque; Lee, Kiwon; Poncz, Mortimer; Rao, A Koneti.

Blood Adv ; 8(7): 1699-1714, 2024 Apr 09.

Article in English | MEDLINE | ID: mdl-38330198

11.

Platelet disorders: the next generation is in.

Rao, A Koneti; Songdej, Natthapol.

Blood ; 127(23): 2781-2, 2016 06 09.

Article in English | MEDLINE | ID: mdl-27282940

12.

Prevalence and outcomes of heparin-induced thrombocytopenia in hospitalized patients with venous thromboembolic disease: Insight from national inpatient sample.

Shah, Neal B; Sharedalal, Parija; Shafi, Irfan; Tang, Alice; Zhao, Huaqing; Lakhter, Vladimir; Kolluri, Raghu; Rao, A Koneti; Bashir, Riyaz.

J Vasc Surg Venous Lymphat Disord ; 11(4): 723-730, 2023 07.

Article in English | MEDLINE | ID: mdl-36893884

13.

Altered Platelet-Megakaryocyte Endocytosis and Trafficking of Albumin and Fibrinogen in RUNX1 Haplodeficiency.

Carpio-Cano, Fabiola Del; Mao, Guangfen; Goldfinger, Lawrence E; Wurtzel, Jeremy; Guan, Liying; Alam, Afaque Mohammad; Lee, Kiwon; Poncz, Mortimer E; Rao, A Koneti.

medRxiv ; 2023 Oct 23.

Article in English | MEDLINE | ID: mdl-37961544

14.

Tissue factor-positive monocytes in children with sickle cell disease: correlation with biomarkers of haemolysis.

Setty, B N Yamaja; Key, Nigel S; Rao, A Koneti; Gayen-Betal, Suhita; Krishnan, Suba; Dampier, Carlton D; Stuart, Marie J.

Br J Haematol ; 157(3): 370-80, 2012 May.

Article in English | MEDLINE | ID: mdl-22360627

15.

RUNX1/core binding factor A2 regulates platelet 12-lipoxygenase gene (ALOX12): studies in human RUNX1 haplodeficiency.

Kaur, Gurpreet; Jalagadugula, Gauthami; Mao, Guangfen; Rao, A Koneti.

Blood ; 115(15): 3128-35, 2010 Apr 15.

Article in English | MEDLINE | ID: mdl-20181616

16.

Regulation of platelet myosin light chain (MYL9) by RUNX1: implications for thrombocytopenia and platelet dysfunction in RUNX1 haplodeficiency.

Jalagadugula, Gauthami; Mao, Guangfen; Kaur, Gurpreet; Goldfinger, Lawrence E; Dhanasekaran, Danny N; Rao, A Koneti.

Blood ; 116(26): 6037-45, 2010 Dec 23.

Article in English | MEDLINE | ID: mdl-20876458

17.

Platelet protein kinase C-theta deficiency with human RUNX1 mutation: PRKCQ is a transcriptional target of RUNX1.

Jalagadugula, Gauthami; Mao, Guangfen; Kaur, Gurpreet; Dhanasekaran, Danny N; Rao, A Koneti.

Arterioscler Thromb Vasc Biol ; 31(4): 921-7, 2011 Apr.

Article in English | MEDLINE | ID: mdl-21252065

18.

Editorial: Platelet Genomics and Disorders of Platelet Number and Function.

Rao, A Koneti.

Platelets ; 28(1): 2, 2017 Jan.

Article in English | MEDLINE | ID: mdl-28095213

19.

Defective RAB31-mediated megakaryocytic early endosomal trafficking of VWF, EGFR, and M6PR in RUNX1 deficiency.

Jalagadugula, Gauthami; Mao, Guangfen; Goldfinger, Lawrence E; Wurtzel, Jeremy; Del Carpio-Cano, Fabiola; Lambert, Michele P; Estevez, Brian; French, Deborah L; Poncz, Mortimer; Rao, A Koneti.

Blood Adv ; 6(17): 5100-5112, 2022 09 13.

Article in English | MEDLINE | ID: mdl-35839075

20.

Effects of simvastatin on tissue factor pathway of blood coagulation in STATCOPE (Simvastatin in the prevention of COPD exacerbations) trial.

Rao, A Koneti; Del Carpio-Cano, Fabiola; Janapati, Sumalaxmi; Zhao, Huaqing; Voelker, Helen; Lu, Xiaoning; Criner, Gerard.

J Thromb Haemost ; 19(7): 1709-1717, 2021 07.

Article in English | MEDLINE | ID: mdl-33638931

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Hematopoietic transcription factor mutations: important players in inherited platelet defects.

Platelet microparticles infiltrating solid tumors transfer miRNAs that suppress tumor growth.

Transcription Factor RUNX1 Regulates Platelet PCTP (Phosphatidylcholine Transfer Protein): Implications for Cardiovascular Events: Differential Effects of RUNX1 Variants.

Gray platelet syndrome: immunity goes awry.

Inherited thrombocytopenias: the beat goes on.

Inherited platelet dysfunction and hematopoietic transcription factor mutations.

P2Y12 receptor inhibition and LPS-induced coagulation.

Spotlight on FLI1, RUNX1, and platelet dysfunction.

Parsing the repertoire of GPIb-IX-V disorders.

Altered platelet-megakaryocyte endocytosis and trafficking of albumin and fibrinogen in RUNX1 haplodeficiency.

Platelet disorders: the next generation is in.

Prevalence and outcomes of heparin-induced thrombocytopenia in hospitalized patients with venous thromboembolic disease: Insight from national inpatient sample.

Altered Platelet-Megakaryocyte Endocytosis and Trafficking of Albumin and Fibrinogen in RUNX1 Haplodeficiency.

Tissue factor-positive monocytes in children with sickle cell disease: correlation with biomarkers of haemolysis.

RUNX1/core binding factor A2 regulates platelet 12-lipoxygenase gene (ALOX12): studies in human RUNX1 haplodeficiency.

Regulation of platelet myosin light chain (MYL9) by RUNX1: implications for thrombocytopenia and platelet dysfunction in RUNX1 haplodeficiency.

Platelet protein kinase C-theta deficiency with human RUNX1 mutation: PRKCQ is a transcriptional target of RUNX1.

Editorial: Platelet Genomics and Disorders of Platelet Number and Function.

Defective RAB31-mediated megakaryocytic early endosomal trafficking of VWF, EGFR, and M6PR in RUNX1 deficiency.

Effects of simvastatin on tissue factor pathway of blood coagulation in STATCOPE (Simvastatin in the prevention of COPD exacerbations) trial.