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Items: 15


GATA1 Binding Kinetics on Conformation-Specific Binding Sites Elicit Differential Transcriptional Regulation.

Hasegawa A, Kaneko H, Ishihara D, Nakamura M, Watanabe A, Yamamoto M, Trainor CD, Shimizu R.

Mol Cell Biol. 2016 Aug 15;36(16):2151-67. doi: 10.1128/MCB.00017-16.


GATA family transcriptional factors: emerging suspects in hematologic disorders.

Gao J, Chen YH, Peterson LC.

Exp Hematol Oncol. 2015 Oct 6;4:28. doi: 10.1186/s40164-015-0024-z. Review.


Hematopoietic transcription factor mutations and inherited platelet dysfunction.

Songdej N, Rao AK.

F1000Prime Rep. 2015 May 26;7:66. doi: 10.12703/P7-66. Review.


Erythro-megakaryocytic transcription factors associated with hereditary anemia.

Crispino JD, Weiss MJ.

Blood. 2014 May 15;123(20):3080-8. doi: 10.1182/blood-2014-01-453167. Review.


Analysis of disease-causing GATA1 mutations in murine gene complementation systems.

Campbell AE, Wilkinson-White L, Mackay JP, Matthews JM, Blobel GA.

Blood. 2013 Jun 27;121(26):5218-27. doi: 10.1182/blood-2013-03-488080.


Normal and malignant megakaryopoiesis.

Wen Q, Goldenson B, Crispino JD.

Expert Rev Mol Med. 2011 Oct 21;13:e32. doi: 10.1017/S1462399411002043. Review.


Pleiotropic platelet defects in mice with disrupted FOG1-NuRD interaction.

Wang Y, Meng R, Hayes V, Fuentes R, Yu X, Abrams CS, Heijnen HF, Blobel GA, Marks MS, Poncz M.

Blood. 2011 Dec 1;118(23):6183-91. doi: 10.1182/blood-2011-06-363580.


Homozygosity mapping with SNP arrays confirms 3p21 as a recessive locus for gray platelet syndrome and narrows the interval significantly.

Fabbro S, Kahr WH, Hinckley J, Wang K, Moseley J, Ryu GY, Nixon B, White JG, Bair T, Schutte B, Di Paola J.

Blood. 2011 Mar 24;117(12):3430-4. doi: 10.1182/blood-2010-12-322990.


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. doi: 10.1111/j.1538-7836.2010.04154.x.


Gray platelet syndrome: natural history of a large patient cohort and locus assignment to chromosome 3p.

Gunay-Aygun M, Zivony-Elboum Y, Gumruk F, Geiger D, Cetin M, Khayat M, Kleta R, Kfir N, Anikster Y, Chezar J, Arcos-Burgos M, Shalata A, Stanescu H, Manaster J, Arat M, Edwards H, Freiberg AS, Hart PS, Riney LC, Patzel K, Tanpaiboon P, Markello T, Huizing M, Maric I, Horne M, Kehrel BE, Jurk K, Hansen NF, Cherukuri PF, Jones M, Cruz P, Mullikin JC, Nurden A, White JG, Gahl WA, Falik-Zaccai T.

Blood. 2010 Dec 2;116(23):4990-5001. doi: 10.1182/blood-2010-05-286534.


The α-granule proteome: novel proteins in normal and ghost granules in gray platelet syndrome.

Maynard DM, Heijnen HF, Gahl WA, Gunay-Aygun M.

J Thromb Haemost. 2010 Aug;8(8):1786-96. doi: 10.1111/j.1538-7836.2010.03932.x.


Differential localization of P-selectin and von Willebrand factor during megakaryocyte maturation.

Zingariello M, Fabucci ME, Bosco D, Migliaccio AR, Martelli F, Rana RA, Zetterberg E.

Biotech Histochem. 2010 Apr 28;85(3):157-70. doi: 10.3109/10520290903149612.


Inherited platelet disorders: thrombocytopenias and thrombocytopathies.

D'Andrea G, Chetta M, Margaglione M.

Blood Transfus. 2009 Oct;7(4):278-92. doi: 10.2450/2009.0078-08. Review. No abstract available.


Platelet alpha-granules: basic biology and clinical correlates.

Blair P, Flaumenhaft R.

Blood Rev. 2009 Jul;23(4):177-89. doi: 10.1016/j.blre.2009.04.001. Review.


Human phenotypes associated with GATA-1 mutations.

Ciovacco WA, Raskind WH, Kacena MA.

Gene. 2008 Dec 31;427(1-2):1-6. doi: 10.1016/j.gene.2008.09.018.

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