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Results: 1 to 20 of 22

Cited In for PubMed (Select 15232614)

1.

Hematopoietic transcription factor mutations and inherited platelet dysfunction.

Songdej N, Rao AK.

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

2.

Human CalDAG-GEFI gene (RASGRP2) mutation affects platelet function and causes severe bleeding.

Canault M, Ghalloussi D, Grosdidier C, Guinier M, Perret C, Chelghoum N, Germain M, Raslova H, Peiretti F, Morange PE, Saut N, Pillois X, Nurden AT, Cambien F, Pierres A, van den Berg TK, Kuijpers TW, Alessi MC, Tregouet DA.

J Exp Med. 2014 Jun 30;211(7):1349-62. doi: 10.1084/jem.20130477. Epub 2014 Jun 23.

3.

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. Epub 2014 Mar 20. Review.

4.

Identification and initial functional characterization of a human vascular cell-enriched long noncoding RNA.

Bell RD, Long X, Lin M, Bergmann JH, Nanda V, Cowan SL, Zhou Q, Han Y, Spector DL, Zheng D, Miano JM.

Arterioscler Thromb Vasc Biol. 2014 Jun;34(6):1249-59. doi: 10.1161/ATVBAHA.114.303240. Epub 2014 Feb 27.

5.

Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defects.

Stockley J, Morgan NV, Bem D, Lowe GC, Lordkipanidzé M, Dawood B, Simpson MA, Macfarlane K, Horner K, Leo VC, Talks K, Motwani J, Wilde JT, Collins PW, Makris M, Watson SP, Daly ME; UK Genotyping and Phenotyping of Platelets Study Group.

Blood. 2013 Dec 12;122(25):4090-3. doi: 10.1182/blood-2013-06-506873. Epub 2013 Oct 7.

6.

Transcription factors in late megakaryopoiesis and related platelet disorders.

Tijssen MR, Ghevaert C.

J Thromb Haemost. 2013 Apr;11(4):593-604. doi: 10.1111/jth.12131. Review.

7.

Identification of unique sensitizing targets for anti-inflammatory CDDO-Me in metastatic melanoma by a large-scale synthetic lethal RNAi screening.

Qin Y, Deng W, Ekmekcioglu S, Grimm EA.

Pigment Cell Melanoma Res. 2013 Jan;26(1):97-112. doi: 10.1111/pcmr.12031. Epub 2012 Nov 6.

8.

Coordinate loss of a microRNA and protein-coding gene cooperate in the pathogenesis of 5q- syndrome.

Kumar MS, Narla A, Nonami A, Mullally A, Dimitrova N, Ball B, McAuley JR, Poveromo L, Kutok JL, Galili N, Raza A, Attar E, Gilliland DG, Jacks T, Ebert BL.

Blood. 2011 Oct 27;118(17):4666-73. doi: 10.1182/blood-2010-12-324715. Epub 2011 Aug 26.

9.

Thrombocytopenia in mice lacking the carboxy-terminal regulatory domain of the Ets transcription factor Fli1.

Moussa O, LaRue AC, Abangan RS Jr, Williams CR, Zhang XK, Masuya M, Gong YZ, Spyropoulos DD, Ogawa M, Gilkeson G, Watson DK.

Mol Cell Biol. 2010 Nov;30(21):5194-206. doi: 10.1128/MCB.01112-09. Epub 2010 Sep 7.

10.

Severe Progressive Autism Associated with Two de novo Changes: A 2.6-Mb 2q31.1 Deletion and a Balanced t(14;21)(q21.1;p11.2) Translocation with Long-Range Epigenetic Silencing of LRFN5 Expression.

de Bruijn DR, van Dijk AH, Pfundt R, Hoischen A, Merkx GF, Gradek GA, Lybæk H, Stray-Pedersen A, Brunner HG, Houge G.

Mol Syndromol. 2010 Feb;1(1):46-57. doi: 10.1159/000280290. Epub 2010 Feb 12.

11.

Megakaryopoiesis.

Geddis AE.

Semin Hematol. 2010 Jul;47(3):212-9. doi: 10.1053/j.seminhematol.2010.03.001. Review.

12.

Dual requirement for the ETS transcription factors Fli-1 and Erg in hematopoietic stem cells and the megakaryocyte lineage.

Kruse EA, Loughran SJ, Baldwin TM, Josefsson EC, Ellis S, Watson DK, Nurden P, Metcalf D, Hilton DJ, Alexander WS, Kile BT.

Proc Natl Acad Sci U S A. 2009 Aug 18;106(33):13814-9. doi: 10.1073/pnas.0906556106. Epub 2009 Jul 31.

13.

Common features of megakaryocytes and hematopoietic stem cells: what's the connection?

Huang H, Cantor AB.

J Cell Biochem. 2009 Aug 1;107(5):857-64. doi: 10.1002/jcb.22184. Review.

14.

Differentiation-dependent interactions between RUNX-1 and FLI-1 during megakaryocyte development.

Huang H, Yu M, Akie TE, Moran TB, Woo AJ, Tu N, Waldon Z, Lin YY, Steen H, Cantor AB.

Mol Cell Biol. 2009 Aug;29(15):4103-15. doi: 10.1128/MCB.00090-09. Epub 2009 May 26.

15.

ETS2 and ERG promote megakaryopoiesis and synergize with alterations in GATA-1 to immortalize hematopoietic progenitor cells.

Stankiewicz MJ, Crispino JD.

Blood. 2009 Apr 2;113(14):3337-47. doi: 10.1182/blood-2008-08-174813. Epub 2009 Jan 23.

16.

Submicroscopic deletions of 11q24-25 in individuals without Jacobsen syndrome: re-examination of the critical region by high-resolution array-CGH.

Tyson C, Qiao Y, Harvard C, Liu X, Bernier FP, McGillivray B, Farrell SA, Arbour L, Chudley AE, Clarke L, Gibson W, Dyack S, McLeod R, Costa T, Vanallen MI, Yong SL, Graham GE, Macleod P, Patel MS, Hurlburt J, Holden JJ, Lewis SM, Rajcan-Separovic E.

Mol Cytogenet. 2008 Nov 11;1:23. doi: 10.1186/1755-8166-1-23.

17.

A role for Fli-1 in B cell proliferation: implications for SLE pathogenesis.

Bradshaw S, Zheng WJ, Tsoi LC, Gilkeson G, Zhang XK.

Clin Immunol. 2008 Oct;129(1):19-30. doi: 10.1016/j.clim.2008.05.010. Epub 2008 Aug 9.

18.
19.

Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius syndrome.

Klopocki E, Schulze H, Strauss G, Ott CE, Hall J, Trotier F, Fleischhauer S, Greenhalgh L, Newbury-Ecob RA, Neumann LM, Habenicht R, König R, Seemanova E, Megarbane A, Ropers HH, Ullmann R, Horn D, Mundlos S.

Am J Hum Genet. 2007 Feb;80(2):232-40. Epub 2006 Dec 21.

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