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Items: 13

1.

The contribution of mouse models to the understanding of constitutional thrombocytopenia.

Léon C, Dupuis A, Gachet C, Lanza F.

Haematologica. 2016 Aug;101(8):896-908. doi: 10.3324/haematol.2015.139394. Review.

2.

Linkage between the mechanisms of thrombocytopenia and thrombopoiesis.

Eto K, Kunishima S.

Blood. 2016 Mar 10;127(10):1234-41. doi: 10.1182/blood-2015-07-607903. Epub 2016 Jan 19. Review.

3.

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.

4.

Distal Deletion of Chromosome 11q Encompassing Jacobsen Syndrome without Platelet Abnormality.

Sheth FJ, Datar C, Andrieux J, Pandit A, Nayak D, Rahman M, Sheth JJ.

Clin Med Insights Pediatr. 2014 Sep 17;8:45-9. doi: 10.4137/CMPed.S18121. eCollection 2014.

5.

The ets transcription factor Fli-1 in development, cancer and disease.

Li Y, Luo H, Liu T, Zacksenhaus E, Ben-David Y.

Oncogene. 2015 Apr 16;34(16):2022-31. doi: 10.1038/onc.2014.162. Epub 2014 Jun 9. Review.

6.

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.

7.

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.

8.

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.

9.

Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome).

Manolakos E, Orru S, Neroutsou R, Kefalas K, Louizou E, Papoulidis I, Thomaidis L, Peitsidis P, Sotiriou S, Kitsos G, Tsoplou P, Petersen MB, Metaxotou A.

Mol Cytogenet. 2009 Dec 9;2:26. doi: 10.1186/1755-8166-2-26.

10.

Epithelial-mesenchymal transitions: the importance of changing cell state in development and disease.

Acloque H, Adams MS, Fishwick K, Bronner-Fraser M, Nieto MA.

J Clin Invest. 2009 Jun;119(6):1438-49. doi: 10.1172/JCI38019. Epub 2009 Jun 1. Review.

11.

Jacobsen syndrome.

Mattina T, Perrotta CS, Grossfeld P.

Orphanet J Rare Dis. 2009 Mar 7;4:9. doi: 10.1186/1750-1172-4-9. Review.

12.

FLI1 monoallelic expression combined with its hemizygous loss underlies Paris-Trousseau/Jacobsen thrombopenia.

Raslova H, Komura E, Le Couédic JP, Larbret F, Debili N, Feunteun J, Danos O, Albagli O, Vainchenker W, Favier R.

J Clin Invest. 2004 Jul;114(1):77-84.

13.

Lonely in Paris: when one gene copy isn't enough.

Shivdasani RA.

J Clin Invest. 2004 Jul;114(1):17-9. Review.

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