Similar articles for PMID: 26316623

Year	Number of Results
1937	1
1993	1
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2001	2
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1

Paris-Trousseau thrombocytopenia is phenocopied by the autosomal recessive inheritance of a DNA-binding domain mutation in FLI1.

Stevenson WS, Rabbolini DJ, Beutler L, Chen Q, Gabrielli S, Mackay JP, Brighton TA, Ward CM, Morel-Kopp MC. Stevenson WS, et al. Blood. 2015 Oct 22;126(17):2027-30. doi: 10.1182/blood-2015-06-650887. Epub 2015 Aug 27. Blood. 2015. PMID: 26316623 Free article.

2

Paris-Trousseau: evidence keeps pointing to FLI1.

Di Paola J. Di Paola J. Blood. 2015 Oct 22;126(17):1973-4. doi: 10.1182/blood-2015-09-667634. Blood. 2015. PMID: 26494917 Free article.

3

Clonal chromosome anomalies affecting FLI1 mimic inherited thrombocytopenia of the Paris-Trousseau type.

Noris P, Valli R, Pecci A, Marletta C, Invernizzi R, Mare L, Balduini CL, Maserati E. Noris P, et al. Eur J Haematol. 2012 Oct;89(4):345-9. doi: 10.1111/j.1600-0609.2012.01833.x. Epub 2012 Aug 3. Eur J Haematol. 2012. PMID: 22775407 Free article.

4

SNP array and phenotype correlation shows that FLI1 deletion per se is not responsible for thrombocytopenia development in Jacobsen syndrome.

Trkova M, Becvarova V, Hynek M, Hnykova L, Hlavova E, Kreckova G, Kulovany E, Cutka D, Zatloukalova J, Markova K, Sukova M, Horacek J, Stejskal D. Trkova M, et al. Am J Med Genet A. 2012 Oct;158A(10):2545-50. doi: 10.1002/ajmg.a.35537. Epub 2012 Aug 7. Am J Med Genet A. 2012. PMID: 22887642

5

MYH10 protein expression in platelets as a biomarker of RUNX1 and FLI1 alterations.

Antony-Debré I, Bluteau D, Itzykson R, Baccini V, Renneville A, Boehlen F, Morabito M, Droin N, Deswarte C, Chang Y, Leverger G, Solary E, Vainchenker W, Favier R, Raslova H. Antony-Debré I, et al. Blood. 2012 Sep 27;120(13):2719-22. doi: 10.1182/blood-2012-04-422352. Epub 2012 Jun 7. Blood. 2012. PMID: 22677128 Free article.

6

11q24.2q24.3 microdeletion in two families presenting features of Jacobsen syndrome, without intellectual disability: Role of FLI1, ETS1, and SENCR long noncoding RNA.

Conrad S, Demurger F, Moradkhani K, Pichon O, Le Caignec C, Pascal C, Thomas C, Bayart S, Perlat A, Dubourg C, Jaillard S, Nizon M. Conrad S, et al. Am J Med Genet A. 2019 Jun;179(6):993-1000. doi: 10.1002/ajmg.a.61113. Epub 2019 Mar 19. Am J Med Genet A. 2019. PMID: 30888095 Free article. Review.

7

Singling out FLI1 in Paris-Trousseau syndrome.

Falet H. Falet H. Blood. 2017 Jun 29;129(26):3399-3401. doi: 10.1182/blood-2017-05-781252. Blood. 2017. PMID: 28663223 Free PMC article.

8

Mice Haploinsufficient for Ets1 and Fli1 Display Middle Ear Abnormalities and Model Aspects of Jacobsen Syndrome.

Carpinelli MR, Kruse EA, Arhatari BD, Debrincat MA, Ogier JM, Bories JC, Kile BT, Burt RA. Carpinelli MR, et al. Am J Pathol. 2015 Jul;185(7):1867-76. doi: 10.1016/j.ajpath.2015.03.026. Am J Pathol. 2015. PMID: 26093983 Free article.

9

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

Shivdasani RA. Shivdasani RA. J Clin Invest. 2004 Jul;114(1):17-9. doi: 10.1172/JCI22292. J Clin Invest. 2004. PMID: 15232606 Free PMC article. Review.

10

FLI1 level during megakaryopoiesis affects thrombopoiesis and platelet biology.

Vo KK, Jarocha DJ, Lyde RB, Hayes V, Thom CS, Sullivan SK, French DL, Poncz M. Vo KK, et al. Blood. 2017 Jun 29;129(26):3486-3494. doi: 10.1182/blood-2017-02-770958. Epub 2017 Apr 21. Blood. 2017. PMID: 28432223 Free PMC article.

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