123 related articles for article (PubMed ID: 26093983)
1. 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
Am J Pathol; 2015 Jul; 185(7):1867-76. PubMed ID: 26093983
[TBL] [Abstract][Full Text] [Related]
2. 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
Am J Med Genet A; 2019 Jun; 179(6):993-1000. PubMed ID: 30888095
[TBL] [Abstract][Full Text] [Related]
3. Partial Jacobsen syndrome phenotype in a patient with a de novo frameshift mutation in the ETS1 transcription factor.
Tootleman E; Malamut B; Akshoomoff N; Mattson SN; Hoffman HM; Jones MC; Printz B; Shiryaev SA; Grossfeld P
Cold Spring Harb Mol Case Stud; 2019 Jun; 5(3):. PubMed ID: 31160359
[TBL] [Abstract][Full Text] [Related]
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
Am J Med Genet A; 2012 Oct; 158A(10):2545-50. PubMed ID: 22887642
[TBL] [Abstract][Full Text] [Related]
5. 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
Blood; 2015 Oct; 126(17):2027-30. PubMed ID: 26316623
[TBL] [Abstract][Full Text] [Related]
6. Case report:
Trachsel T; Prader S; Steindl K; Pachlopnik Schmid J
Front Immunol; 2022; 13():867206. PubMed ID: 36341443
[TBL] [Abstract][Full Text] [Related]
7. Endothelial Loss of ETS1 Impairs Coronary Vascular Development and Leads to Ventricular Non-Compaction.
Wang L; Lin L; Qi H; Chen J; Grossfeld P
Circ Res; 2022 Aug; 131(5):371-387. PubMed ID: 35894043
[TBL] [Abstract][Full Text] [Related]
8. 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
Blood; 2017 Jun; 129(26):3486-3494. PubMed ID: 28432223
[TBL] [Abstract][Full Text] [Related]
9. Paris-Trousseau: evidence keeps pointing to FLI1.
Di Paola J
Blood; 2015 Oct; 126(17):1973-4. PubMed ID: 26494917
[TBL] [Abstract][Full Text] [Related]
10. Gene-targeted deletion in mice of the Ets-1 transcription factor, a candidate gene in the Jacobsen syndrome kidney "critical region," causes abnormal kidney development.
Ye M; Xu L; Fu M; Chen D; Mattina T; Zufardi O; Rossi E; Bush KT; Nigam SK; Grossfeld P
Am J Med Genet A; 2019 Jan; 179(1):71-77. PubMed ID: 30422383
[TBL] [Abstract][Full Text] [Related]
11. Fli1 and Ets1 have distinct roles in connective tissue growth factor/CCN2 gene regulation and induction of the profibrotic gene program.
Nakerakanti SS; Kapanadze B; Yamasaki M; Markiewicz M; Trojanowska M
J Biol Chem; 2006 Sep; 281(35):25259-69. PubMed ID: 16829517
[TBL] [Abstract][Full Text] [Related]
12. FLI1 and EWS-FLI1 function as ternary complex factors and ELK1 and SAP1a function as ternary and quaternary complex factors on the Egr1 promoter serum response elements.
Watson DK; Robinson L; Hodge DR; Kola I; Papas TS; Seth A
Oncogene; 1997 Jan; 14(2):213-21. PubMed ID: 9010223
[TBL] [Abstract][Full Text] [Related]
13. 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. PubMed ID: 15232614
[TBL] [Abstract][Full Text] [Related]
14. 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
Eur J Haematol; 2012 Oct; 89(4):345-9. PubMed ID: 22775407
[TBL] [Abstract][Full Text] [Related]
15. Deregulation of ETS1 and FLI1 contributes to the pathogenesis of diffuse large B-cell lymphoma.
Bonetti P; Testoni M; Scandurra M; Ponzoni M; Piva R; Mensah AA; Rinaldi A; Kwee I; Tibiletti MG; Iqbal J; Greiner TC; Chan WC; Gaidano G; Piris MA; Cavalli F; Zucca E; Inghirami G; Bertoni F
Blood; 2013 Sep; 122(13):2233-41. PubMed ID: 23926301
[TBL] [Abstract][Full Text] [Related]
16. The mouse and human Fli1 genes are similarly regulated by Ets factors in T cells.
Svenson JL; Chike-Harris K; Amria MY; Nowling TK
Genes Immun; 2010 Mar; 11(2):161-72. PubMed ID: 19829305
[TBL] [Abstract][Full Text] [Related]
17. Deletion of ETS-1, a gene in the Jacobsen syndrome critical region, causes ventricular septal defects and abnormal ventricular morphology in mice.
Ye M; Coldren C; Liang X; Mattina T; Goldmuntz E; Benson DW; Ivy D; Perryman MB; Garrett-Sinha LA; Grossfeld P
Hum Mol Genet; 2010 Feb; 19(4):648-56. PubMed ID: 19942620
[TBL] [Abstract][Full Text] [Related]
18. Mouse models in the study of the Ets family of transcription factors.
Bartel FO; Higuchi T; Spyropoulos DD
Oncogene; 2000 Dec; 19(55):6443-54. PubMed ID: 11175360
[TBL] [Abstract][Full Text] [Related]
19. Singling out FLI1 in Paris-Trousseau syndrome.
Falet H
Blood; 2017 Jun; 129(26):3399-3401. PubMed ID: 28663223
[TBL] [Abstract][Full Text] [Related]
20. Diagnosis and fine mapping of a deletion in distal 11q in two Chinese patients with developmental delay.
Ji T; Wu Y; Wang H; Wang J; Jiang Y
J Hum Genet; 2010 Aug; 55(8):486-9. PubMed ID: 20520618
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
