These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
5. Germ-line GATA2 p.THR354MET mutation in familial myelodysplastic syndrome with acquired monosomy 7 and ASXL1 mutation demonstrating rapid onset and poor survival. Bödör C; Renneville A; Smith M; Charazac A; Iqbal S; Etancelin P; Cavenagh J; Barnett MJ; Kramarzová K; Krishnan B; Matolcsy A; Preudhomme C; Fitzgibbon J; Owen C Haematologica; 2012 Jun; 97(6):890-4. PubMed ID: 22271902 [TBL] [Abstract][Full Text] [Related]
6. Acquired ASXL1 mutations are common in patients with inherited GATA2 mutations and correlate with myeloid transformation. West RR; Hsu AP; Holland SM; Cuellar-Rodriguez J; Hickstein DD Haematologica; 2014 Feb; 99(2):276-81. PubMed ID: 24077845 [TBL] [Abstract][Full Text] [Related]
7. MDS-associated mutations in germline GATA2 mutated patients with hematologic manifestations. McReynolds LJ; Yang Y; Yuen Wong H; Tang J; Zhang Y; Mulé MP; Daub J; Palmer C; Foruraghi L; Liu Q; Zhu J; Wang W; West RR; Yohe ME; Hsu AP; Hickstein DD; Townsley DM; Holland SM; Calvo KR; Hourigan CS Leuk Res; 2019 Jan; 76():70-75. PubMed ID: 30578959 [TBL] [Abstract][Full Text] [Related]
8. Prevalence, clinical characteristics, and prognosis of GATA2-related myelodysplastic syndromes in children and adolescents. Wlodarski MW; Hirabayashi S; Pastor V; Starý J; Hasle H; Masetti R; Dworzak M; Schmugge M; van den Heuvel-Eibrink M; Ussowicz M; De Moerloose B; Catala A; Smith OP; Sedlacek P; Lankester AC; Zecca M; Bordon V; Matthes-Martin S; Abrahamsson J; Kühl JS; Sykora KW; Albert MH; Przychodzien B; Maciejewski JP; Schwarz S; Göhring G; Schlegelberger B; Cseh A; Noellke P; Yoshimi A; Locatelli F; Baumann I; Strahm B; Niemeyer CM; Blood; 2016 Mar; 127(11):1387-97; quiz 1518. PubMed ID: 26702063 [TBL] [Abstract][Full Text] [Related]
14. Quantitative and qualitative impairments in GATA2 and myeloid neoplasms. Shimizu R; Yamamoto M IUBMB Life; 2020 Jan; 72(1):142-150. PubMed ID: 31675473 [TBL] [Abstract][Full Text] [Related]
15. GATA2 Deficiency Due to de Novo Complete Monoallelic Deletion in an Adolescent With Myelodysplasia. Vinh DC; Palma L; Storring J; Foulkes WD J Pediatr Hematol Oncol; 2018 May; 40(4):e225-e228. PubMed ID: 29620682 [TBL] [Abstract][Full Text] [Related]
16. Somatic mutations in children with Fisher KE; Hsu AP; Williams CL; Sayeed H; Merritt BY; Elghetany MT; Holland SM; Bertuch AA; Gramatges MM Blood Adv; 2017 Feb; 1(7):443-448. PubMed ID: 29296959 [TBL] [Abstract][Full Text] [Related]
17. Synonymous GATA2 mutations result in selective loss of mutated RNA and are common in patients with GATA2 deficiency. Kozyra EJ; Pastor VB; Lefkopoulos S; Sahoo SS; Busch H; Voss RK; Erlacher M; Lebrecht D; Szvetnik EA; Hirabayashi S; Pasaulienė R; Pedace L; Tartaglia M; Klemann C; Metzger P; Boerries M; Catala A; Hasle H; de Haas V; Kállay K; Masetti R; De Moerloose B; Dworzak M; Schmugge M; Smith O; Starý J; Mejstrikova E; Ussowicz M; Morris E; Singh P; Collin M; Derecka M; Göhring G; Flotho C; Strahm B; Locatelli F; Niemeyer CM; Trompouki E; Wlodarski MW; Leukemia; 2020 Oct; 34(10):2673-2687. PubMed ID: 32555368 [TBL] [Abstract][Full Text] [Related]
18. [Predisposition and progression of myelodysplastic syndromes]. Makishima H Rinsho Ketsueki; 2021; 62(4):278-288. PubMed ID: 33967153 [TBL] [Abstract][Full Text] [Related]
19. Heterogeneity of GATA2-related myeloid neoplasms. Hirabayashi S; Wlodarski MW; Kozyra E; Niemeyer CM Int J Hematol; 2017 Aug; 106(2):175-182. PubMed ID: 28643018 [TBL] [Abstract][Full Text] [Related]
20. [Genomic aberrations in myelodysplastic syndromes and related disorders]. Makishima H Rinsho Ketsueki; 2019; 60(6):600-609. PubMed ID: 31281151 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]