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4. Generalized verrucosis in a patient with GATA2 deficiency. West ES; Kingsbery MY; Mintz EM; Hsu AP; Holland SM; Rady PL; Tyring SK; Grossman ME Br J Dermatol; 2014 May; 170(5):1182-6. PubMed ID: 24359037 [TBL] [Abstract][Full Text] [Related]
5. WILD syndrome is GATA2 deficiency: A novel deletion in the GATA2 gene. Dorn JM; Patnaik MS; Van Hee M; Smith MJ; Lagerstedt SA; Newman CC; Boyce TG; Abraham RS J Allergy Clin Immunol Pract; 2017; 5(4):1149-1152.e1. PubMed ID: 28373026 [No Abstract] [Full Text] [Related]
6. Mutations of the GATA2 and CEBPA genes in paediatric acute myeloid leukaemia. Shiba N; Funato M; Ohki K; Park MJ; Mizushima Y; Adachi S; Kobayashi M; Kinoshita A; Sotomatsu M; Arakawa H; Tawa A; Horibe K; Tsukimoto I; Hayashi Y Br J Haematol; 2014 Jan; 164(1):142-5. PubMed ID: 24033149 [No Abstract] [Full Text] [Related]
7. Differential effects on gene transcription and hematopoietic differentiation correlate with GATA2 mutant disease phenotypes. Chong CE; Venugopal P; Stokes PH; Lee YK; Brautigan PJ; Yeung DTO; Babic M; Engler GA; Lane SW; Klingler-Hoffmann M; Matthews JM; D'Andrea RJ; Brown AL; Hahn CN; Scott HS Leukemia; 2018 Jan; 32(1):194-202. PubMed ID: 28642594 [TBL] [Abstract][Full Text] [Related]
8. Successful umbilical cord blood hematopoietic stem cell transplantation in pediatric patients with MDS/AML associated with underlying GATA2 mutations: two case reports and review of literature. Mallhi K; Dix DB; Niederhoffer KY; Armstrong L; Rozmus J Pediatr Transplant; 2016 Nov; 20(7):1004-1007. PubMed ID: 27416790 [TBL] [Abstract][Full Text] [Related]
9. Classification of CEBPA mutated acute myeloid leukemia by GATA2 mutations. Marceau-Renaut A; Guihard S; Castaigne S; Dombret H; Preudhomme C; Cheok M Am J Hematol; 2015 May; 90(5):E93-4. PubMed ID: 25611491 [No Abstract] [Full Text] [Related]
10. Spectrum of myeloid neoplasms and immune deficiency associated with germline GATA2 mutations. Mir MA; Kochuparambil ST; Abraham RS; Rodriguez V; Howard M; Hsu AP; Jackson AE; Holland SM; Patnaik MM Cancer Med; 2015 Apr; 4(4):490-9. PubMed ID: 25619630 [TBL] [Abstract][Full Text] [Related]
11. GATA2 gene analysis in several forms of hematological malignancies including familial aggregations. Hamadou WS; Mani R; Besbes S; Bourdon V; Youssef YB; Eisinger F; Mari V; Gesta P; Dreyfus H; Bonadona V; Dugast C; Zattara H; Faivre L; Noguchi T; Khélif A; Sobol H; Soua Z Ann Hematol; 2017 Oct; 96(10):1635-1639. PubMed ID: 28752392 [TBL] [Abstract][Full Text] [Related]
17. A Rare Case of Emberger Syndrome Caused By a De Novo Mutation in the GATA2 Gene. Michelini S; Cardone M; Haag M; Agga O; Bruson A; Maltese PE; Bonizzato A; Bertelli M Lymphology; 2016 Mar; 49(1):15-20. PubMed ID: 29906059 [TBL] [Abstract][Full Text] [Related]
18. Genetic predisposition syndromes: when should they be considered in the work-up of MDS? Babushok DV; Bessler M Best Pract Res Clin Haematol; 2015 Mar; 28(1):55-68. PubMed ID: 25659730 [TBL] [Abstract][Full Text] [Related]
19. Low-level GATA2 overexpression promotes myeloid progenitor self-renewal and blocks lymphoid differentiation in mice. Nandakumar SK; Johnson K; Throm SL; Pestina TI; Neale G; Persons DA Exp Hematol; 2015 Jul; 43(7):565-77.e1-10. PubMed ID: 25907033 [TBL] [Abstract][Full Text] [Related]
20. GATA2 null mutation associated with incomplete penetrance in a family with Emberger syndrome. Brambila-Tapia AJL; García-Ortiz JE; Brouillard P; Nguyen HL; Vikkula M; Ríos-González BE; Sandoval-Muñiz RJ; Sandoval-Talamantes AK; Bobadilla-Morales L; Corona-Rivera JR; Arnaud-Lopez L Hematology; 2017 Sep; 22(8):467-471. PubMed ID: 28271814 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]