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.
213 related articles for article (PubMed ID: 21956389)
1. GATA2 mutations lead to MDS and AML. Hyde RK; Liu PP Nat Genet; 2011 Sep; 43(10):926-7. PubMed ID: 21956389 [No Abstract] [Full Text] [Related]
2. Loss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculature. Kazenwadel J; Secker GA; Liu YJ; Rosenfeld JA; Wildin RS; Cuellar-Rodriguez J; Hsu AP; Dyack S; Fernandez CV; Chong CE; Babic M; Bardy PG; Shimamura A; Zhang MY; Walsh T; Holland SM; Hickstein DD; Horwitz MS; Hahn CN; Scott HS; Harvey NL Blood; 2012 Feb; 119(5):1283-91. PubMed ID: 22147895 [TBL] [Abstract][Full Text] [Related]
3. Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia. Hahn CN; Chong CE; Carmichael CL; Wilkins EJ; Brautigan PJ; Li XC; Babic M; Lin M; Carmagnac A; Lee YK; Kok CH; Gagliardi L; Friend KL; Ekert PG; Butcher CM; Brown AL; Lewis ID; To LB; Timms AE; Storek J; Moore S; Altree M; Escher R; Bardy PG; Suthers GK; D'Andrea RJ; Horwitz MS; Scott HS Nat Genet; 2011 Sep; 43(10):1012-7. PubMed ID: 21892162 [TBL] [Abstract][Full Text] [Related]
4. Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome). Ostergaard P; Simpson MA; Connell FC; Steward CG; Brice G; Woollard WJ; Dafou D; Kilo T; Smithson S; Lunt P; Murday VA; Hodgson S; Keenan R; Pilz DT; Martinez-Corral I; Makinen T; Mortimer PS; Jeffery S; Trembath RC; Mansour S Nat Genet; 2011 Sep; 43(10):929-31. PubMed ID: 21892158 [TBL] [Abstract][Full Text] [Related]
5. Heritable GATA2 mutations associated with familial AML-MDS: a case report and review of literature. Gao J; Gentzler RD; Timms AE; Horwitz MS; Frankfurt O; Altman JK; Peterson LC J Hematol Oncol; 2014 Apr; 7():36. PubMed ID: 24754962 [TBL] [Abstract][Full Text] [Related]
6. Donor-derived MDS/AML in families with germline Galera P; Hsu AP; Wang W; Droll S; Chen R; Schwartz JR; Klco JM; Arai S; Maese L; Zerbe C; Parta MJ; Young NS; Holland SM; Hickstein DD; Calvo KR Blood; 2018 Nov; 132(18):1994-1998. PubMed ID: 30232126 [No Abstract] [Full Text] [Related]
7. 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]
8. Genetic predisposition to myelodysplastic syndrome and acute myeloid leukemia in children and young adults. Babushok DV; Bessler M; Olson TS Leuk Lymphoma; 2016; 57(3):520-36. PubMed ID: 26693794 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. First Korean case of Emberger syndrome (primary lymphedema with myelodysplasia) with a novel GATA2 gene mutation. Seo SK; Kim KY; Han SA; Yoon JS; Shin SY; Sohn SK; Moon JH Korean J Intern Med; 2016 Jan; 31(1):188-90. PubMed ID: 26767875 [No Abstract] [Full Text] [Related]
11. High frequency of GATA2 mutations in patients with mild chronic neutropenia evolving to MonoMac syndrome, myelodysplasia, and acute myeloid leukemia. Pasquet M; Bellanné-Chantelot C; Tavitian S; Prade N; Beaupain B; Larochelle O; Petit A; Rohrlich P; Ferrand C; Van Den Neste E; Poirel HA; Lamy T; Ouachée-Chardin M; Mansat-De Mas V; Corre J; Récher C; Plat G; Bachelerie F; Donadieu J; Delabesse E Blood; 2013 Jan; 121(5):822-9. PubMed ID: 23223431 [TBL] [Abstract][Full Text] [Related]
12. Germline GATA2 Mutation and Bone Marrow Failure. McReynolds LJ; Calvo KR; Holland SM Hematol Oncol Clin North Am; 2018 Aug; 32(4):713-728. PubMed ID: 30047422 [TBL] [Abstract][Full Text] [Related]