155 related articles for article (PubMed ID: 32556109)
1. Somatic genetic rescue in hematopoietic cells in GATA2 deficiency.
Catto LFB; Borges G; Pinto AL; Clé DV; Chahud F; Santana BA; Donaires FS; Calado RT
Blood; 2020 Aug; 136(8):1002-1005. PubMed ID: 32556109
[No Abstract] [Full Text] [Related]
2. Breaking the spatial constraint between neighboring zinc fingers: a new germline mutation in GATA2 deficiency syndrome.
Cavalcante de Andrade Silva M; Katsumura KR; Mehta C; Velloso EDRP; Bresnick EH; Godley LA
Leukemia; 2021 Jan; 35(1):264-268. PubMed ID: 32286542
[No Abstract] [Full Text] [Related]
3. Phenotypic heterogeneity associated with germline
Haddox CL; Carr RM; Abraham RS; Perez Botero J; Rodriguez V; Pardanani A; Patnaik MM
Leuk Lymphoma; 2019 Dec; 60(13):3282-3286. PubMed ID: 31246134
[No Abstract] [Full Text] [Related]
4. GATA2 deficiency and human hematopoietic development modeled using induced pluripotent stem cells.
Jung M; Cordes S; Zou J; Yu SJ; Guitart X; Hong SG; Dang V; Kang E; Donaires FS; Hassan SA; Albitar M; Hsu AP; Holland SM; Hickstein DD; Townsley D; Dunbar CE; Winkler T
Blood Adv; 2018 Dec; 2(23):3553-3565. PubMed ID: 30538114
[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. Case Report: Missing zinc finger domains: hemophagocytic lymphohistiocytosis in a GATA2 deficiency patient triggered by non-tuberculous mycobacteriosis.
Huang X; Wu B; Wu D; Huang X; Shen M
Front Immunol; 2023; 14():1191757. PubMed ID: 37680631
[TBL] [Abstract][Full Text] [Related]
7. GATA2 deficiency in a patient with a somatic mutation of GATA2.
Liu Q; Ju X; Peng H
QJM; 2024 Feb; 117(1):66-68. PubMed ID: 37802913
[No Abstract] [Full Text] [Related]
8. GATA2 mutation with recurrent haemophagocytic lymphohistiocytosis and panniculitis: a case report.
Sun L; Xu N; Shen M; Wang R; Sun Y; Zhuang J; Zhao Y; Zeng X; Zhang X
Rheumatology (Oxford); 2021 Jul; 60(7):e229-e231. PubMed ID: 33410496
[No Abstract] [Full Text] [Related]
9. Somatic genetic alterations predict hematological progression in GATA2 deficiency.
Largeaud L; Collin M; Monselet N; Vergez F; Fregona V; Larcher L; Hirsch P; Duployez N; Bidet A; Luquet I; Bustamante J; Dufrechou S; Prade N; Nolla M; Hamelle C; Tavitian S; Habib C; Meynier M; Bellanne-Chantelot C; Donadieu J; De Fontbrune FS; Fieschi C; Ferster A; Delhommeau F; Delabesse E; Pasquet M
Haematologica; 2023 Jun; 108(6):1515-1529. PubMed ID: 36727400
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. MonoMAC Syndrome Caused by a Novel GATA2 Mutation Successfully Treated by Allogeneic Hematopoietic Stem Cell Transplantation.
Moraes-Fontes MF; Caramalho Í; Hsu AP; Holland SM; Abecasis M
J Clin Immunol; 2019 Jan; 39(1):4-6. PubMed ID: 30478525
[No Abstract] [Full Text] [Related]
12. Folliculotropic mycosis fungoides associated with GATA2 deficiency: a new skin manifestation.
Fertitta L; Fontbrune FS; Battistella M; De Masson A; Bergeron A; Ranta D; Vignon-Pennamen MD; Bagot M; Bouaziz JD
Br J Dermatol; 2018 Dec; 179(6):1420-1421. PubMed ID: 30101490
[No Abstract] [Full Text] [Related]
13. Pathogenic human variant that dislocates GATA2 zinc fingers disrupts hematopoietic gene expression and signaling networks.
Jung MM; Shen S; Botten GA; Olender T; Katsumura KR; Johnson KD; Soukup AA; Liu P; Zhang Q; Jensvold ZD; Lewis PW; Beagrie RA; Low JK; Yang L; Mackay JP; Godley LA; Brand M; Xu J; Keles S; Bresnick EH
J Clin Invest; 2023 Apr; 133(7):. PubMed ID: 36809258
[TBL] [Abstract][Full Text] [Related]
14. Inherited GATA2 Deficiency Is Dominant by Haploinsufficiency and Displays Incomplete Clinical Penetrance.
Oleaga-Quintas C; de Oliveira-Júnior EB; Rosain J; Rapaport F; Deswarte C; Guérin A; Sajjath SM; Zhou YJ; Marot S; Lozano C; Branco L; Fernández-Hidalgo N; Lew DB; Brunel AS; Thomas C; Launay E; Arias AA; Cuffel A; Monjo VC; Neehus AL; Marques L; Roynard M; Moncada-Vélez M; Gerçeker B; Colobran R; Vigué MG; Lopez-Herrera G; Berron-Ruiz L; Méndez NHS; O'Farrill Romanillos P; Le Voyer T; Puel A; Bellanné-Chantelot C; Ramirez KA; Lorenzo-Diaz L; Alejo NR; de Diego RP; Condino-Neto A; Mellouli F; Rodriguez-Gallego C; Witte T; Restrepo JF; Jobim M; Boisson-Dupuis S; Jeziorski E; Fieschi C; Vogt G; Donadieu J; Pasquet M; Vasconcelos J; Ardeniz FO; Martínez-Gallo M; Campos RA; Jobim LF; Martínez-Barricarte R; Liu K; Cobat A; Abel L; Casanova JL; Bustamante J
J Clin Immunol; 2021 Apr; 41(3):639-657. PubMed ID: 33417088
[TBL] [Abstract][Full Text] [Related]
15. rs1573858 GATA-2 homozygote variant associated with pulmonary alveolar proteinosis, cytopenia and neurologic dysfunction.
China N; Gurioli C; Maitan S; Poletti V
Pulmonology; 2020; 26(3):178-180. PubMed ID: 31672593
[No Abstract] [Full Text] [Related]
16. GATA2 Deficiency in a Pediatric Patient.
Mojica AM; Elizalde A
J Allergy Clin Immunol Pract; 2019; 7(6):2021-2022. PubMed ID: 30894283
[No Abstract] [Full Text] [Related]
17. Cellular and metabolic characteristics of pre-leukemic hematopoietic progenitors with GATA2 haploinsufficiency.
Rein A; Geron I; Kugler E; Fishman H; Gottlieb E; Abramovich I; Giladi A; Amit I; Mulet-Lazaro R; Delwel R; Gröschel S; Levin-Zaidman S; Dezorella N; Holdengreber V; Rao TN; Yacobovich J; Steinberg-Shemer O; Huang QH; Tan Y; Chen SJ; Izraeli S; Birger Y
Haematologica; 2023 Sep; 108(9):2316-2330. PubMed ID: 36475518
[TBL] [Abstract][Full Text] [Related]
18. Severe influenza in a paediatric patient with GATA2 deficiency and Emberger syndrome.
Jensen MLN; Mathiasen VD; Ifversen M; Nielsen JSA
BMJ Case Rep; 2020 Dec; 13(12):. PubMed ID: 33370941
[TBL] [Abstract][Full Text] [Related]
19. A novel germline GATA2 frameshift mutation with a premature stop codon in a family with congenital sensory hearing loss and myelodysplastic syndrome.
Nakazawa H; Yamaguchi T; Sakai H; Maruyama M; Kawakami T; Kawakami F; Nishina S; Ishikawa M; Kosho T; Ishida F
Int J Hematol; 2021 Aug; 114(2):286-291. PubMed ID: 33759087
[TBL] [Abstract][Full Text] [Related]
20. A Nationwide Study of GATA2 Deficiency in Norway-the Majority of Patients Have Undergone Allo-HSCT.
Jørgensen SF; Buechner J; Myhre AE; Galteland E; Spetalen S; Kulseth MA; Sorte HS; Holla ØL; Lundman E; Alme C; Heier I; Flægstad T; Fløisand Y; Benneche A; Fevang B; Aukrust P; Stray-Pedersen A; Gedde-Dahl T; Nordøy I
J Clin Immunol; 2022 Feb; 42(2):404-420. PubMed ID: 34893945
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]