BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

155 related articles for article (PubMed ID: 34638133)

  • 1. GATA2 deficiency phenotype associated with tandem duplication of GATA2 and overexpression of GATA2-AS1.
    Singh P; Heer M; Resteu A; Mikulasova A; Reza M; Largeaud L; Dufrechou S; Prade N; Dickinson RE; Bustamante J; Neven B; Bigley V; Delabesse E; Rico D; Pasquet M; Collin M
    Blood Adv; 2021 Dec; 5(24):5631-5635. PubMed ID: 34638133
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The evolution of cellular deficiency in GATA2 mutation.
    Dickinson RE; Milne P; Jardine L; Zandi S; Swierczek SI; McGovern N; Cookson S; Ferozepurwalla Z; Langridge A; Pagan S; Gennery A; Heiskanen-Kosma T; Hämäläinen S; Seppänen M; Helbert M; Tholouli E; Gambineri E; Reykdal S; Gottfreðsson M; Thaventhiran JE; Morris E; Hirschfield G; Richter AG; Jolles S; Bacon CM; Hambleton S; Haniffa M; Bryceson Y; Allen C; Prchal JT; Dick JE; Bigley V; Collin M
    Blood; 2014 Feb; 123(6):863-74. PubMed ID: 24345756
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. GATA2 deficiency syndrome: A decade of discovery.
    Homan CC; Venugopal P; Arts P; Shahrin NH; Feurstein S; Rawlings L; Lawrence DM; Andrews J; King-Smith SL; Harvey NL; Brown AL; Scott HS; Hahn CN
    Hum Mutat; 2021 Nov; 42(11):1399-1421. PubMed ID: 34387894
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. A novel GATA2 distal enhancer mutation results in MonoMAC syndrome in 2 second cousins.
    West RR; Bauer TR; Tuschong LM; Embree LJ; Calvo KR; Tillo D; Davis J; Holland SM; Hickstein DD
    Blood Adv; 2023 Oct; 7(20):6351-6363. PubMed ID: 37595058
    [TBL] [Abstract][Full Text] [Related]  

  • 7. GATA2 haploinsufficiency caused by mutations in a conserved intronic element leads to MonoMAC syndrome.
    Hsu AP; Johnson KD; Falcone EL; Sanalkumar R; Sanchez L; Hickstein DD; Cuellar-Rodriguez J; Lemieux JE; Zerbe CS; Bresnick EH; Holland SM
    Blood; 2013 May; 121(19):3830-7, S1-7. PubMed ID: 23502222
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. Heterozygous variants in GATA2 contribute to DCML deficiency in mice by disrupting tandem protein binding.
    Hasegawa A; Hayasaka Y; Morita M; Takenaka Y; Hosaka Y; Hirano I; Yamamoto M; Shimizu R
    Commun Biol; 2022 Apr; 5(1):376. PubMed ID: 35440757
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Lethal Influenza in Two Related Adults with Inherited GATA2 Deficiency.
    Sologuren I; Martínez-Saavedra MT; Solé-Violán J; de Borges de Oliveira E; Betancor E; Casas I; Oleaga-Quintas C; Martínez-Gallo M; Zhang SY; Pestano J; Colobran R; Herrera-Ramos E; Pérez C; López-Rodríguez M; Ruiz-Hernández JJ; Franco N; Ferrer JM; Bilbao C; Andújar-Sánchez M; Álvarez Fernández M; Ciancanelli MJ; Rodríguez de Castro F; Casanova JL; Bustamante J; Rodríguez-Gallego C
    J Clin Immunol; 2018 May; 38(4):513-526. PubMed ID: 29882021
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Disseminated nontuberculous mycobacteriosis and fungemia after second delivery in a patient with MonoMAC syndrome/GATA2 mutation: a case report.
    Haraguchi M; Harada N; Watanabe J; Yoshikawa H; Shirai Y; Komura M; Koyama M; Ito J; Tsukune Y; Horimoto Y; Hayashi T; Nagaoka T; Uekusa T; Takahashi K
    BMC Infect Dis; 2021 May; 21(1):502. PubMed ID: 34051752
    [TBL] [Abstract][Full Text] [Related]  

  • 14. GATA2 mutation in long stand Mycobacterium kansasii infection, myelodysplasia and MonoMAC syndrome: a case-report.
    Mendes-de-Almeida DP; Andrade FG; Borges G; Dos Santos-Bueno FV; Vieira IF; da Rocha LKMDS; Mendes-da-Cruz DA; Zancopé-Oliveira RM; Calado RT; Pombo-de-Oliveira MS
    BMC Med Genet; 2019 Apr; 20(1):64. PubMed ID: 31035956
    [TBL] [Abstract][Full Text] [Related]  

  • 15. GATA2 germline mutations impair GATA2 transcription, causing haploinsufficiency: functional analysis of the p.Arg396Gln mutation.
    Cortés-Lavaud X; Landecho MF; Maicas M; Urquiza L; Merino J; Moreno-Miralles I; Odero MD
    J Immunol; 2015 Mar; 194(5):2190-8. PubMed ID: 25624456
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Sequencing of RNA in single cells reveals a distinct transcriptome signature of hematopoiesis in GATA2 deficiency.
    Wu Z; Gao S; Diamond C; Kajigaya S; Chen J; Shi R; Palmer C; Hsu AP; Calvo KR; Hickstein DD; Holland SM; Young NS
    Blood Adv; 2020 Jun; 4(12):2656-2670. PubMed ID: 32556286
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Connecting the Dots From Fever of Unknown Origin to Myelodysplastic Syndrome: GATA2 Haploinsufficiency.
    Montiel-Esparza R; Reys B; Rogers ZR; Evans AS; Wysocki CA; Timmons C; Dickerson KE
    J Pediatr Hematol Oncol; 2020 Jul; 42(5):e365-e368. PubMed ID: 31033783
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. GATA2 Deficiency in Adult Life Is Characterized by Phenotypic Diversity and Delayed Diagnosis.
    Shamriz O; Zahalka N; Simon AJ; Lev A; Barel O; Mor N; Tal Y; Segel MJ; Somech R; Yonath H; Toker O
    Front Immunol; 2022; 13():886117. PubMed ID: 35603181
    [TBL] [Abstract][Full Text] [Related]  

  • 20. GATA2 and marrow failure.
    Fabozzi F; Strocchio L; Mastronuzzi A; Merli P
    Best Pract Res Clin Haematol; 2021 Jun; 34(2):101278. PubMed ID: 34404529
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.