BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

194 related articles for article (PubMed ID: 22430350)

  • 1. GATA-2 anomaly and clinical phenotype of a sporadic case of lymphedema, dendritic cell, monocyte, B- and NK-cell (DCML) deficiency, and myelodysplasia.
    Ishida H; Imai K; Honma K; Tamura S; Imamura T; Ito M; Nonoyama S
    Eur J Pediatr; 2012 Aug; 171(8):1273-6. PubMed ID: 22430350
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. GATA2 deficiency: a protean disorder of hematopoiesis, lymphatics, and immunity.
    Spinner MA; Sanchez LA; Hsu AP; Shaw PA; Zerbe CS; Calvo KR; Arthur DC; Gu W; Gould CM; Brewer CC; Cowen EW; Freeman AF; Olivier KN; Uzel G; Zelazny AM; Daub JR; Spalding CD; Claypool RJ; Giri NK; Alter BP; Mace EM; Orange JS; Cuellar-Rodriguez J; Hickstein DD; Holland SM
    Blood; 2014 Feb; 123(6):809-21. PubMed ID: 24227816
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. [GATA2 gene mutations: 3 cases].
    Perrard N; Pokeerbux MR; Quesnel B; Duployez N; Fenwarth L; Preudhomme C; Lefèvre G; Baillet C; Launay D; Terriou L
    Rev Med Interne; 2022 Nov; 43(11):677-682. PubMed ID: 36041908
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Loss of B cells and their precursors is the most constant feature of GATA-2 deficiency in childhood myelodysplastic syndrome.
    Nováková M; Žaliová M; Suková M; Wlodarski M; Janda A; Froňková E; Campr V; Lejhancová K; Zapletal O; Pospíšilová D; Černá Z; Kuhn T; Švec P; Pelková V; Zemanová Z; Kerndrup G; van den Heuvel-Eibrink M; van der Velden V; Niemeyer C; Kalina T; Trka J; Starý J; Hrušák O; Mejstříková E
    Haematologica; 2016 Jun; 101(6):707-16. PubMed ID: 27013649
    [TBL] [Abstract][Full Text] [Related]  

  • 8. MonoMAC syndrome in a patient with a GATA2 mutation: case report and review of the literature.
    Camargo JF; Lobo SA; Hsu AP; Zerbe CS; Wormser GP; Holland SM
    Clin Infect Dis; 2013 Sep; 57(5):697-9. PubMed ID: 23728141
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Young woman with mild bone marrow dysplasia, GATA2 and ASXL1 mutation treated with allogeneic hematopoietic stem cell transplantation.
    Lübking A; Vosberg S; Konstandin NP; Dufour A; Graf A; Krebs S; Blum H; Weber A; Lenhoff S; Ehinger M; Spiekermann K; Greif PA; Cammenga J
    Leuk Res Rep; 2015; 4(2):72-5. PubMed ID: 26716079
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Emberger syndrome: A rare association with hearing loss.
    Zawawi F; Sokolov M; Mawby T; Gordon KA; Papsin BC; Cushing SL
    Int J Pediatr Otorhinolaryngol; 2018 May; 108():82-84. PubMed ID: 29605372
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [GATA2 deficiency].
    Nonoyama S
    Nihon Rinsho; 2014 Oct; 72(10):1861-9. PubMed ID: 25509816
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 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. Rheumatologic manifestations of the "MonoMAC" syndrome. a systematic review.
    Johnson JA; Yu SS; Elist M; Arkfeld D; Panush RS
    Clin Rheumatol; 2015 Sep; 34(9):1643-5. PubMed ID: 25739845
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Skin manifestations among GATA2-deficient patients.
    Polat A; Dinulescu M; Fraitag S; Nimubona S; Toutain F; Jouneau S; Poullot E; Droitcourt C; Dupuy A
    Br J Dermatol; 2018 Mar; 178(3):781-785. PubMed ID: 28440875
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cis-element mutated in GATA2-dependent immunodeficiency governs hematopoiesis and vascular integrity.
    Johnson KD; Hsu AP; Ryu MJ; Wang J; Gao X; Boyer ME; Liu Y; Lee Y; Calvo KR; Keles S; Zhang J; Holland SM; Bresnick EH
    J Clin Invest; 2012 Oct; 122(10):3692-704. PubMed ID: 22996659
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Disseminated Mycosis by Arthrocladium fulminans Jeopardizing a Patient with GATA2 Deficiency.
    Egenlauf B; Schuhmann M; Giese T; Junghanss T; Stojkovic M; Tintelnot K; de Hoog S; Greil J; Richter E; Vehresschild M; Heussel CP; Herth FJF; Kreuter M
    Respiration; 2019; 97(5):472-475. PubMed ID: 30928982
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.