BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

359 related articles for article (PubMed ID: 23502222)

  • 21. 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]  

  • 22. 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]  

  • 23. GATA2 zinc finger 1 mutations associated with biallelic CEBPA mutations define a unique genetic entity of acute myeloid leukemia.
    Greif PA; Dufour A; Konstandin NP; Ksienzyk B; Zellmeier E; Tizazu B; Sturm J; Benthaus T; Herold T; Yaghmaie M; Dörge P; Hopfner KP; Hauser A; Graf A; Krebs S; Blum H; Kakadia PM; Schneider S; Hoster E; Schneider F; Stanulla M; Braess J; Sauerland MC; Berdel WE; Büchner T; Woermann BJ; Hiddemann W; Spiekermann K; Bohlander SK
    Blood; 2012 Jul; 120(2):395-403. PubMed ID: 22649106
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. 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]  

  • 26. Myeloid malignancies with somatic
    Alfayez M; Wang SA; Bannon SA; Kontoyiannis DP; Kornblau SM; Orange JS; Mace EM; DiNardo CD
    Leuk Lymphoma; 2019 Aug; 60(8):2025-2033. PubMed ID: 30648453
    [TBL] [Abstract][Full Text] [Related]  

  • 27. GATA2 regulates dendritic cell differentiation.
    Onodera K; Fujiwara T; Onishi Y; Itoh-Nakadai A; Okitsu Y; Fukuhara N; Ishizawa K; Shimizu R; Yamamoto M; Harigae H
    Blood; 2016 Jul; 128(4):508-18. PubMed ID: 27259979
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. GATA2 mutations in patients with acute myeloid leukemia-paired samples analyses show that the mutation is unstable during disease evolution.
    Hou HA; Lin YC; Kuo YY; Chou WC; Lin CC; Liu CY; Chen CY; Lin LI; Tseng MH; Huang CF; Chiang YC; Liu MC; Liu CW; Tang JL; Yao M; Huang SY; Ko BS; Hsu SC; Wu SJ; Tsay W; Chen YC; Tien HF
    Ann Hematol; 2015 Feb; 94(2):211-21. PubMed ID: 25241285
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Haematopoietic and immune defects associated with GATA2 mutation.
    Collin M; Dickinson R; Bigley V
    Br J Haematol; 2015 Apr; 169(2):173-87. PubMed ID: 25707267
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Gata2 haploinsufficiency promotes proliferation and functional decline of hematopoietic stem cells with myeloid bias during aging.
    Abdelfattah A; Hughes-Davies A; Clayfield L; Menendez-Gonzalez JB; Almotiri A; Alotaibi B; Tonks A; Rodrigues NP
    Blood Adv; 2021 Oct; 5(20):4285-4290. PubMed ID: 34496012
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Altered chemotactic response to CXCL12 in patients carrying GATA2 mutations.
    Maciejewski-Duval A; Meuris F; Bignon A; Aknin ML; Balabanian K; Faivre L; Pasquet M; Barlogis V; Fieschi C; Bellanné-Chantelot C; Donadieu J; Schlecht-Louf G; Marin-Esteban V; Bachelerie F
    J Leukoc Biol; 2016 Jun; 99(6):1065-76. PubMed ID: 26710799
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. 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]  

  • 37. Distinct functions of dispersed GATA factor complexes at an endogenous gene locus.
    Grass JA; Jing H; Kim SI; Martowicz ML; Pal S; Blobel GA; Bresnick EH
    Mol Cell Biol; 2006 Oct; 26(19):7056-67. PubMed ID: 16980610
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. 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]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 18.