BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

127 related articles for article (PubMed ID: 38103735)

  • 1. Aggregates of nonmuscular myosin IIA in erythrocytes associate with GATA1- and GFI1B-related thrombocytopenia.
    Zaninetti C; Rivera J; Vater L; Ohlenforst S; Leinøe E; Böckelmann D; Freson K; Thiele T; Makhloufi H; Rath M; Eberl W; Wolff M; Freyer C; Wesche J; Zieger B; Felbor U; Heidel FH; Greinacher A
    J Thromb Haemost; 2024 Apr; 22(4):1179-1186. PubMed ID: 38103735
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Functional characterization of a novel GFI1B mutation causing congenital macrothrombocytopenia.
    Kitamura K; Okuno Y; Yoshida K; Sanada M; Shiraishi Y; Muramatsu H; Kobayashi R; Furukawa K; Miyano S; Kojima S; Ogawa S; Kunishima S
    J Thromb Haemost; 2016 Jul; 14(7):1462-9. PubMed ID: 27122003
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Different substitutions at residue D218 of the X-linked transcription factor GATA1 lead to altered clinical severity of macrothrombocytopenia and anemia and are associated with variable skewed X inactivation.
    Freson K; Matthijs G; Thys C; Mariën P; Hoylaerts MF; Vermylen J; Van Geet C
    Hum Mol Genet; 2002 Jan; 11(2):147-52. PubMed ID: 11809723
    [TBL] [Abstract][Full Text] [Related]  

  • 4. GFI1B mutation causes a bleeding disorder with abnormal platelet function.
    Stevenson WS; Morel-Kopp MC; Chen Q; Liang HP; Bromhead CJ; Wright S; Turakulov R; Ng AP; Roberts AW; Bahlo M; Ward CM
    J Thromb Haemost; 2013 Nov; 11(11):2039-47. PubMed ID: 23927492
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Novel
    Jurk K; Adenaeuer A; Sollfrank S; Groß K; Häuser F; Czwalinna A; Erkel J; Fritsch N; Marandiuc D; Schaller M; Lackner KJ; Rossmann H; Bergmann F
    Cells; 2022 Sep; 11(19):. PubMed ID: 36231035
    [TBL] [Abstract][Full Text] [Related]  

  • 6. X-linked gray platelet syndrome due to a GATA1 Arg216Gln mutation.
    Tubman VN; Levine JE; Campagna DR; Monahan-Earley R; Dvorak AM; Neufeld EJ; Fleming MD
    Blood; 2007 Apr; 109(8):3297-9. PubMed ID: 17209061
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Thrombocytopenia and CD34 expression is decoupled from α-granule deficiency with mutation of the first growth factor-independent 1B zinc finger.
    Rabbolini DJ; Morel-Kopp MC; Chen Q; Gabrielli S; Dunlop LC; Chew LP; Blair N; Brighton TA; Singh N; Ng AP; Ward CM; Stevenson WS
    J Thromb Haemost; 2017 Nov; 15(11):2245-2258. PubMed ID: 28880435
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Platelet characteristics in patients with X-linked macrothrombocytopenia because of a novel GATA1 mutation.
    Freson K; Devriendt K; Matthijs G; Van Hoof A; De Vos R; Thys C; Minner K; Hoylaerts MF; Vermylen J; Van Geet C
    Blood; 2001 Jul; 98(1):85-92. PubMed ID: 11418466
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Diagnosis of inherited platelet disorders on a blood smear: a tool to facilitate worldwide diagnosis of platelet disorders.
    Greinacher A; Pecci A; Kunishima S; Althaus K; Nurden P; Balduini CL; Bakchoul T
    J Thromb Haemost; 2017 Jul; 15(7):1511-1521. PubMed ID: 28457011
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Dominant negative Gfi1b mutations cause moderate thrombocytopenia and an impaired stress thrombopoiesis associated with mild erythropoietic abnormalities in mice.
    Beauchemin H; Shooshtharizadeh P; Pinder J; Dellaire G; Möröy T
    Haematologica; 2020 Oct; 105(10):2457-2470. PubMed ID: 33054086
    [TBL] [Abstract][Full Text] [Related]  

  • 11. An oligogenic case of severe neonatal thrombocytopenia and a purportedly benign variant in
    Frenkel M; Hall A; Meyn MS; Diamond CA
    Platelets; 2023 Dec; 34(1):2237592. PubMed ID: 37577973
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Specific proteome changes in platelets from individuals with GATA1-, GFI1B-, and RUNX1-linked bleeding disorders.
    Van Bergen MGJM; Marneth AE; Hoogendijk AJ; Van Alphen FPJ; Van den Akker E; Laros-Van Gorkom BAP; Hoeks M; Simons A; De Munnik SA; Janssen JJWM; Martens JHA; Jansen JH; Meijer AB; Van der Reijden BA
    Blood; 2021 Jul; 138(1):86-90. PubMed ID: 33690840
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A Novel GATA1 Variant in the C-Terminal Zinc Finger Compared with the Platelet Phenotype of Patients with A Likely Pathogenic Variant in the N-Terminal Zinc Finger.
    Bastida JM; Malvestiti S; Boeckelmann D; Palma-Barqueros V; Wolter M; Lozano ML; Glonnegger H; Benito R; Zaninetti C; Sobotta F; Schilling FH; Morgan NV; Freson K; Rivera J; Zieger B
    Cells; 2022 Oct; 11(20):. PubMed ID: 36291092
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The transcription factor GATA1 regulates NBEAL2 expression through a long-distance enhancer.
    Wijgaerts A; Wittevrongel C; Thys C; Devos T; Peerlinck K; Tijssen MR; Van Geet C; Freson K
    Haematologica; 2017 Apr; 102(4):695-706. PubMed ID: 28082341
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Macrothrombocytopenia associated with a rare GFI1B missense variant confounding the presentation of immune thrombocytopenia.
    Cheng AN; Bao EL; Fiorini C; Sankaran VG
    Pediatr Blood Cancer; 2019 Sep; 66(9):e27874. PubMed ID: 31207059
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel homozygous
    Brøns N; Zaninetti C; Ostrowski SR; Petersen J; Greinacher A; Rossing M; Leinøe E
    Platelets; 2021 Jul; 32(5):701-704. PubMed ID: 32633597
    [TBL] [Abstract][Full Text] [Related]  

  • 17. High-mobility group protein HMGB2 regulates human erythroid differentiation through trans-activation of GFI1B transcription.
    Laurent B; Randrianarison-Huetz V; Maréchal V; Mayeux P; Dusanter-Fourt I; Duménil D
    Blood; 2010 Jan; 115(3):687-95. PubMed ID: 19965638
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Growth factor independence 1b (gfi1b) is important for the maturation of erythroid cells and the regulation of embryonic globin expression.
    Vassen L; Beauchemin H; Lemsaddek W; Krongold J; Trudel M; Möröy T
    PLoS One; 2014; 9(5):e96636. PubMed ID: 24800817
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A dominant-negative GFI1B mutation in the gray platelet syndrome.
    Monteferrario D; Bolar NA; Marneth AE; Hebeda KM; Bergevoet SM; Veenstra H; Laros-van Gorkom BA; MacKenzie MA; Khandanpour C; Botezatu L; Fransen E; Van Camp G; Duijnhouwer AL; Salemink S; Willemsen B; Huls G; Preijers F; Van Heerde W; Jansen JH; Kempers MJ; Loeys BL; Van Laer L; Van der Reijden BA
    N Engl J Med; 2014 Jan; 370(3):245-53. PubMed ID: 24325358
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.