157 related articles for article (PubMed ID: 28880435)
1. 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]
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. 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]
4. 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]
5. 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]
6. Molecular mechanisms of bleeding disorderassociated GFI1B
van Oorschot R; Hansen M; Koornneef JM; Marneth AE; Bergevoet SM; van Bergen MGJM; van Alphen FPJ; van der Zwaan C; Martens JHA; Vermeulen M; Jansen PWTC; Baltissen MPA; Gorkom BAPL; Janssen H; Jansen JH; von Lindern M; Meijer AB; van den Akker E; van der Reijden BA
Haematologica; 2019 Jul; 104(7):1460-1472. PubMed ID: 30655368
[TBL] [Abstract][Full Text] [Related]
7. A novel GFI1B mutation at the first zinc finger domain causes congenital macrothrombocytopenia.
Uchiyama Y; Ogawa Y; Kunishima S; Shiina M; Nakashima M; Yanagisawa K; Yokohama A; Imagawa E; Miyatake S; Mizuguchi T; Takata A; Miyake N; Ogata K; Handa H; Matsumoto N
Br J Haematol; 2018 Jun; 181(6):843-847. PubMed ID: 28439885
[No Abstract] [Full Text] [Related]
8. Differential transcriptional regulation of meis1 by Gfi1b and its co-factors LSD1 and CoREST.
Chowdhury AH; Ramroop JR; Upadhyay G; Sengupta A; Andrzejczyk A; Saleque S
PLoS One; 2013; 8(1):e53666. PubMed ID: 23308270
[TBL] [Abstract][Full Text] [Related]
9. Combined alpha-delta platelet storage pool deficiency is associated with mutations in GFI1B.
Ferreira CR; Chen D; Abraham SM; Adams DR; Simon KL; Malicdan MC; Markello TC; Gunay-Aygun M; Gahl WA
Mol Genet Metab; 2017 Mar; 120(3):288-294. PubMed ID: 28041820
[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. Platelet CD34 expression and α/δ-granule abnormalities in
Marneth AE; van Heerde WL; Hebeda KM; Laros-van Gorkom BA; Barteling W; Willemsen B; de Graaf AO; Simons A; Jansen JH; Preijers F; Jongmans MC; van der Reijden BA
Blood; 2017 Mar; 129(12):1733-1736. PubMed ID: 28096094
[No Abstract] [Full Text] [Related]
13.
Beauchemin H; Shooshtarizadeh P; Vadnais C; Vassen L; Pastore YD; Möröy T
Haematologica; 2017 Mar; 102(3):484-497. PubMed ID: 28082345
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. GFI1B and LSD1 repress myeloid traits during megakaryocyte differentiation.
Venhuizen J; van Bergen MGJM; Bergevoet SM; Gilissen D; Spruijt CG; Wingens L; van den Akker E; Vermeulen M; Jansen JH; Martens JHA; van der Reijden BA
Commun Biol; 2024 Mar; 7(1):374. PubMed ID: 38548886
[TBL] [Abstract][Full Text] [Related]
16. Overexpression of the zinc finger protein MZF1 inhibits hematopoietic development from embryonic stem cells: correlation with negative regulation of CD34 and c-myb promoter activity.
Perrotti D; Melotti P; Skorski T; Casella I; Peschle C; Calabretta B
Mol Cell Biol; 1995 Nov; 15(11):6075-87. PubMed ID: 7565760
[TBL] [Abstract][Full Text] [Related]
17. Direct transcriptional repression of the genes encoding the zinc-finger proteins Gfi1b and Gfi1 by Gfi1b.
Vassen L; Fiolka K; Mahlmann S; Möröy T
Nucleic Acids Res; 2005; 33(3):987-98. PubMed ID: 15718298
[TBL] [Abstract][Full Text] [Related]
18. Erythroid expansion mediated by the Gfi-1B zinc finger protein: role in normal hematopoiesis.
Osawa M; Yamaguchi T; Nakamura Y; Kaneko S; Onodera M; Sawada K; Jegalian A; Wu H; Nakauchi H; Iwama A
Blood; 2002 Oct; 100(8):2769-77. PubMed ID: 12351384
[TBL] [Abstract][Full Text] [Related]
19. Study of inherited thrombocytopenia resulting from mutations in ETV6 or RUNX1 using a human pluripotent stem cell model.
Borst S; Nations CC; Klein JG; Pavani G; Maguire JA; Camire RM; Drazer MW; Godley LA; French DL; Poncz M; Gadue P
Stem Cell Reports; 2021 Jun; 16(6):1458-1467. PubMed ID: 34019812
[TBL] [Abstract][Full Text] [Related]
20. Dysregulation of oncogenic factors by GFI1B p32: investigation of a novel
Faleschini M; Papa N; Morel-Kopp MC; Marconi C; Giangregorio T; Melazzini F; Bozzi V; Seri M; Noris P; Pecci A; Savoia A; Bottega R
Haematologica; 2022 Jan; 107(1):260-267. PubMed ID: 33472357
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
