183 related articles for article (PubMed ID: 36231035)
1. 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]
2. 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]
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. New germline GATA1 variant in females with anemia and thrombocytopenia.
Svidnicki MCCM; Filho MAF; Brandão MM; Dos Santos M; de Oliveira Dias R; Tavares RS; Assis-Mendonça GR; Traina F; Saad STO
Blood Cells Mol Dis; 2021 May; 88():102545. PubMed ID: 33611093
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. GATA1 pathogenic variants disrupt MYH10 silencing during megakaryopoiesis.
Saultier P; Cabantous S; Puceat M; Peiretti F; Bigot T; Saut N; Bordet JC; Canault M; van Agthoven J; Loosveld M; Payet-Bornet D; Potier D; Falaise C; Bernot D; Morange PE; Alessi MC; Poggi M
J Thromb Haemost; 2021 Sep; 19(9):2287-2301. PubMed ID: 34060193
[TBL] [Abstract][Full Text] [Related]
7. Mature erythrocyte membrane homeostasis is compromised by loss of the GATA1-FOG1 interaction.
Hasegawa A; Shimizu R; Mohandas N; Yamamoto M
Blood; 2012 Mar; 119(11):2615-23. PubMed ID: 22279059
[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. Combined variants in factor VIII and prostaglandin synthase-1 amplify hemorrhage severity across three generations of descendants.
Nance D; Campbell RA; Rowley JW; Downie JM; Jorde LB; Kahr WH; Mereby SA; Tolley ND; Zimmerman GA; Weyrich AS; Rondina MT
J Thromb Haemost; 2016 Nov; 14(11):2230-2240. PubMed ID: 27629384
[TBL] [Abstract][Full Text] [Related]
10. Impact of transcription factors KLF1 and GATA1 on red blood cell antigen expression: a review.
Lopez GH; Sarri ME; Flower RL; Hyland CA
Immunohematology; 2024 Apr; 40(1):1-9. PubMed ID: 38739025
[TBL] [Abstract][Full Text] [Related]
11. A novel GATA1 variant p.G229D causing the defect of procoagulant platelet formation.
Ding B; Mao Y; Li Y; Xin M; Jiang S; Hu X; Xu Q; Ding Q; Wang X
Thromb Res; 2024 Feb; 234():39-50. PubMed ID: 38159323
[TBL] [Abstract][Full Text] [Related]
12. Effects of the R216Q mutation of GATA-1 on erythropoiesis and megakaryocytopoiesis.
Balduini CL; Pecci A; Loffredo G; Izzo P; Noris P; Grosso M; Bergamaschi G; Rosti V; Magrini U; Ceresa IF; Conti V; Poggi V; Savoia A
Thromb Haemost; 2004 Jan; 91(1):129-40. PubMed ID: 14691578
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Selective impairment of platelet activation to collagen in the absence of GATA1.
Hughan SC; Senis Y; Best D; Thomas A; Frampton J; Vyas P; Watson SP
Blood; 2005 Jun; 105(11):4369-76. PubMed ID: 15701726
[TBL] [Abstract][Full Text] [Related]
15. Light Transmission Aggregometry Does Not Correlate With the Severity of δ-Granule Platelet Storage Pool Deficiency.
Woods GM; Kudron EL; Davis K; Stanek J; Kerlin BA; O'Brien SH
J Pediatr Hematol Oncol; 2016 Oct; 38(7):525-8. PubMed ID: 27403770
[TBL] [Abstract][Full Text] [Related]
16. Cytopenia: a report of haplo-cord transplantation in twin brothers caused by a novel germline GATA1 mutation and family survey.
Sun XH; Liu Q; Wu SN; Xu WH; Chen K; Shao JB; Jiang H
Ann Hematol; 2023 Nov; 102(11):3177-3184. PubMed ID: 37460606
[TBL] [Abstract][Full Text] [Related]
17. Platelet ultrastructural morphometry for diagnosis of partial delta-storage pool disease in patients with mild platelet dysfunction and/or thrombocytopenia of unknown origin. A study of 24 cases.
Pujol-Moix N; Hernández A; Escolar G; Español I; Martínez-Brotóns F; Mateo J
Haematologica; 2000 Jun; 85(6):619-26. PubMed ID: 10870119
[TBL] [Abstract][Full Text] [Related]
18. Long-term outcome of hemizygous and heterozygous carriers of a germline GATA1 (G208R) mutation.
Dührsen U; Kratz CP; Flotho C; Lauenstein T; Bommer M; König E; Brittinger G; Heimpel H
Ann Hematol; 2011 Mar; 90(3):301-6. PubMed ID: 20922527
[TBL] [Abstract][Full Text] [Related]
19. Regulation of GATA1 levels in erythropoiesis.
Gutiérrez L; Caballero N; Fernández-Calleja L; Karkoulia E; Strouboulis J
IUBMB Life; 2020 Jan; 72(1):89-105. PubMed ID: 31769197
[TBL] [Abstract][Full Text] [Related]
20. Platelet granule disorders.
White JG
Crit Rev Oncol Hematol; 1986; 4(4):337-77. PubMed ID: 3513985
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
