185 related articles for article (PubMed ID: 17209061)
1. 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]
2. Why the disorder induced by GATA1 Arg216Gln mutation should be called "X-linked thrombocytopenia with thalassemia" rather than "X-linked gray platelet syndrome".
Balduini CL; De Candia E; Savoia A
Blood; 2007 Oct; 110(7):2770-1; author reply 2771. PubMed ID: 17881640
[No Abstract] [Full Text] [Related]
3. Platelet proteome and function in X-linked thrombocytopenia with thalassemia and
Bergemalm D; Ramström S; Kardeby C; Hultenby K; Eremo AG; Sihlbom C; Bergström J; Palmblad J; Åström M
Haematologica; 2021 Nov; 106(11):2947-2959. PubMed ID: 33054111
[TBL] [Abstract][Full Text] [Related]
4. Platelet pathology in carriers of the X-linked GATA-1 macrothrombocytopenia.
White JG
Platelets; 2007 Dec; 18(8):620-7. PubMed ID: 18041654
[TBL] [Abstract][Full Text] [Related]
5. X-linked thrombocytopenia with thalassemia displays bone marrow reticulin fibrosis and enhanced angiogenesis: comparisons with primary myelofibrosis.
Åström M; Hahn-Strömberg V; Zetterberg E; Vedin I; Merup M; Palmblad J
Am J Hematol; 2015 Mar; 90(3):E44-8. PubMed ID: 25421114
[TBL] [Abstract][Full Text] [Related]
6. Platelet pathology in sex-linked GATA-1 dyserythropoietic macrothrombocytopenia I ultrastructure.
White JG; Nichols WL; Steensma DP
Platelets; 2007 Jun; 18(4):273-83. PubMed ID: 17538848
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. A novel GATA1 mutation (Stop414Arg) in a family with the rare X-linked blood group Lu(a-b-) phenotype and mild macrothrombocytic thrombocytopenia.
Singleton BK; Roxby DJ; Stirling JW; Spring FA; Wilson C; Poole J; Anstee DJ
Br J Haematol; 2013 Apr; 161(1):139-42. PubMed ID: 23278136
[No Abstract] [Full Text] [Related]
11. 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]
12. Mapping of a syndrome of X-linked thrombocytopenia with Thalassemia to band Xp11-12: further evidence of genetic heterogeneity of X-linked thrombocytopenia.
Raskind WH; Niakan KK; Wolff J; Matsushita M; Vaughan T; Stamatoyannopoulos G; Watanabe C; Rios J; Ochs HD
Blood; 2000 Apr; 95(7):2262-8. PubMed ID: 10733494
[TBL] [Abstract][Full Text] [Related]
13. Intermittent X-linked thrombocytopenia with a novel WAS gene mutation.
Wada T; Itoh M; Maeba H; Toma T; Niida Y; Saikawa Y; Yachie A
Pediatr Blood Cancer; 2014 Apr; 61(4):746-8. PubMed ID: 24115682
[TBL] [Abstract][Full Text] [Related]
14. X-linked thrombocytopenia with thalassemia from a mutation in the amino finger of GATA-1 affecting DNA binding rather than FOG-1 interaction.
Yu C; Niakan KK; Matsushita M; Stamatoyannopoulos G; Orkin SH; Raskind WH
Blood; 2002 Sep; 100(6):2040-5. PubMed ID: 12200364
[TBL] [Abstract][Full Text] [Related]
15. Platelet pathology in sex-linked GATA-1 dyserythropoietic macrothrombocytopenia II. Cytochemistry.
White JG; Nichols WL; Steensma DP
Platelets; 2007 Sep; 18(6):436-50. PubMed ID: 17763153
[TBL] [Abstract][Full Text] [Related]
16. Phenotypic and genetic heterogeneity arising from a novel substitution at amino acid position Val205 in GATA1 related X-linked thrombocytopenia with dyserythropoietic anemia.
Jamwal M; Aggarwal A; Sharma P; Bansal D; Maitra A; Das R
Blood Cells Mol Dis; 2020 Mar; 81():102391. PubMed ID: 31865264
[No Abstract] [Full Text] [Related]
17. 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]
18. Abnormalities of platelet aggregation associated with giant granules in a subset of platelets.
Yang C; Jackups R
Blood; 2018 Apr; 131(14):1626. PubMed ID: 29622538
[No Abstract] [Full Text] [Related]
19. Should any genetic defect affecting α-granules in platelets be classified as gray platelet syndrome?
Nurden AT; Nurden P
Am J Hematol; 2016 Jul; 91(7):714-8. PubMed ID: 26971401
[TBL] [Abstract][Full Text] [Related]
20. First reported co-occurrence of "GATA1-mutated X-linked thrombocytopenia with thalassemia (XLTT)" with heterozygous β-thalassemia.
Singh N; Bhatia P; Jamwal M; Khadwal AR; Chhabra S; Hira JK; Das R; Sharma P
Int J Lab Hematol; 2023 Dec; 45(6):999-1002. PubMed ID: 37382348
[No Abstract] [Full Text] [Related]
[Next] [New Search]
