148 related articles for article (PubMed ID: 26713410)
21. Downregulation of GATA1 drives impaired hematopoiesis in primary myelofibrosis.
Gilles L; Arslan AD; Marinaccio C; Wen QJ; Arya P; McNulty M; Yang Q; Zhao JC; Konstantinoff K; Lasho T; Pardanani A; Stein B; Plo I; Sundaravel S; Wickrema A; Migliaccio A; Gurbuxani S; Vainchenker W; Platanias LC; Tefferi A; Crispino JD
J Clin Invest; 2017 Apr; 127(4):1316-1320. PubMed ID: 28240607
[TBL] [Abstract][Full Text] [Related]
22. Induction of hyperproliferative fetal megakaryopoiesis by an N-terminally truncated GATA1 mutant.
Shimizu R; Kobayashi E; Engel JD; Yamamoto M
Genes Cells; 2009 Sep; 14(9):1119-31. PubMed ID: 19682090
[TBL] [Abstract][Full Text] [Related]
23. An inherited mutation leading to production of only the short isoform of GATA-1 is associated with impaired erythropoiesis.
Hollanda LM; Lima CS; Cunha AF; Albuquerque DM; Vassallo J; Ozelo MC; Joazeiro PP; Saad ST; Costa FF
Nat Genet; 2006 Jul; 38(7):807-12. PubMed ID: 16783379
[TBL] [Abstract][Full Text] [Related]
24. Diamond-Blackfan anaemia caused by a de novo initiation codon mutation resulting in a shorter isoform of GATA1.
Chen T; Zhang Q; Shang X; Zou S; Qin J; Li K; Lin B; Tao Z; Long X; Xu X
Clin Genet; 2022 Dec; 102(6):548-554. PubMed ID: 36029112
[TBL] [Abstract][Full Text] [Related]
25. Novel splice variants in the 5'UTR of Gtf2i expressed in the rat brain: alternative 5'UTRs and differential expression in the neuronal dendrites.
Shirai Y; Watanabe M; Sakagami H; Suzuki T
J Neurochem; 2015 Aug; 134(3):578-89. PubMed ID: 25913238
[TBL] [Abstract][Full Text] [Related]
26. Down syndrome-associated haematopoiesis abnormalities created by chromosome transfer and genome editing technologies.
Kazuki Y; Yakura Y; Abe S; Osaki M; Kajitani N; Kazuki K; Takehara S; Honma K; Suemori H; Yamazaki S; Sakuma T; Toki T; Shimizu R; Nakauchi H; Yamamoto T; Oshimura M
Sci Rep; 2014 Aug; 4():6136. PubMed ID: 25159877
[TBL] [Abstract][Full Text] [Related]
27. Genetic analysis of hierarchical regulation for Gata1 and NF-E2 p45 gene expression in megakaryopoiesis.
Takayama M; Fujita R; Suzuki M; Okuyama R; Aiba S; Motohashi H; Yamamoto M
Mol Cell Biol; 2010 Jun; 30(11):2668-80. PubMed ID: 20351175
[TBL] [Abstract][Full Text] [Related]
28. Gata1s mutant mice display persistent defects in the erythroid lineage.
Ling T; Zhang K; Yang J; Gurbuxani S; Crispino JD
Blood Adv; 2023 Jul; 7(13):3253-3264. PubMed ID: 36350717
[TBL] [Abstract][Full Text] [Related]
29. Morphologic and GATA1 sequencing analysis of hematopoiesis in fetuses with trisomy 21.
Hoeller S; Bihl MP; Tzankov A; Chaffard R; Hirschmann P; Miny P; Kühne T; Bruder E
Hum Pathol; 2014 May; 45(5):1003-9. PubMed ID: 24746204
[TBL] [Abstract][Full Text] [Related]
30. Perturbation of fetal hematopoiesis in a mouse model of Down syndrome's transient myeloproliferative disorder.
Birger Y; Goldberg L; Chlon TM; Goldenson B; Muler I; Schiby G; Jacob-Hirsch J; Rechavi G; Crispino JD; Izraeli S
Blood; 2013 Aug; 122(6):988-98. PubMed ID: 23719302
[TBL] [Abstract][Full Text] [Related]
31. SATB1 Chromatin Loops Regulate Megakaryocyte/Erythroid Progenitor Expansion by Facilitating HSP70 and GATA1 Induction.
Wilkes MC; Chae HD; Scanlon V; Cepika AM; Wentworth EP; Saxena M; Eskin A; Chen Z; Glader B; Grazia Roncarolo M; Nelson SF; Sakamoto KM
Stem Cells; 2023 Jun; 41(6):560-569. PubMed ID: 36987811
[TBL] [Abstract][Full Text] [Related]
32. Surgery of a cyanotic heart defect in an 11-year-old boy with thrombocytopenic thrombocytopathy and severe anemia due to a GATA-1 defect: hemostatic therapy.
Hoefer J; Streif W; Kilo J; Grimm M; Berger G; Velik-Salchner C
Klin Padiatr; 2012 Oct; 224(6):382-5. PubMed ID: 22915449
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. N- and C-terminal transactivation domains of GATA1 protein coordinate hematopoietic program.
Kaneko H; Kobayashi E; Yamamoto M; Shimizu R
J Biol Chem; 2012 Jun; 287(25):21439-49. PubMed ID: 22556427
[TBL] [Abstract][Full Text] [Related]
35. GATA1s goes germline.
Mundschau G; Crispino J
Nat Genet; 2006 Jul; 38(7):741-2. PubMed ID: 16804537
[No Abstract] [Full Text] [Related]
36. Establishment of erythroleukemic GAK14 cells and characterization of GATA1 N-terminal domain.
Mukai HY; Suzuki M; Nagano M; Ohmori S; Otsuki A; Tsuchida K; Moriguchi T; Ohneda K; Shimizu R; Ohneda O; Yamamoto M
Genes Cells; 2013 Oct; 18(10):886-98. PubMed ID: 23890289
[TBL] [Abstract][Full Text] [Related]
37.
Martelli F; Verachi P; Zingariello M; Mazzarini M; Vannucchi AM; Lonetti A; Bacci B; Sarli G; Migliaccio AR
Front Genet; 2021; 12():720552. PubMed ID: 34707640
[TBL] [Abstract][Full Text] [Related]
38. Congenital dyserythropoietic anemia type II (CDAII) is caused by mutations in the SEC23B gene.
Bianchi P; Fermo E; Vercellati C; Boschetti C; Barcellini W; Iurlo A; Marcello AP; Righetti PG; Zanella A
Hum Mutat; 2009 Sep; 30(9):1292-8. PubMed ID: 19621418
[TBL] [Abstract][Full Text] [Related]
39. Enhancement of PRMT6 binding to a novel germline
Lu Y; Zhu Q; Wang Y; Luo M; Huang J; Liang Q; Huang L; Ouyang J; Li C; Tang N; Li Y; Kang T; Song Y; Xu X; Ye L; Zheng G; Chen C; Zhu C
Haematologica; 2024 Feb; ():. PubMed ID: 38385251
[TBL] [Abstract][Full Text] [Related]
40. Blasts in transient leukaemia in neonates with Down syndrome differentiate into basophil/mast-cell and megakaryocyte lineages in vitro in association with down-regulation of truncated form of GATA1.
Miyauchi J; Ito Y; Tsukamoto K; Takahashi H; Ishikura K; Sugita K; Miyashita T
Br J Haematol; 2010 Mar; 148(6):898-909. PubMed ID: 20064153
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
