These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
444 related articles for article (PubMed ID: 25428262)
1. Disruption of SF3B1 results in deregulated expression and splicing of key genes and pathways in myelodysplastic syndrome hematopoietic stem and progenitor cells. Dolatshad H; Pellagatti A; Fernandez-Mercado M; Yip BH; Malcovati L; Attwood M; Przychodzen B; Sahgal N; Kanapin AA; Lockstone H; Scifo L; Vandenberghe P; Papaemmanuil E; Smith CW; Campbell PJ; Ogawa S; Maciejewski JP; Cazzola M; Savage KI; Boultwood J Leukemia; 2015 May; 29(5):1092-103. PubMed ID: 25428262 [TBL] [Abstract][Full Text] [Related]
2. SF3B1 haploinsufficiency leads to formation of ring sideroblasts in myelodysplastic syndromes. Visconte V; Rogers HJ; Singh J; Barnard J; Bupathi M; Traina F; McMahon J; Makishima H; Szpurka H; Jankowska A; Jerez A; Sekeres MA; Saunthararajah Y; Advani AS; Copelan E; Koseki H; Isono K; Padgett RA; Osman S; Koide K; O'Keefe C; Maciejewski JP; Tiu RV Blood; 2012 Oct; 120(16):3173-86. PubMed ID: 22826563 [TBL] [Abstract][Full Text] [Related]
3. SF3B1 mutations in patients with myelodysplastic syndromes: the mutation is stable during disease evolution. Lin CC; Hou HA; Chou WC; Kuo YY; Wu SJ; Liu CY; Chen CY; Tseng MH; Huang CF; Lee FY; Liu MC; Liu CW; Tang JL; Yao M; Huang SY; Hsu SC; Ko BS; Tsay W; Chen YC; Tien HF Am J Hematol; 2014 Aug; 89(8):E109-15. PubMed ID: 24723457 [TBL] [Abstract][Full Text] [Related]
4. Aberrant splicing of genes involved in haemoglobin synthesis and impaired terminal erythroid maturation in SF3B1 mutated refractory anaemia with ring sideroblasts. Conte S; Katayama S; Vesterlund L; Karimi M; Dimitriou M; Jansson M; Mortera-Blanco T; Unneberg P; Papaemmanuil E; Sander B; Skoog T; Campbell P; Walfridsson J; Kere J; Hellström-Lindberg E Br J Haematol; 2015 Nov; 171(4):478-90. PubMed ID: 26255870 [TBL] [Abstract][Full Text] [Related]
5. Distinct iron architecture in SF3B1-mutant myelodysplastic syndrome patients is linked to an SLC25A37 splice variant with a retained intron. Visconte V; Avishai N; Mahfouz R; Tabarroki A; Cowen J; Sharghi-Moshtaghin R; Hitomi M; Rogers HJ; Hasrouni E; Phillips J; Sekeres MA; Heuer AH; Saunthararajah Y; Barnard J; Tiu RV Leukemia; 2015 Jan; 29(1):188-95. PubMed ID: 24854990 [TBL] [Abstract][Full Text] [Related]
6. SF3B1 mutation identifies a distinct subset of myelodysplastic syndrome with ring sideroblasts. Malcovati L; Karimi M; Papaemmanuil E; Ambaglio I; Jädersten M; Jansson M; Elena C; Gallì A; Walldin G; Della Porta MG; Raaschou-Jensen K; Travaglino E; Kallenbach K; Pietra D; Ljungström V; Conte S; Boveri E; Invernizzi R; Rosenquist R; Campbell PJ; Cazzola M; Hellström Lindberg E Blood; 2015 Jul; 126(2):233-41. PubMed ID: 25957392 [TBL] [Abstract][Full Text] [Related]
7. Depletion of Sf3b1 impairs proliferative capacity of hematopoietic stem cells but is not sufficient to induce myelodysplasia. Wang C; Sashida G; Saraya A; Ishiga R; Koide S; Oshima M; Isono K; Koseki H; Iwama A Blood; 2014 May; 123(21):3336-43. PubMed ID: 24735968 [TBL] [Abstract][Full Text] [Related]
8. Cryptic splicing events in the iron transporter ABCB7 and other key target genes in SF3B1-mutant myelodysplastic syndromes. Dolatshad H; Pellagatti A; Liberante FG; Llorian M; Repapi E; Steeples V; Roy S; Scifo L; Armstrong RN; Shaw J; Yip BH; Killick S; Kušec R; Taylor S; Mills KI; Savage KI; Smith CW; Boultwood J Leukemia; 2016 Dec; 30(12):2322-2331. PubMed ID: 27211273 [TBL] [Abstract][Full Text] [Related]
9. Refractory anemia with ring sideroblasts. Malcovati L; Cazzola M Best Pract Res Clin Haematol; 2013 Dec; 26(4):377-85. PubMed ID: 24507814 [TBL] [Abstract][Full Text] [Related]
10. SF3B1-mutated myelodysplastic syndrome with ring sideroblasts harbors more severe iron overload and corresponding over-erythropoiesis. Zhu Y; Li X; Chang C; Xu F; He Q; Guo J; Tao Y; Liu Y; Liu L; Shi W Leuk Res; 2016 May; 44():8-16. PubMed ID: 26970172 [TBL] [Abstract][Full Text] [Related]
11. Activation of targetable inflammatory immune signaling is seen in myelodysplastic syndromes with SF3B1 mutations. Choudhary GS; Pellagatti A; Agianian B; Smith MA; Bhagat TD; Gordon-Mitchell S; Sahu S; Pandey S; Shah N; Aluri S; Aggarwal R; Aminov S; Schwartz L; Steeples V; Booher RN; Ramachandra M; Samson M; Carbajal M; Pradhan K; Bowman TV; Pillai MM; Will B; Wickrema A; Shastri A; Bradley RK; Martell RE; Steidl UG; Gavathiotis E; Boultwood J; Starczynowski DT; Verma A Elife; 2022 Aug; 11():. PubMed ID: 36040792 [TBL] [Abstract][Full Text] [Related]
13. Haploinsufficiency of Sf3b1 leads to compromised stem cell function but not to myelodysplasia. Matsunawa M; Yamamoto R; Sanada M; Sato-Otsubo A; Shiozawa Y; Yoshida K; Otsu M; Shiraishi Y; Miyano S; Isono K; Koseki H; Nakauchi H; Ogawa S Leukemia; 2014 Sep; 28(9):1844-50. PubMed ID: 24535406 [TBL] [Abstract][Full Text] [Related]
15. Mortera-Blanco T; Dimitriou M; Woll PS; Karimi M; Elvarsdottir E; Conte S; Tobiasson M; Jansson M; Douagi I; Moarii M; Saft L; Papaemmanuil E; Jacobsen SEW; Hellström-Lindberg E Blood; 2017 Aug; 130(7):881-890. PubMed ID: 28634182 [TBL] [Abstract][Full Text] [Related]
16. SF3B1 deficiency impairs human erythropoiesis via activation of p53 pathway: implications for understanding of ineffective erythropoiesis in MDS. Huang Y; Hale J; Wang Y; Li W; Zhang S; Zhang J; Zhao H; Guo X; Liu J; Yan H; Yazdanbakhsh K; Huang G; Hillyer CD; Mohandas N; Chen L; Sun L; An X J Hematol Oncol; 2018 Feb; 11(1):19. PubMed ID: 29433555 [TBL] [Abstract][Full Text] [Related]
17. [Gene mutation and myelodysplastic syndromes with ring sideroblast excess]. Meng FK; Huang LF; Zhou JF; Sun HY Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2013 Aug; 21(4):1088-90. PubMed ID: 23998618 [TBL] [Abstract][Full Text] [Related]
18. Altered splicing and cytoplasmic levels of tRNA synthetases in SF3B1-mutant myelodysplastic syndromes as a therapeutic vulnerability. Liberante FG; Lappin K; Barros EM; Vohhodina J; Grebien F; Savage KI; Mills KI Sci Rep; 2019 Feb; 9(1):2678. PubMed ID: 30804405 [TBL] [Abstract][Full Text] [Related]
19. Clinical importance of SF3B1 mutations in Chinese with myelodysplastic syndromes with ring sideroblasts. Cui R; Gale RP; Xu Z; Qin T; Fang L; Zhang H; Pan L; Zhang Y; Xiao Z Leuk Res; 2012 Nov; 36(11):1428-33. PubMed ID: 22921018 [TBL] [Abstract][Full Text] [Related]
20. SF3B1 mutant-induced missplicing of MAP3K7 causes anemia in myelodysplastic syndromes. Lieu YK; Liu Z; Ali AM; Wei X; Penson A; Zhang J; An X; Rabadan R; Raza A; Manley JL; Mukherjee S Proc Natl Acad Sci U S A; 2022 Jan; 119(1):. PubMed ID: 34930825 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]