149 related articles for article (PubMed ID: 33496736)
1. Heterozygous mutation SLFN14 K208N in mice mediates species-specific differences in platelet and erythroid lineage commitment.
Stapley RJ; Smith CW; Haining EJ; Bacon A; Lax S; Pisareva VP; Pisarev AV; Watson SP; Khan AO; Morgan NV
Blood Adv; 2021 Jan; 5(2):377-390. PubMed ID: 33496736
[TBL] [Abstract][Full Text] [Related]
2. Role of the novel endoribonuclease SLFN14 and its disease-causing mutations in ribosomal degradation.
Fletcher SJ; Pisareva VP; Khan AO; Tcherepanov A; Morgan NV; Pisarev AV
RNA; 2018 Jul; 24(7):939-949. PubMed ID: 29678925
[TBL] [Abstract][Full Text] [Related]
3. Ribosome dysfunction underlies SLFN14-related thrombocytopenia.
Ver Donck F; Ramaekers K; Thys C; Van Laer C; Peerlinck K; Van Geet C; Eto K; Labarque V; Freson K
Blood; 2023 May; 141(18):2261-2274. PubMed ID: 36790527
[TBL] [Abstract][Full Text] [Related]
4. SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defects.
Fletcher SJ; Johnson B; Lowe GC; Bem D; Drake S; Lordkipanidzé M; Guiú IS; Dawood B; Rivera J; Simpson MA; Daly ME; Motwani J; Collins PW; Watson SP; Morgan NV;
J Clin Invest; 2015 Sep; 125(9):3600-5. PubMed ID: 26280575
[TBL] [Abstract][Full Text] [Related]
5. Novel SLFN14 mutation associated with macrothrombocytopenia in a patient with severe haemorrhagic syndrome.
Polokhov D; Fedorova D; Ignatova A; Ponomarenko E; Rashevskaya E; Martyanov A; Podoplelova N; Aleksenko M; Mersiyanova I; Seregina E; Poletaev A; Truchina E; Raykina E; Plyasunova S; Novichkova G; Zharkov P; Panteleev M
Orphanet J Rare Dis; 2023 Apr; 18(1):74. PubMed ID: 37041648
[TBL] [Abstract][Full Text] [Related]
6. Characterization of Novel Ribosome-Associated Endoribonuclease SLFN14 from Rabbit Reticulocytes.
Pisareva VP; Muslimov IA; Tcherepanov A; Pisarev AV
Biochemistry; 2015 Jun; 54(21):3286-301. PubMed ID: 25996083
[TBL] [Abstract][Full Text] [Related]
7. Schlafen 14 (SLFN14) is a novel antiviral factor involved in the control of viral replication.
Seong RK; Seo SW; Kim JA; Fletcher SJ; Morgan NV; Kumar M; Choi YK; Shin OS
Immunobiology; 2017 Nov; 222(11):979-988. PubMed ID: 28734654
[TBL] [Abstract][Full Text] [Related]
8.
Stapley RJ; Pisareva VP; Pisarev AV; Morgan NV
Platelets; 2020; 31(3):407-410. PubMed ID: 31378119
[No Abstract] [Full Text] [Related]
9. Distinct, strict requirements for Gfi-1b in adult bone marrow red cell and platelet generation.
Foudi A; Kramer DJ; Qin J; Ye D; Behlich AS; Mordecai S; Preffer FI; Amzallag A; Ramaswamy S; Hochedlinger K; Orkin SH; Hock H
J Exp Med; 2014 May; 211(5):909-27. PubMed ID: 24711581
[TBL] [Abstract][Full Text] [Related]
10. Lysophosphatidic acid receptors 2 and 3 regulate erythropoiesis at different hematopoietic stages.
Chiang JC; Chen WM; Lin KH; Hsia K; Ho YH; Lin YC; Shen TL; Lu JH; Chen SK; Yao CL; Chen BPC; Lee H
Biochim Biophys Acta Mol Cell Biol Lipids; 2021 Jan; 1866(1):158818. PubMed ID: 33035680
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. The spleen is a major site of megakaryopoiesis following transplantation of murine hematopoietic stem cells.
Slayton WB; Georgelas A; Pierce LJ; Elenitoba-Johnson KS; Perry SS; Marx M; Spangrude GJ
Blood; 2002 Dec; 100(12):3975-82. PubMed ID: 12393568
[TBL] [Abstract][Full Text] [Related]
13. FOG-1 and GATA-1 act sequentially to specify definitive megakaryocytic and erythroid progenitors.
Mancini E; Sanjuan-Pla A; Luciani L; Moore S; Grover A; Zay A; Rasmussen KD; Luc S; Bilbao D; O'Carroll D; Jacobsen SE; Nerlov C
EMBO J; 2012 Jan; 31(2):351-65. PubMed ID: 22068055
[TBL] [Abstract][Full Text] [Related]
14. Primitive erythropoiesis and megakaryopoiesis in the yolk sac are independent of c-myb.
Tober J; McGrath KE; Palis J
Blood; 2008 Mar; 111(5):2636-9. PubMed ID: 18174377
[TBL] [Abstract][Full Text] [Related]
15. IDH1 mutation contributes to myeloid dysplasia in mice by disturbing heme biosynthesis and erythropoiesis.
Gu Y; Yang R; Yang Y; Zhao Y; Wakeham A; Li WY; Tseng A; Leca J; Berger T; Saunders M; Fortin J; Gao X; Yuan Y; Xiao L; Zhang F; Zhang L; Gao G; Zhou W; Wang Z; Mak TW; Ye J
Blood; 2021 Feb; 137(7):945-958. PubMed ID: 33254233
[TBL] [Abstract][Full Text] [Related]
16. Transgene insertion in proximity to the c-myb gene disrupts erythroid-megakaryocytic lineage bifurcation.
Mukai HY; Motohashi H; Ohneda O; Suzuki N; Nagano M; Yamamoto M
Mol Cell Biol; 2006 Nov; 26(21):7953-65. PubMed ID: 16940183
[TBL] [Abstract][Full Text] [Related]
17. Distinct circadian time structures characterize myeloid and erythroid progenitor and multipotential cell clonogenicity as well as marrow precursor proliferation dynamics.
Wood PA; Hrushesky WJ; Klevecz R
Exp Hematol; 1998 Jun; 26(6):523-33. PubMed ID: 9620286
[TBL] [Abstract][Full Text] [Related]
18. Homeostatic erythropoiesis by the transcription factor IRF2 through attenuation of type I interferon signaling.
Mizutani T; Tsuji K; Ebihara Y; Taki S; Ohba Y; Taniguchi T; Honda K
Exp Hematol; 2008 Mar; 36(3):255-64. PubMed ID: 18207304
[TBL] [Abstract][Full Text] [Related]
19. Robust hematopoietic progenitor cell commitment in the presence of a conflicting cue.
Shah NA; Levesque MJ; Raj A; Sarkar CA
J Cell Sci; 2015 Aug; 128(16):3009-17. PubMed ID: 26159733
[TBL] [Abstract][Full Text] [Related]
20. Compound heterozygosity for KLF1 mutations is associated with microcytic hypochromic anemia and increased fetal hemoglobin.
Huang J; Zhang X; Liu D; Wei X; Shang X; Xiong F; Yu L; Yin X; Xu X
Eur J Hum Genet; 2015 Oct; 23(10):1341-8. PubMed ID: 25585695
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
