PubMed for id: 821562776

Year	Number of Results
1998	1
2000	2
2001	2
2023	2
2024	3

1

Transcription elongation defects link oncogenic SF3B1 mutations to targetable alterations in chromatin landscape.

Boddu PC, Gupta AK, Roy R, De La Peña Avalos B, Olazabal-Herrero A, Neuenkirchen N, Zimmer JT, Chandhok NS, King D, Nannya Y, Ogawa S, Lin H, Simon MD, Dray E, Kupfer GM, Verma A, Neugebauer KM, Pillai MM. Boddu PC, et al. Mol Cell. 2024 Apr 18;84(8):1475-1495.e18. doi: 10.1016/j.molcel.2024.02.032. Epub 2024 Mar 22. Mol Cell. 2024. PMID: 38521065

2

SF3B1 mutations provide genetic vulnerability to copper ionophores in human acute myeloid leukemia.

Moison C, Gracias D, Schmitt J, Girard S, Spinella JF, Fortier S, Boivin I, Mendoza-Sanchez R, Thavonekham B, MacRae T, Mayotte N, Bonneil E, Wittman M, Carmichael J, Ruel R, Thibault P, Hébert J, Marinier A, Sauvageau G. Moison C, et al. Sci Adv. 2024 Mar 22;10(12):eadl4018. doi: 10.1126/sciadv.adl4018. Epub 2024 Mar 22. Sci Adv. 2024. PMID: 38517966 Free PMC article.

3

IMMUNOPHENOTYPE OF LEUKEMIC CELLS IN CHRONIC LYMPHOCYTIC LEUKEMIA PATIENTS WITH NOTCH1 AND SF3B1 GENE MUTATIONS.

Golyarnik N, Абраменко І, Movchan G, Martina Z, Dyagil I, Chumak A, Bazyka D. Golyarnik N, et al. Exp Oncol. 2023 Dec 28;45(3):322-327. doi: 10.15407/exp-oncology.2023.03.322. Exp Oncol. 2023. PMID: 38186023

4

[Clinical and laboratory features of SF3B1-mutated myeloproliferative neoplasms].

Peng L, Zhang YH, Teng GS, Du CX, Wang Y, Hu NB, Li YQ, Shao ZH, Bai J. Peng L, et al. Zhonghua Yi Xue Za Zhi. 2023 Nov 21;103(43):3472-3477. doi: 10.3760/cma.j.cn112137-20230928-00609. Zhonghua Yi Xue Za Zhi. 2023. PMID: 37981774 Chinese.

5

Erythroid Differentiation Enhances RNA Mis-Splicing in SF3B1-Mutant Myelodysplastic Syndromes with Ring Sideroblasts.

Moura PL, Mortera-Blanco T, Hofman IJ, Todisco G, Kretzschmar WW, Björklund AC, Creignou M, Hagemann-Jensen M, Ziegenhain C, Cabrerizo Granados D, Barbosa I, Walldin G, Jansson M, Ashley N, Mead AJ, Lundin V, Dimitriou M, Yoshizato T, Woll PS, Ogawa S, Sandberg R, Jacobsen SEW, Hellström-Lindberg E. Moura PL, et al. Cancer Res. 2024 Jan 16;84(2):211-225. doi: 10.1158/0008-5472.CAN-23-3038. Cancer Res. 2024. PMID: 37921711 Free PMC article.

6

A novel U2 and U11/U12 snRNP protein that associates with the pre-mRNA branch site.

Will CL, Schneider C, MacMillan AM, Katopodis NF, Neubauer G, Wilm M, Lührmann R, Query CC. Will CL, et al. EMBO J. 2001 Aug 15;20(16):4536-46. doi: 10.1093/emboj/20.16.4536. EMBO J. 2001. PMID: 11500380 Free PMC article.

7

Molecular cloning, genetic mapping, and expression of the mouse Sf3b1 (SAP155) gene for the U2 snRNP component of spliceosome.

Isono K, Abe K, Tomaru Y, Okazaki Y, Hayashizaki Y, Koseki H. Isono K, et al. Mamm Genome. 2001 Mar;12(3):192-8. doi: 10.1007/s003350010258. Mamm Genome. 2001. PMID: 11252167

8

Functional association of U2 snRNP with the ATP-independent spliceosomal complex E.

Das R, Zhou Z, Reed R. Das R, et al. Mol Cell. 2000 May;5(5):779-87. doi: 10.1016/s1097-2765(00)80318-4. Mol Cell. 2000. PMID: 10882114 Free article.

9

Functional Cus1p is found with Hsh155p in a multiprotein splicing factor associated with U2 snRNA.

Pauling MH, McPheeters DS, Ares M Jr. Pauling MH, et al. Mol Cell Biol. 2000 Mar;20(6):2176-85. doi: 10.1128/MCB.20.6.2176-2185.2000. Mol Cell Biol. 2000. PMID: 10688664 Free PMC article.

10

Phosphorylation of spliceosomal protein SAP 155 coupled with splicing catalysis.

Wang C, Chua K, Seghezzi W, Lees E, Gozani O, Reed R. Wang C, et al. Genes Dev. 1998 May 15;12(10):1409-14. doi: 10.1101/gad.12.10.1409. Genes Dev. 1998. PMID: 9585501 Free PMC article.

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