Ellis SR - Search Results

1

Identification of RPS14 as a 5q- syndrome gene by RNA interference screen.

Ebert BL, Pretz J, Bosco J, Chang CY, Tamayo P, Galili N, Raza A, Root DE, Attar E, Ellis SR, Golub TR. Ebert BL, et al. Among authors: ellis sr. Nature. 2008 Jan 17;451(7176):335-9. doi: 10.1038/nature06494. Nature. 2008. PMID: 18202658 Free PMC article.

2

Diminutive somatic deletions in the 5q region lead to a phenotype atypical of classical 5q- syndrome.

Vlachos A, Farrar JE, Atsidaftos E, Muir E, Narla A, Markello TC, Singh SA, Landowski M, Gazda HT, Blanc L, Liu JM, Ellis SR, Arceci RJ, Ebert BL, Bodine DM, Lipton JM. Vlachos A, et al. Among authors: ellis sr. Blood. 2013 Oct 3;122(14):2487-90. doi: 10.1182/blood-2013-06-509935. Epub 2013 Aug 13. Blood. 2013. PMID: 23943650 Free PMC article.

3

Deletion of ribosomal protein genes is a common vulnerability in human cancer, especially in concert with TP53 mutations.

Ajore R, Raiser D, McConkey M, Jöud M, Boidol B, Mar B, Saksena G, Weinstock DM, Armstrong S, Ellis SR, Ebert BL, Nilsson B. Ajore R, et al. Among authors: ellis sr. EMBO Mol Med. 2017 Apr;9(4):498-507. doi: 10.15252/emmm.201606660. EMBO Mol Med. 2017. PMID: 28264936 Free PMC article.

4

Ribosome Levels Selectively Regulate Translation and Lineage Commitment in Human Hematopoiesis.

Khajuria RK, Munschauer M, Ulirsch JC, Fiorini C, Ludwig LS, McFarland SK, Abdulhay NJ, Specht H, Keshishian H, Mani DR, Jovanovic M, Ellis SR, Fulco CP, Engreitz JM, Schütz S, Lian J, Gripp KW, Weinberg OK, Pinkus GS, Gehrke L, Regev A, Lander ES, Gazda HT, Lee WY, Panse VG, Carr SA, Sankaran VG. Khajuria RK, et al. Among authors: ellis sr. Cell. 2018 Mar 22;173(1):90-103.e19. doi: 10.1016/j.cell.2018.02.036. Epub 2018 Mar 15. Cell. 2018. PMID: 29551269 Free PMC article.

5

Rare ribosomopathies: insights into mechanisms of cancer.

Aspesi A, Ellis SR. Aspesi A, et al. Among authors: ellis sr. Nat Rev Cancer. 2019 Apr;19(4):228-238. doi: 10.1038/s41568-019-0105-0. Nat Rev Cancer. 2019. PMID: 30670820 Review.

6

Human RPS19, the gene mutated in Diamond-Blackfan anemia, encodes a ribosomal protein required for the maturation of 40S ribosomal subunits.

Flygare J, Aspesi A, Bailey JC, Miyake K, Caffrey JM, Karlsson S, Ellis SR. Flygare J, et al. Among authors: ellis sr. Blood. 2007 Feb 1;109(3):980-6. doi: 10.1182/blood-2006-07-038232. Epub 2006 Sep 21. Blood. 2007. PMID: 16990592 Free PMC article.

7

Ribosomal RNA analysis in the diagnosis of Diamond-Blackfan Anaemia.

Quarello P, Garelli E, Carando A, Mancini C, Foglia L, Botto C, Farruggia P, De Keersmaecker K, Aspesi A, Ellis SR, Dianzani I, Ramenghi U. Quarello P, et al. Among authors: ellis sr. Br J Haematol. 2016 Mar;172(5):782-5. doi: 10.1111/bjh.13880. Epub 2016 Jan 13. Br J Haematol. 2016. PMID: 26763766 Free article.

8

Abnormalities of the large ribosomal subunit protein, Rpl35a, in Diamond-Blackfan anemia.

Farrar JE, Nater M, Caywood E, McDevitt MA, Kowalski J, Takemoto CM, Talbot CC Jr, Meltzer P, Esposito D, Beggs AH, Schneider HE, Grabowska A, Ball SE, Niewiadomska E, Sieff CA, Vlachos A, Atsidaftos E, Ellis SR, Lipton JM, Gazda HT, Arceci RJ. Farrar JE, et al. Among authors: ellis sr. Blood. 2008 Sep 1;112(5):1582-92. doi: 10.1182/blood-2008-02-140012. Epub 2008 Jun 5. Blood. 2008. PMID: 18535205 Free PMC article.

9

Distinct ribosome maturation defects in yeast models of Diamond-Blackfan anemia and Shwachman-Diamond syndrome.

Moore JB 4th, Farrar JE, Arceci RJ, Liu JM, Ellis SR. Moore JB 4th, et al. Among authors: ellis sr. Haematologica. 2010 Jan;95(1):57-64. doi: 10.3324/haematol.2009.012450. Epub 2009 Aug 27. Haematologica. 2010. PMID: 19713223 Free PMC article.

10

Diamond-Blackfan anemia: diagnosis, treatment, and molecular pathogenesis.

Lipton JM, Ellis SR. Lipton JM, et al. Among authors: ellis sr. Hematol Oncol Clin North Am. 2009 Apr;23(2):261-82. doi: 10.1016/j.hoc.2009.01.004. Hematol Oncol Clin North Am. 2009. PMID: 19327583 Free PMC article. Review.

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