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A new murine Rpl5 (uL18) mutation provides a unique model of variably penetrant Diamond-Blackfan anemia.
Yu L, Lemay P, Ludlow A, Guyot MC, Jones M, Mohamed FF, Saroya GA, Panaretos C, Schneider E, Wang Y, Myers G, Khoriaty R, Li Q, Franceschi R, Engel JD, Kaartinen V, Rothstein TL, Justice MJ, Kibar Z, Singh SA. Yu L, et al. Among authors: khoriaty r. Blood Adv. 2021 Oct 26;5(20):4167-4178. doi: 10.1182/bloodadvances.2021004658. Blood Adv. 2021. PMID: 34464976 Free PMC article.
Sequence analysis of 515 kinase genes in chronic lymphocytic leukemia.
Zhang X, Reis M, Khoriaty R, Li Y, Ouillette P, Samayoa J, Carter H, Karchin R, Li M, Diaz LA Jr, Velculescu VE, Papadopoulos N, Kinzler KW, Vogelstein B, Malek SN. Zhang X, et al. Among authors: khoriaty r. Leukemia. 2011 Dec;25(12):1908-10. doi: 10.1038/leu.2011.163. Epub 2011 Jun 24. Leukemia. 2011. PMID: 21701494 Free PMC article. No abstract available.
Functional overlap between the mammalian Sar1a and Sar1b paralogs in vivo.
Tang VT, Xiang J, Chen Z, McCormick J, Abbineni PS, Chen XW, Hoenerhoff M, Emmer BT, Khoriaty R, Lin JD, Ginsburg D. Tang VT, et al. Among authors: khoriaty r. bioRxiv [Preprint]. 2024 Feb 29:2024.02.27.582310. doi: 10.1101/2024.02.27.582310. bioRxiv. 2024. Update in: Proc Natl Acad Sci U S A. 2024 May 7;121(19):e2322164121. doi: 10.1073/pnas.2322164121. PMID: 38463989 Free PMC article. Updated. Preprint.
The COPII pathway and hematologic disease.
Khoriaty R, Vasievich MP, Ginsburg D. Khoriaty R, et al. Blood. 2012 Jul 5;120(1):31-8. doi: 10.1182/blood-2012-01-292086. Epub 2012 May 14. Blood. 2012. PMID: 22586181 Free PMC article. Review.
An erythroid-to-myeloid cell fate conversion is elicited by LSD1 inactivation.
Yu L, Myers G, Ku CJ, Schneider E, Wang Y, Singh SA, Jearawiriyapaisarn N, White A, Moriguchi T, Khoriaty R, Yamamoto M, Rosenfeld MG, Pedron J, Bushweller JH, Lim KC, Engel JD. Yu L, et al. Among authors: khoriaty r. Blood. 2021 Nov 4;138(18):1691-1704. doi: 10.1182/blood.2021011682. Blood. 2021. PMID: 34324630 Free PMC article.
SEC23A rescues SEC23B-deficient congenital dyserythropoietic anemia type II.
King R, Lin Z, Balbin-Cuesta G, Myers G, Friedman A, Zhu G, McGee B, Saunders TL, Kurita R, Nakamura Y, Engel JD, Reddy P, Khoriaty R. King R, et al. Among authors: khoriaty r. Sci Adv. 2021 Nov 26;7(48):eabj5293. doi: 10.1126/sciadv.abj5293. Epub 2021 Nov 24. Sci Adv. 2021. PMID: 34818036 Free PMC article.
45 results