11 results for author:"Morin R.D." in Literature citations
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| TBL1XR1/TP63: a novel recurrent gene fusion in B-cell non-Hodgkin lymphoma. Scott D.W., Mungall K.L., Ben-Neriah S., Rogic S., Morin R.D., Slack G.W., Tan K.L., Chan F.C., Lim R.S., Connors J.M. et al. Blood 119:4949-4952(2012) · Mapped (7) |
| Whole transcriptome sequencing reveals recurrent NOTCH1 mutations in mantle cell lymphoma. Kridel R., Meissner B., Rogic S., Boyle M., Telenius A., Woolcock B., Gunawardana J., Jenkins C., Cochrane C., Ben-Neriah S. et al. Blood 119:1963-1971(2012) · Mapped (3) |
| BCL2 mutations in diffuse large B-cell lymphoma. Schuetz J.M., Johnson N.A., Morin R.D., Scott D.W., Tan K., Ben-Nierah S., Boyle M., Slack G.W., Marra M.A., Connors J.M. et al. Leukemia 26:1383-1390(2012) · Mapped (4) |
| Frequent mutation of histone-modifying genes in non-Hodgkin lymphoma. Morin R.D., Mendez-Lago M., Mungall A.J., Goya R., Mungall K.L., Corbett R.D., Johnson N.A., Severson T.M., Chiu R., Field M. et al. Nature 476:298-303(2011) · Mapped (6) |
| Somatic mutations at EZH2 Y641 act dominantly through a mechanism of selectively altered PRC2 catalytic activity, to increase H3K27 trimethylation. Yap D.B., Chu J., Berg T., Schapira M., Cheng S.W., Moradian A., Morin R.D., Mungall A.J., Meissner B., Boyle M. et al. Blood 117:2451-2459(2011) · Mapped (9) |
| Hypomorphic temperature-sensitive alleles of NSDHL cause CK syndrome. McLarren K.W., Severson T.M., du Souich C., Stockton D.W., Kratz L.E., Cunningham D., Hendson G., Morin R.D., Wu D., Paul J.E. et al. Am. J. Hum. Genet. 87:905-914(2010) · UniProtKB (1) · Mapped (4) |
| Acquired TNFRSF14 mutations in follicular lymphoma are associated with worse prognosis. Cheung K.J., Johnson N.A., Affleck J.G., Severson T., Steidl C., Ben-Neriah S., Schein J., Morin R.D., Moore R., Shah S.P. et al. Cancer Res. 70:9166-9174(2010) · Mapped (6) |
| System-level analysis of neuroblastoma tumor-initiating cells implicates AURKB as a novel drug target for neuroblastoma. Morozova O., Vojvodic M., Grinshtein N., Hansford L.M., Blakely K.M., Maslova A., Hirst M., Cezard T., Morin R.D., Moore R. et al. Clin. Cancer Res. 16:4572-4582(2010) · Mapped (3) |
| Somatic mutations altering EZH2 (Tyr641) in follicular and diffuse large B-cell lymphomas of germinal-center origin. Morin R.D., Johnson N.A., Severson T.M., Mungall A.J., An J., Goya R., Paul J.E., Boyle M., Woolcock B.W., Kuchenbauer F. et al. Nat. Genet. 42:181-185(2010) · UniProtKB (1) |
| Mutation of FOXL2 in granulosa-cell tumors of the ovary. Shah S.P., Kobel M., Senz J., Morin R.D., Clarke B.A., Wiegand K.C., Leung G., Zayed A., Mehl E., Kalloger S.E. et al. N. Engl. J. Med. 360:2719-2729(2009) · UniProtKB (1) · Mapped (5) |
| The complete genome of Rhodococcus sp. RHA1 provides insights into a catabolic powerhouse. McLeod M.P., Warren R.L., Hsiao W.W.L., Araki N., Myhre M., Fernandes C., Miyazawa D., Wong W., Lillquist A.L., Wang D. et al. Proc. Natl. Acad. Sci. U.S.A. 103:15582-15587(2006) · UniProtKB (9,075) |