11
results
for author:"McLellan M."
in Literature Citations
| Recurring mutations found by sequencing an acute myeloid leukemia genome. Mardis E.R., Ding L., Dooling D.J., Larson D.E., McLellan M.D., Chen K., Koboldt D.C., Fulton R.S., Delehaunty K.D., McGrath S.D. et al. N. Engl. J. Med. 361:1058-1066(2009) · Mapped (10) |
| DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome. Ley T.J., Mardis E.R., Ding L., Fulton B., McLellan M.D., Chen K., Dooling D., Dunford-Shore B.H., McGrath S., Hickenbotham M. et al. Nature 456:66-72(2008) · UniProtKB (36) |
| Novel MEK1 mutation identified by mutational analysis of epidermal growth factor receptor signaling pathway genes in lung adenocarcinoma. Marks J.L., Gong Y., Chitale D., Golas B., McLellan M.D., Kasai Y., Ding L., Mardis E.R., Wilson R.K., Solit D. et al. Cancer Res. 68:5524-5528(2008) · Mapped (3) |
| Somatic mutations and germline sequence variants in the expressed tyrosine kinase genes of patients with de novo acute myeloid leukemia. Tomasson M.H., Xiang Z., Walgren R., Zhao Y., Kasai Y., Miner T., Ries R.E., Lubman O., Fremont D.H., McLellan M.D. et al. Blood 111:4797-4808(2008) · Mapped (41) |
| Identification of somatic JAK1 mutations in patients with acute myeloid leukemia. Xiang Z., Zhao Y., Mitaksov V., Fremont D.H., Kasai Y., Molitoris A., Ries R.E., Miner T.L., McLellan M.D., DiPersio J.F. et al. Blood 111:4809-4812(2008) · Mapped (5) |
| C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy. Richards A., van den Maagdenberg A.M.J.M., Jen J.C., Kavanagh D., Bertram P., Spitzer D., Liszewski M.K., Barilla-Labarca M.-L., Terwindt G.M., Kasai Y. et al. |
| Distinct patterns of mutations occurring in de novo AML versus AML arising in the setting of severe congenital neutropenia. Link D.C., Kunter G., Kasai Y., Zhao Y., Miner T., McLellan M.D., Ries R.E., Kapur D., Nagarajan R., Dale D.C. et al. Blood 110:1648-1655(2007) · Mapped (3) |
| Mutational analysis of EGFR and related signaling pathway genes in lung Adenocarcinomas identifies a novel somatic kinase domain mutation in FGFR4. Marks J.L., McLellan M.D., Zakowski M.F., Lash A.E., Kasai Y., Broderick S., Sarkaria I.S., Pham D., Singh B., Miner T.L. et al. PLoS ONE 2:e426-e426(2007) · Mapped (55) |
| Reduced PU.1 expression causes myeloid progenitor expansion and increased leukemia penetrance in mice expressing PML-RARalpha. Walter M.J., Park J.S., Ries R.E., Lau S.K., McLellan M., Jaeger S., Wilson R.K., Mardis E.R., Ley T.J. Proc. Natl. Acad. Sci. U.S.A. 102:12513-12518(2005) · Mapped (11) |
| Generation and annotation of the DNA sequences of human chromosomes 2 and 4. Hillier L.W., Graves T.A., Fulton R.S., Fulton L.A., Pepin K.H., Minx P., Wagner-McPherson C., Layman D., Wylie K., Sekhon M. et al. Nature 434:724-731(2005) · UniProtKB (4,275) |
| Comparison of genome degradation in Paratyphi A and Typhi, human-restricted serovars of Salmonella enterica that cause typhoid. McClelland M., Sanderson K.E., Clifton S.W., Latreille P., Porwollik S., Sabo A., Meyer R., Bieri T., Ozersky P., McLellan M. et al. Nat. Genet. 36:1268-1274(2004) · UniProtKB (4,083) |
