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22 results for author:"Mardis E.R."Drop in Literature Citations

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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)

A precise reconstruction of the emergence and constrained radiations of Escherichia coli O157 portrayed by backbone concatenomic analysis.

Leopold S.R., Magrini V., Holt N.J., Shaikh N., Mardis E.R., Cagno J., Ogura Y., Iguchi A., Hayashi T., Mellmann A. et al.

Proc. Natl. Acad. Sci. U.S.A. 106:8713-8718(2009) · UniProtKB (4,844)

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)

A sequence motif within chromatin entry sites directs MSL establishment on the Drosophila X chromosome.

Alekseyenko A.A., Peng S., Larschan E., Gorchakov A.A., Lee O.K., Kharchenko P., McGrath S.D., Wang C.I., Mardis E.R., Park P.J. et al.

Cell 134:599-609(2008) · Mapped (9)

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)

Comprehensive genetic variant discovery in the surfactant protein B gene.

Hamvas A., Wegner D.J., Carlson C.S., Bergmann K.R., Trusgnich M.A., Fulton L., Kasai Y., An P., Mardis E.R., Wilson R.K. et al.

Pediatr. Res. 62:170-175(2007) · Mapped (4)

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)

Genome-wide diversity and selective pressure in the human rhinovirus.

Kistler A.L., Webster D.R., Rouskin S., Magrini V., Credle J.J., Schnurr D.P., Boushey H.A., Mardis E.R., Li H., DeRisi J.L.

Virol. J. 4:40-40(2007) · UniProtKB (28)

Expression of a bcr-1 isoform of RARalpha-PML does not affect the penetrance of acute promyelocytic leukemia or the acquisition of an interstitial deletion on mouse chromosome 2.

Walter M.J., Ries R.E., Armstrong J.R., Park J.S., Mardis E.R., Ley T.J.

Blood 109:1237-1240(2007) · Mapped (4)

The complete genome sequence of a chronic atrophic gastritis Helicobacter pylori strain: evolution during disease progression.

Oh J.D., Kling-Baeckhed H., Giannakis M., Xu J., Fulton R.S., Fulton L.A., Cordum H.S., Wang C., Elliott G., Edwards J. et al.

Proc. Natl. Acad. Sci. U.S.A. 103:9999-10004(2006) · UniProtKB (1,541)

Identification of genes subject to positive selection in uropathogenic strains of Escherichia coli: a comparative genomics approach.

Chen S.L., Hung C.-S., Xu J., Reigstad C.S., Magrini V., Sabo A., Blasiar D., Bieri T., Meyer R.R., Ozersky P. et al.

Proc. Natl. Acad. Sci. U.S.A. 103:5977-5982(2006) · UniProtKB (5,193)

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)

A Drosophila model of multiple endocrine neoplasia type 2.

Read R.D., Goodfellow P.J., Mardis E.R., Novak N., Armstrong J.R., Cagan R.L.

Genetics 171:1057-1081(2005) · Mapped (390)

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)

Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution.

Hillier L.W., Miller W., Birney E., Warren W., Hardison R.C., Ponting C.P., Bork P., Burt D.W., Groenen M.A.M., Delany M.E. et al.

Nature 432:695-716(2004) · UniProtKB (10)

The genome sequence of Caenorhabditis briggsae: a platform for comparative genomics.

Stein L.D., Bao Z., Blasiar D., Blumenthal T., Brent M.R., Chen N., Chinwalla A., Clarke L., Clee C., Coghlan A. et al.

PLoS Biol. 1:166-192(2003) · UniProtKB (21,614)

The DNA sequence of human chromosome 7.

Hillier L.W., Fulton R.S., Fulton L.A., Graves T.A., Pepin K.H., Wagner-McPherson C., Layman D., Maas J., Jaeger S., Walker R. et al.

Nature 424:157-164(2003) · UniProtKB (1)

The DNA sequence of human chromosome 7.

Hillier L.W., Fulton R.S., Fulton L.A., Graves T.A., Pepin K.H., Wagner-McPherson C., Layman D., Maas J., Jaeger S., Walker R. et al.

Nature 424:157-164(2003) · UniProtKB (2,635)

Initial sequencing and comparative analysis of the mouse genome.

Waterston R.H., Lindblad-Toh K., Birney E., Rogers J., Abril J.F., Agarwal P., Agarwala R., Ainscough R., Alexandersson M., An P. et al.

Nature 420:520-562(2002) · UniProtKB (1)

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