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6 results on '"Grillot, Marcus"'

1. Clonal Architecture of Secondary Acute Myeloid Leukemia

Author

Walter, Matthew J., Shen, Dong, Ding, Li, Shao, Jin, Koboldt, Daniel C., Chen, Ken, Larson, David E., McLellan, Michael D., Dooling, David, Abbott, Rachel, Fulton, Robert, Magrini, Vincent, Schmidt, Heather, Kalicki-Veizer, Joelle, OʼLaughlin, Michelle, Fan, Xian, Grillot, Marcus, Witowski, Sarah, Heath, Sharon, Frater, John L., Eades, William, Tomasson, Michael, Westervelt, Peter, DiPersio, John F., Link, Daniel C., Mardis, Elaine R., Ley, Timothy J., Wilson, Richard K., and Graubert, Timothy A.

Published
2012
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2. Plerixafor, G-CSF and Azacitidine For The Treatment Of MDS: Results Of a Phase I Trial

Author

Schroeder, Mark A., primary, Grillot, Marcus, additional, Reineck, Teresa, additional, Jacoby, Meagan A, additional, Romee, Rizwan, additional, Pusic, Iskra, additional, Welch, John, additional, Uy, Geoffrey L., additional, Cashen, Amanda F, additional, Stockerl-Goldstein, Keith E., additional, Vij, Ravi, additional, Kulkarni, Shashikant, additional, Westervelt, Peter, additional, Walter, Matthew J., additional, and Dipersio, John F., additional

Published
2013
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3. Recurrent mutations in the U2AF1 splicing factor in myelodysplastic syndromes

Author

Graubert, Timothy A, primary, Shen, Dong, additional, Ding, Li, additional, Okeyo-Owuor, Theresa, additional, Lunn, Cara L, additional, Shao, Jin, additional, Krysiak, Kilannin, additional, Harris, Christopher C, additional, Koboldt, Daniel C, additional, Larson, David E, additional, McLellan, Michael D, additional, Dooling, David J, additional, Abbott, Rachel M, additional, Fulton, Robert S, additional, Schmidt, Heather, additional, Kalicki-Veizer, Joelle, additional, O'Laughlin, Michelle, additional, Grillot, Marcus, additional, Baty, Jack, additional, Heath, Sharon, additional, Frater, John L, additional, Nasim, Talat, additional, Link, Daniel C, additional, Tomasson, Michael H, additional, Westervelt, Peter, additional, DiPersio, John F, additional, Mardis, Elaine R, additional, Ley, Timothy J, additional, Wilson, Richard K, additional, and Walter, Matthew J, additional

Published
2011
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4. Recurrent DNMT3A Mutations In Patients with Myelodysplastic Syndrome

Author

Walter, Matthew J., primary, Shen, Dong, additional, Shao, Jin, additional, Ding, Li, additional, Grillot, Marcus, additional, McLellan, Michael, additional, Fulton, Robert, additional, Schmidt, Heather, additional, Kalicki-Veizer, Joelle, additional, Michelle, O'Laughlin, additional, Westervelt, Peter, additional, DiPersio, John F., additional, Mardis, Elaine R, additional, Wilson, Richard, additional, Ley, Timothy J, additional, and Graubert, Timothy, additional

Published
2010
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5. Recurrent mutations in the U2AF1 splicing factor in myelodysplastic syndromes.

Author

Graubert, Timothy A, Shen, Dong, Ding, Li, Okeyo-Owuor, Theresa, Lunn, Cara L, Shao, Jin, Krysiak, Kilannin, Harris, Christopher C, Koboldt, Daniel C, Larson, David E, McLellan, Michael D, Dooling, David J, Abbott, Rachel M, Fulton, Robert S, Schmidt, Heather, Kalicki-Veizer, Joelle, O'Laughlin, Michelle, Grillot, Marcus, Baty, Jack, and Heath, Sharon

Subjects
MYELODYSPLASTIC syndromes, GENETIC mutation, RNA splicing, HEMATOPOIETIC stem cell transplantation, DRUG therapy, ACUTE myeloid leukemia, NUCLEOTIDE sequence
Abstract

Myelodysplastic syndromes (MDS) are hematopoietic stem cell disorders that often progress to chemotherapy-resistant secondary acute myeloid leukemia (sAML). We used whole-genome sequencing to perform an unbiased comprehensive screen to discover the somatic mutations in a sample from an individual with sAML and genotyped the loci containing these mutations in the matched MDS sample. Here we show that a missense mutation affecting the serine at codon 34 (Ser34) in U2AF1 was recurrently present in 13 out of 150 (8.7%) subjects with de novo MDS, and we found suggestive evidence of an increased risk of progression to sAML associated with this mutation. U2AF1 is a U2 auxiliary factor protein that recognizes the AG splice acceptor dinucleotide at the 3? end of introns, and the alterations in U2AF1 are located in highly conserved zinc fingers of this protein. Mutant U2AF1 promotes enhanced splicing and exon skipping in reporter assays in vitro. This previously unidentified, recurrent mutation in U2AF1 implicates altered pre-mRNA splicing as a potential mechanism for MDS pathogenesis. [ABSTRACT FROM AUTHOR]

Published
2012
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6. Recurrent DNMT3AMutations In Patients with Myelodysplastic Syndrome

Author

Walter, Matthew J., Shen, Dong, Shao, Jin, Ding, Li, Grillot, Marcus, McLellan, Michael, Fulton, Robert, Schmidt, Heather, Kalicki-Veizer, Joelle, Michelle, O'Laughlin, Westervelt, Peter, DiPersio, John F., Mardis, Elaine R, Wilson, Richard, Ley, Timothy J, and Graubert, Timothy

Abstract

Abstract 608

Published
2010
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