Studying clonal dynamics in response to cancer therapy using high-complexity barcoding von Bhang, Hyo-eun C, Ruddy, David A, Krishnamurthy Radhakrishna, Viveksagar, Caushi, Justina X, Zhao, Rui, Hims, Matthew M, Singh, Angad P, Kao, Iris, Rakiec, Daniel, Shaw, Pamela, Balak, Marissa, Raza, Alina, Ackley, Elizabeth, Keen, Nicholas, Schlabach, Michael R, Palmer, Michael, Leary, Rebecca J, Chiang, Derek Y, Sellers, William R, Michor, Franziska, Cooke, Vesselina G, Korn, Joshua M, Stegmeier, Frank

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NxTrim: optimized trimming of Illumina mate pair reads von O'Connell, Jared, Schulz-Trieglaff, Ole, Carlson, Emma, Hims, Matthew M, Gormley, Niall A, Cox, Anthony J

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Loss of Mouse Ikbkap, a Subunit of Elongator, Leads to Transcriptional Deficits and Embryonic Lethality That Can Be Rescued by Human IKBKAP von Chen, Yei-Tsung, Hims, Matthew M., Shetty, Ranjit S., Mull, James, Liu, Lijuan, Leyne, Maire, Slaugenhaupt, Susan A.

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A humanized IKBKAP transgenic mouse models a tissue-specific human splicing defect von Hims, Matthew M., Shetty, Ranjit S., Pickel, James, Mull, James, Leyne, Maire, Liu, Lijuan, Gusella, James F., Slaugenhaupt, Susan A.

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Therapeutic potential and mechanism of kinetin as a treatment for the human splicing disease familial dysautonomia von HIMS, Matthew M, CHERIF IBRAHIM, El, SLAUGENHAUPT, Susan A, LEYNE, Maire, MULL, James, LIJUAN LIU, LAZARO, Conxi, SHETTY, Ranjit S, GILL, Sandra, GUSELLA, James F, REED, Robin

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Specific correction of a splice defect in brain by nutritional supplementation von Shetty, Ranjit S., Gallagher, Cary S., Chen, Yei-Tsung, Hims, Matthew M., Mull, James, Leyne, Maire, Pickel, James, Kwok, David, Slaugenhaupt, Susan A.

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Rescue of a human mRNA splicing defect by the plant cytokinin kinetin von Slaugenhaupt, Susan A., Mull, James, Leyne, Maire, Cuajungco, Math P., Gill, Sandra P., Hims, Matthew M., Quintero, Fabiola, Axelrod, Felicia B., Gusella, James F.

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Mutations in HPRP3, a third member of pre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa von CHAKAROVA, Christina F, HIMS, Matthew M, ROSENBERG, Thomas, WEBSTER, Andrew R, BIRD, Alan C, GAL, Andreas, HUNT, David, VITHANA, Eranga N, BHATTACHARYA, Shomi S, BOLZ, Hanno, ABU-SAFIEH, Leen, PATEL, Reshma J, PAPAIOANNOU, Myrto G, INGLEHEARN, Chris F, KEEN, T. Jeffrey, WILLIS, Catherine, MOORE, Anthony T

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Weak definition of IKBKAP exon 20 leads to aberrant splicing in familial dysautonomia von Ibrahim, El Chérif, Hims, Matthew M., Shomron, Noam, Burge, Christopher B., Slaugenhaupt, Susan A., Reed, Robin

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Mutations in a protein target of the Pim-1 kinase associated with the RP9 form of autosomal dominant retinitis pigmentosa von Keen, T Jeffrey, Hims, Matthew M, McKie, Arthur B, Moore, Anthony T, Doran, Rob M, Mackey, David A, Mansfield, David C, Mueller, Robert F, Bhattacharya, Shomi S, Bird, Alan C, Markham, Alexander F, Inglehearn, Chris F

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Mutations in the RP1 Gene Causing Autosomal Dominant Retinitis Pigmentosa von Bowne, Sara J., Daiger, Stephen P., Hims, Matthew M., Sohocki, Melanie M., Malone, Kimberly A., McKie, Arthur B., Heckenlively, John R., Birch, David G., Inglehearn, Chris F., Bhattacharya, Shomi S., Bird, Alan, Sullivan, Lori S.

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Mutations in a protein target of the Pim-1 kinase associated with the RP9 form of autosomal dominant retinitis pigmentosa

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Weak definition of IKBKAP exon 20 leads to aberrant splicing in familial dysautonomia von Ibrahim, El Chérif, Hims, Matthew M., Shomron, Noam, Burge, Chris B., Slaugenhaupt, Susan A., Reed, Robin

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Mutations in HPRP3, a third member ofpre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa von Chakarova, C. F.

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The Practice of Pre-Therapy von Prouty, Garry F

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Potato virus Y from petunia can cause symptoms of potato tuber necrotic ringspot disease (PTNRD) von Boonham, N. (Central Science Lab., Sand Hutton, York (United Kingdom).), Hims, M, Barker, I, Spence, N

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