Association of Unconventional Myosin MYO15 Mutations with Human Nonsyndromic Deafness DFNB3 von Wang, Aihui, Liang, Yong, Fridell, Robert A., Probst, Frank J., Wilcox, Edward R., Touchman, Jeffrey W., Morton, Cynthia C., Morell, Robert J., Noben-Trauth, Konrad, Camper, Sally A., Friedman, Thomas B.

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Correction of Deafness in shaker-2 Mice by an Unconventional Myosin in a BAC Transgene von Probst, Frank J., Fridell, Robert A., Raphael, Yehoash, Saunders, Thomas L., Wang, Aihui, Liang, Yong, Morell, Robert J., Touchman, Jeffrey W., Lyons, Robert H., Noben-Trauth, Konrad, Friedman, Thomas B., Camper, Sally A.

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Meiotic arrest and aneuploidy in MLH3-deficient mice von Lipkin, Steven M, Cohen, Paula E, Moens, Peter B, Wang, Victoria, Lenzi, Michelle, Shanmugarajah, Dakshine, Gilgeous, Abigail, Thomas, James, Cheng, Jun, Touchman, Jeffrey W, Green, Eric D, Schwartzberg, Pam, Collins, Francis S

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Characterization of the Human and Mouse Unconventional Myosin XV Genes Responsible for Hereditary Deafness DFNB3 and Shaker 2 von Liang, Yong, Wang, Aihui, Belyantseva, Inna A., Anderson, David W., Probst, Frank J., Barber, Thomas D., Miller, Webb, Touchman, Jeffrey W., Jin, Long, Sullivan, Susan L., Sellers, James R., Camper, Sally A., Lloyd, Ricardo V., Kachar, Bechara, Friedman, Thomas B., Fridell, Robert A.

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Comparative analyses of multi-species sequences from targeted genomic regions von Green, E. D, Thomas, J. W, Touchman, J. W, Blakesley, R. W, Bouffard, G. G, Beckstrom-Sternberg, S. M, Margulies, E. H, Blanchette, M, Siepel, A. C, Thomas, P. J, McDowell, J. C, Maskeri, B, Hansen, N. F, Schwartz, M. S, Weber, R. J, Kent, W. J, Karolchik, D, Bruen, T. C, Bevan, R, Cutler, D. J, Schwartz, S, Elnitski, L, Idol, J. R, Prasad, A. B, Lee-Lin, S.-Q, Maduro, V. V. B, Summers, T. J, Portnoy, M. E, Dietrich, N. L, Akhter, N, Ayele, K, Benjamin, B, Cariaga, K, Brinkley, C. P, Brooks, S. Y, Granite, S, Guan, X, Gupta, J, Haghighi, P, Ho, S.-L, Huang, M. C, Karlins, E, Laric, P. L, Legaspi, R, Lim, M. J, Maduro, Q. L, Masiello, C. A, Mastrian, S. D, McCloskey, J. C, Pearson, R, Stantripop, S, Tiongson, E. E, Tran, J. T, Tsurgeon, C, Vogt, J. L, Walker, M. A, Wetherby, K. D, Wiggins, L. S, Young, A. C, Zhang, L.-H, Osoegawa, K, Zhu, B, Zhao, B, Shu, C. L, De Jong, P. J, Lawrence, C. E, Smit, A. F, Chakravarti, A, Haussler, D, Green, P, Miller, W

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Mutation of a new gene causes a unique form of Hermansky-Pudlak syndrome in a genetic isolate of central Puerto Rico von Gahl, William A, Anikster, Yair, Huizing, Marjan, White, James, Shevchenko, Yuriy O, Fitzpatrick, Diana L, Touchman, Jeffrey W, Compton, John G, Bale, Sherri J, Swank, Richard T, Toro, Jorge R

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Analysis of expressed immunoglobulin heavy chain genes in familial B-CLL von Sakai, Akira, Marti, Gerald E., Caporaso, Neil, Pittaluga, Stefania, Touchman, Jeffrey W., Fend, Falko, Raffeld, Mark

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Mutations in the Gene Encoding KRIT1, a Krev-1/rap1a Binding Protein, Cause Cerebral Cavernous Malformations (CCM1) von Sahoo, Trilochan, Johnson, Eric W., Thomas, James W., Kuehl, Peter M., Jones, Thomas L., Dokken, Charles G., Touchman, Jeffrey W., Gallione, Carol J., Lee-Lin, Shih-Queen, Kosofsky, Barry, Kurth, Janice H., Louis, David N., Mettler, Gabrielle, Morrison, Leslie, Gil-Nagel, Antonio, Rich, Steven S., Zabramski, Joseph M., Boguski, Mark S., Green, EricD, Marchuk, Douglas A.

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Human and mouse alpha-synuclein genes: comparative genomic sequence analysis and identification of a novel gene regulatory element von Touchman, J W, Dehejia, A, Chiba-Falek, O, Cabin, D E, Schwartz, J R, Orrison, B M, Polymeropoulos, M H, Nussbaum, R L

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The genomic region encompassing the nephropathic cystinosis gene (CTNS): complete sequencing of a 200-kb segment and discovery of a novel gene within the common cystinosis-causing... von Touchman, J W, Anikster, Y, Dietrich, N L, Maduro, V V, McDowell, G, Shotelersuk, V, Bouffard, G G, Beckstrom-Sternberg, S M, Gahl, W A, Green, E D

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Proximal and Distal Sequences Control UV Cone Pigment Gene Expression in Transgenic Zebrafish von Luo, Wenqin, Williams, John, Smallwood, Philip M, Touchman, Jeffrey W, Roman, Laura M, Nathans, Jeremy

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Systematic sequencing of cDNA clones using the transposon Tn5 von Shevchenko, Yuriy, Bouffard, Gerard G., Butterfield, Yaron S. N., Blakesley, Robert W., Hartley, James L., Young, Alice C., Marra, Marco A., Jones, Steven J. M., Touchman, Jeffrey W., Green, Eric D.

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Pericentromeric duplications in the laboratory mouse von Thomas, James W, Schueler, Mary G, Summers, Tyrone J, Blakesley, Robert W, McDowell, Jennifer C, Thomas, Pamela J, Idol, Jacquelyn R, Maduro, Valerie V B, Lee-Lin, Shih-Queen, Touchman, Jeffrey W, Bouffard, Gerard G, Beckstrom-Sternberg, Stephen M, Green, Eric D

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Comparative analyses of the Dominant megacolon-SOX10 genomic interval in mouse and human von Southard-Smith, E M, Collins, J E, Ellison, J S, Smith, K J, Baxevanis, A D, Touchman, J W, Green, E D, Dunham, I, Pavan, W J

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Identification and Detection of the Common 65-kb Deletion Breakpoint in the Nephropathic Cystinosis Gene (CTNS) von Anikster, Yair, Lucero, Cynthia, Touchman, Jeffrey W., Huizing, Marjan, McDowell, Geraldine, Shotelersuk, Vorasuk, Green, Eric D., Gahl, William A.

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A physical map of human chromosome 7: an integrated YAC contig map with average STS spacing of 79 kb von Bouffard, G G, Idol, J R, Braden, V V, Iyer, L M, Cunningham, A F, Weintraub, L A, Touchman, J W, Mohr-Tidwell, R M, Peluso, D C, Fulton, R S, Ueltzen, M S, Weissenbach, J, Magness, C L, Green, E D

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Branchpoint and polypyrimidine tract mutations mediating the loss and partial recovery of the Moloney murine sarcoma virus MuSVts110 thermosensitive splicing phenotype von Touchman, J W, D'Souza, I, Heckman, C A, Zhou, R, Biggart, N W, Murphy, Jr, E C

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The NIEHS Xenopus maternal EST project: interim analysis of the first 13,879 ESTs from unfertilized eggs von Blackshear, P J, Lai, W S, Thorn, J M, Kennington, E A, Staffa, N G, Moore, D T, Bouffard, G G, Beckstrom-Sternberg, S M, Touchman, J W, Bonaldo, M F, Soares, M B

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Functional analysis of intra-allelic variation at NACP-Rep1 in the α-synuclein gene von CHIBA-FALEK, Ornit, TOUCHMAN, Jeffrey W, NUSSBAUM, Robert L

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2006 expressed-sequence tags derived from human chromosome 7-enriched cDNA libraries von Touchman, J W, Bouffard, G G, Weintraub, L A, Idol, J R, Wang, L, Robbins, C M, Nussbaum, J C, Lovett, M, Green, E D

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