24
results
for author:"Touchman J.W."
in Literature Citations
| Full sequence and comparative analysis of the plasmid pAPEC-1 of avian pathogenic E. coli chi7122 (O78:K80:H9). Mellata M., Touchman J.W., Curtiss R. PLoS ONE 4:e4232-e4232(2009) · UniProtKB (162) |
| The genome of Heliobacterium modesticaldum, a phototrophic representative of the Firmicutes containing the simplest photosynthetic apparatus. Sattley W.M., Madigan M.T., Swingley W.D., Cheung P.C., Clocksin K.M., Conrad A.L., Dejesa L.C., Honchak B.M., Jung D.O., Karbach L.E. et al. J. Bacteriol. 190:4687-4696(2008) · UniProtKB (2,923) |
| Niche adaptation and genome expansion in the chlorophyll d-producing cyanobacterium Acaryochloris marina. Swingley W.D., Chen M., Cheung P.C., Conrad A.L., Dejesa L.C., Hao J., Honchak B.M., Karbach L.E., Kurdoglu A., Lahiri S. et al. Proc. Natl. Acad. Sci. U.S.A. 105:2005-2010(2008) · UniProtKB (8,172) |
| The complete genome sequence of Roseobacter denitrificans reveals a mixotrophic rather than photosynthetic metabolism. Swingley W.D., Sadekar S., Mastrian S.D., Matthies H.J., Hao J., Ramos H., Acharya C.R., Conrad A.L., Taylor H.L., Dejesa L.C. et al. J. Bacteriol. 189:683-690(2007) · UniProtKB (4,118) |
| Functional analysis of intra-allelic variation at NACP-Rep1 in the alpha-synuclein gene. Chiba-Falek O., Touchman J.W., Nussbaum R.L. Hum. Genet. 113:426-431(2003) · Mapped (3) |
| Comparative analyses of multi-species sequences from targeted genomic regions. 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. et al. Nature 424:788-793(2003) · UniProtKB (95) |
| Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Strausberg R.L., Feingold E.A., Grouse L.H., Derge J.G., Klausner R.D., Collins F.S., Wagner L., Shenmen C.M., Schuler G.D., Altschul S.F. et al. Proc. Natl. Acad. Sci. U.S.A. 99:16899-16903(2002) · UniProtKB (500) · Mapped (7,383) |
| Expressed sequence tag analysis of adult human lens for the NEIBank project: over 2000 non-redundant transcripts, novel genes and splice variants. Wistow G., Bernstein S.L., Wyatt M.K., Behal A., Touchman J.W., Bouffard G., Smith D., Peterson K. Mol. Vis. 8:171-184(2002) · UniProtKB (4) |
| Expressed sequence tag analysis of adult human iris for the NEIBank project: steroid-response factors and similarities with retinal pigment epithelium. Wistow G., Bernstein S.L., Ray S., Wyatt M.K., Behal A., Touchman J.W., Bouffard G., Smith D., Peterson K. Mol. Vis. 8:185-195(2002) · UniProtKB (3) |
| Expressed sequence tag analysis of human retina for the NEIBank project: retbindin, an abundant, novel retinal cDNA and alternative splicing of other retina-preferred gene transcripts. Wistow G., Berstein S.L., Wyatt M.K., Ray S., Behal A., Touchman J.W., Bouffard G., Smith D., Peterson K. Mol. Vis. 8:196-204(2002) · UniProtKB (3) |
| Expressed sequence tag analysis of human RPE/choroid for the NEIBank project: over 6000 non-redundant transcripts, novel genes and splice variants. Wistow G., Bernstein S.L., Wyatt M.K., Fariss R.N., Behal A., Touchman J.W., Bouffard G., Smith D., Peterson K. Mol. Vis. 8:205-220(2002) · UniProtKB (3) |
| Meiotic arrest and aneuploidy in MLH3-deficient mice. Lipkin S.M., Moens P.B., Wang V., Lenzi M., Shanmugarajah D., Gilgeous A., Thomas J., Cheng J., Touchman J.W., Green E.D. et al. Nat. Genet. 31:385-390(2002) · Mapped (21) |
| Generation and comparative analysis of approximately 3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11.23 implicated in Williams syndrome. DeSilva U., Elnitski L., Idol J.R., Doyle J.L., Gan W., Thomas J.W., Schwartz S., Dietrich N.L., Beckstrom-Sternberg S.M., McDowell J.C. et al. Genome Res. 12:3-15(2002) · Mapped (103) |
| The human pregnane X receptor: genomic structure and identification and functional characterization of natural allelic variants. Zhang J., Kuehl P., Green E.D., Touchman J.W., Watkins P.B., Daly A., Hall S.D., Maurel P., Relling M., Brimer C. et al. Pharmacogenetics 11:555-572(2001) · UniProtKB (1) |
| Mutation of a new gene causes a unique form of Hermansky-Pudlak syndrome in a genetic isolate of central Puerto Rico. Anikster Y., Huizing M., White J.G., Shevchenko Y.O., Fitzpatrick D.L., Touchman J.W., Comptom J.G., Bale S.J., Swank R.T., Gahl W.A. et al. Nat. Genet. 28:376-380(2001) · UniProtKB (1) |
| The NIEHS Xenopus maternal EST project: interim analysis of the first 13,879 ESTs from unfertilized eggs. Blackshear P.J., Lai W.S., Thorn J.M., Kennington E.A., Staffa N.G. Jr., Moore D.T., Bouffard G.G., Beckstrom-Sternberg S.M., Touchman J.W., Bonaldo M.F. et al. Gene 267:71-87(2001) · UniProtKB (1) |
| Human and mouse alpha-synuclein genes: comparative genomic sequence analysis and identification of a novel gene regulatory element. Touchman J.W., Dehejia A., Chiba-Falek O., Cabin D.E., Schwartz J.R., Orrison B.M., Polymeropoulos M.H., Nussbaum R.L. Genome Res. 11:78-86(2001) · UniProtKB (2) |
| 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 deletion. Touchman J.W., Anikster Y., Dietrich N.L., Maduro V.V.B., McDowell G., Shotelersuk V., Bouffard G.G., Beckstrom-Sternberg S.M., Gahl W.A., Green E.D. Genome Res. 10:165-173(2000) · UniProtKB (5) |
| Comparative genomic sequence analysis of the human and mouse cystic fibrosis transmembrane conductance regulator genes. Ellsworth R.E., Jamison D.C., Touchman J.W., Chissoe S.L., Braden Maduro V.V., Bouffard G.G., Dietrich N.L., Beckstrom-Sternberg S.M., Iyer L.M., Weintraub L.A. et al. Proc. Natl. Acad. Sci. U.S.A. 97:1172-1177(2000) · UniProtKB (4) · Mapped (10) |
| Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2. Liang Y., Wang A., Belyantseva I.A., Anderson D.W., Probst F.J., Barber T.D., Miller W., Touchman J.W., Jin L., Sullivan S.L. et al. |
| Comparative analyses of the Dominant megacolon-SOX10 genomic interval in mouse and human. 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. Mamm. Genome 10:744-749(1999) · Mapped (42) |
| Identification and detection of the common 65-kb deletion breakpoint in the nephropathic cystinosis gene (CTNS). Anikster Y., Lucero C., Touchman J.W., Huizing M., McDowell G., Shotelersuk V., Green E.D., Gahl W.A. Mol. Genet. Metab. 66:111-116(1999) · UniProtKB (1) |
| Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3. Wang A., Liang Y., Fridell R.A., Probst F.J., Wilcox E.R., Touchman J.W., Morton C.C., Morell R.J., Noben-Trauth K., Camper S.A. et al. |
| Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene. Probst F.J., Fridell R.A., Raphael Y., Saunders T.L., Wang A., Liang Y., Morell R.J., Touchman J.W., Lyons R.H., Noben-Trauth K. et al. Science 280:1444-1447(1998) · UniProtKB (1) |
