1 - 25 of 28 results for author:"Thompson E.M." in Literature citations
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| Genotypic and phenotypic analysis of 396 individuals with mutations in Sonic Hedgehog. Solomon B.D., Bear K.A., Wyllie A., Keaton A.A., Dubourg C., David V., Mercier S., Odent S., Hehr U., Paulussen A. et al. J. Med. Genet. 49:473-479(2012) · Mapped (2) |
| Plasticity of animal genome architecture unmasked by rapid evolution of a pelagic tunicate. Denoeud F., Henriet S., Mungpakdee S., Aury J.M., Da Silva C., Brinkmann H., Mikhaleva J., Olsen L.C., Jubin C., Canestro C. et al. Science 330:1381-1385(2010) · UniProtKB (28,572) |
| Local adaptation for body color in Drosophila americana. Wittkopp P.J., Smith-Winberry G., Arnold L.L., Thompson E.M., Cooley A.M., Yuan D.C., Song Q., McAllister B.F. Heredity (Edinb) 106:592-602(2011) · UniProtKB (37) |
| De novo mutations of SETBP1 cause Schinzel-Giedion syndrome. Hoischen A., van Bon B.W., Gilissen C., Arts P., van Lier B., Steehouwer M., de Vries P., de Reuver R., Wieskamp N., Mortier G. et al. Nat. Genet. 42:483-485(2010) · UniProtKB (1) |
| Intraspecific polymorphism to interspecific divergence: genetics of pigmentation in Drosophila. Wittkopp P.J., Stewart E.E., Arnold L.L., Neidert A.H., Haerum B.K., Thompson E.M., Akhras S., Smith-Winberry G., Shefner L. |
| Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9. Luty A.A., Kwok J.B., Thompson E.M., Blumbergs P., Brooks W.S., Loy C.T., Dobson-Stone C., Panegyres P.K., Hecker J., Nicholson G.A. et al. BMC Neurol 8:32-32(2008) · Mapped (5) |
| Altered miRNA repertoire in the simplified chordate, Oikopleura dioica. Fu X., Adamski M., Thompson E.M. Mol. Biol. Evol. 25:1067-1080(2008) · UniProtKB (8) |
| Identification of the novel HLA-C allele Cw*0751. Thompson E.M., Kashi Z.M., Martin R.K., Alcorn J.L., Tidey L. Tissue Antigens 71:178-179(2008) · UniProtKB (1) · Mapped (276) |
| Molecular consequences of dominant Bethlem myopathy collagen VI mutations. Baker N.L., Moergelin M., Pace R.A., Peat R.A., Adams N.E., Gardner R.J., Rowland L.P., Miller G., De Jonghe P., Ceulemans B. et al. Ann. Neurol. 62:390-405(2007) · UniProtKB (2) |
| Rapidly evolving lamins in a chordate, Oikopleura dioica, with unusual nuclear architecture. Clarke T., Bouquet J.M., Fu X., Kallesoe T., Schmid M., Thompson E.M. Gene 396:159-169(2007) · UniProtKB (7) |
| Phosphorylation of the histone H3.3 variant in mitosis and meiosis of the urochordate Oikopleura dioica. Schulmeister A., Schmid M., Thompson E.M. Chromosome Res. 15:189-201(2007) · UniProtKB (1) |
| Plasticity of histone modifications across the invertebrate to vertebrate transition: histone H3 lysine 4 trimethylation in heterochromatin. Spada F., Vincent M., Thompson E.M. Chromosome Res. 13:57-72(2005) · Mapped (2) |
| Spliced-leader RNA trans splicing in a chordate, Oikopleura dioica, with a compact genome. Ganot P., Kallesoe T., Reinhardt R., Chourrout D., Thompson E.M. Mol. Cell. Biol. 24:7795-7805(2004) · UniProtKB (6) |
| Histone mRNAs do not accumulate during S phase of either mitotic or endoreduplicative cycles in the chordate Oikopleura dioica. Chioda M., Spada F., Eskeland R., Thompson E.M. Mol. Cell. Biol. 24:5391-5403(2004) · UniProtKB (4) |
| Cell cycle progression in G1 and S phases is CCR4 dependent following ionizing radiation or replication stress in Saccharomyces cerevisiae. Westmoreland T.J., Marks J.R., Olson J.A. Jr., Thompson E.M., Resnick M.A., Bennett C.B. Eukaryotic Cell 3:430-446(2004) · Mapped (8) |
| Histone gene complement, variant expression, and mRNA processing in a urochordate, Oikopleura dioica, that undergoes extensive polyploidisation. Chioda M., Eskeland R., Thompson E.M. Mol. Biol. Evol. 19:2247-2260(2002) · UniProtKB (11) |
| Diverse genes expressed in distinct regions of the trunk epithelium define a monolayer cellular template for construction of the oikopleurid house. Thompson E.M., Kallesoe T., Spada F. Dev. Biol. 238:260-273(2001) · UniProtKB (13) |
| Miniature genome in the marine chordate Oikopleura dioica. Seo H.C., Kube M., Edvardsen R.B., Jensen M.F., Beck A., Spriet E., Gorsky G., Thompson E.M., Lehrach R., Reinhardt H. et al. Science 294:2506-2506(2001) · UniProtKB (37) |
| Novel TFAP2B mutations that cause Char syndrome provide a genotype-phenotype correlation. Zhao F., Weismann C.G., Satoda M., Pierpont M.E.M., Sweeney E., Thompson E.M., Gelb B.D. Am. J. Hum. Genet. 69:695-703(2001) · UniProtKB (1) · Mapped (2) |
| Molecular patterning of the oikoplastic epithelium of the larvacean tunicate Oikopleura dioica. Spada F., Steen H., Troedsson C., Kallesoe T., Spriet E., Mann M., Thompson E.M. J. Biol. Chem. 276:20624-20632(2001) · UniProtKB (5) |
| Identification of intervals on chromosomes 1, 3, and 13 linked to the development of lupus in BXSB mice. Haywood M.E., Hogarth M.B., Slingsby J.H., Rose S.J., Allen P.J., Thompson E.M., Maibaum M.A., Chandler P., Davies K.A., Simpson E. et al. Arthritis Rheum. 43:349-355(2000) · Mapped (26) |
| Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tarda. Gedeon A.K., Colley A., Jamieson R., Thompson E.M., Rogers J., Sillence D., Tiller G.E., Mulley J.C., Gecz J. Nat. Genet. 22:400-404(1999) · UniProtKB (2) |
| Differential preimplantation regulation of two mouse homologues of the yeast SWI2 protein. LeGouy E., Thompson E.M., Muchardt C., Renard J.P. |
| Homozygous C1q deficiency causes glomerulonephritis associated with multiple apoptotic bodies. Botto M., Dell'Agnola C., Bygrave A.E., Thompson E.M., Cook H.T., Petry F., Loos M., Pandolfi P.P., Walport M.J. Nat. Genet. 19:56-59(1998) · Mapped (3) |
| Mutation in the carboxy-terminal propeptide of the Pro alpha 1(I) chain of type I collagen in a child with severe osteogenesis imperfecta (OI type III): possible implications for protein folding. Oliver J.E., Thompson E.M., Pope F.M., Nicholls A.C. Hum. Mutat. 7:318-326(1996) · UniProtKB (2) |