1 - 25 of
72
results
for author:"Cole J."
in Literature Citations
| Structure of the s5a:k48-linked diubiquitin complex and its interactions with rpn13. Zhang N., Wang Q., Ehlinger A., Randles L., Lary J.W., Kang Y., Haririnia A., Storaska A.J., Cole J.L., Fushman D. et al. Mol. Cell 35:280-290(2009) · Mapped (6) |
| Relation of candidate genes that encode for endothelial function to migraine and stroke: the Stroke Prevention in Young Women study. MacClellan L.R., Howard T.D., Cole J.W., Stine O.C., Giles W.H., O'Connell J.R., Wozniak M.A., Stern B.J., Mitchell B.D., Kittner S.J. Stroke 40:e550-7(2009) · Mapped (12) |
| Worldwide prevalence of class 2 integrases outside the clinical setting is associated with human impact. Rodriguez-Minguela C.M., Apajalahti J.H., Chai B., Cole J.R., Tiedje J.M. Appl. Environ. Microbiol. 75:5100-5110(2009) · UniProtKB (218) |
| RNA dimerization promotes PKR dimerization and activation. Heinicke L.A., Wong C.J., Lary J., Nallagatla S.R., Diegelman-Parente A., Zheng X., Cole J.L., Bevilacqua P.C. J. Mol. Biol. 390:319-338(2009) · Mapped (6) |
| Somatic mutations of the histone H3K27 demethylase gene UTX in human cancer. van Haaften G., Dalgliesh G.L., Davies H., Chen L., Bignell G., Greenman C., Edkins S., Hardy C., O'Meara S., Teague J. et al. Nat. Genet. 41:521-523(2009) · Mapped (12) |
| EGF receptor signaling blocks aryl hydrocarbon receptor-mediated transcription and cell differentiation in human epidermal keratinocytes. Sutter C.H., Yin H., Li Y., Mammen J.S., Bodreddigari S., Stevens G., Cole J.A., Sutter T.R. Proc. Natl. Acad. Sci. U.S.A. 106:4266-4271(2009) · Mapped (17) |
| Allelic variants of streptokinase from Streptococcus pyogenes display functional differences in plasminogen activation. McArthur J.D., McKay F.C., Ramachandran V., Shyam P., Cork A.J., Sanderson-Smith M.L., Cole J.N., Ringdahl U., Sjobring U., Ranson M. et al. FASEB J. 22:3146-3153(2008) · UniProtKB (25) |
| X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment. Dibbens L.M., Tarpey P.S., Hynes K., Bayly M.A., Scheffer I.E., Smith R., Bomar J., Sutton E., Vandeleur L., Shoubridge C. et al. |
| Role of a conserved glutamine residue in tuning the catalytic activity of Escherichia coli cytochrome c nitrite reductase. Clarke T.A., Kemp G.L., Van Wonderen J.H., Doyle R.M., Cole J.A., Tovell N., Cheesman M.R., Butt J.N., Richardson D.J., Hemmings A.M. Biochemistry 47:3789-3799(2008) · Mapped (1) |
| Phylogenetic placement of diverse amoebae inferred from multigene analyses and assessment of clade stability within 'Amoebozoa' upon removal of varying rate classes of SSU-rDNA. Tekle Y.I., Grant J., Anderson O.R., Nerad T.A., Cole J.C., Patterson D.J., Katz L.A. Mol. Phylogenet. Evol. 47:339-352(2008) · UniProtKB (24) |
| Role of group A Streptococcus HtrA in the maturation of SpeB protease. Cole J.N., Aquilina J.A., Hains P.G., Henningham A., Sriprakash K.S., Caparon M.G., Nizet V., Kotb M., Cordwell S.J., Djordjevic S.P. et al. Proteomics 7:4488-4498(2007) · UniProtKB (1) |
| Neuroserpin polymorphisms and stroke risk in a biracial population: the stroke prevention in young women study. Cole J.W., Naj A.C., O'Connell J.R., Stine O.C., Sorkin J.D., Wozniak M.A., Stern B.J., Yepes M., Lawrence D.A., Reinhart L.J. et al. BMC Neurol 7:37-37(2007) · Mapped (1) |
| Barcoding ciliates: a comprehensive study of 75 isolates of the genus Tetrahymena. Chantangsi C., Lynn D.H., Brandl M.T., Cole J.C., Hetrick N., Ikonomi P. Int. J. Syst. Evol. Microbiol. 57:2412-2425(2007) · UniProtKB (53) |
| Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation. Tarpey P.S., Raymond F.L., Nguyen L.S., Rodriguez J., Hackett A., Vandeleur L., Smith R., Shoubridge C., Edkins S., Stevens C. et al. |
| Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephaly. Field M., Tarpey P.S., Smith R., Edkins S., O'Meara S., Stevens C., Tofts C., Teague J., Butler A., Dicks E. et al. Am. J. Hum. Genet. 81:367-374(2007) · UniProtKB (1) |
| A multigene analysis of Corallomyxa tenera sp. nov. suggests its membership in a clade that includes Gromia, Haplosporidia and Foraminifera. Tekle Y.I., Grant J., Cole J.C., Nerad T.A., Anderson O.R., Patterson D.J., Katz L.A. Protist 158:457-472(2007) · UniProtKB (4) |
| Structure of CD84 provides insight into SLAM family function. Yan Q., Malashkevich V.N., Fedorov A., Fedorov E., Cao E., Lary J.W., Cole J.L., Nathenson S.G., Almo S.C. Proc. Natl. Acad. Sci. U.S.A. 104:10583-10588(2007) · UniProtKB (1) |
| The crystal structure of the pentahaem c-type cytochrome NrfB and characterization of its solution-state interaction with the pentahaem nitrite reductase NrfA. Clarke T.A., Cole J.A., Richardson D.J., Hemmings A.M. Biochem. J. 406:19-30(2007) · Mapped (1) |
| Defining how ubiquitin receptors hHR23a and S5a bind polyubiquitin. Kang Y., Chen X., Lary J.W., Cole J.L., Walters K.J. J. Mol. Biol. 369:168-176(2007) · Mapped (10) |
| Recognition of C-terminal amino acids in tubulin by pore loops in Spastin is important for microtubule severing. White S.R., Evans K.J., Lary J., Cole J.L., Lauring B.P. J. Cell Biol. 176:995-1005(2007) · UniProtKB (1) · Mapped (1) |
| T cell immunoglobulin mucin-3 crystal structure reveals a galectin-9-independent ligand-binding surface. Cao E., Zang X., Ramagopal U.A., Mukhopadhaya A., Fedorov A., Fedorov E., Zencheck W.D., Lary J.W., Cole J.L., Deng H. et al. Immunity 26:311-321(2007) · Mapped (7) |
| Patterns of somatic mutation in human cancer genomes. Greenman C., Stephens P., Smith R., Dalgliesh G.L., Hunter C., Bignell G., Davies H., Teague J., Butler A., Stevens C. et al. Nature 446:153-158(2007) · UniProtKB (453) |
| Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremor. Tarpey P.S., Raymond F.L., O'Meara S., Edkins S., Teague J., Butler A., Dicks E., Stevens C., Tofts C., Avis T. et al. Am. J. Hum. Genet. 80:345-352(2007) · UniProtKB (1) · Mapped (2) |
| Mutations in the gene encoding the sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardation. Tarpey P.S., Stevens C., Teague J., Edkins S., O'Meara S., Avis T., Barthorpe S., Buck G., Butler A., Cole J. et al. Am. J. Hum. Genet. 79:1119-1124(2006) · UniProtKB (1) |
| Spectropotentiometric and structural analysis of the periplasmic nitrate reductase from Escherichia coli. Jepson B.J., Mohan S., Clarke T.A., Gates A.J., Cole J.A., Butler C.S., Butt J.N., Hemmings A.M., Richardson D.J. J. Biol. Chem. 282:6425-6437(2007) · Mapped (1) |
