23
results
for author:"Shepherd R."
in Literature Citations
| 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) |
| Fibrogenesis in pediatric cholestatic liver disease: role of taurocholate and hepatocyte-derived monocyte chemotaxis protein-1 in hepatic stellate cell recruitment. Ramm G.A., Shepherd R.W., Hoskins A.C., Greco S.A., Ney A.D., Pereira T.N., Bridle K.R., Doecke J.D., Meikle P.J., Turlin B. et al. Hepatology 49:533-544(2009) · Mapped (2) |
| 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. |
| PAX4 enhances beta-cell differentiation of human embryonic stem cells. Liew C.G., Shah N.N., Briston S.J., Shepherd R.M., Khoo C.P., Dunne M.J., Moore H.D., Cosgrove K.E., Andrews P.W. PLoS ONE 3:e1783-e1783(2008) · Mapped (5) |
| Schwann cells genetically modified to express neurotrophins promote spiral ganglion neuron survival in vitro. Pettingill L.N., Minter R.L., Shepherd R.K. Neuroscience 152:821-828(2008) · Mapped (2) |
| Cochlear implants stimulate activity-dependent CREB pathway in the deaf auditory cortex: implications for molecular plasticity induced by neural prosthetic devices. Tan J., Widjaja S., Xu J., Shepherd R.K. Cereb. Cortex 18:1799-1813(2008) · Mapped (1) |
| 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) |
| Mice deficient for the type II transmembrane serine protease, TMPRSS1/hepsin, exhibit profound hearing loss. Guipponi M., Tan J., Cannon P.Z., Donley L., Crewther P., Clarke M., Wu Q., Shepherd R.K., Scott H.S. Am. J. Pathol. 171:608-616(2007) · Mapped (3) |
| Glucose-dependent modulation of insulin secretion and intracellular calcium ions by GKA50, a glucokinase activator. Johnson D., Shepherd R.M., Gill D., Gorman T., Smith D.M., Dunne M.J. Diabetes 56:1694-1702(2007) · Mapped (1) |
| 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) |
| Aminoglycoside-induced degeneration of adult spiral ganglion neurons involves differential modulation of tyrosine kinase B and p75 neurotrophin receptor signaling. Tan J., Shepherd R.K. Am. J. Pathol. 169:528-543(2006) · Mapped (3) |
| G-CSF and AMD3100 mobilize monocytes into the blood that stimulate angiogenesis in vivo through a paracrine mechanism. Capoccia B.J., Shepherd R.M., Link D.C. Blood 108:2438-2445(2006) · Mapped (6) |
| Sequence analysis of the protein kinase gene family in human testicular germ-cell tumors of adolescents and adults. Bignell G., Smith R., Hunter C., Stephens P., Davies H., Greenman C., Teague J., Butler A., Edkins S., Stevens C. et al. Genes Chromosomes Cancer 45:42-46(2006) · UniProtKB (2) |
| Phylloplanins of tobacco are defensive proteins deployed on aerial surfaces by short glandular trichomes. Shepherd R.W., Bass W.T., Houtz R.L., Wagner G.J. Plant Cell 17:1851-1861(2005) · UniProtKB (1) |
| Lung cancer: intragenic ERBB2 kinase mutations in tumours. Stephens P., Hunter C., Bignell G., Edkins S., Davies H., Teague J., Stevens C., O'Meara S., Smith R., Parker A. et al. Nature 431:525-526(2004) · Mapped (8) |
| The role of hepatic stellate cells and transforming growth factor-beta(1) in cystic fibrosis liver disease. Lewindon P.J., Pereira T.N., Hoskins A.C., Bridle K.R., Williamson R.M., Shepherd R.W., Ramm G.A. Am. J. Pathol. 160:1705-1715(2002) · Mapped (9) |
| Petunia vein-clearing virus: a plant pararetrovirus with the core sequences for an integrase function. Richert-Poggeler K.R., Shepherd R.J. Virology 236:137-146(1997) · UniProtKB (1) |
| Characterization of cassava vein mosaic virus: a distinct plant pararetrovirus. Calvert L.A., Ospina M.D., Shepherd R.J. J. Gen. Virol. 76:1271-1278(1995) · UniProtKB (5) |
| The complete nucleotide sequence of an infectious clone of cauliflower mosaic virus by M13mp7 shotgun sequencing. Gardner R.C., Howarth A.J., Hahn P., Brown-Luedi M., Shepherd R.J., Messing J. Nucleic Acids Res. 9:2871-2888(1981) · UniProtKB (6) |
| Sequence of figwort mosaic virus DNA (caulimovirus group). Richins R.D., Scholthof H.B., Shepherd R.J. Nucleic Acids Res. 15:8451-8466(1987) · UniProtKB (7) |
