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30
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for author:"Buck G."
in Literature Citations
| Prognostic implications of NOTCH1 and FBXW7 mutations in adults with T-cell acute lymphoblastic leukemia treated on the MRC UKALLXII/ECOG E2993 protocol. Mansour M.R., Sulis M.L., Duke V., Foroni L., Jenkinson S., Koo K., Allen C.G., Gale R.E., Buck G., Richards S. et al. J. Clin. Oncol. 27:4352-4356(2009) · Mapped (8) |
| Over-expression and localization of a host protein on the membrane of Cryptosporidium parvum infected epithelial cells. Yang Y.L., Serrano M.G., Sheoran A.S., Manque P.A., Buck G.A., Widmer G. Mol. Biochem. Parasitol. 168:95-101(2009) · Mapped (2) |
| 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) |
| 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. |
| MPL mutations in myeloproliferative disorders: analysis of the PT-1 cohort. Beer P.A., Campbell P.J., Scott L.M., Bench A.J., Erber W.N., Bareford D., Wilkins B.S., Reilly J.T., Hasselbalch H.C., Bowman R. et al. Blood 112:141-149(2008) · Mapped (3) |
| Mutation of sodium channel SCN3A in a patient with cryptogenic pediatric partial epilepsy. Holland K.D., Kearney J.A., Glauser T.A., Buck G., Keddache M., Blankston J.R., Glaaser I.W., Kass R.S., Meisler M.H. Neurosci. Lett. 433:65-70(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) |
| 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) |
| Genome of the opportunistic pathogen Streptococcus sanguinis. Xu P., Alves J.M., Kitten T., Brown A., Chen Z., Ozaki L.S., Manque P., Ge X., Serrano M.G., Puiu D. et al. J. Bacteriol. 189:3166-3175(2007) · UniProtKB (2,269) |
| 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) |
| Definition of subtypes of essential thrombocythaemia and relation to polycythaemia vera based on JAK2 V617F mutation status: a prospective study. The United Kingdom myeloproliferative disorders study group, The medical research council adult leukaemia working party, The Australasian leukaemia and lymphoma group Lancet 366:1945-1953(2005) · UniProtKB (1) |
| 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) |
| The genome of Cryptosporidium hominis. Xu P., Widmer G., Wang Y., Ozaki L.S., Alves J.M., Serrano M.G., Puiu D., Manque P., Akiyoshi D., Mackey A.J. et al. Nature 431:1107-1112(2004) · UniProtKB (3,886) |
| Complete genome sequence of the apicomplexan, Cryptosporidium parvum. Abrahamsen M.S., Templeton T.J., Enomoto S., Abrahante J.E., Zhu G., Lancto C.A., Deng M., Liu C., Widmer G., Tzipori S. et al. Science 304:441-445(2004) · UniProtKB (3,805) |
| Association of erosive hand osteoarthritis with a single nucleotide polymorphism on the gene encoding interleukin-1 beta. Stern A.G., de Carvalho M.R., Buck G.A., Adler R.A., Rao T.P., Disler D., Moxley G. Osteoarthr. Cartil. 11:394-402(2003) · Mapped (8) |
| Evidence for genetic exchange and hybridization in Trypanosoma cruzi based on nucleotide sequences and molecular karyotype. Brisse S., Henriksson J., Barnabe C., Douzery E.J., Berkvens D., Serrano M., De Carvalho M.R., Buck G.A., Dujardin J.C., Tibayrenc M. Infect. Genet. Evol. 2:173-183(2003) · UniProtKB (5) |
| Identification of a spliced leader RNA binding protein from Trypanosoma cruzi. Xu P., Wen L., Benegal G., Wang X., Buck G.A. Mol. Biochem. Parasitol. 112:39-49(2001) · UniProtKB (1) · Mapped (1) |
| PPB1, a putative spliced leader RNA gene transcription factor in Trypanosoma cruzi. Wen L.M., Xu P., Benegal G., Carvalho M.R., Buck G.A. Mol. Biochem. Parasitol. 110:207-221(2000) · UniProtKB (1) |
| Double mutation (A171T and D444H) is a common cause of profound biotinidase deficiency in children ascertained by newborn screening in the United States. Norrgard K.J., Pomponio R.J., Swango K.L., Hymes J., Reynolds T., Buck G.A., Wolf B. Hum. Mutat. 11:410-410(1998) · UniProtKB (1) |
| High prevalence of GB virus C in Brazil and molecular evidence for intrafamilial transmission. Pinho J.R., Zanotto P.M., Ferreira J.L., Sumita L.M., Carrilho F.J., da Silva L.C., Capacci M.L., Silva A.O., Guz B., Goncales F.L. Jr. et al. J. Clin. Microbiol. 37:1634-1637(1999) · UniProtKB (27) |
| Polymorphisms at the topoisomerase II gene locus provide more evidence for the partition of Trypanosoma cruzi into two major groups. Dos Santos W.G., Buck G.A. J. Eukaryot. Microbiol. 46:17-23(1999) · UniProtKB (1) |
| The HSP70 gene family in Pneumocystis carinii: molecular and phylogenetic characterization of cytoplasmic members. Stedman T.T., Butler D.R., Buck G.A. J. Eukaryot. Microbiol. 45:589-599(1998) · UniProtKB (4) · Mapped (6) |
| Structure of the human biotinidase gene. Knight H.C., Reynolds T.R., Meyers G.A., Pomponio R.J., Buck G.A., Wolf B. Mamm. Genome 9:327-330(1998) · UniProtKB (1) |
