14
results
for author:"Blair E."
in Literature Citations
| Identification and functional characterization of cardiac troponin I as a novel disease gene in autosomal dominant dilated cardiomyopathy. Carballo S., Robinson P., Otway R., Fatkin D., Jongbloed J.D., de Jonge N., Blair E., van Tintelen J.P., Redwood C., Watkins H. Circ. Res. 105:375-382(2009) · Mapped (4) |
| The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity. Gordillo M., Vega H., Trainer A.H., Hou F., Sakai N., Luque R., Kayserili H., Basaran S., Skovby F., Hennekam R.C. et al. Hum. Mol. Genet. 17:2172-2180(2008) · Mapped (2) |
| Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma. Bayley J.P., van Minderhout I., Weiss M.M., Jansen J.C., Oomen P.H., Menko F.H., Pasini B., Ferrando B., Wong N., Alpert L.C. et al. BMC Med. Genet. 7:1-1(2006) · Mapped (9) |
| The putidaredoxin reductase-putidaredoxin electron transfer complex: theoretical and experimental studies. Kuznetsov V.Y., Blair E., Farmer P.J., Poulos T.L., Pifferitti A., Sevrioukova I.F. J. Biol. Chem. 280:16135-16142(2005) · UniProtKB (2) |
| Natural variation among human adenoviruses: genome sequence and annotation of human adenovirus serotype 1. Lauer K.P., Llorente I., Blair E., Seto J., Krasnov V., Purkayastha A., Ditty S.E., Hadfield T.L., Buck C., Tibbetts C. et al. J. Gen. Virol. 85:2615-2625(2004) · UniProtKB (36) |
| Mutation analysis of AMP-activated protein kinase subunits in inherited cardiomyopathies: implications for kinase function and disease pathogenesis. Oliveira S.M., Ehtisham J., Redwood C.S., Ostman-Smith I., Blair E.M., Watkins H. J. Mol. Cell. Cardiol. 35:1251-1255(2003) · Mapped (3) |
| Mutations of the light meromyosin domain of the beta-myosin heavy chain rod in hypertrophic cardiomyopathy. Blair E., Redwood C., de Jesus Oliveira M., Moolman-Smook J.C., Brink P., Corfield V.A., Oestman-Smith I., Watkins H. |
| Mutations in cis can confound genotype-phenotype correlations in hypertrophic cardiomyopathy. Blair E., Price S.J., Baty C.J., Oestman-Smith I., Watkins H. J. Med. Genet. 38:385-388(2001) · UniProtKB (1) |
| Mutations in the gamma(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis. Blair E., Redwood C., Ashrafian H., Oliveira M., Broxholme J., Kerr B., Salmon A., Oestman-Smith I., Watkins H. Hum. Mol. Genet. 10:1215-1220(2001) · UniProtKB (1) |
| Identification of the familial cylindromatosis tumor suppressor gene. Bignell G.R., Brown C., Biggs P.J., Lakhani S.R., Jones C., Hansen J., Blair E., Hofmann B., Siebert R., Turner G. et al. Nat. Genet. 25:160-165(2000) · UniProtKB (1) |
| Identification of vaccine candidates against serogroup B meningococcus by whole-genome sequencing. Pizza M., Scarlato V., Masignani V., Giuliani M.M., Arico' B., Comanducci M., Jennings G.T., Baldi L., Bartolini E., Capecchi B. et al. Science 287:1816-1820(2000) · UniProtKB (120) |
| Complete genome sequence of Neisseria meningitidis serogroup B strain MC58. Tettelin H., Saunders N.J., Heidelberg J.F., Jeffries A.C., Nelson K.E., Eisen J.A., Ketchum K.A., Hood D.W., Peden J.F., Dodson R.J. et al. Science 287:1809-1815(2000) · UniProtKB (2,001) |
| Organization of terminal reiterations in the virion DNA of herpesvirus saimiri. Stamminger T., Honess R.W., Young D.F., Bodemer W., Blair E.D., Fleckenstein B. J. Gen. Virol. 68:1049-1066(1987) · UniProtKB (1) |
| Characterization of the genes encoding herpes simplex virus type 1 and type 2 alkaline exonucleases and overlapping proteins. Draper K.G., Devi-Rao G., Costa R.H., Blair E.D., Thompson R.L., Wagner E.K. J. Virol. 57:1023-1036(1986) · UniProtKB (7) |
