13 results for author:"Ross B.M." in Literature citations
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| Predictors of parkin mutations in early-onset Parkinson disease: the consortium on risk for early-onset Parkinson disease study. Marder K.S., Tang M.X., Mejia-Santana H., Rosado L., Louis E.D., Comella C.L., Colcher A., Siderowf A.D., Jennings D., Nance M.A. et al. Arch. Neurol. 67:731-738(2010) · Mapped (15) |
| Motor phenotype of LRRK2 G2019S carriers in early-onset Parkinson disease. Alcalay R.N., Mejia-Santana H., Tang M.X., Rosado L., Verbitsky M., Kisselev S., Ross B.M., Louis E.D., Comella C.L., Colcher A. et al. Arch. Neurol. 66:1517-1522(2009) · Mapped (4) |
| Association of glucocerebrosidase mutations with dementia with lewy bodies. Clark L.N., Kartsaklis L.A., Wolf Gilbert R., Dorado B., Ross B.M., Kisselev S., Verbitsky M., Mejia-Santana H., Cote L.J., Andrews H. et al. Arch. Neurol. 66:578-583(2009) · Mapped (5) |
| Population-based study of SR-BI genetic variation and lipid profile. Morabia A., Ross B.M., Costanza M.C., Cayanis E., Flaherty M.S., Alvin G.B., Das K., James R., Yang A.S., Evagrafov O. et al. Atherosclerosis 175:159-168(2004) · Mapped (8) |
| Association of extreme blood lipid profile phenotypic variation with 11 reverse cholesterol transport genes and 10 non-genetic cardiovascular disease risk factors. Morabia A., Cayanis E., Costanza M.C., Ross B.M., Flaherty M.S., Alvin G.B., Das K., Gilliam T.C. Hum. Mol. Genet. 12:2733-2743(2003) · UniProtKB (10) |
| Association between lipoprotein lipase (LPL) gene and blood lipids: a common variant for a common trait? Morabia A., Cayanis E., Costanza M.C., Ross B.M., Bernstein M.S., Flaherty M.S., Alvin G.B., Das K., Morris M.A., Penchaszadeh G.K. et al. Genet. Epidemiol. 24:309-321(2003) · Mapped (9) |
| Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation. Buiakova O.I., Xu J., Lutsenko S., Zeitlin S., Das K., Das S., Ross B.M., Mekios C., Scheinberg I.H., Gilliam T.C. Hum. Mol. Genet. 8:1665-1671(1999) · Mapped (2) |
| TULP1 mutation in two extended Dominican kindreds with autosomal recessive retinitis pigmentosa. Banerjee P., Kleyn P.W., Knowles J.A., Lewis C.A., Ross B.M., Parano E., Kovats S.G., Lee J.J., Penchaszadeh G.K., Ott J. et al. Nat. Genet. 18:177-179(1998) · UniProtKB (1) |
| Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analyses. Shah A.B., Chernov I., Zhang H.T., Ross B.M., Das K., Lutsenko S., Parano E., Pavone L., Evgrafov O., Ivanova-Smolenskaya I.A. et al. Am. J. Hum. Genet. 61:317-328(1997) · UniProtKB (1) |
| A multicopy transcription-repair gene, BTF2p44, maps to the SMA region and demonstrates SMA associated deletions. Carter T.A., Bonnemann C.G., Wang C.H., Obici S., Parano E., Bonaldo M.F., Ross B.M., Penchaszadeh G.K., Mackenzie A.E., Soares M.B. et al. Hum. Mol. Genet. 6:229-236(1997) · UniProtKB (1) |
| Characterization of the Wilson disease gene encoding a P-type copper transporting ATPase: genomic organization, alternative splicing, and structure/function predictions. Petrukhin K., Lutsenko S., Chernov I., Ross B.M., Kaplan J.H., Gilliam T.C. Hum. Mol. Genet. 3:1647-1656(1994) · UniProtKB (1) |
| ClpB is the Escherichia coli heat shock protein F84.1. Squires C.L., Pedersen S., Ross B.M., Squires C. J. Bacteriol. 173:4254-4262(1991) · UniProtKB (2) |
| Transcriptional termination sequence at the end of the Escherichia coli ribosomal RNA G operon: complex terminators and antitermination. Albrechtsen B., Ross B.M., Squires C., Squires C.L. Nucleic Acids Res. 19:1845-1852(1991) · UniProtKB (3) |