1 - 25 of 26 results for author:"Gilliam T.C." in Literature citations
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| Panic disorder is associated with the serotonin transporter gene (SLC6A4) but not the promoter region (5-HTTLPR). Strug L.J., Suresh R., Fyer A.J., Talati A., Adams P.B., Li W., Hodge S.E., Gilliam T.C., Weissman M.M. Mol. Psychiatry 15:166-176(2010) · Mapped (18) |
| DRD2 C957T polymorphism interacts with the COMT Val158Met polymorphism in human working memory ability. Xu H., Kellendonk C.B., Simpson E.H., Keilp J.G., Bruder G.E., Polan H.J., Kandel E.R., Gilliam T.C. Schizophr. Res. 90:104-107(2007) · Mapped (11) |
| Hardy-Weinberg disequilibrium identified genotyping error of the serotonin transporter (SLC6A4) promoter polymorphism. Yonan A.L., Palmer A.A., Gilliam T.C. Psychiatr. Genet. 16:31-34(2006) · Mapped (3) |
| Gene expression differences in mice divergently selected for methamphetamine sensitivity. Palmer A.A., Verbitsky M., Suresh R., Kamens H.M., Reed C.L., Li N., Burkhart-Kasch S., McKinnon C.S., Belknap J.K., Gilliam T.C. et al. Mamm. Genome 16:291-305(2005) · Mapped (21) |
| Catechol-O-methyltransferase (COMT) genotypes and working memory: associations with differing cognitive operations. Bruder G.E., Keilp J.G., Xu H., Shikhman M., Schori E., Gorman J.M., Gilliam T.C. Biol. Psychiatry 58:901-907(2005) · Mapped (7) |
| Screen for expanded FMR1 alleles in patients with essential tremor. Garcia Arocena D., Louis E.D., Tassone F., Gilliam T.C., Ottman R., Jacquemont S., Hagerman P.J. Mov. Disord. 19:930-933(2004) · Mapped (8) |
| 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) |
| LGI1 mutations in autosomal dominant partial epilepsy with auditory features. Ottman R., Winawer M.R., Kalachikov S., Barker-Cummings C., Gilliam T.C., Pedley T.A., Hauser W.A. Neurology 62:1120-1126(2004) · Mapped (2) |
| 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) |
| Desmoglein 4 in hair follicle differentiation and epidermal adhesion. Evidence from inherited hypotrichosis and acquired pemphigus vulgaris. Kljuic A., Bazzi H., Sundberg J.P., Martinez-Mir A., O'Shaughnessy R., Mahoney M.G., Levy M., Montagutelli X., Ahmad W., Aita V.M. et al. |
| 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) |
| EB simplex superficialis resulting from a mutation in the type VII collagen gene. Martinez-Mir A., Liu J., Gordon D., Weiner M.S., Ahmad W., Fine J.D., Ott J., Gilliam T.C., Christiano A.M. J. Invest. Dermatol. 118:547-549(2002) · UniProtKB (1) |
| Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features. Kalachikov S., Evgrafov O., Ross B., Winawer M., Barker-Cummings C., Boneschi F.M., Choi C., Morozov P., Das K., Teplitskaya E. et al. |
| Positional cloning and characterization of the human DLGAP2 gene and its exclusion in progressive epilepsy with mental retardation. Ranta S., Zhang Y., Ross B., Takkunen E., Hirvasniemi A., de la Chapelle A., Gilliam T.C., Lehesjoki A.-E. Eur. J. Hum. Genet. 8:381-384(2000) · UniProtKB (1) |
| The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8. Ranta S., Zhang Y., Ross B., Lonka L., Takkunen E., Messer A., Sharp J., Wheeler R., Kusumi K., Mole S. et al. |
| 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) |
| Cloning and genomic organization of beclin 1, a candidate tumor suppressor gene on chromosome 17q21. Aita V.M., Liang X.H., Murty V.V.V.S., Pincus D.L., Yu W., Cayanis E., Kalachikov S., Gilliam T.C., Levine B. Genomics 59:59-65(1999) · UniProtKB (1) |
| 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) |
| High-resolution mapping and transcript identification at the progressive epilepsy with mental retardation locus on chromosome 8p. Ranta S., Lehesjoki A.-E., de Fatima Bonaldo M., Knowles J.A., Hirvasniemi A., Ross B., de Jong P.J., Soares M.B., de la Chapelle A., Gilliam T.C. Genome Res. 7:887-896(1997) · 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) |
| Two forms of Wilson disease protein produced by alternative splicing are localized in distinct cellular compartments. Yang X.-L., Miura N., Kawarada Y., Terada K., Petrukhin K., Gilliam T.C., Sugiyama T. Biochem. J. 326:897-902(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) |
| The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene. Tanzi R.E., Petrukhin K., Chernov I., Pellequer J.L., Wasco W., Ross B., Romano D.M., Parano E., Pavone L., Brzustowicz L.M. et al. Nat. Genet. 5:344-350(1993) · 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) |
| Expressed cadherin pseudogenes are localized to the critical region of the spinal muscular atrophy gene. Selig S., Bruno S., Scharf J.M., Wang C.H., Vitale E., Gilliam T.C., Kunkel L.M. Proc. Natl. Acad. Sci. U.S.A. 92:3702-3706(1995) · UniProtKB (1) |