15 results for author:"Duncan A.M.V." in Literature citations
Results Customize
› Repeat search in UniProtKB (16)
| Human microphthalmia associated with mutations in the retinal homeobox gene CHX10. Percin E.F., Ploder L.A., Yu J.J., Arici K., Horsford D.J., Rutherford A., Bapat B., Cox D.W., Duncan A.M.V., Kalnins V.I. et al. |
| Cloning and characterization of human PREB; a gene that maps to a genomic region associated with trisomy 2p syndrome. Taylor Clelland C.L., Levy B., McKie J.M., Duncan A.M.V., Hirschhorn K., Bancroft C. |
| PHR1 encodes an abundant, pleckstrin homology domain-containing integral membrane protein in the photoreceptor outer segments. Xu S., Ladak R., Swanson D.A., Soltyk A., Sun H., Ploder L., Vidgen D., Duncan A.M.V., Garami E., McInnes R.R. et al. J. Biol. Chem. 274:35676-35685(1999) · UniProtKB (2) · Mapped (33) |
| The human mitochondrial elongation factor Tu (EF-Tu) gene: cDNA sequence, genomic localization, genomic structure, and identification of a pseudogene. Ling M., Merante F., Chen H.-S., Duff C., Duncan A.M.V., Robinson B.H. Gene 197:325-336(1997) · UniProtKB (1) |
| Assignment of the PSST subunit gene of human mitochondrial complex I to chromosome 19p13. Hyslop S.J., Duncan A.M.V., Pitkanen S., Robinson B.H. |
| Succinyl CoA:3-oxoacid CoA transferase (SCOT): human cDNA cloning, human chromosomal mapping to 5p13, and mutation detection in a SCOT-deficient patient. Kassovska-Bratinova S., Fukao T., Song X.-Q., Duncan A.M.V., Chen H.S., Robert M.-F., Perez-Cerda C., Ugarte M., Chartrand C., Vobecky S. et al. Am. J. Hum. Genet. 59:519-528(1996) · UniProtKB (1) |
| Mapping of the human NMDA receptor subunit (NMDAR1) and the proposed NMDA receptor glutamate-binding subunit (NMDARA1) to chromosomes 9q34.3 and chromosome 8, respectively. Collins C., Duff C., Duncan A.M.V., Planells-Cases R., Sun W., Norremolle A., Michaelis E., Montal M., Worton R., Hayden M.R. |
| Molecular cloning of the cDNA and chromosomal localization of the gene for a putative seven-transmembrane segment (7-TMS) receptor isolated from human spleen. Federsppiel B., Melhado I.G., Duncan A.M.V., Delaney A.D., Schappert K., Clark-Lewis I., Jirik F.R. Genomics 16:707-712(1993) · UniProtKB (1) |
| Chromosomal localization of the human gene encoding the 51-kDa subunit of mitochondrial complex I (NDUFV1) to 11q13. Ali S.T., Duncan A.M.V., Schappert K.T., Heng H.H.Q., Tsui L.-C., Chow W., Robinson B.H. |
| The adenovirus E1A-associated 130-kD protein is encoded by a member of the retinoblastoma gene family and physically interacts with cyclins A and E. Li Y., Graham C., Lacy S., Duncan A.M.V., Whyte P. Genes Dev. 7:2366-2377(1993) · UniProtKB (1) |
| No title Goyette P., Sumner J.S., Milos R., Duncan A.M.V., Rosenblatt D.S., Matthews R.G., Rozen R. Nat. Genet. 7:551-551(1994) |
| Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification. Goyette P., Sumner J.S., Milos R., Duncan A.M.V., Rosenblatt D.S., Matthews R.G., Rozen R. Nat. Genet. 7:195-200(1994) · UniProtKB (2) |
| A widely distributed putative mammalian transcriptional regulator containing multiple paired amphipathic helices, with similarity to yeast SIN3. Halleck M.S., Pownall S., Harder K.W., Duncan A.M.V., Jirik F.R., Schlegel R.A. |
| Overexpression of a transporter gene in a multidrug-resistant human lung cancer cell line. Cole S.P.C., Bhardwaj G., Gerlach J.H., Mackie J.E., Grant C.E., Almquist K.C., Stewart A.J., Kurz E.U., Duncan A.M.V., Deeley R.G. Science 258:1650-1654(1992) · UniProtKB (1) |
| Characterization of the human 5-hydroxytryptamine1B receptor. Jin H., Oksenberg D., Ashkenazi A., Peroutka S.J., Duncan A.M.V., Rozmahel R., Yang Y., Mengod G., Palacios J.M., O'Dowd B.F. J. Biol. Chem. 267:5735-5738(1992) · UniProtKB (1) |