7 results for author:"Weller P.A." in Literature citations
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| Organization of the human gene encoding the cytoskeletal protein vinculin and the sequence of the vinculin promoter. Moiseyeva E.P., Weller P.A., Zhidkova N.I., Corben E.B., Patel B., Jasinska I., Koteliansky V.E., Critchley D.R. J. Biol. Chem. 268:4318-4325(1993) · UniProtKB (1) |
| The porcine insulin-like growth factor-I gene: characterization and expression of alternate transcription sites. Weller P.A., Dickson M.C., Huskisson N.S., Dauncey M.J., Buttery P.J., Gilmour R.S. J. Mol. Endocrinol. 11:201-211(1993) · UniProtKB (2) |
| Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene. Foster J.W., Dominguez-Steglich M.A., Guioli S., Kowk G., Weller P.A., Stevanovic M., Weissenbach J., Mansour S., Young I.D., Goodfellow P.N. et al. |
| PBDX is the XG blood group gene. Ellis N.A., Tippett P., Petty A., Reid M., Weller P.A., Ye T.Z., German J., Goodfellow P.N., Thomas S., Banting G. Nat. Genet. 8:285-290(1994) · UniProtKB (1) |
| Mutations in SOX9, the gene responsible for Campomelic dysplasia and autosomal sex reversal. Kwok C., Weller P.A., Guioli S., Foster J.W., Mansour S., Zuffardi O., Punnett H.H., Dominguez-Steglich M.A., Brook J.D., Young I.D. et al. Am. J. Hum. Genet. 57:1028-1036(1995) · UniProtKB (1) |
| Complete sequence of human vinculin and assignment of the gene to chromosome 10. Weller P.A., Ogryzko E.P., Corben E.B., Zhidkova N.I., Patel B., Price G.J., Spurr N.K., Koteliansky V.E., Critchley D.R. Proc. Natl. Acad. Sci. U.S.A. 87:5667-5671(1990) · UniProtKB (1) · Mapped (2) |
| An additional exon in the human vinculin gene specifically encodes meta-vinculin-specific difference peptide. Cross-species comparison reveals variable and conserved motifs in the meta-vinculin insert. Koteliansky V.E., Ogryzko E.P., Zhidkova N.I., Weller P.A., Critchley D.R., Vancompernolle K., Vandekerckhove J., Strasser P., Way M., Gimona M. et al. Eur. J. Biochem. 204:767-772(1992) · UniProtKB (1) |