25 results for author:"Putt W." in Literature citations
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| Novel and recurrent LDLR gene mutations in Pakistani hypercholesterolemia patients. Ahmed W., Ajmal M., Sadeque A., Whittall R.A., Rafiq S., Putt W., Khawaja A., Imtiaz F., Ahmed N., Azam M. et al. Mol. Biol. Rep. 39:7365-7372(2012) · Mapped (7) |
| The effects of a single nucleotide polymorphism in SLCO1B1 on the pharmacodynamics of pravastatin. Martin N.G., Li K.W., Murray H., Putt W., Packard C.J., Humphries S.E. Br J Clin Pharmacol 73:303-306(2012) · Mapped (5) |
| Application of statistical and functional methodologies for the investigation of genetic determinants of coronary heart disease biomarkers: lipoprotein lipase genotype and plasma triglycerides as an exemplar. Smith A.J., Palmen J., Putt W., Talmud P.J., Humphries S.E., Drenos F. Hum. Mol. Genet. 19:3936-3947(2010) · Mapped (9) |
| Structure and function of the apoA-IV T347S and Q360H common variants. Gomaraschi M., Putt W.E., Pozzi S., Iametti S., Barbiroli A., Bonomi F., Favari E., Bernini F., Franceschini G., Talmud P.J. et al. Biochem. Biophys. Res. Commun. 393:126-130(2010) · Mapped (2) |
| Effects of six APOA5 variants, identified in patients with severe hypertriglyceridemia, on in vitro lipoprotein lipase activity and receptor binding. Dorfmeister B., Zeng W.W., Dichlberger A., Nilsson S.K., Schaap F.G., Hubacek J.A., Merkel M., Cooper J.A., Lookene A., Putt W. et al. Arterioscler. Thromb. Vasc. Biol. 28:1866-1871(2008) · Mapped (19) |
| The functional interaction on in vitro gene expression of APOA5 SNPs, defining haplotype APOA52, and their paradoxical association with plasma triglyceride but not plasma apoAV levels. Palmen J., Smith A.J., Dorfmeister B., Putt W., Humphries S.E., Talmud P.J. Biochim. Biophys. Acta 1782:447-452(2008) · Mapped (3) |
| Common variants of apolipoprotein A-IV differ in their ability to inhibit low density lipoprotein oxidation. Wong W.M., Gerry A.B., Putt W., Roberts J.L., Weinberg R.B., Humphries S.E., Leake D.S., Talmud P.J. Atherosclerosis 192:266-274(2007) · Mapped (2) |
| Determination of the functionality of common APOA5 polymorphisms. Talmud P.J., Palmen J., Putt W., Lins L., Humphries S.E. J. Biol. Chem. 280:28215-28220(2005) · Mapped (3) |
| Variation in USF1 shows haplotype effects, gene : gene and gene : environment associations with glucose and lipid parameters in the European Atherosclerosis Research Study II. Putt W., Palmen J., Nicaud V., Tregouet D.A., Tahri-Daizadeh N., Flavell D.M., Humphries S.E., Talmud P.J. Hum. Mol. Genet. 13:1587-1597(2004) · Mapped (6) |
| A study of short utrophin isoforms in mice deficient for full-length utrophin. Jimenez-Mallebrera C., Davies K., Putt W., Edwards Y.H. Mamm. Genome 14:47-60(2003) · Mapped (7) |
| Canine TCOF1; cloning, chromosome assignment and genetic analysis in dogs with different head types. Haworth K.E., Islam I., Breen M., Putt W., Makrinou E., Binns M., Hopkinson D., Edwards Y. Mamm. Genome 12:622-629(2001) · UniProtKB (3) |
| Canine homolog of the T-box transcription factor T; failure of the protein to bind to its DNA target leads to a short-tail phenotype. Haworth K.E., Putt W., Cattanach B., Breen M., Binns M., Lingaas F., Edwards Y.H. |
| Up71 and up140, two novel transcripts of utrophin that are homologues of short forms of dystrophin. Wilson J., Putt W., Jimenez C., Edwards Y.H. Hum. Mol. Genet. 8:1271-1278(1999) · Mapped (7) |
| The human TBX6 gene: cloning and assignment to chromosome 16p11.2. Papapetrou C., Putt W., Fox M., Edwards Y.H. |
| Cloning and chromosome assignment of the human CDX2 gene. Drummond F.J., Putt W., Fox M., Edwards Y.H. Ann. Hum. Genet. 61:393-400(1997) · UniProtKB (1) |
| The identification of novel sequences expressed in the mouse notochord. Sowden J.C., Morrison K., Putt W., Beddington R., Edwards Y.H. Mamm. Genome 8:42-44(1997) · Mapped (47) |
| The human homolog T of the mouse T(Brachyury) gene; gene structure, cDNA sequence, and assignment to chromosome 6q27. Edwards Y.H., Putt W., Lekoape K.M., Stott D., Fox M., Hopkinson D.A., Sowden J. |
| The embryonic RNA helicase gene (ERH): a new member of the DEAD box family of RNA helicases. Sowden J.C., Putt W., Morrison K., Beddington R., Edwards Y. |
| A novel cDNA with homology to an RNA polymerase II elongation factors maps to human chromosome 5q31 (TCEB1L) and to mouse chromosome 11 (Tceb1l). Sowden J., Morrison K., Schofield J., Putt W., Edwards Y. |
| Phosphoglucomutase 1: a gene with two promoters and a duplicated first exon. Putt W., Ives J.H., Hollyoake M., Hopkinson D.A., Whitehouse D.B., Edwards Y.H. Biochem. J. 296:417-422(1993) · UniProtKB (1) |
| The classical human phosphoglucomutase (PGM1) isozyme polymorphism is generated by intragenic recombination. March R.E., Putt W., Hollyoake M., Ives J.H., Lovegrove J.U., Hopkinson D.A., Edwards Y.H., Whitehouse D.B. Proc. Natl. Acad. Sci. U.S.A. 90:10730-10733(1993) · UniProtKB (1) |
| Complete sequence and in vitro expression of a tissue-specific phosphatidylinositol-linked N-CAM isoform from skeletal muscle. Barton C.H., Dickson G., Gower H.J., Rowett L.H., Putt W., Elsom V., Moore S.E., Goridis C., Walsh F.S. Development 104:165-173(1988) · UniProtKB (1) |
| Human muscle neural cell adhesion molecule (N-CAM): identification of a muscle-specific sequence in the extracellular domain. Dickson G., Gower H.J., Barton C.H., Prentice H.M., Elsom V.L., Moore S.E., Cox R.D., Quinn C., Putt W., Walsh F.S. Cell 50:1119-1130(1987) · UniProtKB (1) |
| N-cadherin gene maps to human chromosome 18 and is not linked to the E-cadherin gene. Walsh F.S., Barton C.H., Putt W., Moore S.E., Kelsell D., Spurr N., Goodfellow P.N. J. Neurochem. 55:805-812(1990) · UniProtKB (1) |
| Phosphoglucomutase 1: complete human and rabbit mRNA sequences and direct mapping of this highly polymorphic marker on human chromosome 1. Whitehouse D.B., Putt W., Lovegrove J.U., Morrison K.E., Hollyoake M., Fox M.F., Hopkinson D.A., Edwards Y.H. Proc. Natl. Acad. Sci. U.S.A. 89:411-415(1992) · UniProtKB (2) |