Kate V Everett

Summary

Affiliation: St George's
Country: UK

Publications

  1. doi request reprint Confirmation of two novel loci for infantile hypertrophic pyloric stenosis on chromosomes 3 and 5
    Kate V Everett
    Human Genetics Research Centre, Division of Biomedical Sciences, St George s University of London, London, UK
    J Hum Genet 58:236-7. 2013
  2. doi request reprint Transient receptor potential genes and human inherited disease
    Kate V Everett
    St George s University of London, London, UK
    Adv Exp Med Biol 704:1011-32. 2011
  3. doi request reprint Infantile hypertrophic pyloric stenosis: evaluation of three positional candidate genes, TRPC1, TRPC5 and TRPC6, by association analysis and re-sequencing
    Kate V Everett
    Molecular Medicine Unit, University College London Institute of Child Health, London, UK
    Hum Genet 126:819-31. 2009

Collaborators

Detail Information

Publications3

  1. doi request reprint Confirmation of two novel loci for infantile hypertrophic pyloric stenosis on chromosomes 3 and 5
    Kate V Everett
    Human Genetics Research Centre, Division of Biomedical Sciences, St George s University of London, London, UK
    J Hum Genet 58:236-7. 2013
    ..Here, we report our confirmation of two of these significant results thus providing further support for new loci for IHPS on chromosome 3p25.1 and chromosome 5q35.2...
  2. doi request reprint Transient receptor potential genes and human inherited disease
    Kate V Everett
    St George s University of London, London, UK
    Adv Exp Med Biol 704:1011-32. 2011
    ..This feedback loop of information will serve to enhance our knowledge of disease and elucidate basic gene and protein function of the TRPs...
  3. doi request reprint Infantile hypertrophic pyloric stenosis: evaluation of three positional candidate genes, TRPC1, TRPC5 and TRPC6, by association analysis and re-sequencing
    Kate V Everett
    Molecular Medicine Unit, University College London Institute of Child Health, London, UK
    Hum Genet 126:819-31. 2009
    ..Fine mapping of all three genes using a tagSNP approach and re-sequencing identified a SNP in the promoter region of TRPC6 and a missense variant in exon 4 of TRPC6 which may be putative causal variants...