Search Results - Wadey, K.

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  1. 1
    Protein kinase CK2 inhibition suppresses neointima formation via a proline-rich homeodomain-dependent mechanism

    Protein kinase CK2 inhibition suppresses neointima formation via a proline-rich homeodomain-dependent mechanism by Wadey, K.S., Brown, B.A., Sala-Newby, G.B., Jayaraman, P.-S., Gaston, K., George, S.J.

    Published in Vascular pharmacology
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  2. 2
    Elevation of PRH and inhibition of CK2 retards smooth muscle cell proliferation

    Elevation of PRH and inhibition of CK2 retards smooth muscle cell proliferation by Wadey, K, Jayaraman, P.-S, Gaston, K, George, S.J

    Published in Atherosclerosis
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  3. 3
    Identification of prh as a novel inhibitor of smooth muscle cell proliferation

    Identification of prh as a novel inhibitor of smooth muscle cell proliferation by Wadey, K, Sawasdichai, A, Jayaraman, P.-S, Gaston, K, George, S.J

    Published in Atherosclerosis
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  4. 4
    Periodontal pathogens enhance Wnt/ -Catenin signalling and thereby may exacerbate atherogenesis

    Periodontal pathogens enhance Wnt/ -Catenin signalling and thereby may exacerbate atherogenesis by Wadey, K., Cameron, O., Brittan, J.L., Hellin, N., Johnson, J.L., Jenkinson, H.F., Nobbs, A.H., George, S.J.

    Published in Atherosclerosis
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  5. 5
    Proline-rich homeodomain and protein kinase CK2 as mediators of vascular smooth muscle cell proliferation and pathophysiological neointima formation

    Proline-rich homeodomain and protein kinase CK2 as mediators of vascular smooth muscle cell proliferation and pathophysiological neointima formation by Wadey, K.S, Jayaraman, P.-S, Gaston, K, George, S.J

    Published in Atherosclerosis
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  6. 6
    Molecular Definition of 22q11 Deletions in 151 Velo-Cardio-Facial Syndrome Patients

    Molecular Definition of 22q11 Deletions in 151 Velo-Cardio-Facial Syndrome Patients by Carlson, C., Sirotkin, H., Pandita, R., Goldberg, R., McKie, J., Wadey, R., Patanjali, S.R., Weissman, S.M., Anyane-Yeboa, K., Warburton, D., Scambler, P., Shprintzen, R., Kucherlapati, R., Morrow, B.E.

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  7. 7
    Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11

    Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11 by Burn, J, Takao, A, Wilson, D, Cross, I, Momma, K, Wadey, R, Scambler, P, Goodship, J

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  8. 8
    Identification of a novel transcript disrupted by a balanced translocation associated with DiGeorge syndrome

    Identification of a novel transcript disrupted by a balanced translocation associated with DiGeorge syndrome by SUTHERLAND, H. F, WADEY, R, SCAMBLER, P. J, MCKIE, J. M, TAYLOR, C, ATIF, U, JOHNSTONE, K. A, HALFORD, S, KIM, U.-J, GOODSHIP, J, BALDINI, A

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  9. 9
    Isolation and regional localisation of DNA sequences from a human chromosome 11-specific cosmid library

    Isolation and regional localisation of DNA sequences from a human chromosome 11-specific cosmid library by WADEY, R. B, LITTLE, P. F. R, PRITCHARD, J, COWELL, J. K

    Published in Human genetics
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  10. 10
    A high-density YAC contig map of human chromosome 22

    A high-density YAC contig map of human chromosome 22 by Collins, J E, Cole, C G, Smink, L J, Garrett, C L, Leversha, M A, Soderlund, C A, Maslen, G L, Everett, L A, Rice, K M, Coffey, A J

    Published in Nature (London)
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  11. 11
    Hepatitis C virus testing of plasma pools by nucleic acid amplification technology: external quality assessment

    Hepatitis C virus testing of plasma pools by nucleic acid amplification technology: external quality assessment by Gentili, G., Pisani, G., Bisso, G., Cristiano, K., Wirz, M., Mele, C.

    Published in Vox sanguinis
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  12. 12
    Molecular analysis of chromosome region 11p13 in patients with Drash syndrome

    Molecular analysis of chromosome region 11p13 in patients with Drash syndrome by Jadresic, L, Wadey, R B, Buckle, B, Barratt, T M, Mitchell, C D, Cowell, J K

    Published in Human genetics
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  13. 13
    The aniridia-Wilms' tumour association: molecular and genetic analysis of chromosome deletions on the short arm of chromosome 11

    The aniridia-Wilms' tumour association: molecular and genetic analysis of chromosome deletions on the short arm of chromosome 11 by COWELL, J. K, WADEY, R. B, BUCKLE, B. B, PRITCHARD, J

    Published in Human genetics
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  14. 14
    A MspI RFLP associated with the human catalase gene

    A MspI RFLP associated with the human catalase gene by WADEY, R. B, COWELL, J. K

    Published in Nucleic acids research
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  15. 15
    A MspI RFLP associated with the human catatase gene

    A MspI RFLP associated with the human catatase gene by Wadey, R.B., Cowell, J.K.

    Published in Nucleic acids research
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  16. 16
    Molecular analysis of chromosome region 11q13 in patients with Drash syndrome

    Molecular analysis of chromosome region 11q13 in patients with Drash syndrome by JADRESIC, L, WADEY, R. B, BUCKLE, B, BARRATT, T. M, MITCHELL, C. D, COWELL, J. K

    Published in Human genetics
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  17. 17
    A high-density YAC contig map of human chromosome 22: The genome directory

    A high-density YAC contig map of human chromosome 22: The genome directory by COLLINS, J. E, COLE, C. G, GREGORY, S. G, GWILLIAM, R, DUNHAM, A, DAVIES, A. F, HASSOCK, S, TODD, C. M, LEHRACH, H, HULSEBOS, T. J. M, WEISSENBACH, J, MORROW, B, SMINK, L. J, KUCHERLAPATI, R. S, WADEY, R, SCAMBLER, P. J, UNG-JIN KIM, SIMON, M. I, PEYRARD, M, YA-GANG XIE, CARTER, N. P, DURBIN, R, DUMANSKI, J. P, GARRETT, C. L, BENTLEY, D. R, DUNHAM, I, LEVERSHA, M. A, SODERLUND, C. A, MASLEN, G. L, EVERETT, L. A, RICE, K. M, COFFEY, A. J

    Published in Nature (London)
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