IgM associated primary diffuse mesangial proliferative glomerulonephritis.

Por Lawler, W, Williams, G, Tarpey, P, Mallick, N P
Publicado em 1980

Amino acid sequence and the cellular location of the Na(+)-dependent D-glucose symporters (SGLT1) in the ovine enterocyte and the parotid acinar cell.

Por Tarpey, P S, Wood, I S, Shirazi-Beechey, S P, Beechey, R B
Publicado em 1995

Diseases and histological normality of the renal glomerulus: a clinicopathological study.

Por Lawler, W, Tarpey, P, Williams, G, Acheson, E J, Mallick, N P
Publicado em 1976

IgA localisation in glomerular diseases.

Por Lawler, W, Williams, G, Tarpey, P, Acheson, E J, Mallick, N P
Publicado em 1977

Re: Pitfalls of automated comparative sequence analysis as a single platform for routine clinical testing for NF1 (Messiaen and Wimmer)

Por Whittaker, J, Mattocks, C, Baralle, D, Tarpey, P, ffrench-Constant, C, Bobrow, M
Publicado em 2005

Re: Pitfalls of automated comparative sequence analysis as a single platform for routine clinical testing for NF1 (Messiaen and Wimmer)

Por Whittaker, J, Mattocks, C, Baralle, D, Tarpey, P, ffrench-Constant, C, Bobrow, M
Publicado em 2005

Automated comparative sequence analysis identifies mutations in 89% of NF1 patients and confirms a mutation cluster in exons 11–17 distinct from the GAP related domain

Por Mattocks, C, Baralle, D, Tarpey, P, ffrench-Constant, C, Bobrow, M, Whittaker, J
Publicado em 2004

Mutations in the RSK2(RPS6KA3) gene cause Coffin–Lowry syndrome and nonsyndromic X-linked mental retardation

Por Field, M, Tarpey, P, Boyle, J, Edkins, S, Goodship, J, Luo, Y, Moon, J, Teague, J, Stratton, MR, Futreal, PA, Wooster, R, Raymond, FL, Turner, G
Publicado em 2006

Mutations in a novel member of the FERM family, FRMD7 cause X-linked idiopathic congenital nystagmus (NYS1)

Por Tarpey, P, Thomas, S, Sarvananthan, N, Mallya, U, Lisgo, S, Talbot, CJ, Roberts, EO, Awan, M, Surendran, M, McLean, RJ, Reinecke, RD, Langmann, A, Lindner, S, Koch, M, Woodruff, G, Gale, R, Degg, C, Droutsas, K, Asproudis, I, Zubcov, AA, Pieh, C, Veal, CD, Machado, RD, Backhouse, OC, Baumber, L, Jain, S, Constantinescu, CS, Brodsky, MC, Hunter, DG, Hertle, RW, Read, RJ, Edkins, S, O’Meara, S, Parker, A, Stevens, C, Teague, J, Wooster, R, Futreal, PA, Trembath, RC, Stratton, MR, Raymond, FL, Gottlob, I
Publicado em 2006

Somatic SF3B1 Mutation in Myelodysplasia with Ring Sideroblasts

Por Papaemmanuil, E., Cazzola, M., Boultwood, J., Malcovati, L., Vyas, P., Bowen, D., Pellagatti, A., Wainscoat, J.S., Hellstrom-Lindberg, E., Gambacorti-Passerini, C., Godfrey, A.L., Rapado, I., Cvejic, A., Rance, R., McGee, C., Ellis, P., Mudie, L.J., Stephens, P.J., McLaren, S., Massie, C.E., Tarpey, P.S., Varela, I., Nik-Zainal, S., Davies, H.R., Shlien, A., Jones, D., Raine, K., Hinton, J., Butler, A.P., Teague, J.W., Baxter, E.J., Score, J., Galli, A., Della Porta, M.G., Travaglino, E., Groves, M., Tauro, S., Munshi, N.C., Anderson, K.C., El-Naggar, A., Fischer, A., Mustonen, V., Warren, A.J., Cross, N.C.P., Green, A.R., Futreal, P.A., Stratton, M.R., Campbell, P.J.
Publicado em 2011

Somatic CALR Mutations in Myeloproliferative Neoplasms with Nonmutated JAK2

Por Nangalia, J., Massie, C.E., Baxter, E.J., Nice, F.L., Gundem, G., Wedge, D.C., Avezov, E., Li, J., Kollmann, K., Kent, D.G., Aziz, A., Godfrey, A.L., Hinton, J., Martincorena, I., Van Loo, P., Jones, A.V., Guglielmelli, P., Tarpey, P., Harding, H.P., Fitzpatrick, J.D., Goudie, C.T., Ortmann, C.A., Loughran, S.J., Raine, K., Jones, D.R., Butler, A.P., Teague, J.W., O’Meara, S., McLaren, S., Bianchi, M., Silber, Y., Dimitropoulou, D., Bloxham, D., Mudie, L., Maddison, M., Robinson, B., Keohane, C., Maclean, C., Hill, K., Orchard, K., Tauro, S., Du, M.-Q., Greaves, M., Bowen, D., Huntly, B.J.P., Harrison, C.N., Cross, N.C.P., Ron, D., Vannucchi, A.M., Papaemmanuil, E., Campbell, P.J., Green, A.R.
Publicado em 2013