Urinary Tract Effects of HPSE2 Mutations

Autor: Stuart, H. M., Roberts, N. A., Hilton, E. N., Mckenzie, E. A., Daly, S. B., Hadfield, K. D., Rahal, J. S., Gardiner, N. J., Tanley, S. W., Lewis, M. A., Sites, E., Angle, B., Alves, C., Lourenço, T., Rodrigues, M., Calado, A., Amado, M., Guerreiro, N., Serras, I., Beetz, C., Varga, R. -E., Silay, M. S., Darlow, J. M., Dobson, M. G., Barton, D. E., Hunziker, M., Puri, P., Feather, S. A., Goodship, J. A., Goodship, T. H. J., Lambert, H. J., Cordell, H. J., Saggar, A., Kinali, M., Lorenz, C, Moeller, K, Schaefer, F, Bayazit, Ak, Weber, S, Newman, Wg, Woolf, As, Beattie, J, Bradbuty, M, Coad, N, Coulthard, M, Cuckow, P, Dossetor, J, Dudley, J, Hughes, D, Feather, S, Fitzpatrick, M, Goodship, Ja, Goodship, Th, Griffin, N, Gullett, Am, Haycock, G, Hodes, D, Houtman, P, Hughes, A, Hulton, S, Hunter, E, Iqbal, J, Inward, C, Jackson, J, Jadresic, L, Jaswon, M, Jones, C, Jones, R, Judd, B, Kier, M, Kilby, A, Lambert, H, Lewis, M, Malcolm, S, Marks, S, Maxwell, H, Mcgraw, M, Milford, D, Moghal, N, O'Connor, M, O'Donoghue, Dj, Ognanovic, M, Plant, N, Postlethwaite, R, Rees, L, Reid, C, Rfidah, E, Rigdon, S, Sandford, R, Savage, M, Scanlan, J, Sinha, S, Stephens, S, Stewart, A, Storr, J, Taheri, S, Taylor, Cm, Tizard, J, Trompeter, R, Tullus, K, Verber, I, Van't Hoff, W, Vernon, S, Verrier-Jones, K, Watson, A, Webb, N, Wilcox, D, Aksu, N, Alpay, H, Anarat, A, Arbeiter, K, Ardissino, Gl, Balat, A, Baskin, E, Bayazit, A, Büscher, R, Cakar, N, Caldas Afonso, A, Caliskan, S, Candan, C, Canpolat, N, Donmez, O, Doyon, A, Drozdz, D, Dusek, J, Duzova, A, Emre, S, Erdogan, H, Feldkötter, M, Fischbach, M, Galiano, G, Haffner, D, Harambat, J, Jankauskiene, A, Jeck, N, John, U, Jungraithmair, T, Kemper, M, Kiyak, A, Kracht, D, Kranz, B, Laube, G, Litwin, M, Matteucci, Cm, Montini, G, Melk, A, Mir, S, Niemirska, A, Peco-Antic, A, Ozcelik, G, Pelan, E, Picca, S, Pohl, M, Querfeld, U, Ranchin, B, Shroff, R, Simonetti, G, Sözeri, B, Soylemezoglu, O, Tabel, Y, Testa, S, Trivelli, A, Vidal, E, Wigger, M, Wühl, E, Wygoda, S, Yalcinkaya, F, Yilmaz, E, Zeller, R, Zurowska, Am.

Publikováno v: Europe PubMed Central
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP

PubMedID: 25145936 Urofacial syndrome (UFS) is an autosomal recessive congenital disease featuring grimacing and incomplete bladder emptying. Mutations of HPSE2, encoding heparanase 2, a heparanase 1 inhibitor, occur in UFS, but knowledge about the H

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4796319029029e10fd14a07767d3d461
http://europepmc.org/abstract/med/25145936

Combining X‐rays, neutrons and electrons, and NMR, for precision and accuracy in structure–function studies.

Autor: Helliwell, John R.¹ (AUTHOR) john.helliwell@manchester.ac.uk

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Re-refinement of 4xan: hen egg-white lysozyme with carboplatin in sodium bromide solution.

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