Impaired endothelium‐dependent relaxation in isolated resistance arteries of spontaneously diabetic rats von Heygate, Katherine M., Lawrence, Ian G., Bennett, Michael A., Thurston, Herbert

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The effect of insulin treatment and of islet transplantation on the resistance artery function in the STZ‐induced diabetic rat von Heygate, Katherine M., Davies, Joanne, Holmes, Michael, James, Roger F.L., Thurston, Herbert

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Impaired endothelium-dependent relaxation in isolated resistance arteries of spontaneously diabetic rats von HEYGATE, K. M, LAWRENCE, I. G, BENNETT, M. A, THURSTON, H

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Heterozygous lamin B1 and lamin B2 variants cause primary microcephaly and define a novel laminopathy von Parry, David A., Martin, Carol-Anne, Greene, Philip, Marsh, Joseph A., Blyth, Moira, Cox, Helen, Donnelly, Deirdre, Greenhalgh, Lynn, Greville-Heygate, Stephanie, Harrison, Victoria, Lachlan, Katherine, McKenna, Caoimhe, Quigley, Alan J., Rea, Gillian, Robertson, Lisa, Suri, Mohnish, Jackson, Andrew P.

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Clinical delineation of the PACS1-related syndrome-Report on 19 patients von Schuurs-Hoeijmakers, Janneke H. M., Landsverk, Megan L., Foulds, Nicola, Kukolich, Mary K., Gavrilova, Ralitza H., Greville-Heygate, Stephanie, Hanson-Kahn, Andrea, Bernstein, Jonathan A., Glass, Jennifer, Chitayat, David, Burrow, Thomas A., Husami, Ammar, Collins, Kathleen, Wusik, Katie, van der Aa, Nathalie, Kooy, Frank, Brown, Kate Tatton, Gadzicki, Dorothea, Kini, Usha, Alvarez, Sara, Fernández-Jaén, Alberto, McGehee, Frank, Selby, Katherine, Tarailo-Graovac, Maja, Van Allen, Margot, van Karnebeek, Clara D. M., Stavropoulos, Dimitri J., Marshall, Christian R., Merico, Daniele, Gregor, Anne, Zweier, Christiane, Hopkin, Robert J., Chu, Yoyo Wing-Yiu, Chung, Brian Hon-Yin, de Vries, Bert B. A., Devriendt, Koenraad, Hurles, Matthew E., Brunner, Han G.

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Extent of investigation and management of cases of ‘unexplained’ mismatch repair deficiency (u-dMMR): a UK Cancer Genetics Group consensus von McVeigh, TP, Monahan, KJ, Christopher, J, West, N, Scott, M, Murray, J, Hanson, H, Armstrong, R, Beggs, A, Berlin, C, Boyde, A, Brady, A, Bulmer, J, Burghel, G, Burn, J, Catherwood, M, Cleaver, R, Coad, B, Conti, H, Cook, J, Cope, W, Corbett, G, Crosbie, E, Davidson, R, DeSouza, B, Donaldson, A, Durkie, M, Eccles, D, Foot, N, Frayling, I, George, A, Gerrard, G, Gibson, S, Green, A, Greville-Heygate, S, Hamilton, S, Hart, R, Hodgson, S, Holliday, D, Hoyle, J, Jewell, R, Kemp, Z, Kiely, L, Kiesel, V, Kohut, K, Kristeleit, R, Kumar, A, Lalloo, F, Latchford, A, Lee, N, Lobo, D, Loughrey, M, MacMahon, S, Martin, R, Martin, S, McVeigh, T, Miedzybrodzka, Z, Minshall, E, Monahan, K, Monje-Garcia, L, Morgan, M, Mugalaasi, H, Musgrave, H, Nastali, E, Norbury, G, Ong, KR, Onyeador, N, Pagan, J, Quigley, K, Ratsma, E, Rea, G, Repana, D, Rosenthal, A, Searle, C, Shaw, A, Side, L, Simon, K, Smith, K, Solomons, J, Varde, A, Wiggins, J, Wren, D, Yarram-Smith, L

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Extent of investigation and management of cases of ‘unexplained’ mismatch repair deficiency (u-dMMR): a UK Cancer Genetics Group consensus von McVeigh, T.P, Monahan, K.J, Christopher, J, West, N, Scott, M, Murray, J, Hanson, H, Attendees, U.D.C.M, Armstrong, R, Beggs, A, Berlin, C, Boyde, A, Brady, A, Bulmer, J, Burghel, G, Burn, J, Catherwood, M, Cleaver, R, Coad, B, Conti, H, Cook, J, Cope, W, Corbett, G, Crosbie, E, Davidson, R, DeSouza, B, Donaldson, A, Durkie, M, Eccles, D, Foot, N, Frayling, I, George, A, Gerrard, G, Gibson, S, Green, A, Greville-Heygate, S, Hamilton, S, Hart, R, Hodgson, S, Holliday, D, Hoyle, J, Jewell, R, Kemp, Z, Kiely, L, Kiesel, V, Kohut, K, Kristeleit, R, Kumar, A, Lalloo, F, Latchford, A, Lee, N, Lobo, D, Loughrey, M, MacMahon, S, Martin, R, Martin, S, McVeigh, T, Miedzybrodzka, Z, Minshall, E, Monahan, K, Monje-Garcia, L, Morgan, M, Mugalaasi, H, Musgrave, H, Nastali, E, Norbury, G, Ong, K.R, Onyeador, N, Pagan, J, Quigley, K, Ratsma, E, Rea, G, Repana, D, Rosenthal, A, Searle, C, Shaw, A, Side, L, Simon, K, Smith, K, Solomons, J, Varde, A, Wiggins, J, Wren, D, Yarram-Smith, L

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Heterozygous lamin B1 and lamin B2 variants cause primary microcephaly and define a novel laminopathy von Parry, DA, Martin, CA, Greene, P, Marsh, JA, Ambrose, JC, Arumugam, P, Baple, EL, Bleda, M, Boardman-Pretty, F, Boissiere, JM, Boustred, CR, Brittain, H, Caulfield, MJ, Chan, GC, Craig, CEH, Daugherty, LC, de Burca, A, Devereau, A, Elgar, G, Foulger, RE, Fowler, T, Furió-Tarí, P, Giess, A, Hackett, JM, Halai, D, Hamblin, A, Henderson, S, Holman, JE, Hubbard, TJP, Ibáñez, K, Jackson, R, Jones, LJ, Kasperaviciute, D, Kayikci, M, Kousathanas, A, Lahnstein, L, Lawson, K, Leigh, SEA, Leong, IUS, Lopez, FJ, Maleady-Crowe, F, Mason, J, McDonagh, EM, Moutsianas, L, Mueller, M, Murugaesu, N, Need, AC, Odhams, CA, Orioli, A, Patch, C, Perez-Gil, D, Pereira, MB, Polychronopoulos, D, Pullinger, J, Rahim, T, Rendon, A, Riesgo-Ferreiro, P, Rogers, T, Ryten, M, Savage, K, Sawant, K, Scott, RH, Siddiq, A, Sieghart, A, Smedley, D, Smith, KR, Smith, SC, Sosinsky, A, Spooner, W, Stevens, HE, Stuckey, A, Sultana, R, Tanguy, M, Thomas, ERA, Thompson, SR, Tregidgo, C, Tucci, A, Walsh, E, Watters, SA, Welland, MJ, Williams, E, Witkowska, K, Wood, SM, Zarowiecki, M, Blyth, M, Cox, H, Donnelly, D, Greenhalgh, L, Greville-Heygate, S, Harrison, V, Lachlan, K, McKenna, C, Quigley, AJ, Rea, G, Robertson, L, Suri, M, Jackson, AP

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