Cowpox virus von Dugmore, W N, Dabir, Z M

Volltext

Cowpox virus von Simcock, P R, Noble, J L, Tullo, A B, Morris, D J, Morgan-Capner, P, Dugmore, W N, Dabir, Z M

Volltext

Cowpox virus von Dugmore, W N, Dabir, Z M

Volltext

Large-scale discovery of novel genetic causes of developmental disorders von van Kogelenberg, M, Goudie, D, Gray, E, Harrison, L, Hawkins, R, Henderson, A, Holder, S, Irving, M, Bayzetinova, T, Jones, D, Kini, U, Kinning, E, Kirby, G, Kirk, C, Kumar, D, Lachlan, K, Lees, M, Lim, D, Coomber, E L, Lowther, G, Lynch, S A, Maher, E, Mansour, S, Maye, U, McCann, E, McMullan, D J, McNerlan, S, Metcalfe, K, Mohammed, S, Jones, P, Moore, D, Morton, J, Mugalaasi, H, Newbury-Ecob, R, Ogilvie, C, Park, S, Parker, M J, Patel, C, Porteous, D, Mason, L E, Ragge, N, Rankin, J, Raymond, L, Rosser, E, Miller, R, Sarkar, A, Scott, C, Scott, R, Selby, A, Shannon, N, Simpkin, D, Singzon, R, Skitt, Z, Rajan, D, Splitt, M, Stewart, F, Swaminathan, G J, Tatton-Brown, K, Temple, I K, Torokwa, A, Turner, C, Turnpenny, P, Tysoe, C, Vandersteen, A, Walker, D, Ahmed, M, Widaa, S, Williams, N, Wragg, C, Yau, M, FitzPatrick, D R, Anjum, U, Balasubramanian, M, Banerjee, R, Baralle, D, Baty, D, Bennett, C, Berg, J, Bevan, A P, Bourdon, L, Brady, A, Burton, J, Chandler, K, Cooper, N, Cross, G, D'Alessandro, M, Dabir, T, Davidson, R, Davies, S, Dean, J, Deshpande, C, Donnelly, C, Douglas, A, Eason, J, Edkins, S, Foulds, N, Fryer, A, Gardiner, C, Pereira, S L Gomes, Goodship, J

Volltext

Development of a CHP/DH system for the new town of Parand: An opportunity to mitigate global warming in Middle East von Mostafavi Tehrani, S. Saeed, Saffar-Avval, M., Mansoori, Z., Behboodi Kalhori, S., Abbassi, A., Dabir, B., Sharif, M.

Volltext

Mutations in the PP2A regulatory subunit B family genes PPP2R5B, PPP2R5C and PPP2R5D cause human overgrowth von Loveday, Chey, Tatton-Brown, Katrina, Clarke, Matthew, Westwood, Isaac, Renwick, Anthony, Ramsay, Emma, Nemeth, Andrea, Campbell, Jennifer, Joss, Shelagh, Gardner, McKinlay, Zachariou, Anna, Elliott, Anna, Ruark, Elise, van Montfort, Rob, Rahman, Nazneen

Volltext

Finding Diagnostically Useful Patterns in Quantitative Phenotypic Data von Aitken, Stuart, McRae, Jeremy, Kini, Usha, Parker, Michael J., Joss, Shelagh, Scott, Richard H., Hurles, Matthew E., FitzPatrick, David R., Morley, K.I., Al-Turki, S., Ambridge, K., Barrett, D.M., Bayzetinova, T., Krishnappa, N., Mason, L.E., Middleton, A., Prigmore, E., Tivey, A.R., Akawi, N., Andrews, R., Armstrong, R., Balasubramanian, M., Banerjee, R., Baty, D., Bernhard, B., Blair, E., Bourn, D., Brady, A., Brewer, C., Burn, J., Connell, F., Cooper, N., Cross, G., Dixit, A., Ellis, P., Fendick, T., Fisher, R., Greenhalgh, L., Hawkins, R., Hobson, E., Holden, S., Holder, S., Hurst, J., Ingram, S., Jarvis, J., Johnson, D., Joss, S., Kaemba, B., Kirby, G., Kraus, A., Kumar, D., Lim, D., Lowther, G., Marks, K., Maye, U., McConnell, V., McGowan, R., McMullan, D.J., Metcalfe, K., Mohammed, S., Nevitt, L., Newbury-Ecob, R., Ogilvie, C., Paterson, J., Payne, S., Porteous, D., Raymond, L., Roberts, E., Roberts, G., Roberts, P., Ross, A., Saggar, A., Sandford, R., Schweiger, S., Scott, C., Selby, A., Seller, A., Shears, D., Singzon, R., Smith, B., Sneddon, L., Stewart, F., Stewart, H., Suri, M., Swaminathan, G.J., Sweeney, E., Tolmie, J., Turner, C., Tysoe, C., Vasudevan, P., Vogt, J., Waters, J., Wellesley, D., Widaa, S., Wilcox, S., Williams, N., Yang, F., Wright, C.F., Barrett, J.C., Hurles, M.E.

Volltext

Inter-particle heat transfer in a riser of gas–solid turbulent flows von Mansoori, Z., Saffar-Avval, M., Basirat Tabrizi, H., Dabir, B., Ahmadi, G.

Volltext

Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human height von Tatton-Brown, Katrina, Hanks, Sandra, Ruark, Elise, Zachariou, Anna, Duarte, Silvana Del Vecchio, Ramsay, Emma, Snape, Katie, Murray, Anne, Perdeaux, Elizabeth R, Seal, Sheila, Loveday, Chey, Banka, Siddharth, Clericuzio, Carol, Flinter, Frances, Magee, Alex, McConnell, Vivienne, Patton, Michael, Raith, Wolfgang, Rankin, Julia, Splitt, Miranda, Strenger, Volker, Taylor, Clare, Wheeler, Patricia, Temple, Karen I, Cole, Trevor, Douglas, Jenny, Rahman, Nazneen

Volltext

T1 values in discrimination between health and disease using different T1 sequences: comparison between 3'3'5-MOLLI, 3'5-MOLLI, shMOLLI and SASHA von Mahmoud, Islam Z, Cummins, Ciara, Hussain, Zakir, Rogers, Toby, Dabir, Darius, Voigt, Tobias, Higgins, David M, Nagel, Eike, Schaeffter, Tobias, Puntmann, Valentina

Volltext

Eight Years of Lung Transplantation: Experience of the National Research Institute of Tuberculosis and Lung Diseases von Shadmehr, M.B, Arab, M, Pejhan, S, Daneshvar, A, Javaherzadeh, N, Abbasi, A, Ahmadi, Z.H, Radpay, B, Dabir, S, Parsa, T, Mohammadi, F, Mansoori, S.D, Tabarsi, P, Amiri, M. Valiollahpour, Marjani, M, Kashani, B. Sharif, Najafizadeh, K, Shafaghi, S, Ghorbani, F, Masjedi, M.R, Velayati, A.A

Volltext

Age-gender normal values of native and post-contrast myocardial T1 relaxation times (lambda) on 1.5T and 3T using MOLLI: a multicenter, single vendor cardiovascular magnetic resona... von Dabir, Darius, Child, Nicholas, Kalra, Ashwin, Mahmoud, Islam Z, Rogers, Toby, Gebker, Rolf, Kidambi, Ananth, Plein, Sven, Jabbour, Andrew, Higgins, David M, Schnackenburg, Bernhard, Schaeffter, Tobias, Nagel, Eike, Puntmann, Valentina

Volltext

The contribution of X-linked coding variation to severe developmental disorders von Martin, HC, Gardner, EJ, Samocha, KE, Kaplanis, J, Akawi, N, Sifrim, A, Eberhardt, RY, Tavares, ALT, Neville, MDC, Niemi, MEK, Gallone, G, McRae, J, Borras, S, Clark, C, Dean, J, Miedzybrodzka, Z, Ross, A, Tennant, S, Dabir, T, Donnelly, D, Humphreys, M, Magee, A, McConnell, V, McKee, S, McNerlan, S, Morrison, PJ, Rea, G, Stewart, F, Cole, T, Cooper, N, Cooper-Charles, L, Cox, H, Islam, L, Jarvis, J, Keelagher, R, Lim, D, McMullan, D, Morton, J, Naik, S, O’Driscoll, M, Ong, KR, Osio, D, Ragge, N, Turton, S, Vogt, J, Williams, D, Bodek, S, Donaldson, A, Hills, A, Low, K, Newbury-Ecob, R, Norman, AM, Roberts, E, Scurr, I, Smithson, S, Tooley, M, Abbs, S, Armstrong, R, Dunn, C, Holden, S, Park, SM, Paterson, J, Raymond, L, Reid, E, Sandford, R, Simonic, I, Tischkowitz, M, Woods, G, Bradley, L, Comerford, J, Green, A, Lynch, S, McQuaid, S, Mullaney, B, Berg, J, Goudie, D, Mavrak, E, McLean, J, McWilliam, C, Reavey, E, Azam, T, Cleary, E, Jackson, A, Lam, W, Lampe, A, Moore, D, Porteous, M, Baple, E, Baptista, J, Brewer, C, Castle, B, Kivuva, E, Owens, M, Rankin, J, Shaw-Smith, C, Turner, C, Turnpenny, P, Tysoe, C, Bradley, T, Davidson, R

Volltext bestellen

Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons von Bell, S, Rousseau, J, Peng, H, Aouabed, Z, Priam, P, Theroux, J-F, Jefri, M, Tanti, A, Wu, H, Kolobova, I, Silviera, H, Manzano-Vargas, K, Ehresmann, S, Hamdan, FF, Hettige, N, Zhang, X, Antonyan, L, Nassif, C, Ghaloul-Gonzalez, L, Sebastian, J, Vockley, J, Begtrup, AG, Wentzensen, IM, Crunk, A, Nicholls, RD, Herman, KC, Deignan, JL, Al-Hertani, W, Efthymiou, S, Salpietro, V, Miyake, N, Makita, Y, Matsumoto, N, Ostern, R, Houge, G, Hafstrom, M, Fassi, E, Houlden, H, Wassink-Ruiter, JSK, Nelson, D, Goldstein, A, Dabir, T, van Gils, J, Bourgeron, T, Delorme, R, Cooper, GM, Martinez, JE, Finnila, CR, Carmant, L, Lortie, A, Oegema, R, van Gassen, K, Mehta, SG, Huhle, D, Abou Jamra, R, Martin, S, Brunner, HG, Lindhout, D, Au, M, Graham, JM, Coubes, C, Turecki, G, Gravel, S, Mechawar, N, Rossignol, E, Michaud, JL, Lessard, J, Ernst, C, Campeau, PM

Volltext bestellen