Potential for forage diet manipulation in New Zealand pasture ecosystems to mitigate ruminant urine derived N2O emissions: a review von Gardiner, CA, Clough, TJ, Cameron, KC, Di, HJ, Edwards, GR, de Klein, CAM

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A novel functional assay using etoposide plus nutlin-3a detects and distinguishes between ATM and TP53 mutations in CLL von Best, O G, Gardiner, A C, Majid, A, Walewska, R, Austen, B, Skowronska, A, Ibbotson, R, Stankovic, T, Dyer, M J S, Oscier, D G

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Increased inbreeding and inter-species gene flow in remnant populations of the rare Eucalyptus benthamii von Butcher, P. A., Skinner, A. K., Gardiner, C. A.

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Day 3 serum inhibin-B is predictive of assisted reproductive technologies outcome von Seifer, David B., Lambert-Messerlian, Geralyn, Hogan, Joseph W., Gárdiner, Alice C., Blazar, Andrew S., Berk, Carol A.

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P2X7 polymorphism and chronic lymphocytic leukaemia: lack of correlation with incidence, survival and abnormalities of chromosome 12 von Zhang, L Y, Ibbotson, R E, Orchard, J A, Gardiner, A C, Seear, R V, Chase, A J, Oscier, D G, Cross, N C P

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A subset of Binet stage A CLL patients with TP53 abnormalities and mutated IGHV genes have stable disease von Best, O G, Gardiner, A C, Davis, Z A, Tracy, I, Ibbotson, R E, Majid, A, Dyer, M J S, Oscier, D G

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The mutation spectrum in Holt-Oram syndrome von CROSS, STEPHEN J, CHING, YUNG-HAO, LI, QUAN YI, ARMSTRONG-BUISSERET, LINDSAY, SPRANGER, STEPHANIE, LYONNET, STANISLAW, BONNET, DAMIEN, PENTTINEN, MAILA, JONVEAUX, PHILIPPE, LEHEUP, BRUNO, MORTIER, GEERT, VAN RAVENSWAAIJ, CONNY, GARDINER, CAROL-ANNE, BROOK, J DAVID, NEWBURY-ECOB, RUTH

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Apoptosis as a function of ovarian reserve in women undergoing in vitro fertilization von Seifer, David B., Gardiner, Alice C., Ferreira, Karen A., Peluso, John J.

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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

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Differential secretion of dimeric inhibin in cultured luteinized granulosa cells as a function of ovarian reserve von SEIFER, D. B, GARDINER, A. C, LAMBERT-MESSERLIAN, G, SCHNEYER, A. L

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Germline mutations in RAD51D confer susceptibility to ovarian cancer von Loveday, Chey, Turnbull, Clare, Ramsay, Emma, Hughes, Deborah, Ruark, Elise, Frankum, Jessica R, Bowden, Georgina, Kalmyrzaev, Bolot, Warren-Perry, Margaret, Snape, Katie, Adlard, Julian W, Barwell, Julian, Berg, Jonathan, Brady, Angela F, Brewer, Carole, Brice, Glen, Chapman, Cyril, Cook, Jackie, Davidson, Rosemarie, Donaldson, Alan, Douglas, Fiona, Greenhalgh, Lynn, Henderson, Alex, Izatt, Louise, Kumar, Ajith, Lalloo, Fiona, Miedzybrodzka, Zosia, Morrison, Patrick J, Paterson, Joan, Porteous, Mary, Rogers, Mark T, Shanley, Susan, Walker, Lisa, Eccles, Diana, Evans, D Gareth, Renwick, Anthony, Seal, Sheila, Lord, Christopher J, Ashworth, Alan, Reis-Filho, Jorge S, Antoniou, Antonis C, Rahman, Nazneen

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Analysis of rare disruptive germline mutations in 2135 enriched BRCA-negative breast cancers excludes additional high-impact susceptibility genes von Loveday, C., Garrett, A., Hanks, S., Berg, J., Brady, A.F., Cook, J., Donaldson, A., Douglas, F., Greenhalgh, L., Miedzybrodzka, Z., Morrison, P.J., Paterson, J., Ahmed, M., Bardsley, C., Barton, D., Bartlett, M., Baxter, L., Belk, R., Berg, J., Brant, S., Brewer, C., Brice, G., Brooks, C., Campbell, J., Castle, B., Cole, T., Collins, A., Cruger, D., Cummings, C., Davidson, R., Day, L., Dolling, C., Douglas, F., Drummond, S., Edwards, M., Edwards, E., Edwardson, J., Elmslie, F., Evans, G., Ghali, N., Greenhalgh, L., Henderson, A., Hodgson, S., Houlston, R.S., Hunt, V., Izatt, L., Jacobs, C., Jobson, I., Kennedy, M.J., Kightley, C., Kohut, K., Kumar, A., Levene, S., Logan, P., Magee, A., Mansour, S., McBride, D., McEntagart, M., McKeown, C., McLeod, D., Melville, A., Miedzybrodzka, Z., Murday, V., Myhill, K., Myring, J., Pearson, P., Pichert, G., Platt, K., Porteous, M., Protheroe, L., Pugh, S., Randhawa, K., Riddick, C., Robertson, L., Robinson, A., Rowe, S., Schofield, A., Scott, G., Sharif, S., Shaw, A., Shaw, J., Shea-Simonds, J., Side, L., Simon, K., Slater, S., Smith, K., Soloway, J., Steel, M., Stewart, H., Thomas, M., Turner, H., Wakeling, E., Watt, C., Watts, S., Whyte, C., Eccles, D., Evans, D.G., Hanson, H., Houlston, R.S., Turnbull, C.

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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

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Mutations in NONO lead to syndromic intellectual disability and inhibitory synaptic defects von Mircsof, Dennis, Langouët, Maéva, Rio, Marlène, Moutton, Sébastien, Siquier-Pernet, Karine, Bole-Feysot, Christine, Cagnard, Nicolas, Nitschke, Patrick, Gaspar, Ludmila, Žnidarič, Matej, Alibeu, Olivier, Fritz, Ann-Kristina, Wolfer, David P, Schröter, Aileen, Bosshard, Giovanna, Rudin, Markus, Koester, Christina, Crestani, Florence, Seebeck, Petra, Boddaert, Nathalie, Prescott, Katrina, Hines, Rochelle, Moss, Steven J, Fritschy, Jean-Marc, Munnich, Arnold, Amiel, Jeanne, Brown, Steven A, Tyagarajan, Shiva K, Colleaux, Laurence

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Autologous granulosa cell coculture demonstrates zygote suppression of granulosa cell steroidogenesis von Seifer, David B., Freeman, Melanie R., Gardiner, Alice C., Hill, George A., Schneyer, Alan L., Vanderhyden, Barbara C.

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BRCA1 testing should be offered to individuals with triple-negative breast cancer diagnosed below 50 years von Robertson, L, Hanson, H, Seal, S, Warren-Perry, M, Hughes, D, Howell, I, Turnbull, C, Houlston, R, Shanley, S, Butler, S, Evans, D G, Ross, G, Eccles, D, Tutt, A, Rahman, N

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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.

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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

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Mayer - Rokitansky - Kuster - Hauser syndrome von Chandiramani, M., Gardiner, C. A., Padfield, C. J. H., Ikhena, S. E.

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Detailed molecular delineation of 13q14.3 loss in B-cell chronic lymphocytic leukemia von Corcoran, M M, Rasool, O, Liu, Y, Iyengar, A, Grander, D, Ibbotson, R E, Merup, M, Wu, X, Brodyansky, V, Gardiner, A C, Juliusson, G, Chapman, R M, Ivanova, G, Tiller, M, Gahrton, G, Yankovsky, N, Zabarovsky, E, Oscier, D G, Einhorn, S

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