Resultados da busca - Algar, Elizabeth M

Rare Childhood Malignancy por Algar, Elizabeth M

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Rapid detection of SMARCB1 sequence variation using high resolution melting por Dagar, Vinod, Chow, Chung-Wo, Ashley, David M, Algar, Elizabeth M

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Cancer Risks for Relatives of Children with Cancer por Heath, John A., Smibert, Elizabeth, Algar, Elizabeth M., Dite, Gillian S., Hopper, John L.

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PDTM-06. TARGETED CATALYTIC INHIBITION OF EZH2 SYNERGIZES WITH LOW-DOSE PANOBINOSTAT IN MALIGNANT RHABDOID TUMOR por Popovski, Dean, Cochrane, Catherine R, Algar, Elizabeth M, Szczepny, Anette, Jayasekara, W Samantha, Ashley, David M, Downie, Peter, Watkins, D Neil, Cain, Jason E

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The evolutionary pattern of mutations in glioblastoma reveals therapy-mediated selection por Muscat, Andrea M., Wong, Nicholas C., Drummond, Katharine J., Algar, Elizabeth M., Khasraw, Mustafa, Verhaak, Roel, Field, Kathryn, Rosenthal, Mark A., Ashley, David M.

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Imprinted CDKN1C Is a Tumor Suppressor in Rhabdoid Tumor and Activated by Restoration of SMARCB1 and Histone Deacetylase Inhibitors por Algar, Elizabeth M., Muscat, Andrea, Dagar, Vinod, Rickert, Christian, Chow, C. W., Biegel, Jaclyn A., Ekert, Paul G., Saffery, Richard, Craig, Jeff, Johnstone, Ricky W., Ashley, David M.

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High expression of BMP pathway genes distinguishes a subset of atypical teratoid/rhabdoid tumors associated with shorter survival por Birks, Diane K., Donson, Andrew M., Patel, Purvi R., Dunham, Christopher, Muscat, Andrea, Algar, Elizabeth M., Ashley, David M., Kleinschmidt-DeMasters, B. K., Vibhakar, Rajeev, Handler, Michael H., Foreman, Nicholas K.

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Genome wide methylation profiling of selected matched soft tissue sarcomas identifies methylation changes in metastatic and recurrent disease por Vargas, Ana Cristina, Gray, Lesley-Ann, White, Christine L., Maclean, Fiona M., Grimison, Peter, Ardakani, Nima Mesbah, Bonar, Fiona, Algar, Elizabeth M., Cheah, Alison L., Russell, Peter, Mahar, Annabelle, Gill, Anthony J.

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Atypical Teratoid Rhabdoid Tumours Are Susceptible to Panobinostat-Mediated Differentiation Therapy por Chong, Wai C., Jayasekara, W. Samantha N., Vaghjiani, Vijesh G., Parackal, Sarah, Sun, Claire, Popovski, Dean, Algar, Elizabeth M., Firestein, Ron, Wood, Paul J., Khan, Sara, Huang, Annie, Ashley, David M., Downie, Peter, Cain, Jason E.

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Nemaline myopathy and distal arthrogryposis associated with an autosomal recessive TNNT3 splice variant por Sandaradura, Sarah A, Bournazos, Adam, Mallawaarachchi, Amali, Cummings, Beryl B, Waddell, Leigh B, Jones, Kristi J, Troedson, Christopher, Sudarsanam, Annapurna, Nash, Benjamin M, Peters, Gregory B, Algar, Elizabeth M, MacArthur, Daniel G, North, Kathryn N, Brammah, Susan, Charlton, Amanda, Laing, Nigel G, Wilson, Meredith J, Davis, Mark R, Cooper, Sandra T

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Genetic variation affecting DNA methylation and the human imprinting disorder, Beckwith-Wiedemann syndrome por Dagar, Vinod, Hutchison, Wendy, Muscat, Andrea, Krishnan, Anita, Hoke, David, Buckle, Ashley, Siswara, Priscillia, Amor, David J., Mann, Jeffrey, Pinner, Jason, Colley, Alison, Wilson, Meredith, Sachdev, Rani, McGillivray, George, Edwards, Matthew, Kirk, Edwin, Collins, Felicity, Jones, Kristi, Taylor, Juliet, Hayes, Ian, Thompson, Elizabeth, Barnett, Christopher, Haan, Eric, Freckmann, Mary-Louise, Turner, Anne, White, Susan, Kamien, Ben, Ma, Alan, Mackenzie, Fiona, Baynam, Gareth, Kiraly-Borri, Cathy, Field, Michael, Dudding-Byth, Tracey, Algar, Elizabeth M.

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