Mutation analysis of 24 known cancer genes in the NCI-60 cell line set
Ikediobi, Ogechi N, Davies, Helen, Bignell, Graham, Edkins, Sarah, Stevens, Claire, O'Meara, Sarah, Santarius, Thomas, Avis, Tim, Barthorpe, Syd, Brackenbury, Lisa, Buck, Gemma, Butler, Adam, Clements, Jody, Cole, Jennifer, Dicks, Ed, Forbes, Simon, Gray, Kristian, Halliday, Kelly, Harrison, Rachel, Hills, Katy, Hinton, Jonathan, Hunter, Chris, Jenkinson, Andy, Jones, David, Kosmidou, Vivienne, Lugg, Richard, Menzies, Andrew, Mironenko, Tatiana, Parker, Adrian, Perry, Janet, Raine, Keiran, Richardson, David, Shepherd, Rebecca, Small, Alex, Smith, Raffaella, Solomon, Helen, Stephens, Philip, Teague, Jon, Tofts, Calli, Varian, Jennifer, Webb, Tony, West, Sofie, Widaa, Sara, Yates, Andy, Reinhold, William, Weinstein, John N, Stratton, Michael R, Futreal, P Andrew, Wooster, Richard
Published in Molecular cancer therapeutics (01.11.2006)
Published in Molecular cancer therapeutics (01.11.2006)
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Mutations in UPF3B , a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation
Gécz, Jozef, Perry, Janet, Smith, Raffaella, Edkins, Sarah, Pearson, Pauline, Nguyen, Lam S, Shepherd, Rebecca, West, Sofie, Bobrow, Martin, Teague, John, Sanderson, Tracy, Richardson, David, Wooster, Richard, Varian, Jennifer, Rodriguez, Jayson, Bhat, Shambhu S, Jenkinson, Andrew, Vandeleur, Lucianne, Dicks, Ed, Srivastava, Anand K, Warner, John P, O'Meara, Sarah, Skinner, Cindy, Tarpey, Patrick S, Raine, Keiran, Stevenson, Roger E, Luo, Yin, Barthorpe, Syd, Butler, Adam, Moon, Jenny, Hackett, Anna, Parnau, Josep, Hoganson, George, Thomas, Paul, Hills, Katy, Brooks, Doug, Widaa, Sara, Halliday, Kelly, Lucy Raymond, F, Tofts, Calli, Andrew Futreal, P, Jones, David, Cole, Jennifer, Porteous, Mary E, Menzies, Andrew, Superneau, Duane, Corbett, Mark, Shoubridge, Cheryl, Schwartz, Charles E, Gardner, Alison, Stevens, Claire, Turner, Gillian, Parkinson-Lawrence, Emma, Stratton, Michael R, Buck, Gemma, Mironenko, Tatiana, Simensen, Richard J
Published in Nature genetics (01.09.2007)
Published in Nature genetics (01.09.2007)
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Mutations in the Gene Encoding the Sigma 2 Subunit of the Adaptor Protein 1 Complex, AP1S2, Cause X-Linked Mental Retardation
Tarpey, Patrick S., Stevens, Claire, Teague, Jon, Edkins, Sarah, O’Meara, Sarah, Avis, Tim, Barthorpe, Syd, Buck, Gemma, Butler, Adam, Cole, Jennifer, Dicks, Ed, Gray, Kristian, Halliday, Kelly, Harrison, Rachel, Hills, Katy, Hinton, Jonathon, Jones, David, Menzies, Andrew, Mironenko, Tatiana, Perry, Janet, Raine, Keiran, Richardson, David, Shepherd, Rebecca, Small, Alexandra, Tofts, Calli, Varian, Jennifer, West, Sofie, Widaa, Sara, Yates, Andy, Catford, Rachael, Butler, Julia, Mallya, Uma, Moon, Jenny, Luo, Ying, Dorkins, Huw, Thompson, Deborah, Easton, Douglas F., Wooster, Richard, Bobrow, Martin, Carpenter, Nancy, Simensen, Richard J., Schwartz, Charles E., Stevenson, Roger E., Turner, Gillian, Partington, Michael, Gecz, Jozef, Stratton, Michael R., Futreal, P. Andrew, Raymond, F. Lucy
Published in American journal of human genetics (01.12.2006)
Published in American journal of human genetics (01.12.2006)
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Patterns of somatic mutation in human cancer genomes
Futreal, P. Andrew, Stratton, Michael R, Greenman, Christopher, Stephens, Philip, Smith, Raffaella, Dalgliesh, Gillian L, Hunter, Christopher, Bignell, Graham, Davies, Helen, Teague, Jon, Butler, Adam, Stevens, Claire, Edkins, Sarah, O'Meara, Sarah, Vastrik, Imre, Schmidt, Esther E, Avis, Tim, Barthorpe, Syd, Bhamra, Gurpreet, Buck, Gemma, Choudhury, Bhudipa, Clements, Jody, Cole, Jennifer, Dicks, Ed, Forbes, Simon, Gray, Kris, Halliday, Kelly, Harrison, Rachel, Hills, Katy, Hinton, Jon, Jenkinson, Andy, Jones, David, Menzies, Andy, Mironenko, Tatiana, Perry, Janet, Raine, Keiran, Richardson, Dave, Shepherd, Rebecca, Small, Alexandra, Tofts, Calli, Varian, Jennifer, Webb, Tony, West, Sofie, Widaa, Sara, Yates, Andy, Cahill, Daniel P, Louis, David N, Goldstraw, Peter, Nicholson, Andrew G, Brasseur, Francis, Looijenga, Leendert, Weber, Barbara L, Chiew, Yoke-Eng, deFazio, Anna, Greaves, Mel F, Green, Anthony R, Campbell, Peter, Birney, Ewan, Easton, Douglas F, Chenevix-Trench, Georgia, Tan, Min-Han, Khoo, Sok Kean, Teh, Bin Tean, Yuen, Siu Tsan, Leung, Suet Yi, Wooster, Richard
Published in Nature (08.03.2007)
Published in Nature (08.03.2007)
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Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders
BAXTER, E, SCOTT, L, CAMPBELL, P, EAST, C, FOUROUCLAS, N, SWANTON, S, VASSILIOU, G, BENCH, A, BOYD, E, CURTIN, N
Published in The Lancet (British edition) (25.03.2005)
Published in The Lancet (British edition) (25.03.2005)
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X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment
Jenkinson, Andrew, Varian, Jennifer, Shoubridge, Cheryl, Vandeleur, Lucianne, Shepherd, Rebecca, Hynes, Kim, Shaw, Marie, Gusella, James F, Teague, John, Edkins, Sarah, Dicks, Ed, Dibbens, Leanne M, Haan, Eric, Gécz, Jozef, Halliday, Kelly, Lerman-Sagie, Tally, Sutton, Edwina, Corbett, Mark, Wray, Paul, Bomar, Jamee, Stevens, Claire, Scheffer, Ingrid E, Barthorpe, Syd, Butler, Adam, Tarpey, Patrick S, Jones, David, Bayly, Marta A, Madison, Mark, West, Sofie, Lev, Dorit, Stratton, Michael R, Neufeld, Miriam Y, Korczyn, Amos D, Tofts, Calli, Futreal, P Andrew, Turner, Samantha J, Kim, Hyung-Goo, Berkovic, Samuel F, Buck, Gemma, O'Meara, Sarah, Friend, Kathryn, Kivity, Sara, Afawi, Zaid, Mironenko, Tatiana, McKee, Shane, Cole, Jennifer, Lee, Rebecca, Geschwind, Daniel H, Widaa, Sara, Ryan, Stephen, Smith, Raffaella, Sutherland, Grant R, Menzies, Andrew, Mulley, John C, Mazarib, Aziz, Derry, Christopher P, Thomas, Paul
Published in Nature genetics (01.06.2008)
Published in Nature genetics (01.06.2008)
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Lung cancer Intragenic ERBB2 kinase mutations in tumours
Futreal, P. Andrew, Stephens, Philip, Hunter, Chris, Bignell, Graham, Edkins, Sarah, Davies, Helen, Teague, Jon, Stevens, Claire, O'Meara, Sarah, Smith, Raffaella, Parker, Adrian, Barthorpe, Andy, Blow, Matthew, Brackenbury, Lisa, Butler, Adam, Clarke, Oliver, Cole, Jennifer, Dicks, Ed, Dike, Angus, Drozd, Anja, Edwards, Ken, Forbes, Simon, Foster, Rebecca, Gray, Kristian, Greenman, Chris, Halliday, Kelly, Hills, Katy, Kosmidou, Vivienne, Lugg, Richard, Menzies, Andy, Perry, Janet, Petty, Robert, Raine, Keiran, Ratford, Lewis, Shepherd, Rebecca, Small, Alexandra, Stephens, Yvonne, Tofts, Calli, Varian, Jennifer, West, Sofie, Widaa, Sara, Yates, Andrew, Brasseur, Francis, Cooper, Colin S, Flanagan, Adrienne M, Knowles, Margaret, Leung, Suet Y, Louis, David N, Looijenga, Leendert H. J, Malkowicz, Bruce, Pierotti, Marco A, Teh, Bin, Chenevix-Trench, Georgia, Weber, Barbara L, Yuen, Siu T, Harris, Grace, Goldstraw, Peter, Nicholson, Andrew G, Wooster, Richard, Stratton, Michael R
Published in Nature (30.09.2004)
Published in Nature (30.09.2004)
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Intragenic ERBB2 kinase mutations in tumours
Stephens, Philip, Hunter, Chris, Bignell, Graham, Edkins, Sarah, Davies, Helen, Teague, Jon, Stevens, Claire, O'Meara, Sarah, Smith, Raffaella, Parker, Adrian, Barthorpe, Andy, Blow, Matthew, Brackenbury, Lisa, Butler, Adam, Clarke, Oliver, Cole, Jennifer, Dicks, Ed, Dike, Angus, Drozd, Anja, Edwards, Ken, Forbes, Simon, Foster, Rebecca, Gray, Kristian, Greenman, Chris, Halliday, Kelly, Hills, Katy, Kosmidou, Vivienne, Lugg, Richard, Menzies, Andy, Perry, Janet, Petty, Robert, Raine, Keiran, Ratford, Lewis, Shepherd, Rebecca, Small, Alexandra, Stephens, Yvonne, Tofts, Calli, Varian, Jennifer, West, Sofie, Widaa, Sara, Yates, Andrew, Brasseur, Francis, Cooper, Colin S., Flanagan, Adrienne M., Knowles, Margaret, Leung, Suet Y., Louis, David N., Looijenga, Leendert H. J., Malkowicz, Bruce, Pierotti, Marco A., Teh, Bin, Chenevix-Trench, Georgia, Weber, Barbara L., Yuen, Siu T., Harris, Grace, Goldstraw, Peter, Nicholson, Andrew G., Futreal, P. Andrew, Wooster, Richard, Stratton, Michael R.
Published in Nature (London) (30.09.2004)
Published in Nature (London) (30.09.2004)
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A hypermutation phenotype and somatic MSH6 mutations in recurrent human malignant gliomas after alkylator chemotherapy
HUNTER, Chris, SMITH, Raffaella, O'MEARA, Sarah, PARKER, Adrian, AVIS, Tim, BARTHORPE, Syd, BRACKENBURY, Lisa, BUCK, Gemma, BUTLER, Adam, CLEMENTS, Jody, COLE, Jennifer, DICKS, Ed, CAHILL, Daniel P, FORBES, Simon, GORTON, Matthew, GRAY, Kristian, HALLIDAY, Kelly, HARRISON, Rachel, HILLS, Katy, HINTON, Jonathon, JENKINSON, Andy, JONES, David, KOSMIDOU, Vivienne, STEPHENS, Philip, LAMAN, Ross, LUGG, Richard, MENZIES, Andrew, PERRY, Janet, PETTY, Robert, RAINE, Keiran, RICHARDSON, David, SHEPHERD, Rebecca, SMALL, Alexandra, SOLOMON, Helen, STEVENS, Claire, TOFTS, Calli, VARIAN, Jennifer, WEST, Sofie, WIDAA, Sara, YATES, Andy, EASTON, Douglas F, RIGGINS, Gregory, ROY, Jennifer E, LEVINE, Kymberly K, MUELLER, Wolf, TEAGUE, Jon, BATCHELOR, Tracy T, LOUIS, David N, STRATTON, Michael R, FUTREAL, P. Andrew, WOOSTER, Richard, GREENMAN, Chris, EDKINS, Sarah, BIGNELL, Graham, DAVIES, Helen
Published in Cancer research (Chicago, Ill.) (15.04.2006)
Published in Cancer research (Chicago, Ill.) (15.04.2006)
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Mutations in CUL4B, Which Encodes a Ubiquitin E3 Ligase Subunit, Cause an X-linked Mental Retardation Syndrome Associated with Aggressive Outbursts, Seizures, Relative Macrocephaly, Central Obesity, Hypogonadism, Pes Cavus, and Tremor
Tarpey, Patrick S., Raymond, F. Lucy, O’Meara, Sarah, Edkins, Sarah, Teague, Jon, Butler, Adam, Dicks, Ed, Stevens, Claire, Tofts, Calli, Avis, Tim, Barthorpe, Syd, Buck, Gemma, Cole, Jennifer, Gray, Kristian, Halliday, Kelly, Harrison, Rachel, Hills, Katy, Jenkinson, Andrew, Jones, David, Menzies, Andrew, Mironenko, Tatiana, Perry, Janet, Raine, Keiran, Richardson, David, Shepherd, Rebecca, Small, Alexandra, Varian, Jennifer, West, Sofie, Widaa, Sara, Mallya, Uma, Moon, Jenny, Luo, Ying, Holder, Susan, Smithson, Sarah F., Hurst, Jane A., Clayton-Smith, Jill, Kerr, Bronwyn, Boyle, Jackie, Shaw, Marie, Vandeleur, Lucianne, Rodriguez, Jayson, Slaugh, Rachel, Easton, Douglas F., Wooster, Richard, Bobrow, Martin, Srivastava, Anand K., Stevenson, Roger E., Schwartz, Charles E., Turner, Gillian, Gecz, Jozef, Futreal, P. Andrew, Stratton, Michael R., Partington, Michael
Published in American journal of human genetics (01.02.2007)
Published in American journal of human genetics (01.02.2007)
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Mutations in ZDHHC9, Which Encodes a Palmitoyltransferase of NRAS and HRAS, Cause X-Linked Mental Retardation Associated with a Marfanoid Habitus
Raymond, F. Lucy, Tarpey, Patrick S., Edkins, Sarah, Tofts, Calli, O’Meara, Sarah, Teague, Jon, Butler, Adam, Stevens, Claire, Barthorpe, Syd, Buck, Gemma, Cole, Jennifer, Dicks, Ed, Gray, Kristian, Halliday, Kelly, Hills, Katy, Hinton, Jonathon, Jones, David, Menzies, Andrew, Perry, Janet, Raine, Keiran, Shepherd, Rebecca, Small, Alexandra, Varian, Jennifer, Widaa, Sara, Mallya, Uma, Moon, Jenny, Luo, Ying, Shaw, Marie, Boyle, Jackie, Kerr, Bronwyn, Turner, Gillian, Quarrell, Oliver, Cole, Trevor, Easton, Douglas F., Wooster, Richard, Bobrow, Martin, Schwartz, Charles E., Gecz, Jozef, Stratton, Michael R., Futreal, P. Andrew
Published in American journal of human genetics (01.05.2007)
Published in American journal of human genetics (01.05.2007)
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Mutations in the BRWD3 Gene Cause X-Linked Mental Retardation Associated with Macrocephaly
Field, Michael, Tarpey, Patrick S., Smith, Raffaella, Edkins, Sarah, O’Meara, Sarah, Stevens, Claire, Tofts, Calli, Teague, Jon, Butler, Adam, Dicks, Ed, Barthorpe, Syd, Buck, Gemma, Cole, Jennifer, Gray, Kristian, Halliday, Kelly, Hills, Katy, Jenkinson, Andrew, Jones, David, Menzies, Andrew, Mironenko, Tatiana, Perry, Janet, Raine, Keiran, Richardson, David, Shepherd, Rebecca, Small, Alexandra, Varian, Jennifer, West, Sofie, Widaa, Sara, Mallya, Uma, Wooster, Richard, Moon, Jenny, Luo, Ying, Hughes, Helen, Shaw, Marie, Friend, Kathryn L., Corbett, Mark, Turner, Gillian, Partington, Michael, Mulley, John, Bobrow, Martin, Schwartz, Charles, Stevenson, Roger, Gecz, Jozef, Stratton, Michael R., Andrew Futreal, P., Lucy Raymond, F.
Published in American journal of human genetics (01.08.2007)
Published in American journal of human genetics (01.08.2007)
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Sequence analysis of the protein kinase gene family in human testicular germ-cell tumors of adolescents and adults
Bignell, Graham, Smith, Raffaella, Hunter, Chris, Stephens, Philip, Davies, Helen, Greenman, Chris, Teague, Jon, Butler, Adam, Edkins, Sarah, Stevens, Claire, O'Meara, Sarah, Parker, Adrian, Avis, Tim, Barthorpe, Syd, Brackenbury, Lisa, Buck, Gemma, Clements, Jody, Cole, Jennifer, Dicks, Ed, Edwards, Ken, Forbes, Simon, Gorton, Matthew, Gray, Kristian, Halliday, Kelly, Harrison, Rachel, Hills, Katy, Hinton, Jonathon, Jones, David, Kosmidou, Vivienne, Laman, Ross, Lugg, Richard, Menzies, Andrew, Perry, Janet, Petty, Robert, Raine, Keiran, Shepherd, Rebecca, Small, Alexandra, Solomon, Helen, Stephens, Yvonne, Tofts, Calli, Varian, Jennifer, Webb, Anthony, West, Sofie, Widaa, Sara, Yates, Andy, Gillis, Ad J. M., Stoop, Hans J., van Gurp, Ruud J. H. L. M., Oosterhuis, J. Wolter, Looijenga, Leendert H. J., Futreal, P. Andrew, Wooster, Richard, Stratton, Michael R.
Published in Genes chromosomes & cancer (01.01.2006)
Published in Genes chromosomes & cancer (01.01.2006)
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Anthraquinones related to rhein inhibit glucose uptake into chondrocytes. A mechanism for anti-osteoarthritis drugs?
Carney, Stephen L., Broadmore, Richard J., Tomlinson, Rosemarie, Kingston, Ann, Gallagher, Peter T., Owton, W.Martin, Miles, Martin V., Brunavs, Michael, Smith, Colin W., Hicks, Terry A., Dobson, David R., Steggles, David J., Ambler, Samantha J., Halliday, Kelly A.
Published in Bioorganic & medicinal chemistry letters (08.04.1997)
Published in Bioorganic & medicinal chemistry letters (08.04.1997)
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