Microarray analysis of human leucocyte subsets: the advantages of positive selection and rapid purification von Lyons, Paul A, Koukoulaki, Maria, Hatton, Alexander, Doggett, Karen, Woffendin, Hayley B, Chaudhry, Afzal N, Smith, Kenneth G C

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Novel expression signatures identified by transcriptional analysis of separated leucocyte subsets in systemic lupus erythematosus and vasculitis von Lyons, Paul A, McKinney, Eoin F, Rayner, Tim F, Hatton, Alexander, Woffendin, Hayley B, Koukoulaki, Maria, Freeman, Thomas C, Jayne, David R W, Chaudhry, Afzal N, Smith, Kenneth G C

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Mutations in the DLG3 Gene Cause Nonsyndromic X-Linked Mental Retardation von Tarpey, Patrick, Parnau, Josep, Blow, Matthew, Woffendin, Hayley, Bignell, Graham, Cox, Charles, Cox, James, Davies, Helen, Edkins, Sarah, Holden, Simon, Korny, Angelique, Mallya, Uma, Moon, Jenny, O’Meara, Sarah, Parker, Adrian, Stephens, Philip, Stevens, Claire, Teague, Jon, Donnelly, Andrew, Mangelsdorf, Marie, Mulley, John, Partington, Michael, Turner, Gillian, Stevenson, Roger, Schwartz, Charles, Young, Ian, Easton, Douglas, Bobrow, Martin, Futreal, P. Andrew, Stratton, Michael R., Gecz, Jozef, Wooster, Richard, Raymond, F. Lucy

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A novel PCR approach for prenatal detection of the common NEMO rearrangement in incontinentia pigmenti von Steffann, Julie, Raclin, Valérie, Smahi, Asmae, Woffendin, Hayley, Munnich, Arnold, Kenwrick, Sue J., Grebille, Anne-Gaelle, Benachi, Alexandra, Dumez, Yves, Bonnefont, Jean-Paul, Hadj-Rabia, Smaïl

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Mutations of the BRAF gene in human cancer von Wooster, Richard, Davies, Helen, Bignell, Graham R, Cox, Charles, Stephens, Philip, Edkins, Sarah, Clegg, Sheila, Teague, Jon, Woffendin, Hayley, Garnett, Mathew J, Bottomley, William, Davis, Neil, Dicks, Ed, Ewing, Rebecca, Floyd, Yvonne, Gray, Kristian, Hall, Sarah, Hawes, Rachel, Hughes, Jaime, Kosmidou, Vivian, Menzies, Andrew, Mould, Catherine, Parker, Adrian, Stevens, Claire, Watt, Stephen, Hooper, Steven, Wilson, Rebecca, Jayatilake, Hiran, Gusterson, Barry A, Cooper, Colin, Shipley, Janet, Hargrave, Darren, Pritchard-Jones, Katherine, Maitland, Norman, Chenevix-Trench, Georgia, Riggins, Gregory J, Bigner, Darell D, Palmieri, Giuseppe, Cossu, Antonio, Flanagan, Adrienne, Nicholson, Andrew, Ho, Judy W. C, Leung, Suet Y, Yuen, Siu T, Weber, Barbara L, Seigler, Hilliard F, Darrow, Timothy L, Paterson, Hugh, Marais, Richard, Marshall, Christopher J, Stratton, Michael R, Futreal, P. Andrew

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A recurrent deletion in the ubiquitously expressed NEMO (IKK-γ) gene accounts for the vast majority of incontinentia pigmenti mutations von ARADHYA, Swaroop, WOFFENDIN, Hayley, LEWIS, Richard A, KENWRICK, Sue, NELSON, David L, JAKINS, Tracy, BARDARO, Tiziana, ESPOSITO, Teresa, SMAHI, Asmae, SHAW, Christine, LEVY, Moise, MUNNICH, Arnold, D'URSO, Michele

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Physical and Genetic Characterization Reveals a Pseudogene, an Evolutionary Junction, and Unstable Loci in Distal Xq28 von Aradhya, Swaroop, Woffendin, Hayley, Bonnen, Penelope, Heiss, Nina S., Yamagata, Takanori, Esposito, Teresa, Bardaro, Tiziana, Poustka, Annemarie, D'Urso, Michele, Kenwrick, Sue, Nelson, David L.

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X-inactivation and marker studies in three families with incontinentia pigmenti: implications for counselling and gene localisation von Woffendin, Hayley, Jakins, Tracy, Jouet, Monique, Stewart, Helen, Landy, Sarah, Haan, Eric, Harris, Ann, Donnai, Dian, Read, Andrew, Kenwrick, Sue

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Molecular analysis of the mature T cell proliferation-1 (MTCP-1) gene in Xq28-linked incontinentia pigmenti von Woffendin, H, Esposito, T, Jakins, T, Bardaro, T, Stern, M H, Kenwrick, S

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Mutation analysis of the DKC1 gene in incontinentia pigmenti von HEISS, NINA S, POUSTKA, ANNEMARIE, KNIGHT, STUART W, ARADHYA, SWAROOP, NELSON, DAVID L, LEWIS, RICHARD A, ESPOSITO, TERESA, CICCODICOLA, ALFREDO, D’URSO, MICHELE, SMAHI, ASMAE, HEUERTZ, SOLANGE, MUNNICH, ARNOLD, VABRES, PIERRE, WOFFENDIN, HAYLEY, KENWRICK, SUSAN

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Screen and identification of proteins interacting with ADAM19 cytoplasmic tail von Huang, Li, Feng, Libing, Yang, Limin, Zhou, Weiguo, Zhao, Shouyuan, Li, Changben

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Genomic rearrangement in NEMO impairs NF-κB activation and is a cause of incontinentia pigmenti von Smahi, Asmae, Courtois, G, Vabres, P, Yamaoka, S, Heuertz, S, Munnich, A, Israel, A, Heiss, Nina S, Klauck, S. M, Kioschis, P, Wiemann, S, Poustka, A, Esposito, Teresa, Bardaro, T, Gianfrancesco, F, Ciccodicola, A, D'Urso, M, Woffendin, Hayley, Jakins, T, Donnai, D, Stewart, H, Kenwrick, S. J, Aradhya, Swaroop, Yamagata, T, Levy, M, Lewis, R. A, Nelson, D. L

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Genomic rearrangement in NEMO impairs NF-B activation and is a cause of incontinentia pigmenti von Smahi, Asmae, Courtois, G, Vabres, P, Yamaoka, S, Heuertz, S, Munnich, A, Israel, A, Heiss, Nina S, Klauck, S M, Kioschis, P, Wiemann, S, Poustka, A, Esposito, Teresa, Bardaro, T, Gianfrancesco, F, Ciccodicola, A, D'Urso, M, Woffendin, Hayley, Jakins, T, Donnai, D, Stewart, H, Kenwrick, S J, Aradhya, Swaroop, Yamagata, T, Levy, M, Lewis, R A, Nelson, D L

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Somatic and germ line mosaicism and mutation origin for a mutation in the L1 gene in a family with X-linked hydrocephalus von Du, Jian-Sheng, Bason, Lynne, Woffendin, Hayley, Zackai, Elaine, Kenwrick, Susan

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Combined Hardening of Composite Materials Based on Aluminum von Lysyi, M V, Zuzyak, P M

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Microarray analysis of human leucocyte subsets: the advantages of positive selection and rapid purification von Lyons, Paul A, Koukoulaki, Maria, Hatton, Alexander, Doggett, Karen, Woffendin, Hayley B, Chaudhry, Afzal N, Smith, Kenneth GC

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Somatic and germ line mosaicism and mutation origin for a mutation in theL1 gene in a family with X-linked hydrocephalus von Du, Jian-Sheng, Bason, Lynne, Woffendin, Hayley, Zackai, Elaine, Kenwrick, Susan

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Diagnosis and treatment of medical conditions associated with defective NFkappa B(NF- B) activation von Kenwrick, Sue J, Woffendin, Hayley, Munnich, Arnold, Smahi, Asmae, Israel, Alain, Poustka, Annemarie, Heiss, Nina, D'Urso, Michele, Lewis, Richard A, Nelson, David L, Aradhya, Swaroop, Levy, Moise

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Diagnosis and treatment of medical conditions associated with defective NFkappa B(NF-kappaB) activation von HEISS NINA, KENWRICK SUE J, ISRAEL ALAIN, LEWIS RICHARD A, POUSTKA ANNEMARIE, WOFFENDIN HAYLEY, SMAHI ASMAE, NELSON DAVID L, MUNNICH ARNOLD, D'URSO MICHELE, LEVY MOISE, ARADHYA SWAROOP

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Diagnosis and treatment of medical conditions associated with defective NFkappa B(NF-kappaB) activation von HEISS NINA, KENWRICK SUE J, LEWIS RICHARD ALAN, ISRAEL ALAIN, POUSTKA ANNEMARIE, WOFFENDIN HAYLEY, SMAHI ASMAE, NELSON DAVID L, MUNNICH ARNOLD, D'URSO MICHELE, LEVY MOISE, ARADHYA SWAROOP

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