Discovery and pharmacophoric characterization of chemokine network inhibitors using phage-display, saturation mutagenesis and computational modelling von Vales, Serena, Kryukova, Jhanna, Chandra, Soumyanetra, Smagurauskaite, Gintare, Payne, Megan, Clark, Charlie J., Hafner, Katrin, Mburu, Philomena, Denisov, Stepan, Davies, Graham, Outeiral, Carlos, Deane, Charlotte M., Morris, Garrett M., Bhattacharya, Shoumo

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Quiet as a mouse: dissecting the molecular and genetic basis of hearing von Brown, Steve D. M., Hardisty-Hughes, Rachel E., Mburu, Philomena

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Pleiotropic brain function of whirlin identified by a novel mutation von Aguilar, Carlos, Williams, Debbie, Kurapati, Ramakrishna, Bains, Rasneer S., Mburu, Philomena, Parker, Andy, Williams, Jackie, Concas, Danilo, Tateossian, Hilda, Haynes, Andrew R., Banks, Gareth, Vikhe, Pratik, Heise, Ines, Hutchison, Marie, Atkins, Gemma, Gillard, Simon, Starbuck, Becky, Oliveri, Simona, Blake, Andrew, Sethi, Siddharth, Kumar, Saumya, Bardhan, Tanaya, Jeng, Jing-Yi, Johnson, Stuart L., Corns, Lara F., Marcotti, Walter, Simon, Michelle, Wells, Sara, Potter, Paul K., Lad, Heena V.

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The actin-binding proteins eps8 and gelsolin have complementary roles in regulating the growth and stability of mechanosensory hair bundles of mammalian cochlear outer hair cells von Olt, Jennifer, Mburu, Philomena, Johnson, Stuart L, Parker, Andy, Kuhn, Stephanie, Bowl, Mike, Marcotti, Walter, Brown, Steve D M

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Gelsolin plays a role in the actin polymerization complex of hair cell stereocilia von Mburu, Philomena, Romero, María Rosario, Hilton, Helen, Parker, Andrew, Townsend, Stuart, Kikkawa, Yoshiaki, Brown, Steve D M

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Whirlin Complexes with p55 at the Stereocilia Tip during Hair Cell Development von Mburu, Philomena, Kikkawa, Yoshiaki, Townsend, Stuart, Romero, Rosario, Yonekawa, Hiromichi, Brown, Steve D. M.

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Mutations in the myosin VIIA gene cause non-syndromic recessive deafness von Liu, Xue-Zhong, Walsh, James, Mburu, Philomena, Kendrick-Jones, John, Cope, M. Jamie T.V., Steel, Karen P., Brown, Steve D.M.

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Mutant analysis reveals whirlin as a dynamic organizer in the growing hair cell stereocilium von Kikkawa, Yoshiaki, Mburu, Philomena, Morse, Sue, Kominami, Ryo, Townsend, Stuart, Brown, Steve D.M.

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Protein 4.1 expression in the developing hair cells of the mouse inner ear von Okumura, Kazuhiro, Mochizuki, Eiji, Yokohama, Michinari, Yamakawa, Hisashi, Shitara, Hiroshi, Mburu, Philomena, Yonekawa, Hiromichi, Brown, Steve D.M, Kikkawa, Yoshiaki

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Otitis media in the Tgif knockout mouse implicates TGFβ signalling in chronic middle ear inflammatory disease von Tateossian, Hilda, Morse, Susan, Parker, Andrew, Mburu, Philomena, Warr, Nick, Acevedo-Arozena, Abraham, Cheeseman, Michael, Wells, Sara, Brown, Steve D M

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Otitis media in the Tgif knockout mouse implicates TGF[beta] signalling in chronic middle ear inflammatory disease von Tateossian, Hilda, Morse, Susan, Parker, Andrew, Mburu, Philomena, Warr, Nick, Acevedo-Arozena, Abraham, Cheeseman, Michael, Wells, Sara, Brown, Steve DM

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Clarin‐2 is essential for hearing by maintaining stereocilia integrity and function von Dunbar, Lucy A, Patni, Pranav, Aguilar, Carlos, Mburu, Philomena, Corns, Laura, Wells, Helena RR, Delmaghani, Sedigheh, Parker, Andrew, Johnson, Stuart, Williams, Debbie, Esapa, Christopher T, Simon, Michelle M, Chessum, Lauren, Newton, Sherylanne, Dorning, Joanne, Jeyarajan, Prashanthini, Morse, Susan, Lelli, Andrea, Codner, Gemma F, Peineau, Thibault, Gopal, Suhasini R, Alagramam, Kumar N, Hertzano, Ronna, Dulon, Didier, Wells, Sara, Williams, Frances M, Petit, Christine, Dawson, Sally J, Brown, Steve DM, Marcotti, Walter, El‐Amraoui, Aziz, Bowl, Michael R

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Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31 von Mburu, Philomena, Mustapha, Mirna, Varela, Anabel, Weil, Dominique, El-Amraoui, Aziz, Holme, Ralph H, Rump, Andreas, Hardisty, Rachel E, Blanchard, Stéphane, Coimbra, Roney S, Perfettini, Isabelle, Parkinson, Nick, Mallon, Ann-Marie, Glenister, Pete, Rogers, Mike J, Paige, Adam J, Moir, Lee, Clay, Jo, Rosenthal, Andre, Liu, Xue Zhong, Blanco, Gonzalo, Steel, Karen P, Petit, Christine, Brown, Steve D M

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Light and Electron Microscopy Methods for Examination of Cochlear Morphology in Mouse Models of Deafness von Parker, Andrew, Chessum, Lauren, Mburu, Philomena, Sanderson, Jeremy, Bowl, Michael R.

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A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse von Nolan, Patrick M., Peters, Jo, Strivens, Mark, Rogers, Derek, Hagan, Jim, Spurr, Nigel, Gray, Ian C., Vizor, Lucie, Brooker, Debra, Whitehill, Elaine, Washbourne, Rebecca, Hough, Tertius, Greenaway, Simon, Hewitt, Mazda, Liu, Xinhong, McCormack, Stefan, Pickford, Karen, Selley, Rachael, Wells, Christine, Tymowska-Lalanne, Zuzanna, Roby, Phil, Glenister, Peter, Thornton, Claire, Thaung, Caroline, Stevenson, Julie-Anne, Arkell, Ruth, Mburu, Philomena, Hardisty, Rachel, Kiernan, Amy, Erven, Alexandra, Steel, Karen P., Voegeling, Stephanie, Guenet, Jean-Louis, Nickols, Carole, Sadri, Ramin, Naase, Mahmood, Isaacs, Adrian, Davies, Kay, Browne, Mick, Fisher, Elizabeth M.C., Martin, Jo, Rastan, Sohaila, Brown, Steve D.M., Hunter, Jackie

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Mutation analysis of the mouse myosin VIIA deafness gene von Mburu, Philomena, Liu, Xue Zhong, Walsh, James, Saw, Dennis, Cope, M., Gibson, Fernando, Kendrick-Jones, John, Steel, Karen, Brown, Steve

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Defective myosin VIIA gene responsible for Usher syndrome type IB von Well, Dominique, Blanchard, Stéphane, Kaplan, Josseline, Guilford, Parry, Gibson, Fernando, Walsh, James, Mburu, Philomena, Varela, Anabel, Levilliers, Jacqueline, Weston, Michael D., Kelley, Phillip M., Kimberling, William J., Wagenaar, Mariette, Levi-Acobas, Fabienne, Larget-Piet, Dominique, Munnich, Arnold, Steel, Karen P., Brown, Steve D. M., Petit, Christine

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The mouse slalom mutant demonstrates a role for Jagged1 in neuroepithelial patterning in the organ of Corti von TSAI, Hsun, HARDISTY, Rachel E, STEEL, Karen P, RHODES, Charlotte, KIERNAN, Amy E, ROBY, Phil, TYMOWSKA-LALANNE, Zuzanna, MBURU, Philomena, RASTAN, Sohaila, HUNTER, A. Jackie, BROWN, Steve D. M

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Models of congenital deafness: Mouse and zebrafish von Whitfield, Tanya T., Mburu, Philomena, Hardisty-Hughes, Rachel E., Brown, Steve D.M.

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Towards a mutant map of the mouse--new models of neurological, behavioural, deafness, bone, renal and blood disorders von Rastan, Sohaila, Hough, Tertius, Kierman, Amy, Hardisty, Rachel, Erven, Alexandra, Gray, Ian C, Voeling, Stepanie, Isaacs, Adrian, Tsai, Hsun, Strivens, Mark, Washbourne, Rebecca, Thornton, Claire, Greenaway, Simon, Hewitt, Mazda, McCormick, Stefan, Selley, Rachael, Wells, Christine, Tymowska-Lalanne, Zuzanna, Roby, Phil, Mburu, Philomena, Rogers, Derek, Hagan, Jim, Reavill, Charlie, Davies, Kay, Glenister, Peter, Fisher, Elizabeth M C, Martin, Josephine, Vizor, Lucy, Bouzyk, Mark, Kelsell, David, Guenet, J L, Steel, Karen P, Sheardown, Steve, Spurr, Nigel, Gray, Ian, Peters, Jo, Nolan, Patrick M, Hunter, A Jacqueline, Brown, Steve D M

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