Symmetrically reduced stiffness and increased extensibility in compression and tension at the mineralized fibrillar level in rachitic bone von Karunaratne, A, Boyde, A, Esapa, C.T, Hiller, J, Terrill, N.J, Brown, S.D.M, Cox, R.D, Thakker, R.V, Gupta, H.S

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Reduced climbing and increased slipping adaptation in cochlear hair cells of mice with Myo7a mutations von Kros, C. J, Marcotti, W, van Netten, S. M, Self, T. J, Libby, R. T, Brown, S. D. M, Richardson, G. P, Steel, K. P

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Hypophosphatemic rickets is associated with disruption of mineral orientation at the nanoscale in the flat scapula bones of rachitic mice with development von Karunaratne, A, Davis, G.R, Hiller, J, Esapa, C.T, Terrill, N.J, Brown, S.D.M, Cox, R.D, Thakker, R.V, Gupta, H.S

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Multiscale alterations in bone matrix quality increased fragility in steroid induced osteoporosis von Karunaratne, A, Xi, L, Bentley, L, Sykes, D, Boyde, A, Esapa, C.T, Terrill, N.J, Brown, S.D.M, Cox, R.D, Thakker, R.V, Gupta, H.S

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Bone matrix development in steroid-induced osteoporosis is associated with a consistently reduced fibrillar stiffness linked to altered bone mineral quality von Xi, L., De Falco, P., Barbieri, E., Karunaratne, A., Bentley, L., Esapa, C.T., Terrill, N.J., Brown, S.D.M., Cox, R.D., Davis, G.R., Pugno, N.M., Thakker, R.V., Gupta, H.S.

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impending crisis in the provision of histopathology expertise for mouse functional genomics von Warren, MV, Studley, ML, Dubus, P, Fiette, L, Rozell, B, Quintanilla-Martinez, L, Raspa, M, Breuer, M, Song, J.Y, Gates, H, Brown, SDM, Schofield, PN

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Myosin VIIA Is Required for Aminoglycoside Accumulation in Cochlear Hair Cells von Richardson, G. P, Forge, A, Kros, C. J, Fleming, J, Brown, S. D. M, Steel, K. P

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Surface-enhanced and normal stokes and anti-stokes Raman spectroscopy of single-walled carbon nanotubes von Kneipp, K, Kneipp, H, Corio, P, Brown, S D, Shafer, K, Motz, J, Perelman, L T, Hanlon, E B, Marucci, A, Dresselhaus, G, Dresselhaus, M S

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The Opdc missense mutation of Pax2 has a milder than loss-of-function phenotype von CROSS, Sally H, MCKIE, Lisa, WEST, Katrine, COGHILL, Emma L, FAVOR, Jack, BHATTACHARYA, Shoumo, BROWN, Steve D. M, JACKSON, Ian J

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A type VII myosin encoded by the mouse deafness gene shaker-1 von Gibson, F, Walsh, J, Mburu, P, Varela, A, Brown, K. A, Antonio, M, Beisel, K. W, Steel, K. P, Brown, S. D. M

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Mouse models of genetic disease: New approaches, new paradigms von Brown, S. D. M.

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Analysis of the mouse mutant Cloth‐ears shows a role for the voltage‐gated sodium channel Scn8a in peripheral neural hearing loss von Mackenzie, F. E., Parker, A., Parkinson, N. J., Oliver, P. L., Brooker, D., Underhill, P., Lukashkina, V. A., Lukashkin, A. N., Holmes, C., Brown, S. D. M.

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Structural characterization of milled mesophase pitch-based carbon fibers von Endo, M, Kim, C, Karaki, T, Kasai, T, Matthews, M.J, Brown, S.D.M, Dresselhaus, M.S, Tamaki, T, Nishimura, Y

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Structural characterization of carbons obtained from polyparaphenylenes prepared by the Kovacic and Yamamoto methods von Endo, M., Kim, C., Hiraoka, T., Karaki, T., Nishimura, K., Matthews, M. J., Brown, S. D. M., Dresselhaus, M. S.

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Polarization effects in surface-enhanced resonant Raman scattering of single-wall carbon nanotubes on colloidal silver clusters von Kneipp, K., Jorio, A., Kneipp, H., Brown, S. D. M., Shafer, K., Motz, J., Saito, R., Dresselhaus, G., Dresselhaus, M. S.

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Enu Mutagenesis and the Search for Deafness Genes von Hardisty, R. E., Mburu, P., Brown, S. D. M.

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The anomalous dispersion of the disorder-induced and the second-order Raman Bands in Carbon Nanotubes von Pimenta, M. A., Hanlon, E. B., Marucci, A., Corio, P., Brown, S. D. M., Empedocles, S. A., Bawendi, M. G., Dresselhaus, G., Dresselhaus, M. S.

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EMPReSS: standardized phenotype screens for functional annotation of the mouse genome von Brown, S D M, Chambon, P, de Angelis, M Hrabé

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Relationship Between Resuscitation Team Members' Self-Efficacy and Team Competence During In-Hospital Cardiac Arrest von Hooper, Gabriel A, Butler, Allison M, Guidry, David, Kumar, Naresh, Brown, Katie, Beninati, William, Brown, Samuel M, Peltan, Ithan D

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A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse von Brown, Steve D.M, 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, Hunter, Jackie

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