Very mild muscular dystrophy associated with the deletion of 46% of dystrophin von England, S. B, Nicholson, L. V. B, Johnson, M. A, Forrest, S. M, Love, D. R, Zubrzycka-Gaarn, E. E, Bulman, D. E, Harris, J. B, Davies, K.E

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Heterogeneity of dystrophin expression in patients with Duchenne and Becker muscular dystrophy von NICHOLSON, L. V. B, JOHNSON, M. A, GARDNER-MEDWIN, D, BHATTACHARYA, S, HARRIS, J. B

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Ultrastructural Localization of Dystrophin in Human Muscle by Using Gold Immunolabelling von Cullen, M. J., Walsh, J., Nicholson, L. V. B., Harris, J. B.

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The clinical, genetic and dystrophin characteristics of Becker muscular dystrophy. II: Correlation of phenotype with genetic and protein abnormalities von BUSHBY, K. M. D, GARDNER-MEDWIN, D, NICHOLSON, L. V. B, JOHNSON, M. A, HAGGERTY, I. D, CLEGHORN, N. J, HARRIS, J. B, BHATTACHARYA, S. S

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Immunogold localization of the 43-kDa dystroglycan at the plasma membrane in control and dystrophic human muscle von CULLEN, M. J, WALSH, J, NICHOLSON, L. V. B

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Severe mental retardation in a young boy with an in-frame deletion in the dystrophin gene von COLOMER, J, GALLANO, P, NICHOLSON, L. V. B, TIZZANO, E, BAIGET, M

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Different distributions of dystrophin and related proteins at nerve-muscle junctions von Bewick, Guy S, Nicholson, Louise V. B, Young, Carol, OʼDonnell, Elizabeth, Slater, Clarke R

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Dystrophin in skeletal muscle I. Western blot analysis using a monoclonal antibody von Nicholson, Louise V.B., Davison, Keith, Falkous, Gavin, Harwood, Colin, O'Donnell, Elizabeth, Slater, Clarke R., Harris, John B.

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A homologue of dystrophin is expressed at the neuromuscular junctions of normal individuals and DMD patients, and of normal and mdx mice Immunological evidence von Pons, F., Augier, N., Léger, J.O.C., Robert, A., Tome, F.M.S., Fardeau, M., Voit, T., Nicholson, L.V.B., Mornet, D., Léger, J.J.

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Dystrophin in skeletal muscle II. Immunoreactivity in patients with Xp21 muscular dystrophy von Nicholson, Louise V.B., Davison, Keith, Johnson, Margaret A., Slater, Clarke R., Young, Carol, Bhattacharya, Shomi, Gardner-Medwin, David, Harris, John B.

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Functional significance of dystrophin positive fibres in Duchenne muscular dystrophy von Nicholson, L V, Johnson, M A, Bushby, K M, Gardner-Medwin, D

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Are cysteine-rich and COOH-terminal domains of dystrophin critical for sarcolemmal localization ? von RECAN, D, CHAFEY, P, FARDEAU, M, KAPLAN, J.-C, CHELLY, J, LETURCQ, F, HUGNOT, J.-P, VINCENT, N, TOME, F, COLLIN, H, SIMON, D, CZERNICHOW, P, NICHOLSON, L. V. B

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Immunohistological evidence for second or somatic mutations as the underlying cause of dystrophin expression by isolated fibres in Xp21 muscular dystrophy of Duchenne-type severity von Wallgren-Pettersson, Carina, Jasani, Bharat, Rosser, Lyndon G., Lazarou, Lazarus Pavlou, Nicholson, Louise V.B., Clarke, Angus

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The fate of dystrophin during the degeneration and regeneration of the soleus muscle of the rat von Vater, R, Cullen, M J, Nicholson, L V, Harris, J B

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Predicted and observed sizes of dystrophin in some patients with gene deletions that disrupt the open reading frame von Nicholson, L V, Bushby, K M, Johnson, M A, den Dunnen, J T, Ginjaar, I B, van Ommen, G J

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Is dystrophin labelling always discontinuous in Becker muscular dystrophy? von Slater, Clarke R., Nicholson, Louise V.B.

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Identification of a mutation in the promoter region of the dystrophin gene in a patient with atypical becker muscular dystrophy von BUSHBY, K. M. D, CLEGHORN, N. J, CURTIS, A, HAGGERTY, I. D, NICHOLSON, L. V. B, JOHNSON, M. A, HARRIS, J. B, BHATTACHARYA, S. S

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Fetal dystrophin to diagnose carrier status von Ginjaar, IekeB, Soffers, Sylvia, Moorman, AntoonF.M., Nicholson, LouiseV.B., Morris, GlennE, Bakker, Egbert, Van Haeringen, Arie, Van Ommen, Gert-JanB

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The fate of dystrophin during the degeneration and regeneration ofthe soleus muscle of the rat von VATER, R, CULLEN, M. J, NICHOLSON, L. V. B, HARRIS, J. B

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A homologue of dystrophin is expressed at the blood vessel membrane of DMD and BMD patients: Immunological evidence von Augier, Nathalie, Boucraut, José, Léger, Jocelyne, Anoal, Monique, Nicholson, Louise V.B., Voelkel, Marie A., Léger, Jean J., Pellissier, Jean F.

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