p62 overexpression induces TDP-43 cytoplasmic mislocalisation, aggregation and cleavage and neuronal death von Foster, A. D., Flynn, L. L., Cluning, C., Cheng, F., Davidson, J. M., Lee, A., Polain, N., Mejzini, R., Farrawell, N., Yerbury, J. J., Layfield, R., Akkari, P. A., Rea, S. L.

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A mutation in the α tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy von Laing, Nigel G, Akkari, Patrick A, Love, Donald R, Watkins, Hugh, Wilton, Stephen D, Dorosz, Shellie, Kneebone, Chris, White, Sue, Haan, Eric, Boundy, Karyn, Blumbergs, Peter

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Early onset chromosome 14-linked distal myopathy (Laing) von Mastaglia, F.L., Phillips, B.A., Cala, L.A., Meredith, C., Egli, S., Akkari, P.A., Laing, N.G.

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Mutations in the Nebulin Gene Associated with Autosomal Recessive Nemaline Myopathy von Pelin, Katarina, Hilpela, Pirta, Donner, Kati, Sewry, Caroline, Akkari, Patrick A., Wilton, Stephen D., Wattanasirichaigoon, Duangrurdee, Bang, Marie-Louise, Centner, Thomas, Hanefeld, Folker, Odent, Sylvie, Fardeau, Michel, Urtizberea, J. Andoni, Muntoni, Francesco, Dubowitz, Victor, Beggs, Alan H., Laing, Nigel G., Labeit, Siegfried, de la Chapelle, Albert, Wallgren-Pettersson, Carina

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A splice-site mutation causing ovine McArdle's disease von Tan, P, Allen, J.G, Wilton, S.D, Akkari, P.A, Huxtable, C.R, Laing, N.G

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Production of human skeletal α-actin proteins by the baculovirus expression system von Anthony Akkari, P, Nowak, Kristen J, Beckman, Kaye, Walker, Kendall R, Schachat, Fred, Laing, Nigel G

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Bridging the gap: Short structural variants in the genetics of anorexia nervosa von Berthold, Natasha, Pytte, Julia, Bulik, Cynthia M., Tschochner, Monika, Medland, Sarah E., Akkari, Patrick Anthony

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Assignment of a gene (NEM1) for autosomal dominant nemaline myopathy to chromosome 1 von Laing, NG, Majda, B T, Akkari, P A, Layton, M G, Mulley, J C, Phillips, H, Haan, E A, White, S J, Kakulas, BA

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Assignment of a gene (NEMI) for autosomal dominant nemaline myopathy to chromosome I von Laing, N G, Majda, B T, Akkari, P A, Layton, M G, Mulley, J C, Phillips, H, Haan, E A, White, S J, Beggs, A H, Kunkel, L M

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An αtropomyosin mutation alters dimer preference in nemaline myopathy von Corbett, Mark A., Anthony Akkari, P., Domazetovska, Ana, Cooper, Sandra T., North, Kathryn N., Laing, Nigel G., Gunning, Peter W., Hardeman, Edna C.

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Identification of Duchenne muscular dystrophy genomic probe P20 constant Taql fragment corresponding to the EcoRV and Mspl polymorphisms von LAING, N. G, WALKER, A. P, WAPENAAR, M. C, VAN OMMEN, G, ROSES, A. D, KAKULAS, B. A, AKKARI, P. A, CHANDLER, D. C, LAYTON, M. G, MEARS, M. E, YAMADA, T, BARTLETT, R. J, PERICAK-VANCE, M. A, HUNG, W.-Y

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Expression and biological activity of Baculovirus generated wild-type human slow α tropomyosin and the Met9Arg mutant responsible for a dominant form of nemaline myopathy von Anthony Akkari, P, Song, Yuhua, Hitchcock-DeGregori, Sarah, Blechynden, Lori, Laing, Nigel

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A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy NEM1 von Laing, N G, Wilton, S D, Akkari, P A, Dorosz, S, Boundy, K, Kneebone, C, Blumbergs, P, White, S, Watkins, H, Love, D R

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Duchenne muscular dystrophy (DMD) gene cDNA 8 Pstl and Taql polymorphisms involve exon 51 of the hindIII map von LAING, N. G, AKKARI, P. A, CHANDLER, D. C, THOMAS, H. E, LAYTON, M. G, MEARS, M. E, KAKULAS, B. A

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Duchenne muscular dystrophy (DMD) gene cDNA 8 PstI and TaqI polymorphisms involve exon 51 of the HindIII map von Laing, N G, Akkari, P A, Chandler, D C, Thomas, H E, Layton, M G, Mears, M E, Kakulas, B A

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Expression of caltrin in the baculovirus system and its purification in high yield and purity by cobalt (II) affinity chromatography von Phan, Tony C.A., Nowak, Kristen J., Anthony Akkari, P., Zheng, Ming H., Xu, Jiake

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Duchenne muscular dystrophy (DMD) gene cDNA 8 Pstl and Taql Polymorphisms involve exon 51 of the Hindlll map von Laing, N.G., Akkari, P.A., Chandler, D.C., Thomas, H.E., Layton, M.G., Mears, M.E., Kakulas, B.A.

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Assignment of a gene (NEMI) for autosomal dominant nemaline myopathy to chromosone I von LAING, N. G, MAJDA, B. T, GROTH, D. M, BOUNDAY, K. L, KNEEBONE, C. S, BLUMBERG, P. C, WILTON, S. D, SPEER, M. C, KAKULAS, B. A, AKKARI, P. A, LAYTON, M. G, MULLEY, J. C, PHILLIPS, H, HAAN, E. A, WHITE, S. J, BEGGS, A. H, KUNKEL, L. M

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Identification of duchenne muscular dystrophy genomic probe P20 constant Taq1 fragment corresponding to the EcoRV and Msp1 polymorphisms von Laing, N. G., Walker, A. P., Akkari, P. A., Chandler, D. C., Layton, M. G., Mears, M. E., Yamada, T., Bartlett, R. J., Pericak-Vance, M. A., Hung, W.-Y., Wapenaar, M. C., van Ommen, G., Roses, A. D., Kakulas, B. A.

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ALS Genetics, Mechanisms, and Therapeutics: Where Are We Now? von Mejzini, Rita, Flynn, Loren L, Pitout, Ianthe L, Fletcher, Sue, Wilton, Steve D, Akkari, P Anthony

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