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Results: 1-13 |
Results: 13
Cryptic splicing involving the splice site mutation in the canine model ofDuchenne muscular dystrophy
Authors: Fletcher, S Ly, T Duff, RM Howell, JM Wilton, SD
Citation: S. Fletcher et al., Cryptic splicing involving the splice site mutation in the canine model ofDuchenne muscular dystrophy, NEUROMUSC D, 11(3), 2001, pp. 239-243
Antisense-induced exon skipping and synthesis of dystrophin in the mdx mouse
Authors: Mann, CJ Honeyman, K Cheng, AJ Ly, T Lloyd, F Fletcher, S Morgan, JE Partridge, TA Wilton, SD
Citation: Cj. Mann et al., Antisense-induced exon skipping and synthesis of dystrophin in the mdx mouse, P NAS US, 98(1), 2001, pp. 42-47
The regrowth of axons within tissue defects in the CNS is promoted by implanted hydrogel matrices that contain BDNF and CNTF producing fibroblasts
Authors: Loh, NK Woerly, S Bunt, SM Wilton, SD Harvey, AR
Citation: Nk. Loh et al., The regrowth of axons within tissue defects in the CNS is promoted by implanted hydrogel matrices that contain BDNF and CNTF producing fibroblasts, EXP NEUROL, 170(1), 2001, pp. 72-84
Evaluation of a short interspersed nucleotide element in the 3 ' untranslated region of the defective dystrophin gene of dogs with muscular dystrophy
Authors: Fletcher, S Carville, KS Howell, JM Mann, CJ Wilton, SD
Citation: S. Fletcher et al., Evaluation of a short interspersed nucleotide element in the 3 ' untranslated region of the defective dystrophin gene of dogs with muscular dystrophy, AM J VET RE, 62(12), 2001, pp. 1964-1968
Gene therapy and molecular approaches to the treatment of hereditary muscular disorders
Authors: Fletcher, S Wilton, SD Howell, JM
Citation: S. Fletcher et al., Gene therapy and molecular approaches to the treatment of hereditary muscular disorders, CURR OP NEU, 13(5), 2000, pp. 553-560
Severe gamma-sarcoglycanopathy caused by a novel missense mutation and a large deletion
Authors: Nowak, KJ Walsh, P Jacob, RL Johnsen, RD Peverall, J McNally, EM Wilton, SD Kakulas, BA Laing, NG
Citation: Kj. Nowak et al., Severe gamma-sarcoglycanopathy caused by a novel missense mutation and a large deletion, NEUROMUSC D, 10(2), 2000, pp. 100-107
Massive idiosyncratic exon skipping corrects the nonsense mutation in dystrophic mouse muscle and produces functional revertant fibers by clonal expansion
Authors: Lu, QL Morris, GE Wilton, SD Ly, T Artem'yeva, OV Strong, P Partridge, TA
Citation: Ql. Lu et al., Massive idiosyncratic exon skipping corrects the nonsense mutation in dystrophic mouse muscle and produces functional revertant fibers by clonal expansion, J CELL BIOL, 148(5), 2000, pp. 985-995
Homozygosity for a nonsense mutation in the alpha-tropomyosin slow gene TPM3 in a patient with severe infantile nemaline myopathy
Authors: Tan, P Briner, J Boltshauser, E Davis, MR Wilton, SD North, K Wallgren-Pettersson, C Laing, NG
Citation: P. Tan et al., Homozygosity for a nonsense mutation in the alpha-tropomyosin slow gene TPM3 in a patient with severe infantile nemaline myopathy, NEUROMUSC D, 9(8), 1999, pp. 573-579
Molecular analysis of a spontaneous dystrophin 'knockout' dog
Authors: Schatzberg, SJ Olby, NJ Breen, M Anderson, LVB Langford, CF Dickens, HF Wilton, SD Zeiss, CJ Binns, MM Kornegay, JN Morris, GE Sharp, NJH
Citation: Sj. Schatzberg et al., Molecular analysis of a spontaneous dystrophin 'knockout' dog, NEUROMUSC D, 9(5), 1999, pp. 289-295
Specific removal of the nonsense mutation from the mdx dystrophin mRNA using antisense oligonucleotides
Authors: Wilton, SD Lloyd, F Carville, K Fletcher, S Honeyman, K Agrawal, S Kole, R
Citation: Sd. Wilton et al., Specific removal of the nonsense mutation from the mdx dystrophin mRNA using antisense oligonucleotides, NEUROMUSC D, 9(5), 1999, pp. 330-338
Mutations in the nebulin gene associated with autosomal recessive nemalinemyopathy
Authors: Pelin, K Hilpela, P Donner, K Sewry, C Akkari, PA Wilton, SD Wattanasirichaigoon, D Bang, ML Centner, T Hanefeld, F Odent, S Fardeau, M Urtizberea, JA Muntoni, F Dubowitz, V Beggs, AH Laing, NG Labeit, S de la Chapelle, A Wallgren-Pettersson, C
Citation: K. Pelin et al., Mutations in the nebulin gene associated with autosomal recessive nemalinemyopathy, P NAS US, 96(5), 1999, pp. 2305-2310
Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathy
Authors: Mastaglia, FL Nowak, KJ Stell, R Phillips, BA Edmondston, JE Dorosz, SM Wilton, SD Hallmayer, J Kakulas, BA Laing, NG
Citation: Fl. Mastaglia et al., Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathy, J NE NE PSY, 67(2), 1999, pp. 174-179
Development of a snapback method of single-strand conformation polymorphism analysis for genotyping Golden Retrievers for the X-linked muscular dystrophy allele
Authors: Honeyman, K Carville, KS Howell, JM Fletcher, S Wilton, SD
Citation: K. Honeyman et al., Development of a snapback method of single-strand conformation polymorphism analysis for genotyping Golden Retrievers for the X-linked muscular dystrophy allele, AM J VET RE, 60(6), 1999, pp. 734-737
Risultati: 1-13 |