C. Meredith | Researchain

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Featured researches published by C. Meredith.

Cytogenetic and Genome Research | 1995

Assignment of the human beta tropomyosin gene (TPM2) to band 9p13 by fluorescence in situ hybridisation

C.C.J. Hunt; Helen J. Eyre; P.A. Akkari; C. Meredith; S.M. Dorosz; S.D. Wilton; D.F. Callen; Nigel G. Laing; Elizabeth Baker

A sequence tagged site (STS) was developed for the human beta tropomyosin gene (TPM2). The STS was used to amplify DNA from somatic cell hybrids to localise TPM2 to human chromosome 9. Genomic clones isolated with the STS product were in turn used in fluorescence in situ hybridisation to metaphase chromosome spreads to further localise TPM2 to 9p13.

Cytogenetic and Genome Research | 1993

Assignment of the human slow skeletal muscle troponin gene (TNNI1) to 1q32 by fluorescence in situ hybridisation

H.J. Eyre; P.A. Akkari; C. Meredith; S.D. Wilton; D.C. Callen; L. Kedes; Nigel G. Laing

The human gene for slow-twitch skeletal muscle troponin I (TNNI1) has previously been mapped to 1q12-->qter using somatic cell hybrids. The TNNI1 locus has now been further localised to 1q32 using fluorescence in situ hybridization. This result confirms the previous assignment of this locus and maps the gene to a single chromosome band.

American Journal of Human Genetics | 1995

Autosomal dominant distal myopathy: Linkage to chromosome 14

Nigel G. Laing; B.A. Laing; C. Meredith; S.D. Wilton; Peter D. Robbins; K. Honeyman; S Dorosz; H. Kozman; F.L. Mastaglia; Byron Kakulas

Cytogenetic and Genome Research | 1994

Assignment of the human skeletal muscle alpha actin gene (ACTA1) to 1q42 by fluorescence in situ hybridisation

P.A. Akkari; H.J. Eyre; S.D. Wilton; D.F. Callen; S.A. Lane; C. Meredith; L. Kedes; Nigel G. Laing

Autosomal dominant distal myopathy linkage on Chromosome 14 | 1994

Autosomal dominant distal myopathy linkage on Chromosome 14

C. Meredith; B.A. Laing; S.D. Wilton; Francis Mastaglia; Peter Robbins; H. Kozman; K. Honeyman; S.M. Dorosz; Byron Kakulas; Nigel G. Laing

Laing, N.G., Laing, B.A., Meredith, C., Wilton, S.D. <http://researchrepository.murdoch.edu.au/view/author/Wilton, Steve.html>, Mastaglia, F.L. <http://researchrepository.murdoch.edu.au/view/author/Mastaglia, Frank.html>, Robbins, P., Honeyman, K., Dorosz, S. and Kakulas, B.A. (1993) Autosomal dominant distal myopathy: linkage to chromosome 14. Clinical Biochemist Reviews, 14 . | 1993

Autosomal dominant distal myopathy: linkage to chromosome 14

Nigel G. Laing; B.A. Laing; C. Meredith; S.D. Wilton; F.L. Mastaglia; Peter D. Robbins; K. Honeyman; S.M. Dorosz; Byron Kakulas

Hereditary distal myopathy | 1993

Hereditary distal myopathy

B.A. Laing; C. Meredith; Francis Mastaglia; Nigel G. Laing; Peter Robbins

Mitrpant, C., Fletcher, S. <http://researchrepository.murdoch.edu.au/view/author/Fletcher, Susan.html>, Meredith, C., Bittles, A. <http://researchrepository.murdoch.edu.au/view/author/Bittles, Alan.html> and Wilton, S. <http://researchrepository.murdoch.edu.au/view/author/Wilton, Steve.html> (2007) Antisense induced exon skipping restores dystrophin in the 4CV mouse model of muscular dystrophy. In: 5th Australasian Gene Therapy Society Meeting, 18 - 20 April 2007, Shine Dome Academy of Science, Canberra. | 2007