C. Duff

发表

Human ribosomal RNA genes: orientation of the tandem array and conservation of the 5' end.

R G Worton, H. Willard, P. Ray, 1988, Science.

Protein-tyrosine phosphatase SH-PTP2 (PTPN11) is localized to 12q24.1–24.3

A. Duncan, F. Jirik, U. Dechert, 1995, Human Genetics.

Chromosomal localization of the human liver form cytochrome c oxidase subunit VIIa gene.

J. Rommens, A. Duncan, G. Mitchell, 1997, Genome.

Moderate-level gene amplification in methotrexate-resistant Chinese hamster ovary cells is accompanied by chromosomal translocations at or near the site of the amplified DHFR gene

W. Flintoff, E. Livingston, R. Worton, 1984, Molecular and cellular biology.

Microcell-mediated cotransfer of genes specifying methotrexate resistance, emetine sensitivity, and chromate sensitivity with Chinese hamster chromosome 2

W. Flintoff, R. Worton, C. Duff, 1981, Molecular and cellular biology.

Duchenne muscular dystrophy involving translocation of the dmd gene next to ribosomal RNA genes.

H. Willard, R. Schmickel, J. Sylvester, 1984, Science.

Cloning, characterization, and chromosomal localization of human liver form cytochrome c oxidase subunit VIa related genes.

A. Duncan, B. Robinson, C. Duff, 1997, Genome.

Condensation of plasmid DNA with polylysine improves liposome-mediated gene transfer into established and primary muscle cells.

L. Vitiello, A. Chonn, J. Wasserman, 1996, Gene therapy.

Localization of the human gene for inducible nitric oxide synthase (NOS2) to chromosome 17q11.2-q12.

H. Heng, L. Tsui, P. Marsden, 1994, Genomics.

Marker segregation without chromosome loss at theemt locus in Chinese hamster cell hybrids

R. Worton, C. Campbell, C. Duff, 1980, Somatic cell genetics.

Ryanodine receptor gene is a candidate for predisposition to malignant hyperthermia

M. Phillips, B. Britt, J. Fujii, 1990, Nature.

Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the Duchenne muscular dystrophy (DMD) gene.

M. W. Thompson, J. Chamberlain, J. Sutherland, 1989, American journal of human genetics.

Polymorphisms and deduced amino acid substitutions in the coding sequence of the ryanodine receptor (RYR1) gene in individuals with malignant hyperthermia.

B. Britt, K. Otsu, J. Fujii, 1992, Genomics.

The human mitochondrial elongation factor tu (EF-Tu) gene: cDNA sequence, genomic localization, genomic structure, and identification of a pseudogene.

A. Duncan, B. Robinson, C. Duff, 1997, Gene.

Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy

M. W. Thompson, P. Ray, R. Schmickel, 1985, Nature.

TheHumanRyanodine Receptor Gene:ItsMapping to19ql3.1, Placement ina Chromosome19Linkage Group,andExclusion as theGeneCausing Myotonic Dystrophy

M. Phillips, J. Fujii, F. Zorzato, 1990 .

Linkage analysis of polymorphisms within the DNA fragment XJ cloned from the breakpoint of an X;21 translocation associated with X linked muscular dystrophy.

M. W. Thompson, P. Ray, R. Worton, 1986, Journal of medical genetics.

Chromosome stability in CHO cells

R. Worton, C. Duff, C. Ho, 1977, Somatic cell genetics.

A substitution of cysteine for arginine 614 in the ryanodine receptor is potentially causative of human malignant hyperthermia.

B. Britt, K. Otsu, J. Fujii, 1991, Genomics.

Mechanism for the Expression of Recessive Phenotypes

R. Worton, S. G. Grant, C. Duff, 2006 .

Myoblast transfer in duchenne muscular dystrophy

George Karpati, E. Shoubridge, M. Abrahamowicz, 1993, Annals of neurology.

Assignment of the gene (UQCRFS1) for the Rieske iron-sulfur protein subunit of the mitochondrial cytochrome bc1 complex to the 22q13 and 19q12-q13.1 regions of the human genome.

R. Rozen, A. Duncan, T. Ozawa, 1994, Genomics.

Chromosomal alterations associated with overproduction of asparagine synthetase in albizziin-resistant Chinese hamster ovary cells

I. Andrulis, L. Siminovitch, R. Worton, 1983, Molecular and cellular biology.

Mapping of the human NMDA receptor subunit (NMDAR1) and the proposed NMDA receptor glutamate-binding subunit (NMDARA1) to chromosomes 9q34.3 and chromosome 8, respectively.

C. Collins, M. Hayden, A. Duncan, 1993, Genomics.