MS Core Research Facilities

The C134W (402 C > G) FOXL2 mutation is absent in ovarian gynandroblastoma: insights into the genesis of an unusual tumour

Oparka, R., Cassidy, A., Reilly, S., Stenhouse, A., McCluggage, W. G. & Herrington, C. S. Apr-2012 In : Histopathology. 60, 5, p. 838-842, 5 p.

Research output: Contribution to journal › Article

Epithelial IgG and its relationship to the loss of F508 in the common mutant form of the cystic fibrosis transmembrane conductance regulator

Treharne, K. J., Cassidy, D., Goddard, C., Colledge, W. H., Cassidy, A. & Mehta, A. 6-Aug-2009 In : FEBS Letters. 583, 15, p. 2493-2499, 7 p.

Research output: Contribution to journal › Article

MDM2 SNP309 is associated with high grade node positive breast tumours and is in linkage disequilibrium with a novel MDM2 intron 1 polymorphism

Paulin, F. E. M., O'Neill, M., McGregor, G., Cassidy, A., Ashfield, A., Ali, C. W., Munro, A. J., Baker, L., Purdie, C. A., Lane, D. P. & Thompson, A. M. 1-Oct-2008 In : BMC Cancer. 8, p. -, 10 p., 281

Research output: Contribution to journal › Article

The human intermediate filament database: Comprehensive information on a gene family involved in many human diseases

Szeverenyi, I. , Cassidy, A. J. , Chung, C. W. , Lee, B. T. , Common, J. E. A. , Ogg, S. C. , Chen, H. , Sim, S. Y. , Goh, W. L. R. , Ng, K. W. , Simpson, J. A. , Chee, L. L. , Eng, G. H. , Li, B. , Lunny, D. P. , Chuon, D. , Venkatesh, A. , Khoo, K. H. , McLean, W. H. I. , Lim, Y. P. & 1 others Lane, E. B. Mar-2008 In : Human Mutation. 29, 3, p. 351-360, 10 p.

Research output: Contribution to journal › Article

Novel Mdm2 intron 1 single nucleotide polymorphisms and their role in breast cancer

Paulin, F., O'Neill, M., McGregor, G., Cassidy, A., Ashfield, A., Ali, C. W., Baker, L., Munro, A. J., Lane, D. & Thompson, A. M. Dec-2007 In : Breast Cancer Research and Treatment. 106, p. S285-S285, 1 p., 6114

Research output: Contribution to journal › Book/Film/Article review

Prevalent and rare mutations in the gene encoding filaggrin cause ichthyosis vulgaris and predispose individuals to atopic dermatitis

Sandilands, A., O'Regan, G. M., Liao, H., Zhao, Y., Terron-Kwiatkowski, A., Watson, R. M., Cassidy, A. J., Goudie, D. R., Smith, F. J. D., McLean, W. H. I. & Irvine, A. D. 2006 In : Journal of Investigative Dermatology. 126, 8, p. 1770-1775, 6 p.

Research output: Contribution to journal › Article

A homozygous missense mutation in TGM5 abolishes epidermal transglutaminase 5 activity and causes acral peeling skin syndrome

Cassidy, A., van Steensel, M. A. M., Steijlen, P. M., van Geel, M., van der Velden, J., Morley, S., Terrinoni, A., Melino, G., Candi, E. & McLean, I. Dec-2005 In : American Journal of Human Genetics. 77, 6, p. 909-917, 9 p.

Research output: Contribution to journal › Article