Publication Venue For
- Distinct roles for Toll and autophagy pathways in double-stranded RNA toxicity in a Drosophila model of expanded repeat neurodegenerative diseases. 2013
- Mutations in mouse Ift144 model the craniofacial, limb and rib defects in skeletal ciliopathies. 2012
- Drosophila orthologue of WWOX, the chromosomal fragile site FRA16D tumour suppressor gene, functions in aerobic metabolism and regulates reactive oxygen species. 2011
- Perturbation of the Akt/Gsk3-ß signalling pathway is common to Drosophila expressing expanded untranslated CAG, CUG and AUUCU repeat RNAs. 2011
- Common chromosomal fragile site FRA16D mutation in cancer cells. 2005
- Common chromosomal fragile site FRA16D sequence: identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells. 2000
- The t(8;13)(p11;q11-12) rearrangement associated with an atypical myeloproliferative disorder fuses the fibroblast growth factor receptor 1 gene to a novel gene RAMP. 1998
- Isolation of a candidate human telomerase catalytic subunit gene, which reveals complex splicing patterns in different cell types. 1997
- Diverse phenotypes associated with exon 10 mutations of the RET proto-oncogene. 1994
- Mitochondrial DNA polymorphism in disease: a possible contributor to respiratory dysfunction. 1994