T. Ward

Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux

W. Dobyns, M. Eccles, M. Pierpont, 1995, Nature Genetics.

Differential regulation of the human Wilms tumour suppressor gene (WT1) promoter by two isoforms of PAX2

H. Cunliffe, M. Eccles, T. Ward, 1997, Oncogene.

Primary renal hypoplasia in humans and mice with PAX2 mutations: evidence of increased apoptosis in fetal kidneys of Pax2(1Neu) +/- mutant mice.

H. Cunliffe, M. Eccles, N. Cho, 2000, Human molecular genetics.

The prevalence of PAX2 mutations in patients with isolated colobomas or colobomas associated with urogenital anomalies.

H. Cunliffe, M. Eccles, K. Devriendt, 1998, Journal of medical genetics.

Erratum: Mutation of the gene in a family with optic nerve colobomas, renal anomolies and vesicoureteral reflux (Nature Genetics (1995) 9 (358- 364))

W. Dobyns, M. Eccles, M. Pierpont, 1996 .

Cloning and Characterization of the Human PAX2Promoter*

H. Cunliffe, M. Eccles, T. Ward, 1998, The Journal of Biological Chemistry.

Genomic structure of the human PAX2 gene.

M. Eccles, A. Nebel, P. Sanyanusin, 1996, Genomics.

Alternative messenger RNA forms and open reading frames within an additional conserved region of the human PAX-2 gene.

M. Eccles, A. Reeve, A. Nebel, 1994, Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research.

Further delineation of renal-coloboma syndrome in patients with extreme variability of phenotype and identical PAX2 mutations.

H. Cunliffe, K. Devriendt, M. Masuno, 1997, American journal of human genetics.