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J Prosser

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Publications

TOP 3
J Prosser; Veronica van Heyningen
PAX6 mutations reviewed.
A Brown; M McKie; Veronica van Heyningen; J Prosser
The Human PAX6 Mutation Database.
RA Axton; Isabel M Hanson; J Love; Anne Seawright; J Prosser; Veronica van Heyningen
Combined SSCP/heteroduplex analysis in the screening for PAX6 mutations.

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All Publications

1998: J Prosser; Veronica van Heyningen
PAX6 mutations reviewed.
Human mutation 1998;11(2):93-108.
1998: A Brown; M McKie; Veronica van Heyningen; J Prosser
The Human PAX6 Mutation Database.
Nucleic acids research 1998;26(1):259-64.
1997: RA Axton; Isabel M Hanson; J Love; Anne Seawright; J Prosser; Veronica van Heyningen
Combined SSCP/heteroduplex analysis in the screening for PAX6 mutations.
Molecular and cellular probes 1997;11(4):287-92.
1997: RA Axton; Isabel M Hanson; S Danes; Grant C Sellar; Veronica van Heyningen; J Prosser
The incidence of PAX6 mutation in patients with simple aniridia: an evaluation of mutation detection in 12 cases.
Journal of medical genetics 1997;34(4):279-86.
1996: J Prosser; J D Inglis; A Condie; K Ma; S Kerr; R Thakrar; K Taylor; J M Cameron; Howard J Cooke
Degeneracy in human multicopy RBM (YRRM), a candidate spermatogenesis gene.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(11):835-42.
1994: J Prosser; A Condie; M Wright; J M Horn; Judy A Fantes; A H Wyllie; M G Dunlop
APC mutation analysis by chemical cleavage of mismatch and a protein truncation assay in familial adenomatous polyposis.
British journal of cancer 1994;70(5):841-6.
1994: Jillian M Birch; A L Hartley; KJ Tricker; J Prosser; A Condie; Anna M Kelsey; M Harris; P H Jones; A Binchy; Derek Crowther
Prevalence and diversity of constitutional mutations in the p53 gene among 21 Li-Fraumeni families.
Cancer research 1994;54(5):1298-304.
1993: T Bhagirath; A Condie; M G Dunlop; A H Wyllie; J Prosser
Exclusion of constitutional p53 mutations as a cause of genetic susceptibility to colorectal cancer.
British journal of cancer 1993;68(4):712-4.
1993: A Condie; R Eeles; A L Borresen; C Coles; C Cooper; J Prosser
Detection of point mutations in the p53 gene: comparison of single-strand conformation polymorphism, constant denaturant gel electrophoresis, and hydroxylamine and osmium tetroxide techniques.
Human mutation 1993;2(1):58-66.
1992: H J Evans; J Prosser
Tumor-suppressor genes: cardinal factors in inherited predisposition to human cancers.
Environmental health perspectives 1992;98():25-37.
1992: C Coles; A Condie; U Chetty; C M Steel; H J Evans; J Prosser
p53 mutations in breast cancer.
Cancer research 1992;52(19):5291-8.
1992: T Jordan; Isabel M Hanson; D Zaletayev; S Hodgson; J Prosser; Anne Seawright; Nicholas D Hastie; Veronica van Heyningen
The human PAX6 gene is mutated in two patients with aniridia.
Nature genetics 1992;1(5):328-32.
1992: Melissa H Little; J Prosser; A Condie; P J Smith; Veronica van Heyningen; Nicholas D Hastie
Zinc finger point mutations within the WT1 gene in Wilms tumor patients.
Proceedings of the National Academy of Sciences of the United States of America 1992;89(11):4791-5.
1992: J Prosser; D Porter; C Coles; A Condie; A M Thompson; U Chetty; C M Steel; H J Evans
Constitutional p53 mutation in a non-Li-Fraumeni cancer family.
British journal of cancer 1992;65(4):527-8.
1992: A M Thompson; T J Anderson; A Condie; J Prosser; U Chetty; DC Carter; H J Evans; C M Steel
p53 allele losses, mutations and expression in breast cancer and their relationship to clinico-pathological parameters.
International journal of cancer. Journal international du cancer 1992;50(4):528-32.
1992: Robert E Hill; J Favor; B L Hogan; C C Ton; Grady F Saunders; Isabel M Hanson; J Prosser; T Jordan; Nicholas D Hastie; Veronica van Heyningen
Mouse Small eye results from mutations in a paired-like homeobox-containing gene.
Nature 1992;355(6362):750.
1991: Robert E Hill; J Favor; B L Hogan; C C Ton; Grady F Saunders; Isabel M Hanson; J Prosser; T Jordan; Nicholas D Hastie; Veronica van Heyningen
Mouse small eye results from mutations in a paired-like homeobox-containing gene.
Nature 1991;354(6354):522-5.
1991: E Weir-Thompson; A Condie; R C F Leonard; J Prosser
A familial RB1 mutation detected by the HOT technique is homozygous in a second primary neoplasm.
Oncogene 1991;6(12):2353-6.
1991: J Prosser; A Condie
Biallelic ApaI polymorphism of the human p53 gene (TP53).
Nucleic acids research 1991;19(17):4799.
1991: J Prosser; P A Elder; A Condie; I MacFadyen; C M Steel; H J Evans
Mutations in p53 do not account for heritable breast cancer: a study in five affected families.
British journal of cancer 1991;63(2):181-4.
1990: J Prosser; A M Thompson; G Cranston; H J Evans
Evidence that p53 behaves as a tumour suppressor gene in sporadic breast tumours.
Oncogene 1990;5(10):1573-9.