J. Prosser

发表

Mutations in Breast Cancer

H. J. Evans, U. Chetty, C. Steel, 2006 .

p53 mutations in breast cancer.

H. J. Evans, U. Chetty, C. Steel, 1992, Cancer research.

Biallelic ApaI polymorphism of the human p53 gene (TP53).

A. Condie, J. Prosser, 1991, Nucleic acids research.

Evidence that p53 behaves as a tumour suppressor gene in sporadic breast tumours.

H. J. Evans, A. Thompson, G. Cranston, 1990, Oncogene.

Nonsense and missense mutations in the muscular chloride channel gene Clc-1 of myotonic mice.

H. Jockusch, T. Jentsch, K. Steinmeyer, 1994, The Journal of biological chemistry.

Detecting single-base mutations.

J. Prosser, 1993, Trends in biotechnology.

Nucleic Acids Research

M. Frommer, J. Prosser, Kanematsu, 2003 .

Zinc finger point mutations within the WT1 gene in Wilms tumor patients.

P. Smith, M. Little, A. Condie, 1992, Proceedings of the National Academy of Sciences of the United States of America.

Degeneracy in human multicopy RBM (YRRM), a candidate spermatogenesis gene

J. Cameron, H. Cooke, A. Condie, 1996, Mammalian Genome.

APC mutation analysis by chemical cleavage of mismatch and a protein truncation assay in familial adenomatous polyposis.

A. Wyllie, M. Dunlop, A. Condie, 1994, British Journal of Cancer.

Combined SSCP/heteroduplex analysis in the screening for PAX6 mutations.

R. Axton, J. Love, I. Hanson, 1997, Molecular and cellular probes.

Human satellite I sequences include a male specific 2.47 kb tandemly repeated unit containing one Alu family member per repeat.

M. Frommer, P. Vincent, J. Prosser, 1984, Nucleic acids research.

Exclusion of constitutional p53 mutations as a cause of genetic susceptibility to colorectal cancer.

A. Wyllie, M. Dunlop, A. Condie, 1993, British Journal of Cancer.

Mouse Small eye results from mutation in a paired-like homebox-containing gene

G. Saunders, B. Hogan, I. Hanson, 1992, Nature.

Monovalent cation induced structural transitions in telomeric DNAs: G-DNA folding intermediates.

C. C. Hardin, E. Henderson, J. Prosser, 1991, Biochemistry.

The human PAX6 gene is mutated in two patients with aniridia

S. Hodgson, I. Hanson, N. Hastie, 1992, Nature Genetics.

Mouse Small eye results from mutations in a paired-like homeobox-containing gene

G. Saunders, B. Hogan, I. Hanson, 1991, Nature.

The incidence of PAX6 mutation in patients with simple aniridia: an evaluation of mutation detection in 12 cases.

R. Axton, I. Hanson, V. van Heyningen, 1997, Journal of medical genetics.

Prevalence and diversity of constitutional mutations in the p53 gene among 21 Li-Fraumeni families.

A. Craft, M. Santibanez-Koref, P. H. Jones, 1994, Cancer research.

Sequence relationships of three human satellite DNAs.

M. Frommer, P. Vincent, J. Prosser, 1986, Journal of molecular biology.

Simple repeated sequences in human satellite DNA.

M. Frommer, A. Reisner, P. Vincent, 1982, Nucleic acids research.

Buoyant density and hybridization analysis of human DNA sequences, including three satellite DNAs.

K. Ho, A. Reisner, P. Vincent, 1981, Biochimica et biophysica acta.

Constitutional p53 mutation in a non-Li-Fraumeni cancer family.

H. J. Evans, U. Chetty, C. Steel, 1992, British Journal of Cancer.

PAX6 mutations reviewed

V. van Heyningen, J. Prosser, 1998, Human mutation.

The Human PAX6 Mutation Database

Veronica van Heyningen, Alastair Brown, Mark McKie, 1998, Nucleic Acids Res..

Tumor-suppressor genes: cardinal factors in inherited predisposition to human cancers.

H. J. Evans, H. Evans, J. Prosser, 1992, Environmental health perspectives.

p53 allele losses, mutations and expression in breast cancer and their relationship to clinico‐pathological parameters

H. J. Evans, U. Chetty, D. Carter, 1992, International journal of cancer.

Mutations in p53 do not account for heritable breast cancer: a study in five affected families.

H. J. Evans, P. Elder, C. Steel, 1991, British Journal of Cancer.

Satellite sequences in chimpanzee (Pan troglodytes).

M. Bobrow, K. Jones, J. Prosser, 1973, Biochimica et biophysica acta.

Identification of a potential RNA intermediate for transposition of the LINE‐like element I factor in Drosophila melanogaster.

D. Finnegan, A. Bucheton, J. Prosser, 1990, The EMBO journal.

Identification of a novel gene, ETX1, from Xp21.1, a candidate gene for X-linked retinitis pigmentosa (RP3)

K. Dry, A. Lennon, M. Aldred, 1995 .

The chromosomal localisation of human satellite DNA I

I. Purdom, K. Jones, G. Corneo, 2004, Chromosoma.

Localization of human satellite DNA I.

I. Purdom, K. Jones, G. Corneo, 1975, Cytogenetics and Cell Genetics.

The chromosomal location of human satellite DNA III

K. Jones, G. Corneo, J. Prosser, 1973, Chromosoma.

A familial RB1 mutation detected by the HOT technique is homozygous in a second primary neoplasm.

A. Condie, R. Leonard, J. Prosser, 1991, Oncogene.

Detection of point mutations in the p53 gene: Comparison of single‐strand conformation polymorphism, constant denaturant gel electrophoresis, and hydroxylamine and osmium tetroxide techniques

R. Eeles, A. Børresen, A. Condie, 1993, Human mutation.

Cloning and sequencing of the mouse Gli2 gene: localization to the Dominant hemimelia critical region.

M. Farrall, M. Mattei, D. C. Hughes, 1997, Genomics.

Satellite III DNA hybridised to chromosomes from patients with acute leukemia

P. Vincent, J. Prosser, F. Gunz, 1978 .

Mutations in p53 do not account for heritable breast cancer: a study in five affected families.

P. Elder, C. Steel, A. Condie, 1991, British Journal of Cancer.