J. Parrington

发表

Human myosin heavy chain genes assigned to chromosome 17 using a human cDNA clone as probe

S. Povey, E. Solomon, Y. Edwards, 1985, Annals of human genetics.

Overrepresentation of chromosome 12p sequences and karyotypic evolution in i(12p)-negative testicular germ-cell tumors revealed by fluorescence in situ hybridization.

R. Sinke, A. Sandberg, R. Suijkerbuijk, 1993, Cancer genetics and cytogenetics.

Development and characterization of cisplatin-resistant human testicular and bladder tumour cell lines.

R. Knuechel, S. Povey, J. Masters, 1990, European journal of cancer.

Growth, DNA repair, sister chromatid exchange and chromosome studies in fibroblasts fromHuntington's disease patients

J. Attwood, J. Delhanty, J. Delhanty, 1981, Annals of Human Genetics.

Loss of heterozygosity in hypotriploid cell cultures from testicular tumours

S. Povey, L. West, J. Parrington, 1987, Human Genetics.

The genetics of peptidase C in man

S. Povey, H. Harris, G. Corney, 1972, Annals of human genetics.

The human glucosamine-6-phosphate deaminase gene: cDNA cloning and expression, genomic organization and chromosomal localization.

R. Ekong, J. Parrington, J. Parrington, 1998, Gene.

Loss of heterozygosity on chromosome arms 5q, IIp, IIq, I3q, and I6p in Human Testicular Germ Cell Tumors

S. Povey, J. Delhanty, J. Parrington, 1995 .

A xeroderma pigmentosum patient having a high residual activity of unscheduled DNA synthesis after UV is assigned to complementation group A.

D. Bootsma, M. Sabour, J. Parrington, 1976, Mutation research.

Chromosome analysis of parallel short-term cultures from four testicular germ-cell tumors.

E. Heyderman, L. West, J. Parrington, 1994, Cancer genetics and cytogenetics.

Molecular cytogenetic analysis of five newly established cervical cancer cell lines using G banding and fluorescence in situ hybridization.

E. Heyderman, J. Parrington, A. Thein, 1996, Cancer genetics and cytogenetics.

The origin of ovarian teratomas.

S. Povey, L. West, J. Parrington, 1984, Journal of medical genetics.

Diverse origins of multiple ovarian teratomas in a single individual.

S. Povey, J. Parrington, B. Carritt, 1982, Proceedings of the National Academy of Sciences of the United States of America.

Linkage relationships between the three phosphoglucomutase loci PGM1, PGM2 and PGM3

H. Harris, D. Hopkinson, E. Robson, 1968 .

Homologies between human and marmoset (Callithrix jacchus) chromosomes revealed by comparative chromosome painting.

D. Griffin, J. Delhanty, J. Sherlock, 1996, Genomics.

The origin of isochromosomes

J. Delhanty, J. Parrington, 1988, Clinical genetics.

Loss of heterozygosity on chromosome arms 5q, 11p, 11q, 13q, and 16p in human testicular germ cell tumors.

S. Povey, J. Delhanty, J. Parrington, 1995, Genes, chromosomes & cancer.

Theorigin ofovarian teratomas

S. Povey, L. West, J. Parrington, 1984 .

DNA synthesis in normal and xeroderma pigmentosum fibroblasts following treatment with 8-methoxypsoralen and long wave ultraviolet light.

J. Delhanty, H. Baden, J. Parrington, 1972, Biochimica et biophysica acta.

Specific chromosome aberrations in ataxia telangiectasia.

J. Delhanty, D. Harnden, J. Parrington, 1975, Journal of medical genetics.

Locus Control Region Function and Heterochromatin-Induced Position Effect Variegation

D. Kioussis, A. Miliou, R. Festenstein, 1996, Science.

Chromosome assignment, biochemical and immunological studies on a human aldehyde dehydrogenase, ALDH3

S. Povey, D. Hopkinson, L. West, 1985, Annals of human genetics.

Isolation and characterization of a multipotent clone of human embryonal carcinoma cells.

M. Pera, J. Mills, M F Pera, 1989, Differentiation; research in biological diversity.

Patau's syndrome with D1 duplication‐deficiency derived from a maternal D group pericentric inversion

J. Edwards, J. Parrington, 1971, Annals of human genetics.

XH1--a new cervical carcinoma cell line and xenograft model of tumour invasion, 'metastasis' and regression.

R. Lyle, R. Jewers, S. Money, 1991, British Journal of Cancer.

Chromosome 1 in relation to human disease.

S. Povey, J. Parrington, 1986, Journal of medical genetics.

Chromosome I in relation to human disease the normal human genome essential for suppression of hamster cell transformation

S. Povey, J. Parrington, 2022 .

Anomalous cellular proliferation in vitro associated with Huntington's disease

G. Corney, J. Parrington, D. Kirk, 1977, Human Genetics.

Diverse origins ofmultiple ovarian teratomas inasingle individual (dermoid cyst/C-band heteromorphism/enzyme electrophoresis/somatic cell hybrid)

J. Parrington, B. Carritt, H. M. Welch, 1982 .

Molecular and cytological investigations of phosphoglucomutase (PGM1) in the K562 cell line

M. Fox, J. Tomkins, D. Whitehouse, 1997, Annals of human genetics.

Correlation of loss of heterozygosity with cytogenetic analysis using G-banding and fluorescence in situ hybridization in aneuploid cultures from two human testicular germ-cell tumors.

D. Wells, D. Wells, J. Parrington, 1995, Cancer genetics and cytogenetics.

Cytogenetic investigation of five newly established cell lines from cervical cancer with G-banding and fluorescence in situ hybridisation (FISH), using chromosome-specific paint probes

E. Heyderman, J. Parrington, A. Thein, 1994 .

Elucidation of a pericentric inversion of a D‐group chromosome in the mother of a child with Patau's syndrome

J. Parrington, A. Mcdermott, 1975, Annals of human genetics.

Unscheduled DNA synthesis, u.v.‐induced chromosome aberrations adn SV40 transformation in cultured cells from xeroderma pigmentosum

J. Delhanty, H. Baden, J. Parrington, 1971, Annals of human genetics.

The application of comparative genomic hybridization to previously karyotyped cervical cancer cell lines.

M. Trková, J. Parrington, A. Thein, 2000, Cancer genetics and cytogenetics.

Ultraviolet-induced chromosome aberrations and mitotic delay in human fibroblast cells.

J. Parrington, 1972, Cytogenetics.