Loss of heterozygosity for alleles on chromosome II in cervical carcinoma.

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1975 • 33,059 citations

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1983 • 26,063 citations

Genetic Alterations during Colorectal-Tumor Development

1988 • 6,691 citations

A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma

1986 • 2,968 citations

Chromosome 17 Deletions and p53 Gene Mutations in Colorectal Carcinomas

1989 • 2,081 citations

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

1983 • 1,952 citations

Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus

1990 • 1,882 citations

SUPERCOILED CIRCULAR DNA-PROTEIN COMPLEX IN Escherichia coli : PURIFICATION AND INDUCED CONVERSION TO AN OPEN CIRCULAR DNA FORM

1969 • 1,847 citations

Identification of a Chromosome 18q Gene that Is Altered in Colorectal Cancers

1990 • 1,747 citations

The Molecular Genetics of Cancer

1987 • 1,729 citations

Human Retinoblastoma Susceptibility Gene: Cloning, Identification, and Sequence

1987 • 1,436 citations

Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping

1990 • 1,300 citations

Hereditary cancer, oncogenes, and antioncogenes.

1985 • 1,261 citations

The isolation and characterization of linked δ- and β-globin genes from a cloned library of human DNA

1978 • 1,055 citations

Cancer statistics, 1990

1990 • 818 citations

Structural Evidence for the Authenticity of the Human Retinoblastoma Gene

1987 • 809 citations

Chromosome 5 allele loss in human colorectal carcinomas

1987 • 566 citations

Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism

1985 • 555 citations

Retinoblastoma: Clues to Human Oncogenesis

1984 • 495 citations

Tumor Suppressor Genes: The Puzzle and the Promise

1989 • 488 citations

Loss of heterozygosity of chromosome 3p markers in small-cell lung cancer

1987 • 472 citations

Somatic deletion and duplication of genes on chromosome 11 in Wilms' tumours

1984 • 426 citations

Development of homozygosity for chromosome 11p markers in Wilms' tumour

1984 • 411 citations

Loss of heterozygosity for the short arm of chromosome 1 in human neuroblastomas: correlation with N-myc amplification.

1989 • 395 citations

Loss of a Harvey ras allele in sporadic Wilms' tumour

1984 • 336 citations

Introduction of human chromosome 11 via microcell transfer controls tumorigenic expression of HeLa cells.

1986 • 301 citations

Charles S. Mott prize papillomaviruses in human cancer

1987 • 283 citations

Specific chromosome loss associated with the expression of tumorigenicity in human cell hybrids

1981 • 234 citations

Deletion mapping of a locus on human chromosome 22 involved in the oncogenesis of meningioma.

1987 • 216 citations

Loss of heterozygosity on the short arm of chromosome 3 in carcinoma of the uterine cervix.

1989 • 192 citations

Human Papillomaviruses And Genital Cancer

1987 • 186 citations

Normal human chromosome 11 suppresses tumorigenicity of human cervical tumor cell line SiHa

1989 • 144 citations

Amplification of FGF-related genes in human tumors: possible involvement of HST in breast carcinomas.

1989 • 134 citations

High correlation between molecular alterations of the c-myc oncogene and carcinoma of the uterine cervix.

1987 • 127 citations

Human papillomaviruses and cervical cancer: Analysis of histopathologic features associated with different viral types

1988 • 123 citations

Frequent loss of heterozygosity on chromosome 14q in neuroblastoma.

1989 • 119 citations

The amplification unit on chromosome 11q13 in aggressive primary human breast tumors entails the bcl-1, int-2 and hst loci.

1989 • 114 citations

Human HST1 (HSTF1) gene maps to chromosome band 11q13 and coamplifies with the INT2 gene in human cancer.

1988 • 111 citations

Implication of chromosome 11 in the suppression of neoplastic expression in human cell hybrids.

1986 • 108 citations

Somatic deletions and mutations of c-Ha-ras gene in human cervical cancers.

1988 • 98 citations

Chromosomal rearrangements, genes, and fragile sites in cancer: clinical and biologic implications.

1986 • 75 citations

Human papillomavirus types 16 and 18 sequences in early cervical neoplasia

1986 • 61 citations

Localization of HeLa cell tumor-suppressor gene to the long arm of chromosome II.

1989 • 57 citations

Chromosome 1 abnormalities in cervical carcinoma

1988 • 56 citations

A guide to fragile sites on human chromosomes

1990 • 52 citations

Nonrandom chromosome changes in carcinoma of the cervix uteri. II. Ten tumors in the triploid-tetraploid range

1984 • 44 citations

Chromosome analysis and alkaline phosphatase of C41, a cell line of human cervical origin distinct from HeLa.

1977 • 33 citations

Karyotypic analysis of two related cervical carcinoma cell lines that contain human papillomavirus type 18 DNA and express divergent differentiation

1989 • 23 citations

Future trends in cervical cancer

1988 • 23 citations

Chromosomal rearrangements, genes, and fragile sites in cancer: clinical and biologic implications.

1986 • 14 citations