Imprinting of the gene encoding a human cyclin-dependent kinase inhibitor, p57KIP2, on chromosome 11p15.

WAF1, a potential mediator of p53 tumor suppression

1993 • 8,360 citations

The p21 Cdk-interacting protein Cip1 is a potent inhibitor of G1 cyclin-dependent kinases

1993 • 5,680 citations

Mice Lacking p21CIP1/WAF1 undergo normal development, but are defective in G1 checkpoint control

1995 • 2,115 citations

5′ CpG island methylation is associated with transcriptional silencing of the tumour suppressor p16/CDKN2/MTS1 in human cancers

1995 • 2,000 citations

Parental imprinting of the mouse insulin-like growth factor II gene

1991 • 1,773 citations

Germline p16 mutations in familial melanoma

1994 • 1,241 citations

p57KIP2, a structurally distinct member of the p21CIP1 Cdk inhibitor family, is a candidate tumor suppressor gene.

1995 • 956 citations

Cloning of p57KIP2, a cyclin-dependent kinase inhibitor with unique domain structure and tissue distribution.

1995 • 910 citations

Relaxation of imprinted genes in human cancer

1993 • 792 citations

Disruption of imprinting caused by deletion of the H19 gene region in mice

1995 • 765 citations

Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour

1993 • 710 citations

Genomic imprinting and the strange case of the insulin-like growth factor II receptor

1991 • 494 citations

Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour

1994 • 466 citations

Epigenetic lesions at the H19 locus in Wilms' tumour patients

1994 • 318 citations

Genomic imprinting of p57KIP2, a cyclin–dependent kinase inhibitor, in mouse

1995 • 288 citations

A model for embryonal rhabdomyosarcoma tumorigenesis that involves genome imprinting.

1989 • 260 citations

Nonrandom loss of maternal chromosome 11 alleles in Wilms tumors.

1987 • 212 citations

Tumor Cell Growth Arrest Caused by Subchromosomal Transferable DNA Fragments from Chromosome 11

1993 • 177 citations

Autosomal and X-chromosome imprinting

1990 • 176 citations

Functional imprinting and epigenetic modification of the human SNRPN gene

1993 • 158 citations

Parental Imprinting of Human Chromosome Region 11p15.3-pter Involved in the Beckwith-Wiedemann Syndrome and Various Human Neoplasia

1994 • 111 citations

Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments.

1995 • 108 citations

Imprinting: a gamete's point of view

1994 • 95 citations

Genomic imprinting and candidate genes in the Prader-Willi and Angelman syndromes

1993 • 85 citations