Genomic imprinting of human p57KIP2 and its reduced expression in Wilms' tumors

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

1987 • 64,270 citations

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

1991 • 1,773 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

The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus

1991 • 904 citations

DIFFERENTIAL IMPRINTING AND EXPRESSION OF MATERNAL AND PATERNAL GENOMES

1988 • 451 citations

Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.

1989 • 448 citations

Uniparental paternal disomy in a genetic cancer-predisposing syndrome

1991 • 432 citations

DNA methylation and genomic imprinting

1994 • 349 citations

Genetic linkage of Beckwith-Wiedemann syndrome to 11p15.

1989 • 306 citations

Tumours and hemihypertrophy associated with Wiedemann-Beckwith syndrome

1983 • 289 citations

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

1995 • 288 citations

High resolution visual mapping of stretched DNA by fluorescent hybridization

1993 • 286 citations

A model for embryonal rhabdomyosarcoma tumorigenesis that involves genome imprinting.

1989 • 260 citations

The Molecular Basis of the Sparse Fur Mouse Mutation

1987 • 253 citations

Dynamics of GATA transcription factor expression during erythroid differentiation

1993 • 238 citations

Abnormality of chromosome 11 in patients withfeatures of Beckwith-Wiedemann syndrome

1983 • 236 citations

R-banding and nonisotopic in situ hybridization: precise localization of the human type II collagen gene (COL2A1)

1990 • 234 citations

Nonrandom loss of maternal chromosome 11 alleles in Wilms tumors.

1987 • 212 citations

Parental imprinting of autosomal mammalian genes

1994 • 208 citations

A third Wilms' tumor locus on chromosome 16q.

1992 • 201 citations

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

1993 • 177 citations

Report of the committee on chromosome and gene loss in human neoplasia

1991 • 158 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

Beckwith-Wiedemann syndrome: a demonstration of the mechanisms responsible for the excess of transmitting females.

1992 • 70 citations

Preferential loss of maternal alleles in sporadic Wilms' tumour.

1990 • 63 citations

Wiedemann‐Beckwith syndrome: Autosomal‐dominant inheritance in a family

1981 • 57 citations

Physical Ordering of Three Polymorphic DNA Markers Spanning the Regions Containing a Tumor Suppressor Gene of Renal Cell Carcinoma by Three‐color Fluorescent in situ Hybridization

1992 • 50 citations

High resolution ordering of DNA markers by multi-color fluorescent in situ hybridization of prophase chromosomes

1994 • 47 citations

An infant with Beckwith-Wiedemann syndrome and chromosomal duplication 11p13→pter.: Correlation of symptoms between 11p trisomy and Beckwith-Wiedemann syndrome

1986 • 33 citations

An Integrated Physical Map of 210 Markers Assigned to the Short Arm of Human Chromosome 11

1994 • 27 citations