Two Novel Genes in the Center of the 11p15 Imprinted Domain Escape Genomic Imprinting

Basic local alignment search tool

1990 • 87,358 citations

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

1983 • 26,063 citations

Basic Local Alignment Search Tool

1990 • 12,947 citations

The Genetic Basis of Human Cancer

1997 • 1,113 citations

Relaxation of imprinted genes in human cancer

1993 • 792 citations

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

1993 • 710 citations

Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15

1995 • 606 citations

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

1994 • 466 citations

Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region

1994 • 430 citations

Parental genomic imprinting of the human IGF2 gene

1993 • 422 citations

Monoallelic expression of the human H19 gene

1992 • 409 citations

An imprinted gene p57KIP2 is mutated in Beckwith–Wiedemann syndrome

1996 • 390 citations

Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements

1997 • 354 citations

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

1996 • 302 citations

IGF2 is parentally imprinted during human embryogenesis and in the Beckwith–Wiedemann syndrome

1993 • 290 citations

Multiple Mechanisms Regulate Imprinting of the Mouse Distal Chromosome 7 Gene Cluster

1998 • 245 citations

A Novel Gene Product that Couples TCR Signaling to Fas(CD95) Expression in Activation-Induced Cell Death

1996 • 196 citations

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

1993 • 177 citations

The IPL Gene on Chromosome 11p15.5 is Imprinted in Humans and Mice and is Similar to TDAG51, Implicated in Fas Expression and Apoptosis

1997 • 164 citations

Low Frequency of p57KIP2 Mutation in Beckwith-Wiedemann Syndrome

1997 • 141 citations

Coding Mutations in p57 Are Present in Some Cases of Beckwith-Wiedemann Syndrome but Are Rare or Absent in Wilms Tumors

1997 • 140 citations

Genomic Imprinting and Cancer

2006 • 128 citations

Aberrant splicing but not mutations of TSG101 in human breast cancer.

1997 • 113 citations

IMPT1, an imprinted gene similar to polyspecific transporter and multi- drug resistance genes

1998 • 101 citations

Imprinting of mouse Kvlqt1 is developmentally regulated

1998 • 98 citations

New p57 KIP2 mutations in Beckwith-Wiedemann syndrome

1997 • 96 citations

A 2.5-Mb Transcript Map of a Tumor-Suppressing Subchromosomal Transferable Fragment from 11p15.5, and Isolation and Sequence Analysis of Three Novel Genes

1997 • 89 citations

Genomic imprinting of a human apoptosis gene homologue, TSSC3.

1998 • 79 citations

The Human Achaete-Scute Homologue 2 (ASCL2, HASH2) Maps to Chromosome 11p15.5, Close to IGF2 and is Expressed in Extravillus Trophoblasts

1997 • 79 citations

Reduced expression of the cyclin-dependent kinase inhibitor gene p57KIP2 in Wilms' tumor.

1996 • 74 citations

Divergently Transcribed Overlapping Genes Expressed in Liver and Kidney and Located in the 11p15.5 Imprinted Domain

1998 • 68 citations

Somatic mutation of TSSC5, a novel imprinted gene from human chromosome 11p15.5.

1998 • 44 citations