Expression of three mRNA species from a single rat aldolase A gene, differing in their 5′ non-coding regions
Keiichiro Joh, Katsuji Hori(Saga Medical School Hospital), Yuji Arai(National Cerebral and Cardiovascular Center), Tsunehiro Mukai(Nishikyushu University)
Cited by 65
Related Papers
An imprinted gene p57KIP2 is mutated in Beckwith–Wiedemann syndrome
|Nature Genetics|1996|385
Genomic imprinting of p57KIP2, a cyclin–dependent kinase inhibitor, in mouse
|Nature Genetics|1995|291
Analysis of germline CDKN1C (p57<sup>KIP2</sup>) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation
|Journal of Medical Genetics|1999|178
A Comprehensive Analysis of Allelic Methylation Status of CpG Islands on Human Chromosome 21q
|Genome Research|2004|169
Restriction landmark genomic scanning method and its various applications
|Electrophoresis|1993|159