A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis

The HECT Domain of TRIP12 Ubiquitinates Substrates of the Ubiquitin Fusion Degradation Pathway

Fine localization of a new cataract locus, Kec, on mouse chromosome 14 and exclusion of candidate genes as the gene that causes cataract in the Kec mouse

Association of a-adducin Gly460Trp polymorphism with coronary artery disease in a Korean population

Establishment and characterization of an in vivo model for Epstein-Barr virus positive gastric carcinoma

Interaction between GNB3 C825T and ACE I/D Polymorphisms in Essential

Lack of association between Y-chromosomal haplogroups and prostate cancer in the Korean population

Genomic organization of the region spanning D14Mit262 and D14Mit86 on mouse chromosome 14 and exclusion of Adam28 and Adamdec1 as the cataract-causing

A novel mutation in the SCN5A gene is associated with Brugada Syndrome.

A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hr(m1Enu).