Showing results 1 to 12 of 12
|Clinical characterization and molecular classification of 12 Korean patients with pseudohypoparathyroidism and pseudopseudohypoparathyroidism.
|Connexin26 mutations associated with nonsyndromic hearing loss.
|박기현, 박홍준, 전영명, 한시훈
|Deletion of SNAP-23 results in pre-implantation embryonic lethality in mice
|Deletion of the alpha subunit of the heterotrimeric Go protein impairs cerebellar cortical development in mice
|김성수, 서해영, 최정미
|Development of the main olfactory system and main olfactory epithelium-dependent male mating behavior are altered in Go-deficient mice
|김성수, 이영돈, 최정미
|Hrp3, a chromodomain helicase/ATPase DNA binding protein, is required for heterochromatin silencing in fission yeast.
|Loss of Dfg5 glycosylphosphatidylinositol-anchored membrane protein confers enhanced heat tolerance in Saccharomyces cerevisiae.
|Molecular cytogenetic analysis of Korean patients with Waldenström macroglobulinemia.
|Parthanatos mediates AIMP2-activated age-dependent dopaminergic neuronal loss.
|Reversion from precore/core promoter mutants to wild-type hepatitis B virus during the course of lamivudine therapy.
|김진홍, 조성원, 함기백
|Simultaneous deletion of floxed genes mediated by CaMKIIα-Cre in the brain and in male germ cells: application to conditional and conventional disruption of Goα.
|김성수, 서해영, 이영돈, 최정미
|Spontaneous fractures in the mouse mutant sfx are caused by deletion of the gulonolactone oxidase gene, causing vitamin C deficiency.