Browsing by Keyword : Gene Deletion
Showing results 1 to 12 of 12
| Pub Year | | Title | Author(s) |
| 2013 | | Clinical characterization and molecular classification of 12 Korean patients with pseudohypoparathyroidism and pseudopseudohypoparathyroidism. | 손영배 |
| 2000 | | Connexin26 mutations associated with nonsyndromic hearing loss. | 박기현, 박홍준, 전영명, 한시훈 |
| 2011 | | Deletion of SNAP-23 results in pre-implantation embryonic lethality in mice | 서영호 |
| 2019 | | Deletion of the alpha subunit of the heterotrimeric Go protein impairs cerebellar cortical development in mice | 김성수, 서해영, 최정미 |
| 2016 | | Development of the main olfactory system and main olfactory epithelium-dependent male mating behavior are altered in Go-deficient mice | 김성수, 이영돈, 최정미 |
| 2002 | | Hrp3, a chromodomain helicase/ATPase DNA binding protein, is required for heterochromatin silencing in fission yeast. | 이명애 |
| 2015 | | Loss of Dfg5 glycosylphosphatidylinositol-anchored membrane protein confers enhanced heat tolerance in Saccharomyces cerevisiae. | 김완기 |
| 2010 | | Molecular cytogenetic analysis of Korean patients with Waldenström macroglobulinemia. | 조성란 |
| 2013 | | Parthanatos mediates AIMP2-activated age-dependent dopaminergic neuronal loss. | 강호철 |
| 2000 | | Reversion from precore/core promoter mutants to wild-type hepatitis B virus during the course of lamivudine therapy. | 김진홍, 조성원, 함기백 |
| 2014 | | 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 |
| 2005 | | Spontaneous fractures in the mouse mutant sfx are caused by deletion of the gulonolactone oxidase gene, causing vitamin C deficiency. | 정윤석 |
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