Browsing "Pharmacology" by Keyword : Mutation

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Showing results 1 to 17 of 17

Pub YearTitleAuthor(s)
2014A Korean case of neurofibromatosis type 1 with an exonic splicing enhancer site mutation박상욱, 손영배, 정선용
2009Accumulation of labile zinc in neurons and astrocytes in the spinal cords of G93A SOD-1 transgenic mice.곽병주
2021Caveolin-1 deficiency impairs synaptic transmission in hippocampal neurons박상면
2010Cell cycle-regulated expression and subcellular localization of a kinesin-8 member human KIF18B.김완기
2005Characterization of thiol-specific antioxidant 1 (TSA1) of Candida albicans.김완기
1995Contribution of B cell subsets to delayed development of MAIDS in xid mice.김완기
2018DJ-1 deficiency impairs synaptic vesicle endocytosis and reavailability at nerve terminals박상면, 조은혜, 주일로, 최동주, 하태영
2016G2385R and I2020T Mutations Increase LRRK2 GTPase Activity조은혜
2015Loss of parkin promotes lipid rafts-dependent endocytosis through accumulating caveolin-1: implications for Parkinson's disease.박상면, 조은혜, 주일로, 차선희
2015LRRK2 G2019S mutation attenuates microglial motility by inhibiting focal adhesion kinase.강호철, 박상면, 조은혜, 주일로
2013Mutations of the TATA-binding protein confer enhanced tolerance to hyperosmotic stress in Saccharomyces cerevisiae.김완기
2006Neuronal nitric oxide synthase (nNOS) modulates the JNK1 activity through redox mechanism: a cGMP independent pathway.곽병주
2019Parkinson's disease-associated LRRK2-G2019S mutant acts through regulation of SERCA activity to control ER stress in astrocytes김현미, 박상면, 이지훈, 조은혜, 주일로
2021Small heterodimer partner (SHP) aggravates ER stress in Parkinson’s disease-linked LRRK2 mutant astrocyte by regulating XBP1 SUMOylation이지훈, 조은혜, 주일로
1998The cDNA cloning and ontogeny of mouse alpha-synuclein.곽병주, 조은혜
2023The in-silico evaluation of important GLUT9 residue for uric acid transport based on renal hypouricemia type 2조성권
2015Tolerance to acetic acid is improved by mutations of the TATA-binding protein gene.김완기
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