Browsing "Research Organization" by Keyword : Mutation

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Showing results 1 to 11 of 11

Pub YearTitleAuthor(s)
2007A role of the Lowe syndrome protein OCRL in early steps of the endocytic pathway.이상윤
2000Correlation between structure of Bcl-2 and its inhibitory function of JNK and caspase activity in dopaminergic neuronal apoptosis.진병관
2018DJ-1 deficiency impairs synaptic vesicle endocytosis and reavailability at nerve terminals박상면, 조은혜, 주일로, 최동주, 하태영
2006ERK1/2 is an endogenous negative regulator of the gamma-secretase activity.백은주, 정민환
1999Histochemically reactive zinc in plaques of the Swedish mutant beta-amyloid precursor protein transgenic mice.묵인희
2018Identification of a rare homozygous c.790C>T variation in the TFB2M gene in Korean patients with autism spectrum disorder김정현, 박찬배, 이영수, 임신영, 정선용
2016Pacemaker-neuron-dependent disturbance of the molecular clockwork by a Drosophila CLOCK mutant homologous to the mouse Clock mutation김은영, 조은주
2019Parkinson's disease-associated LRRK2-G2019S mutant acts through regulation of SERCA activity to control ER stress in astrocytes김현미, 박상면, 이지훈, 조은혜, 주일로
1999Presenilin 1 mediates protein kinase C dependent alpha-secretase derived amyloid precursor protein secretion and mitogen-activated protein kinase activation in presenilin 1 transfected human embryonic kidney 293 cell.묵인희
2021Small heterodimer partner (SHP) aggravates ER stress in Parkinson’s disease-linked LRRK2 mutant astrocyte by regulating XBP1 SUMOylation이지훈, 조은혜, 주일로
2007The dual phosphatase activity of synaptojanin1 is required for both efficient synaptic vesicle endocytosis and reavailability at nerve terminals.이상윤
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